Kurahashi Hiroki 倉橋浩樹

… Alternative Names

KURAHAS Hihiroki 倉橋浩樹

KURAHASHI Hiroki 倉橋浩樹

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Researcher Number	30243215
Other IDs
Affiliation (Current)	2025: 藤田医科大学, 医科学研究センター, 教授
Affiliation (based on the past Project Information) *help	2022 – 2024: 藤田医科大学, 医科学研究センター, 教授 2018 – 2021: 藤田医科大学, 総合医科学研究所, 教授 2017: 藤田保健衛生大学, 総合医科学研究所・分子遺伝学, 教授 2007 – 2017: Fujita Health University, 総合医科学研究所, 教授 2012: 藤田保健衛生大学, 医療科学部, 教授 … More 2011: 藤田保健衛生大学, 総合医科学研究所, 助教 2003 – 2005: Fujita Health University, Institute For Comprehensive Medical Science, Professor, 総合医科学研究所, 教授 2002: 大阪大学, 医学系研究科, 助手 1999: Osaka University Medical Schoo., Research Associate, 医学部, 助手 1993 – 1997: 大阪大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Human genetics / Biological Sciences / Pediatrics / Basic Section 56040:Obstetrics and gynecology-related / Human genetics Except Principal Investigator Digestive surgery / Experimental pathology / Pathological medical chemistry / Basic Section 50010:Tumor biology-related / Basic Section 56040:Obstetrics and gynecology-related / Basic Section 48040:Medical biochemistry-related / Basic Section 53040:Nephrology-related / Medical genome science
Keywords	Principal Investigator 習慣流産 / パリンドローム / 回文配列 / 切断点 / 染色体転座 / t(11;22) / 染色体構造異常 / 22q11 / CATCH22 / DiGeorge症候群 … More / chromosome 22 / 22番染色体 / 十字架型 / 染色体再構成 / 非B型DNA / 十字架型DNA / 減数分裂 / 不育症 / 不妊症 / 染色体欠失 / 円錐動脈幹異常顔貌 / chromosome 11 / cruciform / palindrome / breakpoint / translocation / chromosome / 11番染色体 / cDNA / 染色体 / FoSTeS / 多型 / プロモーター / 対合 / SYCP3 / 異数体 / マイクロアレイ / 共通欠失領域 / 反復配列 / 隣接遺伝子症候群 / Velo-cardio-facial症候群 / Genomic rearrangement / Structural variant / Spermatogenesis / Molecular cytogenetics / Cytogenomics / MMBIR / 逆位重複 / 端部欠失 / 遺伝学 / 遺伝子 / 鋳型乗り換え / 複製の停止 / 複雑構造異常 / クロモスリプシス / 端部欠失・逆位重複 / 挿入 / 構造異常 / ゲノム / 十字加型 / PATRR / AT rich / 転座切断点 / 神経線維腫症1型 / t(17;22) / Repetivive seguence / Deletion / Contiguous gene syndrome / Velo-cardio-facial syndrome / Contruncal anomaly face / DiGeorge syndrome / transcriptional factor / leucine zipper / microdeletion / conotruncal anomaly face / DiGeorge syndrome(DGS) / マイクロダイセクション / コスミドライブラリー / 転写因子 / ロイシンジッパー / DiGeorge症候群(DGS) / 2次構造 / バイサルファイト法 / ２次構造 / アネキシンV / エピゲノム / アネキシン / DNA二次構造 / グアニン四重鎖 / ゲノム不安定性 / 脆弱部位 / パリンドローム配列 / マイクロホモロジー / 複製のストール / DNA複製 / SNP / 二次構造 / 遺伝子多型 / グアニン4重鎖 / アネキシンA5 / 円旋光二色性 / グアニン 4 重鎖 / アネキシン A5 / 遺伝子導入 / 器官培養 / 卵巣 / アレイCGH / 無精子症 / コピー数多型 / 流産 / 異数性 / ダウン症候群 / 発現プロファイリング / 網羅的解析 / 2重鎖DNA切断 / 相同組換え / VNTR … More Except Principal Investigator 染色体 / メタボロミクス / Mutation search / EB3 / EB1 / 53BP2 / APCL / LKB1 / STK11 / PJS / 多発性嚢胞腎 / 酵母モデル / ゲノム / de novo型癌 / 癌遺伝子 / LOH / p53遺伝子 / 癌抑制遺伝子 / 表面型大腸癌 / APC遺伝子 / 核内トポロジー / 染色体再構成 / 核内配置編集 / 染色体配置編集 / ゲノム編集 / 染色体配置 / 胚培養液 / 着床前診断 / CRISPR / iPS細胞 / Down症候群 / トリソミー / CRISPR/Cas / 染色体消去 / 疾患モデル / バイオマーカー / キヌレニン / トリプトファン / NMDA受容体拮抗薬 / トリプトファン代謝 / NMDA受容体 / 尿細管障害 / 糖尿性腎臓病 / メタボローム解析 / トリプトファン代謝物 / 糖尿病性腎臓病 / 糖尿病性腎症 / 網羅的解析 / りん酸化タンパク質 / オミックス解析 / 塩分摂取 / 環境因子 / メタボローム / 多発性嚢胞腎症 / リン酸化 / プロテオミクス / 慢性腎臓病 / 遺伝子 / 先天奇形 / Ｘ染色体不活化 / 染色体構造異常 / PCR-SSCP法 / 遺伝子診断 / LKB1遺伝子 / Peutz-Jeghers syndrome / Mutaition search / S6 / polycystic liver / polycystic kidney / 細胞内情報伝達 / 嚢胞 / 線維化 / 核内受容体 / 線維 / 細胞増殖 / SCD1 / TGF / mTOR / ERK / PPAR / 減数分裂 / 不分離 / 染色体転座 / 高次構造 / 重複配列 / 染色体欠失 Less

胚培養液中cell-freeRNAの解析による異数性胚細胞制御メカニズムの解明
- Principal Investigator
  
  真里谷奨
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Sapporo Medical University
染色体の核内配置編集による染色体転座の発生機序の解明
- Principal Investigator
  
  河村理恵
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 50010:Tumor biology-related
- Research Institution
  Fujita Health University
Elucidation of mechanism for gross chromosomal rearrangements by genomic and epigenomic studiesPrincipal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Fujita Health University
Establishing the type I CRISPR platform for extra chromosome elimination through epigenetic modulation
- Principal Investigator
  
  橋詰令太郎
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 48040:Medical biochemistry-related
- Research Institution
  Mie University
Elucidation of the role of tryptophan metabolism in diabetic nephropathy: Towards a development of novel treatment of diabetic nephropathy targeting tryptophan metabolism
- Principal Investigator
  
  Yuzawa Yukio
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Fujita Health University
Study for chromosomal instability leading to human disorders
- Principal Investigator
  
  Fukami Maki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Medical genome science
- Research Institution
  National Center for Child Health and Development
Establishment of new classification for structural variation based on next generation sequencingPrincipal Investigator
- Principal Investigator
  
  Kurahashi Hiroki
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
Omics analysis applicable to preemptive medicine of chronic kidney disease -focusing on comprehensive analysis of phosphorylated proteins-
- Principal Investigator
  
  Nagao Shizuko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Experimental pathology
- Research Institution
  Fujita Health University
Transcriptional regulation via DNA secondary structure: novel epigenetic mechanismPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
DNA replication-dependent/independent mechanism of gross chromosomal rearrangementPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
変異型SYCP3が相同染色体分配に与えるインパクトと習慣流産Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Fujita Health University
Recurrent pregnancy loss -associated promoter polymorphisms affect ANXA5 ge ne expression via G -quadruplex propensityPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
A novel therapeutic approach for cystic disease:Inhibition of intracellular signal transduction pathways by a nuclear receptor cascade
- Principal Investigator
  
  SHIZUKO Nagao
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Experimental pathology
- Research Institution
  Fujita Health University
加齢依存性第1減数分裂不分離と変異型SYCP3Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Fujita Health University
Sperm-specific mechanism that induces the gross chromosomal rearrangementsPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
Analysis of interchromosomal effect in human using yeast model
- Principal Investigator
  
  OHYE Tamae
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Fujita Health University
コピー数多型は相同染色体対合・組換え不全によるヒト不妊・不育症をおこすか?Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
DNA secondary structure drives chromosomal dynamicsPrincipal Investigator
- Principal Investigator
  
  KURAHAS Hihiroki
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
Non-B form DNA structure at the region of 22q11 deletion
- Principal Investigator
  
  OHYE Tamae
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Fujita Health University
不妊症原因遺伝子の同定を目的とした、減数分裂関連遺伝子の網羅的解析Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  2004
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Fujita Health University
Etiology of the translocation mediated by cruciform DNAPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
Etiology of the most common constitutional translocation in human, t(11;22)Principal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
  Osaka University
Isolation and characterization of Peutz-Jeghers Syndrome Gene
- Principal Investigator
  
  KOYAMA Kumiko
- Project Period (FY)
  1998 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Digestive surgery
- Research Institution
  Japanese Foundation for Cancer Research
  Osaka University
CATCH22症候群における遺伝子レベルでの発生機構の解析Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  1997
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Osaka University
CATCH22症候群の染色体欠失領域(22q11)のゲノム構造の解析Principal Investigator
- Principal Investigator
  
  倉橋浩樹
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Osaka University
表面型早期大腸癌の発生・進展と癌関連遺伝子変異の検討
- Principal Investigator
  
  西圧勇
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Digestive surgery
- Research Institution
  Osaka University
Molecular genetics of Digeorge syndrome and related disordersPrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Osaka University
大腸癌の進展様式と癌遺伝子・癌抑制遺伝子の変異の関連性の検討
- Principal Investigator
  
  NISHISYO Isamu
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Digestive surgery
- Research Institution
  Osaka University
Analysis of molecular abnormalities in DiGeorge syndromePrincipal Investigator
- Principal Investigator
  
  KURAHASHI Hiroki
- Project Period (FY)
  1993 – 1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Osaka University

[Book] Clinical Genomics: Practical Applications in Adult Patient Care2014
- Author(s)
  Nisizawa H, Kurahashi H
- Total Pages
  928
- Publisher
  McGraw-Hill Professional
- Data Source
  KAKENHI-PROJECT-24390085
[Book] Clinical Genomics: Practical Applications in Adult Patient Care2014
- Author(s)
  Nisizawa H, Kurahashi H
- Total Pages
  928
- Publisher
  McGraw-Hill Professional
- Data Source
  KAKENHI-PROJECT-26670171
[Book] 生殖細胞系列の細胞分裂一体細胞分裂と減数分裂の違い、遺伝カウンセリングハンドブック2011
- Author(s)
  大江瑞恵、倉橋浩樹
- Total Pages
  2
- Publisher
  メディカルドゥ
- Data Source
  KAKENHI-PROJECT-21590346
[Book] 産婦人科臨床で扱われる染色体異常、産婦人科の実際2011
- Author(s)
  西山幸江、西澤春紀、大江瑞恵、宇田川康博、倉橋浩樹
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-21590346
[Book] エマヌエル症候群の臨床像と遺伝、小児科2010
- Author(s)
  大江瑞恵、倉橋浩樹
- Total Pages
  8
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-21590346
[Book] ここまでわかった染色体異常症の発生メカニズム、小児内科2009
- Author(s)
  倉橋浩樹、大江瑞恵、ボロル・ハスバイラ、加藤武馬
- Publisher
  東京医学社
- Data Source
  KAKENHI-PROJECT-21590346
[Book] Cruciform DNA. Encyclopedia of Genetics, 2nd Edition
- Author(s)
  Inagaki H, Kurahashi H
- Publisher
  Elsevier(in press)
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] The age-related required number of zygotes estimated from prior clinical studies of preimplantation genetic testing for aneuploidy (PGT-A)2023
- Author(s)
  Mariya Tasuku、Sugimoto Takeshi、Kato Takema、Endo Toshiaki、Kurahashi Hiroki
- Journal Title
  
  Systems Biology in Reproductive Medicine
  
  Volume: 69 Issue: 1 Pages: 50-56
- DOI
  10.1080/19396368.2022.2151387
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K08855
[Journal Article] A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome2023
- Author(s)
  Kawano Yusuke、Seki Atsuhito、Kuroiwa Takashi、Maeda Atsushi、Funahashi Takuya、Shizu Kanae、Suzuki Katsuji、Inagaki Hidehito、Kurahashi Hiroki、Fujita Nobuyuki
- Journal Title
  
  JSES International
  
  Volume: 7 Issue: 4 Pages: 714-718
- DOI
  10.1016/j.jseint.2023.03.021
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K08855
[Journal Article] Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm2023
- Author(s)
  Sugimoto Takeshi、Inagaki Hidehito、Mariya Tasuku、Kawamura Rie、Taniguchi-Ikeda Mariko、Mizuno Seiji、Muramatsu Yukako、Tsuge Ikuya、Ohashi Hirofumi、Saito Nakamichi、Hasegawa Yuiko、Ochi Nobuhiko、Yamaguchi Masatoshi、Murotsuki Jun、Kurahashi Hiroki
- Journal Title
  
  Human Genetics
  
  Volume: 142 Issue: 10 Pages: 1451-1460
- DOI
  10.1007/s00439-023-02591-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K08855
[Journal Article] Clinical application of long‐read nanopore sequencing in a?preimplantation genetic testing pre‐clinical workup to identify the junction for complex Xq chromosome rearrangement‐related disease2023
- Author(s)
  Mariya Tasuku、Shichiri Yui、Sugimoto Takeshi、Kawamura Rie、Miyai Syunsuke、Inagaki Hidehito、Sugihara Eiji、Ikeda Keiko、Baba Tsuyoshi、Ishikawa Aki、Ammae Michiko、Nakaoka Yoshiharu、Saito Tsuyoshi、Sakurai Akihiro、Kurahashi Hiroki
- Journal Title
  
  Prenatal Diagnosis
  
  Volume: 43 Issue: 3 Pages: 304-313
- DOI
  10.1002/pd.6334
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K07179, KAKENHI-PROJECT-23K08855
[Journal Article] Mitochondrial DNA mutations can influence the post-implantation development of human mosaic embryos2023
- Author(s)
  Ijuin Akifumi、Ueno Hiroe、Hayama Tomonari、Miyai Shunsuke、Miyakoshi Ai、Hamada Haru、Sueyoshi Sumiko、Tochihara Shiori、Saito Marina、Hamanoue Haruka、Takeshima Teppei、Yumura Yasushi、Miyagi Etsuko、Kurahashi Hiroki、Sakakibara Hideya、Murase Mariko
- Journal Title
  
  Frontiers in Cell and Developmental Biology
  
  Volume: 11 Pages: 1215626-1215626
- DOI
  10.3389/fcell.2023.1215626
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K08855, KAKENHI-PROJECT-21K09474
[Journal Article] Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant2022
- Author(s)
  Enkhjargal Sarantuya、Sugahara Kana、Khaledian Behnoush、Nagasaka Miwako、Inagaki Hidehito、Kurahashi Hiroki、Koshimizu Hisatsugu、Toda Tatsushi、Taniguchi-Ikeda Mariko
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 32 Issue: 8 Pages: 1301-1312
- DOI
  10.1093/hmg/ddac286
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K21430, KAKENHI-PROJECT-23K08855
[Journal Article] Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique2022
- Author(s)
  Sachiko Wakita, Mari Hara, Yasuji Kitabatake, Keiji Kawatani, Hiroki Kurahashi, Ryotaro Hashizume
- Journal Title
  
  Journal of human genetics
  
  Volume: 67 Issue: 10 Pages: 565-572
- DOI
  10.1038/s10038-022-01049-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06835, KAKENHI-PROJECT-20K06758
[Journal Article] Development of aortic valve stenosis in myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis with renal involvement2021
- Author(s)
  Hasegawa Midori、Iwasaki Jin、Sugiyama Satoshi、Ishihara Takuma、Yamamoto Yoshihiro、Asada Hiroaki、Koide Shigehisa、Hayashi Hiroki、Takahashi Kazuo、Inaguma Daijo、Yuzawa Yukio、Tsuboi Naotake
- Journal Title
  
  PLOS ONE
  
  Volume: 16 Issue: 1 Pages: e0245869-e0245869
- DOI
  10.1371/journal.pone.0245869
- Data Source
  KAKENHI-PROJECT-19K08715
[Journal Article] Long-term changes in renal function after treatment initiation and the importance of early diagnosis in maintaining renal function among IgG4-related tubulointerstitial nephritis patients in Japan2020
- Author(s)
  Arai Haruna、Ogata Soshiro、Ozeki Takaya、Takahashi Kazuo、Tsuboi Naotake、Maruyama Shoichi、Inaguma Daijo、Hasegawa Midori、Yuzawa Yukio、Hayashi Hiroki
- Journal Title
  
  Arthritis Research & Therapy
  
  Volume: 22 Issue: 1
- DOI
  10.1186/s13075-020-02320-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08715, KAKENHI-PROJECT-20K08600
[Journal Article] Comparison of the 2018 and 2003 International Society of Nephrology/Renal Pathology Society classification in terms of renal prognosis in patients of lupus nephritis: a retrospective cohort study2020
- Author(s)
  Umeda Ryosuke、Ogata Soshiro、Hara Shigeo、Takahashi Kazuo、Inaguma Daijo、Hasegawa Midori、Yasuoka Hidetaka、Yuzawa Yukio、Hayashi Hiroki、Tsuboi Naotake
- Journal Title
  
  Arthritis Research & Therapy
  
  Volume: 22 Issue: 1
- DOI
  10.1186/s13075-020-02358-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08715, KAKENHI-PROJECT-20K08600
[Journal Article] Extreme hyperuricemia is a risk factor for infection-related deaths in incident dialysis patients: a multicenter prospective cohort study2020
- Author(s)
  Yoshida Hiroyuki、Inaguma Daijo、Koshi-Ito Eri、Ogata Soshiro、Kitagawa Akimitsu、Takahashi Kazuo、Koide Shigehisa、Hayashi Hiroki、Hasegawa Midori、Yuzawa Yukio、Tsuboi Naotake
- Journal Title
  
  Renal Failure
  
  Volume: 42 Issue: 1 Pages: 646-655
- DOI
  10.1080/0886022x.2020.1788582
- Data Source
  KAKENHI-PROJECT-19K08715
[Journal Article] Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events.2018
- Author(s)
  Fukami M, Kurahashi H.
- Journal Title
  
  Methods Mol Biol.
  
  Volume: 1769 Pages: 21-33
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H03616
[Journal Article] Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders2018
- Author(s)
  Terasawa Sumire、Kato Asuka、Nishizawa Haruki、Kato Takema、Yoshizawa Hikari、Noda Yoshiteru、Miyazaki Jun、Ito Mayuko、Sekiya Takao、Fujii Takuma、Kurahashi Hiroki
- Journal Title
  
  Congenital Anomalies
  
  Volume: - Issue: 1 Pages: 1-7
- DOI
  10.1111/cga.12278
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-17K11300, KAKENHI-PROJECT-15H04710
[Journal Article] Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome2017
- Author(s)
  Nagasaka M, Taniguchi-Ikeda M, Inagaki H, Ouchi Y, Kurokawa D, Yamana K, Harada R, Nozu K, Sakai Y, Mishra SK, Yamaguchi Y, Morikoka I, Toda T, Kurahashi H, Iijima K
- Journal Title
  
  J Hum Genet
  
  Volume: 62 Issue: 9 Pages: 869-869
- DOI
  10.1038/jhg.2017.59
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis2017
- Author(s)
  Kato Takema、Ouchi Yuya、Inagaki Hidehito、Makita Yoshio、Mizuno Seiji、Kajita Mitsuharu、Ikeda Toshiro、Takeuchi Kazuhiro、Kurahashi Hiroki
- Journal Title
  
  Cytogenetic and Genome Research
  
  Volume: 153 Issue: 1 Pages: 1-9
- DOI
  10.1159/000481586
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-16K12941, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287
[Journal Article] The DNA Damage Checkpoint Eliminates Mouse Oocytes with Chromosome Synapsis Failure2017
- Author(s)
  Vera Rinaldi, Ewelina Bolcun-Filas, Hiroshi Kogo, Hiroki Kurahashi, John C.Schimenti
- Journal Title
  
  Molecular Cell
  
  Volume: 67 Issue: 6 Pages: 1026-1036.e2
- DOI
  10.1016/j.molcel.2017.07.027
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K08461, KAKENHI-PROJECT-15H04710
[Journal Article] PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene2017
- Author(s)
  Kato Maki、Kato Takema、Hosoba Eriko、Ohashi Masanao、Fujisaki Midori、Ozaki Mamoru、Yamaguchi Masatoshi、Sameshima Hiroshi、Kurahashi Hiroki
- Journal Title
  
  Human Genome Variation
  
  Volume: 4 Issue: 1 Pages: 17021-17021
- DOI
  10.1038/hgv.2017.21
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-15H04710
[Journal Article] Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromes.2017
- Author(s)
  Azuma Y, Topf A, Evangelista T, Lorenzoni PJ, Roos A, Viana P, Inagaki H, Kurahashi H, Lochmuller H
- Journal Title
  
  Neurol Genet
  
  Volume: 3 Issue: 3
- DOI
  10.1212/nxg.0000000000000152
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287
[Journal Article] PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene.2017
- Author(s)
  Kato M, Kato T, Hosoba E, Ohashi M, Fujisaki M, Ozaki M, Yamaguchi M, Sameshima H, *Kurahashi H.
- Journal Title
  
  Hum Genome Var
  
  Volume: 印刷中
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements2017
- Author(s)
  Kohmoto T, Okamoto N, Naruto T, Murata C, Ouchi Y, Fujita N, Inagaki H, Satomura S, Okamoto N, Saito M, Masuda K, Kurahashi H, Imoto I
- Journal Title
  
  Mol Cytogenet
  
  Volume: 10 Issue: 1 Pages: 15-15
- DOI
  10.1186/s13039-017-0316-6
- NAID
  120006937633
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-15K08949, KAKENHI-PROJECT-16K15618
[Journal Article] Analysis of the origin of inherited chromosomally integrated human herpesvirus 6 in the Japanese population.2017
- Author(s)
  Kawamura Y, Ohye T, Miura H, Ihira M, Kato Y, Kurahashi H, Yoshikawa T.
- Journal Title
  
  J Gen Virol.
  
  Volume: 98(7) Issue: 7 Pages: 1823-1830
- DOI
  10.1099/jgv.0.000834
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K08981, KAKENHI-PROJECT-15H04710
[Journal Article] Remote intracranial recurrence of <i>IDH</i> mutant gliomas is associated with <i>TP53</i> mutations and an 8q gain2017
- Author(s)
  Nakae Shunsuke、Kato Takema、Murayama Kazuhiro、Sasaki Hikaru、Abe Masato、Kumon Masanobu、Kumai Tadashi、Yamashiro Kei、Inamasu Joji、Hasegawa Mitsuhiro、Kurahashi Hiroki、Hirose Yuichi
- Journal Title
  
  Oncotarget
  
  Volume: 8 Issue: 49 Pages: 84729-84742
- DOI
  10.18632/oncotarget.20951
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K10343, KAKENHI-PROJECT-16K20029
[Journal Article] A Family With Craniofrontonasal Syndrome: The First Report of Familial Cases of Craniofrontonasal Syndrome With Bilateral Cleft Lip and Palate.2017
- Author(s)
  Inoue Y, Sakamoto Y, Sugimoto M, Inagaki H, Boda H, Miyata M, Kato H, Kurahashi H, *Okumoto T.
- Journal Title
  
  Cleft Palate Craniofac J
  
  Volume: 印刷中 Issue: 7 Pages: 15347-15347
- DOI
  10.1597/15-347
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287
[Journal Article] Palindrome-mediated translocations in humans: a new mechanistic model for gross chromosomal rearrangements.2016
- Author(s)
  Inagaki H, Kato T, Tsutsumi M, Ouchi Y, Ohye T, *Kurahashi H.
- Journal Title
  
  Front Genet
  
  Volume: 7 Pages: 125-125
- DOI
  10.3389/fgene.2016.00125
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-16K08981
[Journal Article] A simple cytogenetic method to detect chromosomally integrated human herpesvirus-6.2016
- Author(s)
  Ohye T, et al.
- Journal Title
  
  J Virol Methods
  
  Volume: 228 Pages: 74-78
- DOI
  10.1016/j.jviromet.2015.11.001
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-25460705, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-16K08947, KAKENHI-PROJECT-16K08981
[Journal Article] Successful living donor liver transplantation for classical maple syrup urine disease.2016
- Author(s)
  Yasui T, Suzuki T, Hara F, Watanabe S, Uga N, Naoe A, Yoshikawa T, Ito T, Nakajima Y, Miura H, Sugioka A, Kato Y, Tokoro T, Tanahashi Y, Kasahara M, Fukuda A, Kurahashi H. Successful living donor liver transplantation for classical maple syrup urine disease.
- Journal Title
  
  Pediatr Transplant
  
  Volume: 20 Issue: 5 Pages: 707-710
- DOI
  10.1111/petr.12738
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] Annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?2016
- Author(s)
  *Markoff A, Kurahashi H, Grandone E, Bogdanova N.
- Journal Title
  
  Reprod Biomed Online
  
  Volume: 32 Issue: 5 Pages: 469-73
- DOI
  10.1016/j.rbmo.2016.02.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016
- Author(s)
  Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 61 Issue: 4 Pages: 351-355
- DOI
  10.1038/jhg.2015.157
- NAID
  40020802923
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
[Journal Article] Authors' response to the letter of Nagirnaja et al., "Response to annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?"2016
- Author(s)
  Markoff A, Kurahashi H, Grandone E, Bogdanova N.
- Journal Title
  
  Reprod Biomed Online
  
  Volume: 33 Issue: 1 Pages: 116-7
- DOI
  10.1016/j.rbmo.2016.05.006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] A PDE3A mutation in familial hypertension and brachydactyly syndrome2016
- Author(s)
  Boda H, Uchida H, Takaiso N, Ouchi Y, Fujita N, Kuno A, Hata T, et al.
- Journal Title
  
  J Hum Gene
  
  Volume: Apr 7 Issue: 8 Pages: 1-6
- DOI
  10.1038/jhg.2016.32
- NAID
  40020923782
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26350944, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287
[Journal Article] Mutation analysis of the JUNO gene in female infertility of unknown etiology.2016
- Author(s)
  Takaiso N, Nishizawa H, Nishiyama S, Sawada T, Hosoba E, Ohye T, Sato T, Inagaki H, *Kurahashi H.
- Journal Title
  
  Fujita Med J
  
  Volume: 2 Pages: 59-61
- NAID
  130005264393
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04710
[Journal Article] Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.2016
- Author(s)
  Suzuki E, Shima H, Toki M, Hanew K, Matsubara K, Kurahashi H, Narumi S, Ogata T, Kamimaki T, *Fukami M.
- Journal Title
  
  Cytogenet Genome Res
  
  Volume: 150 Issue: 2 Pages: 86-92
- DOI
  10.1159/000455026
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K19538, KAKENHI-PROJECT-15K09734
[Journal Article] Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy.2016
- Author(s)
  Tsutsumi M, Yokoi S, Miya F, Miyata M, Kato M, Okamoto N, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Saitoh S, *Kurahashi H.
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 24 Issue: 12 Pages: 1702-1706
- DOI
  10.1038/ejhg.2016.119
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-16K07211
[Journal Article] Increased levels of soluble corin in pre-eclampsia and fetal growth restriction.2016
- Author(s)
  Miyazaki J, *Nishizawa H, Kambayashi A, Ito M, Noda Y, Terasawa S, Kato T, Miyamura H, Shiogama K, Sekiya T, Kurahashi H, Fujii T.
- Journal Title
  
  Placenta
  
  Volume: 48 Pages: 20-25
- DOI
  10.1016/j.placenta.2016.10.002
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K19042
[Journal Article] PCSK5 mutation in a patient with the VACTERL association2015
- Author(s)
  Nakamura Y. et al.
- Journal Title
  
  BMC Res Notes
  
  Volume: 8 Issue: 1 Pages: 228-228
- DOI
  10.1186/s13104-015-1166-0
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-25462289, KAKENHI-PROJECT-26670171
[Journal Article] A unique TBX5 microdeletion with microinsertion detected in patient with Holt-Oram syndrome.2015
- Author(s)
  Morine M, et al.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 167 Issue: 12 Pages: 3192-3196
- DOI
  10.1002/ajmg.a.37359
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-15K08949, KAKENHI-PROJECT-26670171, KAKENHI-PROJECT-26293304
[Journal Article] Novel FATP4 mutations responsible for ichthyosis prematurity syndrome in a Japanese patient2015
- Author(s)
  Tsuge I, Morishita M, Kato T, Tsutsumi M, Inagaki H, Mori Y, Yamawaki K, Inuo C, Ieda K, Ohye T, Hayakawa A, Kurahashi H
- Journal Title
  
  Human Genome Variation
  
  Volume: 2 Issue: 1 Pages: 15003-15003
- DOI
  10.1038/hgv.2015.3
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26670171
[Journal Article] Nine-year follow-up in a child with chromosomal integration of human herpesvirus 6 transmitted from an unrelated donor through the Japan Marrow Donor Program2015
- Author(s)
  Yagasaki H, Shichino H, Shimizu N, Ohye T, Kurahashi H, Yoshikawa T, Takahashi S
- Journal Title
  
  Transpl Infect Dis
  
  Volume: 17 Issue: 1 Pages: 160-161
- DOI
  10.1111/tid.12338
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26670171
[Journal Article] Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand2015
- Author(s)
  Komoto S, Tacharoenmuang R, Guntapong R, Ide T, Haga K, Katayama K, Kato T, Ouchi Y, Kurahashi H, Tsuji T, Sangkitporn S, Taniguchi K.
- Journal Title
  
  PLoS One
  
  Volume: 10(11) Issue: 11 Pages: 1-22
- DOI
  10.1371/journal.pone.0141739
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08505, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Preimplantation genetic diagnosis/screening by comprehensive molecular testing2015
- Author(s)
  Kurahashi H, Kato T, Miyazaki J, Nishizawa H, Nishio E, Furukawa H, Miyamura H, Ito M, Endo T, Ouchi Y, Inagaki H, Fujii T
- Journal Title
  
  Reprod Med Biol
  
  Volume: 15 Issue: 1 Pages: 13-19
- DOI
  10.1007/s12522-015-0216-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reassortment Events2015
- Author(s)
  Tacharoenmuang R, Komoto S, Guntapong R, Ide T, Haga K, Katayama K, Kato T, Ouchi Y, Kurahashi H, Tsuji T, Sangkitporn S, Taniguchi K.
- Journal Title
  
  PLoS One
  
  Volume: 10(9) Issue: 9 Pages: 1-23
- DOI
  10.1371/journal.pone.0139381
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08505, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] TUBA1A mutation can cause a hydranencephaly-likesevere form of cortical dysgenesis.2015
- Author(s)
  Yokoi S, Ishihara N, Miya F, Tsutsumi M, Yanagihara I, Fujita N, Yamamoto H, Kato M, Okamoto N, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Kojima S, Saitoh S, Kurahashi H, Natsume J.
- Journal Title
  
  Sci Rep.
  
  Volume: 23 Issue: 1 Pages: 1-10
- DOI
  10.1038/srep15165
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461652, KAKENHI-PROJECT-26670171
[Journal Article] Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.2015
- Author(s)
  Miyazaki J, et al.
- Journal Title
  
  BMC Med Genet
  
  Volume: 16 Issue: 1 Pages: 98-98
- DOI
  10.1186/s12881-015-0245-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.2014
- Author(s)
  Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Uchino S, Kosugi S, Kurahashi H, Iwase K.
- Journal Title
  
  Surg Today
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis2014
- Author(s)
  Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Kurahashi H, Iwase K
- Journal Title
  
  Endocr J
  
  Volume: 61 Pages: 19-23
- NAID
  130004443932
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26670171
[Journal Article] A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis2014
- Author(s)
  Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Kurahashi H, Iwase K
- Journal Title
  
  Endocr J
  
  Volume: 61 Pages: 19-23
- NAID
  130004443932
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Analysis of the t(3;8) of hereditary renal cell carcinoma: A palindrome mediated translocation2014
- Author(s)
  Kato T, Franconi CP, Sheridan MB, Hacker AM, Inagakai H, Glover TW, Arlt MF, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Journal Title
  
  Cancer Genet
  
  Volume: 207 Issue: 4 Pages: 133-140
- DOI
  10.1016/j.cancergen.2014.03.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171
[Journal Article] Molecular and virological evidence of viral activation from chromosomally integrated human herpesvirus 6A in a patient with X-linked severe combined immunodeficiency2014
- Author(s)
  Endo A, Watanabe K, Ohye T, Suzuki K, Matsubara T, Shimizu N, Kurahashi H, Yoshikawa T, Katano H, Inoue N, Imai K, Takagi M, Morio T, Mizutani S
- Journal Title
  
  Clin Infect Dis
  
  Volume: 59 Issue: 4 Pages: 545-548
- DOI
  10.1093/cid/ciu323
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25460578, KAKENHI-PROJECT-26293244, KAKENHI-PROJECT-26670171
[Journal Article] Prevalence of Emanuel syndrome: theoretical frequency and surveillance result2014
- Author(s)
  Ohye T, Inagaki H, Kato T, Tsutsumi M, Kurahashi H
- Journal Title
  
  Pediatr Int
  
  Volume: 56 Issue: 4 Pages: 462-466
- DOI
  10.1111/ped.12437
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171
[Journal Article] Age-related decrease of meiotic cohesins in human oocyte2014
- Author(s)
  Tsutsumi M, Fujiwara R, Nishizawa H, Ito M, Kogo H, Inagaki H, Ohye T, Kato T, Fujii T, Kurahashi H
- Journal Title
  
  PLoS One
  
  Volume: 9, Issue: 5 Pages: 1-8
- DOI
  10.1371/journal.pone.0096710
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263, KAKENHI-PROJECT-25860255, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26462540, KAKENHI-PROJECT-26670171
[Journal Article] Signature of backward replication slippage at the copy number variation junction.2014
- Author(s)
  Ohye T, Inagaki H, Ozaki M, Ikeda T, Kurahashi H
- Journal Title
  
  J Hum Genet
  
  Volume: in press Issue: 5 Pages: 247-250
- DOI
  10.1038/jhg.2014.20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307, KAKENHI-PROJECT-26670171
[Journal Article] A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis.2014
- Author(s)
  Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Kurahashi H, Iwase K.
- Journal Title
  
  Endocr J
  
  Volume: 61 Pages: 19-23
- NAID
  130004443932
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation2014
- Author(s)
  Mishra D, Kato T, Inagaki H, Kosho T, Wakui K, Kido Y, Sakazume S, Taniguchi-Ikeda M, Morisada N, Iijima K, Fukushima Y, Emanuel BS, Kurahashi H
- Journal Title
  
  Mol Cytogenet
  
  Volume: 7 Issue: 1 Pages: 55-55
- DOI
  10.1186/s13039-014-0055-x
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171, KAKENHI-PROJECT-221S0002
[Journal Article] Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case2014
- Author(s)
  Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Uchino S, Kosugi S, Kurahashi H, Iwase K
- Journal Title
  
  Surg Today
  
  Volume: 44 Issue: 11 Pages: 2195-2200
- DOI
  10.1007/s00595-013-0826-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590694, KAKENHI-PROJECT-26670171
[Journal Article] Serum liver-type fatty acid-binding protein predicts recovery of graft function after kidney transplantation from donors after cardiac death2014
- Author(s)
  Kawai A, Kusaka M, Kitagawa F, Ishii J, Fukami N, Maruyama T, Sasaki H, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Clin Transplant
  
  Volume: 28 Issue: 6 Pages: 749-754
- DOI
  10.1111/ctr.12375
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-26293355, KAKENHI-PROJECT-26670171
[Journal Article] Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6.2014
- Author(s)
  Ohye T, Inagaki H, Ihira M, Higashimoto Y, Kato K, Oikawa J, Yagasaki H, Niizuma T, Takahashi Y, Kojima S, Yoshikawa T, Kurahashi H
- Journal Title
  
  Sci Rep
  
  Volume: 4 Issue: 1 Pages: 4559-4559
- DOI
  10.1038/srep04559
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25460705, KAKENHI-PROJECT-25461610, KAKENHI-PROJECT-26670171
[Journal Article] Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.2014
- Author(s)
  Tsuge I, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A
- Journal Title
  
  Pediatr Pulmonol
  
  Volume: 49 Issue: 3
- DOI
  10.1002/ppul.22814
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-26670171
[Journal Article] Age-related decrease of meiotic cohesins in human oocytes.2014
- Author(s)
  Tsutsumi M, Fujiwara R, Nishizawa H, Kogo H, Inagaki H, Ohye T, Kato T, Fujii T, Kurahashi H
- Journal Title
  
  PLoS One
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient2013
- Author(s)
  Tsuge I, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A
- Journal Title
  
  Pediatric Pulmonology
  
  Volume: In press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182
[Journal Article] MTA3 regulates CGB5 and Snail genes in trophoblast2013
- Author(s)
  Chen Y, Miyazaki J, Nishizawa H, Kurahashi H, Leach R, Wang K
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: (In press) Issue: 4 Pages: 379-384
- DOI
  10.1016/j.bbrc.2013.02.102
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085
[Journal Article] Decreased expression of apelin in placentas from severe pre-eclampsia patients2013
- Author(s)
  Inuzuka H, Nishizawa H, Inagaki A, SuzukiM,Ota S,Miyamura H, Miyazaki J, Sekiya T, Kurahashi H, Udagawa Y
- Journal Title
  
  Hypertens Pregnancy
  
  Volume: 32 Issue: 4 Pages: 410-421
- DOI
  10.3109/10641955.2013.813535
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations2013
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Journal Title
  
  Nat Commun
  
  Volume: 4 Issue: 1 Pages: 1592-1592
- DOI
  10.1038/ncomms2595
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307, KAKENHI-PROJECT-24590263, KAKENHI-PROJECT-25860256
[Journal Article] Contribution of fetal genotype of promoter polymorphisms in ANXA5gene to the onset of pre-eclampsia2013
- Author(s)
  Ota S,Miyamura H, Nishizawa H, Inagaki H, Inagaki A,Inuzuka H, SuzukiM, Miyazaki J, Sekiya T, Udagawa Y, Kurahashi H
- Journal Title
  
  Placenta
  
  Volume: 34 Issue: 12 Pages: 1202-1210
- DOI
  10.1016/j.placenta.2013.09.010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307
[Journal Article] Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient2013
- Author(s)
  Tsuge l, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A
- Journal Title
  
  Pediatric Pulmonology
  
  Volume: (In press) (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient2013
- Author(s)
  Tsuge I, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A
- Journal Title
  
  Pediatric Pulmonology
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Definition and refinement of the 7q36.3 duplication region associated with schizophrenia2013
- Author(s)
  Aleksic B, Kushima I, Ohye T, Ikeda M, Kunimoto S, Nakamura Y, Yoshimi A, Koide T, Iritani S, Kurahashi H, Iwata N, Ozaki N
- Journal Title
  
  Sci Rep
  
  Volume: 3 Issue: 1 Pages: 2587-2587
- DOI
  10.1038/srep02587
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591701, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24791210, KAKENHI-PLANNED-25117010, KAKENHI-PROJECT-25253072, KAKENHI-PROJECT-25670516, KAKENHI-PROJECT-25860999
[Journal Article] Global gene expression profiling in PPAR-γ agonist-treated kidneys in an orthologous rat model of human autosomal recessive polycystic kidney disease2012
- Author(s)
  Yoshihara D, Kugita M, Yamaguchi T, Aukema H.M., Kurahashi H., Morita M., Hiki Y., Calvet J.P., Wallace D.P., Toyohara T., TAbe T., Nagao S.
- Journal Title
  
  PPAR Research
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] Upregulation of HtrA4 in the placentas of patients with severe pre-eclampsia2012
- Author(s)
  Inagaki A, Nishizavva H, Ota S, Suzuki M, Inuzuka H, Miyamura H, Sekiya T, Kurahashi H, Udagawa Y
- Journal Title
  
  Placenta
  
  Volume: 33 Pages: 919-926
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390085
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.2012
- Author(s)
  Tsutsumi M, Kowa-Sugiyama H, Bolor H, Kogo H, Inagaki H, Ohye T, Yamada K, Taniguchi-Ikeda M, Toda T, Kurahashi H.
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Issue: 8 Pages: 515-522
- DOI
  10.1038/jhg.2012.61
- NAID
  10031056588
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
[Journal Article] Molecular basis of maternal age-related increase in oocyte aneuploidy2012
- Author(s)
  Kurahashi, H., Tsutsumi, M., Nishiyama, S., Kogo, H., Inagaki, H., Ohye, T.
- Journal Title
  
  Congenit. Anom
  
  Volume: 52 Pages: 8-15
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Global Gene ExpressionProfiling in PPAR-γ Agonist-TreatedKidneys in an Orthologous Rat Model of Human Autosomal Recessive Polycystic Kidney Disease.2012
- Author(s)
  Yoshihara D, Kugita M, Yamaguchi T, Aukema HM, Kurahashi H, Morita M, Hiki Y, Calvet JP, Wallace DP, Toyohara T, Abe T, Nagao S.
- Journal Title
  
  PPAR Res
  
  Volume: 2012 Pages: 695898-695898
- DOI
  10.1155/2012/695898
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24790393
[Journal Article] A Functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan2012
- Author(s)
  Ahmed WA, Tsutsumi M, Nakata S, Mori T, Nishimura Y, Fujisawa T, Kato I, Nakashima M, Kurahashi H, Suzuki K
- Journal Title
  
  Laryngoscope
  
  Volume: 122 Issue: 4 Pages: 925-929
- DOI
  10.1002/lary.23179
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085
[Journal Article] HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes2012
- Author(s)
  Kogo, H., Tsutsumi, M., Ohye, T., Inagaki, H., Abe, T., Kurahashi, H.
- Journal Title
  
  Genes Cells
  
  Volume: 17 Issue: 6 Pages: 439-454
- DOI
  10.1111/j.1365-2443.2012.01600.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790192, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
[Journal Article] Molecular basis of maternal age-related increase in oocyte aneuploidy2012
- Author(s)
  Kurahashi H, Tsutsumi M, Nishiyama S, Kogo H, Inagaki H, Ohye T
- Journal Title
  
  Congenit Anom (Kyoto)
  
  Volume: 52 Issue: 1 Pages: 8-15
- DOI
  10.1111/j.1741-4520.2011.00350.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-21590346, KAKENHI-PROJECT-22790192, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
[Journal Article] Failure of homologous synapsis and sex-specific reproduction problems2012
- Author(s)
  Kurahashi H, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  Front Genet
  
  Volume: 3 Pages: 112-112
- DOI
  10.3389/fgene.2012.00112
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085
[Journal Article] HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity2012
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Kiyonari H, Kurahashi H
- Journal Title
  
  Genes Cells
  
  Volume: 17 Issue: 11 Pages: 897-912
- DOI
  10.1111/gtc.12005
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
[Journal Article] Chromosomal translocations and palindromic AT-rich repeats2012
- Author(s)
  Kato T, Kurahashi H, Emanuel BS
- Journal Title
  
  Curr Opin Genet Dev
  
  Volume: 22 Issue: 3 Pages: 221-228
- DOI
  10.1016/j.gde.2012.02.004
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-24390085
[Journal Article] Chromosomal translocations and palindromic AT-rich repeats2012
- Author(s)
  Kato T, Kurahashi H, Emanuel BS
- Journal Title
  
  Curr Opin Genet Dev
  
  Volume: 22 Pages: 221-228
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182
[Journal Article] Mechanism of complex gross chromosomal rearrangements : a commentary on concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation2012
- Author(s)
  Kurahashi, H., Ohye, T., Inagaki, H., Kogo, H., Tsutsumi, M.
- Journal Title
  
  J. Hum. Genet
  
  Volume: 57 Pages: 81-83
- NAID
  10030711395
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Serum neutrophil gelatinase-associated lipocalin during the early postoperative period predicts the recovery of graft function after kidney transplantation from donors after cardiac death2012
- Author(s)
  Kusaka M, Iwamatsu F, Kuroyanagi Y, Nakaya M, Ichino M, Marubashi S, Nagano H, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  J Urol
  
  Volume: 187 Issue: 6 Pages: 2261-2267
- DOI
  10.1016/j.juro.2012.01.033
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23592385, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085
[Journal Article] Mechanism of complex gross chromosomal rearrangements : A commentary on Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation2012
- Author(s)
  Kurahashi H, Ohye T, Inagaki H, Kogo H, Tsutsumi M
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Issue: 2 Pages: 81-83
- DOI
  10.1038/jhg.2011.143
- NAID
  10030711395
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-21590346, KAKENHI-PROJECT-22790192, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085
[Journal Article] Failure of homologous synapsis and sex-specific reproduction problems2012
- Author(s)
  Kurahashi H, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  Front Genet
  
  Volume: 3 Pages: 112-112
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Upregulation of HtrA4 in the placentas of patients with severe pre-eclampsia2012
- Author(s)
  Inagaki A, Nishizawa H, Ota S, Suzuki M, Inuzuka H, Miyamura H, Sekiya T, Kurahashi H, Udagawa Y
- Journal Title
  
  Placenta
  
  Volume: 33 Issue: 11 Pages: 919-926
- DOI
  10.1016/j.placenta.2012.08.003
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] Chromosomal translocations and palindromic...2012
- Author(s)
  Kato T, Kurahashi H, Emanuel BS.
- Journal Title
  
  Curr Opin Genet Dev.
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling.2011
- Author(s)
  Kugita M, Nishii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] A rare synaptonemal complex protein 3 gene variant is associated with unexplained female infertility.2011
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Bolor H, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Yoshihara D., Kurahashi H., Morita M., Kugita M., Hiki Y., Aukema HM., Yamaguchi T., Calvet JP., Wallace DP., Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol.
  
  Volume: 300(2)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] DNA secondary structure is influencec by genetic variation and alters susceptibility to de novo translocation2011
- Author(s)
  Kato, T., Inagaki, H., Tong, M., Kogo, H., Ohye, T., Yamada, K., Tsutsumi, M., Emanuel, B. S., Kurahashi, H.
- Journal Title
  
  Mol. Cytogenet
  
  Volume: 4 Pages: 18-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease.2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease.2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease.2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling.2011
- Author(s)
  Kugita M, Nshii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] A rare synaptonemal complex protein 3 gene variant in unexplained female infertility2011
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Bolor H, Udagawa Y, Kurahashi H
- Journal Title
  
  Mol Hum Reprod
  
  Volume: 17 Issue: 4 Pages: 266-271
- DOI
  10.1093/molehr/gaq098
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling.2011
- Author(s)
  Kugita M, Nishii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 300(1)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation2011
- Author(s)
  Kato T, Inagaki H, Tong M, Kogo H, Ohye T, Yamada K, Tsutsumi M, Emanuel BS, Kurahashi H
- Journal Title
  
  Mol Cytoenet
  
  Volume: 4 Pages: 18-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] A rare synaptonemal complex protein 3 gene variant is associated with unexplained female infertility.2011
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Bolor H, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011
- Author(s)
  Taniguchi-Ikeda M, Kobayashi K, Kanagawa M, Yu CC, Mori K, Oda T, Kuga A, Kurahashi H, Akman HO, DiMauro S, Kaji R, Yokota T, Takeda S, Toda T
- Journal Title
  
  Nature
  
  Volume: 478 Issue: 7367 Pages: 127-131
- DOI
  10.1038/nature10456
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-21390269, KAKENHI-PROJECT-21689030, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-22790980, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182
[Journal Article] Lack of Association between Orexin Receptor Genes Polymorphisms and Obstructive Sleep Apnea Syndrome in Japanese2011
- Author(s)
  Ahmed WA, Mori T, Nishimura Y, Kitanaka T, Kato T, Bhardwaj KA, Kurahashi H, Suzuki K.
- Journal Title
  
  Sleep Biol Rhythms
  
  Volume: 9 Pages: 73-77
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182
[Journal Article] Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY Body to the nucleolus during prophase of male meiosis2011
- Author(s)
  Tsutsumi, M., Kogo, H., Kowa-Sugiyama, H., Inagaki, H., Ohye, T., Kurahashi, H.
- Journal Title
  
  I. Biol. Reprod
  
  Volume: 85 Pages: 165-171
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling.2011
- Author(s)
  Kugita M., Nishii K., Morita M., Yoshihara D., Kowa-Sugiyama H., Yamada K., Yamaguchi T., Wallace D.P., Calvet J.P., Kurahashi H., Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol.
  
  Volume: 300(1)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] Polymorphism in annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Polymorphism in annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H
- Journal Title
  
  Mol Hum Reprod
  
  Volume: 17 Issue: 7 Pages: 447-452
- DOI
  10.1093/molehr/gar008
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23591609, KAKENHI-PROJECT-23659182
[Journal Article] Lack of Association between Orexin Receptor Genes Polymorphisms and Obstructive Sleep Apnea Syndrome in Japanese2011
- Author(s)
  Ahmed WA, Mori T, Nishimura Y, Kitanaka T, Kato T, Bhardwaj KA, Kurahashi H, Suzuki K
- Journal Title
  
  Sleep Biol Rhythms
  
  Volume: 9 Pages: 73-77
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Polymorphism in annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction2011
- Author(s)
  Nishizawa H, Ota S, Suzuki M, Kato T, Sekiya T, Kurahashi H, Udagawa Y
- Journal Title
  
  Reprod Biol Endocrinol
  
  Volume: 9 Issue: 1 Pages: 107-107
- DOI
  10.1186/1477-7827-9-107
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling2011
- Author(s)
  Kugita M, Nishii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 300 Issue: 1 Pages: F177-F188
- DOI
  10.1152/ajprenal.00470.2010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] Lack of Association between Orexin Receptor Genes Polymorphisms and Obstructive Sleep Apnea Syndrome in Japanese2011
- Author(s)
  Ahmed WA, Mori T, Nishimura Y, Kitanaka T, Kato T, Bhardwaj KA, Kurahashi H, Suzuki K
- Journal Title
  
  Sleep Biol Rhythms
  
  Volume: 9 Pages: 73-77
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 300 Issue: 2 Pages: F465-F474
- DOI
  10.1152/ajprenal.00460.2010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation2011
- Author(s)
  Kato T, Inagaki H, Tong M, Kogo H, Ohye T, Yamada K, Tsutsumi M, Emanuel BS, Kurahashi H
- Journal Title
  
  Mol Cytogenet
  
  Volume: 4 Issue: 1 Pages: 18-18
- DOI
  10.1186/1755-8166-4-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-22790192, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] Characterization of a novel mouse gene encoding an SYCP3-like protein that re-localizes from the XY body to the nucleolus during prophase of male meiosis I2011
- Author(s)
  Tsutsumi M, Kogo H, Kowa-Sugiyama H, Inagaki H, Ohye T, Kurahashi H
- Journal Title
  
  Biol Reprod
  
  Volume: 85 Issue: 1 Pages: 165-171
- DOI
  10.1095/biolreprod.110.087270
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-22790192, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] PPAR-{gamma} agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M,Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 300(2)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] Impact of indoleamine 2,3-dioxygenase on the antioxidant system in the placentas of severely pre-eclamptic patients2011
- Author(s)
  Nishizawa H, Suzuki M, Pryor-Koishi K, Sekiya T, Tada S, Kurahashi H, Udagawa Y
- Journal Title
  
  Syst Biol Reprod Med
  
  Volume: 57 Issue: 4 Pages: 174-178
- DOI
  10.3109/19396368.2011.587590
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182
[Journal Article] A rare synaptonemal complex protein 3 gene variant is associated with unexplained female infertility.2011
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Bolor H, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Global gene expression profiling in early-stage polycystic kidney disease in the Han : SPRD Cy rat identifies a role for RXR signaling.2011
- Author(s)
  Kugita M, Nishii K, Morita M, Yoshihara D, Kowa-Sugiyama H, Yamada K, Yamaguchi T, Wallace DP, Calvet JP, Kurahashi H, Nagao S.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Polymorphism in annexin A5 gene promoter in Japanese women with recurrent pregnancy loss.2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H.
- Journal Title
  
  Mol Hum Reprod
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Polycystic kidney disease in Han : SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.2010
- Author(s)
  Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
- Journal Title
  
  Am J Physiol Renal Physiol.
  
  Volume: 299(5)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.2010
- Author(s)
  Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H.
- Journal Title
  
  Hum Mol Genet
  
  Volume: 19 Pages: 2630-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] A new palindrome-mediated recurrent translocation with 3 : 1 meiotic non-disjunction : the t(8 ; 22)(q24.13 ; q11.21)2010
- Author(s)
  Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS
- Journal Title
  
  Am J Hum Genet
  
  Volume: 87(2) Pages: 209-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.2010
- Author(s)
  Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H.
- Journal Title
  
  Hum Mol Genet
  
  Volume: 19 Pages: 2630-7
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11 ; 22) s in sperm2010
- Author(s)
  Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H
- Journal Title
  
  Hum Mol Genet
  
  Volume: 19(13) Pages: 2630-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11 ; 22) s in sperm2010
- Author(s)
  Tong, M., Kato, T., Yamada, K., Inagaki, H., Kogo, H., Ohye, T., Tsutsumi, M., Wang, J., Emanuel, B. S. Kurahashi, H.
- Journal Title
  
  Hum. Mol. Genet
  
  Volume: 19 Pages: 2630-2637
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia (Reply).2010
- Author(s)
  Nishizawa H, Kurahashi H.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 317-317
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Angiotensin converting enzyme 2 gene expression increased compensatory for left ventricular remodeling in patients with end-stage heart failure.2010
- Author(s)
  Ohtsuki M, Morimoto S, Izawa H, Ismail TF, Ishibashi-Ueda H, Kato Y, Horii T, Isomura T, Suma H, Nomura M, Hishida H, Kurahashi H, Ozaki Y.
- Journal Title
  
  Int J Cardiol
  
  Volume: 145 Pages: 333-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Correlation of axillary osmidrosis to a SNP in the ABCC11 gene determined by the smart-amplification process (SMAP).2010
- Author(s)
  Inoue Y, Mori T, Sakurai A, Mitani Y, Toyoda Y, Ishikawa T, Hayashizaki Y, Yoshimura Y, Kurahashi H, Sakai Y.
- Journal Title
  
  J Plast Reconstr Aesthet Surg
  
  Volume: 63 Pages: 1369-74
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Polycystic kidney disease in Han : SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.2010
- Author(s)
  Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 299
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] CD9 gene variations are not associated with female infertility in humans2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H
- Journal Title
  
  Gynecologic and Obstetric Investigation 69
  
  Pages: 116-121
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Urinary neutrophil gelatinase-associated lipocalin is a potential non-invasive marker for renal scarring in patients with vesicoureteral reflux.2010
- Author(s)
  Ichino M, Kusaka M, Kuroyanagi Y, Mori T, Morooka M, Sasaki H, Shiroki R, Shishido S, Kurahashi H, Hoshinaga K.
- Journal Title
  
  J Urol
  
  Volume: 183 Pages: 2001-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] CD9 gene variations are not associated with female infertility in humans.2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H.
- Journal Title
  
  Gynecol Obstet Invest
  
  Volume: 69 Pages: 116-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Urinary neutrophil gelatinase-associated lipocalin is a potential non-invasive marker for renal scarring in patients with vesicoureteral reflux.2010
- Author(s)
  Ichino M, Kusaka M, Kuroyanagi Y, Mori T, Morooka M, Sasaki H, Shiroki R, Shishido S, Kurahashi H, Hoshinaga K.
- Journal Title
  
  J Urol
  
  Volume: 183 Pages: 2001-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Serum tissue inhibitor of metalloproteinases 1 (TIMP-1) predicts organ recovery from delayed graft function after kidney transplantation from donors after cardiac death.2010
- Author(s)
  Kusaka M, Kuroyanagi Y, Ichino M, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Sugitani A, Kurahashi H, Hoshinaga K.
- Journal Title
  
  Cell Transplant
  
  Volume: 19 Pages: 723-9
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Serum tissue inhibitor of metalloproteinases 1 (TIMP-1) predicts organ recovery from delayed graft function after kidney transplantation from donors after cardiac death.2010
- Author(s)
  Kusaka M, Kuroyanagi Y, Ichino M, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Sugitani A, Kurahashi H, Hoshinaga K.
- Journal Title
  
  Cell Transplant
  
  Volume: 19 Pages: 723-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] CD9 gene variations are not associated with female infertility in humans2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H
- Journal Title
  
  Gynecologic and Obstetric Investigation 69
  
  Pages: 116-121
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Paternal origin of the de now constitutional t(11 ; 22)(q23 ; q11)2010
- Author(s)
  Ohye, T., Inagaki, H., Kogo, H., Tsutsumi, M., Kato, T., Tong, M., Macville, M. V. E., Medne, L., Zackai, E. H., Emanuel, B. S., Kurahashi, K.
- Journal Title
  
  Eur. J. Hum. Genet
  
  Volume: 18 Pages: 783-787
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia.2010
- Author(s)
  Nishizawa H, Kato T, Ohta S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 68-76
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Urinary neutrophil gelatinase-associated lipocalin is a potential non-invasive marker for renal scarring in patients with vesicoureteral reflux.2010
- Author(s)
  Ichino M, Kusaka M, Kuroyanagi Y, Mori T, Morooka M, Sasaki H, Shiroki R, Shishido S, Kurahashi H, Hoshinaga K.
- Journal Title
  
  J Urol
  
  Volume: 183 Pages: 2001-7
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] The constitutional t(11 ; 22): implications for a novel mechanism responsible for gross chromosomal rearrangements2010
- Author(s)
  Kurahashi, H., Inagaki, H., Ohye, T., Kogo, H., Tsutsumi, M., Kato, T., Emanuel, B. S.
- Journal Title
  
  Clin. Genet
  
  Volume: 78 Pages: 299-309
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Paternal origin of the de novo constitutional t(11;22)(q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville M, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 18 Pages: 783-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia (Reply).2010
- Author(s)
  Nishizawa H, Kurahashi H.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 317-317
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] CD9 gene variations are not associated with female infertility in humans2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H
- Journal Title
  
  Gynecologic and Obstetric Investigation 69
  
  Pages: 116-121
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I : towards the identification of genes responsible for infertility in humans.2010
- Author(s)
  Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H.
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 293-9
- NAID
  10030734983
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia (Reply).2010
- Author(s)
  Nishizawa H, Kurahashi H.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 317-317
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Polycystic kidney disease in Han : SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.2010
- Author(s)
  Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 299
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Angiotensin converting enzyme 2 gene expression increased compensatory for left ventricular remodeling in patients with end-stage heart failure.2010
- Author(s)
  Ohtsuki M, Morimoto S, Izawa H, Ismail TF, Ishibashi-Ueda H, Kato Y, Horii T, Isomura T, Suma H, Nomura M, Hishida H, Kurahashi H, Ozaki Y.
- Journal Title
  
  Int J Cardiol
  
  Volume: 145 Pages: 333-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I : towards the identification of genes responsible for infertility in humans.2010
- Author(s)
  Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Tada T, Kurahashi H.
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 293-9
- NAID
  10030734983
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Polycystic kidney disease in Han : SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.2010
- Author(s)
  Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 299
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia.2010
- Author(s)
  Nishizawa H, Kato T, Ohta S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 68-76
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I : towards the identification of genes responsible for infertility in humans2010
- Author(s)
  Kogo, H., Kowa-Sugiyama, H., Yamada, K., Bolor, H., Tsutsumi, M., Ohye, T., Inagaki, H., Taniguchi, M., Toda, T., Kurahashi, H.
- Journal Title
  
  J. Hum. Genet
  
  Volume: 55 Pages: 293-299
- NAID
  10030734983
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] CD9 gene variations are not associated with female infertility in humans.2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H.
- Journal Title
  
  Gynecol Obstet Invest
  
  Volume: 69 Pages: 116-21
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I : towards the identification of genes responsible for infertility in humans.2010
- Author(s)
  Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Tada T, Kurahashi H.
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 293-9
- NAID
  10030734983
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] The constitutional t(11;22) : implications for a novel mechanism responsible for gross chromosomal rearrangements2010
- Author(s)
  Kurahashi, H.
- Journal Title
  
  Clin.Genet.
  
  Volume: 78 Pages: 299-309
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Paternal origin of the de novo constitutional t(11;22)(q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville M, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 18 Pages: 783-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Correlation of axillary osmidrosis to a SNP in the ABCC11 gene determined by the smart-amplification process (SMAP).2010
- Author(s)
  Inoue Y, Mori T, Sakurai A, Mitani Y, Toyoda Y, Ishikawa T, Hayashizaki Y, Yoshimura Y, Kurahashi H, Sakai Y.
- Journal Title
  
  J Plast Reconstr Aesthet Surg
  
  Volume: 63 Pages: 1369-74
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Paternal origin of the de novo constitutional t(11 ; 22)(q23 ; q11)2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville M, Medne L, Zackai EH, Emanuel BS, Kurahashi H
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 18(7) Pages: 783-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] 絨毛検査で偶然見つかり切断点の解析を必要とした胎児t(11 ; 22)新生転座2010
- Author(s)
  大江瑞恵, Livija Medne, Beverly S. Emanuel, 倉橋浩樹
- Journal Title
  
  遺伝カウンセリング学会誌
  
  Volume: 31巻 Pages: 169-173
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] The constitutional t(11;22) : implications for a novel mechanism responsible for gross chromosomal rearrangement.2010
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Emanuel BS.
- Journal Title
  
  Clin Genet
  
  Volume: 78 Pages: 299-309
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Correlation of axillary osmidrosis to a SNP in the ABCC11 gene determined by the smart-amplification process (SMAP).2010
- Author(s)
  Inoue Y, Mori T, Sakurai A, Mitani Y, Toyoda Y, Ishikawa T, Hayashizaki Y, Yoshimura Y, Kurahashi H, Sakai Y.
- Journal Title
  
  J Plast Reconstr Aesthet Surg
  
  Volume: 63 Pages: 1369-74
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Serum tissue inhibitor of metalloproteinases 1 (TIMP-1) predicts organ recovery from delayed graft function after kidney transplantation from donors after cardiac death.2010
- Author(s)
  Kusaka M, Kuroyanagi Y, Ichino M, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Sugitani A, Kurahashi H, Hoshinaga K.
- Journal Title
  
  Cell Transplant
  
  Volume: 19 Pages: 723-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.2010
- Author(s)
  Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H.
- Journal Title
  
  Hum Mol Genet
  
  Volume: 19 Pages: 2630-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Polycystic kidney disease in Han : SPRD Cy rats is associated with elevated expression and mislocalization of SamCystin.2010
- Author(s)
  Nagao S, Morita M, Kugita M, Yoshihara D, Yamaguchi T, Kurahashi H, Calvet JP, Wallace DP.
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 299(5)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590351
[Journal Article] The constitutional t(11;22) : implications for a novel mechanism responsible for gross chromosomal rearrangement.2010
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Emanuel BS.
- Journal Title
  
  Clin Genet
  
  Volume: 78 Pages: 299-309
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia.2010
- Author(s)
  Nishizawa H, Kato T, Ohta S, Nishiyama S, Pryor-Koishi K, Suzuki M, Tsutsumi M, Inagaki H, Kurahashi H, Udagawa Y.
- Journal Title
  
  Am J Reprod Immunol
  
  Volume: 64 Pages: 68-76
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] A new palindrome-mediated recurrent translocation with 3:1 meiotic non-disjunction : the t(8;22)(q24.13;q11.21).2010
- Author(s)
  Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS.
- Journal Title
  
  Am J Hum Genet
  
  Volume: 87 Pages: 209-18
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] A new palindrome -mediated recurrent translocation with 3:1 meiotic non-disjunction : the t(8;22)(q24.13 ; q11.21).2010
- Author(s)
  Sheridan MB, Kato T, Haldem an-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS.
- Journal Title
  
  Am J Hum Genet
  
  Volume: 87 Pages: 209-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] CD9 gene variations are not associated with female infertility in humans.2010
- Author(s)
  Nishiyama S, Kishi T, Kato T, Suzuki M, Nishizawa H, Pryor-Koishi K, Sawada T, Nishiyama Y, Iwata N, Udagawa Y, Kurahashi H.
- Journal Title
  
  Gynecol Obstet Invest
  
  Volume: 69 Pages: 116-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Paternal origin of the de novo constitutional t(11;22)(q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville M, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 18 Pages: 783-7
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] The constitutional t(11 ; 22): implications for a novel mechanism responsible for gross chromosomal rearrangement2010
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Emanuel BS
- Journal Title
  
  Clin Genet
  
  Volume: 78(4) Pages: 299-309
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] The constitutional t(11;22) : implications for a novel mechanism responsible for gross chromosomal rearrangement.2010
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Kato T, Tong M, Emanuel BS.
- Journal Title
  
  Clin Genet
  
  Volume: 78 Pages: 299-309
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Angiotensin converting enzyme 2 gene expression increased compensatory for left ventricular remodeling in patients with end-stage heart failure.2010
- Author(s)
  Ohtsuki M, Morimoto S, Izawa H, Ismail TF, Ishibashi-Ueda H, Kato Y, Horii T, Isomura T, Suma H, Nomura M, Hishida H, Kurahashi H, Ozaki Y.
- Journal Title
  
  Int J Cardiol
  
  Volume: 145 Pages: 333-4
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] A new palindrome -mediated recurrent translocation with 3:1 meiotic non-disjunction : the t(8;22)(q24.13 ; q11.21).2010
- Author(s)
  Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS.
- Journal Title
  
  Am J Hum Genet
  
  Volume: 87 Pages: 209-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi, H., Inagaki, H., Kato, T., Hosoba, E., Kogo, H., Ohye, T., Tsutsumi, M., Bolor, H., Tong, M., Emanuel, B. S.
- Journal Title
  
  Hum. Mol. Genet
  
  Volume: 18 Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Global expression profiles in 1-hour biopsy specimens of human kidney transplantation from donors after cardiac death2009
- Author(s)
  Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Cell Transplantation 18
  
  Pages: 647-656
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Chromosomal instability mediated by non-B DNA : cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki, H., Ohye, T., Kogo, H., Kato, T., Bolor, H., Taniguchi, M., Shaikh, T. H., Emanuel, B. S., Kurahashi, H.
- Journal Title
  
  Genome. Res
  
  Volume: 19 Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Global expression profiles in 1-hour biopsy specimens of human kidney transplantation from donors after cardiac death2009
- Author(s)
  Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Cell Transplantation 18
  
  Pages: 647-656
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS
- Journal Title
  
  Human Molecular Genetics 18
  
  Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Impaired DNA replication prompts deletions within palindrom is sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS
- Journal Title
  
  Human Molecular Genetics 18
  
  Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H
- Journal Title
  
  Genome Research 19
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia2009
- Author(s)
  Nishizawa H, Pryor-Koishi K, Suzuki M, Kato T, Sekiya T, Tada S, Kurahashi H, Udagawa Y
- Journal Title
  
  Gynecologic and Obstetric Investigation 68
  
  Pages: 239-247
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS
- Journal Title
  
  Hum Mol Genet
  
  Volume: 18(18) Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Makiko T, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H
- Journal Title
  
  American Journal of Human Genetics 84
  
  Pages: 14-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi, H., Bolor, H., Kato, T., Kogo, H., Tsutsumi, M., Inagaki, H., Ohye, T.
- Journal Title
  
  J. Hum. Genet
  
  Volume: 54 Pages: 253-260
- NAID
  10030730167
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H
- Journal Title
  
  Genome Res
  
  Volume: 19(2) Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia2009
- Author(s)
  Nishizawa H, Pryor-Koishi K, Suzuki M, Kato T, Sekiya T, Tada S, Kurahashi H, Udagawa Y
- Journal Title
  
  Gynecologic and Obstetric Investigation 68
  
  Pages: 239-247
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Makiko T, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y-, Kurahashi H
- Journal Title
  
  American Journal of Human Genetics 84
  
  Pages: 14-20
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Bolor, H., Mori, T., Nishiyama, S., Ito, Y., Hosoba, E., Inagaki, H., Kogo, H., Ohye, T., Tsutsumi, M., Kato, T., Tong, M., Nishizawa, H., Pryor-Koishi, K., Kitaoka, E., Sawada, T., Nishiyama, Y., Udagawa, Y., Kurahashi, H.
- Journal Title
  
  Am. J. Hum. Genet
  
  Volume: 84 Pages: 14-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Increased urinary neutrophil gelatinase-associated lipocalin levels in a rat model of upper urinary tract infection2009
- Author(s)
  Ichino M, Kuroyanagi Y, Kusaka M, Mori T, Ishikawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Journal of Urology 181
  
  Pages: 2326-2331
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  Journal of Human Genetics 54
  
  Pages: 253-260
- NAID
  10030730167
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Increased urinary neutrophil gelatinase-associated lipocalin levels in a rat model of upper urinary tract infection2009
- Author(s)
  Ichino M, Kuroyanagi Y, Kusaka M, Mori T, Ishikawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Journal of Urology 181
  
  Pages: 2326-2331
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  J Hum Genet
  
  Volume: 54(5) Pages: 253-260
- NAID
  10030730167
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS
- Journal Title
  
  Human Molecular Genetics 18
  
  Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells2009
- Author(s)
  Kurahashi, H.
- Journal Title
  
  Hum.Mol.Genet. 18
  
  Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  Journal of Human Genetics 54
  
  Pages: 253-260
- NAID
  10030730167
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Bolor H, Mori T, Nishiyama S, Ito Y, Hosoba E, Inagaki H, Kogo H, Ohye T, Makiko T, Kato T, Tong M, Nishizawa H, Pryor-Koishi K, Kitaoka E, Sawada T, Nishiyama Y, Udagawa Y, Kurahashi H
- Journal Title
  
  American Journal of Human Genetics 84
  
  Pages: 14-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H
- Journal Title
  
  Genome Research 19
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21659085
[Journal Article] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H
- Journal Title
  
  Genome Research 19
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi, H.
- Journal Title
  
  J.Hum.Genet. 54
  
  Pages: 253-260
- NAID
  10030730167
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] Increased urinary neutrophil gelatinase-associated lipocalin levels in a rat model of upper urinary tract infection2009
- Author(s)
  Ichino M, Kuroyanagi Y, Kusaka M, Mori T, Ishikawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Journal of Urology 181
  
  Pages: 2326-2331
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia2009
- Author(s)
  Nishizawa H, Pryor-Koishi K, Suzuki M, Kato T, Sekiya T, Tada S, Kurahashi H, Udagawa Y
- Journal Title
  
  Gynecologic and Obstetric Investigation 68
  
  Pages: 239-247
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Global expression profiles in 1-hour biopsy specimens of human kidney transplantation from donors after cardiac death2009
- Author(s)
  Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  Cell Transplantation 18
  
  Pages: 647-656
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028020
[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2009
- Author(s)
  Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T
- Journal Title
  
  Journal of Human Genetics 54
  
  Pages: 253-260
- NAID
  10030730167
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Two different forms of palindrome resolution in the human genome : deletion or translocation.2008
- Author(s)
  Kato T, Inagaki H, Kogo H, Ohye T, Yamada K, Emanuel BS, Kurahashi H
- Journal Title
  
  Human Molecular Genetics 17
  
  Pages: 1184-91
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients2008
- Author(s)
  Nishizawa, H., Pryor-Koishi, K., Suzuki, M., Kato, T., Kogo, H., Sekiya, T., Kurahashi, H., Udagawa, Y.
- Journal Title
  
  Mol. Hum. Reprod 14
  
  Pages: 595-602
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients.2008
- Author(s)
  Nishizawa H, Pryor-Koishi K, S uzuki M, Kato T, Kogo H, Sekiya T, Kurahashi H, Udagawa Y
- Journal Title
  
  Molecular Human Reproduction 14
  
  Pages: 595-602
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Global gene expression profiling on renal scarring in rat model of pyelonephritis.2008
- Author(s)
  Ichino M, Mori T, Kusaka M, Kuroyanagi Y, Ishikawa K, Shiroki R, Kurahashi H, et al.
- Journal Title
  
  Pediatric Nephrology 23
  
  Pages: 1059-71
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Calcium channel inhibition with verapamil accelerates polycystic kidney disease progression in the Cy/+rat.2008
- Author(s)
  Nagao s, Nishii K, Yoshihara D, Kurahashi H, et al.
- Journal Title
  
  Kidney Int 73
  
  Pages: 269-77
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Serum neutrophil gelatinase-associated lipocalin as a predictor of organ recovery from delayed graft function after kidney tran splantation applying donation after cardiac death2008
- Author(s)
  Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Kurahashi H, et al.
- Journal Title
  
  Cell Transplantation 17
  
  Pages: 129-34
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Mouse model for allogeneic fetal rejection recapitulates humanpre-eclampsia.2008
- Author(s)
  Nishizawa H, Hasegawa K, Suzuki M, Achiwa Y, Kato T, Saito K, Kurahashi H, Udagawa Y
- Journal Title
  
  Journal of Obstetrics Gynaecology Research 34
  
  Pages: 1-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Two different forms of palindrome resolution in the human genome : deletion or translocation2008
- Author(s)
  Kato, T., Inagaki, H., Kogo, H., Ohye, T., Yamada, K., Emanuel, B. S., Kurahashi, H.
- Journal Title
  
  Hum. Mol. Genet 17
  
  Pages: 1184-1191
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Up-regulated cytokine inducible SH2-containing protein expression in allergen-stimulated T cells from hen's egg-allergic patients.2008
- Author(s)
  Nakajima Y, Tsuge I, Kondo Y, Komatsubara R, Hirata N, Kakami M, Kurahashi H., et al.
- Journal Title
  
  Clinical Experimental Allergy 38
  
  Pages: 1499-506
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] The etiological role of allogeneic fetal rejection in pre-eclampsia.2007
- Author(s)
  Nishizawa, H., Hasegawa, K. Kurahashi, H., et. al.
- Journal Title
  
  American Journal of Reproductive Immunology 58
  
  Pages: 11-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Age has no effect on de novo constitutional t(11;22)translocation frequency in sperm.2007
- Author(s)
  Kato, T., Yamada, K., Kurahashi, H., et. al.
- Journal Title
  
  Fertility & Sterility 88
  
  Pages: 1446-1448
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Overproduction of the follistatin-related gene protein in the placenta and maternal serum of women with pre-eclampsia.2007
- Author(s)
  Pryor-Koishi, K., Nishizawa, H., Kurahashi, H., et. al.
- Journal Title
  
  BJOG 114
  
  Pages: 1128-1137
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Molecular clonong of a translocation hotspot in 22q11.2007
- Author(s)
  Kurahashi, H., Inagaki, H., Hosoba. E., et. al.
- Journal Title
  
  Genome Research 17
  
  Pages: 461-469
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Genome-wide expression profile in rat model of renal isografts from brain dead donors.2007
- Author(s)
  Kusaka, M., Kuroyanagi, Y., Kurahashi, H., et. al.
- Journal Title
  
  Transplantation 83
  
  Pages: 62-70
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Molecular cloning of a translocation breakpoint hotspot in 22q11.2007
- Author(s)
  Kurahashi H.
- Journal Title
  
  Genome Res. 17
  
  Pages: 461-469
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590322
[Journal Article] CDH1 is a specific marker for undifferentiated spermatogonia in mouse testes2007
- Author(s)
  Tokuda, M., Kadokawa, Y., Kurahashi, H., Marunouchi, T.
- Journal Title
  
  Biol. Reprod. 76
  
  Pages: 130-141
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Age has no effect on de novo constitutional t(11 ; 22) translocation frequency in sperm2007
- Author(s)
  Kato, T., Yamada, K., Inagaki, H., Kogo, H., Ohye, T., Emanuel, B.S., Kurahashi, H.
- Journal Title
  
  Fertil Steril 88
  
  Pages: 1446-1448
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] CDH1 is a specific marker for undifferentiated spermatogonia in mouse testes.2007
- Author(s)
  Tokuda, M., Kadokawa, Y., Kurahashi, H., et. al.
- Journal Title
  
  Biology of Reproduction 76
  
  Pages: 130-141
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype2007
- Author(s)
  Kano, H., Kurahashi, H., Toda, T.
- Journal Title
  
  Proc. Natl. Acad. Sci. U.S.A. 104
  
  Pages: 19034-19039
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.2007
- Author(s)
  Kogo, H., Inagaki, H., Kurahashi, H., et. al.
- Journal Title
  
  Nucleic Acids Research 35
  
  Pages: 1198-1208
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Molecular cloning of a translocation breakpoint hotspot in 22q112007
- Author(s)
  Kurahashi H. Inagaki H. (他5人)
- Journal Title
  
  Genome Research 17
  
  Pages: 461-469
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590322
[Journal Article] 染色体構造異常の発生メカニズム2007
- Author(s)
  大江瑞恵, 倉橋浩樹
- Journal Title
  
  藤田学園医学会誌 31
  
  Pages: 89-97
- Data Source
  KAKENHI-PROJECT-19590322
[Journal Article] Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype.2007
- Author(s)
  Kano, H., Kurahashi, H., Toda, T.
- Journal Title
  
  Proceedings of National Academy of Science of the U.S.A., 104
  
  Pages: 19034-19039
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia.2007
- Author(s)
  Nishizawa, H., Pryor-Koishi, K., Kurahashi, H., et. al.
- Journal Title
  
  Placenta 28
  
  Pages: 487-497
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Molecular clonong of a translocation hotspot in 22q112007
- Author(s)
  Kurahashi, H., Inagaki, H., Hosoba. E., Kato, T., Ohye, T., Kogo, H., Emanuel, B. S.
- Journal Title
  
  Genome Res 17
  
  Pages: 461-469
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Cruciform extrusion propensity of human translocationmediating palindromic AT-rich repeats2007
- Author(s)
  Kogo, H., Inagaki, H., Ohye, T., Kato, T., Emanuel, B.S., Kurahashi, H.
- Journal Title
  
  Nucleic Acids Res 35
  
  Pages: 1198-1208
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?2006
- Author(s)
  Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, et al.
- Journal Title
  
  Biochemical and Biophysical Research Communications 342・2
  
  Pages: 489-502
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Molecular analysis of a mouse orthologue of HSFY, a candidate for the azoospermic factor on the human Y chromosome2006
- Author(s)
  Kinoshita K, Shinka T, Sato Y, Kurahashi H, Kowa H, Chen G, Umeno M, Toida K, Kiyokage E, Nakano T, Ito S, Nakahori Y.
- Journal Title
  
  Journal of Medical Investigation 53(1-2)
  
  Pages: 117-122
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Genetic variation affects de novo translocation frequency.2006
- Author(s)
  Kato T, Inagaki H, Yamada K, Kogo H, Ohye T, Kowa H, Nagaoka K, Taniguchi M, Emanuel BS, Kurahashi H
- Journal Title
  
  Science 311(5763)
  
  Pages: 971-971
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy ; is congenital muscular dystrophy a primary fibrotic disease?2006
- Author(s)
  Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
- Journal Title
  
  Biochemical and Biophysical Research Communication 342(2)
  
  Pages: 489-502
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Molecular analysis of a mouse orthologue of HSFY,a candidate for the azoospermic factor on the human Y chromosome.2006
- Author(s)
  Kinoshita K, Shinka T, Sato Y, Kurahashi H, Kowa H et al.
- Journal Title
  
  Journal of Medical Investigation 53・1-2
  
  Pages: 117-122
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] A palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved among primates.2005
- Author(s)
  Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H.
- Journal Title
  
  Human Mutation 26(4)
  
  Pages: 332-342
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Basement membrane fragility underlies embryonic lethality in fukutin-null mice.2005
- Author(s)
  Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, Horie M, Otani H, Toda T.
- Journal Title
  
  Neurobiology of the Disease 19(1-2)
  
  Pages: 208-217
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Gene expression profile in rat renal isografts from brain death donors.2005
- Author(s)
  Kusaka M, Yamada K, Kuroyanagi A, Terauchi H, Kowa H, Kurahashi H., Hoshinaga K.
- Journal Title
  
  Transplantation Proceedings 37(1)
  
  Pages: 364-366
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Androgen Receptor Pathway in Rats with Autosomal Dominant Polycystic Kidney Disease.2005
- Author(s)
  Nagao S, Kusaka M, Nishii K, Marunouchi T, Kurahashi H, et al.
- Journal Title
  
  Journal of American Society of Nephrology 16・7
  
  Pages: 2052-2062
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Androgen Receptor Pathway in Rats with Autosomal Dominant Polycystic Kidney Disease.2005
- Author(s)
  Nagao S, Kusaka M, Nishii K, Marunouchi T, Kurahashi H, Takahashi H, Grantham J.
- Journal Title
  
  Journal of American Society of Nephrology 16(7)
  
  Pages: 2052-2062
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Basement membrane fragility underlies embryonic lethality in fukutin-null mice.2005
- Author(s)
  Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, et al.
- Journal Title
  
  Neurobiology of the Disease 19・1-2
  
  Pages: 208-217
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation (SHFM).2005
- Author(s)
  Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T.
- Journal Title
  
  Human Genetics 118(3-4)
  
  Pages: 477-483
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Fukutin and α-dystroglycanopahties.2005
- Author(s)
  Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, Endo T.
- Journal Title
  
  Acta Myology 24(2)
  
  Pages: 60-63
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.2004
- Author(s)
  Kurahashi H, Inagaki H, Yamada K, Ohye T, et al.
- Journal Title
  
  Journal of Biological Chemistry 279・34
  
  Pages: 35377-35383
- Data Source
  KAKENHI-PROJECT-16012262
[Journal Article] Human herpesvirus 6 (HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.2004
- Author(s)
  Tanaka-Taya K, Sashihara J, Kurahashi H, Amo K, Miyagawa H, Kondo K, Okada S, Yamanishi K.
- Journal Title
  
  Journal of Medical Virology 73(3)
  
  Pages: 465-473
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.2004
- Author(s)
  Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T.
- Journal Title
  
  Journal of Biological Chemistry 279(34)
  
  Pages: 35377-35383
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Human herpesvirus 6(HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.2004
- Author(s)
  Tanaka-Taya K, Sashihara J, Kurahashi H, Amo K, Miyagawa H, et al.
- Journal Title
  
  Journal of Medical Virology 73・3
  
  Pages: 465-473
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Human herpesvirus 6 (HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.2004
- Author(s)
  Tanaka-Taya K, Sashihara J, Kurahashi H, Amo K, Miyagawa H, et al.
- Journal Title
  
  Journal of Medical Virology. 73・3
  
  Pages: 465-473
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Human herpesvirus 6 (HHV-6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV-6 DNA.2004
- Author(s)
  Tanaka-Taya K, Sashihara J, Kurahashi H, Amo K, Miyagawa H, et al.
- Journal Title
  
  Journal of Medical Virology 73・3
  
  Pages: 465-473
- Data Source
  KAKENHI-PROJECT-16012262
[Journal Article] Cruciform DNA structure underlies the etiology for palindrome mediated human chromosomal translocations.2004
- Author(s)
  Kurahashi H, Inagaki H, Yamada K, Ohye T, et al.
- Journal Title
  
  Journal of Biological Chemistry 279・34
  
  Pages: 35377-35383
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Ras/MEK pathway is required for NGF-induced expression of tyrosine hydroxylase gene.2004
- Author(s)
  Suzuki T, Kurahashi H, Ichinose H.
- Journal Title
  
  Biochemical and Biophysical Research Communication 315(2)
  
  Pages: 389-396
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Ras/MEK pathway is required for NGF-induced expression of tyrosine hydroxylase gene.2004
- Author(s)
  Suzuki T, Kurahashi H, Ichinose H
- Journal Title
  
  Biochemical and Biophysical Research Communications 315・2
  
  Pages: 389-396
- Data Source
  KAKENHI-PROJECT-16012262
[Journal Article] Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.2004
- Author(s)
  Kurahashi H, Inagaki H, Yamada K, Ohye T, et al.
- Journal Title
  
  Journal of Biological Chemistry 279・34
  
  Pages: 35377-35383
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Ras/MEK pathway is required for NGF-induced expression of tyrosine hydroxylase gene.2004
- Author(s)
  Suzuki T, Kurahashi H, Ichinose H
- Journal Title
  
  Biochemical and Biophysical Research Communications 315・2
  
  Pages: 389-396
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Calcium channel inhibition with verapamil accelerates polycystic kidney disease progression in the Cy/+rat.
- Author(s)
  Nagao, S., Nishii, K., Kurahashi, H., et. al.
- Journal Title
  
  Kidney International (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Two different forms of palindrome resolution in the human genome: deletion or translocation.
- Author(s)
  Kato, T., Inagaki, H., Kurahashi, H., et. al.
- Journal Title
  
  Human Molecular Genetics (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy ; is congenital muscular dystrophy a primary fibrotic disease?
- Author(s)
  Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, et al.
- Journal Title
  
  Biochemical and Biophysical Research Communications (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Mouse model for allogeneic fetal rejection recapitulates human pre-eclampsia.
- Author(s)
  Nishizawa, H., Hasegawa, K., Kurahashi, H., et. al.
- Journal Title
  
  Journal of Obstetrics and Gynaecology Research (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Serum neutrophil gelatinase-associated lipocalin during the early postoperative period predicts the recovery of graft function after kidney transplantation from donors after cardiac death
- Author(s)
  Kusaka M, Iwamatsu F, Kuroyanagi Y, Nakaya M, Ichino M, Marubashi S, Nagano H, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  J Urol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Abe T, Kurahashi H
- Journal Title
  
  Genes Cells
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Global gene expression profiling on renal scarring in rat model of pyelonephritis.
- Author(s)
  Ichino, M., Mori, T., Kurahashi, H., et. al.
- Journal Title
  
  Pediatric Nephrology (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] A Functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan
- Author(s)
  Ahmed WA, Tsutsumi M, Nakata S, Mori T, Nishimura Y, Fujisawa T, Kato I, Nakashima M, Kurahashi H, Suzuki K
- Journal Title
  
  Laryngoscope
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Basement membrane fragility underlies embryonic lethality in fukutin-null mice.
- Author(s)
  Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, et al.
- Journal Title
  
  Neurobiology of the Disease (印刷中)
- Data Source
  KAKENHI-PROJECT-16012262
[Journal Article] Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies.
- Author(s)
  Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, et al.
- Journal Title
  
  Human Molecular Genetics (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Palindrome-mediated chromosomal translocations in humans
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS
- Journal Title
  
  DNA Repair (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Molecular analysis of a mouse orthologue of HSFY, a candidate for the azoospermic factor on the human Y chromosome.
- Author(s)
  Kinoshita K, Shinka T, Sato Y, Kurahashi H, Kowa H, et al.
- Journal Title
  
  Journal of Medical Investigation (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Palindrome-mediated chromosomal translocations in humans
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS
- Journal Title
  
  DNA Repair (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Differential expression of caveolin-3 in mouse smooth muscle cells in vivo.
- Author(s)
  Kogo H, Ito S, Moritoki Y, Kurahashi H, Fujimoto T
- Journal Title
  
  Cell Tissue Research (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Basement membrane fragility underlies embryonic lethality in fukutin-null mice.
- Author(s)
  Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, et al.
- Journal Title
  
  Neurobiology of the Disease (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Palindrome-mediated chromosomal translocations in humans.
- Author(s)
  Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS
- Journal Title
  
  DNA Repair (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Chromosomal translocations and palindromic AT-rich repeats
- Author(s)
  Kato T, Kurahashi H, Emanuel BS
- Journal Title
  
  Curr Opin Genet Dev
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Differential expression of caveolin-3 in mouse smooth muscle cells in vivo.
- Author(s)
  Kogo H, Ito S, Moritoki Y, Kurahashi H, Fujimoto T
- Journal Title
  
  Cell Tissue Research (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Gene expression profile in rat renal isografts from brain death donors.
- Author(s)
  Kusaka M, Yamada K, Kuroyanagi A, Terauchi H, Kowa H, Kurahashi K.et al.
- Journal Title
  
  Transplantation Proceedings (印刷中)
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Gene expression profile in rat renal isografts from brain death donors.
- Author(s)
  Kusaka M, Yamada K, Kuroyanagi A, Terauchi H, Kowa H, Kurahashi K, et al.
- Journal Title
  
  Transplantation Proceedings (印刷中)
- Data Source
  KAKENHI-PROJECT-16012262
[Journal Article] HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Abe T, Kurahashi H
- Journal Title
  
  Genes Cells
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Chromosomal translocations and palindromic AT-rich repeats
- Author(s)
  Kato T, Kurahashi H, Emanuel BS
- Journal Title
  
  Curr Opin Genet Dev.
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.
- Author(s)
  Tsuge I, Ito K, Ohye T, Kando N, Kondo Y, Nakajima Y, Inuo C, Kurahashi H, Urisu A.
- Journal Title
  
  Pediatric Pulmonology
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659182
[Journal Article] The constitutional t(11 ; 22) : implications for a novel mechanism responsible for gross chromosomal rearrangements
- Author(s)
  Kurahashi, H.
- Journal Title
  
  Clin.Genet. (In press)
- Data Source
  KAKENHI-PROJECT-21590346
[Journal Article] A Functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan
- Author(s)
  Ahmed WA, Tsutsumi M, Nakata S, Mori T, Nishimura Y, Fujisawa T, Kato I, Nakashima M, Kurahashi H, Suzuki K
- Journal Title
  
  Laryngoscope
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101
[Journal Article] Differential expression of caveolin-3 in mouse smooth muscle cells in vivo.
- Author(s)
  Kogo H, Ito S, Moritoki Y, Kurahashi H, Fujimoto T
- Journal Title
  
  Cell Tissue Research (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Serum neutrophil gelatinase-associated lipocalin during the early postoperative period predicts the recovery of graft function after kidney transplantation from donors after cardiac death
- Author(s)
  Kusaka M, Iwamatsu F, Kuroyanagi Y, Nakaya M, Ichino M, Marubashi S, Nagano H, Shiroki R, Kurahashi H, Hoshinaga K
- Journal Title
  
  J Urol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019
[Journal Article] Serum neutrophil gelatinase-associated lipocalin as a predictor of organ recovery from delayed graft function after kidney transplantation applying donation after cardiac death.
- Author(s)
  Kusaka, M., Kuroyanagi, Y., Kurahashi, H., et. al.
- Journal Title
  
  Cell Transplantation (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390097
[Journal Article] Analysis of gene expression profiles by oligonucleotide microarray in children with influenza
- Author(s)
  Kawada J, Kimura H, Kamachi Y, Kojima S, Nishikawa K, Nagaoka K, Taniguchi M, Kurahashi H, Morishima T
- Journal Title
  
  Journal of General Virology (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Journal Article] Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies
- Author(s)
  Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T
- Journal Title
  
  Human Molecular Genetics (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390102
[Patent] 胚の染色体異数性の検査方法2023
- Inventor(s)
  倉橋浩樹、真里谷奨
- Industrial Property Rights Holder
  倉橋浩樹、真里谷奨
- Industrial Property Rights Type
  特許
- Filing Date
  2023
- Overseas
- Data Source
  KAKENHI-PROJECT-23K08855
[Presentation] 不妊・不育症のゲノム医療を目指して2023
- Author(s)
  倉橋浩樹
- Organizer
  第68回日本生殖医学会学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-23K08855
[Presentation] Gene signatures in genetically homogeneous trisomy 21 and euploid at the induced pluripotent stem cell level2023
- Author(s)
  Ryotaro Hashizume, Sachiko Wakita, Mari Hara, Hirofumi Sawada, Shin-ichiro Takebayashi, Yasuji Kitabatake, Yoshitaka Miyagawa, Yoshifumi S Hirokawa, Hiroshi Imai, and Hiroki Kurahashi
- Organizer
  Human Genetics Asia 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06835
[Presentation] PGT-M　技術革新の恩恵と陥穽2023
- Author(s)
  倉橋浩樹
- Organizer
  第9回日本産科婦人科遺伝診療学会
- Invited
- Data Source
  KAKENHI-PROJECT-23K08855
[Presentation] 全ゲノムシークエンスで同定されたエンハンサー領域欠失によるOTC欠損症の１例2023
- Author(s)
  河村理恵,中島葉子,稲垣秀人,七里由衣,村瀬悠理,倉橋浩樹
- Organizer
  第46回日本小児遺伝学会　学術集会
- Data Source
  KAKENHI-PROJECT-23K06619
[Presentation] Presence of small 21p-21p chromosome in mosaic rob(21;21) carrier2023
- Author(s)
  Rie Kawamura, Ikumi Moriyama, Shunsaku Fujii, Takeshi Iwasa, Akira Kuwahara, Minoru Irahara, Ei Yuzawa, Hiroki Kurahashi
- Organizer
  日本人類遺伝学会　第68回大会
- Data Source
  KAKENHI-PROJECT-23K06619
[Presentation] ゲノム編集技術によるダウン症候群由来細胞の核型修正を通じた細胞再生2023
- Author(s)
  脇田幸子、原万里、宮川世志幸、北畠康司、倉橋浩樹、橋詰令太郎
- Organizer
  第2回ダウン症基礎研究会
- Data Source
  KAKENHI-PROJECT-21K06835
[Presentation] CRISPR/Cas9を用いた染色体切断による異数性細胞からの染色体除去は可能か？2022
- Author(s)
  橋詰令太郎、脇田幸子、原万里、北畠康司、宮川世志幸、倉橋浩樹
- Organizer
  第111回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-21K06835
[Presentation] CRISPR/Cas9システムの染色体削減と核型修正への応用 Extra chromosome 21 elimination using the CRISPR-Cas9 platform in the iPS cell model for Down syndrome2022
- Author(s)
  橋詰令太郎、脇田幸子、原万里、澤田博文、竹林慎一郎、北畠康司、宮川世志幸、倉橋浩樹
- Organizer
  日本人類遺伝学会第6７回大会
- Data Source
  KAKENHI-PROJECT-21K06835
[Presentation] 次世代型PGD/PGSの現状と問題点2017
- Author(s)
  倉橋浩樹
- Organizer
  第62回日本生殖医学会学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Recent advance in our understanding of the molecular nature of chromosomal abnormalities2017
- Author(s)
  倉橋浩樹
- Organizer
  日本人類遺伝学会第62回大会
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 網羅的手法による次世代型PGD ~PGDの実際とこれから2017
- Author(s)
  倉橋浩樹
- Organizer
  JISARTシンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Screening for Genetic Disease within the Asian Context2017
- Author(s)
  Hiroki Kurahashi
- Organizer
  ASPIRE 3rd Masterclass
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 造血器腫瘍のクリニカルシーケンスにおける遺伝診療体制の構築2017
- Author(s)
  倉橋浩樹
- Organizer
  第59回日本小児血液・がん学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 網羅的手法による次世代型PGD ～PGDの実際とこれから2017
- Author(s)
  倉橋浩樹
- Organizer
  JISARTシンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 造血器腫瘍のクリニカルシーケンスにおける遺伝診療体制の構築2017
- Author(s)
  倉橋浩樹
- Organizer
  第５９回日本小児血液・がん学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 着床前診断の現状と今後の展望2017
- Author(s)
  倉橋浩樹
- Organizer
  第19回日本イアンドナルド超音波講座
- Invited
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD -mutation screening with long preserved dried umbilical cord and detection of mosaicism-.2016
- Author(s)
  Unzaki A, Taniguchi-Ikeda M, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] 13q22.2q34 tetrasomy mosaicism due to an inverted duplication with a neocentromere.2016
- Author(s)
  Hattori T, Togawa T, Togawa Y, Kawabe H, Kato T, Kurahashi H, Saitoh S, Kouwaki M, Koyama N.
- Organizer
  ASHG2016
- Place of Presentation
  Vancouver, Canada
- Year and Date
  2016-10-18
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Spermatogenic failure by impaired meiotic sex chromosome inactivation in a mouse with reciprocal translocation.2016
- Author(s)
  Tsutsumi M, Kato T, Inagaki H, Ohye T, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Palindrome-mediated recurrent translocations in humans.2016
- Author(s)
  Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Gene expression analysis reveals molecular phenotypes related to schizophrenia in Neurogranin knockout mice.2016
- Author(s)
  Hattori S, Hagihara H, Kameyama T, Ouchi Y, Inagaki H, Kurahashi H, Huang FL, Huang KP, Miyakawa T.
- Organizer
  Neuroscience 2016
- Place of Presentation
  San Diego, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Relationship between various clinical features in a genotyped population investigated for tuberous sclerosis complex.2016
- Author(s)
  Ishihara N, Sasaki H, Kato T, Inagaki H, Tsutsumi M, Shiroki R, Kurahashi H.
- Organizer
  ASHG2016
- Place of Presentation
  Vancouver, Canada
- Year and Date
  2016-10-18
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Mechanism for Structural Variation.2016
- Author(s)
  Kurahashi H.
- Organizer
  APAC RGH Symposium Singapore
- Place of Presentation
  Singapore
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Cell culture model for X-linked disorder: craniofrontonasal dysplasia and severe phenotype in female.2016
- Author(s)
  Sugimoto M, Inagaki H, Tsutsumi M, Inoue Y, Taguchi Y, Boda H, Miyata M, Okumoto T, Yoshikawa T, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Prenatal diagnosis of the Premature chromosome separation/ mosaic variegated aneuploidy (PCS/MVA) syndrome in fetus with microcephalus.2016
- Author(s)
  Ohashi M, Yamaguchi M, Ishii M, Yamaguchi T, Akeno K, Fijisaki M, Sumiyoshi C, Sameshima H, Ozaki M, Kato T, Inagaki H, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Mechanisms of interchromosomal insertional translocation.2016
- Author(s)
  Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] A PDE3A mutation in familial hypertension and brachydactyly syndrome.2016
- Author(s)
  Inagaki H, Boda H, Uchida H, Takaiso N, Ouchi Y, Fujita N, Kuno A, Hata T, Nagatani A, Funamoto Y, Miyata M, Yoshikawa T, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] De novo translocation frequency of the recurrent constitutional t(11;22)(q23;q11.2) in normal somatic tissues.2016
- Author(s)
  Kurahashi H, Kato T, Suzuki M, Tsutsumi M, Ohye T, Inagaki H.
- Organizer
  ESHG2016
- Place of Presentation
  Barcelona, Spain
- Year and Date
  2016-05-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Sex determination of the fetus by noninvasive prenatal testing (NIPT) with maternal blood.2016
- Author(s)
  Noda Y, Nishizawa H, Kato T, Kambayashi A, Terasawa S, Miyazaki J, Ito M, Kurahashi H, Fujii T.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] A child presenting distinct phenotype in severe alternating hemiplegia with a novel ATP1A3 mutation.2016
- Author(s)
  Ishihara N, Inagaki H, Miyake M, Ouchi Y, Ohye T, Tsutsumi M, Yoshikawa T, Kurahashi H.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Increased levels of soluble corin in patients with pre-eclampsia and fetal growth restriction.2016
- Author(s)
  Miyazaki J, Nishizawa H, Kambayashi A, Ito M, Noda Y, Terasawa S, Kato T, Miyamura H, Sekiya T, Kurahashi H, Fujii T.
- Organizer
  ICHG2016
- Place of Presentation
  Kyoto, Japan、京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Mechanistic analysis and prediction of interchromosomal insertional translocation.2016
- Author(s)
  Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kurahashi H.
- Organizer
  ASHG2016
- Place of Presentation
  Vancouver, Canada
- Year and Date
  2016-10-18
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Missense mutations in the PLK4 gene identified in a patient with autosomal recessive microcephaly and chorioretinopathy.2016
- Author(s)
  Tsutsumi M, Yokoi S, Miya F, Miyata M, Kato M, Okamoto N, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Saitoh S, Kurahashi H.
- Organizer
  ASHG2016
- Place of Presentation
  Vancouver, Canada
- Year and Date
  2016-10-18
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04710
[Presentation] Massive parallel sequencing revealed the conformational dynamics of the non-B form DNA at the promoter2015
- Author(s)
  Inagaki H, Miyamura H, Tsutsumi M, Kato T, Nishizawa H, Kurahashi H
- Organizer
  ASHG2015
- Place of Presentation
  Baltimore
- Year and Date
  2015-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Age-related increase of aneuploidy in human oocytes2015
- Author(s)
  Kurahashi H
- Organizer
  IFFS/JSRM International Meeting 2015
- Place of Presentation
  Yokohama
- Year and Date
  2015-04-26
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Breakpoint analysis of the recurrent constitutional t(8;22) (q24.13;q11.21) translocation2015
- Author(s)
  Kurahashi H, Mishra D, Kato T, Inagaki H, Kosho T, Wakui K et al.
- Organizer
  ESHG2015
- Place of Presentation
  Glasgow
- Year and Date
  2015-06-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Towards the identification of novel palindrome-mediated translocations2013
- Author(s)
  Kurahashi H, Inagaki H, Ohye T, Tsutsumi M, Kato T, Okamoto N
- Organizer
  European Human Genetics Conference 2013
- Place of Presentation
  Paris, France
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Age-related decrease of meiotic cohesins in human oocytes2013
- Author(s)
  Tsutsumi M, Fujiwara R, Nishizawa H, Kogo H, Inagaki H, Ohye T, Kato T, Kurahashi H
- Organizer
  ASHG 2013
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] HORMAD2 phosphorylation may be involved in the initiation of meiotic silencing of unsynapsed chromatin2013
- Author(s)
  Kogo H, Tsutsumi M, Iizuka-Kogo A, Kurahashi H, Matsuzaki T
- Organizer
  EMBO Conference Meiosis
- Place of Presentation
  Dresden, Germany
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Disease-causing candidate genes in the patients with congenital vertebral anomalies2013
- Author(s)
  Nakamura Y, Kikugawa S, Seki S, Takahata M, Terai H, Akaoka Y, Matsubara M, Fujioka F, Inagaki H, Kurahashi H, Kobayashi T, Kato H
- Organizer
  ASHG 2013
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromes2012
- Author(s)
  Inagaki, H., Ohye, T., Kogo, H., Tsutsum,i Kurahashi H
- Organizer
  FASEB SRC:“Dynamic DNA structures in biology”
- Place of Presentation
  Saxtons River, USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Faukuyama muscular dystrophy2012
- Author(s)
  Taniguchi M, Kobayashi K, Kanagawa M, Yu CC, Oda T, Kuga A, Kurahashi H, Akmen HO,DiMauro S, Yokota T, Takeda S, Toda T
- Organizer
  ASHG 2012, annual meeting
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with pre-eclampsia2012
- Author(s)
  Kurahashi H, Miyamura H, Nishizavva H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Udagawa Y
- Organizer
  European Society of Human Genetics Conference 2012
- Place of Presentation
  Nurnberg, Germany
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with preeclampsia2012
- Author(s)
  Miyamura H, Nishizawa H, Ota S,Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kurahashi H, Udagawa Y.
- Organizer
  The XX FIGO World Congress
- Place of Presentation
  Rome, Italy
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with Pre-eclampsia2012
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Udagawa Y
- Organizer
  European Society of Human Genetics Conference 2012
- Place of Presentation
  Nurnberg, Germany
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Faukuyama muscular dystrophy2012
- Author(s)
  Taniguchi M, Kobayashi K, Kanagawa M, Yu CC, Oda T, Kuga A, Kurahashi H, Akmen HO, DiMauro S, Yokota T, Takeda S, Toda T
- Organizer
  ASHG 2012, annual meeting
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with preeclampsia2012
- Author(s)
  Miyamura H, Nishizavva H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kurahashi H, Udagawa Y
- Organizer
  The XX FIGO World Congress
- Place of Presentation
  Rome, Italy
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Mechanism of recurrent translocation t(11; 22) initiated by cruciform conformation of palindromes2012
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kurahashi H
- Organizer
  FASEB SRC : "Dynamic DNA structures in biology"
- Place of Presentation
  Saxtons River, USA
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromes2012
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kurahashi H.
- Organizer
  FASEB SRC:"Dynamic DNA structures in biology
- Place of Presentation
  Saxtons River, USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with preeclampsia2012
- Author(s)
  Miyamura H, Nishizavva H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kurahashi H, Udagawa Y
- Organizer
  The XX FIGO World Congress
- Place of Presentation
  Rome, Italy
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Faukuyama muscular dystrophy2012
- Author(s)
  Taniguchi M, Kobayashi K, Kanagawa M, Yu CC, Oda T, Kuga A, Kurahashi H, Akmen HO, DiMauro S, Yokota T, Takeda S, Toda T
- Organizer
  ASHG 2012, annual meeting
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] ラット多発性嚢胞腎における PPARγアゴニスト投与の治療効果に関する網羅的遺伝子発現プロファイリング.2012
- Author(s)
  吉原大輔、釘田雅則、倉橋浩樹、森田美和、比企能之、山口太美雄、豊原敬文、阿部高明、長尾静子(枝澄香)
- Organizer
  第55回日本腎臓学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromes2012
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kurahashi H
- Organizer
  FASEB SRC : "Dynamic DNA structures in biology"
- Place of Presentation
  Saxtons River, USA
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Obstetric complication-associated ANXA5promoter polymorphisms affect gene expression via DNA secondary structures2012
- Author(s)
  Inagaki H, Ota S, Nishizawa H, Miyamura H, Nakahira K, Suzuki M, Nishiyama S, Udagawa Y, Yanagihara I, Kurahashi H.
- Organizer
  ASHG 2012, annual meeting
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with pre-eclampsia2012
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S,Suzuki M, Inagaki A, Egusa H, Nishiyama S, Udagawa Y
- Organizer
  European Society of Human Genetics Conference 2012
- Place of Presentation
  Nurnberg, Germany
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Faukuyama muscular dystrophy2012
- Author(s)
  Taniguchi M, Kobayashi K, Kanagawa M, Yu CC, Oda T, Kuga A, Kurahashi H, Akmen H0, DiMauro S, Yokota T, Takeda S, Toda T
- Organizer
  ASHG 2012, annual meeting
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] ラット多発性嚢胞腎におけるPPARγアゴニスト投与の治療効果に関する網羅的遺伝子発現プロファイリング2012
- Author(s)
  吉原大輔、釘田雅則、倉橋浩樹、森田美和、比企能之、山口太美雄、豊原敬文、阿部高明、長尾静子 (枝澄香)
- Organizer
  第55回日本腎臓学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Global gene expression profiling in kidneys of PPAR-γ agonist-treated PCK rats, an orthologous model of human ARPKD.2011
- Author(s)
  Yoshihara D, Kugita M, Kurahashi H, Morita M, Hiki Y, Yamaguchi T, Aukema HM, Wallace DP, Calvet JP, Toyohara T, Abe T, Nagao S.
- Organizer
  American Society of Nephrology 44th Annual Meeting & Scientific Exposition 2011
- Place of Presentation
  Philadelphia, PA USA
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Identification of a recombination hotspot sequence at the breakpoint region of the 22q11 deletion using a yeast model2011
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Emanuel BS, Kurahashi H.
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal,Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] 対合不全のチェックポイントの男女間の違いと不妊・習慣流産2011
- Author(s)
  倉橋浩樹
- Organizer
  文部科学省科学研究費補助金特定領域研究特定領域研究「生殖系列の世代サイクルとエピゲノムネットワーク」第4回公開シンポジウム
- Place of Presentation
  豊中
- Data Source
  KAKENHI-PROJECT-21590346
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Negi R, Markoff A, Yanagihara I, Udagawa, Y
- Organizer
  European Society of Human Genetics Conference 2011.
- Place of Presentation
  Amsterdam, Netherlands
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] 多発性嚢胞腎ラット PCK の腎臓における PPARγアゴニスト投与の治療効果に関する網羅的遺伝子発現プロファイリング2011
- Author(s)
  吉原大輔、釘田雅則、山口太美雄、倉橋浩樹、長尾枝澄香(静子)
- Organizer
  第43回藤田医学会総会
- Place of Presentation
  豊明
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  Keystone Symposia : Functional Consequences of Structural Variation in the Genome
- Place of Presentation
  Steamboat Springs, Colorado, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] PPAR-γagonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease.2011
- Author(s)
  Daisuke Yoshihara, Hiroki Kurahashi, M iwa Morita, Masano r i K ugit a, Yoshiyuki Hiki, Harold M Aukema, Tamio Yamaguchi, James P Calvet, Darren PWallace, Shizuko Nagao.
- Organizer
  World Congress of Nephrology 2011
- Place of Presentation
  Vancouver, Canada
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  Keystone Symposia : Functional Consequences of Structural Variation in the Genome
- Place of Presentation
  Steamboat Springs, Colorado, USA
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] Identification of a recombination hotspot sequence at the breakpoint region of the 22q11 deletion using a yeast model2011
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Emanuel BS, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H
- Organizer
  27th Annual Meeting of ESHRE-Stockholm 2011
- Place of Presentation
  Stockholm, Sweden
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromic sequences2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H
- Organizer
  27th Annual Meeting of ESHRE-Stockholm 2011
- Place of Presentation
  Stockholm, Sweden
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans. Keystone Symposia: Functional Consequences of Structural Variation in the Genome2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  Steamboat Springs
- Place of Presentation
  Colorado, USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] ヒト多発性嚢胞腎症のラットモデルにおける PPAR-γアゴニストの治療効果2011
- Author(s)
  吉原大輔、倉橋浩樹、森田美和、釘田雅則、比企能之、Aukema Harold、山口太美雄、Calvet James、Wallace Darren、長尾枝澄香(静子)
- Organizer
  第54回日本腎臓学会学術総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Polymorphisms in the annexin A5 gene promoter...2011
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, et al.
- Organizer
  European Society of Human Genetics Conference
- Place of Presentation
  Amsterdam, Netherlands
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  Kyestone Symposia : Functional consequences of structural variation in the genome
- Place of Presentation
  Steamboat Springs, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutation in the SYCP3 gene identified in a woman with recurrent pregnancy loss affect the synaptonemal complex conformation at meiotic prophase I2011
- Author(s)
  Tsutsumi M, Kogo H, Inagaki H, Ohye T, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mechanism of recurrent translocation t(11 ; 22) initiated by cruciform conformation of palindromic sequences2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H.
- Organizer
  59th Annual Clinical Meeting, ACOG
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Global gene expression profiling in kidneys of PPAR-gamma agonist-treated PCK rats, an orthologous model of human ARPKD2011
- Author(s)
  Yoshihara D, Kugita M, Kurahashi H, Morita M, Hiki Y, Yamaguchi T, Aukema HM, Wallace DP, Calvet JP, Toyohara T, Abe T, Nagao S
- Organizer
  American Society of Nephrology 44th Annual Meetine & Scientific Exposition
- Place of Presentation
  Philadelphia, PA USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama s, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H
- Organizer
  59th Annual Clinical Meeting, ACOG
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T,Imayoshi Y, Markoff A, Yanagihara I,Udagawa Y, Kurahashi H.
- Organizer
  27th Annual Meeting of ESHRE - Stockholm 2011
- Place of Presentation
  Stockholm, Sweden
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromic sequences2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] PPAR-gamma agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S
- Organizer
  World Congress of Nephrology 2011
- Place of Presentation
  Vancouver, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Identification of a novel palindrome mediated translocation associated with the t(3 ; 8) of hereditary renal cancer2011
- Author(s)
  Kato T, Sheridan MB, Hacker AM, Inagaki H, Glover TW, Plon SE, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] HORMAD1-dependent synapsis checkpoint in mammalian meiosis2011
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Kurahashi H
- Organizer
  2011 FASEB Summer Research Conferences, Genetic Recombination & Genome Rearrangements
- Place of Presentation
  Steamboat Springs, USA
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Identification of a novel palindrome mediated translocation associated with the t(3;8) of hereditary renal cancer2011
- Author(s)
  Kato T, Sheridan MB, Hacker AM, Inagaki H, Glover TW, Plon SE, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromic sequences2011
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal,Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] HORMAD1-deficiency causes azoospermia in males and pregnancy loss in females2011
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Global gene expression profiling in kidneys of PPAR-gamma agonist-treated PCK rats, an orthologous model of human ARPKD2011
- Author(s)
  Yoshihara D, Kugita M, Kurahashi H, Morita M, Hiki Y, Yamaguchi T, Aukema HM, Wallace DP, Calvet JP, Toyohara T, Abe T, Nagao S
- Organizer
  American Society of Nephrology 44th Annual Meeting & Scientific Exposition
- Place of Presentation
  Philadelphia, PA USA
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Mutation in the SYCP3 gene identified in a woman with recurrent pregnancy loss affect the synaptonemal complex conformation at meiotic prophase I2011
- Author(s)
  Tsutsumi M, Kogo H, Inagaki H, Ohye T,Kurahashi H.
- Organizer
  The 12th International Congress of Human Genetics, Montreal
- Place of Presentation
  Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the ANXA5gene promoter in Japanese women with pre-eclampsia2011
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S,Suzuki M, Inagaki A, Egusa H, Nishiyama S, Udagawa Y.
- Organizer
  European Society of Human Genetics Conference 2012.
- Place of Presentation
  Nurnberg,Germany
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Mutation in the SYCP3 gene identified in a woman with recurrent pregnancy loss affect the synaptonemal complex conformation at meiotic prophase I2011
- Author(s)
  Tsutsumi M, Kogo H, Inagaki H, Ohye T, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Global gene expression profiling in kidneys of...2011
- Author(s)
  Yoshihara D, Kugita M, Kurahashi H, et al.
- Organizer
  American Society of Nephrology 44th Annual Meeting
- Place of Presentation
  Philadelphia, PA USA
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] HORMAD1-dependent synapsis checkpoint in mammalian meiosis2011
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Kurahashi H
- Organizer
  2011 FASEB Summer Research Conferences, Genetic Recombination & Genome Rearrangements
- Place of Presentation
  Steamboat Spring, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Global gene expression profiling in kidneys of PPAR-gamma agonist-treated PCK rats, an orthologous model of human ARPKD2011
- Author(s)
  Yoshihara D., Kugita M., Kurahashi H, Morita M, Hiki Y, Yamaguchi T, Aukema HM, Wallace DP, Calvet JP, Toyohara T., Abe T., Nagao S.
- Organizer
  American Society of Nephrology 44th Annual Meeting & Scientific Exposition
- Place of Presentation
  Philadelphia, PA USA
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] 多発性嚢胞腎ラットPCKの腎臓におけるPPARγアゴニスト投与の治療効果に関する網羅的遺伝子発現プロファイリング2011
- Author(s)
  吉原大輔、釘田雅則、山口太美雄、倉橋浩樹、長尾枝澄香(静子)
- Organizer
  第43回藤田医学会総会
- Place of Presentation
  豊明、日本
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] ヒト多発性嚢胞腎症のラットモデルにおけるPPAE-γアゴニストの治療効果2011
- Author(s)
  吉原大輔、倉橋浩樹、森田美和、釘田雅則、比企能之、Aukema Harold、山口太美雄、Calvet James、Wallace Darren、長尾枝澄香(静子)
- Organizer
  第54回日本腎臓学会学術総会
- Place of Presentation
  横浜、日本
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] 網羅的遺伝子発現解析を用いた多発性嚢胞腎ラットPCKにおけるPPARγアゴニストによる治療機序の検証2011
- Author(s)
  吉原大輔、釘田雅則、倉橋浩樹、森田美和、比企能之、山口太美雄、豊原敬文、阿部高明、長尾枝澄香(静子)
- Organizer
  第19回嚢胞性腎疾患研究会
- Place of Presentation
  東京、日本
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] PPAE-γ agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Daisuke Yoshihara., Hiroki Kurahashi., Miwa Morita., Masanori Kugita., Yoshiyuki Hiki., Harold M.Aukema., Tamio Yamaguchi., James P.Calvet, Darren P.Wallace., Shizuko Nagao.
- Organizer
  World Congress of Nephrology 2011
- Place of Presentation
  Vancouver, Canada
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] PPAR-gamma agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S
- Organizer
  World Congress of Nephrology 2011
- Place of Presentation
  Vancouver, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] 羅的遺伝子発現解析を用いた多発性嚢胞腎ラット PCK における PPAR-γアゴニストによる治療機序の検証2011
- Author(s)
  吉原大輔、釘田雅則、倉橋浩樹、森田美和、比企能之、山口太美雄、豊原敬文、阿部高明、長尾枝澄香(静子)
- Organizer
  第19回嚢胞性腎疾患研究会
- Place of Presentation
  東京
- Year and Date
  2011-09-11
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Identification of a novel palindrome mediated translocation associated with the t(3;8) of hereditary renal cancer2011
- Author(s)
  Kato T, Sheridan MB, Hacker AM, Inagaki H, Glover TW, Plon SE, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Negi R, Markoff A, Yanagihara I, Udagawa, Y.
- Organizer
  European Society of Human Genetics Conference 2011.
- Place of Presentation
  Amsterdam, Netherlands
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Kurahashi H, Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Negi R, Markoff A, Yanagihara I, Udagawa, Y
- Organizer
  European Society of Human Genetics Conference 2011
- Place of Presentation
  Amsterdam, Netherlands
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Identification of a novel palindrome mediated translocation associated with the t(3;8) of hereditary renal cancer2011
- Author(s)
  Kato T, Sheridan MB, Hacker AM, Inagaki H, Glover TW, Plon SE, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] Identification of a recombination hotspot sequence at the breakpoint region of the 22q11 deletion using a yeast model2011
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Emanuel BS, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] PPAR-gamma agonist ameliorates kidney and liver...2011
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, et al.
- Organizer
  World Congress of Nephrology 2011
- Place of Presentation
  Vancouver, Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] HORMAD1-deficiency causes azoospermia in males and pregnancy loss in females2011
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H,Kurahashi H.
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-23659182
[Presentation] Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss2011
- Author(s)
  Miyamura H, Nishizawa H, Ota S, Suzuki M, Inagaki A, Egusa H, Nishiyama S, Kato T, Pryor-Koishi K, Nakanishi I, Fujita T, Imayoshi Y, Markoff A, Yanagihara I, Udagawa Y, Kurahashi H
- Organizer
  59th Annual Clinical Meeting, ACOG
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] HORMAD1-deficiency causes azoospermia in males and pregnancy loss in females2011
- Author(s)
  Kogo H, Tsutsumi M, Ohye T, Inagaki H, Kurahashi H
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PUBLICLY-23013019
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The American Society of Human Genetics 60th Annual Meeting
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The 7th 3R Symposium
- Place of Presentation
  Toyama, Japan
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] 多発性嚢胞腎ラットモデルPCKの腎臓と肝臓における細胞情報伝達系の解析2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、山口太美雄、倉橋浩樹、長尾静子
- Organizer
  第42回藤田医学会総会
- Place of Presentation
  豊明
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Paternal origin of the de novo constitutional t(11;22)(q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MVE, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Organizer
  European Society of Human Genetics Conference 2010.
- Place of Presentation
  Gothenburg, Sweden
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The American Society of Human Genetics 60th Annual Meeting
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] 多発性嚢胞腎ラットモデル PCK の腎臓と肝臓における細胞情報伝達系の解析.2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、山口太美雄、倉橋浩樹、長尾静子
- Organizer
  第42回藤田医学会総会
- Place of Presentation
  豊明
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] 嚢胞性腎臓疾患モデル Cy ラットにおける嚢胞形成と RXR との関連性についての検討.2010
- Author(s)
  釘田雅則、西井一宏、森田美和、吉原大輔、山口太美雄、日下守、倉橋浩樹、長尾静子
- Organizer
  第42回藤田医学会総会
- Place of Presentation
  豊明
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] PCK ラットの腎臓と肝臓における PPAR-γアゴニストの治療効果2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、山口太美雄、倉橋浩樹、長尾静子
- Organizer
  第18回嚢胞性腎疾患研究会
- Place of Presentation
  東京
- Year and Date
  2010-10-31
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Mutation of the SYCP3 gene in women with recurrent pregnancy loss.2010
- Author(s)
  Kurahashi H, Tsutsumi M, Egusa H, Nishiyama S, Suzuki M, Kogo H, Inagaki H, Ohye T.
- Organizer
  International Symposium on Epigenome Network, Development and Reprogramming of Germ Cells.
- Place of Presentation
  Fukuoka, Japan
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] PCKラットの腎臓と肝臓におけるPPAR-γアゴニストの治療効果2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、山口太美雄、倉橋浩樹、長尾静子
- Organizer
  第18回嚢胞性腎疾患研究会
- Place of Presentation
  東京
- Year and Date
  2010-10-31
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] 嚢胞性腎臓疾患モデルCyラットにおける嚢胞形成とRXRとの関連性についての検討2010
- Author(s)
  釘田雅則、西井一宏、森田美和、吉原大輔、山口太美雄、日下守、倉橋浩樹、長尾静子
- Organizer
  第42回藤田医学会総会
- Place of Presentation
  豊明
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Palindrome-mediated chromosomal translocation in humans.2010
- Author(s)
  Kurahashi H.
- Organizer
  FASEB Summer Research Conferences. Biological Impact of Alternatively Structured DNA.
- Place of Presentation
  Steamboat Springs, Colorado, USA(招待講演)
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Paternal origin of the de novo constitutional t(11;22) (q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MVE, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Organizer
  European Society of Human Genetics Conference 2010.
- Place of Presentation
  Gothenburg, Sweden
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  The 7th 3R Symposium
- Place of Presentation
  Toyama, Japan
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Thiazolidinedione Ameliorates Autosomal Recessive Polycystic Kidney and Liver Disease in the PCK Rat, an Orthologous Model of Human ARPKD.2010
- Author(s)
  Yoshihara D., Kurahashi H., Morita M., Kugita M., Hiki Y., Aukema H.M., Yamaguchi T., Calvet J.P., Wallace D.P., Nagao S.
- Organizer
  American Society of Nephrology 43rd Annual Meeting & Scientific Exposition
- Place of Presentation
  Denver, CO USA
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Palindrome-mediated chromosomal translocation in humans.2010
- Author(s)
  Kurahashi H
- Organizer
  FASEB Summer Research Conferences. Biological Impact of Alternatively Structured DNA
- Place of Presentation
  Colorado, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Palindrome-mediated chromosomal translocation in humans.2010
- Author(s)
  Kurahashi H.
- Organizer
  FASEB Summer Research Conferences. Biological Impact of Alternatively Structured DNA.
- Place of Presentation
  Steamboat Springs, Colorado, USA(招待講演)
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  Keystone Symposia : Functional Consequences of Structural Variation in the Crenome
- Place of Presentation
  Steamboat Springs, Colorado, USA
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] ヒトARPKDとオーソログな遺伝子変異モデルであるPCKラットの腎・肝組織における情報伝達系の検討2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、倉橋浩樹、山口太美雄、長尾静子
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The American Society of Human Genetics 60th Annual Meeting
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Palindrome-mediated chromosomal translocation in humans.2010
- Author(s)
  Kurahashi H.
- Organizer
  FASEB Summer Research Conferences. Biological Impact of Alternatively Structured DNA.
- Place of Presentation
  Steamboat Springs, Colorado, USA(招待講演)
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] ヒト ARPKDとオーソログな遺伝子変異モデルである PCK ラットの腎・肝組織における情報伝達系の検討.2010
- Author(s)
  吉原大輔、森田美和、釘田雅則、倉橋浩樹、山口太美雄、長尾静子
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] Paternal origin of the de novo constitutional t(11;22) (q23;q11).2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MVE, Medne L, Zackai EH, Emanuel BS, Kurahashi H.
- Organizer
  European Society of Human Genetics Conference 2010.
- Place of Presentation
  Gothenburg, Sweden
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutation of the SYCP3 gene in women with recurrent pregnancy loss.2010
- Author(s)
  Kurahashi H, Tsutsumi M, Egusa H, Nishiyama S, Suzuki M, Kogo H, Inagaki H, Ohye T.
- Organizer
  International Symposium on Epigenome Network, Development and Reprogramming of Germ Cells.
- Place of Presentation
  Fukuoka, Japan
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  The American Society of Human Genetics 60th Annual Meeting
- Place of Presentation
  Washington DC, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The 7th 3R Symposium
- Place of Presentation
  Toyama, Japan
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Thiazolidinedione Ameliorates Autosomal Recessive Polycystic Kidney and Liver Disease in the PCK Rat, an Orthologous Model of Human ARPKD.2010
- Author(s)
  Yoshihara D, Kurahashi H, Morita M, Kugita M, Hiki Y, Aukema HM, Yamaguchi T, Calvet JP, Wallace DP, Nagao S.
- Organizer
  American Society of Nephrology 43rd Annual Meeting & Scientific Exposition.
- Place of Presentation
  Denver, CO USA
- Data Source
  KAKENHI-PROJECT-22590351
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to a recurrent translocation in humans.2010
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H.
- Organizer
  The 7th 3R Symposium
- Place of Presentation
  Toyama, Japan
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] Paternal origin of the de novo constitutional t(11 ; 22)(q23 ; q11)2010
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MVE, Medne L, Zackai EH, Emanuel BS, Kurahashi H
- Organizer
  European Society of Human Genetics Conference 2010
- Place of Presentation
  Gothenburg, Sweden
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutation of the SYCP3 gene in women with recurrent pregnancy loss2010
- Author(s)
  Kurahashi H, Tsutsumi M, Egusa H, Nishiyama S, Suzuki M, Kogo H, Inagaki H, Ohye T.
- Organizer
  International Symposium on Epigenome Network, Development and Reprogramming of Germ Cells.
- Place of Presentation
  Fukuoka, Japan
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Parental origin of de novo t(11 ; 22)(q23 ; q11)2009
- Author(s)
  Ohye T, Inagaki H, Kogo H, Tsutsumi M, Kato T, Tong M, Macville MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H
- Organizer
  59th annual meeting of American Society of Human Genetics
- Place of Presentation
  Hawai, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Kurahashi H, Bolor H, Mori T, Nishiyama S, Inagaki H, Kogo H, Tsutsumi M, Ohye T
- Organizer
  European Society of Human Genetics conference 2009
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Kurahashi H, Bolor H, Mori T, Nishiyama S, Inagaki H, Kogo H, Tsutsumi M, Ohye T
- Organizer
  European Society of Human Genetics conference 2009
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Kurahashi, H.
- Organizer
  European Human Genetics Conferences
- Place of Presentation
  Austria
- Year and Date
  2009-05-25
- Data Source
  KAKENHI-PROJECT-21590346
[Presentation] Two successive cleavages in palindrome-mediated translocation2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Ohye T, Kogo H, Shaikh TH, Emanuel BS
- Organizer
  Genome Instability and DNA Repair
- Place of Presentation
  Taos, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Parental origin of de novo t(11 ; 22)(q23 ; q11)2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Ohye T, Kogo H, Shaikh TH, Emanuel BS
- Organizer
  59th annual meeting of American Society of Human Genetics
- Place of Presentation
  Honolulu, Hawai, USA
- Data Source
  KAKENHI-PROJECT-21659085
[Presentation] Parental origin of de novo t(11;22)(q23;q11)2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Ohye T, Kogo H, Shaikh TH, Emanuel BS
- Organizer
  59th annual meeting of American Society of Human Genetics
- Place of Presentation
  Honolulu, Hawai, USA
- Data Source
  KAKENHI-PROJECT-21390101
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2009
- Author(s)
  Kurahashi H, Bolor H, Mori T, Nishiyama S, Inagaki H, Kogo H, Tsutsumi M, Ohye T
- Organizer
  European Society of Human Genetics conference 2009
- Place of Presentation
  Vienna, Austria
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Parental origin of de novo t(11;22)(q23;q11)2009
- Author(s)
  Kurahashi H, Inagaki H, Kato T, Ohye T, Kogo H, Shaikh TH, Emanuel BS
- Organizer
  59th annual meeting of American Society of Human Genetics
- Place of Presentation
  Honolulu, Hawai, USA
- Data Source
  KAKENHI-PUBLICLY-21028020
[Presentation] Possible post-meiotic origin of the constitutional t(11 ; 22)2008
- Author(s)
  Kato, T., Inagaki, H., Kogo, H., Ohye, T., Yamada, K., Emanuel, B.S., Kurahashi, H.
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Barcelona, Spain
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Artemis cleaves cruciform-forming palindromic DNA leading to recurrent translocation in humans.2008
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Tong M, Tsutsumi M, Emanuel BS, Kurahashi H
- Organizer
  ASHG AT/GI Satellite Meeting
- Place of Presentation
  Philadelphia, PA
- Year and Date
  2008-11-11
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss.2008
- Author(s)
  Kurahashi H. Bolor H, Mori T, Nishiyama S, Inagaki H, Kogo H, Tsutsumi M, Ohye T
- Organizer
  58th annual meeting of ASHG
- Place of Presentation
  Philadelphia, PA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.2008
- Author(s)
  Kurahashi H.
- Organizer
  FASEB SRC. DNA Palindromes.
- Place of Presentation
  Saxtons River, VT
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Possible post-meiotic origin of the constitutionalt(11 ; 22).2008
- Author(s)
  Kato T, Inagaki H, Kogo H, Ohye T, Yamada K, Emanuel BS, Kurahashi H
- Organizer
  European Human Genetics Conference
- Place of Presentation
  Barcelona, Spain
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Artemis cleaves cruciform-forming palindromic DNA leading to recurrent translocation in humans.2008
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Tong M, Tsutsumi M, Emanuel BS, Kurahashi H
- Organizer
  58th annual meeting of ASHG
- Place of Presentation
  Philadelphia, PA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Chromosomal instability mediated by non-B DNA : Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans. DNA Palindromes : Roles, consequences and implications of structurally ambivalent DNA2008
- Author(s)
  Kurahashi, H.
- Organizer
  FASEB Summer Research Conferences
- Place of Presentation
  Saxtons River, USA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Artemis cleaves cruciform-forming palindromic DNA leading to recurrent translocation in humans2008
- Author(s)
  Inagaki, H., Ohye, T., Kogo, H., Kato, T., Tong, M., Tsutsumi, M., Emanuel., B. S., Kurahashi, H.
- Organizer
  58th annual meeting of American Society of Human Genetics
- Place of Presentation
  Philadelphia, USA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Mutations of the SYCP3 gene in women with recurrent pregnancy loss2008
- Author(s)
  Kurahashi, H.
- Organizer
  58th annual meeting of American Society of Human Genetics
- Place of Presentation
  Philadelphia, USA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Artemis cleaves cruciform-forming palindromic DNA leading to recurrent translocation in humans.2008
- Author(s)
  Inagaki H, Ohye T, Kogo H, Kato T, Tong M, Tsutsumi M, Emanuel BS, Kurahashi H
- Organizer
  The 6th 3R Symposium
- Place of Presentation
  Kakegawa, Japan
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] DNA secondary structure-forming propensity dictates translocation frequency2007
- Author(s)
  Kato, T., Inagaki, H., Kogo, H., Ohye, T., Yamada, K., Emanuel, B. S., Kurahashi, H.
- Organizer
  European Human Genetics Conference 2007
- Place of Presentation
  Nice, France
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] DNA secondary structure-forming propensity dictates translocation frequency.2007
- Author(s)
  Kato, T., Inagaki, H., Kurahashi, H., et. al.
- Organizer
  European Human Genetics Conference 2007
- Place of Presentation
  Nice, France
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Possible post-meiotic origin of the constitutional t(11 ; 22)2007
- Author(s)
  Kato, T., Inagaki, H., Kogo, H., Ohye, T., Tong, M., Emanuel, B. S., Kurahashi, H.
- Organizer
  57th Annual Meeting of American Society of Human Genetics
- Place of Presentation
  San Diego, USA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Possible post-meiotic origin of the constitutional t(11;22).2007
- Author(s)
  Kato, T., Inagaki, H., Kurahashi, H., et. al.
- Organizer
  57th Annual Meeting of American Society of Human Genetics
- Place of Presentation
  San Diego, USA
- Data Source
  KAKENHI-PROJECT-19390097
[Presentation] Age-related decrease of meiotic cohesins in human oocytes
- Author(s)
  Kurahashi H, Tsutsumi M, Fujiwara R, Nishizawa H, Kogo H, Inagaki H, Ohye T, Kato T, Fujii T
- Organizer
  Eshre 2014
- Place of Presentation
  Munich, Germany
- Year and Date
  2014-06-29 – 2014-07-02
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Cytogenetic analysis of monopronucleated (1PN) zygotes after intracytoplasmic sperm injection and conventional in-vitro fertilization
- Author(s)
  Nishiyama S, Kato T, Kani C, Miyazaki J, Nishizawa H, Ochi M, Fujii T, Kurahashi H
- Organizer
  International Society for Mild Approaches in Assisted Reproduction
- Place of Presentation
  Sydney, Australia
- Year and Date
  2014-09-10 – 2014-09-12
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Age-related decrease of meiotic cohesins in human oocyte
- Author(s)
  Kurahashi H, Tsutsumi M, Fujiwara R, Nishizawa H, Kogo H, Inagaki H, Ohye T, Kato T, Fujii T
- Organizer
  Eshre 2014
- Place of Presentation
  Munich, Germany
- Year and Date
  2014-06-29 – 2014-07-02
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Two cases of lissencephaly with marked hydrocephalus caused by TUBA1A mutation
- Author(s)
  Ishihara N, Yokoi S, Yamamoto H, Natsume J, Tsutsumi M, Ohye T, Kato M, Saito S, Kurahashi H
- Organizer
  ASHG 2014
- Place of Presentation
  San Diego, CA
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Obstetric complication-associated ANXA5 promoter polymorphisms affect gene expression via G-quadruplex structure in vivo
- Author(s)
  Inagaki H, Ota S, Nishizawa H, Miyamura H, Nakahira K, Suzuki M, Tsutsumi M, Kato T, Nishiyama S, Udagawa Y, Yanagihara I, Kurahashi H
- Organizer
  FASEB SRC, Dynamic DNA Structures in Biology
- Place of Presentation
  Itasca, Illinois
- Year and Date
  2014-07-20 – 2014-07-25
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Detection of in vivo G-quadruplex structure of the ANXA5 promoter that contributes to the recurrent pregnancy loss
- Author(s)
  Inagaki H, Ota S, Miyamura H, Tsutsumi M, Kato T, Nishizawa H, Yanagihara I, Kurahashi H
- Organizer
  ASHG 2014
- Place of Presentation
  San Diego, CA
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Cytogenetic analysis of monopronucleated (1PN) zygotes after intracytoplasmic sperm injection and conventional in-vitro fertilization
- Author(s)
  Nishiyama S, Kato T, Kani C, Miyazaki J, Nishizawa H, Ochi M, Fujii T, Kurahashi H
- Organizer
  International Society for Mild Approaches in Assisted Reproduction
- Place of Presentation
  Sydney, Australia
- Year and Date
  2014-09-10 – 2014-09-12
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] EFNB1 mutation found in patients with craniofrontonasal syndrome in a Japanese family
- Author(s)
  Kato H, Okumoto T, Yoshimura Y, Taguchi Y, Sugimoto M, Inagaki H, Kurahashi H
- Organizer
  The　10th　Asian Pacific Craniofacial Association Conference
- Place of Presentation
  Adelaide, Australia
- Year and Date
  2014-10-03 – 2014-10-05
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Obstetric complication-associated ANXA5 promoter polymorphisms affect gene expression via G-quadruplex structure in vivo
- Author(s)
  Inagaki H, Ota S, Nishizawa H, Miyamura H, Nakahira K, Suzuki M, Tsutsumi M, Kato T, Nishiyama S, Udagawa Y, Yanagihara I, Kurahashi H
- Organizer
  FASEB SRC, Dynamic DNA Structures in Biology
- Place of Presentation
  Itasca, Illinois
- Year and Date
  2014-07-20 – 2014-07-25
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] EFNB1 mutation found in patients with craniofrontonasal syndrome in a Japanese family
- Author(s)
  Kato H, Okumoto T, Yoshimura Y, Taguchi Y, Sugimoto M, Inagaki H, Kurahashi H
- Organizer
  The　10th　Asian Pacific Craniofacial Association Conference
- Place of Presentation
  Adelaide, Australia
- Year and Date
  2014-10-03 – 2014-10-05
- Data Source
  KAKENHI-PROJECT-24390085
[Presentation] Two cases of lissencephaly with marked hydrocephalus caused by TUBA1A mutation
- Author(s)
  Ishihara N, Yokoi S, Yamamoto H, Natsume J, Tsutsumi M, Ohye T, Kato M, Saito S, Kurahashi H. Two cases of lissencephaly with marked hydrocephalus caused by TUBA1A mutation
- Organizer
  ASHG 2014
- Place of Presentation
  San Diego, CA
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-26670171
[Presentation] Detection of in vivo G-quadruplex structure of the ANXA5 promoter that contributes to the recurrent pregnancy loss
- Author(s)
  Inagaki H, Ota S, Miyamura H, Tsutsumi M, Kato T, Nishizawa H, Yanagihara I, Kurahashi H. Detection of in vivo G-quadruplex structure of the ANXA5 promoter that contributes to the recurrent pregnancy loss
- Organizer
  ASHG 2014
- Place of Presentation
  San Diego, CA
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-24390085
[]

1. NISHISYO Isamu (10228182)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
2. SHIZUKO Nagao (20183527)

# of Collaborated Projects: 3 results

# of Collaborated Products: 30 results
3. KOYAMA Kumiko (90294066)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. OHYE Tamae (10247661)

# of Collaborated Projects: 2 results

# of Collaborated Products: 19 results
5. MASANORI Kugita (50440681)

# of Collaborated Projects: 2 results

# of Collaborated Products: 29 results
6. YOSHIHARA Daisuke (70454402)

# of Collaborated Projects: 2 results

# of Collaborated Products: 30 results
7. Yuzawa Yukio (00191479)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
8. Saito Kuniaki (80262765)

# of Collaborated Projects: 2 results

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9. 三好康雄 (50283784)

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10. MORITA Miwa (90329699)

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11. YAGYU Shigeru (10200479)

# of Collaborated Projects: 1 results

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12. YAMAGUCHI Tamio (70536292)

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# of Collaborated Products: 30 results
13. HIKI Yoshiyuki (20156566)

# of Collaborated Projects: 1 results

# of Collaborated Products: 16 results
14. Fukami Maki (40265872)

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# of Collaborated Products: 1 results
15. Suzuki Atsushi (90340265)

# of Collaborated Projects: 1 results

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16. 坪井直毅 (50566958)

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# of Collaborated Products: 4 results
17. 鍋島俊隆 (70076751)

# of Collaborated Projects: 1 results

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18. 高橋和男 (90631391)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
19. 橋詰令太郎 (50456662)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
20. 河野光雄 (00234097)

# of Collaborated Projects: 1 results

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21. 脇田幸子 (20782981)

# of Collaborated Projects: 1 results

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22. 北畠康司 (80506494)

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# of Collaborated Products: 5 results
23. 宮川世志幸 (90415604)

# of Collaborated Projects: 1 results

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24. 真里谷奨 (50836757)

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25. 馬場剛 (60404654)

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26. 斉藤豪 (90145566)

# of Collaborated Projects: 1 results

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27. 河村理恵 (20735534)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
28. 稲垣秀人 (70308849)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
29. UCHIDA Hidetoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
30. IRITANI Syuji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
31. TANIGUCHI Mariko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
32. 戸田達史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
33. 加藤武馬

# of Collaborated Projects: 0 results

# of Collaborated Products: 5 results
34. 向後寛

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
35. 野津寛大

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
36. 飯島一誠

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
37. 畑忠善

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
38. 河本聡志

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
39. 尾崎紀夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
40. 杉原英志

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
41. 長坂美和子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
42. 柳原格

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kurahashi Hiroki 倉橋 浩樹

KURAHAS Hihiroki 倉橋 浩樹

KURAHASHI Hiroki 倉橋 浩樹

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Elucidation of mechanism for gross chromosomal rearrangements by genomic and epigenomic studiesPrincipal Investigator

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Establishment of new classification for structural variation based on next generation sequencingPrincipal Investigator

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Transcriptional regulation via DNA secondary structure: novel epigenetic mechanismPrincipal Investigator

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DNA replication-dependent/independent mechanism of gross chromosomal rearrangementPrincipal Investigator

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変異型SYCP3が相同染色体分配に与えるインパクトと習慣流産Principal Investigator

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Recurrent pregnancy loss -associated promoter polymorphisms affect ANXA5 ge ne expression via G -quadruplex propensityPrincipal Investigator

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加齢依存性第1減数分裂不分離と変異型SYCP3Principal Investigator

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Kurahashi Hiroki 倉橋浩樹

KURAHAS Hihiroki 倉橋浩樹

KURAHASHI Hiroki 倉橋浩樹