HIDEHITO INAGAKI 稲垣秀人

… Alternative Names

INAGAKI Hidehito 稲垣秀人

稲垣秀人イナガキヒデヒト

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Researcher Number	70308849
Other IDs	https://orcid.org/0000-0002-2383-0619
Affiliation (Current)	2024: 藤田医科大学, 医科学研究センター, 講師
Affiliation (based on the past Project Information) *help	2022 – 2023: 藤田医科大学, 医科学研究センター, 講師 2019 – 2021: 藤田医科大学, 総合医科学研究所, 講師 2014 – 2017: 藤田保健衛生大学, 総合医科学研究所, 講師 2012 – 2013: 藤田保健衛生大学, 総合医科学研究所, 助教 2008 – 2009: Fujita Health University, 総合医科学研究所, 助教 2004 – 2006: 藤田保健衛生大学, 総合医科学研究所, 助手 1999 – 2001: 藤田保健衛生大学, 総合医科学研究所, 助手
Review Section/Research Field	Principal Investigator Basic Section 50010:Tumor biology-related / General medical chemistry / Carcinogenesis / Molecular biology / Applied genomics / Human genetics Except Principal Investigator Basic Section 52010:General internal medicine-related / Neuroscience in general / Basic Section 50010:Tumor biology-related / Basic Section 52050:Embryonic medicine and pediatrics-related / Rehabilitation science/Welfare engineering
Keywords	Principal Investigator 染色体転座 / DNA高次構造 / ゲノム / モデル細胞 / 相分離 / クロマチン / 染色体構造異常 / がん / 染色体複雑構造異常 / chromothripsis … More / 染色体再構成 / モザイク / migration / 細胞移動 / ephrin / X不活化 / X連鎖 / アメリカ / 国際情報交換 / ポジショナルエフェクト / Chromosome conformation / Translocation / DNA secondary structure / 染色体 / 動物 / 発生・分化 / 核酸 / DNA二重鎖切断 / DNAの高次構造 / 遺伝子導入 / パリンドローム / ビオプテリン / GTPシクロヒドロラーゼ / 多型 / BAC / ジストニア / セロトニン / ドーパミン … More Except Principal Investigator ゲノム編集 / Nurr1 / dopaminergic neuron / tyrosine hydroxylase / Cre-loxP / Cre-ERT / ドーパミンニューロン / カテコールアミン / チロシン水酸化酵素 / DNA複製 / テロメア / icIHHV-6 / 核内トポロジー / 染色体再構成 / 核内配置編集 / タンパク構造解析 / タンパク３次元構造解析 / West症候群 / 三次元タンパク解析 / 網羅的遺伝子解析 / ウエスト症候群 / 表現型 / 発生メカニズム / 発症メカニズム / 遺伝子発現 / 過剰マーカー染色体 / UPLC / 遺伝子産物 / 質量分析 / 微量検体分析 / 生体成分 / 神経変性 / 脳卒中回復期リハビリ / 遺伝子産物検索 / マウス用重心動揺 / マウス用歩行解析 / 遊離アミノ酸 / 小脳性運動失調 / シナプス受容体 / セリン / メイトペアライブラリ / ＮＧＳエクソーム解析 / アンキリンＧ / 原因遺伝子 / リハビリ訓練 / 小脳失調 / 強制運動負荷 / D型セリン / 神経栄養 / 神経シナプス / 次世代シークエンサー解析 / 運動失調症 / 小脳変性マウス / 染色体構造異常 / 原因遺伝子解析 / 環境エンリッチメント飼育 / 歩行解析 / 運動失調 / プルキンエ細胞変性 / リハ運動訓練 / 小脳失調症 / nuclear receptor / 発達 / ドーパミン / 核内受容体 / catecholamine / 条件付き遺伝子破壊 / 相同組み換え Less

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
テロメアでのDNA複製ストールはiciHHV-6を誘発するのか？
- Principal Investigator
  
  大江瑞恵
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52010:General internal medicine-related
- Research Institution
  Fujita Health University
Production of chromosomal structural abnormalities using cultured cell systemPrincipal Investigator
- Principal Investigator
  
  稲垣秀人
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 50010:Tumor biology-related
- Research Institution
  Fujita Health University
ゲノム編集による過剰マーカー染色体の病因解明
- Principal Investigator
  
  大江瑞恵
- Project Period (FY)
  2019 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52010:General internal medicine-related
- Research Institution
  Fujita Health University
網羅的遺伝子解析と三次元タンパク構造解析を用いたウエスト症候群の基礎病態解析
- Principal Investigator
  
  石原尚子
- Project Period (FY)
  2019 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Fujita Health University
Cell culture model elucidates severe phenotype of female in X-linked disorderPrincipal Investigator
- Principal Investigator
  
  INAGAKI Hidehito
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  General medical chemistry
- Research Institution
  Fujita Health University
The study trains rehabilitation training to perform to spino- cerebellar degeneration patient to a cerebellar degenerative mouse
- Principal Investigator
  
  Hidehiro(hidehiko) Beppu
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Rehabilitation science/Welfare engineering
- Research Institution
  Fujita Health University
Analysis of chromosome conformation and breakpoints of balanced translocations in humanPrincipal Investigator
- Principal Investigator
  
  INAGAKI Hidehito
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Carcinogenesis
- Research Institution
  Fujita Health University
Analysis of chromosomal translocation in humans by using medaka germ cell and its applicationPrincipal Investigator
- Principal Investigator
  
  INAGAKI Hidehito
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Molecular biology
- Research Institution
  Fujita Health University
十字架型DNAを利用した安全な遺伝子治療ベクターの開発Principal Investigator
- Principal Investigator
  
  稲垣秀人
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Applied genomics
- Research Institution
  Fujita Health University
BACを用いたGTPシクロヒドロラーゼI変異疾患の変異同定系の確立Principal Investigator
- Principal Investigator
  
  稲垣秀人
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
Alteration in neural function by an inducible knock-out of tyrosine hydroxylase.
- Principal Investigator
  
  ICHINOSE Hiroshi
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neuroscience in general
- Research Institution
  Fujita Health University
Role of Neurotransmitters and orphan receptors in neural cytoarchitecture of the brain..
- Principal Investigator
  
  ICHINOSE Hiroshi
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (B).
- Research Field
  
  Neuroscience in general
- Research Institution
  Fujita Health University

[Journal Article] A case of 46, <scp>XY</scp> disorders of sex development with congenital heart disease caused by a <i>GATA4</i> variant2022
- Author(s)
  Shichiri Yui、Kato Yoshimi、Inagaki Hidehito、Kato Takema、Ishihara Naoko、Miyata Masafumi、Boda Hiroko、Kojima Arisa、Miyake Misa、Kurahashi Hiroki
- Journal Title
  
  Congenital Anomalies
  
  Volume: 62 Issue: 5 Pages: 203-207
- DOI
  10.1111/cga.12482
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08285
[Journal Article] Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes2022
- Author(s)
  Mariya T, Kato T, Sugimoto T, Miyai S, Inagaki H, Ohye T, Sugihara E, Muramatsu Y, Mizuno S, Kurahashi H.
- Journal Title
  
  Journal of human genetics
  
  Volume: Jan 14 Issue: 6 Pages: 363-368
- DOI
  10.1038/s10038-021-01004-x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-21K06283, KAKENHI-PROJECT-19K07902
[Journal Article] Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.2017
- Author(s)
  Taniguchi-Ikeda M, Nagasaka 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
  
  Journal of Human Genetics
  
  Volume: 未定 Issue: 9 Pages: 851-855
- DOI
  10.1038/jhg.2017.48
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-16H04758
[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] 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] 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] 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] 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] 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] Identification of an enhancer region for immune activation in the human GTP cyclohydrolase I gene.2013
- Author(s)
  Liang Y, Inagaki H, Hao Q, Sakamoto M, Ohye T, Suzuki T, Ichinose H.
- Journal Title
  
  Biochem Biophys Res Commun.
  
  Volume: 442 Issue: 1-2 Pages: 72-78
- DOI
  10.1016/j.bbrc.2013.11.002
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24501307
[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] 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 MV, Medne L, Zackai EH, Emanuel BS, Kurahashi H
- Journal Title
  
  Eur J Hum Genet (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20770141
[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 Vol.18、No.18
  
  Pages: 3397-3406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20770141
[Journal Article] Chromosomal instability mediated by non- B DNA : cruciform conformation and DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki, H., et.al.
- Journal Title
  
  Genome Research 19
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20770141
[Journal Article] Choromosomal 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 Vol.19、No.2
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20770141
[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 Vol.54、No.5
  
  Pages: 253-260
- NAID
  10030730167
- Data Source
  KAKENHI-PROJECT-20770141
[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 T, Emanuel BS, Kurahashi H
- Journal Title
  
  Hum Mol Genet Vol.17、no.8
  
  Pages: 1184-1191
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20770141
[Journal Article] Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats2007
- Author(s)
  Kogo H, Inagaki H, Ohye T他3名
- Journal Title
  
  Nucleic Acids Res. (in press)
- Data Source
  KAKENHI-PROJECT-16710148
[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他4名
- Journal Title
  
  Fertil. Steril. (In press)
- Data Source
  KAKENHI-PROJECT-16710148
[Journal Article] Molecular cloning of a translocation hotspot in 22q11.2007
- Author(s)
  Kurahashi H, Inagaki H, Hosoba E他4名
- Journal Title
  
  Genome Res. 17・4
  
  Pages: 461-469
- Data Source
  KAKENHI-PROJECT-16710148
[Journal Article] Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)2006
- Author(s)
  Ashley T, Gaet AP, Inagaki H他5名
- Journal Title
  
  Am.J.Hum.Genet. 79・3
  
  Pages: 524-538
- Data Source
  KAKENHI-PROJECT-16710148
[Journal Article] Chromosomal translocation mediated by palindromic DNA.2006
- Author(s)
  Kurahashi H, Inagaki H, Kogo H他3名
- Journal Title
  
  Cell Cycle 5・12
  
  Pages: 1297-1303
- Data Source
  KAKENHI-PROJECT-16710148
[Journal Article] Palindrome-mediated chromosomal translocation in humans.2006
- Author(s)
  Kurahashi H, Inagaki H, Kogo H他3名
- Journal Title
  
  DNA Repair 5・9-10
  
  Pages: 1136-1145
- Data Source
  KAKENHI-PROJECT-16710148
[Journal Article] Palindromic AT-rich Repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates2005
- Author(s)
  Inagaki, H. et al.
- Journal Title
  
  Human mutation 26・4
  
  Pages: 332-342
- Data Source
  KAKENHI-PROJECT-16710148
[Presentation] Chromosome conformation affects the clustered breakage and complex chromosomal rearrangement in germline2023
- Author(s)
  Hidehito Inagaki, Takema Kato, Atsushi Toyoda, Yoshio Makita, and Hiroki Kurahashi
- Organizer
  ICHG 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07108
[Presentation] Chromatin-domains affect the clustered breakpoint formation in complex chromosomal rearrangement2021
- Author(s)
  Inagaki H, Kato T, Toyoda A, Makita Y, Kurahashi H
- Organizer
  ASHG 2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07108
[Presentation] 妊娠出産に至った筋拘縮型エーラス・ダンロス症候群女性の報告2020
- Author(s)
  森山育実、河村理恵、大江瑞恵、長坂美和子、石原尚子、宮井俊介、岸野洋祐、加藤武馬、堤真紀子、稲垣秀人、佐藤労、倉橋浩樹、池田真理子
- Organizer
  日本人類遺伝学会第65回大会
- Data Source
  KAKENHI-PROJECT-19K07902
[Presentation] 細胞培養モデルが明らかにしたX連鎖の疾患での女性重症化2017
- Author(s)
  Hidehito Inagaki
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-15K08287
[Presentation] 小脳変性マウスへのＤ型セリンおよび強制歩行訓練の単独・併用介入が運動失調改善を示す機序の検討2017
- Author(s)
  別府秀彦、新里昌功、千原猛、水谷謙明、玉井育子、稲垣秀人、園田茂、高橋久英
- Organizer
  第27回生物試料分析科学会
- Place of Presentation
  新潟・朱鷺メッセ
- Year and Date
  2017-02-11
- Data Source
  KAKENHI-PROJECT-25282166
[Presentation] Cell culture model for X-linked disorder: craniofrontonasal dysplasia and severe phenotype in female2016
- Author(s)
  Sugimoto M, Inagaki H, Tsutsumi M et al
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto International Conferece Center (京都府京都市）
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08287
[Presentation] 小脳変性マウスへのＤ型セリン投与および強制歩行訓練による運動失調改善の検討とその機序2016
- Author(s)
  別府秀彦、新里昌功、水谷謙明、千原猛、稲垣秀人、園田茂
- Organizer
  第48回藤田学園医学会
- Place of Presentation
  豊明・藤田保健衛生大学
- Year and Date
  2016-10-06
- Data Source
  KAKENHI-PROJECT-25282166
[Presentation] A PDE3A mutation in familial hypertension and brachydactyly syndrome2016
- Author(s)
  Inagaki H, Boda H, Uchida H et al
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto International Conferece Center (京都府京都市）
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08287
[Presentation] NGS analysis of DNA secondary structure dynamics at the promoter region2015
- Author(s)
  稲垣秀人他
- Organizer
  BMB2015
- Place of Presentation
  神戸ポートアイランド
- Year and Date
  2015-12-01
- Data Source
  KAKENHI-PROJECT-15K08287
[Presentation] Massive parallel sequencing revealed the conformational dynamics of the non-B form DNA at the promoter2015
- Author(s)
  Inagaki H, et al.
- Organizer
  ASHG2015
- Place of Presentation
  アメリカボルティモア
- Year and Date
  2015-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08287
[Presentation] パリンドロームを介した染色体転座の発生メカニズムの解明.2013
- Author(s)
  稲垣秀人、加藤武馬、倉橋浩樹.
- Organizer
  新学術領域「ゲノム支援」２０１３年度拡大班会議
- Place of Presentation
  神戸市
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] Bisulfite法を用いたプロモータ部位のグアニン四重鎖ＤＮＡ構造の解析.2013
- Author(s)
  稲垣秀人、太田小百合、宮村浩徳、大江瑞恵、堤真紀子、加藤武馬、西澤春紀、倉橋浩樹.
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台市
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] ゲノム中に存在するDNA高次構造と疾患：習慣流産の例.2013
- Author(s)
  稲垣秀人、太田小百合、宮村浩徳、大江瑞恵、堤真紀子、加藤武馬、西澤春紀、倉橋浩樹.
- Organizer
  第２２回 DNA複製・組換え・修復ワークショップ
- Place of Presentation
  仙台市
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] DNA Quadruplex structure at promoter region analyzed by bisulfite method.2013
- Author(s)
  稲垣秀人、太田小百合、宮村浩徳、大江瑞恵、堤真紀子、加藤武馬、西澤春紀、倉橋浩樹.
- Organizer
  第３６回日本分子生物学会年会
- Place of Presentation
  神戸市
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] 妊娠合併症に関連したANXA5プロモーター多型はDNA高次構造を介して発現量に影響する2012
- Author(s)
  稲垣秀人、太田小百合、宮村浩徳、西澤春紀、中平久美子、柳原格、宇田川康博、倉橋浩樹
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡市
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] Mechanism of recurrent translocation t(11;22) initiated by cruciform conformation of palindromes2012
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Organizer
  FASEB Science Research Conference
- Place of Presentation
  アメリカ・サクストンズリバー
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] Obstetric complication-associated ANXA5 promoter 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
  American Society of Human Genetics 62nd Annual Meeting
- Place of Presentation
  アメリカ・サンフランシスコ
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] GEN1 resolves cruciform-forming palindromic DNA leading to recurrent translocation in human2009
- Author(s)
  稲垣, 他
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  神奈川県横浜市
- Year and Date
  2009-12-12
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] GEN1 resolves cruciformforming palindromic DNA leading to recurrent translocation in human2009
- Author(s)
  稲垣秀人
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  横浜市
- Year and Date
  2009-12-12
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Non-B型DNAが引き起こすヒト染色体転座の発生機構2009
- Author(s)
  稲垣秀人
- Organizer
  日本分子生物学会第9回春季シンポジウム
- Place of Presentation
  宮崎市
- Year and Date
  2009-05-11
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Artemisは十字架型のパリンドローム構造を切断し染色体転座を誘発する2008
- Author(s)
  稲垣秀人
- Organizer
  第31回日本分子生物学会年会
- Place of Presentation
  神戸市
- Year and Date
  2008-12-11
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Artemis cleaves cruciform- forming palindromic DNA leading to recurrent translocation in humans2008
- Author(s)
  Inagaki, H., et.al.
- Organizer
  58^<th> Annual meeting of The American Sciety of Human Genetics
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-13
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Artemis cleaves cruciform- forming palindromic DNA leading to recurrent translocation in humans2008
- Author(s)
  Inagaki H.
- Organizer
  58th Meeting of The American Society of Human Genetics
- Place of Presentation
  Philadelphia
- Year and Date
  2008-11-13
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Artemisは十字架型のパリンドローム構造を切断し染色体転座を誘発する2008
- Author(s)
  稲垣秀人, 他
- Organizer
  第31回日本分子生物学会年会
- Place of Presentation
  兵庫県神戸市
- Year and Date
  2008-12-11
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] Artemis cleaves cruciform- forming palindromic DNA leading to recurrent translocation in humans2008
- Author(s)
  Inagaki H.
- Organizer
  ASHG Ataxia-Telangiectasia/Genome Instability Satellite Meeting
- Place of Presentation
  Philadelphia
- Year and Date
  2008-11-11
- Data Source
  KAKENHI-PROJECT-20770141
[Presentation] 生体内でのDNA高次構造形成の探索
- Author(s)
  稲垣秀人、加藤武馬、大内雄矢、西澤春紀、倉橋浩樹
- Organizer
  ゲノム支援2014拡大班会議
- Place of Presentation
  神戸ポートピアホテル (神戸市)
- Year and Date
  2014-08-20 – 2014-08-21
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] Detection of in vivo G-quadruplex structure of the ANXA5 promoter that contributes to the recurrent pregnancy loss
- Author(s)
  H. Inagaki1, S. Ota1, H. Nishizawa2, H. Miyamura1,2, K. Nakahira3, M. Suzuki1, M. Tsutsumi1, T. Kato1, S. Nishiyama2, Y. Udagawa2, I. Yanagihara3, H. Kurahashi
- Organizer
  The American Society of Human Genetics
- Place of Presentation
  San Diego (USA)
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-24501307
[Presentation] Obstetric complication-associated ANXA5 promoter polymorphisms affect gene expression via G-quadruplex structure in vivo
- Author(s)
  H. Inagaki, S. Ota, H. Nishizawa, H. Miyamura, K. Nakahira, M. Suzuki, M. Tsutsumi, T. Kato, S. Nishiyama, Y. Udagawa, I. Yanagihara, H. Kurahashi
- Organizer
  FASEB Summer Reseach Conference
- Place of Presentation
  Itasca (USA)
- Year and Date
  2014-07-20 – 2014-07-25
- Data Source
  KAKENHI-PROJECT-24501307

1. OHYE Tamae (10247661)

# of Collaborated Projects: 4 results

# of Collaborated Products: 1 results
2. ICHINOSE Hiroshi (90192492)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
3. SUZUKI Takahiro (70298545)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. ICHINOSE Chiho (10247653)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. Hidehiro(hidehiko) Beppu (30142582)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
6. SINZATO MASANORI (80148288)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
7. CHIHARA TAKESHI (00217241)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
8. MIZUTANI KENMEI (30351068)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. SHIMPO HIROSHI (10142580)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. SONODA SHIGERU (10197022)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
11. 林宣宏 (80267955)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 石原尚子 (30393143)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
13. 河村理恵 (20735534)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 倉橋浩樹 (30243215)

# of Collaborated Projects: 1 results

# of Collaborated Products: 8 results
15. 河村吉紀 (30581475)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. TANIGUCHI Mariko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. 原田理沙

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
19. 宮井俊輔

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

HIDEHITO INAGAKI 稲垣 秀人

INAGAKI Hidehito 稲垣 秀人

稲垣 秀人 イナガキ ヒデヒト

Research Projects

Research Products

Co-Researchers

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

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テロメアでのDNA複製ストールはiciHHV-6を誘発するのか？

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Production of chromosomal structural abnormalities using cultured cell systemPrincipal Investigator

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ゲノム編集による過剰マーカー染色体の病因解明

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網羅的遺伝子解析と三次元タンパク構造解析を用いたウエスト症候群の基礎病態解析

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Cell culture model elucidates severe phenotype of female in X-linked disorderPrincipal Investigator

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The study trains rehabilitation training to perform to spino- cerebellar degeneration patient to a cerebellar degenerative mouse

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Analysis of chromosome conformation and breakpoints of balanced translocations in humanPrincipal Investigator

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Analysis of chromosomal translocation in humans by using medaka germ cell and its applicationPrincipal Investigator

Principal Investigator

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十字架型DNAを利用した安全な遺伝子治療ベクターの開発Principal Investigator

Principal Investigator

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BACを用いたGTPシクロヒドロラーゼI変異疾患の変異同定系の確立Principal Investigator

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Alteration in neural function by an inducible knock-out of tyrosine hydroxylase.

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Role of Neurotransmitters and orphan receptors in neural cytoarchitecture of the brain..

Principal Investigator

HIDEHITO INAGAKI 稲垣秀人

INAGAKI Hidehito 稲垣秀人

稲垣秀人イナガキヒデヒト