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Ohta Toru  太田 亨

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… Alternative Names

OHTA Tohru  太田 亨

OTA Toru  太田 徹

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Researcher Number 10223835
Other IDs
Affiliation (Current) 2025: 北海道医療大学, 先端研究推進センター, 教授
2025: 北海道医療大学, 健康科学研究所, 教授
Affiliation (based on the past Project Information) *help 2017 – 2022: 北海道医療大学, 健康科学研究所, 教授
2013 – 2016: 北海道医療大学, 個体差健康科学研究所, 教授
2015: 北海道医療大学, 個体差健康科学研究所, 准教授
2013: 北海道医療大学, 公私立大学の部局等, 教授
2006 – 2013: Inst. of Personalized Medicine, Associate Professor, 個体差健康科学研究所, 准教授 … More
2012: 北海道医療大学, 公私立大学の部局等, 准教授
2009: 個体差健康科学研究所, 准教授
2007: 個体差健康科学研究所, 准教授
2006: 北海道医療大学, 個体差健康科学研究所, 助手
2004 – 2005: Health Sciences University of Hokkaido, The Research Institute of Personalized Health Sciences, Associate Professor, 個体差健康科学研究所, 助教授
2003: 長崎大学, 先導生命科学研究支援センター, 助手 Less
Review Section/Research Field
Principal Investigator
Human genetics
Except Principal Investigator
Human genetics / Pathobiological dentistry/Dental radiology / Basic Section 57060:Surgical dentistry-related / Surgical dentistry / Otorhinolaryngology / Hematology / Periodontology / Experimental pathology / Biological Sciences
Keywords
Principal Investigator
CTCF / insulator / imprinting control center / genomic imprinting / 刷り込み調節中枢 / Snrpn isoform / ゲノム刷り込み / インプリティング調節中枢 / ゲノムインプリティング / 転写因子 … More / インスレーター / インプリンティング調節中枢 / ゲノムインプリンティング / 薬剤耐性遺伝子 / マウスモデル / ABCC11遺伝子 / モデル細胞 / 乳がん / 耳垢 / ABCC11 … More
Except Principal Investigator
エピジェネティクス / 転写因子 / 歌舞伎症候群 / 関連解析 / Gfi-1 / Ets-1 / 分化 / PU.1 / 歯周病原菌 / DNAメチル化 / 線維芽細胞 / FOXP2 / 連鎖解析 / 膵臓 / 海馬 / 口腔内病原菌内毒素 / DNA / 国際協力 / 口唇口蓋裂 / バンキング / 遺伝子解析 / 口蓋裂 / 口唇裂 / 先天異常 / 脳・神経 / 再生医療 / 聴神経様細胞 / Tlx3 / ES細胞 / hematopoiesis / apoptosis / cross-talk / GfilB / ETS / transcription factors / 血球分化 / アポトーシス / bax / 増殖 / 赤血球 / 骨髄球 / Gfi-1B / クロストーク / 口腔 / 炎症性疾患 / エピジェネティック / シェーグレン症候群 / 歯肉上皮 / 歯肉線維芽細胞 / 歯周病 / P.gingivalis / 歯周組織 / LPS / 歯周疾患 / エピジェネティック変化 / 変異 / ヒストンメチル化 / ゲノム編集 / グリア細胞 / 言語関連遺伝子 / 多型 / 遺伝形質 / ヒト正常形質 / ヒトゲノム / 遺伝子 / 遺伝学 / 軟口蓋裂 / 脳動静脈奇形 / 遺伝子座マッピング / 骨髄異形成症 / SOLiD / emulsion PCR / 筋萎縮性側索硬化症 / エキソンキャプチャー法 / 次世代型シーケンサー / ゲノム医科学 / 脳神経 / 言語 / ABCC11アレルの全国地図 / 腋窩臭症 / 初乳量 / 乳がん / 遺伝子多型 / 耳垢型 / ABCC11遺伝子 / 分子遺伝学 / 精神遅滞症 / Kabuki make-up症候群 / 家族性心房中隔欠損症 / 染色体構造異常 / 一過性運動誘発性コレオアテトーシス / 特発性手掌多汗症 / 遺伝子単離 / 合指症 / 多指趾症 / 染色体 / 因子疾患 / 疾患感受性遺伝子 / 多因子疾患 / 単因子疾患 / 疾患遺伝子 / 染色体異常 Less
  • Research Projects

    (16 results)
  • Research Products

    (103 results)
  • Co-Researchers

    (74 People)
  •  Epigenetic alterations of pancreas induced by oral bacterial endotoxin

    • Principal Investigator
      ABIKO Yoshihiro
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 57060:Surgical dentistry-related
    • Research Institution
      Health Sciences University of Hokkaido
  •  Genome-wide analysis of epigenetic modification in hippocampus by oral pathogen endotoxin

    • Principal Investigator
      ABIKO Yoshihiro
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pathobiological dentistry/Dental radiology
    • Research Institution
      Health Sciences University of Hokkaido
  •  Elucidation of the mechanism underlying differentiation of auditory neurons toward the realization of regenerative therapy for Auditory Neuropathy

    • Principal Investigator
      SHIMOMURA Atsushi
    • Project Period (FY)
      2016 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      Health Sciences University of Hokkaido
  •  Genome-wide analysis of epigenetics in the sialadenitis from Sjogren's syndrome

    • Principal Investigator
      ABIKO Yoshihiro
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pathobiological dentistry/Dental radiology
    • Research Institution
      Health Sciences University of Hokkaido
  •  Whole genome epigenetic analysis in Kabuki syndrome and model cell line construction

    • Principal Investigator
      YOSHIURA Koh-ichiro
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Nagasaki University
  •  Elucidation of epigenetic mechanism in gingival epithelium by periodontal pathogen

    • Principal Investigator
      Michiko Nishimura
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Periodontology
    • Research Institution
      Health Sciences University of Hokkaido
  •  Genomic analysis of genes relating to oral and maxillofacial congenital anomalies - Establishing a center of human genome resource banking

    • Principal Investigator
      NATSUME Nagato
    • Project Period (FY)
      2012 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Surgical dentistry
    • Research Institution
      Aichi Gakuin University
  •  Identification and characterization of target genes for the language-related human and chimpanzee FOXP2

    • Principal Investigator
      OIKAWA TSUNEYUKI
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Health Sciences University of Hokkaido
  •  Molecular genetic study of normal morphological variants

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Health Sciences University of Hokkaido
  •  Mapping of the disease loci using SNP genotyping and identification of the gene by the sequence capture method

    • Principal Investigator
      YOSHIURA Koichiro
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Nagasaki University
  •  Genetic, medical and anthropological study of human earwax gene, ABCC11

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Health Sciences University of Hokkaido
  •  Establishment of model system including human ABCC11 transgenePrincipal Investigator

    • Principal Investigator
      OHTA Tohru
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Health Sciences University of Hokkaido
  •  Identification of target genes for the language-related FOXP2 transcription factor

    • Principal Investigator
      OIKAWA Tsuneyuki
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Experimental pathology
    • Research Institution
      Health Sciences University of Hokkaido
  •  A family-analysis-based search for genes susceptible to mono-, oligo- and polygenic disorders

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      2005 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Health Sciences University of Hokkaido
      Nagasaki University
  •  Cross-talks between ETS and GFI family of transcription factors in hematopoietic cell differentiation

    • Principal Investigator
      OIKAWA Tsuneyuki
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Hematology
    • Research Institution
      Health Sciences University of Hokkaido
      Sasaki Institute
  •  Functional analysis of trans-acting factor binding to imprinting control region.Principal Investigator

    • Principal Investigator
      OHTA Tohru
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Health Sciences University of Hokkaido
      Nagasaki University

All 2017 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 Other

All Journal Article Presentation Patent

  • [Journal Article] Epigenetics of oral infection and inflammatory diseases―DNA methylation changes in infections and inflammation diseases.2014

    • Author(s)
      Abiko Y, Uehara O, Fukumoto S,Ohta T
    • Journal Title

      J Oral Biosci

      Volume: 56 Issue: 4 Pages: 105-109

    • DOI

      10.1016/j.job.2014.06.004

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26462852
  • [Journal Article] Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosis.2014

    • Author(s)
      Kaname T, Ki CS, Niikawa N, Baillie GS, Day JP, Yamamura KI, Ohta T, Nishimura G, Mastuura N, Kim OH, Sohn YB, Kim HW, Cho SY, Ko AR, Lee JY, Kim HW, Ryu SH, Rhee H, Yang KS, Joo K, Lee J, Kim CH, Cho KH, Kim D, Yanagi K, Naritomi K, Yoshiura KI, Kondoh T, Nii E, Tonoki H, Houslay MD, Jin DK.
    • Journal Title

      Cellular Signaling

      Volume: 26 (11) Issue: 11 Pages: 2446-2459

    • DOI

      10.1016/j.cellsig.2014.07.025

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293084, KAKENHI-PROJECT-25550033, KAKENHI-PROJECT-26430194
  • [Journal Article] Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.2014

    • 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

      Clin Genet.

      Volume: 8 Issue: 3 Pages: 1-1

    • DOI

      10.1111/cge.12496

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-26670169, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293084
  • [Journal Article] MLL2 and KDM6A mutations in patients with Kabuki syndrome.2013

    • Author(s)
      Miyake N*, Koshimizu E, Okamoto N, Mizuno S, Ogata T,at all
    • Journal Title

      Am J Med Genet A

      Volume: 161 Issue: 9 Pages: 2234-2243

    • DOI

      10.1002/ajmg.a.36072

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-23390268, KAKENHI-PROJECT-23590383, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-24249019, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591531, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25293084, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-25860915
  • [Journal Article] Clinical correlations of mutations affecting six components of the SWI/SNF complex : Detailed description of 21 patients and a review of the literature2013

    • Author(s)
      Kosho T, Okamoto N, Ohashi H, Yamagata T, Matsumoto N (27人中11番目)
    • Journal Title

      Am J Med Genet A

      Volume: 161 Issue: 6 Pages: 1221-1237

    • DOI

      10.1002/ajmg.a.35933

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23390275, KAKENHI-PROJECT-23590383, KAKENHI-PROJECT-23591506, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-24249019, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-25860915
  • [Journal Article] Clinical correlations of mutations affecting six components of the SW1/SNF complex: detailed description of 21 patients and a review of the literature2013

    • Author(s)
      Kosho T, Okamoto N, Ohashi H, Tsurusaki Y, Imai Y,Hibi-Ko Y, Kawame H, Homma T, Tanabe S, Kato M, Hiraki Y, Yamagata T, Yono S, Sakazume S, Ishii T, Nagai T, Ohta T, Niikawa N, Mizuno S, Kaname T, Naritomi K, Narumi Y, Wakui K, Fukushima Y, Miyatake S, Mizuguchi T, Saitsu H, Miyake N, Mstsumoto N
    • Journal Title

      Am J Med Genet

      Volume: 161A: 1221-1237

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] MLL2 and KDM6A mutations in patients with Kabuki syndrome2013

    • Author(s)
      Miyake N, Koshimizu E, Okamoto N, Mizuno S, Ogata T, Nagai T, Kosho T, Ohashi H, Kato M, Sasaki G, Mabe H, Watanabe Y, Yoshino M, Matsuishi T, Takanashi J, Shotelersuk V, Tekin M, Ochi N, Kubota M, Ito N, Ihara K, Hara T, Tonoki H, Ohta T, Saito K, Matsuo M, Urano M, Enokizono T, Sato A, Tanaka H, Ogawa A, Fujita T, Hiraki Y, Kitanaka S, Matsubara Y, Makita T, Taguri M, Nakashima M, Tsurusaki Y, Saitsu H, Yoshiura K, Matsumoto N, Niikawa N
    • Journal Title

      Am J Med Genet A

      Volume: 161(9) Pages: 2234-2243

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] エピジェネティクスが関連する先天異常Angelman症候群とPrader Willi症候群2013

    • Author(s)
      太田 亨
    • Journal Title

      小児科臨床

      Volume: 66 Pages: 1297-1307

    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Clinical correlations of mutations affecting six components of the SWI/SNF complex : detailed description of 21 patients and a review of the literature2013

    • Author(s)
      Kosho T, Okamoto N, Ohashi H, Tsurusaki Y, Imai Y, Hibi-Ko Y, Kawame H, Homma T, Tanabe S, Kato M, Hiraki Y, Yamagata T, Yano S, Sakazume S, Ishii T, Nagai T, Ohta T, Niikawa N, Mizuno S, Kaname T, Naritomi K, Narumi Y, Wakui K, Fukushima Y, Miyatake S, Mizuguchi T, Saitsu H, Miyake N, Matsumoto N
    • Journal Title

      Am J Med Genet A

      Volume: 161(6) Pages: 1221-1237

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome2012

    • Author(s)
      Tsurusaki Y, Okamoto N, Ohashi H, Kosho T, Imai Y, Hibi-Ko Y, Kaname T, Naritomi K, Kawame H, Wakui K, Fukushima Y, Homma T, Kato M, Hiraki Y, Yamagata T, Yano S, Mizuno S, Sakazume S, Ishii T, Nagai T, Shiina M, Ogata K, Ohta T, Niikawa N, Miyatake S, Okada I, Mizuguchi T, Doi H, Saitsu H, Miyake N, Matsumoto N
    • Journal Title

      Nat Genet

      Volume: 44(4) Pages: 376-378

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome2012

    • Author(s)
      Hosoki K, Ohta T, Fujita K, Nishigaki S, Shiomi M, Niikawa N, Saitoh S.
    • Journal Title

      Pediatr Int

      Volume: 54(3) Issue: 3 Pages: 22-25

    • DOI

      10.1111/j.1442-200x.2011.03550.x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Mutations in PRRT2responsible for paroxysmal kinesinic dyskinesias also cause benign familial infantile convulsions2012

    • Author(s)
      Ono S, Yoshiura K, Kinoshita A, Kikuchi T, Nakane Y, Kato N, Sadamatsu M, Konishi T, Nagamitsu S, Matsuura M, Yasuda A, Komine M, Kanai K, Inoue T, Osamura T, Saito K, Hirose S, Koide H, Tomita H, Ozawa H, Niikawa N, Kurotaki N
    • Journal Title

      J Hum Genet

      Volume: 57: 338-341

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome2012

    • Author(s)
      Tsurusaki Y, Okamoto N, Ohashi H, Kosho T, Imai Y, Hibi-Ko Y, Kaname T, Naritomi K, Kawame H, Wakui K, Fukushima Y, Homma T, Kato M, Hiraki Y, Yamagata T, Yano S, Mizuno S, Sakazume S, Ishii T, Nagai T, Shiina M, Ogata K, Ohta T, Niikawa N, Miyatake S, Okada I, Mizuguchi T, Doi H, Saitsu H, Miyake N, Matsumoto N
    • Journal Title

      Nat Genet

      Volume: 44 Issue: 4 Pages: 376-378

    • DOI

      10.1038/ng.2219

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390104, KAKENHI-PROJECT-21591329, KAKENHI-PROJECT-22790823, KAKENHI-PROJECT-23390275, KAKENHI-PROJECT-23590383, KAKENHI-PROJECT-23591506, KAKENHI-PROJECT-23689052, KAKENHI-PROJECT-24249019, KAKENHI-PROJECT-24591500, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118005, KAKENHI-PLANNED-24118007
  • [Journal Article] (Japanese Archipelago Human Population Genetics Consortium):The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations2012

    • Author(s)
      Jinam T, Nishida N, Hirai M, Kawamura S, Oota H, Umetsu K, Kimura R, Ohashi J, Tajima A, Yamamoto T, Tanabe H, Mano S, Suto Y, Kaname T, Naritomi K, Yanagi K, Niikawa N, Omoto K, Tokunaga K, Saitou N
    • Journal Title

      J Hum Genet

      Volume: 57: 1-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome2012

    • Author(s)
      Hosoki K, Ohta T, Natsume J, Imai S, Okumura A, Matsui T, Harada N, Bacino CA, Scaglia F, Jones JY, Niikawa N, Saitoh S
    • Journal Title

      Am J Med Genet A

      Volume: 158A(8) Pages: 1891-1896

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Hand-foot-genital syndrome with a 7p15 deletion : clinically recognizable syndrome2012

    • Author(s)
      Hosoki K, Ohta T, Fujita K, Nishigaki S, Shiomi M, Niikawa N, Saitoh S
    • Journal Title

      Pediatr Int

      Volume: 54(3)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] 遺伝学的基礎Prader-Willi症候群の基礎と臨床2011

    • Author(s)
      太田亨
    • Journal Title

      診断と治療社

      Pages: 7-14

    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Identification of Novel Schizophrenia Loci by Homozygosity Mapping Using DNA Microarray Analysis2011

    • Author(s)
      Kurotaki N, Tasaki S, Mishima H, Ono S, Imamura A, Kikuchi T, Nishida N, Tokunaga K, Yoshiura K, Hiroki Ozawa H
    • Journal Title

      PLos One

      Volume: 6(5)

    • NAID

      120006985084

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome2011

    • Author(s)
      Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, Liang D, Sudo A, Morris CA, Banka S, Black GC, Clayton-Smith J, Nickerson DA, Zackai EH, Shaikh TH, Donnai D, Niikawa N, Shendure J, Bamshad MJ
    • Journal Title

      Am J Med Genet A

      Volume: 155A(7) Pages: 1511-1516

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Down-regulation of ABCC11 protein(MRP8) in human breast cancer2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D.
    • Journal Title

      Exp Oncol

      Volume: 33(1) Pages: 42-6

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome2011

    • Author(s)
      Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, Liang D, Sudo A, Morris CA, Banka S, Black GC, Clayton-Smith J, Nickerson DA, Zackai EH, Shaikh TH, Donnai D, Niikawa N, Shendure J, Bamshad MJ
    • Journal Title

      Am J Med Genet A

      Volume: 155A(7):1511-1516

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Spectrum of MLL2(ALR) mutations in 110 cases of Kabuki syndrome2011

    • Author(s)
      Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, et al.
    • Journal Title

      Am J Med Genet A

      Volume: 155A(7) Pages: 1511-6

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Spectrum of MLL2(ALR) mutations in 110 cases of Kabuki syndrome2011

    • Author(s)
      Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, Lian
    • Journal Title

      Am J Med Genet A

      Volume: 155A(7) Pages: 1511-1516

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Mutation and copy number analysis in paroxysmal kinesigenic dyskinesia families2011

    • Author(s)
      Ono S, Yoshiura K, Kurotaki N, Kikuchi T, Niikawa N, Kinoshita A
    • Journal Title

      Mov Disord

      Volume: 26: 761-763

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Down-regulation of ABCC11 protein (MEP8) in human breast cancer2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T Niikawa N, Starenki D
    • Journal Title

      Exp Oncol

      Volume: 33 Pages: 42-46

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Mutation and Copy Number Analysis in Paroxysmal Kinesigenic Dyskinesia Families2011

    • Author(s)
      Ono S, Yoshiura K, Kurotaki N, Kikuchi T, Niikawa N, Kinoshita A
    • Journal Title

      Movement Disorders

      Volume: 26(4) Pages: 762-764

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Identification of Novel Schizophrenia Loci by Homozygosity Mapping Using DNA Microarray Analysis2011

    • Author(s)
      Kurotaki, et al
    • Journal Title

      PLos One

      Volume: 6(5) Issue: 5 Pages: e20589-e20589

    • DOI

      10.1371/journal.pone.0020589

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390100, KAKENHI-PROJECT-22659071, KAKENHI-PROJECT-23791230
  • [Journal Article] A polymerase chain reaction-based method for constructing a linear vector with site-specific DNA methylation2011

    • Author(s)
      Arakawa T, Ohta T, Abiko Y, Okayama M, Mizoguchi I, Takuma T
    • Journal Title

      Anal Biochem

      Volume: 416(2) Pages: 211-217

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Down-regulation of ABCC11 protein (MRP8) in human breast cancer.2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D.
    • Journal Title

      Exp Oncol. 33(1)

      Pages: 42-46

    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Down-regulation of ABCC11 protein (MRP8) in human breast cancer2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D
    • Journal Title

      Exp Oncol

      Volume: 33: 42-46

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Down-regulation of ABCC11 protein (MRP8) in human breast cancer.2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D.
    • Journal Title

      Exp Oncol

      Volume: 33(1) Pages: 42-46

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Down-regulation of ABCC11 protein (MRP8) in human breast cancer2011

    • Author(s)
      Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D
    • Journal Title

      Exp Oncol

      Volume: 33(1) Pages: 42-46

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Journal Article] Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome2011

    • Author(s)
      Hannibal, et al
    • Journal Title

      Am J Med Genet A

      Volume: 115A(7) Issue: 7 Pages: 1511-1516

    • DOI

      10.1002/ajmg.a.34074

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390100, KAKENHI-PROJECT-21591329, KAKENHI-PROJECT-22659071, KAKENHI-PROJECT-23590383, KAKENHI-PROJECT-23591506, KAKENHI-PROJECT-23689052
  • [Journal Article] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.2010

    • Author(s)
      Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, Niikawa N, Nickerson DA, Bamshad MJ, Shendure J.
    • Journal Title

      Nat.Genet. 42(9)

      Pages: 790-793

    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome2010

    • Author(s)
      Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, et al.
    • Journal Title

      Nat. Genet

      Volume: 42(9) Pages: 790-793

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome2010

    • Author(s)
      Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, NiikawaN, Nickerson DA, BamshadMJ, Shendure J
    • Journal Title

      Nature Genet

      Volume: 42: 790-793

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390066
  • [Journal Article] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome2010

    • Author(s)
      Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, Niikawa N, Nickerson DA, Bamshad MJ, Shendure J
    • Journal Title

      Nat Genet

      Volume: 42(9) Pages: 790-793

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Failure to Confirm CNVs as of Aetiological Significance in Twin Pairs Discordant for Schizophrenia2010

    • Author(s)
      Ono S, Imamura A, Tasaki S, Kurotaki N, Ozawa H, Yoshiura K, Okazaki Y
    • Journal Title

      Twin Res Hum Genet

      Volume: 13(5) Pages: 455-460

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Endo I and Shimada H. Association between breast cancer risk and the wild-type allele of human ABC transporter ABCC112010

    • Author(s)
      Ota I, Sakurai A, Toyoda Y, Morita S, Sasaki T, Chishima T, Yamakado M, Kawai Y, Ishidao T, Lezhava A, Yoshiura K-i, Togo S, Hayashizaki Y, Ishikawa T, Ishikawa T
    • Journal Title

      Anticancer Res

      Volume: 30(12) Pages: 5189-5194

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene2009

    • Author(s)
      Miyazaki K, Mapendano CK, Fuchigami Y, Kondo S, Ohta T, Kinoshita A, Tsukamoto K, Yoshiura K, Niikawa N, Kishino T.
    • Journal Title

      Gene

      Volume: 432 Pages: 97-101

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene.2009

    • Author(s)
      Miyazaki K, Ohta T., et al.
    • Journal Title

      Gene. 432

      Pages: 97-101

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Earwax, osmidrosis, and breast cancer why does one SNP(538G> A) in the human ABC transporter ABCC11 gene determine earwax type?2009

    • Author(s)
      Toyoda Y, Sakurai A, Mitani Y, Nakashima M, Yoshiura KI, Nakagawa H, Sakai Y, Ota I, Lezhava A, Hayashizaki Y, Niikawa N, Ishikawa T.
    • Journal Title

      FASEB J

      Volume: 23(6) Pages: 2001-2013

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] The Super Science High School (SSH) Consortium Japanese map of the earwax gene frequency : a nation-wide collaborative study by Super Science High School (SSH) Consortium.2009

    • Author(s)
      S Sakai, K Imai, T Ogawa, H Iwaoka, M Ishii, S Komori, T Yoshida, H Jumonji, K Iizumi, H Ohshima, T Maeda, A Kanno, K Takahashi, H Kubota, Y Inoue, Y Takahashi, H Onoda, R Uchiyama, M Matsuda, T Akazawa, N Kawamura, T Odagiri, Y Watanabe, Y Matsumoto, S Shinoda, M Terada, M Matsuoka, C Ueno, E Ozaki, S Takaya, T Takeyama, T Hujita, K Kawakatsu, J Takemura, H Maekawa, T Doei, S Ihara, Y Sakaguchi, Y Hirota, A Shindo, H Araki, J Miura, T Morita, T Fujiwara, H Akiyama, S Itome, Y Tanaka, K Nakagawa, S Okamoto, S Yamamoto, T Aoyagi, T Noda, Inoue, I Hirota, K Tanaka, T Nagashima, I Koga, K Watanabe, H Kusadome, H Otsuka, T Takayama, H Miwa, A Hamakawa, K China, N Niikawa, T Ohta, D Starenki, K Umehara, K Yamada, Y Shimada, H Nagasawa, T Minato, T Ogino, K Yoshiura, N Miwa, M Nomura, H Kuniba, Y Noguchi, S Ono, M Tsuda, M Nakashima, T Kikuchi, D Satoh, T Kishino, S Kondo, A Kinoshita
    • Journal Title

      J Hum Genet 54

      Pages: 499-503

    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene2009

    • Author(s)
      Miyazaki K, Mapendano CK, Fuchigami Y, Kondo S, Ohta T, Kinoshita A, Tsukamoto K, Yoshiura K, Niikawa N, Kishino T
    • Journal Title

      Gene 432

      Pages: 97-101

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] 新川詔夫 DNAメチル化と遺伝子発現制御のしくみを探る2009

    • Author(s)
      太田亨
    • Journal Title

      Biophilia 5(3)

      Pages: 11-15

    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Earwax, osmidrosis, and breast cancer : Why does one SNP (538G>A) in the human ABC transporter ABCC11 gene determine earwax type?2009

    • Author(s)
      Toyoda Y, Sakurai A, Mitani Y, Nakashima M, Yoshiura K, Nakagawa H, Sakai Y, Ota I, Lezhava A, Hayashizaki Y, Niikawa N, Ishikawa T
    • Journal Title

      FASEB J 23(6)

      Pages: 2001-2013

    • Data Source
      KAKENHI-PROJECT-19390095
  • [Journal Article] Japanese map of the earwax gene frequency: a nation-wide collaborative study by Super Science High School (SSH) Consortium.2009

    • Author(s)
      Yoshiura K, Kinoshita A, Ohta T, Niikawa N, et al
    • Journal Title

      J Hum Genet 54

      Pages: 499-503

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Earwax, osmidrosis, and breast cancer : Why does one SNP (538G>A) in the human ABC transporter ABCC11 gene determine earwax type?2009

    • Author(s)
      Toyoda Y, Sakurai A, Mitani Y, Nakashima M, Yoshiura K, Nakagawa H, Sakai Y, Ota I, Lezhava A, Hayashizaki Y, Niikawa N, Ishikawa T
    • Journal Title

      FASEB J 23(6)

      Pages: 2001-2013

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] DNAメチル化と遺伝子発現制御のしくみを探る2009

    • Author(s)
      太田亨、新川詔夫
    • Journal Title

      Biophilia

      Volume: 5(3) Pages: 11-15

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene.2009

    • Author(s)
      Miyazaki K, Mapendano CK, Fuchigami Y, Kondo S, Ohta T, Kinoshita A, Tsukamoto K, Yoshiura K, Niikawa N, Kishino T
    • Journal Title

      Gene 432

      Pages: 97-101

    • Data Source
      KAKENHI-PROJECT-20590409
  • [Journal Article] Developmentally dynamic changes of DNA methylation in the mouse Snurf/ Snrpn gene2009

    • Author(s)
      Miyazaki K, Mapendano CK, Fuchigami T, Kondo S, Ohta T, Kinoshita A, Tsukamoto K, Yoshiura KI, Niikawa N, Kishino T
    • Journal Title

      Gene

      Volume: 432(1-2) Pages: 97-101

    • Data Source
      KAKENHI-PROJECT-21390100
  • [Journal Article] nese map of the earwax gene frequency : a nation-wide collaborative study by Super Science High School(SSH) Consortium2009

    • Author(s)
      S Sakai, K Imai, T Ogawa, H Iwaoka, M Ishii, S Komori, T Yoshida, H Jumonji, K Iizumi, H Ohshima, T Maeda, A Kanno, K Takahashi, H Kubota, Y Inoue, Y Takahashi, H Onoda, R Uchiyama, M Matsuda, T Akazawa, N Kawamura, T Odagiri, Y Watanabe, Y Matsumoto, S Shinoda, M Terada, M Matsuoka, C Ueno, E Ozaki, S Takaya, T Takeyama, T Hujita, K Kawakatsu, J Takemura, H Maekawa, T Doei, S Ihara, Y Sakaguchi, Y Hirota, A Shindo, H Araki, J Miura, T Morita, T Fujiwara, H Akiyama, S Itome, Y Tanaka, K Nakagawa, S Okamoto, S Yamamoto, T Aoyagi, T Noda, Inoue, I Hirota, K Tanaka, T Nagashima, I Koga, K Watanabe, H Kusadome, H Otsuka, T Takayama, H Miwa, A Hamakawa, K China, N Niikawa, T Ohta, et al.
    • Journal Title

      J Hum Genet

      Volume: 54 Pages: 499-503

    • Data Source
      KAKENHI-PROJECT-20590332
  • [Journal Article] Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb102007

    • Author(s)
      Yamasaki Y, Kayashima T, Mapendano CK, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T
    • Journal Title

      Mol Cell Biol 27(2)

      Pages: 732-742

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Opitz C (trigonocephaly) syndrome caused by deficiency of a member of the immunoglobulin superfamily, CD962007

    • Author(s)
      Kaname T, Yanagi K, Chinen Y, Makita Y, Okamoto N, Maehara H, Ohwan I, Kanaya F, Kubota Y, Oike Y, Yamamoto T, Kurosawa K, Fuku shima Y, Bohring A, Opitz JM, Yoshiura K, Niikawa N, Naritomi K
    • Journal Title

      Am J Hum Genet 81(4)

      Pages: 835-841

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb102007

    • Author(s)
      YamasaKi Y, Kayashima T, Mapendano CK, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T
    • Journal Title

      Moleculr Cell Biology 27 (2)

      Pages: 732-742

    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.2006

    • Author(s)
      Miyake N, Yoshiura K, Ohta T, Niikawa N, et al
    • Journal Title

      Am J Med Genet 140A

      Pages: 291-293

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrom patients2006

    • Author(s)
      Miyake N, Yoshiura K, Ohta T, Niikawa N et al.
    • Journal Title

      American Journal of Medical Genetics 140A

      Pages: 205-211

    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] SNP in the ABCC11 gene is the determinant of human earwax type.2006

    • Author(s)
      Yoshiura K, Kinoshita A, Ohta T, Niikawa N, et al
    • Journal Title

      Nat Genet 38

      Pages: 324-330

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] BAC array CGH reveals genomic aberrations in idiopathic mental retardation.2006

    • Author(s)
      Miyake N, Yoshiura K, Ohta T, Niikawa N, et al
    • Journal Title

      Am J Med Genet 140A

      Pages: 205-211

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] BAC array CGH reveals genomic aberrations in idiopathic mental retardation2006

    • Author(s)
      Miyake N, Yoshiura K, Ohta T, Niikawa N et al.
    • Journal Title

      American Journal of Medical Genetics 140A

      Pages: 291-293

    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Molecular characterization of del(8)(p23. 1p23. 1) in a case of congenital diaphragmatic hernia.2005

    • Author(s)
      Shimokawa O, Ohta T, Kinoshita A, Yoshiura K, Niikawa N, et al
    • Journal Title

      Am J Med Genet 136A

      Pages: 49-51

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion2005

    • Author(s)
      Visser R, Ohta T, Niikawa N, Matsumoto N et al.
    • Journal Title

      American Journal of Human Genetics 76

      Pages: 52-67

    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Identification of a 3. 0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1. 9-Mb microdeletion.2005

    • Author(s)
      Visser R, Kinoshita A, Ohta T, Niikawa N, et al
    • Journal Title

      Am J Hum Genet 76(1)

      Pages: 52-67

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Sotes syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats2005

    • Author(s)
      Kurotaki N, Stankiewicz P, Wakui K, Niikawa N, Lupsli JR
    • Journal Title

      Human Molecular Genetics 14

      Pages: 535-542

    • Data Source
      KAKENHI-PROJECT-17019055
  • [Journal Article] Japan map of the earwax gene frequency : A nation-wide collaborative study by Super Science High School(SSH)

    • Author(s)
      Satoshi Sakai, Kazumi Imai, Takashi Ogawa, Hiroshi Iwaoka, Mikiko Ishii, Shinichiro Komori, Toyohiko Yoshida, Hideyuki Jumonji, Keiji Iizumi, Hiroshi Ohshima, Toshiaki Maeda, Akira Kanno, Kenji Takahashi, Hiroto Kubota, Yoko Inoue, Yoshiyuki Takahashi, Hiroshi Onoda, Rie Uchiyama, Michihiko Matsuda, Takashi Akazawa, Naohiro Kawamura, Toru Odagiri, Yasuharu Watanabe, Yukihiro Matsumoto, Seiji Shinoda, * Masato Terada, Manabu Matsuoka, Chikara Ueno, Etsuo Ozaki, Sadafusa Takaya, Tetsuharu Takeyama, Toshiaki Hujita, Kazuya Kawakatsu, Junichi Takemura, Hitonori Maekawa, Tomoko Doei, Shigeru Ihara, Yuji Sakaguchi, Yasuyuki Hirota, Akihiko Shindo, Hiroko Araki, Junko Miura, Tatsumi Morita, Takayuki Fujiwara, Haruhiko Akiyama, Shinya Itome, Yoshihisa Tanaka, Kazunori Nakagawa, Sumito Okamoto, Shushi Yamamoto, Takaaki Aoyagi, Toru Noda, Shinichi Inoue, Isao Hirota, Kiyoshi Tanaka, Tetsuya Nagashima, Iwao Koga, Kayo Watanabe, Hideto Kusadome, Hirosi Otsuka, Tosifumi Takayama, Hiroshi Miwa, Atsushi Hamakawa, Katsunori China, Norio Niikawa, Tohru Ohta, Dmytro Starenki, Ken Umehara, Kensuke Yamada, Yoichi Shimada, Hiroyuki Nagasawa, Takashi Minato, Toshihiko Ogino, Koh-ichiro Yoshiura, Nobutomo Miwa, Masayo Nomura, Hideo Kuniba, Yasuko Noguchi, Shinji Ono, Masayoshi Tsuda, Mitsuko Nakashima, Taeko Kikuchi, Daisuke Satoh, Tatsuya Kishino, Shinji Kondo, Akira Kinoshita
    • Journal Title

      Consortium(J Hum Genet) (in press)

    • Data Source
      KAKENHI-PROJECT-19390095
  • [Patent] 体臭抑制剤2012

    • Inventor(s)
      長田和実、新川詔夫、太田亨
    • Industrial Property Rights Holder
      (特許出願人)学校法人東日本学園北海道医療大学
    • Industrial Property Number
      2012-016299
    • Filing Date
      2012-01-30
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] Polyamines Remove DNA Methylation of COL15A1 Caused by LPS.2017

    • Author(s)
      R. Takai, O. Uehara, T. Morikawa, F. Harada, K. Yoshida, J. Sato, M. Nishimura, I. Chiba, Y. Abiko, T.Ohta.
    • Organizer
      95th IADR
    • Place of Presentation
      Sanfrancisco, USA
    • Year and Date
      2017-03-22
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25463223
  • [Presentation] Van der Woude症候群に関する基礎的臨床的研究-第4報 披裂の関係を中心とした分析-2015

    • Author(s)
      大野磨弥,新美照幸,古川博雄,南克浩,井村英人,早川統子,森明弘,太田亨,夏目長門
    • Organizer
      第39回日本口蓋裂学会総会学術集会
    • Place of Presentation
      シェーンバッハ・サボー(東京都千代田区)
    • Year and Date
      2015-05-21
    • Data Source
      KAKENHI-PROJECT-24249092
  • [Presentation] Identification of target genes for the language-related FOXP2 and its isoform.2013

    • Author(s)
      T. Ohta, N. Niikawa, T. Oikawa
    • Organizer
      ASHG 2013
    • Place of Presentation
      Boston, USA
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 過去8年間(2004~2012年)に天使病院小児科遺伝外来を受診しマイクロアレイを用いたゲノム解析を行った患者の検討2012

    • Author(s)
      徳富智明, 太田亨, 齋藤伸治, 奥原宏治, 飯塚進, 高橋伸浩, 小畑慶子, 新川詔夫, 外木秀文
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 微細染色体異常の同定されたAngelman症候群様表現型を呈する症例2012

    • Author(s)
      細木華奈, 太田亨, 新川詔夫, 小崎健次郎, 齋藤伸治
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 過去8 年間(2004 ~ 2012 年)に天使病院小児科遺伝外来を受診しマイクロアレイを用いたゲノム解析を行った患者の検討2012

    • Author(s)
      徳富 智明、太田 亨、齋藤 伸治、奥原 宏治、飯塚 進、高橋 伸浩、小畑 慶子、新川 詔夫、外木 秀文
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] ホルモン非抵抗性先端異骨症のエクソーム解析2012

    • Author(s)
      要匡, 柳久美子, 小口良子, 成富研二, 當間隆也, 近藤達郎, 二井英二, 外木秀文, 西村玄, 吉浦孝一郎, 太田亨, 新川詔夫, 松浦信夫, Dong-Kyu Jin
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] Identification of target genes for the language-related FOXP2 and its isoform2012

    • Author(s)
      Ohta T. Niikawa N. Oikawa T
    • Organizer
      The 62nd Annual Meeting of the American Society of Human Geetics
    • Place of Presentation
      BOSTON, USA
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 言語関連転写因子FOXP2のisoformの機能と標的遺伝子の同定2012

    • Author(s)
      太田亨, 及川恒之, 新川詔夫
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 言語関連転写因子FOXP2 のisoform の機能と標的遺伝子の同定2012

    • Author(s)
      太田 亨、及川 恒之、新川 詔夫
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] Angelman症候群とPrader-Willi症候群のエピジェネティックス2012

    • Author(s)
      太田亨
    • Organizer
      第54回歯科基礎医学会学術大会・総会・サテライトシンポジウム
    • Place of Presentation
      郡山市
    • Invited
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 微細染色体異常の同定されたAngelman 症候群様表現型を呈する症例2012

    • Author(s)
      細木 華奈、太田 亨、新川 詔夫、小崎 健次郎、齋藤 伸治
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 5q31.3 microdeletion syndrome is a clinically discernible new syndrome characterized by severe neonatal hypotonia, feeding difficulties, respiratory distress, and severe developmental delay2011

    • Author(s)
      Hosoki K, Ohta T, Natsume J, Imai S, Okumura A, Matsui T, Harada N, Scaglia F, Bacino CA, Niikawa N, Saitoh S
    • Organizer
      The 12th International Congress of Human Genetics / The 61st Annual Meeting of the American Society of Human Geetics
    • Place of Presentation
      Montreal, CANADA
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 言語関連転写因子FOXP2の標的遺伝子の同定2011

    • Author(s)
      太田亨, 松田律史, 及川恒之, 新川詔夫
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 5q31.3 microdeletion syndrome is a clinically discernible new syndrome characterized by severe neonatal hypotonia, feeding difficulties, respiratory distress, and severe developmental delay.2011

    • Author(s)
      K. Hosoki, T.Ohta, J. Natsume, S. Imai, A. Okumura, T. Matsui, N. Harada, F. Scaglia, C.A. Bacino, N. Niikawa, S. Saitoh.
    • Organizer
      12th ICHG/61th ASHG2011
    • Place of Presentation
      Montreal
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] ポアソン回帰及びモデル選択の多因子マイクロアレイ実験への適応2011

    • Author(s)
      松田律史,加茂憲一,太田亨,及川恒之,新川詔夫
    • Organizer
      第34回日本分子生物学会年回
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 5q31.3欠失症候群は新規の染色体微細欠失症候群である2011

    • Author(s)
      細木華奈, 太田亨, 夏目淳, 今井純好, 奥村彰久, 松井健, 原田直樹, Scaglia Fernando, Bacino Carlos, 新川詔夫, 齋藤伸治
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] Identification of novel schizophrenia loci by homozygosity mapping using DNA microarray analysis2011

    • Author(s)
      Kurotaki, et al
    • Organizer
      12^<th> Unternational Congress of Human Genetics and The American Society of Human Genetics, 61^<st> Annual Meeting
    • Place of Presentation
      Montoreal
    • Data Source
      KAKENHI-PROJECT-21390100
  • [Presentation] 日本人におけるヒト耳垢遺伝子ABCC11のΔ27アリル頻度2010

    • Author(s)
      山田愛子, 堀佑輔, 小野佑輔, 松田律史, ストランキーディマ, ソソンキナナディア, 吉浦孝一郎, 新川詔夫, 太田亨
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] Discovery of a gene for Kabuki syndrome by exome sequencing and genotype-phenotype relationship in 110 cases2010

    • Author(s)
      M. J. Bamshad. M. C. Hannibal, K. J. Buckingham, A. E. Beck, S. B. Ng, M. McMillin, H. Gildersleeve, A. W. Bigham, H. K. Tabor, K. Yoshiura, T. Matsumot, N. Matsumoto, H. Tonoki, K. Naritomi, T. Kaname, T. Nagai, H. Ohashi, K. Kurosawa, J. Hou, T. Ohta, e
    • Organizer
      日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] 歌舞伎メーキャップ症候群のエクソーム解析2010

    • Author(s)
      要匡, 塚原正俊, 柳久美子, 藤森一浩, 喜久里育也, 照屋盛実, 今田有美, 鼠尾まい子, 矢野修一, 佐藤友紀, 三輪有希乃, 平野隆, 吉浦孝一郎, 太田亨, 新川詔夫, 成富研二
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] 日本人におけるヒト耳垢遺伝子ABCC11のΔ27アリルの新たな見解2010

    • Author(s)
      松田律史, 山田愛子, 小野佑輔, 堀佑輔, スタレンキディミトロ, ソソンキナナディア, 吉浦孝一郎, 太田亨, 新川詔夫
    • 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
      神戸ポートアイランド,神戸
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] ABCC11 expression and 538G/A poly-morphism in human breast cancer.2010

    • Author(s)
      Sosonkina Nadiya, Starenki Dmytro, 太田亨, 吉浦孝一郎, 新川詔夫
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] ホールエクソンキャプチャーによる歌舞伎メーキャップ症候群の解析2010

    • Author(s)
      要匡, 塚原正俊, 柳久美子, 藤森一浩, 喜久里育也, 照屋盛実, 今田有美, 鼠尾まい子, 矢野修一, 佐藤友紀, 三輪有希乃, 平野隆, 吉浦孝一郎, 太田亨, 新川詔夫, 成富研二
    • 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
      神戸ポートアイランド,神戸
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] 日本人におけるヒト耳垢遺伝子ABCC11のΔ27アリル頻度2010

    • Author(s)
      山田愛子, 堀佑輔, 小野佑輔, 松田律史, ストランキーディマ, ソソンキナナディア, 吉浦孝一郎, 新川詔夫, 太田亨
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] ABCC11 expression and 538G/A poly-morphism in human breast cancer. Sosonkina Nadiya, Starenki Dmytro2010

    • Author(s)
      太田亨, 吉浦孝一郎, 新川詔夫
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] Frequency of 27-bp deletion mutation, another earwax determinant, in ABCC11 among the Japanese population2010

    • Author(s)
      A. Yamada, Y. Hori, Y. Ono, N. Matsuda, D. Starenki, N. Sosonkina, K. Yoshiura, T. Ohta, N. Niikawa
    • Organizer
      The American Society of Human Genetics, 59th Annual Meeting
    • Place of Presentation
      Washigton D. C., Baltimore
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] ホールエクソンキャプチャーによる歌舞伎メーキャップ症候群の解析2010

    • Author(s)
      要匡, 塚原正俊, 柳久美子, 藤森一浩, 喜久里育也, 照屋盛実, 今田有美, 鼠尾まい子, 矢野修一, 佐藤友紀, 三輪有希乃, 平野隆, 吉浦孝一郎, 太田亨, 新川詔夫, 成富研二
    • 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
      神戸ポートアイランド,神戸
    • Data Source
      KAKENHI-PROJECT-20590332
  • [Presentation] Discovery of a gene for Kabuki syndrome by exome sequencing and genotype-phenotype relationship in 110 cases.2010

    • Author(s)
      M.J. Bamshad. M.C. Hannibal, K.J. Buckingham, A.E. Beck, S.B. Ng, M. McMillin, H. Gildersleeve, A.W. Bigham, H.K. Tabor, K.Yoshiura, T. Matsumot, N. Matsumoto, H. Tonoki, K.Naritomi, T. Kaname, T. Nagai, H. Ohashi, K. Kurosawa, J. Hou, T.Ohta, C.A. Morris, J.E. Ming, T.H. Shikh, S. Banka, G. Black, J. Clayton-Smith, E.H. Zackai, D. Donnai, N.Niikawa, D.A. Nickerson, J. Shendure.
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] 歌舞伎メーキャップ症候群のエクソーム解析2010

    • Author(s)
      要匡, 塚原正俊, 柳久美子, 藤森一浩, 喜久里育也, 照屋盛実, 今田有美, 鼠尾まい子, 矢野修一, 佐藤友紀, 三輪有希乃, 平野隆, 吉浦孝一郎, 太田亨, 新川詔夫, 成富研二
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティー,大宮
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] 日本人におけるヒト耳垢遺伝子ABCC11のΔ27アリルの新たな見解2010

    • Author(s)
      松田律史, 山田愛子, 小野佑輔, , スタレンキディミトロ, ソソンキナナディア, 吉浦孝一郎, 太田亨, 新川詔夫
    • 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
      神戸ポートアイランド,神戸
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] Frequency of 27-bp deletion mutation, another earwax determinant, in ABCC11 among the Japanese population.2010

    • Author(s)
      A.Yamada, Y.Hori, Y.Ono, N.Matsuda, D. Starenki, N. Sosonkina, K.Yoshiura, T.Ohta, N.Niikawa
    • Organizer
      The American Society of Human Genetics, 59th Annual Meeting
    • Place of Presentation
      Washigton D.C., Baltimore
    • Data Source
      KAKENHI-PROJECT-20590409
  • [Presentation] A strong association of axillary osmidrosis with genotype of the ABCC11 gene defining the earwax type.2008

    • Author(s)
      Tsuda M, Mivva N, Nakano M, Nakashima M, Yoshiura K, Ohta T, Niikawa N
    • Organizer
      The 2008 EAUHGS Symposium & the 8^<th> EAUHGS Annual Meeting
    • Place of Presentation
      Sapporo
    • Year and Date
      2008-07-19
    • Data Source
      KAKENHI-PROJECT-19390095
  • [Presentation] 歌舞伎症候群 第1報-歌舞伎症候群の責任遺伝子解析を中心にして-

    • Author(s)
      加藤大貴,太田亨,吉浦孝一郎,古川博雄,新美照幸,南克浩,村田幸枝,鈴木聡,井村英人,夏目長門
    • Organizer
      第38回日本口蓋裂学会総会・学術大会
    • Place of Presentation
      札幌
    • Year and Date
      2014-05-29 – 2014-05-30
    • Data Source
      KAKENHI-PROJECT-24249092
  • [Presentation] ポアソン回帰及びモデル選択の多因子マイクロアレイ実験への適応

    • Author(s)
      松田 律史,加茂 憲一,太田 亨,及川 恒之,新川 詔夫
    • Organizer
      第34回日本分子生物学会年回
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 5q31.3欠失症候群は新規の染色体微細欠失症候群である

    • Author(s)
      細木華奈)、太田亨、夏目淳、今井純好、奥村彰久、松井健、原田 直樹、Scaglia Fernando、Bacino Carlos、新川詔夫、齋藤伸治
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23590383
  • [Presentation] 言語関連転写因子FOXP2の標的遺伝子の同定

    • Author(s)
      太田亨、松田律史、及川恒之、新川詔夫
    • Organizer
      第56回日本人類遺伝学会・第11回東アジア人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-23590383
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  • 44.  YAMAMOTO Masahiko (40378039)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 45.  INOUE Makoto (50191888)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 46.  MAEDA Hatsuhiko (30175591)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 47.  FUJIWARA Kumiko (60404737)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 48.  HAYAKAWA Toko (90609710)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 49.  YOSHIDA Waka (10513210)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 50.  SUZUKI Satoshi (30468996)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 51.  IMURA Hideto (10513187)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 52.  ONO Maya (70760718)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 53.  荒川 俊哉 (40306254)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 54.  古市 保志 (80305143)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 55.  田隈 泰信 (40095336)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 56.  齊藤 正人 (50337036)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 57.  斎藤 一郎 (60147634)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 58.  向後 晶子 (20340242)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 59.  新美 照幸 (60291762)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 60.  古川 博雄 (70291763)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 61.  南 克浩 (70346162)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 62.  道川 誠 (40270912)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 63.  藏滿 保宏 (50281811)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 64.  MORI Akihiro
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 65.  YAMAUCHI Fuko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 66.  SAKUMA Chisato
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 67.  ITO Masaaki
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 68.  AKASHI Junko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 69.  NATSUME Nagana
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 70.  OGATA Tsutomu
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 71.  山形 崇倫
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 72.  福嶋 義光
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 73.  副島 英伸
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 74.  大塚 泰史
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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