• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

KISHINO Tatsuya  木住野 達也

ORCIDConnect your ORCID iD *help
Researcher Number 70315232
Other IDs
External Links
Affiliation (Current) 2025: 長崎大学, 医歯薬学総合研究科(医歯薬学総合研究系), 准教授
Affiliation (based on the past Project Information) *help 2021 – 2025: 長崎大学, 医歯薬学総合研究科(医歯薬学総合研究系), 准教授
2013 – 2016: 長崎大学, 先導生命科学研究支援センター, 准教授
2007 – 2011: Nagasaki University, Center for Frontier Life Sciences, Division of Functional Genomics, Associate Professor
2006: 長崎大学, 先端生命科学研究支援センター, 助教授
2003 – 2006: Nagasaki University, Center for Frontier Life Sciences, Division of Functional Genomics, Assistant Professor, 先導生命科学研究支援センター, 助教授
2004: 長崎大学, 先導生命科学支援センター, 助教授
2000 – 2002: 長崎大学, 遺伝子実験施設, 助教授
Review Section/Research Field
Principal Investigator
Biological Sciences / Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Pediatrics / General medical chemistry
Except Principal Investigator
Human genetics / Basic Section 59040:Nutrition science and health science-related / Human genetics / Biological Sciences
Keywords
Principal Investigator
インプリンティング / 神経細胞 / Ube3a / プラダーウィリー症候群 / Snrpn / Atp10a / ヒストン修飾 / Snord116 / Magel2 / モデルマウス … More / トランスジェニックマウス / アンジェルマン症候群 / UBE3A / DNAメチル化 / プラダー・ウィリー症候群 / 遺伝子改変マウス / プラダーウウィリー症候群 / CTCF / neuron / histone modifications / DNA methvyation / epigenetics / imprinting / MeCP2 / 脳 / メチル化 / エピジェネティクス / Histone modification / Gliall cells / Neuron / Angelman syndrome / Imprinting / アンジェルマシ症候群 / グリア細胞 / BACトランスジェニックマウス / mkrn3 / magel2 / ゲノムインプリンティング / G9a阻害剤 / necdin / Mkrn3 / Necdin / 前駆細胞 / 神経幹細胞 / 母親由来2倍体ES細胞 / エンハンサー / 卵 / IC-transcript / クロマチン病 / エピジェネテクス / Silver-Russell症侯群 / 自閉性 / TSGA14 / 自閉症 / PEG1 / MEST / 7q32 / ゲノム刷り込み … More
Except Principal Investigator
ハプロタイプ解析 / インプリンティング / Sexual dimorphism / Visceral fat / Neuropeptide Y / Aging / Longevity / familial cases of genetic diseases / disease genes / gene mapping / single-gene disorders / linkage analysis / ITGA3B遺伝子 / 遺伝性難聴 / WFS1遺伝子 / 疾病遺伝子 / 変異解析 / マイクロサテライトマーカー / 単一遺伝子疾患 / 疾患遺伝子座 / 緊張性四肢麻痺 / 無臭覚症 / 家族性側索硬化症 / 心房中隔欠損症 / 無嗅覚症 / 下顎前突症 / 多汗症 / 家族性心房中核欠損症 / 遺伝病家系 / 疾患遺伝子 / 遺伝子マッピング / 遺伝子病 / 連鎖解析 / 7q32 region / genomic imprinting / single nucleotide polymorphism (SNP) / association study / haplotype analysis / LRP5 gene / bone-mineral-density determinant / osteoporosis / TGFBR1 / TGF-β1蛋白 / 多因子疾患 / ゲノムインプリンティング / 自閉症 / モデルマウス / 連関解析 / TGFB1 / 骨軟化症 / 1塩基多型(SNP) / TGFB1遺伝子 / TGFB遺伝子 / 刷り込み遺伝子 / マウスAtp10a遺伝子 / 刷り込み関連遺伝子 / LRP5遺伝子SNP / 骨粗鬆症発症危険因子 / 発症危険因子 / ハプロタイプ / 7q32領域 / ゲノム刷り込み / SNP / 関連解析 / LRP5遺伝子 / 骨密度決定因子 / 骨粗鬆症 / 発生・分化 / 細胞・組織 / 神経細胞 / 脳 Less
  • Research Projects

    (15 results)
  • Research Products

    (61 results)
  • Co-Researchers

    (15 People)
  •  Generation of Prader-Wili syndrome model mice and molecular genetic analysis of the disease pathologyPrincipal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2025 – 2027
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Nagasaki University
  •  The role of macrophage-derived NPY from the perspective of gender differences in lipid metabolism, which holds the key to extending healthy lifespan

    • Principal Investigator
      朴 盛浚
    • Project Period (FY)
      2024 – 2026
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 59040:Nutrition science and health science-related
    • Research Institution
      Nagasaki University
  •  Molecular analysis of Prader-Willi syndrome by model micePrincipal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2021 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Nagasaki University
  •  molecular analysis of Prader-Willi syndrome model mice with imprinting mutationPrincipal Investigator

    • Principal Investigator
      KISHINO Tatsuya
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  Molecular and behavioral analysis of transgenic mice of Angelman syndrome gene, Ube3aPrincipal Investigator

    • Principal Investigator
      KISHINO Tatsuya
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  The regulation of bone formation by epigenetic factor MeCP2

    • Principal Investigator
      HIGASHIMOTO Ken
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Human genetics
    • Research Institution
      Saga University
  •  ヒト、マウスにおける神経細胞特異的インプリンティング遺伝子の探索Principal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  過排卵が及ぼす未受精卵インプリントへの影響Principal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  Molecular analysis of tissue-specific imprintingPrincipal Investigator

    • Principal Investigator
      KISHINO Tatsuya
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      General medical chemistry
    • Research Institution
      Nagasaki University
  •  脳高次機能に関与するエピジェネティクス調節因子の解析Principal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2005
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  脳における系統的インプリンティング解析を可能にする片親由来2倍体神経細胞の作製

    • Principal Investigator
      宮崎 和美
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Human genetics
    • Research Institution
      Nagasaki University
  •  Functional and Imprinting Analysis in Brain of Angelman Syndrome Gene UBE3APrincipal Investigator

    • Principal Investigator
      KISHINO Tatsuya
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  CONSORTIUM-BACED LINKAGE ANALYSIS AND IDENTIFICATION OF GENES FOR SINGEL-GENE DISEASES

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      2001 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (S)
    • Research Field
      Human genetics
    • Research Institution
      NAGASAKI UNIVERSITY
  •  自閉症の原因遺伝子の単離Principal Investigator

    • Principal Investigator
      木住野 達也
    • Project Period (FY)
      2000 – 2001
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  Genome study on osteoporosis and on imprinted genes

    • Principal Investigator
      NIKAWA Norio
    • Project Period (FY)
      2000 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki Universty

All 2023 2022 2017 2016 2015 2014 2013 2011 2009 2007 2006 2005 2004 2003 2002 2001 Other

All Journal Article Presentation Book

  • [Book] 転写因子・転写制御キーワードブック2006

    • Author(s)
      木住野 達也, 他
    • Publisher
      東京羊土社
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590273
  • [Journal Article] Proline-rich transmembrane protein 2 knock-in mice present dopamine-dependent motor deficits2023

    • Author(s)
      Hatta Daisuke、Kanamoto Kaito、Makiya Shiho、Watanabe Kaori、Kishino Tatsuya、Kinoshita Akira、Yoshiura Koh-Ichiro、Kurotaki Naohiro、Shirotani Keiro、Iwata Nobuhisa
    • Journal Title

      The Journal of Biochemistry

      Volume: 174 Issue: 6 Pages: 561-570

    • DOI

      10.1093/jb/mvad074

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21K07296, KAKENHI-PROJECT-21K07848, KAKENHI-PROJECT-23K08680, KAKENHI-PROJECT-21H02809
  • [Journal Article] Imprinting analysis of the mouse chromosome 7C region inDNMT1-null embryos2014

    • Author(s)
      Nakagaki A, Osanai H, Kishino T
    • Journal Title

      GENE

      Volume: 553 Issue: 1 Pages: 63-68

    • DOI

      10.1016/j.gene.2014.10.006

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Journal Article] Disruption of the LTD dialogue between the cerebellum and the cortex in Angelman syndrome model: a timing hypothesis.2014

    • Author(s)
      Cheron G, Márquez-Ruiz J, Kishino T, Dan B
    • Journal Title

      Front Syst Neurosci.

      Volume: 8 Pages: 221-229

    • DOI

      10.3389/fnsys.2014.00221

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Journal Article] No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.2006

    • Author(s)
      Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Ohashi H, Kurosawa K, Naritomi K, Kaname T, Nagai T, Shotelersuk V, Hou J-W, Fukushima Y, Kondoh T, Matsumoto T, Shinoki T, Kato M, Tonoki H, Nomura M, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N.
    • Journal Title

      Am J Med Genet 140A

      Pages: 291-293

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] BAC array CGH reveals genomic aberrations in idiopathic mental retardation.2006

    • Author(s)
      Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N.
    • Journal Title

      Am J Med Genet 140A

      Pages: 205-211

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.2006

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

      Am J Med Genet 140A

      Pages: 291-293

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] BAC array CGH reveals genomic aberrations in idiopathic mental retardation.2006

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

      Am J Med Genet 140A

      Pages: 205-211

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] PAX9 and TGFB3 are susceptible to nonsyndromic cleft lip with or without cleft palate in the Japanese : Population-based and family-based candidate gene analyses.2006

    • Author(s)
      Ichikawa E, Watanabe A, Nakano Y, Hirano A, Akita S, Kinoshita A, Kondo, S, Kishino, T, Uchiyama T, Niikawa N, Yoshiura K
    • Journal Title

      J Hum Genet 51

      Pages: 38-46

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Expression of the Snurf-Snrpn IC transcript in the oocyte and putative role in the imprinting establishment of the mouse 7C imprinting domain2006

    • Author(s)
      Mapendano CK, Kishino T, Miyazaki K, Kondo S, Yoshiura K, Hishikawa Y, Koji T, Niikawa N
    • Journal Title

      J Hum Genet (In press)

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Neuron-specific relaxation of Igf2r imprinting is associated with neuron-specific histone modifications and lack of its antisense transcript Air.2005

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

      Hum Mol Genet 14

      Pages: 2511-2530

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Neuron-specific relaxation of Igf2r imprinting is associated with neuron-specific histone modifications and lack of its antisense transcript Air2005

    • Author(s)
      Yamasaki Y, Kayashima T, Niikawa N, Kishino T, et al.
    • Journal Title

      Hum Mol Genet 14

      Pages: 2511-2530

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] LRP5, low density lipoprotein receptor-related protein 5, is a determinant for bone mineral density (BMD).2004

    • Author(s)
      Mizuguchi T, Furuta I, Watanabe Y, Tsukamoto K, Tomita H, Tsujihata M, Ohta T, Kishino T, Matsumoto N, Minakami H, Niikawa N, Yoshiura K
    • Journal Title

      J Hum Genet 49

      Pages: 80-86

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q322004

    • Author(s)
      Yamada T, Niikawa N, Kishino T, et al.
    • Journal Title

      Genomics 83

      Pages: 402-412

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Heterozygous TGFBR2 mutations in Marfan syndrome.2004

    • Author(s)
      Mizuguchi T, Collod-Beroud G, Abifadel M, Akiyama T, Harada N, Morisaki T, Allard D, Varret M, Claustres M, Morisaki H, Ihara M, Kinoshita A, Yoshiura K, Junien C, Kajii T, Jondeau G, Ohta T, Kishino T, Fukukawa Y, Nakamura Y, Niikawa N, Boileau C, Matsumoto N
    • Journal Title

      Nat Genet 36(8)

      Pages: 855-860

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] LRP5, low density lipoprotein receptor-related protein 5, is a determinant for bone mineral density (BMD)2004

    • Author(s)
      Mizuguchi T, Kishino T, Matsumoto N, Minakami H, Niikawa N, et al.
    • Journal Title

      J Hum Genet 49

      Pages: 80-86

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] A novel GATA4 mutation completely segregated with atrial septal defect in a large Japnese family.2004

    • Author(s)
      Okubo A, Yoshiura K, Kishino T, Niikawa N, et al.
    • Journal Title

      J Med Genet 41

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family.2004

    • Author(s)
      Okubo A, Miyoshi O, Baba K, Takagi M, Tsukamoto K, Kinoshita A, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N
    • Journal Title

      J Med Genet 41(7)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Heterozygous TGFBR2 mutations in Marfan syndrome.2004

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

      Nat Genet 36

      Pages: 855-860

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Fifty microdeletions among 112 cases of Sotos syndrome : Low copy repeats possibly mediate the common deletion.2003

    • Author(s)
      Kurotaki N, Harada N, Shimokawa O, Miyake N, Kawame H, Uetake K, Makita Y, Kondoh T, Ogata T, Hasegawa T, Nagai T, Ozaki T, Touyama M, Shenhav R, Ohashi H, Medne L, Shiihara T, Ohtsu S, Kato Z, Okamoto N, Nishimoto J, Lev D, Miyoshi Y, Ishikiriyama S, Sonoda T, Sakazume S, Fukushima Y, Kurosawa K, Cheng J-F, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N
    • Journal Title

      Hum Mut 22(5)

      Pages: 378-387

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] On the conflicting reports of imprinting status of mouse ATP10a in the adult brain Strain-background-dependent imprinting?2003

    • Author(s)
      Kayashima T, Ohta T, Niikawa N, kishino T
    • Journal Title

      J Hum Genet 48(9)

      Pages: 492-493

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] The novel imprinted carboxypeptidase A4 gene (CPA4) in the 7q32 imprinting domain.2003

    • Author(s)
      Kayashima T, Yamasaki K, Yamada T, Sakai H, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Kanetake H, Niikawa N, Kishino T
    • Journal Title

      Hum Genet 112

      Pages: 220-226

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Atp1Oa, the mouse ortholog of the human imprinted ATP10C gene, escapes genomic imprinting.2003

    • Author(s)
      Kayashima T, Yamasaki K, Joh K, Yamada T, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Mukai T, Niikawa N, Kishino T
    • Journal Title

      Genomics 81

      Pages: 644-647

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a2003

    • Author(s)
      Yamasaki K, Niikawa N, Ogawa M, Wagstaff J, Kishino T, et al.
    • Journal Title

      Hum Mol Genet 12

      Pages: 837-847

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] On the conflicting reports of imprinting status of mouse ATP10a in the adult brain : Strain-background-dependent imprinting?2003

    • Author(s)
      Kayashima T, Ohta T, Niikawa N, Kishino T
    • Journal Title

      J Hum Genet 48

      Pages: 492-493

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] The novel imprinted carboxypeptidase A4 gene (CPA4) in the 7q32 imprinting domain2003

    • Author(s)
      Kayashima T, Yamasaki K, Niikawa N, Kishino T, et al.
    • Journal Title

      Hum Genet 112

      Pages: 220-226

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.2003

    • Author(s)
      Yamasaki K, Joh K, Ohta T, Masuzaki H, Ishimaru T, Mukai T, Niikawa N, Ogawa M, Wagstaff J, Kishino T
    • Journal Title

      Hum Mol Genet 12

      Pages: 837-847

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Atp10a, the mouse ortholog of the human imprinted ATP10C gene, escapes genomic imprinting2003

    • Author(s)
      Kayashima T, Yamasaki K, Niikawa N, Kishino T, et al.
    • Journal Title

      Genomics 81

      Pages: 644-647

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Fifty microdeletions among 112 cases of Sotos syndrome : Lo copy repeats possibly mediate the common deletion.2003

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

      Hum Mut 22

      Pages: 378-387

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A catalog of 106 single nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-β1 (TGF-β1) and its signaling pathway.2002

    • Author(s)
      Watanabe Y, Kinoshita A, Yamada T, Ohta T, Kishino T, Matsumoto N, Ishikawa M, Niikawa N, Yoshiura K
    • Journal Title

      J Hum Genet 47

      Pages: 478-483

    • NAID

      50000630975

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Confirmation of genetic homogeneity of non-syndromic low frequency sensorineural hearing loss by linkage analysis and DFNA6/14 mutations in a Japanese family.2002

    • Author(s)
      Komatsu K, Nakamura N, Ghadami M, Matsumoto N, Kishino K, Ohta T, Niikawa N, Yoshiura K
    • Journal Title

      J Hum Genet 47

      Pages: 395-399

    • NAID

      50000580507

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations : report of a Thai family.2002

    • Author(s)
      Kantaputra PN, Yamasaki K, Ishida T, Kishino T, Niikawa N
    • Journal Title

      Am J Med Genet 111(3)

      Pages: 301-306

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, an absence of TBX5 mutations : report of a Thai family.2002

    • Author(s)
      Kantaputra PN, Yamasaki K, Ishida T, Kishino T, Niikawa I'
    • Journal Title

      Am J Med Genet 111

      Pages: 301-306

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] The novel gene,TSGA14, adjacent to the imprinted gene MEST escapes genomic imprinting2002

    • Author(s)
      Yamada T, Kayashima T, Nilkawa N, Kishino T, et al.
    • Journal Title

      Gene 288

      Pages: 57-63

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Confirmation of genetic homogeneity of non-syndromic low frequency sensorineural hearing loss by linkage analysis an DFNA6/14 mutations in a Japanese family.2002

    • Author(s)
      Komatsu K Kishino K, Niikawa N, Yoshiura K, et al.
    • Journal Title

      J Hum Genet 47

      Pages: 395-399

    • NAID

      50000580507

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Haploinsufficiency of the NSD1 gene causes Sotos syndrome.2002

    • Author(s)
      Kyrotaki N, Naritomi K, Yoshiura K, Kishino T, Niikawa N. et al.
    • Journal Title

      Nat Genet 30

      Pages: 365-366

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] The novel gene, TSGA14, adjacent to the imprinted gene MEST escapes genomic imprinting.2002

    • Author(s)
      Yamada T, Kayashima T, Yamasaki K, Ohta T, Yoshiura K, Matsumoto N, Fujimoto S, Niikawa N, Kishino T
    • Journal Title

      Gene 288 (1-2)

      Pages: 57-63

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Journal Article] Haploinsufficiency of the NSD1 gene causes Sotos syndrome.2002

    • Author(s)
      Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita H-A, Kinoshita A, Mizuguchi T, Yoshiura K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N
    • Journal Title

      Nat Genet 30(April)

      Pages: 365-366

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Two Thai families with Norrie disease (ND) : Association of two novel missense mutations with severe ND phenotype, epileptic seizures, and manifesting female carrier.2001

    • Author(s)
      Yamada K, Limprasert P, Ratanasukon M, Tengtrisorn S, Yingchareonpukdee J, Vasiknanonte P, Kitaoka T, Ghadami M, Niikawa N, Kishino T
    • Journal Title

      Am J Med Genet 100

      Pages: 52-55

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Two Thai families with Norrie disease (ND) : Association of two novel missense mutations with severe ND phenotype, epileptic seizures, and manifesting female carrier.2001

    • Author(s)
      Yamada K, Niikawa N, Kishino T, et al.
    • Journal Title

      Am J Med Genet 100

      Pages: 52-55

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Imprinting in neurons

    • Author(s)
      Kishino T
    • Journal Title

      Cytogenet.Genome Res. in press

    • Data Source
      KAKENHI-PROJECT-17024046
  • [Journal Article] Expression of the Snurf-Snrpn IC transcript in the oocyte and putative role in the imprinting establishment of the mouse 7C imprinting domain.

    • Author(s)
      Mapendano CK, Kishino T, Miyazaki K, Kondo S, Yoshiura K, Hishikawa Y, Koji T, Niikawa N, Ohta T
    • Journal Title

      J Hum Genet (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12204010
  • [Presentation] プラダー・ウィリー症候群のマウス責任領域におけるに新規インプリンティング遺伝子の同定とその表現型解析2023

    • Author(s)
      木住野達也
    • Organizer
      日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-21K07848
  • [Presentation] プラダー・ウィリー症候群のマウス責任領域におけるに新規インプリンティング遺伝子の同定とその表現型解析2023

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Data Source
      KAKENHI-PROJECT-21K07848
  • [Presentation] Snrpnインイントロン1領域に存在するエンハンサー配列欠失マウスにおける遺伝子発現解析2022

    • Author(s)
      木住野達也
    • Organizer
      日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-21K07848
  • [Presentation] BACトランスジェニック(Tg)マウス作製過程に同定されたメイプルシロップ尿症モデルマウス2017

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      大阪国際会議場(大阪府・大阪市)
    • Year and Date
      2017-06-15
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] ドロップレットデジタルPCR(ddPCR)を用いたアンジェルマン症候群責任遺伝子Ube3a のアレル別発現の絶対定量解析2016

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      京王プラザホテル(東京都・新宿区)
    • Year and Date
      2016-06-03
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] Mkrn3ノックアウト(KO)及びトランスジェニック(Tg)マウスの解析2016

    • Author(s)
      斉藤亜佑美、木住野達也
    • Organizer
      日本分子生物学会
    • Place of Presentation
      パシフィコ横浜(神奈川県・横浜市)
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] Angelman症候群原因遺伝子UBE3Aトランスジェニックマウスの解析2015

    • Author(s)
      木住野達也,齋藤伸治
    • Organizer
      日本小児神経学会
    • Place of Presentation
      帝国ホテル大阪(大阪市)
    • Year and Date
      2015-05-29
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] Dnmt1 欠失マウスにおける染色体7Cインプリンティング領域の解析2014

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      アクトシティ浜松コングレスセンター(静岡県浜松市)
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] Dnmt1 欠失マウスにおける染色体7Cインプリンティング領域の解析2013

    • Author(s)
      木住野達也
    • Organizer
      日本分子生物学会
    • Place of Presentation
      神戸ポートピアホテル(兵庫県神戸市)
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] アンジェルマン症候群原因遺伝子UBE3AトランスジェニックマウスによるUbe3aノックアウトマウスレスキュー2011

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      横浜
    • Year and Date
      2011-05-26
    • Data Source
      KAKENHI-PROJECT-21591327
  • [Presentation] Angelman症候群原因遺伝子UBE3Aトランスジェニックマウスの解析2009

    • Author(s)
      木住野達, 也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      鳥取県米子市
    • Year and Date
      2009-05-28
    • Data Source
      KAKENHI-PROJECT-21591327
  • [Presentation] Angelman症候群原因遺伝子UBE3Aトランスジェニックマウスの解析2009

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      鳥取県米子市
    • Year and Date
      2009-05-28
    • Data Source
      KAKENHI-PROJECT-20022032
  • [Presentation] Mechanisms of imprinting of the Angelman/Prader-Willi region2007

    • Author(s)
      Kishino, T., et. al.
    • Organizer
      Angelman syndrome foundation 10th Biennial conference & scientific symposium
    • Place of Presentation
      St.Louis. U.S.A.
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590273
  • [Presentation] プラダーウィリ症候群/アンジェルマン症候群責任領域のインプリント確立機構の解析2007

    • Author(s)
      Kishino T
    • Organizer
      日本小児神経学会
    • Place of Presentation
      大阪
    • Year and Date
      2007-07-07
    • Data Source
      KAKENHI-PROJECT-18051012
  • [Presentation] プラダーウィリ症候群/アンジェルマン症候群責任領域のインプリント確立機構の解析2007

    • Author(s)
      木住野 達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      大阪
    • Year and Date
      2007-07-07
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590273
  • [Presentation] 初代培養神経細胞を用いたChIP法によるクロマチン病の病態解析2006

    • Author(s)
      木住野 達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      東京
    • Year and Date
      2006-06-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590273
  • [Presentation] Dynamic developmental changes of DNA methylation in the Snurf-Snrpn locus2006

    • Author(s)
      Kishino, T., et. al.
    • Organizer
      The American Society of Human Genetics 54th Annual meeting
    • Place of Presentation
      New Orleans, U.S.A.
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590273
  • [Presentation] アンジェルマン症候群モデルマウス(Ube3a KOマウス)のUBE3Aトランスジェニックレスキュー

    • Author(s)
      木住野達也
    • Organizer
      第50回高血圧関連疾患モデル学会学術総会
    • Place of Presentation
      和歌山県立医大(和歌山市)
    • Year and Date
      2014-12-05 – 2014-12-06
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461555
  • [Presentation] Dnmt1欠失マウスにおける染色体7C領域のインプリンティング解析

    • Author(s)
      木住野達也
    • Organizer
      日本小児神経学会
    • Place of Presentation
      アクトシティ浜松(浜松市)
    • Year and Date
      2014-05-28 – 2014-05-30
    • Data Source
      KAKENHI-PROJECT-25461555
  • 1.  NIKAWA Norio (00111170)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 36 results
  • 2.  HIGASHIMOTO Ken (30346887)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 3.  KOMORI Toshihisa (00252677)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 4.  MIYAZAKI Toshihiro (10174161)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 5.  YOSHIURA Koh-ichiro (00304931)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 15 results
  • 6.  TSUKAMOTO Kazuhiro (30253305)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 7.  MATSUMOTO Tadashi (70190535)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 7 results
  • 8.  NARITOMI Kenji (20101446)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 9.  FUKUSHIMA Yoshimitsu (70273084)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 4 results
  • 10.  宮崎 和美 (60398154)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  高雄 啓三 (80420397)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  辻田 高宏 (40304919)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  朴 盛浚 (60635853)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  奥崎 大介 (00346131)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  城谷 圭朗
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

URL: 

Are you sure that you want to link your ORCID iD to your KAKEN Researcher profile?
* This action can be performed only by the researcher himself/herself who is listed on the KAKEN Researcher’s page. Are you sure that this KAKEN Researcher’s page is your page?

この研究者とORCID iDの連携を行いますか?
※ この処理は、研究者本人だけが実行できます。

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi