SOEJIMA HIDENOBU 副島英伸

… Alternative Names

SOEJIMA Hidenobu 副島英伸

HIGASHIMOTO Ken 東元健

副島英伸ソエジマヒデノブ

Less

Researcher Number	30304885
Other IDs
External Links
Affiliation (Current)	2022: 佐賀大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2006 – 2022: 佐賀大学, 医学部, 教授 2016: 佐賀大学, 医学部, 助教 2015: 佐賀大学, 医学部分子遺伝学エピジェネティクス分野, 教授 2007: Saga University, 医学部, 助教 2004 – 2005: 佐賀大学, 医学部, 助手 2000 – 2002: 佐賀医科大学, 医学部, 助手 1998: Saga Medical School, Department of Biochemistry, assistant professor, 医学部, 助手
Review Section/Research Field	Principal Investigator Human genetics / Pathological medical chemistry / Biological Sciences / Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 52:General internal medicine and related fields Except Principal Investigator Biological Sciences / Obstetrics and gynecology / Embryonic/Neonatal medicine / Cerebral neurosurgery / Pathological medical chemistry / Basic Section 56040:Obstetrics and gynecology-related
Keywords	Principal Investigator DNAメチル化 / ゲノム刷り込み / non-coding RNA / ゲノムインプリンティング / 刷り込みドメイン / エピジェネティクス / KIP2 / Wilms腫瘍 / siRNAライブラリー / ヒストンメチル化 … More / LIT1刷り込みドメイン / ソトス症候群 / 遺伝子発現 / Beckwith-Wiedemann症候群 / Beckwith-Wiedemann syndrome / WT1 / プロモーター / OBPH1 / Obph1 / 腫瘍抑制遺伝子 / Bisulfite-Sequencing法 / ルシフェラーゼレポーターアッセイ / iPS細胞 / 肝芽腫 / インプリントDMR / 分化万能性 / ヒストンメチル化酵素 / 歌舞伎症候群 / 癌 / ヒストンH3K9メチル化 / ヒストンH3K27トリメチル化 / Genomic imprinting / DNA methylation / Histone methylation / cancer / Wilms tumor / non-coding RNA / non-codin RNA / genomic imprinting / LIT1 imprinted domain / 体細胞性インプリントＤＭＲ / メチル化可変領域 / NSD1 / エピゲノム / 精神発達遅滞 / コンディショナルノックアウトマウス / トランスクリプトーム / インプリンティング制御領域 / DNAメチル化バウンダリー / SOX2/OCT4 / CTCF … More Except Principal Investigator インプリンティング / Beckwith-Wiedemann症候群 / Lit1 / DNAメチル化 / インプリント疾患 / Obp-rs,FISH解析 / DNAのメチル化 / p57kip2 / p57^<kip2> / インプリンティングセンター / 脳・神経 / 脳腫瘍 / 遺伝子 / 蛋白質 / プロテオミクス / 胎児性腫瘍 / DNAメチレーション / Beckwith-wiedemann症候群 / 、ベックウィズ・ウィードマン症候群 / サイクリンキナーゼインヒビター / genomic imprinting / Beckwith-Wiedemann syndrome / embryonal tumor / DNA methylation / 間葉性異形成胎盤 / 胎盤 / 早産 / 胎児発育不全 / エピジェネティック変異 / インプリント遺伝子 / 出生前診断 / 胞状奇胎 / 間葉性異型性胎盤 / 出世前診断 / 片親性ダイソミー / ゲノムワイド父性ダイソミー / エクソーム解析 / メチル化解析 / 父性ダイソミー / 次世代シークエンサー / エピジェネティック / 全ゲノム父性ダイソミー / Beckwith-Wiedemann 症候群 / 生殖補助医療(ART) / 生殖補助医療（ART） / インプリント異常症 / 胎児異常 / 糖尿病 / エピゲノム変異 / 尾部退行症候群 Less

インプリンティング疾患の異常高メチル化が境界領域を超えて伸展する分子機構の解明Principal Investigator
- Principal Investigator
  
  副島英伸
- Project Period (FY)
  2021 – 2022
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Saga University
エピゲノム修飾因子NSD1の標的遺伝子同定に基づく精神発達遅滞の分子病態解明Principal Investigator
- Principal Investigator
  
  副島英伸
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Saga University
Study on epigenetic changes of the genes involved in the malformations of the fetus affected by diabetes
- Principal Investigator
  
  大場隆
- Project Period (FY)
  2019 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Kumamoto University
Identification of regulatory factors for somatic imprinted DMR establishment and elucidation of their molecular mechanismsPrincipal Investigator
- Principal Investigator
  
  Soejima Hidenobu
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Saga University
Clinicopathological features of placental mesenchymal dysplasia
- Principal Investigator
  
  Ohba Takashi
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Kumamoto University
A search for target genes of aberrant histone methylation diseases and the establishment of drug discovery platform based on elucidation of pathological conditionsPrincipal Investigator
- Principal Investigator
  
  Soejima Hidenobu
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  Saga University
Epigenetic analyses in patients with imprinting disorders conceived by assisted reproduction technologies
- Principal Investigator
  
  Hiura Hitoshi
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Embryonic/Neonatal medicine
  Obstetrics and gynecology
- Research Institution
  Tohoku University
Molecular biological analysis of genome wide paternal uniparental disomy
- Principal Investigator
  
  Ohtsuka Yasufumi
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Saga University
Drawing a differentiation potency index of iPSC based on genomic imprintingPrincipal Investigator
- Principal Investigator
  
  SOEJIMA Hidenobu
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  Saga University
Identification of regulatory factors for genomic imprinting using siRNA libraryPrincipal Investigator
- Principal Investigator
  
  SOEJIMA Hidenobu
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Saga University
Bidirectional approach for elucidation of genomic imprinting mechanismPrincipal Investigator
- Principal Investigator
  
  SOEJIMA Hidenobu
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Saga University
siRNAライブラリーを用いた刷り込み遺伝子発現調節分子の同定Principal Investigator
- Principal Investigator
  
  副島英伸
- Project Period (FY)
  2005
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Saga University
グリオーマ細胞核内蛋白質のプロテオミクスと核内蛋白質ネットワークの解析
- Principal Investigator
  
  香畑智彦
- Project Period (FY)
  2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cerebral neurosurgery
- Research Institution
  Saga University
A molecular base of epigenetic gene expression control in imprinted domainPrincipal Investigator
- Principal Investigator
  
  SOEJIMA Hidenobu
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Saga University
細胞機能を司るゲノムDNAメチル化によるインプリンティング制御と疾患発症機構
- Principal Investigator
  
  向井常博
- Project Period (FY)
  2001
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  佐賀医科大学
腫瘍抑制遺伝子WT1のエピジェネティック変化による発現制御機構の解明Principal Investigator
- Principal Investigator
  
  副島英伸
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  佐賀医科大学
ヒト11p15.5(セントロメア側)に対応するマウスゲノム領域の構造解析
- Principal Investigator
  
  MUKAI Tsunehiro
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (A)
- Research Institution
  佐賀医科大学
細胞機能を司るゲノムDNAメチル化の生理的動態ならびに病態解析
- Principal Investigator
  
  向井常博
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  佐賀医科大学
Molecular genetic analysis of the disease resulted from abnomal genomic imprinting
- Principal Investigator
  
  MUKAI Tsunehiro
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Saga Medical School

[Book] Fetal Morph Functional Diagnosis2021
- Author(s)
  Soejima H, Ohba T
- Total Pages
  346
- Publisher
  Springer
- ISBN
  9789811581700
- Data Source
  KAKENHI-PROJECT-20H03643
[Book] 遺伝子医学MOOK36　エピゲノムで新たな解明が進む「先天性疾患」2021
- Author(s)
  原聡史、副島英伸
- Total Pages
  218
- Publisher
  メディカルドゥ
- ISBN
  9784909508119
- Data Source
  KAKENHI-PROJECT-21K19451
[Book] 遺伝子医学MOOK36　エピゲノムで新たな解明が進む「先天性疾患」2021
- Author(s)
  原聡史、副島英伸
- Total Pages
  218
- Publisher
  メディカルドゥ
- ISBN
  9784909508119
- Data Source
  KAKENHI-PROJECT-20H03643
[Book] Fetal Morph Functional Diagnosis2021
- Author(s)
  Soejima H, Ohba T
- Total Pages
  346
- Publisher
  Springer
- ISBN
  9789811581700
- Data Source
  KAKENHI-PROJECT-21K19451
[Book] コアカリ準拠臨床遺伝学テキストノート　第６講義エピジェネティクス2018
- Author(s)
  副島英伸
- Total Pages
  192
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-17K08687
[Book] DNA and Histone Methylation as Cancer Targets2017
- Author(s)
  Higashimoto K, Joh K, Soejima H
- Total Pages
  622
- Publisher
  Humana Press
- Data Source
  KAKENHI-PROJECT-17K08687
[Book] エピジェネティクスの産業応用　第Ⅳ編疾患エピゲノム研究　第12章インプリンティング疾患のエピジェネティクス2014
- Author(s)
  副島英伸
- Total Pages
  14
- Publisher
  シーエムシー出版
- Data Source
  KAKENHI-PROJECT-26670169
[Book] Beckwith-Wiedemann症候群．別冊日本臨牀　新領域別症候群シリーズNo.29　神経症候群（第２版）Ⅳ-その他の神経疾患を含めて-2014
- Author(s)
  東元健、副島英伸
- Total Pages
  4
- Publisher
  日本臨牀社
- Data Source
  KAKENHI-PROJECT-26670169
[Book] Silver-Russell症候群．別冊日本臨牀　新領域別症候群シリーズNo.29　神経症候群（第２版）Ⅳ-その他の神経疾患を含めて-2014
- Author(s)
  前田寿幸、副島英伸
- Total Pages
  4
- Publisher
  日本臨牀社
- Data Source
  KAKENHI-PROJECT-26670169
[Book] 遺伝子医学MOOK252013
- Author(s)
  東元健、副島英伸
- Total Pages
  280
- Publisher
  メディカルドゥ
- Data Source
  KAKENHI-PROJECT-23659181
[Book] Beckwith-Wiedemann症候群と小児腫瘍.遺伝子医学MOOK25エピジェネティクスと病気第2 章エピジェネティクスと病気 4.不妊・先天異常(監修:佐々木裕之, 編集:中尾光善, 中島欽一)2013
- Author(s)
  東元健, 副島英伸
- Publisher
  メディカルドゥ, 大阪
- Data Source
  KAKENHI-PROJECT-23659181
[Book] ベックウィズ・ヴィーデマン症候群第XIV 章先天異常・奇形症候群ハンドブック.(井村裕夫総編集, 福井次矢・辻省次編集.)2011
- Author(s)
  副島英伸
- Total Pages
  679
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-23659181
[Book] 症候群ハンドブック、第XIV章先天異常・奇形、シルバー・ラッセル症候群2011
- Author(s)
  副島英伸
- Total Pages
  757
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-23659181
[Book] シルバー・ラッセル症候群第XIV 章先天異常・奇形症候群ハンドブック.(井村裕夫総編集, 福井次矢・辻省次編集)2011
- Author(s)
  副島英伸
- Total Pages
  685
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-23659181
[Book] 症候群ハンドブック、第XIV章先天異常・奇形、ベックウィズ・ヴィーデマン症候群2011
- Author(s)
  副島英伸
- Total Pages
  757
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-23659181
[Book] 23章エピジェネティクスとヒト疾患(エピジェネティクス.D.アリス・T.ジェニュワイン・D.ラインバーグ共編, 堀越正美監訳)2010
- Author(s)
  副島英伸, 城圭一郎, 中尾光善
- Publisher
  培風館.東京
- Data Source
  KAKENHI-PROJECT-20590330
[Book] エピジェネティクス 23章エピジェネティクスとヒト疾患(D.アリス・T.ジェニュワイン・D.ラインバーグ共編,堀越正美監訳)2010
- Author(s)
  副島英伸
- Total Pages
  573
- Publisher
  培風館
- Data Source
  KAKENHI-PROJECT-20590330
[Book]2009
- Author(s)
  副島英伸
- Publisher
  メディカル・サイエンス・インターナショナル.東京(第2部ゲノミクスカラー図解基礎から疾憩までわかる遺伝学)(新川詔夫,吉浦孝一郎監訳)
- Data Source
  KAKENHI-PROJECT-20590330
[Book] 実験医学増刊ゲノムワイドに展開するエピジェネティクス医科学中尾光善、塩田邦郎、牛島俊和、佐々木裕之編集2006
- Author(s)
  副島英伸
- Publisher
  羊土社
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Book] 実験医学増刊ゲノムワイドに展開するエピゲネティクス医科学中尾光善, 塩田邦郎, 牛島俊和, 佐々木裕之編集2006
- Author(s)
  副島英伸
- Publisher
  羊土社
- Data Source
  KAKENHI-PROJECT-18590313
[Book] Disruption of imprinting domain and diseases (Epigenetics)(Ed.Hiroyuki Sasaki)2004
- Author(s)
  Soejima H
- Total Pages
  8
- Publisher
  Springer-Veglag
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Book] エピジェネティクス(佐々木裕之編)2004
- Author(s)
  副島英伸
- Total Pages
  8
- Publisher
  シュプリンガー・フェアラーク
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] An analysis of the demographic history of the risk allele R4810K of moyamoya disease2021
- Author(s)
  K. Koganebuchi, K. Sato, K. Fujii, T. Kumabe, K. Haneji, T. Toma, H. Ishida, K. Joh, H. Soejima, S. Mano, M. Ogawa, H. Oota
- Journal Title
  
  Annals of Human Genetics
  
  Volume: 1-12 Pages: 1-12
- DOI
  10.1111/ahg.12424
- NAID
  120007168800
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H03590, KAKENHI-PROJECT-21H04352, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-21K19289, KAKENHI-PROJECT-21K19451, KAKENHI-PROJECT-21K13141, KAKENHI-PROJECT-20KK0166
[Journal Article] Lecture（臨床遺伝学・人類遺伝学誌上講義）エピゲノム2021
- Author(s)
  副島英伸
- Journal Title
  
  遺伝子医学
  
  Volume: 38 Pages: 108-115
- Data Source
  KAKENHI-PROJECT-21K19451
[Journal Article] TYK2 promoter variant is associated with impaired insulin secretion and lower insulin resistance in Japanese type 2 diabetes patients2021
- Author(s)
  Mori H, Takahashi H, Mine K, Higashimoto K, Inoue K, Kojima M, Kuroki S, Eguchi T, Ono Y, Inuzuka S, Soejima H, Nagafuchi S, Anzai K.
- Journal Title
  
  Genes
  
  Volume: 12 Pages: 400-400
- DOI
  10.3390/genes12030400
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-18H02853, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-21K19451
[Journal Article] Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series2021
- Author(s)
  Kodera C, Aoki S, Ohba T, Higashimoto K, Mikami Y, Fukunaga M, Soejima H, Katabuchi H.
- Journal Title
  
  Journal of Obstetrics and Gynaecology Research
  
  Volume: 47 Pages: 1118-1125
- DOI
  10.1111/jog.14647
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-21K19451
[Journal Article] Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.2021
- Author(s)
  Sun Feifei、Hara Satoshi、Tomita Chiyoko、Tanoue Yuka、Yatsuki Hitomi、Higashimoto Ken、Soejima Hidenobu
- Journal Title
  
  Am J Med Genet A.
  
  Volume: 185 Pages: 3062-3067
- DOI
  10.1002/ajmg.a.62364
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K06451, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-21K19451
[Journal Article] Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome2021
- Author(s)
  Higashimoto K, Watanabe H, Tanoue Y, Tonoki H, Tokutomi T, Hara S, Yatsuki H, Soejima H.
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: - Pages: 422-425
- DOI
  10.1136/jmedgenet-2020-106907
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-21K19451
[Journal Article] Short‐term running exercise alters DNA methylation patterns in neuronal nitric oxide synthase and brain‐derived neurotrophic factor genes in the mouse hippocampus and reduces anxiety‐like behaviors2021
- Author(s)
  Tomiga Yuki、Sakai Kazuya、Ra Song‐Gyu、Kusano Masaki、Ito Ai、Uehara Yoshinari、Takahashi Hirokazu、Kawanaka Kentaro、Soejima Hidenobu、Higaki Yasuki
- Journal Title
  
  The FASEB Journal
  
  Volume: 35
- DOI
  10.1096/fj.202100630r
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19H04012, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-20H04085, KAKENHI-PROJECT-20J00439, KAKENHI-PROJECT-21K19451, KAKENHI-PROJECT-20K19502
[Journal Article] Lecture（臨床遺伝学・人類遺伝学誌上講義）エピゲノム2021
- Author(s)
  副島英伸
- Journal Title
  
  遺伝子医学
  
  Volume: 38 Pages: 108-115
- Data Source
  KAKENHI-PROJECT-20H03643
[Journal Article] DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2 ‐DMR0 as a DNA methylation‐dependent, P0 promoter‐specific enhancer2020
- Author(s)
  Watanabe H, Higashimoto K, Miyake N, Morita S, Horii T, Kimura M, Suzuki T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Uemura T, Hatada I, Matsumoto N, Soejima H.
- Journal Title
  
  The FASEB Journal
  
  Volume: 34 Pages: 960-973
- DOI
  10.1096/fj.201901757r
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K06607, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-18H02487, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-20H03643
[Journal Article] One week, but not 12?hours, of cast immobilization alters promotor DNA methylation patterns in the nNOS gene in mouse skeletal muscle2019
- Author(s)
  Tomiga Yuki、Ito Ai、Sudo Mizuki、Ando Soichi、Eshima Hiroaki、Sakai Kazuya、Nakashima Shihoko、Uehara Yoshinari、Tanaka Hiroaki、Soejima Hidenobu、Higaki Yasuki
- Journal Title
  
  The Journal of Physiology
  
  Volume: 597 Pages: 5145-5159
- DOI
  10.1113/jp277019
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19H04012, KAKENHI-PROJECT-17K08687
[Journal Article] Beckwith-Wiedemann syndrome with asymmetric mosaic of paternal disomy causing hemihyperplasia2019
- Author(s)
  Yamada Tomohiro、Sugiyama Goro、Higashimoto Ken、Nakashima Azusa、Nakano Hiroyuki、Sumida Tomoki、Soejima Hidenobu、Mori Yoshihide
- Journal Title
  
  Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
  
  Volume: 127
- DOI
  10.1016/j.oooo.2018.07.053
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687
[Journal Article] Habitual Light-intensity Physical Activity and ASC Methylation in a Middle-aged Population2019
- Author(s)
  Nishida Y, Hara M, Higaki Y, Taguchi N, Nakamura K, Nanri H, Horita M, Shimanoe C, Yasukata J, Miyoshi N, Yamada Y, Higashimoto K, Soejima H, Tanaka K
- Journal Title
  
  Int. J. Sports Med.
  
  Volume: 40 Pages: 670-677
- DOI
  10.1055/a-0965-1374
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K10049, KAKENHI-PROJECT-17H01554, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16H06277
[Journal Article] The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome2019
- Author(s)
  Sun Feifei、Higashimoto Ken、Awaji Atsuko、Ohishi Kenji、Nishizaki Naoto、Tanoue Yuka、Aoki Saori、Watanabe Hidetaka、Yatsuki Hitomi、Soejima Hidenobu
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 64 Pages: 937-943
- DOI
  10.1038/s10038-019-0634-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08687
[Journal Article] Unbiased shRNA screening, using a combination of FACS and high-throughput sequencing, enables identification of novel modifiers of Polycomb silencing2018
- Author(s)
  Nishioka Kenichi、Miyazaki Hitomi、Soejima Hidenobu
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Pages: 12128-12128
- DOI
  10.1038/s41598-018-30649-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16K07451
[Journal Article] Growing oocyte specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.2018
- Author(s)
  Joh K, Matsuhisa F, Kitajima S, Nishioka K, Higashimoto K, Yatsuki H, Kono T, Koseki H, Soejima H
- Journal Title
  
  Epigenetics Chromatin
  
  Volume: 11 Pages: 28-28
- DOI
  10.1186/s13072-018-0200-6
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K07138, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16H02622, KAKENHI-PROJECT-16K09970, KAKENHI-PROJECT-18H00338
[Journal Article] Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.2018
- Author(s)
  Hidaka H, Higashimoto K, Aoki S, Mishima H, Hayashida C, Maeda T, Koga Y, Yatsuki H, Joh K, Noshiro H, lwakiri R, Kawaguchi A, Yoshiura K, Fujimoto K, Soejima H
- Journal Title
  
  Clin Epigenetics
  
  Volume: 10 Pages: 150-150
- DOI
  10.1186/s13148-018-0578-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-18K07850, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-16K09970, KAKENHI-PROJECT-18H00338
[Journal Article] Hepatoblastoma in an extremely low birth-weight infant with Beckwith?Wiedemann syndrome2018
- Author(s)
  Kawasaki Yukako、Makimoto Masami、Samejima Azusa、Yoneda Noriko、Higashimoto Ken、Soejima Hidenobu、Yoshida Taketoshi
- Journal Title
  
  Pediatrics & Neonatology
  
  Volume: 59 Pages: 523-524
- DOI
  10.1016/j.pedneo.2017.11.012
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687
[Journal Article] Mbf1 ensures Polycomb silencing by protecting E(z) mRNA from degradation by Pacman2018
- Author(s)
  Nishioka Kenichi、Wang Xian-Feng、Miyazaki Hitomi、Soejima Hidenobu、Hirose Susumu
- Journal Title
  
  Development
  
  Volume: 145 Pages: 162461-162461
- DOI
  10.1242/dev.162461
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16F16703, KAKENHI-PROJECT-16K07451
[Journal Article] Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan2017
- Author(s)
  TAKAMATSU Yuichiro、HIGASHIMOTO Ken、MAEDA Toshiyuki、KAWASHIMA Masatou、MATSUO Muneaki、ABE Tatsuya、MATSUSHIMA Toshio、SOEJIMA Hidenobu
- Journal Title
  
  Neurologia medico-chirurgica
  
  Volume: 57 Issue: 11 Pages: 607-611
- DOI
  10.2176/nmc.oa.2017-0036
- NAID
  130006201788
- ISSN
  0470-8105, 1349-8029
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-15K10337
[Journal Article] The allele frequency of ALDH2* Glu504Lys and ADH1B* Arg47His for the Ryukyu islanders and their history of expansion among East Asians2017
- Author(s)
  Koganebuchi, K., Haneji, K., Toma, T., Joh, K., Soejima, H., Fujimoto, K., Ishida, H., Ogawa, M., Hanihara, T., Harada, S., Kawamura, S. and *Oota, H.
- Journal Title
  
  American Journal of Human Biology,
  
  Volume: 29 Pages: 1-14
- DOI
  10.1002/ajhb.22933
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H02421, KAKENHI-PROJECT-25251046, KAKENHI-PROJECT-15J10824, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16H01954
[Journal Article] Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain ofDIS3L22017
- Author(s)
  Soma Noriko、Higashimoto Ken、Imamura Masaru、Saitoh Akihiko、Soejima Hidenobu、Nagasaki Keisuke
- Journal Title
  
  Am J Med Genet Part A
  
  Volume: 173 Pages: 1077-1081
- DOI
  10.1002/ajmg.a.38111
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08687
[Journal Article] CTCFdeletion syndrome: clinical features and epigenetic delineation2017
- Author(s)
  Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S
- Journal Title
  
  J Med Genet.
  
  Volume: 54 Pages: 836-842
- DOI
  10.1136/jmedgenet-2017-104854
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K07248, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-26293365, KAKENHI-PROJECT-15K08330
[Journal Article] Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.2017
- Author(s)
  Eri Imagawa, Ken Higashimoto, Yasunari Sakai, Chikahiko Numakura, Nobuhiko Okamoto, Satoko Matsunaga, Akihide Ryo, Yoshinori Sato, Masafumi Sanefuji, Kenji Ihara, Yui Takada, Gen Nishimura, Hirotomo Saitsu, Takeshi Mizuguchi, Satoko Miyatake, Mitsuko Nakashima, Noriko Miyake, Hidenobu Soejima, Naomichi Matsumoto
- Journal Title
  
  Hum Mut
  
  Volume: 印刷中 Pages: 637-648
- DOI
  10.1002/humu.23200
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H06533, KAKENHI-PROJECT-26461549, KAKENHI-PROJECT-15K09624, KAKENHI-PROJECT-16K09991, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-17K15630, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05198, KAKENHI-PROJECT-16H05357
[Journal Article] An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression2017
- Author(s)
  Akiyama Tokiho、Katsumura Takafumi、Nakagome Shigeki、Lee Sang-il、Joh Keiichiro、Soejima Hidenobu、Fujimoto Kazuma、Kimura Ryosuke、Ishida Hajime、Hanihara Tsunehiko、Yasukouchi Akira、Satta Yoko、Higuchi Shigekazu、Oota Hiroki
- Journal Title
  
  PLOS ONE
  
  Volume: 12
- DOI
  10.1371/journal.pone.0178373
- NAID
  120006891149
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-16K21352, KAKENHI-PROJECT-25251046, KAKENHI-PROJECT-16J07227
[Journal Article] The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.2016
- Author(s)
  Rumbajan JM, Yamaguchi Y, Nakabayashi K, Higashimoto K, Yatsuki H, Nishioka K, Matsuoka K, Aoki S, Toda S, Takeda S, Seki H, Hatada I, Hata K, Soejima H, Joh K.
- Journal Title
  
  Gene
  
  Volume: 583 Pages: 141-146
- DOI
  10.1016/j.gene.2016.02.025
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461554, KAKENHI-PROJECT-26670169
[Journal Article] ldentification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.2016
- Author(s)
  Ohtsuka Y, Higashimoto K, Oka T, Yatsuki H, Jozaki K, Maeda T, Kawahara K, Hamasaki Y, Matsuo M, Nishioka K, Joh K, Mukai T, Soejima H.
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 25 Pages: 1406-1419
- DOI
  10.1093/hmg/ddw023
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-26670169, KAKENHI-PROJECT-16H00598
[Journal Article] Novel nonsense mutation in the NLRP7 gene associated with recurrent hydatidiform mole.2016
- Author(s)
  Ito Y, Maehara K, Kaneki E, Matsuoka K, Sugahara N, Miyata T, Kamura H, Yamaguchi Y, Kono A, Nakabayashi K, Migita O, Higashimoto K, Soejima H, Okamoto A, Nakamura H, Kimura T, Wake N, Taniguchi T, Hata K.
- Journal Title
  
  Gynecol. Obstet. Invest.
  
  Volume: Epub ahead of print Pages: 353-358
- DOI
  10.1159/000441780
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25860258, KAKENHI-PROJECT-24592494, KAKENHI-PROJECT-26670169, KAKENHI-PROJECT-16K11086, KAKENHI-PROJECT-16K11087, KAKENHI-PROJECT-16K11120
[Journal Article] Beckwith-Wiedemann syndrome2015
- Author(s)
  東元健、副島英伸
- Journal Title
  
  日本臨床家族性腫瘍学―家族性腫瘍の最新研究動向―
  
  Volume: 73 Pages: 59-63
- Data Source
  KAKENHI-PROJECT-26670169
[Journal Article] Beckwith-Wiedemann 症候群（BWS）2015
- Author(s)
  東元健、副島英伸
- Journal Title
  
  臨床画像
  
  Volume: 31 Pages: 189-191
- Data Source
  KAKENHI-PROJECT-26670169
[Journal Article] Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.2015
- Author(s)
  Ohtsuka Y, Higashimoto K, Sasaki K, Jozaki K, Yoshinaga H, Okamoto N, Takama Y, Kubota A, Nakayama M, Yatsuki H, Nishioka K, Joh K, Mukai T, Yoshiura KI, Soejima H.
- Journal Title
  
  Clinical Genetics
  
  Volume: 8 Pages: 1-1
- DOI
  10.1111/cge.12496
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-26670169, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293084
[Journal Article] A Clinical Study of Beckwith-Wiedemann Syndrome2014
- Author(s)
  加藤大貴、井村英人、東元健、八木ひとみ、芝崎龍典、古川博雄、新美照幸、藤原久美子、鈴木聡、外山佳孝、南克浩、井上知佐子、早川統子、副島英伸、夏目長門
- Journal Title
  
  J.Jpn.Cleft Palate Assoc.
  
  Volume: 39 Issue: 1 Pages: 21-27
- DOI
  10.11224/cleftpalate.39.21
- NAID
  130004567685
- ISSN
  0386-5185, 2186-5701
- Language
  Japanese
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26670169
[Journal Article] Beckwith-Wiedemann症候群2014
- Author(s)
  東元健、副島英伸
- Journal Title
  
  周産期医学
  
  Volume: 44 Pages: 258-260
- Data Source
  KAKENHI-PROJECT-26670169
[Journal Article] Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of the human imprintome and suggests a germline methylation independent establishment of imprinting2014
- Author(s)
  Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simon C, Moore H, Harness J, Keirstead H, Vicente Sanchez-Mut J, Kaneki E, Lapunzina P, Soejima H, Wake N, Esteller M, Ogata T, Hata K, Nakabayashi K, Monk D*
- Journal Title
  
  Genome Reserch.
  
  Volume: in press Pages: 54-569
- DOI
  10.1101/gr.164913.113
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-23249075, KAKENHI-PROJECT-23770273, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-26670169
[Journal Article] Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.2014
- Author(s)
  Rumbajan JM, Maeda T, Souzaki R, Mitsui K, Higashimoto K, Nakabayashi K, Yatsuki H, Nishioka K, Harada R, Aoki S, Kohashi K, Oda Y, Hata K, Saji T, Taguchi T, Tajiri T, Soejima H, Joh K.
- Journal Title
  
  BioMed Cancer
  
  Volume: 13 Pages: 608-608
- DOI
  10.1186/1471-2407-13-608
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23256006, KAKENHI-PROJECT-23592631, KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-24592698, KAKENHI-PROJECT-25461554
[Journal Article] Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions (DMRs) to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.2014
- Author(s)
  Maeda T, Higashimoto K, Jozaki K, Hitomi H, Nakabayashi K, Makita Y, Tonoki H, Okamoto N, Takada F, Ohashi H, Migita M, Kosaki R, Matsubara K, Ogata T, Matsuo M, Hamasaki Y, Ohtsuka Y, Nishioka K, Joh K, Mukai T, Hata K, Soejima H
- Journal Title
  
  Genetics in Medicine
  
  Volume: 16(12) Pages: 903-12
- DOI
  10.1038/gim.2014.46
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-25461554, KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-25860898, KAKENHI-PROJECT-26670169
[Journal Article] Fibroadenoma in a Beckwith-Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5.2014
- Author(s)
  Takama Y, Kubota A, Nakayama M, Higashimoto K, Jozaki K, Soejima H.
- Journal Title
  
  Pediatr Int
  
  Volume: 56 Pages: 931-934
- DOI
  10.1111/ped.12406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461554, KAKENHI-PROJECT-26670169
[Journal Article] A novel de novo point mutation of OCT-binding site in the IGF2/H19-imprinting control region in a patient with Beckwith-Wiedemann syndrome2014
- Author(s)
  Higashimoto K, Jozaki K, Kosho T, Matsubara K, Sato T, Yamada D, Yatsuki H, Maeda T, Ohtsuka Y, Nishioka K, Joh K, Koseki H, Ogata T, SoejimaH*
- Journal Title
  
  Clin Genet.
  
  Volume: in press Pages: 539-44
- DOI
  10.1111/cge.12318
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-23249015, KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25461554, KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-25860898, KAKENHI-PROJECT-26670169
[Journal Article] 間葉性異形成胎盤Placental mesenchymal dysplasia (PMD)の診断と原因遺伝子2014
- Author(s)
  大場隆、片渕秀隆、副島英伸
- Journal Title
  
  病理と臨床
  
  Volume: 32 Pages: 535-540
- Data Source
  KAKENHI-PROJECT-26670169
[Journal Article] Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation2014
- Author(s)
  Ohnishi K, Semi K, Yamamoto T, Shimizu M, Tanaka A, Mitsunaga K, Okita K, Osafune K, Arioka Y, Maeda T, Soejima H, Moriwaki H, Yamanaka S, Woltjen K, Yamada Y.
- Journal Title
  
  Cell
  
  Volume: 156 Pages: 663-677
- DOI
  10.1016/j.cell.2014.01.005
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-24390096, KAKENHI-PROJECT-24880023, KAKENHI-PROJECT-25460987, KAKENHI-PROJECT-25460988, KAKENHI-PROJECT-25893084, KAKENHI-PROJECT-26670169, KAKENHI-PROJECT-221S0001
[Journal Article] Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation2014
- Author(s)
  Ohnishi K, Semi K, Yamamoto T, Shimizu M, Tanaka A, Mitsunaga K, Okita K, Osafune K, Arioka Y, Maeda T, Soejima H, Moriwaki H, Yamanaka S, Woltjen K, Yamada Y
- Journal Title
  
  Cell
  
  Volume: 156(4) Pages: 663-677
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome2013
- Author(s)
  Higashimoto, K, Maeda, T, Okada, J, Ohtsuka, Y, Sasaki, K, Hirose, A, Nomiyama, M, Takayanagi, T, Fukuzawa, R, Yatsuki, H, Koide, K, Nishioka, K, Joh, K, Watanabe, Y, Yoshiura, ICI, Soejima, H.
- Journal Title
  
  Eur J Hum Genet.
  
  Volume: 21 Pages: 1316-1319
- DOI
  10.1038/ejhg.2013.45
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-13J11173, KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-25461554
[Journal Article] Novel Mutations of CDKN1C in Japanese Patients with Beckwith-Wiedemann Syndrome2013
- Author(s)
  Yatsuki H, Higashimoto K, Jozaki K, Koide K, Okada J, Watanabe Y, Okamoto N, Tsuno Y, Yoshida Y, Ueda K, Shimizu K, Ohashi H, Mukai T, Soejima H
- Journal Title
  
  Genes & Genomics
  
  Volume: 35(2) Pages: 141-147
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Beckwith-Wiedemann 症候群とSilver-Russell 症候群2013
- Author(s)
  前田寿幸, 東元健, 副島英伸
- Journal Title
  
  小児科臨床
  
  Volume: 66(増刊号) Pages: 1308-1314
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome2013
- Author(s)
  Soejima H
- Journal Title
  
  J Hum Genet
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract Polycomb silencing2013
- Author(s)
  Miyazaki H, Higashimoto K, Yada Y, A. Endo T¶, Sharif J¶, Komori T, Matsuda M, Koseki Y, Nakayama M, Soejima H, Handa H, Koseki H, Hirose S, Nishioka K
- Journal Title
  
  PLoS Genet
  
  Volume: 9(11)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Beckwith-Wiedemann症候群とSilver-Russell症候群2013
- Author(s)
  前田寿幸、東元健、副島英伸
- Journal Title
  
  小児科臨床
  
  Volume: 66 Pages: 1308-1314
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome2013
- Author(s)
  Higashimoto K, Maeda T, Okada J, Ohtsuka Y, Sasaki K, Hirose A, Nomiyama M, Takayanagi T, Fukuzawa R, Yatsuki H, Koide K, Nishioka K, Joh K, Watanabe Y, Yoshiura KI, Soejima H
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 21(11) Pages: 1316-1319
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Epigenetic and genetic alterations of the imprinting disorder Beckwith–Wiedemann syndrome and related disorders.2013
- Author(s)
  Soejima H, Higashimoto K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 58 Pages: 402-409
- DOI
  10.1038/jhg.2013.51
- NAID
  10031190033
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-25461554
[Journal Article] Regional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes2013
- Author(s)
  Fukuda K, Ichiyanagi K, Yamada Y, Go Y, Udono T, Wada S, Maeda T, Soejima H, Saitou N, Ito T, Sasaki H
- Journal Title
  
  J Hum Genet
  
  Volume: 58(7) Pages: 446-454
- NAID
  10031190040
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Beckwith-Wiedemann 症候群, Sotos 症候群2013
- Author(s)
  副島英伸
- Journal Title
  
  周産期医学
  
  Volume: 43(3) Pages: 377-382
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Beckwith-Wiedemann症候群，Sotos症候群2013
- Author(s)
  副島英伸
- Journal Title
  
  周産期医学
  
  Volume: 43(3) Pages: 377-382
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 : Few clinical features suggestive of Beckwith-Wiedemann syndrome2013
- Author(s)
  Adachi H, Takahashi I, Higashimoto K, Tsuchida S, Noguchi A, Tamura H, Arai H, Ito T, Masue M, Nishibori H, Takahashi T, Soejima H
- Journal Title
  
  Endocr J
  
  Volume: 60(4) Pages: 403-408
- NAID
  10031170628
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders2013
- Author(s)
  Soejima H, Higashimoto K
- Journal Title
  
  J Hum Genet
  
  Volume: 58(7) Pages: 402-409
- NAID
  10031190033
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient2013
- Author(s)
  Higashimoto K, Jozaki K, Kosho T, Matsubara K, Fuke T, Yamada D, Yatsuki H, Maeda T, Ohtsuka Y, Nishioka K, Joh K, Koseki H, Ogata T, Soejima H
- Journal Title
  
  Clin Genet
  
  Volume: (published online)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma2013
- Author(s)
  Rumbajan JM, Maeda T, Souzaki R, Mitsui K, Higashimoto K, Nakabayashi K, Yatsuki H, Nishioka K, Harada R, Aoki S, Kohashi K, Oda Y, Hata K, Saji T, Taguchi T, Tajiri T, Soejima H, Joh K
- Journal Title
  
  BMC Cancer
  
  Volume: 13 Pages: 608-608
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.2013
- Author(s)
  Higashimoto K, Maeda T, Okada J, Ohtsuka Y, Sasaki K, Hirose A, Nomiyama M, Takayanagi T, Fukuzawa R, Yatsuki H, Koide K, Nishioka K, Joh K, Watanabe Y, Yoshiura K, Soejima H.
- Journal Title
  
  Eur J Hum Genet.
  
  Volume: 21（11） Pages: 1316-1319
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461648
[Journal Article] Regional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes2013
- Author(s)
  福田渓
- Journal Title
  
  J Hum Genet
  
  Volume: 58 Pages: 446-454
- DOI
  10.1038/jhg.2013.55
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-13J03253, KAKENHI-PROJECT-22247037, KAKENHI-PROJECT-23249019, KAKENHI-PROJECT-23659181, KAKENHI-PUBLICLY-24113511, KAKENHI-PROJECT-24510266, KAKENHI-PROJECT-24650234, KAKENHI-PROJECT-25711027
[Journal Article] Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract Polycomb silencing.2013
- Author(s)
  H. Miyazaki, K. Higashimoto, Y. Yada, T. A. Endo, J. Sharif, T. Komori, M. Matsuda, Y. Koseki, M. Nakayama, H. Soejima, H. Handa, H. Koseki, S. Hirose, K. Nishioka
- Journal Title
  
  PLoS Genet
  
  Volume: 9
- DOI
  10.1371/journal.pgen.1003897
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-23102002, KAKENHI-PROJECT-23659181, KAKENHI-PROJECT-25461554
[Journal Article] Aberrant methylation of H19-DMR acquired after2012
- Author(s)
  Higashimoto K, et al.
- Journal Title
  
  Am J Med Genet A
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome2012
- Author(s)
  Higashimoto K, Nakabayashi K, Yatsuki H, Yoshinaga H, Jozaki K, Okada J, Watanabe Y, Aoki A, Shiozaki A, Saito S, Koide K, Mukai T, Hata K, Soejima H
- Journal Title
  
  Am J Med Genet Part A
  
  Volume: 158A(7) Pages: 1670-1675
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome2012
- Author(s)
  Higashimoto K
- Journal Title
  
  Am J Med Genet A
  
  Volume: 158A Pages: 1670-1675
- DOI
  10.1002/ajmg.a.35335
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies2012
- Author(s)
  Hiura H, Okae H, Miyauchi N, Sato F, Sato A, Van De Pette M, John RM, Kagami M, Nakai K, Soejima H, Ogata T, Arima T
- Journal Title
  
  Hum Reprod
  
  Volume: 27(8) Pages: 2541-2548
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659181
[Journal Article] Acute megakaryocytic leukemia (AMKL, FAB ; M7) with Beckwith-wiedemann syndrome.2010
- Author(s)
  Yamamoto S, Soejima H, Isoyama K
- Journal Title
  
  Pediatr Blood Cancer. 55(4)
  
  Pages: 733-735
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] Organotypic culture of human bone marrow adipose tissue for analyzing its biological roles.2010
- Author(s)
  Uchihashi K, Soejima H, Toda S
- Journal Title
  
  Pathol Int 60(4)
  
  Pages: 259-267
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] エピジェネティクス関連疾患と解析方法2009
- Author(s)
  副島英伸
- Journal Title
  
  臨床紡理 57(8)
  
  Pages: 769-778
- NAID
  10026337428
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] Antisense transcription occurs at the promoter of a mouse imprinted gene, Commdl, on the repressed paternal allele.2009
- Author(s)
  Joh K, Yatsuki H, Higashimoto K, Mukai T, Soejima H
- Journal Title
  
  J Biochem 146(6)
  
  Pages: 771-774
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] 小児秤特集小児疾患における臨床遺伝学の進歩2009
- Author(s)
  東元健、副島英伸
- Journal Title
  
  Beckwith-Wiedemann症候群 50(7)
  
  Pages: 1046-1052
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] Wiedemann-Beckwith症候群2009
- Author(s)
  副島英伸
- Journal Title
  
  ビジュアル疾患解説目で見る遺伝病とターナー症候群株式会社メディアート(新川詔夫,緒方勤監修) No.5
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] 特集小児疾患における臨床遺伝学の進歩Beckwith-Wiedemann症候群2009
- Author(s)
  東元健
- Journal Title
  
  小児科 50
  
  Pages: 1046-1052
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] エピジェネティクス関連疾患と解析方法2009
- Author(s)
  副島英伸
- Journal Title
  
  臨床病理 57
  
  Pages: 769-778
- NAID
  10026337428
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article]2009
- Author(s)
  副島英伸(新川詔夫, 吉浦孝一郎監訳)
- Journal Title
  
  カラー図解基礎から疾患までわかる遺伝学第2部ゲノミクス(メディカル・サイエンス・インターナショナル)
  
  Pages: 240-269
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article]2009
- Author(s)
  副島英伸(新川詔夫, 緒方勤監修)
- Journal Title
  
  ビジュアル疾患解説目で見る遺伝病とターナー症候群Wiedemann-Beckwith症候群(株式会社メディアート)
  
  Pages: 6-7
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities.2008
- Author(s)
  Haruta M, Soejima H, Kaneko Y
- Journal Title
  
  Genes Chromosomes Cancer 47(8)
  
  Pages: 712-727
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] 特集エピジェネティクス-最近の動向と疾患-ゲノムインプリンティング異常と疾患2008
- Author(s)
  副島英伸
- Journal Title
  
  最新医学 63(4)
  
  Pages: 83-90
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products.2008
- Author(s)
  Yakabe S, Soejima H, Higashimoto K, Joh K
- Journal Title
  
  Genes Genet Syst 83(2)
  
  Pages: 199-208
- NAID
  10024396087
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] ゲノムインプリンティング機構と疾患2008
- Author(s)
  副島英伸
- Journal Title
  
  臨床検査 52(6)
  
  Pages: 683-688
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] A BHD Germline Mutation Identified in an Asian Family with Birt-Hogg-Dube Syndrome.2008
- Author(s)
  Misago N, Joh K, Soejima H
- Journal Title
  
  Acta Dermato-Venereologica 88(4)
  
  Pages: 423-425
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] ゲノム刷り込みとBeckwith-Wiedemann症候群2008
- Author(s)
  東元健, 副島英伸
- Journal Title
  
  日本小児血液学会雑誌 22(3)
  
  Pages: 139-143
- NAID
  10029309180
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] 特集エピジェネティクス-最近の動向と疾患- ゲノムインプリンティング異常と疾患2008
- Author(s)
  副島英伸
- Journal Title
  
  最新医学 63
  
  Pages: 83-90
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] ゲノム刷り込みとBeckwith-Wiedemann症候群2008
- Author(s)
  東元健
- Journal Title
  
  日本小児血液学会雑誌 22
  
  Pages: 139-143
- NAID
  10029309180
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] MeCP2-dependent repression of an imprinted miR-184 released by depolarization.2008
- Author(s)
  Nomura T, Soejima H, Hatada I
- Journal Title
  
  Hum Mol Genet 17(8)
  
  Pages: 1192-1199
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] A new organotypic culture of adipose tissue fragments maintains viable mature adipocytes for a long term, together with development of immature adipocytes and mesenchymal stem cell-like cells.2008
- Author(s)
  Sonoda E, Soejima H, Toda S
- Journal Title
  
  Endocrinology 149(10)
  
  Pages: 4794-4798
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] ゲノムインプリンティング機構と疾患2008
- Author(s)
  副島英伸
- Journal Title
  
  臨床検査 52
  
  Pages: 683-688
- Data Source
  KAKENHI-PROJECT-20590330
[Journal Article] Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations.2007
- Author(s)
  Sasaki, K, Soejima, H, Higashimoto, K, Yatsuki, H, Ohashi, H, Yakabe, S, Joh, K, Niikawa, N, Mukai, T
- Journal Title
  
  Eur JHum Genet 15(12)
  
  Pages: 1205-10
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Role of DNA methylation and histone H3 Lysine 27 methylation in tissue-specific imprinting of mouse Grb 10.2007
- Author(s)
  Yamasaki-Ishizaki, Y, Kayashima, T, Mapendano, CK, Soejima, H, Ohta, T, Masuzaki, H, Kinoshita, A, Urano, T, Yoshiura, KI, Matsumoto, N, Ishimaru, T, Mukai, T, Niikawa, N, Kishino, T
- Journal Title
  
  Mol Cell Biol 27(2)
  
  Pages: 732-742
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] 特集エピジェネティクスの最新テクノロジーヒストン修飾の個別およびゲノム網羅的解析法-ChIP法とChIP on chip法2007
- Author(s)
  副島英伸
- Journal Title
  
  バイオテクノロジージャーナル 7
  
  Pages: 433-439
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Leading-edge technology for epigenetics-site specific and genome wide analysis of the histone modification-ChIP and ChIP on chip(in Japanese)2007
- Author(s)
  Soejima, H
- Journal Title
  
  Biotechnology Journal 7(4)
  
  Pages: 433-439
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type2007
- Author(s)
  Watanabe, N, Haruta, M, Soejima, H, Fukushi, D, Yokomori, K, Nakadate, H, Okita, H, Hata, J, Fukuzawa, M, Kaneko, Y
- Journal Title
  
  Genes, Chromosomes and Cancer 46(10)
  
  Pages: 929-935
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] 特集エピジェネティクスの最新テクノロジーヒストン修飾の個別およびゲノム網羅的解析法〜ChIP法とChIP on chip法2007
- Author(s)
  副島英伸
- Journal Title
  
  バイオテクノロジージャーナル 7
  
  Pages: 433-439
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 11q : Comparison with chromosome 21q.2006
- Author(s)
  Yamada, Y, Shirakawa, T, Taylor, Td, Okamura, K, Soejima, H, Uchiyama, M., Iwasaka, T, Mukai, T, Muramoto, Ki, Sakaki, Y, Ito, T
- Journal Title
  
  DNA Sequence 17(4)
  
  Pages: 300-306
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] 4 Imprinting related diseases, Chapter 5 Epigenetics and diseases, Genome Wide Development of Epigenetic Medical Science.(in Japanese)2006
- Author(s)
  Soejima, H, Ohta, T, Mukai, T
- Journal Title
  
  (M, Nakao, K, Shiota, T, Ushijima, Sasaki H ed.)(Yodo-sha, Tokyo, Experimental Medicine) 24(8)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumors2006
- Author(s)
  Satoh, Y, Nakadate, H, Nakagawachi, T, Higashimoto, K, Joh, K, Masaki, Z, Uozumi, J, Kaneko, Y, Mukai, T, Soejima, H
- Journal Title
  
  Brit J Cancer 95(4)
  
  Pages: 541-547
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers.2006
- Author(s)
  Nakano, S, Murakami, K, Meguro, M, Soejima, H, Higashimoto, K, Urano, T, Kugoh, H, Mukai, T, Ikeguchi, M., Oshimura, M
- Journal Title
  
  Cancer Science 97(11)
  
  Pages: 1147-1154
- NAID
  10019376824
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Imprinting disruption of the KIP2/LIT1 domain : the molecular mechanism causing Beckwith-Wiedemann syndrome and cancer.2006
- Author(s)
  Higashimoto K
- Journal Title
  
  Cytogenet Genome Res 113(1-4)
  
  Pages: 306-312
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Association of 11q loss, trisomy 12 and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.2006
- Author(s)
  Watanabe, N, Nakadate, H, Haruta, M, Sugawara, W, Sasaki, F, Tsunematsu, Y, Kikuta, A, Fukuzawa, M, Okita, H, Hata, Ji, Soejima, H, Kaneko, Y
- Journal Title
  
  Gene Chromosome Cancer 45(6)
  
  Pages: 592-601
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] Imprinting disruption of the KIP2/LIT1 domain : the molecular mechanism causing Beckwith-Wiedemann syndrome and cancer2006
- Author(s)
  Higashimoto K
- Journal Title
  
  Cytogenet Genome Res 113・1-4
  
  Pages: 306-312
- Data Source
  KAKENHI-PROJECT-18590313
[Journal Article] インプリンティングと先天異常、癌2005
- Author(s)
  副島英伸
- Journal Title
  
  Molecular Medicine 42・2
  
  Pages: 201-208
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Imprinting, Chromatin Structure, and Disease.2005
- Author(s)
  Soejima H
- Journal Title
  
  J Cell Biochem 95・2
  
  Pages: 226-233
- Data Source
  KAKENHI-PROJECT-17019054
[Journal Article] インプリンティングと先天異常、癌.2005
- Author(s)
  副島英伸
- Journal Title
  
  Molecular Medicine 42・2
  
  Pages: 201-208
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] インプリンティングと先天異常、癌2005
- Author(s)
  副島英伸
- Journal Title
  
  Molecular Medicine 42・2
  
  Pages: 201-208
- Data Source
  KAKENHI-PROJECT-17019054
[Journal Article] Imprinting, Chromatin Structure, and Disease.2005
- Author(s)
  Soejima H
- Journal Title
  
  J Cell Biochem 95・2
  
  Pages: 226-233
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Genomic imprinting and congenital abnormality and cancer.2005
- Author(s)
  Soejima H
- Journal Title
  
  Molecular Medicine 42・2
  
  Pages: 201-208
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Epigenetic silencing of the MGMT gene in cancer.2005
- Author(s)
  Soejima H
- Journal Title
  
  Biochem Cell Biol 83・4
  
  Pages: 429-437
- Data Source
  KAKENHI-PROJECT-17019054
[Journal Article] Epigenetic silencing of the MGMT gene in cancer.2005
- Author(s)
  Soejima H
- Journal Title
  
  Biochem Cell Biol 83・4
  
  Pages: 429-437
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.2004
- Author(s)
  Soejima H
- Journal Title
  
  Oncogene 23・25
  
  Pages: 4380-4388
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Gene silencing in DNA damage repair2004
- Author(s)
  Soejima H
- Journal Title
  
  Cellular and Molecular Life Science 61・17
  
  Pages: 2168-2172
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer2004
- Author(s)
  Soejima H
- Journal Title
  
  Oncogene 23・25
  
  Pages: 4380-4388
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Molecular genetics of Beckwith -Wiedenman syndrome.2004
- Author(s)
  Soejima H
- Journal Title
  
  The Cell 36・7
  
  Pages: 278-281
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Journal Article] Beckwith-Wiedenmann症候群の分子遺伝学2004
- Author(s)
  副島英伸
- Journal Title
  
  細胞 36・7
  
  Pages: 278-281
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590263
[Presentation] 遺伝子検査と遺伝カウンセリング2022
- Author(s)
  副島英伸
- Organizer
  第19回佐賀県新生児聴覚スクリーニング研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] 遺伝子検査と遺伝カウンセリング2022
- Author(s)
  副島英伸
- Organizer
  第19回佐賀県新生児聴覚スクリーニング研究会
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] エピゲノム異常疾患とゲノム異常2022
- Author(s)
  副島英伸
- Organizer
  第３回Chubu Cytogenetics Conference
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] エピゲノム異常疾患とゲノム異常2022
- Author(s)
  副島英伸
- Organizer
  第３回Chubu Cytogenetics Conference
- Invited
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] IGF2-DMR0はDNAメチル化依存的なIGF2 P0プロモーター特異的エンハンサーである―ソトス症候群のインプリントDMRのDNAメチル化解析から―2021
- Author(s)
  東元健、渡邊英孝、三宅紀子、森田純代、堀居拓郎、畑田出穂、松本直通、副島英伸
- Organizer
  第14回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] 表現型は一致するがDNAメチル化状態が一致しないBeckwith-Wiedemann症候群双胎（二絨毛膜二羊膜）の1例2021
- Author(s)
  原聡史、孫菲菲、富田知世子、田上由香、八木ひとみ、東元健、副島英伸．
- Organizer
  日本人類遺伝学会第66回大会・第28回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] Beckwith-Wiedemann症候群に合併した副腎性クッシング症候群の_例．2021
- Author(s)
  八木弘子、佐藤知彦、神尾卓哉、東元健、副島英伸、照井君典
- Organizer
  第29回特定非営利活動法人東北内分泌研究会・第41回日本内分泌学会東北地方会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.2021
- Author(s)
  Soejima H, Sun F, Yatsuki H, Higashimoto K, Hara S.
- Organizer
  European Society of Human Genetics Conference
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] Beckwith-Wiedemann症候群に合併した副腎性クッシング症候群の_例．2021
- Author(s)
  八木弘子、佐藤知彦、神尾卓哉、東元健、副島英伸、照井君典
- Organizer
  第29回特定非営利活動法人東北内分泌研究会・第41回日本内分泌学会東北地方会
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] IGF2-DMR0はDNAメチル化依存的なIGF2 P0プロモーター特異的エンハンサーである―ソトス症候群のインプリントＤＭＲのＤNAメチル化解析から―2021
- Author(s)
  東元健，渡邊英孝, 三宅紀子, 森田純代, 堀居拓郎, 畑田出穂, 松本直通, 副島英伸．
- Organizer
  第14回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.2021
- Author(s)
  Soejima H, Sun F, Yatsuki H, Higashimoto K, Hara S.
- Organizer
  European Society of Human Genetics Conference
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] 前立腺癌におけるBRCA1/2遺伝子検査と遺伝カウンセリング2021
- Author(s)
  副島英伸
- Organizer
  日本泌尿器科学会第86回佐賀地方会専門医制度対応泌尿器科領域講習会
- Invited
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] 前立腺癌におけるBRCA1/2遺伝子検査と遺伝カウンセリング2021
- Author(s)
  副島英伸
- Organizer
  日本泌尿器科学会第86回佐賀地方会専門医制度対応泌尿器科領域講習会
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] エピゲノム異常疾患―基礎、解析、診断―2021
- Author(s)
  副島英伸
- Organizer
  第２８回臨床細胞遺伝学セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] エピゲノム異常疾患―基礎、解析、診断―2021
- Author(s)
  副島英伸
- Organizer
  第２８回臨床細胞遺伝学セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] 表現型は一致するがDNAメチル化状態が一致しないBeckwith-Wiedemann症候群双胎（二絨毛膜二羊膜）の1例2021
- Author(s)
  原聡史、孫菲菲、富田知世子、田上由香、八木ひとみ、東元健、副島英伸．
- Organizer
  日本人類遺伝学会第66回大会・第28回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-21K19451
[Presentation] IGF2-DMR0はDNAメチル化依存的なIGF2 P0プロモーター特異的エンハンサーである―ソトス症候群のインプリントＤＭＲのＤNAメチル化解析から―2021
- Author(s)
  東元健，渡邊英孝, 三宅紀子, 森田純代, 堀居拓郎, 畑田出穂, 松本直通, 副島英伸．
- Organizer
  第14回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] 羊水・胎盤・新_児末梢_の染_体検査結果に相違を認めた性染_体モザイクの１例2020
- Author(s)
  山本徒子、大隈恵美、副島英伸、横山正俊
- Organizer
  第44回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] 子宮体癌再発症例におけるがんゲノムプロファイリング検査2020
- Author(s)
  大隈恵美、中尾佳史、大隈良一、栗原麻希子、光貴子、田中智子、山本徒子、橋口真理子、中村秀明、佐藤朋美、横山正俊、副島英伸、荒金尚子
- Organizer
  日本人類遺伝学会第65回大会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.2020
- Author(s)
  Watanabe H, Higashimoto K, Miyake N, Morita S, Horii T, Kimura M, Suzuki T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Uemura T, Hatada I, Matsumoto N, Soejima H.
- Organizer
  European Society of Human Genetics Conference
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] ICR1のセントロメア側のDNA低メチル化によって生じたシルバーラッセル症候群の1例2020
- Author(s)
  東元健、渡邉聖、田上由香、外木秀文、徳富智明、原聡史、八木ひとみ、副島英伸
- Organizer
  日本人類遺伝学会第65回大会
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] ヒト疾患のエピゲノム2020
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第65回大会
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] 遺伝の基礎とエピジェネティクスの基礎2020
- Author(s)
  副島英伸
- Organizer
  日本遺伝看護学会第19回学術大会Web開催
- Invited
- Data Source
  KAKENHI-PROJECT-20H03643
[Presentation] The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome.2019
- Author(s)
  Sun F, Higashimoto K, Soejima H.
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Methylation anticipation extends to the outside of ICR1 in familial Beckwith-Wiedemann syndrome patients with ICR1 mutation.2019
- Author(s)
  Sun F, Higashimoto K, Soejima H.
- Organizer
  European Society of Human Genetics Conference 2019
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] IGF2-DMR0はDNAメチル化依存的なIGF2 P0プロモーター特異的エンハンサーである-ソトス症候群のインプリントＤＭＲのＤNAメチル化解析から-2019
- Author(s)
  東元健、渡邊英孝、三宅紀子、森田純代、堀居拓郎、畑田出穂、松本直通、副島英伸．
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 本邦の間葉性異形成胎盤症例における妊娠高血圧症候群の発症に関する検討―PMD全国調査の副次的解析―．2019
- Author(s)
  小寺千聡、大場隆、副島英伸、片渕秀隆．
- Organizer
  第40回日本妊娠高血圧学会学術集会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] IGF2 overexpression due to IGF2-DMR0 hypomethylation in Sotos syndrome.2019
- Author(s)
  Higashimoto K, Watanabe H, Miyake N, Morita S, Horii T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Hatada I, Matsumoto N, Soejima H.
- Organizer
  The 59th Annual Meeting of The Japanese Teratology Society, The 13th World Congress of The International Cleft Lip and Palate Foundation
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] HBOCの遺伝カウンセリング2019
- Author(s)
  副島英伸
- Organizer
  第11回佐賀乳腺フォーラム
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] FACSと次世代シークエンサーを用いたshRNAライブラリースクリーニングによるポリコームサイレンシング制御因子の探索2019
- Author(s)
  西岡憲一、宮_仁美、副島英伸．
- Organizer
  第13回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] ヒト疾患のエピゲノム2019
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第64回大会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 先天異常症候群のエピゲノム異常2019
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第64回大会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Atypical DNA methylation defects of ICR1 cause two opposite imprinting disorders, Beckwith-Wiedemann syndrome and Silver-Russell syndrome．2019
- Author(s)
  Soejima H, Sun F, Tanoue Y, Yatsuki H, Higashimoto K.
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 乳癌と卵巣癌を合併する症例の検討．2019
- Author(s)
  大隈恵美、橋口真理子、山本徒子、西山哲、光貴子、中尾佳史、副島英伸、横山正俊．
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] DNA methylation anticipation due to ICR1 mutation in familial Beckwith-Wiedemann syndrome patients.2019
- Author(s)
  Sun F, Higashimoto K, Soejima H. The extended
- Organizer
  第13回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR occurs in the growing oocyte, but not in early embryonic cells.2018
- Author(s)
  Soejima H, Matsuhisa F, Kitajima S, Nishioka K, Higashimoto K, Yatsuki H, Kono T, Koseki, H Joh K.
- Organizer
  European Society of Human Genetics Conference 2018.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] エピゲノム―基礎と疾患―2018
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第63回大会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Clinicopathological features and genomic/epigenetic aspects of placental mesenchymal dysplasia2018
- Author(s)
  Kodera C, Aoki S, Ohba T, Higashimoto K, Soejima H, Katabuchi H.
- Organizer
  IFPA 2018
- Data Source
  KAKENHI-PROJECT-15K10678
[Presentation] FACSと次世代シークエンサーを用いたshRNAライブラリースクリーニングによるポリコームサイレンシング制御因子の探索2018
- Author(s)
  西岡憲一、宮崎仁美、副島英伸
- Organizer
  第41回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 眼瞼腫脹を契機に神経芽細胞腫が判明したBeckwith-Wiedemann症候群の女児．2018
- Author(s)
  米田堅佑、川口晃司、高橋郁子、小倉妙美、堀越泰雄、宮林和紀、左藤由梨亜、東元健、副島英伸、渡邉健一郎
- Organizer
  第121回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 佐賀大学におけるHBOCの遺伝カウンセリング2018
- Author(s)
  副島英伸
- Organizer
  BRCA遺伝子変異陽性乳癌診療セミナー in Saga
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] エピジェネティクス_基礎と疾患_2018
- Author(s)
  副島英伸
- Organizer
  第42回日本産婦人科栄養・代謝研究会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] NSD1 haploinsufficiency evokes DNA hypomethylation at imprinted DMRs and the increased expression of imprinted genes.2018
- Author(s)
  Watanabe H, Higashimoto K, Nagano Y, Kurokawa M, Uemura T, Soejima H
- Organizer
  EURAPS Research Meeting 2018.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 超早産児で出生した11p15.5重複によるBeckwith-Wiedemann症候群の一例2018
- Author(s)
  香田翼、三崎真衣子、柴田暁男、川本久美、東元健、副島英伸、竹島泰弘
- Organizer
  日本人類遺伝学会第63回大会 2017.10.10-13. パシフィコ横浜（ポスターP-195、プログラム・抄録集 p152/p353）
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Beckwith-Wiedemann syndrome and placental mesenchymal dysplasia.2018
- Author(s)
  Soejima H.
- Organizer
  International Federation of Placenta Associations (IFPA 2018 Tokyo Meeting)
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Beckwith-Wiedemann症候群とゲノムインプリンティング2018
- Author(s)
  副島英伸
- Organizer
  第175回染色体研究会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] ポリコーム抑制複合体２の構成蛋白質の遺伝子変異がWeaver症候群を引き起こす2017
- Author(s)
  今川英里、東元健、酒井康成、沼倉周彦、岡本伸彦、松永智子、梁明秀、佐藤由典、實藤雅文、井原健二、高田結、西村玄、才津浩智、水口剛、宮武聡子、中島光子、三宅紀子、副島英伸、松本直通
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Mbf1はPacmanからE(z) mRNAを保護することでポリコームサイレンシングの堅牢性を担保している2017
- Author(s)
  西岡憲一、宮崎仁美、副島英伸、広瀬進
- Organizer
  第11回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] NSD1ハプロ不全はDNAメチル化インプリント異常と遺伝子発現異常を惹起する2017
- Author(s)
  渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、松本直通、副島英伸
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Mbf1はPacmanからE(z) mRNAを保護することでポリコームサイレンシングの堅牢性を担保している2017
- Author(s)
  西岡憲一、宮崎仁美、副島英伸、広瀬進
- Organizer
  2017年度生命科学系学会合同年次大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Germline mutations associated with polycomb repressive complex 2 cause Weaver syndrome2017
- Author(s)
  Imagawa E, Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N
- Organizer
  The 67th Annual Meeting of the American Society of Human Genetics
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 大腸癌におけるインプリントDMRの包括的メチル化解析2017
- Author(s)
  樋高秀憲、東元健、青木早織、渡邊英孝、前田寿幸、古賀靖大、岩切龍一、能城浩和、藤本一眞、副島英伸
- Organizer
  第11回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] マウスCommd1とZrsr1のゲノムインプリンティング機構の研究2017
- Author(s)
  城圭一郎、西岡憲一、北嶋修司、松久葉一、古関明彦、河野友宏、副島英伸
- Organizer
  2017年度生命科学系学会合同年次大会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] NSD1 haploinsufficiency evokes DNA hypomethylation at imprinted DMRs and the increased expression of imprinted genes2017
- Author(s)
  Watanabe H, Higashimoto K, Miyake N, Maeda T, Hidaka H, Aoki S, Matsumoto N, Soejima H
- Organizer
  The 67th Annual Meeting of the American Society of Human Genetics
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] マウスCommd1とZrsr1のゲノムインプリンティング機構の研究2017
- Author(s)
  城圭一郎、西岡憲一、北嶋修司、松久葉一、古関明彦、河野友宏、副島英伸
- Organizer
  第11回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] NSD1ハプロ不全はDNAメチル化インプリント異常と遺伝子発現異常を惹起する2017
- Author(s)
  渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、松本直通、副島英伸
- Organizer
  第11回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] Beckwith-Wiedemann症候群に合併した後縦隔神経芽腫の1例2017
- Author(s)
  川口晃司、卜部馨介、高橋郁子、小倉妙美、堀越泰雄、東元健、副島英伸、渡邉健一郎
- Organizer
  第73回東海小児がん研究会
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 間葉性異形成胎盤とインプリンティング異常2017
- Author(s)
  副島英伸
- Organizer
  第25回日本胎盤学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] ゲノムインプリンティングのoverviewとBeckwith-Wiedemann症候群2017
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第62回大会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08687
[Presentation] 大腸癌におけるインプリントDMRの包括的メチル化解析（Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer）2016
- Author(s)
  樋高秀憲、東元健、古賀靖大、副島英伸．
- Organizer
  第75回日本癌学会学術総会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2016-10-06
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Novel MCA/ID syndrome with ASH1L mutation.2016
- Author(s)
  Okamoto N, Miya F, Nishioka K, Soejima H, Tsunoda T, Kato M, Saitoh S, Yamasaki M, Kanemura Y, Kosaki K.
- Organizer
  The 13th International Congress of Human Genetics.
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] DNAメチル化異常不一致を示す一卵性2絨毛膜2羊膜双胎のBeckwith-Wiedemann syndrome2016
- Author(s)
  東元　健、八木ひとみ、副島英伸
- Organizer
  第23回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  長崎大学医学部
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 大腸癌におけるインプリントDMRの包括的メチル化解析2016
- Author(s)
  樋高秀憲、東元健、青木早織、渡邊英孝、前田寿幸、古賀靖大、岩切龍一、能城浩和、藤本一眞、副島英伸
- Organizer
  第10回日本エピジェネティクス研究会年会
- Place of Presentation
  千里ライフサイエンスセンター
- Year and Date
  2016-05-19
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] ソトス症候群とベックウィズ・ビーデマン症候群でオーバーラップする表現型の原因探索2016
- Author(s)
  渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、松本直通、副島英伸
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  慶應義塾大学三田キャンパス
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] NSD1ハプロ不全はDNAメチル化インプリント異常と遺伝子発現異常を惹起する2016
- Author(s)
  渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、森田純代、堀居拓郎、木村美香、畑田出穂、松本直通、副島英伸
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.2016
- Author(s)
  Hidaka H, Higashimoto K, Takara Y, Takedomi H, Okamoto N, Kawakubo H, Yamamoto K, Yamanouchi K, Koga Y, Iwakiri R, Noshiro H, Fujimoto K, Soejima H
- Organizer
  24th United European Gastroenterology Week
- Place of Presentation
  Vienna, Austria
- Year and Date
  2016-10-15
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 間葉性異形成胎盤のゲノム・エピゲノム解析2016
- Author(s)
  青木早織、東元　健、樋高秀憲、大塚泰史、渡邊英孝、三嶋博之、吉浦孝一郎、大場　隆、片渕秀隆、副島英伸
- Organizer
  第10回日本エピジェネティクス研究会年会
- Place of Presentation
  千里ライフサイエンスセンター
- Year and Date
  2016-05-19
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.2016
- Author(s)
  Hidaka H, Higashimoto K, Aoki S, Watanabe H, Yatsuki H, Nishioka K, Joh K, Maeda T, Koga Y, Iwakiri R, Noshiro H, Fujimoto K, Soejima H.
- Organizer
  The 13th International Congress of Human Genetics.
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Aberrant methylation at imprinted DMRs is associated with placental mesenchymal dysplasia.2016
- Author(s)
  Aoki S, Higashimoto K, Hidaka H, Watanabe H, Ohtsuka Y, Mishima H, Yoshiura KI, Yatsuki H, Nishioka K, Joh K, Ohba T, Katabuchi H, Soejima H.
- Organizer
  The 13th International Congress of Human Genetics.
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] DIS3L2複合ヘテロ変異を同定した長期生存Perlman症候群の１例2016
- Author(s)
  長崎啓祐、東元健、相馬規子、今村勝、齋藤昭彦、副島英伸
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  慶應義塾大学三田キャンパス
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] CTCF遺伝子欠失を認めた2女児の臨床的および遺伝学的検討2016
- Author(s)
  堀いくみ, 河村理恵, 中林一彦, 家田大輔, 大橋圭, 根岸豊, 服部文子, 杉尾嘉嗣, 涌井敬子, 黒澤健司, 秦健一郎，副島英伸, 齋藤伸治
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  慶應義塾大学三田キャンパス
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 間葉性異形成胎盤の分子遺伝学的解析2015
- Author(s)
  青木早織、東元健、樋高秀憲、渡邊英孝、大塚泰史、三嶋博之、吉浦孝一郎、八木ひとみ、西岡憲一、城圭一郎、大場隆、片渕秀隆、副島英伸
- Organizer
  第23回日本胎盤学会学術集会
- Place of Presentation
  JA共済ビル（東京）
- Year and Date
  2015-11-05
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Beckwith-Wiedemann症候群エピ変異症例におけるインプリントDMRの包括的メチル化解析2015
- Author(s)
  前田寿幸、城崎幸介、八木ひとみ、東元　健、松尾宗明、副島英伸
- Organizer
  第57回日本小児神経学会学術集会
- Place of Presentation
  帝国ホテル大阪（大阪）
- Year and Date
  2015-05-28
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 間葉性異形成胎盤の分子遺伝学的解析2015
- Author(s)
  青木早織、東元健、樋高秀憲、渡邊英孝、大塚泰史、三嶋博之、吉浦孝一郎、八木ひとみ、西岡憲一、城圭一郎、大場隆、片渕秀隆、副島英伸
- Organizer
  第23回日本胎盤学会学術集会
- Place of Presentation
  JA共済ビル、東京都
- Year and Date
  2015-11-05
- Data Source
  KAKENHI-PROJECT-15K10678
[Presentation] Beckwith-Wiedemann症候群の原因となる片親性父性ダイソミーの切断点領域の解析2015
- Author(s)
  大塚泰史、岡岳彦、川原弘三、八木ひとみ、東元健、副島英伸
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル（東京）
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] シスチン尿症を伴うゲノムワイド父性片親性ダイソミー症例の遺伝子解析2015
- Author(s)
  副島英伸
- Organizer
  第22回日本遺伝子診療学会大会
- Place of Presentation
  かながわ労働プラザ（横浜）
- Year and Date
  2015-07-17
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Beckwith-Wiedemann症候群の原因となる片親性父性ダイソミーの切断点領域の解析．2015
- Author(s)
  大塚泰史、岡岳彦、川原弘三、八木ひとみ、東元健、副島英伸．
- Organizer
  第60回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-25461648
[Presentation] 間葉性異形成胎盤に関するゲノム・エピゲノム解析2015
- Author(s)
  青木早織、東元健、樋高秀憲、渡邊英孝、大塚泰史、三嶋博之、吉浦孝一郎、八木ひとみ、西岡憲一、城圭一郎、大場隆、片渕秀隆、副島英伸．
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル、東京都
- Year and Date
  2015-10-15
- Data Source
  KAKENHI-PROJECT-15K10678
[Presentation] 間葉性異形成胎盤におけるインプリントDMRのエピジェノタイプ変化2015
- Author(s)
  青木早織、東元健、樋高秀憲、大塚泰史、三嶋博之、吉浦孝一郎、大場隆、片渕秀隆、副島英伸
- Organizer
  第22回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  九州大学医学部同窓会館、福岡市
- Year and Date
  2015-10-03
- Data Source
  KAKENHI-PROJECT-15K10678
[Presentation] Beckwith-Wiedemann症候群における新生児期低血糖合併機序の検討2015
- Author(s)
  長嶋一昭、田中大祐、東元　健、八木ひとみ、杉崎　和、田原裕美子、副島英伸、稲垣暢也
- Organizer
  第112回日本内科学会総会
- Place of Presentation
  京都
- Year and Date
  2015-04-10
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Clinical and histopathlogical features of placental mesenchymal dysplasia.2015
- Author(s)
  Aoki S, Ohba T, Okajima M, Higashimoto K, Soejima H, Katabuchi H.
- Organizer
  The 6th Asan-Kumamoto Joint Symposium
- Place of Presentation
  Kumamoto, Japan
- Year and Date
  2015-05-23
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] インプリンティング関連疾患のゲノム・エピゲノム解析2015
- Author(s)
  副島英伸
- Organizer
  第19回日本内分泌病理学会
- Place of Presentation
  アバンセ（佐賀市）
- Year and Date
  2015-10-24
- Invited
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 大腸癌におけるインプリントDMRの包括的メチル化解析2015
- Author(s)
  樋高秀憲、東元健、青木早織、渡邊英孝、八木ひとみ、西岡憲一、城圭一郎、前田寿幸、古賀靖大、岩切龍一、能城浩和、藤本一眞、副島英伸
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル（東京）
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 間葉性異形成胎盤のゲノム・エピゲノム解析2015
- Author(s)
  青木早織、東元健、樋高秀憲、渡邊英孝、大塚泰史、三嶋博之、吉浦孝一郎、八木ひとみ、西岡憲一、城圭一郎、大場隆、片渕秀隆、副島英伸
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル（東京）
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Beckwith-Wiedemann症候群と診断した1絨毛膜2羊膜性双胎の一女児例2015
- Author(s)
  吉村歩、松原理沙、田中秀門、今市悠太郎、吉田悟、荻田薫、野村武雅、側島健宏、松下博亮、白井憲司、南野初香、元重京子、木部哲也、東元健、副島英伸
- Organizer
  第137回日本小児科学会静岡地方会
- Place of Presentation
  静岡県職員会館
- Year and Date
  2015-06-07
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] 間葉性異形成胎盤におけるインプリントDMRのエピジェノタイプ変化2015
- Author(s)
  青木早織、東元健、樋高秀憲、大塚泰史、三嶋博之、吉浦孝一郎、大場隆、片渕秀隆、副島英伸
- Organizer
  第22回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  九州大学
- Year and Date
  2015-10-03
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Beckwith-Wiedemann 症候群と関連疾患におけるゲノム・エピゲノム異常2013
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第58回大会「シンポジウム8 先天異常とゲノム・エピゲノム」
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 間葉性異形成胎盤における11p15インプリント領域の分子遺伝学的解析2013
- Author(s)
  副島英伸、東元健、城﨑幸介、八木ひとみ、大塚泰史、前田寿幸、青木早織、岡島翠、坂口勲、大場隆、片渕秀隆
- Organizer
  第21回日本胎盤学会学術集会
- Place of Presentation
  名古屋市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] H19DMR メチル化異常で発症するインプリント疾患におけるH19DMR の変異解析2013
- Author(s)
  東元健, 城崎幸介, 八木ひとみ, 古庄知己, 松原圭子, 山田大輔, 前田寿幸, 大塚泰史, 古関明彦, 緒方勤, 副島英伸
- Organizer
  第7回日本エピジェネティクス研究会年会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群におけるインプリントDMRのマルチローカスメチル化解析2013
- Author(s)
  前田寿幸、東元健、中林一彦、城崎幸介、八木ひとみ、緒方勤、秦健一郎、副島英伸
- Organizer
  第7回日本エピジェネティクス研究会年会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Practical use of pyrosequencing analysis to detect Moyamoya disease susceptible gene RNF213 variant c.14576G>A2013
- Author(s)
  Takamatsu Y, Maeda T, Matsuo M, Higashimoto K, Kawashima M, Matsushima T, Soejima H
- Organizer
  3rd International Moyamoya Meeting
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] シスチン尿症を伴うゲノムワイド父性片親性ダイソミー症例の遺伝子解析.2013
- Author(s)
  大塚泰史、佐々木健作、城崎幸介、東元健、岡本伸彦、高間勇一、窪田昭男、松本富美、中山雅弘、吉浦孝一郎、副島英伸.
- Organizer
  第58回日本人類遺伝学会.
- Place of Presentation
  日本、宮城
- Data Source
  KAKENHI-PROJECT-25461648
[Presentation] 間葉性異形成胎盤における11p15刷り込み領域の分子遺伝学的解析2013
- Author(s)
  副島英伸、東元健、城﨑幸介、八木ひとみ、大塚泰史、前田寿幸、青木早織、岡島翠、坂口勲、大場隆、片渕秀隆
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 新生児期低血糖合併Beckwith-Wiedemann症候群患者における病態形成機序の検討2013
- Author(s)
  長嶋一昭、田中大祐、東元　健、八木ひとみ、杉崎　和、田原裕美子、小倉かさね、佐藤広規、佐藤雄一、山野　言、副島英伸、稲垣暢也
- Organizer
  第56回日本糖尿病学会年次学術集会
- Place of Presentation
  熊本
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] シスチン尿症を伴うゲノムワイド父性片親性ダイソミー症例の遺伝子解析.2013
- Author(s)
  大塚泰史、佐々木健作、城崎幸介、東元健、岡本伸彦、高間勇一、窪田昭男、松本富美中山雅弘、吉浦孝一郎、副島英伸.
- Organizer
  第48回日本小児腎臓病学会学術集会
- Place of Presentation
  日本、徳島
- Data Source
  KAKENHI-PROJECT-25461648
[Presentation] H19DMRメチル化異常で発症するインプリント疾患におけるH19DMRの変異解析2013
- Author(s)
  東元　健、城崎幸介、八木ひとみ、古庄知己、松原圭子、山田大輔、前田寿幸、大塚泰史、古関明彦、緒方勤、副島英伸
- Organizer
  第7回日本エピジェネティクス研究会年会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] インプリンティング疾患Beckwith-Wiedemann症候群と類縁疾患におけるエピゲノム・ゲノム異常2013
- Author(s)
  副島英伸
- Organizer
  第5回金沢大学学際科学実験センターシンポジウム「深遠なる疾患エピジェネティクス」
- Place of Presentation
  金沢大学
- Invited
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] ゲノムワイドDNAメチル化解析によるヒトインプリントーム解明2013
- Author(s)
  中林一彦、Trujillo Alex Martin、田山千春、兼城英輔、和氣徳夫、副島英伸、緒方勤、Monk David、秦健一郎
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 11p15インプリントドメインのメチル化異常を認めた間葉性異形成胎盤の1例2013
- Author(s)
  副島英伸、東元健、八木ひとみ、青木早織、鮫島梓、齋藤滋、夫律子、中山雅弘、坂口勲、大場隆、片渕秀隆
- Organizer
  第20回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  鹿児島
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 母体血中sFlt-1が異常高値を示したPlacental Mesenchymal Dysplasiaの一例2013
- Author(s)
  鮫島梓、米田徳子、森尻昌人、米澤理可、米田哲、塩崎有宏、夫律子、中山雅弘、副島英伸、齋藤滋
- Organizer
  第21回日本胎盤学会学術集会
- Place of Presentation
  名古屋市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract Polycomb silencing2013
- Author(s)
  宮崎仁美, 東元健, 矢田有加里, 遠藤高帆, Sharif Jafar, 小森敏治, , 松田正史, 古関庸子, 中山学, 副島英伸, 半田宏, 古関明彦, 広瀬進, 西岡憲一
- Organizer
  第36回日本分子生物学会年会
- Place of Presentation
  神戸
- Year and Date
  2013-03-06
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群と関連疾患におけるゲノム・エピゲノム異常2013
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann 症候群におけるインプリントDMR のマルチローカスメチル化解析2013
- Author(s)
  前田寿幸, 東元健, 中林一彦, 城崎幸介, 八木ひとみ, 緒方勤, 秦健一郎, 副島英伸
- Organizer
  第7回日本エピジェネティクス研究会年会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] モヤモヤ病原因遺伝子RNF213の琉球諸島・北部九州ヒト集団における遺伝的多型2013
- Author(s)
  小金渕佳江、中込滋樹、間野修平、石崎直也、河村正二、木村亮介、石田肇、城圭一郎、副島英伸、藤本一真、佐藤公俊、湯澤泉、安井美江、隈部俊宏、藤井清孝、秋山辰穂、埴原恒彦、太田博樹
- Organizer
  第67回日本人類学会大会
- Place of Presentation
  筑波
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] シスチン尿症を伴うゲノムワイド父性片親性ダイソミー症例の遺伝子解析2013
- Author(s)
  大塚泰史、佐々木健作、城崎幸介、東元健、岡本信彦、高間勇一、窪田昭男、松本富美、中山雅弘、吉浦孝一郎、副島英伸
- Organizer
  第48回日本小児腎臓病学会
- Place of Presentation
  徳島
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 本邦における間葉性異形成胎盤の臨床像2013
- Author(s)
  青木早織、大場隆、岡島翠、坂口勲、東元健、副島英伸、福永真治、片渕秀隆
- Organizer
  第21回日本胎盤学会学術集会
- Place of Presentation
  名古屋市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] シスチン尿症を伴うゲノムワイド父性片親性ダイソミー症例の遺伝子解析2013
- Author(s)
  大塚泰史, 佐々木健作, 城崎幸介, 東元健, 岡本信彦, 高間勇一, 窪田昭男, 松本富美, 中山雅弘, 吉浦孝一郎, 副島英伸
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 時計遺伝子 PERIOD2 の多型と光刺激応答の生理的多様性の関係及びその人類学的考察2013
- Author(s)
  秋山辰穂、勝村啓史、埴原恒彦、太田博樹、中込滋樹、藤本一真、副島英伸、城圭一郎、木村亮介、石田肇、安河内朗、樋口重和
- Organizer
  第67回日本人類学会大会
- Place of Presentation
  筑波
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 胎児発育異常症例の網羅的ゲノム・エピゲノム解析2013
- Author(s)
  佐々木かりん、右田王介、中林一彦、東元健、前田寿幸、橋本和法、松井英雄、副島英伸、高田史男、秦健一郎
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 経過観察中にWilms腫瘍を発症した父性ダイソミー型Beckwith-Wiedemann症候群の1例2013
- Author(s)
  中山真悠子、岡陽一郎、近藤剛、村守克己、岩田はるか、城賀本敏宏、石田也寸志、東元健，副島英伸
- Organizer
  第88回日本小児外科学会愛媛地方会
- Place of Presentation
  愛媛
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] ゲノム・インプリンティングとヒト疾患―間葉性異形成胎盤の分子遺伝学的解析2013
- Author(s)
  副島英伸
- Organizer
  群馬大学生体調節研究所内分泌・代謝学共同研究拠点セミナー
- Place of Presentation
  群馬大学
- Invited
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 肝芽腫におけるメチル化インプリントDMR のゲノムワイド検索2012
- Author(s)
  副島英伸, 東元健, 田尻達郎
- Organizer
  第71回日本癌学会学術総会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Genome-wide quantitative DNA methylation analysis of imprinted DMRs in patients with Beckwith-Wiedemann Syndrome by MALDI-TOF MS technology2012
- Author(s)
  Maeda T, Jozaki K, Yatsuki H, Higashimoto K, Soejima H
- Organizer
  The American Society of Human Genetics 62nd Annual Meeting (poster 3432T)
- Place of Presentation
  San Francisco, California, USA
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] H19-DMR メチル化異常で発症するインプリント疾患におけるH19-DMR の変異解析2012
- Author(s)
  東元健, 城崎幸介, 八木ひとみ, 古庄知己, 松原圭子, 山田大輔, 前田寿幸, 大塚泰史, 古関明彦, 緒方勤, 副島英伸
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 肝芽腫におけるメチル化インプリントDMRのゲノムワイド検索2012
- Author(s)
  副島英伸
- Organizer
  第71回日本癌学会学術総会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Genome-wide Screening of Aberrant Methylations of Imprinted DMRs in Hepatoblastomas2012
- Author(s)
  Rumbajan JM, Maeda T, Tajiri T, Higashimoto K, Souzaki R, Taguchi T, Soejima H, Joh K
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] H19-DMRメチル化異常で発症するインプリント疾患におけるH19-DMRの変異解析2012
- Author(s)
  東元　健
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann 症候群における片親性父性ダイソミーの多様性と臨床症状との関連2012
- Author(s)
  大塚泰史, 城崎幸介, 前田寿幸, 八木ひとみ, 東元健, 副島英伸
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] The relationship between paternal uniparental disomy and clinical features in patients with Beckwith-Wiedemann syndrome2012
- Author(s)
  Ohtsuka Y, Jozaki K, Maeda T, Yatsuki H, Higashimoto K, Soejima H
- Organizer
  The American Society of Human Genetics 62nd Annual Meeting (poster 3519T)
- Place of Presentation
  San Francisco, California, USA
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 19-DMRにメチル化異常を認めたインプリント疾患におけるH19-DMRの変異解析2012
- Author(s)
  東元　健
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 肝芽腫におけるインプリントDMRメチル化異常のゲノムワイド検索2012
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Perlman症候群におけるDIS3L2のエクソン9の欠失はLINE-1間の非相同組換えによって生じる2012
- Author(s)
  東元　健
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Aberrant methylation of H19-DMR acquired after2011
- Author(s)
  Soejima H, et al.
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群の臨床像と遺伝子解析2011
- Author(s)
  副島英伸
- Organizer
  BWS親の会勉強会(招待講演)
- Place of Presentation
  鹿児島市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Role of Histone H3 Lys36 methylation by Ash1l2011
- Author(s)
  Higashimoto K, et al.
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Hemihypertrophyにおける11番染色体短腕BWS領域の異常について2011
- Author(s)
  蒔田芳男、副島英伸
- Organizer
  日本人類遺伝学会第56回大会第11回東アジア人類遺伝学会
- Place of Presentation
  幕張
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 本邦Beckwith-Wiedemann 症候群の臨床像とゲノム・エピゲノム解析.180 超例の解析により明らかとなった本邦Beckwith-Wiedemann 症候群の臨床像とゲノム・エピゲノム変異2011
- Author(s)
  副島英伸, 城崎幸介, 八木ひとみ, 前田寿幸, 大塚泰史, 東元健
- Organizer
  日本人類遺伝学会第56回大会第11回東アジア人類遺伝学会
- Place of Presentation
  幕張
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Clinical features and genome/epigenome analyses of2011
- Author(s)
  Soejima H
- Organizer
  The 9th Korean PWS Symposium(招待講演)
- Place of Presentation
  Seoul, Korea
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Acquisition of aberrant hypermethylation after implantation induces discordant hypermethylation at H19-DMR between bodies and placentas in Beckwith-Wiedemann syndrome patients2011
- Author(s)
  Soejima H, Nakabayashi K, Yatsuki H, Jozaki K, Hata K, Higashimoto K
- Organizer
  Idibell Cancer Conferences on Imprinting and Beyond; "Mono-allelic expression in Health and Disease"
- Place of Presentation
  Barcelona, Spain
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 本邦Beckwith-Wiedemann症候群の臨床像とゲノム・エピゲノム解析2011
- Author(s)
  副島英伸、他
- Organizer
  遺伝医学合同学術集会2011
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Acquisition of aberrant hypermethylation after2011
- Author(s)
  Soejima H, et al.
- Organizer
  Idibell Cancer Conferences
- Place of Presentation
  Barcelona, Spain
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 本邦Beckwith-Wiedemann症候群の臨床像とゲノム・エピゲノム解析2011
- Author(s)
  副島英伸、他
- Organizer
  日本人類遺伝学会第56回大会第11回東アジア人類遺伝学会
- Place of Presentation
  幕張
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] 本邦における間葉性異形成胎盤の臨床像2011
- Author(s)
  岡島　翠、大場　隆、片渕秀隆、東元　健、副島英伸
- Organizer
  第18回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  佐賀
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群の臨床像と遺伝子解析2011
- Author(s)
  副島英伸
- Organizer
  BWS親の会勉強会(招待講演)
- Place of Presentation
  旭川市
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群の臨床像とゲノム・エピゲノム解析2010
- Author(s)
  副島英伸
- Organizer
  第17回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  那覇
- Year and Date
  2010-11-20
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Beckwith-Wiedemann症候群のインプリンティング機構と患者解析2010
- Author(s)
  副島英伸
- Organizer
  九州大学母子総合研究リサーチコアカンファレンス
- Place of Presentation
  福岡
- Year and Date
  2010-03-19
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] enome and epigenome analyses of an imprinting disease Beckwith-Wiedemann syndrome.2010
- Author(s)
  副島英伸
- Organizer
  The 4^<th> Asian Chromosome Colloquium.
- Place of Presentation
  Beijing, China
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Genome and epigenome analyses of an imprinting disease Beckwith-Wiedemann syndrome2010
- Author(s)
  Soejima H
- Organizer
  The 4^<th> Asian Chromosome Colloquium
- Place of Presentation
  Beijing, China
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] インプリンティング疾患Beckwith-Wiedemann症候群本邦例の臨床像とゲノム・エピゲノム解析2010
- Author(s)
  副島英伸
- Organizer
  第69回日本癌学会学術総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] A role of histone methylation by Ash1L in the establishment of transcriptional memory.2010
- Author(s)
  Higashimoto K
- Organizer
  2010 Cold Spring Harbor Asia Conference "Epigenetics, Chromatin & Transcription"
- Place of Presentation
  Suzhou, China
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] インプリンティング異常と疾患2010
- Author(s)
  副島英伸
- Organizer
  ヒューマンサイエンス振興財団ポストゲノム医薬品開発WG勉強会
- Place of Presentation
  東京
- Year and Date
  2010-10-29
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] 腫瘍細胞におけるエピジェネティックな遺伝子発現異常の分子機構2010
- Author(s)
  副島英伸
- Organizer
  第49回日本婦人科腫瘍学会学術集会
- Place of Presentation
  佐賀
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] ゲノム刷り込み疾患Beckwith-Wiedemann症候群およびPlacental mesenchymal dysplasiaのゲノム・エピゲノム解析2010
- Author(s)
  副島英伸
- Organizer
  第18回日本胎盤学会学術集会
- Place of Presentation
  熊本
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Role of Ash1l for transcriptional pause release2010
- Author(s)
  Higashimoto K
- Organizer
  第33回日本分子生物学会年会第83回日本生化学会大会合同大会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] 本邦Beckwith-Wiedemann症候群の臨床像とゲノム・エピゲノム解析2010
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第55回大会
- Place of Presentation
  大宮
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] HISTONE METHYLATION BY MAMMALIAN ASH1L FACILITATES IN DUCTION OF HOX GENES IN RESPONSE TO RETINOIC ACID, THEREBY CONTRIBUTES TO ACQUISITION OF PROPER IDENTITIES OF CERVICAL VERTEBRAE.2009
- Author(s)
  Higashimoto K
- Organizer
  Cold Spring Harbor Meeting 2009 Mechanism of Eukaryotic Transcription
- Place of Presentation
  NewYork
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] H19-DMRのメチル化インプリントは正常発生過程で変化しうる2009
- Author(s)
  東元健
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Regulation of imprinted domains, mouse Murr1/U2af1-rs1, Human KIF2/LIT1 and IGF2/H19.2009
- Author(s)
  副島英伸
- Organizer
  18th Lake Shirakaba Conference
- Place of Presentation
  Vedbaek, Denmark
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] HISTONE METHYLATION BY MAMMALIAN ASH1L FACILITATES IN DUCTION OF HOX GENES IN RESPONSE TO RETINOIC ACID, TH EREBY CONTRIBUTES TO ACQUISITION OF PROPER IDENTITIES OF CERVICAL VERTEBRA.2009
- Author(s)
  東元健
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] エピジェネティクス関連疾患と解析方法2009
- Author(s)
  副島英伸
- Organizer
  第19回日本臨床化学会九州支部総会,第53回日本臨床検査医学会九州地方会
- Place of Presentation
  福岡
- Year and Date
  2009-02-14
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Regulation of imprinted domains, mouse Murr1/U2af1-rs1, Human KIP2/LIT1 and IGF2/H19.2009
- Author(s)
  Soejima H
- Organizer
  18th Lake Shirakaba Conference
- Place of Presentation
  Vedbaek, Denmark
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] H19メチル化インプリントが患児と胎盤で異なるBeckkwith-Wiedemann症候群の1例2009
- Author(s)
  東元健
- Organizer
  第16回日本遺伝子診療学会大会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] H19-DMRのメチル化インプリントは正常発生過程で変化しうる2009
- Author(s)
  東元健
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Different control mechanisms of two imprinted domains, KIP2/LIT1 and Murrl/U2af1-rs1.2008
- Author(s)
  Soejima H
- Organizer
  INTERNATIONAL SYMPOSIUM「Decoding Epigenetic Code」
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] ベックウィズ・ヴィーデマン症候群のインプリンティング機序2008
- Author(s)
  副島英伸
- Organizer
  大阪大学蛋白研セミナー「インプリンティング疾患発症機序の解明と治療に向けて」
- Place of Presentation
  吹田市
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] ベックウィズ・ヴィーデマン症候群のインプリンティング機序2008
- Author(s)
  副島英伸
- Organizer
  大阪大学蛋白研セミナー「インプリンティング疾患発症機序の解明と治療に向けて」
- Place of Presentation
  大阪大学医学部
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Imprinted non-coding RNA LITl is required for paternal repression of genes within human KIP2/LIT1 imprinted domain.2008
- Author(s)
  Soejima H
- Organizer
  The 2008 EAUHGS Symposium & the 8th EAUHGS Annual Meeting
- Place of Presentation
  札幌
- Year and Date
  2008-07-19
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Regulation of imprinting in Beckwith-Wiedemann syndrome.2008
- Author(s)
  副島英伸
- Organizer
  Northeastern Asian Symposium on "Cancer Epigenetics".
- Place of Presentation
  Jeju, Korea
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] 胎盤と臍帯血でDNAメチル化状態が異なったBeckwith-Wiedemann症候群の1例2008
- Author(s)
  副島英伸
- Organizer
  第15回遺伝性疾患に関する出生前診断研究会
- Place of Presentation
  大分市
- Year and Date
  2008-10-19
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Regulation of imprinting in Beckwith-Wiedemann syndrome2008
- Author(s)
  Soejima H
- Organizer
  Northeastern Asian Symposium on “Cancer Epigenetics"
- Place of Presentation
  Jeju, Korea
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] Different control mechanisms of two imprinted domains, KIP2/LIT1-and Murrl/U2af1-rs1.2008
- Author(s)
  副島英伸
- Organizer
  INTERNATIONAL SYMPOSIUM 「Decoding Epigenetic Code」
- Place of Presentation
  Tokyo
- Data Source
  KAKENHI-PROJECT-20590330
[Presentation] A case with partial trisomy of 11p15 transmitted from mother2007
- Author(s)
  Shimokawa, O., Fu, R., Soejima, H., Sasaki, K., Kondo, T., Matsumoto, N., Yoshiura, K., Niikawa, N., Harada, N
- Organizer
  The 52nd Annual Meeting of the Japanese Society of Human Genetics
- Place of Presentation
  Tokyo
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] SNP array analysis and H19-DMR CTCF6 methylation analysis revealed genetic and clinical heterogeneity of Wilms tumors with WT1 aberration2007
- Author(s)
  Kaneko, Y., Haruta, M., Arai, Y., Soejima, H., Watanabe, N., Fukuzawa, M
- Organizer
  The 52nd Annual Meeting of the Japanese Society of Human Genetics
- Place of Presentation
  Tokyo
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] What molecular mechanism contributes to the different incidence rates between Japanese and Caucasian Wilms tumors?2007
- Author(s)
  Haruta, M., Watanabe, N., Nakadate, N., Fukuzwa, M., Soejima, H., Kaneko, Y
- Organizer
  66th Annual Meeting of the Japanese Cancer Association
- Place of Presentation
  Yokohama
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Regulation mechanism of mouse Murrl/U2afl-rsl imprinted region.2007
- Author(s)
  Yatsuki, H., Joh, K., Soejima, H., Mukai, T
- Organizer
  1st Annual Meeting of the Japanese Society for Epigenetics
- Place of Presentation
  Osaka
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Different incidence of some epigenetic and genetic alterations between Japanese and Caucasian patients with Beckwith- Wiedemann syndrome2006
- Author(s)
  Soejima, H., Sasaki, K., Higashimoto, K., Yatsuki, H., Joh, K., Niikawa, N., Mukai, T
- Organizer
  International Genomic Imprinting Workshop 2006
- Place of Presentation
  Tokyo, Japan
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Different incidence of epigenetic and genetic alterations between Japanese and Caucasian patients with Beckwith-Wiedemann syndrome.2006
- Author(s)
  Soejima, H, Sasaki, K, Higashimoto, K, Joh, K, Niikawa N, Mukai, T
- Organizer
  11th International Congress of Human Genetics
- Place of Presentation
  Brisbane, Australia
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Loss of imprinting(LOI) of IGF2 and structural aberration of WT1 in Wilms tumors2006
- Author(s)
  Haruta, M, Nakadate, N, Watanabe, N, Fukuzawa, M, Soejima, H, Kaneko, Y
- Organizer
  65th Annual Meeting of the Japanese Cancer Association
- Place of Presentation
  Yokohama
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Bgckwith-Wiedemann症候群本邦例の包括的解析2006
- Author(s)
  副島英伸
- Organizer
  日本人類遺伝学会第51回大会
- Place of Presentation
  米子
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Different incidence of epigenetic and genetic alterations between Japanese and Caucasian patients with Beckwith-Wiedemann syndrome2006
- Author(s)
  Soejima H
- Organizer
  11th International Congress of Human Genetics
- Place of Presentation
  Brisbane,Australia
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] U2afl-rsl/Murr1 loci are newly imprinted loci formed in mouse after the divergence between human and mouse.2006
- Author(s)
  Joh, K., Wang, Y., Zhang, Z., Yatsuki, H., Soejima, H., Mukai, T
- Organizer
  International Genomic Imprinting Workshop 2006
- Place of Presentation
  Tokyo, Japan
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Expression of imprinted LI1/KCNQlOTl gene and Epigenetics of KvDMR12006
- Author(s)
  Nakano, S, Murakami, K, Meguro, M., Soejima, H., Higashimoto, K., Urano, T., Kugoh, H., Mukai, T., Ikeguchi, M., Oshimura, M
- Organizer
  The 51st Annual Meeting of the Japanese Society of Human Genetics
- Place of Presentation
  Yonago
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Comprehensive analyses of Japanese patients with Beckwith-Wiedemann syndrome.2006
- Author(s)
  Soejima, H, Sasaki, K, Higashimoto, K, Niikawa, N, Mukai, T
- Organizer
  The 51st Annual Meeting of the Japanese Society of Human Genetics
- Place of Presentation
  Yonago
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Different incidence of some epigenetic and genetic alterations between Japanese and Caucasian patients with Beckwith-Wiedemann syndrome2006
- Author(s)
  Soejima H
- Organizer
  International Genomic Imprinting Workshop 2006
- Place of Presentation
  Tokyo,Japan
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590313
[Presentation] Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract Polycomb silencing.
- Author(s)
  Kenichi Nishioka、Hitomi Miyazaki, Ken Higashimoto, Yukari Yada, Takaho A. Endo, Jafar Sharif, Manabu Nakayama, Hidenobu Soejima, Haruhiko Koseki, Susumu Hirose．
- Organizer
  第8回日本エピジェネティクス研究会年会
- Place of Presentation
  東京大学
- Year and Date
  2014-05-25 – 2014-05-27
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] ゲノムインプリンティングとヒト疾患―ベックウィズ・ビーデマン症候群と間葉性異形成胎盤の解析を中心に
- Author(s)
  副島英伸
- Organizer
  第８回遺伝医学セミナー
- Place of Presentation
  別府
- Invited
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Beckwith-Wiedemann症候群と肝芽腫におけるmultiple methylation defectの解析
- Author(s)
  前田寿幸、Rumbajan Janette Mareska、東元　健、中林一彦、八木ひとみ、秦健一郎、城圭一郎、副島英伸．
- Organizer
  第8回日本エピジェネティクス研究会年会
- Place of Presentation
  東京大学
- Year and Date
  2014-05-25 – 2014-05-27
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] ゲノム・エピゲノム解析による間葉性異形成胎盤の原因遺伝子探索の現状
- Author(s)
  副島英伸
- Organizer
  熊本大学医学部産婦人科セミナー
- Place of Presentation
  熊本
- Invited
- Data Source
  KAKENHI-PROJECT-23659181
[Presentation] Small for gestational age（SGA）胎盤のゲノムワイドDNAメチル化解析
- Author(s)
  副島英伸、Rumbajan Janette Mareska、畑田出穂、中林一彦、泰健一郎、青木茂久、関博之、竹田省、城圭一郎
- Organizer
  日本人類遺伝学会第59回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-19 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-26670169
[Presentation] Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of the human imprintome and suggests a germline methylation independent control of imprinting in the placenta．
- Author(s)
  中林一彦、Court Franck、田山千春、Romanelli Valeria、副島英伸、和氣徳夫、Esteller Manel、緒方勤、秦健一郎、Monk David．
- Organizer
  第8回日本エピジェネティクス研究会年会
- Place of Presentation
  東京大学
- Year and Date
  2014-05-25 – 2014-05-27
- Data Source
  KAKENHI-PROJECT-26670169

1. MUKAI Tsunehiro (40108741)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
2. YOSHIURA Ko-ichiro (00304931)

# of Collaborated Projects: 2 results

# of Collaborated Products: 11 results
3. JOH Keiichiro (90124809)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
4. HIGASHIMOTO Ken (30346887)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. Ohba Takashi (50244132)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
6. YATSUKI Hitomi

# of Collaborated Projects: 2 results

# of Collaborated Products: 18 results
7. KUGOH Hiroyuki (40225131)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. KOSEKI Haruhiko (40225446)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. OGURA Atsuo (20194524)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. MATSUMOTO Naomichi (80325638)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
11. Ohtsuka Yasufumi (50448479)

# of Collaborated Projects: 1 results

# of Collaborated Products: 8 results
12. Hiura Hitoshi (70451523)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. ARIMA Takahiro (80253532)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. OGATA Tustomu (40169173)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
15. 三ツ矢幸造 (30375191)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 押村光雄 (20111619)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 香畑智彦 (50380762)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 田渕和雄 (50116480)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 峯田寿裕 (20264187)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 片渕秀隆 (90224451)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
21. 荒木喜美 (90211705)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. WATANABE Hidetaka

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
23. 白石哲也

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. SATO Hiroyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. WAKE Norio

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. TAYAMA Chiharu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. SUGAHARA Naoko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. SOUZAKI Ryota

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. KOHASHI Kenichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
30. TAKADA Shuji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
31. MATSUBARA Keiko

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
32. WAKUI Keiko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
33. SUZUKI Takayuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
34. MIGITA Ohsuke

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
35. MAEHARA Kayoko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
36. KAMURA Hiromi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
37. MISHIMA Hiroyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
38. SANEFUJI Masafumi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
39. SEMI Katsunori

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
40. SHIMIZU Masahito

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
41. TANAKA Hideo

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
42. KITA Yoshikuni

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
43. GO Yasuhiro

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
44. ICHIYANAGI Kenji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
45. NISHIDA Yuichiro

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
46. OHTA Tohru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
47. 阿部竜也

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
48. 太田博樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
49. 石田肇

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
50. 小金渕佳江

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
51. 河村正二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
52. 永淵正法

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
53. 高橋宏和

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
54. 安西慶三

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
55. 岡村浩司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
56. 中林一彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
57. 田尻達郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
58. 田口智章

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
59. 西岡憲一

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
60. 冨川順子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
61. 秦健一郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
62. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
63. 河村理恵

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
64. 堀居拓郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
65. 森田純代

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
66. 木村正

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
67. 中村仁美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
68. 北嶋修司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
69. 松久葉一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
70. 上原吉就

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
71. 桧垣靖樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
72. 冨賀裕貴

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
73. 原聡史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
74. WANG XIAN-FENG

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
75. 今川英里

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
76. 宮武聡子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
77. 酒井康成

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
78. 水口剛

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
79. 梁明秀

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
80. 三宅紀子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
81. 森脇久隆

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
82. 有岡祐子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
83. 森満

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
84. 山田泰広

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
85. 田中恵太郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
86. 田中祐吉

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
87. 田中勇悦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
88. 川中健太郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
89. 福田渓

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
90. 佐々木裕之

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
91. 山田洋一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
92. 勝村啓史

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
93. 安河内朗

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
94. 樋口重和

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
95. 半田宏

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
96. 原めぐみ

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
97. 島ノ江千里

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

SOEJIMA HIDENOBU 副島 英伸

SOEJIMA Hidenobu 副島 英伸

HIGASHIMOTO Ken 東元 健

副島 英伸 ソエジマ ヒデノブ

Research Projects

Research Products

Co-Researchers

インプリンティング疾患の異常高メチル化が境界領域を超えて伸展する分子機構の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

エピゲノム修飾因子NSD1の標的遺伝子同定に基づく精神発達遅滞の分子病態解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identification of regulatory factors for somatic imprinted DMR establishment and elucidation of their molecular mechanismsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

A search for target genes of aberrant histone methylation diseases and the establishment of drug discovery platform based on elucidation of pathological conditionsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Drawing a differentiation potency index of iPSC based on genomic imprintingPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of regulatory factors for genomic imprinting using siRNA libraryPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Bidirectional approach for elucidation of genomic imprinting mechanismPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

siRNAライブラリーを用いた刷り込み遺伝子発現調節分子の同定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

SOEJIMA HIDENOBU 副島英伸

SOEJIMA Hidenobu 副島英伸

HIGASHIMOTO Ken 東元健

副島英伸ソエジマヒデノブ

[Book] 遺伝子医学MOOK36　エピゲノムで新たな解明が進む「先天性疾患」2021

[Book] 遺伝子医学MOOK36　エピゲノムで新たな解明が進む「先天性疾患」2021

[Book] コアカリ準拠臨床遺伝学テキストノート　第６講義エピジェネティクス2018