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Matsuura Shinya  松浦 伸也

… Alternative Names

MATSUURA Shinya  松浦 伸也

松浦 信也  マツウラ シンヤ

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Researcher Number 90274133
Other IDs
  • ORCIDhttps://orcid.org/0000-0001-5294-081X
External Links
Affiliation (Current) 2025: 広島大学, 原爆放射線医科学研究所, 名誉教授
Affiliation (based on the past Project Information) *help 2002 – 2024: 広島大学, 原爆放射線医科学研究所, 教授
2009: 国立国際医療研究センター, 原爆放射線医科学研究所, 教授
1999 – 2001: Research Institute for Radiation Biology and Medicine, Hiroshima University, Associate Professor, 原爆放射能医学研究所, 助教授
1996 – 1998: Res.Inst.Rad.Biol.Med., Hiroshima Univ., Assistant Prof., 原爆放射能医学研究所, 助手
Review Section/Research Field
Principal Investigator
Biological Sciences / Human genetics / Basic Section 63020:Radiation influence-related / Risk sciences of radiation/Chemicals / Human genetics / Pathological medical chemistry / Medium-sized Section 48:Biomedical structure and function and related fields / Medical genome science / Biological Sciences / Medical genome science … More
Except Principal Investigator
… More 環境影響評価(含放射線生物学) / Biological Sciences / Nuclear fusion studies / Human genetics / Basic Section 49030:Experimental pathology-related / Basic Section 63020:Radiation influence-related / Medium-sized Section 63:Environmental analyses and evaluation and related fields / Basic Section 49010:Pathological biochemistry-related / General anatomy (including histology/embryology) / Risk sciences of radiation and chemicals / Cerebral neurosurgery / Risk sciences of radiation/Chemicals Less
Keywords
Principal Investigator
染色体 / 放射線感受性 / NBS1 / Nbs1 / 遺伝病 / BubR1 / BUB1B / 高発癌性遺伝病 / p55cdc / ATM … More / dsb / AT / NBS / テロメア / Ataxia-telangiectasia / 個人差 / 中心体 / ナイミーヘン症候群 / Wilms腫瘍 / キネトコア / 異数性モザイク / 医療放射線防護 / ゲノム編集 / ノックアウトマウス / 染色体不安定性 / 放射線高感受性 / フォーカス / 電離放射線 / Nijmegen syndrome / Xrs2 / 毛細血管拡張性運動失調症 / Model mouse / Xist / モデルマウス / 遺伝子標的法 / DNA修復 / 細胞周期 / チェックポイント / 高発がん性遺伝病 / Nijmegen症候群 / 紡錘体形成チェックポイント / PCS症候群 / 染色体不安定症候群 / モザイク / 細胞競合 / 異数性 / 細胞周期チェックポイント / モデル動物 / モデル生物 / 細胞老化 / chromosome instability / Wilms tumor / PCS syndrome / Mitotic checkpoint / Mosaic variegated aneuploidy / MAD2 / Dandy-Walker奇形 / 分裂期 / PCS / BubRl / M期チェックポイント / Nuclear foci / Histone H2AX / Homologous recombination / DT40 cells / Radiation scnsitivity / Knockout mouse / Nijmegen breakage syndrome / DN二重鎖切断 / 核内フォーカス / ヒストンH2AX / 相同組換え修復 / DT40細胞 / focus / telomere / Radiation / 免疫不全 / 高発癌性 / Ku70 / Atm / Embryonic lethal / Gene targeting / Rodiation sensitivity / Cancer prone disease / Nbs 1 / 胎生致死 / Positional cloning / Radiosensitivity / Cancer prone disorder / 減数分裂 / 8q21 / NBSI / Nijmegen breakage症候群 / ポジショナルクローニング / Counting mechanism / X inactivation / microinjection / transgenic mouse / カウンティング機構 / X不活化 / シリア / エクソーム解析 / 人工ヌクレアーゼ / 次世代シーケンサー / 遺伝性小頭症 / GWAS / 微小核形成法 / クロマチン / ヒストン / ATR / エピジェネティックス / 紡錘体軸 / BUBR1 / 変異 / 小頭症 / 分子遺伝学 / 紡錘体 / Plk1 / RecQヘリケース遺伝子 / Bloom症候群 / Rothmund-Thomson症候群 / ウエルナー症候群 / VTM / 稀少性染色体不安定症候群 / 高発ガン性遺伝病 / 相補性試験 / 不死化細胞 / hTERT / バリアント / M期紡錘体チェックポイント / 染色分体早期解離症候群 / YACコンティグ / 創始者ハプロタイプ / スフェロプラスト融合法 / 微小核移入法 / 連鎖解析候群 … More
Except Principal Investigator
放射線感受性 / NBS1 / ATM / WRN / NBS / 相同組換え / 中心体 / 放射線 / SMC1 / DNA修復 / ゲノム編集 / がん / BRCA1 / dsb / AT / 電離放射線 / RBE / p53 / 二重鎖切断 / DNA二重鎖切断 / ポジショナルクローニング / ゲノム編集技術 / 繊毛病 / MRE11 / Homologous recombination / シグナル伝達 / 細胞・組織 / 遺伝子 / テロメア / 染色体異常 / S期チェックポイント / ナイミーヘン症候群 / ionizing radiation / DNA repair / Radiation sensitivity / Nijmegen breakage syndrome / gene mutation / 遺伝子突然変異 / 細胞工学 / 遺伝子マッピング / 染色体 / centrosome / 染色体不安定性 / ナイミーヘン染色体不安定症候群 / 染色体異数性レスキュー / 染色体異数性可塑性 / 一次繊毛 / 染色体数レスキュー / 繊毛抑制遺伝子 / Patau症候群 / 13番染色体 / トリソミーレスキュー / iPS細胞 / 家族性乳がん卵巣がん症候群 / 遺伝的個人差 / FIB-SEM技術 / 染色体微細構造 / 集束イオンビーム-走査電子顕微鏡 / FIBーSEM / BubR1 / UFB構造 / 遺伝子改変動物 / DNA損傷修復 / 疾患モデル / DNA修復遺伝子 / DNA損傷修復欠損症 / DNA修復遺伝子欠損症 / DNA修復欠損症 / chromosome / mouse A9 cell line / suppressor / re-duplication / M期 / S期 / FISH / 細胞 / 遺伝学 / 再複製抑制 / Ataxia-telangiectasia / Genome stability / チェックポイント / 相同組換え修復 / ゲノム不安定性 / 毛細血管拡張性運動失調症 / ゲノム安定性 / Gene knockout / 遺伝疾患 / 相同組み換え / 遺伝子ノックアウト / Chromosomal instability / DNA double strand break / Homologous Recombination / Nijmegen Breakage Syndrome / フォーカス / Bloom syndrome / Gene homing / Shaffron / Transposition / Transposon / Mobile genetic elements / DNA end-Joining / Illegitimate recombination / エンドヌクレアーゼ / DNAヘリカーゼ / DNA切断再結合 / RecQヘリカーゼ / DNAの切断と再結合 / シャフロン / ブルーム症候群 / トランスポゼース / 遺伝的組換え / DNAエンドジョイニング / DNA二本鎖切断 / トランスポゾン / 遺伝病 / 遺伝子ホーミング / 遺伝子スイッチ / 転移 / トラシスポゾン / 動く遺伝子 / エンドジョイニング / 非相同組換え / linkage analysis / YAC / ア-Tバリアント / Xrs2 / NBSI / p21 / MDM2 / AT-Fresno / 家系分析 / HPRT mutation / hybrid cells / tritium / 6-thioguanin resistance / a human X-chromosome / ホルミ-シス効果 / 遺伝的影響 / hprt遺伝子 / 染色体移入 / Cu炭素粒子線 / HPRT / 6-チオグアニン / ハイブリッド細胞 / HPRT変異 / ハイブリット細胞 / トリチウム / 6-TG耐性 / 高感度突然変異 / ヒトX染色体 / double strand break / genetic instability / teratogenesis protein / hyperthermia / V (D) J recombination / murine scid / DNA dependent protein kinase / Ku80 / OK1035 / 温熱感受性 / DNA2重鎖切断 / scid / DNA-PK / 遺伝的不安定性 / 催奇形成 / ハイパーサーミア / V(D)J組換え / scidマウス / DNA依存性蛋白キナーゼ / YAC contig / Homozygosity mapping / Founder effect / Chromosome transfer uia microcell / p53 tumor suppressor protein / Positional cloning / 劣性遺伝病 / 8番染色体 / 放射線高感受性 / ATバリアント / アタキシアテランジェクタシア / ヒト染色体微小核移入 / YACコンティグ / ホモ接合体マッピング / 始祖効果 / 染色体微小核移入 / p53がん制御蛋白 / ナイミ-ヘン染色体不安定症候群 / p-gal positive selection / plasmid vector / Radiation effect / lacZ gene / Ingeno mouse / transgenic mouse / P-gal選択法 / プラスミドベクター / 放射線影響 / lacZ / インジェノマウス / トランスジェニックマウス / 小頭症 / DNA複製 / DNA修復制御 / ナイメーヘン症候群 / RAD18ドメイン / ドメイン解析 / 非相同末端再結合 / 損傷乗越えDNA合成 / クロマチン・リモデリング / キネシン / PLK1 / 紡錘体 / 細胞分裂 / 紡錘体形成 / Kif2a / PLKl / 抑制遺伝子 / 中心体過剰複製 / 微小核移入法 / タイムラプス観察 / グリオーマ / survivin / radiosensitivity / p16 / mitotic cell death / chromosome instability / malignant glioma / p27 / 腫瘍幹細胞 / Survivin / 悪性グリオーマ / トポイソメレース阻害剤 / 多環芳香族炭化水素付加体 / 感興変異原 / DNA鎖架橋 / 紫外線 / H2AX リン酸化 / DNA 修復 / 環境変異原 / クロマチンリモデリング / H2Bユビキチン化 / 損傷乗り越え合成 / 環境変異原,NBS1 / H2AXリン酸化 / 複製阻害 / 機能的相補性 / A-Tバリアント / Xrs2遺伝子 / NBSI遺伝子 Less
  • Research Projects

    (45 results)
  • Research Products

    (464 results)
  • Co-Researchers

    (47 People)
  •  Genetic basis of individual differences of radiosensitivity for medical radiation protectionPrincipal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2022 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 63020:Radiation influence-related
    • Research Institution
      Hiroshima University
  •  Pathological mechanism of ciliopathy in Patau syndrome using aneuploidy rescue technology

    • Principal Investigator
      Miyamoto Tatsuo
    • Project Period (FY)
      2021 – 2023
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 49030:Experimental pathology-related
    • Research Institution
      Yamaguchi University
  •  Morphological characteristics of the genome stress-induced chromosomal tether structure

    • Principal Investigator
      Miyamoto Tatsuo
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Challenging Research (Exploratory)
    • Review Section
      Medium-sized Section 63:Environmental analyses and evaluation and related fields
    • Research Institution
      Yamaguchi University
      Hiroshima University
  •  Quantitative assessment of genetic factors underlying individual differences of radiosensitivity

    • Principal Investigator
      藤田 和将
    • Project Period (FY)
      2020
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 63020:Radiation influence-related
    • Research Institution
      Hiroshima University
  •  Cell competition analysis using model cells of mosaic aneuploidyPrincipal Investigator

    • Principal Investigator
      Matsuura Shinya
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Challenging Research (Exploratory)
    • Review Section
      Medium-sized Section 48:Biomedical structure and function and related fields
    • Research Institution
      Hiroshima University
  •  Identification of radiation-sensitive genes for achieving precision medicine for medical radiation protectionPrincipal Investigator

    • Principal Investigator
      Matsuura Shinya
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 63020:Radiation influence-related
    • Research Institution
      Hiroshima University
  •  Neuro-pathological mechanism caused by impaired DNA damage response signaling

    • Principal Investigator
      Miyamoto Tatsuo
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 49010:Pathological biochemistry-related
    • Research Institution
      Hiroshima University
  •  Molecular basis underlying ciliopathy in 13 trisomy syndrome

    • Principal Investigator
      Miyamoto Tatsuo
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      General anatomy (including histology/embryology)
    • Research Institution
      Hiroshima University
  •  Telomere function in premature aging phenotypes of BubR1 deficiencyPrincipal Investigator

    • Principal Investigator
      MATSUURA SHINYA
    • Project Period (FY)
      2015 – 2016
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pathological medical chemistry
    • Research Institution
      Hiroshima University
  •  Rescue of 21 trisomy in Down syndrome cells using spindle assembly checkpointPrincipal Investigator

    • Principal Investigator
      Matsuura Shinya
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Medical genome science
    • Research Institution
      Hiroshima University
  •  Role of NBS1 C-terminal domain in genomic stability

    • Principal Investigator
      Komatsu Kenshi
    • Project Period (FY)
      2014 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Risk sciences of radiation and chemicals
    • Research Institution
      Kyoto University
  •  キネシン分子が制御するシリア形成と中心小体接着の分子機構Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  Identification of genetic determinant for individual radiosensitivityPrincipal Investigator

    • Principal Investigator
      MATSUURA SHINYA
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Risk sciences of radiation/Chemicals
    • Research Institution
      Hiroshima University
  •  Molecular analysis of primary microcephaly using genome editing techniquePrincipal Investigator

    • Principal Investigator
      MATSUURA SHINYA
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Medical genome science
    • Research Institution
      Hiroshima University
  •  M期紡錘体チェックポイント分子BUBR1による紡錘体軸形成機構Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2010 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  Epigenetic dysregulation in disorder with defective ATR signalingPrincipal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      2010 – 2011
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Risk sciences of radiation/Chemicals
    • Research Institution
      Hiroshima University
  •  中心体分離に関わる微小管系モーター分子の同定とその制御機構Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  PLK1による分裂期における両極性紡垂体形成機構のメカニズムの解明

    • Principal Investigator
      泉 秀樹
    • Project Period (FY)
      2008 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Research Institute, International Medical Center of Japan
      Hiroshima University
  •  Toward the identification of the genes for hereditary microcephalyPrincipal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Hiroshima University
  •  Effect of centrosome amplification/chromosome instability on the radiosensitivity in human glioma cells

    • Principal Investigator
      KURISU Kaoru
    • Project Period (FY)
      2007 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Cerebral neurosurgery
    • Research Institution
      Hiroshima University
  •  Molecular cloning of the gene on chromosome 8, which suppresses centrosome re-duplication

    • Principal Investigator
      IZUMI Hideki
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Hiroshima University
  •  BUB1Bによる紡錘体チェックポイントと中心体複製の分子連携機構Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  Induction of DNA double strand break by environmental genotoxic and carcinogenic agents

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      2006 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (S)
    • Research Field
      Risk sciences of radiation/Chemicals
    • Research Institution
      Kyoto University
  •  Identification and characterization of centrosome re-duplication suppressor gene(s)

    • Principal Investigator
      IZUMI Hideki
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Hiroshima University
  •  遺伝性Wilms腫瘍症候群(PCS)のM期紡錘体チェックポイント異常の分子機構Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  稀少性染色体不安定症候群バリアントの病因解明と国内調査Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2004
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Human genetics
    • Research Institution
      Hiroshima University
  •  姉妹染色体早期分離と異数性モザイクを特徴とする高発癌性遺伝病の原因遺伝子の解明Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2003
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  Nijmegen症候群バリアントの不死化細胞株の樹立と病因の解明Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      2003
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pathological medical chemistry
    • Research Institution
      Hiroshima University
  •  Origin of radiation-induced genomic instability

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      2002 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      Kyoto University
  •  Molecular cloning of the gene for cancer-prone syndrome characterized by abnormal mitotic spindle checkpoint.Principal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      2002 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  DNA double strand break repair by NBS1 complex.Principal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Hiroshima University
  •  Cancersusceptibility disease Nijmegen Breakage Syndrome and the function of underlying gene.

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      2000 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      KYOTO UNIVERSITY
      Hiroshima University
  •  Molecular mechanism for chromosome stability using Nbs1 knockout micePrincipal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      2000 – 2001
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Role of NBS1 in Repair of DNA damage Induced by Ionizing Radiation

    • Principal Investigator
      TAUCHI Hiroshi
    • Project Period (FY)
      2000 – 2001
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      IBARAKI UNIVERSITY
      Hiroshima University
  •  Generation of knockout mice for Nijmegen breakage syndrome gene, NBS1.Principal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      1999
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Hiroshima University
  •  染色体8q21上の放射線誘発DNA二重鎖切断からの修復遺伝子のクローニング

    • Principal Investigator
      小松 賢志
    • Project Period (FY)
      1998
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      Hiroshima University
  •  Study on underlying gene of Nijmegen Breakage Syndrome

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      1998 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Novel developments on genetic recombination : DNA double-strand break and DNA end-joining

    • Principal Investigator
      OHTSUBO Eichi, 池田 日出男
    • Project Period (FY)
      1998 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      The University of Tokyo
      Kitasato Institute
  •  Complementation assisted positional cloning of the gene for AT variant.Principal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      1998 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Hiroshima University
  •  高発癌遺伝病ナイミ-ヘン染色体不安定症候群の原因遺伝子の単離Principal Investigator

    • Principal Investigator
      松浦 伸也
    • Project Period (FY)
      1997
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Hiroshima University
  •  Development of (a human X-chromosome * hamster) hybrid cell assay system, which is sensitive to tritium exposure.

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Nuclear fusion studies
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Molecular study on Nijmegen breakage sybdrome

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for international Scientific Research
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Multi-functions of DNA-dependent protein kinase (DNA-PK) and the association of radiation sensitivity

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      環境影響評価(含放射線生物学)
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Molecular mechanism of initiation of X inactivation using Xist YAC transgenic mousePrincipal Investigator

    • Principal Investigator
      MATSUURA Shinya
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      HIROSHIMA UNIVERSITY
  •  Research and development of transgenic mouse for biological effect assesment of tritium

    • Principal Investigator
      KOMATSU Kenshi
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Nuclear fusion studies
    • Research Institution
      HIROSHIMA UNIVERSITY

All 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation Book

  • [Book] 実験医学別冊・完全版 ゲノム編集実験スタンダード (山本卓、佐久間哲史 編)2019

    • Author(s)
      宮本達雄、藤田和将、阿久津シルビア夏子、松浦伸也
    • Total Pages
      386
    • Publisher
      羊土社
    • ISBN
      9784758122443
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Book] Genome and Disease, Nijmegen breakage syndrome and functions of the responsible protein, NBS12006

    • Author(s)
      A.Antoccia, J, Kobayashi, H.Tauchi, S.Matsuura, K.Komatsu
    • Total Pages
      246
    • Publisher
      Kerger (Basel)
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis2023

    • Author(s)
      Kume Kodai Kurashige Takashi Muguruma Keiko Morino Hiroyuki、...Kawakami Hideshi
    • Journal Title

      The American Journal of Human Genetics

      Volume: 110 Issue: 7 Pages: 1086-1097

    • DOI

      10.1016/j.ajhg.2023.05.014

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21H04818, KAKENHI-PROJECT-21H02718, KAKENHI-PROJECT-21H03812, KAKENHI-PROJECT-23K24996
  • [Journal Article] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2022

    • Author(s)
      Akutsu Silvia Natsuko、Miyamoto Tatsuo、Oba Daiju、Tomioka Keita、Ochiai Hiroshi、Ohashi Hirofumi、Matsuura Shinya
    • Journal Title

      PLOS ONE

      Volume: 17 Issue: 3 Pages: 1-20

    • DOI

      10.1371/journal.pone.0264965

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K06612, KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-19K16520, KAKENHI-PUBLICLY-21H05753, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-21H02718, KAKENHI-PROJECT-20K21845, KAKENHI-PLANNED-18H05531
  • [Journal Article] Imaging of the Ciliary Cholesterol Underlying the Sonic Hedgehog Signal Transduction2022

    • Author(s)
      Miyamoto T, Hosoba K, Akutsu SN, Matsuura S
    • Journal Title

      Methods Mol Biol

      Volume: 2374 Pages: 49-57

    • DOI

      10.1007/978-1-0716-1701-4_5

    • ISBN
      9781071617007, 9781071617014
    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-19K16520, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-21H02718, KAKENHI-PROJECT-20K21845
  • [Journal Article] NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations2021

    • Author(s)
      Tomioka K, Miyamoto T, Akutsu SN, Yanagihara H, Fujita K, Royba E, Tauchi H, Yamamoto T, Koh I, Hirata E, Kudo Y, Kobayashi M, Okada S, Matsuura S
    • Journal Title

      Scientific Reports

      Volume: 11 Issue: 1 Pages: 1-13

    • DOI

      10.1038/s41598-021-98673-7

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-19K16520, KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-21H02718, KAKENHI-PROJECT-20K21845
  • [Journal Article] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の定量的評価2020

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内広、山本卓、工藤美樹、小林正夫、宮本達雄、松浦伸也
    • Journal Title

      広島医学

      Volume: 73(4) Pages: 224-227

    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Journal Article] ゲノム編集技術を用いた培養細胞における疾患モデリング2020

    • Author(s)
      宮本達雄、藤田和将、松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 273(9) Pages: 20977-20982

    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Journal Article] A novel CDK-independent function of p27Kip1 in preciliary vesicle trafficking during ciliogenesis2020

    • Author(s)
      Yukimoto Hiroki、Miyamoto Tatsuo、Kiyono Tohru、Wang Shujie、Matsuura Shinya、Mizoguchi Akira、Katayama Naoyuki、Inagaki Masaki、Kasahara Kousuke
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 527 Issue: 3 Pages: 716-722

    • DOI

      10.1016/j.bbrc.2020.05.048

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-18H02624, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-20H03448, KAKENHI-PROJECT-19K09990
  • [Journal Article] ゲノム編集技術を用いた培養細胞における疾患モデリング2020

    • Author(s)
      宮本達雄、藤田和将、松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 273(9) Pages: 20977-20982

    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Journal Article] Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders2020

    • Author(s)
      Akutsu Silvia Natsuko、Fujita Kazumasa、Tomioka Keita、Miyamoto Tatsuo、Matsuura Shinya
    • Journal Title

      Cells

      Volume: 9 Issue: 1 Pages: 239-239

    • DOI

      10.3390/cells9010239

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PUBLICLY-18H04979, KAKENHI-PROJECT-18H02624, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-19K16520, KAKENHI-ORGANIZER-15H05935
  • [Journal Article] ゲノム編集技術を用いた培養細胞における疾患モデリング2020

    • Author(s)
      宮本達雄, 藤田和将, 松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 273 Pages: 20977-20982

    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Journal Article] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の定量的評価2020

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内広、山本卓、工藤美樹、小林正夫、宮本達雄、松浦伸也
    • Journal Title

      広島医学

      Volume: 73(4) Pages: 224-227

    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Journal Article] Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation2020

    • Author(s)
      Fujita Harumi、Sasaki Takashi、Miyamoto Tatsuo、Akutsu Silvia Natsuko、Sato Showbu、Mori Takehiko、Nakabayashi Kazuhiko、Hata Kenichiro、Suzuki Hisato、Kosaki Kenjiro、Matsuura Shinya、Matsubara Yoichi、Amagai Masayuki、Kubo Akiharu
    • Journal Title

      Aging Cell

      Volume: 19 Issue: 11 Pages: 1-13

    • DOI

      10.1111/acel.13251

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-20K21845, KAKENHI-PROJECT-18H02624, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-18K16040
  • [Journal Article] Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome.2020

    • Author(s)
      Miyamoto T, Hosoba K, Itabashi T, Iwane AH, Akutsu AN, Ochiai H, Saito Y, Yamamoto T, Matsuura S
    • Journal Title

      EMBO Journal

      Volume: - Issue: 12

    • DOI

      10.15252/embj.2019103499

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K06612, KAKENHI-PROJECT-19K06739, KAKENHI-PROJECT-19K22515, KAKENHI-PUBLICLY-18H04979, KAKENHI-PROJECT-18H02624, KAKENHI-PROJECT-19H04270, KAKENHI-PROJECT-17K07372, KAKENHI-PROJECT-19K16521, KAKENHI-PROJECT-17H01409, KAKENHI-PLANNED-18H05531, KAKENHI-ORGANIZER-15H05935, KAKENHI-WRAPUP-20H05615
  • [Journal Article] Familial rhabdomyosarcoma due to germline bi-allelic variants of BUB1B2019

    • Author(s)
      Yoshida K, Yamaoka S, Yoshida M, Nakabayashi K, Shirai R, Osumi T, Kiyotani C, Akutsu SN, Miyamoto T, Hata K, Kiyokawa N, Yoza Y, Matsumoto K, Matsuura S, Kato M
    • Journal Title

      Pediatric Blood & Cancer

      Volume: 66 Issue: S5

    • DOI

      10.1002/pbc.28049

    • Data Source
      KAKENHI-PROJECT-19K22515, KAKENHI-PROJECT-19H04270
  • [Journal Article] ゲノム編集 実験スタンダード「培養細胞でのゲノム編集」2019

    • Author(s)
      宮本達雄、藤田和将、阿久津シルビア夏子、松浦伸也
    • Journal Title

      実験医学別冊

      Volume: - Pages: 173-183

    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Journal Article] ゲノム編集 実験スタンダード「培養細胞でのゲノム編集」2019

    • Author(s)
      宮本達雄、藤田和将、阿久津シルビア夏子、松浦伸也
    • Journal Title

      実験医学別冊

      Volume: - Pages: 173-183

    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Journal Article] Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology.2018

    • Author(s)
      Miyamoto T, Akutsu SN, Tauchi H, Kudo Y, Tashiro S, Yamamoto T, Matsuura S.
    • Journal Title

      J Radiat Res.

      Volume: Epub ahead of print Issue: suppl_2 Pages: 1-8

    • DOI

      10.1093/jrr/rry007

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H02821, KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-15K09122
  • [Journal Article] ゲノム編集を用いた遺伝性疾患の治療2018

    • Author(s)
      宮本達雄、阿久津シルビア夏子、松浦伸也
    • Journal Title

      生物の科学 遺伝

      Volume: 6 Pages: 599-605

    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Journal Article] Albatross/FBF1 contributes to both centriole duplication and centrosome separation.2018

    • Author(s)
      Inoko A, Yano T, Miyamoto T, Matsuura S, Kiyono T, Goshima N, Inagaki M, Hayashi Y.
    • Journal Title

      Genes Cells.

      Volume: 23 Issue: 12 Pages: 1023-1042

    • DOI

      10.1111/gtc.12648

    • Peer Reviewed
    • Data Source
      KAKENHI-PUBLICLY-18H04979, KAKENHI-PROJECT-18H02624, KAKENHI-ORGANIZER-15H05935
  • [Journal Article] Wilms tumor accompanied by premature chromatid separation2017

    • Author(s)
      Shimada K, Yanagisawa R, Kubota N, Hidaka E, Sakashita K, Ishii E, Matsuura S, Ogiso Y
    • Journal Title

      Pediatr Blood Cancer

      Volume: 64 Issue: 3

    • DOI

      10.1002/pbc.26255

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K15082, KAKENHI-PROJECT-16K10021, KAKENHI-PROJECT-15K15017, KAKENHI-PROJECT-15H04321
  • [Journal Article] PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation2017

    • Author(s)
      Miyamoto Tatsuo、Akutsu Silvia Natsuko、Fukumitsu Akihiro、Morino Hiroyuki、Masatsuna Yoshinori、Hosoba Kosuke、Kawakami Hideshi、Yamamoto Takashi、Shimizu Kenji、Ohashi Hirofumi、Matsuura Shinya
    • Journal Title

      Human Molecular Genetics

      Volume: 26 Issue: 22 Pages: 4429-4440

    • DOI

      10.1093/hmg/ddx330

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26242085, KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-15K15017, KAKENHI-PROJECT-15K15083
  • [Journal Article] Updated summary of genome editing technology in human cultured cells linked to human genetics studies2017

    • Author(s)
      Miyamoto Tatsuo、Akutsu Silvia Natsuko、Matsuura Shinya
    • Journal Title

      Journal of Human Genetics

      Volume: 63 Issue: 2 Pages: 133-143

    • DOI

      10.1038/s10038-017-0349-z

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-15K15017
  • [Journal Article] Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.2017

    • Author(s)
      Royba E, Miyamoto T, Natsuko Akutsu S, Hosoba K, Tauchi H, Kudo Y, Tashiro S, Yamamoto T, Matsuura S.
    • Journal Title

      Sci Rep.

      Volume: 7 Issue: 1 Pages: 5996-5996

    • DOI

      10.1038/s41598-017-06393-8

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H02821, KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-15K15017
  • [Journal Article] Induction of somatic mutations by low-dose X-rays: the challenge in recognizing radiation-induced events2017

    • Author(s)
      Nagashima Haruki、Shiraishi Kumiko、Ohkawa Saori、Sakamoto Yuki、Komatsu Kenshi、Matsuura Shinya、Tachibana Akira、Tauchi Hiroshi
    • Journal Title

      J Radiat Res

      Volume: 58 Issue: suppl_2 Pages: 1-7

    • DOI

      10.1093/jrr/rrx053

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26241013, KAKENHI-PROJECT-15H04321
  • [Journal Article] Analysis of individual differences in radiosensitivity using genome editing.2016

    • Author(s)
      Matsuura S, Royba E , Akutsu SN, Ynanagihara H, Ochiai H, Kudo Y, Tashiro H, Miyamoto T
    • Journal Title

      Ann ICRP

      Volume: in press

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Journal Article] Analysis of individual differences in radio sensitivity using genome editing2016

    • Author(s)
      Matsuura S, Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro H, Miyamoto T
    • Journal Title

      Annals of the ICRP

      Volume: Published online before print Issue: 1_suppl Pages: 1-7

    • DOI

      10.1177/0146645316633941

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K15082, KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-26701006, KAKENHI-PROJECT-15K15017
  • [Journal Article] Ciliopathy in PCS(MVA) syndrome2015

    • Author(s)
      Miyamoto T, Matsuura S
    • Journal Title

      Oncotarget

      Volume: 6(28) Issue: 28 Pages: 24582-24583

    • DOI

      10.18632/oncotarget.5244

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K15017, KAKENHI-PUBLICLY-15H01216, KAKENHI-PROJECT-15H04321, KAKENHI-PROJECT-26701006
  • [Journal Article] 新規一塩基置換導入法による高発癌性遺伝病の原因変異の同定2015

    • Author(s)
      落合 博、松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 252 Pages: 153-158

    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Journal Article] YAP is essential for tissue tension to ensure vertebrate 3D body shape2015

    • Author(s)
      Sean Porazinski, Huijia Wang, Yoichi Asaoka, Martin Behrndt, Tatsuo Miyamoto, Hitoshi Morita, Shoji Hata et al.
    • Journal Title

      Nature

      Volume: 印刷中 Issue: 7551 Pages: 217-221

    • DOI

      10.1038/nature14215

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-13J08895, KAKENHI-PROJECT-24310043, KAKENHI-PROJECT-24651222, KAKENHI-PUBLICLY-25113521, KAKENHI-PROJECT-25460358, KAKENHI-PLANNED-26114005, KAKENHI-PROJECT-15K15017, KAKENHI-PUBLICLY-15H01216, KAKENHI-PROJECT-26251024, KAKENHI-PROJECT-26293012, KAKENHI-PROJECT-26701006
  • [Journal Article] 新規一塩基置換導入法による高発癌性遺伝病の原因変異の同定2015

    • Author(s)
      落合 博、松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 252 Pages: 153-158

    • Data Source
      KAKENHI-PROJECT-24651222
  • [Journal Article] The microtubule depolymerizing activity of a mitotic kinesin protein KIF2A drives primary cilia disassembly coupled with cell proliferation2015

    • Author(s)
      Miyamoto T, Hosoba K, Ochiai H, Royba E, Izumi H, Sakuma T, Yamamoto T, Matsuura S
    • Journal Title

      Cell Reports

      Volume: 10 Issue: 5 Pages: 664-673

    • DOI

      10.1016/j.celrep.2015.01.003

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-24310043, KAKENHI-PROJECT-24651222, KAKENHI-PUBLICLY-25113521, KAKENHI-PROJECT-25830138, KAKENHI-PROJECT-25890014, KAKENHI-PROJECT-26701006, KAKENHI-PROJECT-15K09674
  • [Journal Article] 新規一塩基置換導入法による高発癌性遺伝病の原因変異の同定2015

    • Author(s)
      落合 博、松浦伸也
    • Journal Title

      医学のあゆみ

      Volume: 252 Pages: 153-158

    • Data Source
      KAKENHI-PROJECT-24310043
  • [Journal Article] Ciliopathy in PCS (MVA) syndrome2015

    • Author(s)
      Miyamoto T, Matsuura S
    • Journal Title

      Oncotarget

      Volume: 6 Pages: 24582-24583

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Journal Article] PCS(MVA)症候群2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 411-414

    • Data Source
      KAKENHI-PROJECT-24651222
  • [Journal Article] Nijgemen(ナイミーヘン)染色体不安定症候群2014

    • Author(s)
      松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 617-620

    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Journal Article] DNA修復障害概論2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 28 Pages: 642-645

    • Data Source
      KAKENHI-PROJECT-24310043
  • [Journal Article] Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxia.2014

    • Author(s)
      Miyamoto R, Morino H, Yoshizawa A, Miyazaki Y, Maruyama H, Murakami N, Fukada K, Izumi Y, Matsuura S, Kaji R, Kawakami H.
    • Journal Title

      J Neurol Sci.

      Volume: 337 Issue: 1-2 Pages: 219-223

    • DOI

      10.1016/j.jns.2013.11.032

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-23111008, KAKENHI-PROJECT-23591246, KAKENHI-PROJECT-24310043, KAKENHI-PROJECT-24390223, KAKENHI-PROJECT-24651222, KAKENHI-PUBLICLY-25113521
  • [Journal Article] Nijgemen(ナイミーヘン)染色体不安定症候群2014

    • Author(s)
      松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 617-620

    • Data Source
      KAKENHI-PROJECT-24651222
  • [Journal Article] PCS(MVA)症候群2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 411-414

    • Data Source
      KAKENHI-PROJECT-24310043
  • [Journal Article] TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.2014

    • Author(s)
      Ochiai H, Miyamoto T, Kanai A, Hosoba K, Sakuma T, Kudo Y, Asami K, Ogawa A, Watanabe A, Kajii T, Yamamoto T, Matsuura S.
    • Journal Title

      Proc Natl Acad Sci U S A.

      Volume: 111(4) Issue: 4 Pages: 1461-6

    • DOI

      10.1073/pnas.1317008111

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23710068, KAKENHI-PROJECT-24310043, KAKENHI-PROJECT-24651222, KAKENHI-PROJECT-24657156, KAKENHI-PUBLICLY-25113521, KAKENHI-PROJECT-25830138, KAKENHI-PROJECT-25890014
  • [Journal Article] DNA修復障害概論2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 28 Pages: 642-645

    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Journal Article] Nijgemen(ナイミーヘン)染色体不安定症候群2014

    • Author(s)
      松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 617-620

    • Data Source
      KAKENHI-PROJECT-24310043
  • [Journal Article] PCS(MVA)症候群2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 29 Pages: 411-414

    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Journal Article] DNA修復障害概論2014

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      別冊日本臨床 新領域別症候群シリーズ

      Volume: 28 Pages: 642-645

    • Data Source
      KAKENHI-PROJECT-24651222
  • [Journal Article] Repeating pattern of non-RVD variations in DNA-binding modules enhances TALEN activity.2013

    • Author(s)
      Sakuma T, Ochiai H, Kaneko T, Mashimo T, Tokumasu D, Sakane Y, Suzuki K, Miyamoto T, Sakamoto N, Matsuura S, Yamamoto T
    • Journal Title

      Sci Rep.

      Volume: 3 Issue: 1 Pages: 3379-3379

    • DOI

      10.1038/srep03379

    • Peer Reviewed
    • Data Source
      KAKENHI-ORGANIZER-22124001, KAKENHI-PROJECT-23710068, KAKENHI-PROJECT-24310043, KAKENHI-PROJECT-24651222, KAKENHI-PROJECT-24657156, KAKENHI-PROJECT-24700427, KAKENHI-PUBLICLY-25113521, KAKENHI-PUBLICLY-25124708, KAKENHI-PROJECT-25890014
  • [Journal Article] NBS1recruitsRAD18viaaRAD6-likedomainandregulatesPolη-dependenttranslesionDNAsynthesis2011

    • Author(s)
      Yanagihara H, Kobayashi J, Tateishi S, KatoA, Matsuura S, Tauchi H, Yamada K, Takezawa J, Sugasawa K, Masutani C, Hanaoka F, WeemaesC M, MoriT, Zou L, Komatsu K.
    • Journal Title

      Mol Cell

      Volume: 43 Pages: 788-789

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Journal Article] Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.2011

    • Author(s)
      Matsumoto Y, Miyamoto T, Sakamoto H, Izumi H, Nakazawa Y, Ogi T, Tahara H, Oku S, Hiramoto A, Shiiki T, Fujisawa Y, Ohashi H, Sakemi Y, Matsuura S.
    • Journal Title

      DNA Repair (Amst) 10

      Pages: 314-321

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Insufficie ncyofBUBR1, amito ticspindle checkpointre gulator, causesim pairedciliogene sisinvertebrates2011

    • Author(s)
      Miyamoto T, Porazinski S, Wang H, Boravina A, Ciruna B, Shimizu A, KajiiT, Kikuchi A, Furutani-Seiki M, Matsuura S
    • Journal Title

      Hum Mol Genet

      Volume: 20 Pages: 2058-2070

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Journal Article] Twounre atedpatie ntswithMRE11Amutationsand Nijmegenbreakage syndrome-likese vere micro cephaly2011

    • Author(s)
      Matsumoto Y, Miyamoto T, Sakamoto H, Izumi H, Nakazawa Y, OgiT, Tahara H, OkuS, Hiramoto A, ShiikiT, Fujisawa Y, OhashiH, Sakemi Y, Matsuura S.
    • Journal Title

      DNA Re pair(Amst)

      Volume: 10 Pages: 314-321

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Journal Article] Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.2011

    • Author(s)
      Matsumoto Y, Miyamoto T, Sakamoto H, Izumi H, Nakazawa Y, Ogi T, Tahara H, Oku S, Hiramoto A, Shiiki T, Fujisawa Y, Ohashi H, Sakemi Y, Matsuura S
    • Journal Title

      DNA Repair (Aast) 10

      Pages: 314-321

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Insufficiency of BUBR1, amitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.2011

    • Author(s)
      Miyamoto T, Porazinski S, Wang H, Boravina A, Ciruna B, Shimizu A, Kajii T, Kikuchi A, Furutani-Seiki M, Matsuura S
    • Journal Title

      Hum Mol Genet 20

      Pages: 2058-2070

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] WRN partici patesintransl sionsyn the sispathway through interac tionwith NBS12010

    • Author(s)
      KobayashiJ, OkuiM, AsaithambyA, BurmaS, ChenBP, TanimotoK, MatsuuraS, KomatsuK, ChenDJ.
    • Journal Title

      Mech Ageing Dev

      Volume: 131 Pages: 436-444

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Journal Article] Mutatio nsofo ptineurininam yotro phiclateral sclerosis2010

    • Author(s)
      MaruyamaH, MorinoH, ItoH, IzumiY, KatoH, WatanabeY, KinoshitaY, KamadaM, NoderaH, SuzukiH, KomureO, MatsuuraS, KobatakeK, MorimotoN, AbeK, SuzukiN, AokiM, KawataA, HiraiT, KatoT, OgasawaraK, HiranoA, TakumiT, KusakaH, HagiwaraK, KajiR, KawakamiH.
    • Journal Title

      Nature

      Volume: 465 Pages: 223-226

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Journal Article] Sporadic neonatal Fanconi's anemia with VACTERL association.2010

    • Author(s)
      Kanemoto N, Fukushima T, Imoto N, Koike K, Kanemoto K, Matsuura S.
    • Journal Title

      Pediatr Int 52

      Pages: 141-142

    • NAID

      10028181433

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] HpSulf, a heparan sulfate 6-0-endosulfatase, is involved in the regulation of VEGF signaling during sea urchin development.2010

    • Author(s)
      Fujita K, Takechi E, Sakamoto N, Sumiyoshi N, Izumi S, Miyamoto T, Matsuura S, Tsurugaya T, Akasaka K, Yamamoto T.
    • Journal Title

      Mech Dev 127

      Pages: 235-245

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Mutations of optineurin in amyotrophic lateral sclerosis.2010

    • Author(s)
      Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure 0, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H.
    • Journal Title

      Nature 465

      Pages: 223-226

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] WRN participates in translesion synthesis pathway through interaction with NBS1.2010

    • Author(s)
      J.Kobayashi, M.Okui, A.Asaithamby, S.Burma, B.P.Chen, K.Tanimoto, S.Matsuura, K.Komatsu, D.J.Chen.
    • Journal Title

      Mechanisms of Ageing and Development 131

      Pages: 436-444

    • NAID

      120002426896

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] HpSulf, a heparan sulfate 6-O-endosulfatase, is involved in the regulation of VEGF signaling during sea urchin development.2010

    • Author(s)
      Fujita K, Takechi E, Sakamoto N, Sumiyoshi N, Izumi S, Miyamoto T, Matsuura S, Tsurugaya T, Akasaka K, Yamamoto T.
    • Journal Title

      Mech Dev 127

      Pages: 235-245

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] WRN participates in translesion synthesis pathway through interaction with NBS1.2010

    • Author(s)
      Kobayashi J, Okui M, Asaithamby A, Burma S, Chen BP, Tanimoto K, Matsuura S, Komatsu K, Chen DJ.
    • Journal Title

      Mech Ageing Dev 131

      Pages: 436-444

    • NAID

      120002426896

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Mutations of optineurin in amyotrophic lateral sclerosis.2010

    • Author(s)
      Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H.
    • Journal Title

      Nature 465

      Pages: 223-226

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Sporadic neonatal Fanconi's anemia with VACTERL association.2010

    • Author(s)
      Kanemoto N, Fukushima T, Imoto N, Koike K, Kanemoto K, Matsuura S
    • Journal Title

      Pediatr Int 52

      Pages: 141-142

    • NAID

      10028181433

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] 日本人が発見に関わった疾患遺伝子.Njimegen症候群2009

    • Author(s)
      松浦伸也
    • Journal Title

      小児科 50

      Pages: 953-957

    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Histone H2AX participates the DNA damage-induced ATM activation through interaction with NBS12009

    • Author(s)
      Kobayashi, J., Tauchi, H., Chen, B. Burma, S., Tashiro, S., Matsuura, S., Tanimoto, K., Chen, D. J., Komatsu, K.
    • Journal Title

      Biochem Biophys Res Commun 380

      Pages: 752-757

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Histone H2AX participates the DNA damage-induced ATM activation through interaction with NBS1.2009

    • Author(s)
      Kobayashi J, Tauchi H, Chen B, Bruma S, Tashiro S, Matsuura S, Tanimoto K, Chen DJ, Komatsu K.
    • Journal Title

      Biochem Biophys Res Commun. 380

      Pages: 752-757

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Histone H2AX participates the DNA damage-induced ATM activation through interaction with NBS1.2009

    • Author(s)
      Kobayashi J, Tauchi H, Chen B, Burma S, Tashiro S, Matsuura S, Tanimoto K, Chen DJ, Komatsu K.
    • Journal Title

      Biochem Biophys Res Commun 380

      Pages: 752-757

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plkl activity in interphase cells.2009

    • Author(s)
      Izumi H, Matsumoto Y, Ikeuchi T, Saya H, Kajii T, Matsuura S
    • Journal Title

      Oncogene 28

      Pages: 2806-2820

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] セッケル症候群2009

    • Author(s)
      松浦伸也
    • Journal Title

      小児科診療 72

      Pages: 85-85

    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] 遺伝性小頭症におけるDNA損傷シグナル経路の破綻2009

    • Author(s)
      宮本達雄、松浦伸也
    • Journal Title

      放射線生物 44

      Pages: 330-342

    • NAID

      40016838876

    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Histone H2AX participates the DNA damage-induced ATM activation through interaction with NBS12009

    • Author(s)
      Kobayashi J, Tauchi H, Chen B, Bruma S, Tashiro S, Matsuura S, Tanimoto K, Chen DJ, Komatsu K
    • Journal Title

      Biochem Biophys Res Commun. (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] セッケル症候群2009

    • Author(s)
      松浦伸也
    • Journal Title

      小児科診療 72

      Pages: 85-85

    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] NBS1 regulates a novel apoptotic pathway through Bax activation.2008

    • Author(s)
      Iijima K, Muranaka C, Kobayashi J, Sakamoto S, Komatsu K, Matsuura S, Kubota N, Tauchi H.
    • Journal Title

      DNA Repair 7

      Pages: 1705-1716

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC1.2008

    • Author(s)
      Antoccia A, Sakamoto S, Matsuura S, Tauchi H, Komatsu K.
    • Journal Title

      Radiat Res. 170

      Pages: 345-352

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC12008

    • Author(s)
      Antoccia A, Sakamoto S, Matsuura S, Tauchi H, Komatsu K
    • Journal Title

      Radiat Res 170

      Pages: 345-352

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues.2008

    • Author(s)
      Uehara Y, Ikehata H, Komura J, Ito A, Ogata M, Itoh T, Hirayama R, Furusawa Y, Ando K, Paunesku T, Woloschak GE, Komatsu K, Matsuura S, Ikura T, Kamiya K, Ono T.
    • Journal Title

      Radiat Res 170

      Pages: 216-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues.2008

    • Author(s)
      Uehara Y, Ikehata H, Komura J, Ito A, Ogata M, Itoh T, Hirayama R, Furusawa Y, Ando K, Paunesku T, Woloschak GE, Komatsu K, Matsuura S, Ikura T, Kamiya K, Ono T.
    • Journal Title

      Radiat Res. 170

      Pages: 216-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes2008

    • Author(s)
      Haruta, M., Matsumoto, Y., Izumi, H., Watanabe, N., Fukuzawa, M., Matsuura, S., Kaneko, Y.
    • Journal Title

      Mol Carcinog 47

      Pages: 660-666

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Centrosome amplification induced by survivin suppression enhances both chromosome instability and radiosensitivity in glioma cells.2008

    • Author(s)
      Saito T, Hama S, Izumi H, Yamasaki F, Kajiwara Y, Matsuura S, Morishima K, Hidaka T, Shrestha P, Sugiyama K, Kurisu K.
    • Journal Title

      Br J Cancer. 98(2)

      Pages: 345-355

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390379
  • [Journal Article] MRE11遺伝子変異を原因とする放射線高感受性遺伝病の2例2008

    • Author(s)
      松本祥幸、川田純也、泉秀樹、松浦伸也
    • Journal Title

      長崎医学会雑誌 83

      Pages: 273-276

    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Centrosome amplification induced by survivin suppression enhances both chromosome instability and radiosensitivity in glioma cells.2008

    • Author(s)
      Saito T, Hama S, Izumi H, Yamasaki F, Kajiwara Y, Matsuura S, Morishima K, Hidaka T, Shrestha P, Sugiyama K, Kurisu K.
    • Journal Title

      Br J Cancer. 98

      Pages: 345-355

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Centrosome amplification induced by survivin suppression enhances both chromosome instability and radiosensitivity in glioma cells2008

    • Author(s)
      Saito, T., Hama, S., Izumi, H., Yamasaki, F., Kajiwara, Y., Matsuura, S., Morishima, K., Hidaka, T., shrestha, P., Sugiyama, K., Kurisu, K.
    • Journal Title

      Br J Cancer 98

      Pages: 345-355

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] NBS1 regulates a novel apoptotic pathway through Bax activation2008

    • Author(s)
      Iijima, K., Muranaka, C., Kobayashi, J., Sakamoto, S., Komatsu, K., Matsuura, S., Kubota, N., Tauchi, H.
    • Journal Title

      DNA repair 7

      Pages: 1705-1716

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] BubR1は間期の中心体に局在し、Polo-like kinase 1(Plk1)の活性を制御して中心体の過剰複製を抑制する2008

    • Author(s)
      泉秀樹、松本祥幸、池内達郎、梶井正、松浦伸也
    • Journal Title

      広島医学 61

      Pages: 345-318

    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC1.2008

    • Author(s)
      Antoccia A, Sakamoto S, Matsuura S, Tauchi H, Komatsu K.
    • Journal Title

      Radiat Res 170

      Pages: 345-352

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Journal Article] NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC12008

    • Author(s)
      Antoccia, A., Sakamoto, S., Matsuura, S., Tauchi, H., Komatsu, K.
    • Journal Title

      Radiat Res 170

      Pages: 345-352

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues2008

    • Author(s)
      Uehara, Y., Ikehata, H., Komura, J., Ito, A., Ogata, M., Itoh, T., Hirayama, R., Furusawa, Y., Ando, K., Paunesku, T., Woloschak, G. E., Komatsu, K., Matsuura, S., Ikura, T., Kamiya, K., Ono, T.
    • Journal Title

      Radiat Res 170

      Pages: 216-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.2008

    • Author(s)
      Haruta M, Matsumoto Y, Izumi H, Watanabe N, Fukuzawa M, Matsuura S, Kaneko Y.
    • Journal Title

      Mol Carcinog. 47

      Pages: 660-666

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] ATRによるDNA損傷シグナルと疾患2007

    • Author(s)
      松浦伸也ら
    • Journal Title

      ゲノム医学 7・1

      Pages: 11-15

    • Data Source
      KAKENHI-PROJECT-17590286
  • [Journal Article] Homologous recombination repair is regulated by domains at the N- and C-terminus of NBS1 and is dissociated with ATM functions.2007

    • Author(s)
      Sakamoto.S., Iijima.K., Mochizuki.D., Nakamura.K., Teshigawara.K., Kobayashi.J., Matsuura.S., Tauchi.H.Komatsu K.
    • Journal Title

      Oncogene. 26

      Pages: 6002-6009

    • NAID

      130007001459

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] TopBP1 associates with NBS1 and is involved in homologous recombination repair2007

    • Author(s)
      Morishima, K., Sakamoto, S., Kobayashi, J., Izumi, H., Suda, T., Matsumoto, Y., Tauchi, H., Ide, H., Komatsu, K., Matsuura, S.
    • Journal Title

      Biochem Biophys Res Commun 362

      Pages: 872-879

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] TopBP1 associates with NBS1 and is involved in homologous recombination repair.2007

    • Author(s)
      Morisima.K., Sakamoto.S., Kobayashi.J., Izumi.H., Suda.T., Matsumoto.Y., Tauchi.H., Ide.H., Komatsu K.Matsuura.S.
    • Journal Title

      Biochem Biophys Res Commun. 362

      Pages: 872-879

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] PCS(MVA)症候群染色体数の不安定性が癌の原因であることを実証した疾患2007

    • Author(s)
      松浦伸也、泉秀樹、池内達郎、梶井正
    • Journal Title

      実験医学 25

      Pages: 2925-2931

    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Homologous recombination repair is regulated by domains at the N- and C-terminus of NBS1 and is dissociated with ATM functions2007

    • Author(s)
      Sakamoto S., Iijima K., Mochizuki D., Nakamura K., Teshigawara K., Kobayashi J., Matsuura S., Tauchi H., Komatsu K.
    • Journal Title

      Oncogene 26

      Pages: 6002-9

    • NAID

      130007001459

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] PCS(MVA)症候群-染色体数の不安定性が癌の原因であることを実証した疾患-2007

    • Author(s)
      松浦伸也, ほか
    • Journal Title

      実験医学 25

      Pages: 2925-2931

    • Data Source
      KAKENHI-PROJECT-19590334
  • [Journal Article] Monoallelic BUB1B Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families with Premature Chromotid Separation (PCP) Syndrome.2006

    • Author(s)
      Shinya Matsuura
    • Journal Title

      American Journal of Medical Genetics 140(4)

      Pages: 358-367

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Nijmegen Breakage Syndrome and Functions of the Responsible Protein, NBS1.2006

    • Author(s)
      Antoccia, J.Kobayashi, H.Tauchi, S.Matsuura, K.Komatsu.
    • Journal Title

      Genome Dyn.Basel, Karger. 1

      Pages: 191-205

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Monoallelic BUB1B Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families With Premature Chromatid Separation(PCS)Syndrome2006

    • Author(s)
      Matsuura, S., et. al.
    • Journal Title

      Am.J.Med.Genet. A140・4

      Pages: 358-367

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17590286
  • [Journal Article] Monoallelic BUB1B Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families With Premature Chromatid Separation (PCS) Syndrome.2006

    • Author(s)
      S.Matsuura, Y.Matsumoto, K.Morishima, H.Izumi, H.Matsumoto, E.Ito, K.Tsutsui, J.Kobayashi, H.Tauchi, Y.Kajiwara, S.Hama, K.Kurisu, H.Tahara, M.Oshimura, K.Komatsu, Tatsuro Ikeuchi, Tadashi Kajii.
    • Journal Title

      Amer J Med Genet. 140(4)

      Pages: 358-367

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Monoallelic BUBIB Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families With Premature Chromatid Separation(PCP) Syndrome.2006

    • Author(s)
      S.Matsuura
    • Journal Title

      Amer J Med Genet. 140(4)

      Pages: 358-367

    • Data Source
      KAKENHI-PROJECT-18101002
  • [Journal Article] Monoallelic BUB1B Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families With Premature Chromatid Separation(PCS) Syndrome.2006

    • Author(s)
      Matsuura, S., et. al.
    • Journal Title

      Am. J. Med. Genet A140(4)

      Pages: 358-367

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17590286
  • [Journal Article] Monoallelic BUBIB Mutations and Defective Mitotic-Spindle Checkpoint in Seven Families with Premature Chromatid Separation(PCP) Syndrome.2006

    • Author(s)
      Shinya Matsuura
    • Journal Title

      American Journal of Medical Genetics 140(4)

      Pages: 358-367

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome2006

    • Author(s)
      Matsuura, S., et al.
    • Journal Title

      Am.J.Med.Genet. 140A

      Pages: 358-367

    • Data Source
      KAKENHI-PROJECT-17590286
  • [Journal Article] Monoallelic BUB1B Mutations and Defective Mitotic-spindle Checkpoint in Seven Families With Premature Chromatid Separation(PCS) Syndrome.2005

    • Author(s)
      Shinya Matsuura
    • Journal Title

      American Journal Medical Genetics (in press)

    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex.2004

    • Author(s)
      Shinya Matsuura
    • Journal Title

      Advances in biophysics 38

      Pages: 65-80

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex.2004

    • Author(s)
      Matsuura S, Kobayashi J, et al.
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex2004

    • Author(s)
      Matsuura S, Kobayashi J, et al.
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Data Source
      KAKENHI-PROJECT-12213087
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair By NBS1 complex2004

    • Author(s)
      Matsuura, S.et al.
    • Journal Title

      Advances in Biophysics 35

      Pages: 65-80

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14370776
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex.2004

    • Author(s)
      Shinya Matsuura
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14208068
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex2004

    • Author(s)
      Matsuura, S.
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Data Source
      KAKENHI-PROJECT-16021240
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex2004

    • Author(s)
      Matsuura, S.
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Data Source
      KAKENHI-PROJECT-14370776
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex2004

    • Author(s)
      Matsuura, s.
    • Journal Title

      Advances in Biophysics 38

      Pages: 65-80

    • Data Source
      KAKENHI-PROJECT-16659090
  • [Journal Article] Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex2004

    • Author(s)
      Matsuura, S.et al.
    • Journal Title

      Advances in Biophysics 35

      Pages: 65-80

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370776
  • [Journal Article] BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells

    • Author(s)
      Izumi, H., Matsumoto, Y., Ikeuchi, T., Saya, H., Kajii, T., Matsuura, S.
    • Journal Title

      Oncogene (Epub ahead of print)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] Inborn error of human CYLD causes combined immunodeficiency with syndromic features2024

    • Author(s)
      Takaki Asano, Risa Matsumura, Silvia Natsuko Akutsu, Shinya Matsuura
    • Organizer
      The 8th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] Development of a model cell system for tracking iPSC reprogramming-mediated trisomy correction in aneuploidy syndrome2023

    • Author(s)
      Silvia Natsuko Akutsu, Risa Matsumura, Shinya Matsuura
    • Organizer
      The 7th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis2023

    • Author(s)
      Kume K, Kurashige T, Muguruma K, Morino H, Tada Y, Kikumoto M, Miyamoto T, Akutsu SN, Matsuda Y, Matsuura S, Nakamori M, Nishiyama A, Izumi R, Niihori T, Ogasawara M, Eura N, Kato T, Yokomura M, Nakayama Y, Ito H, Nakamura M, Saito K, Riku Y, Iwasaki Y, Maruyama H, Aoki Y, Nishino I, Izumi Y, Aoki M, Kawakami H
    • Organizer
      日本人類遺伝学会第68回大会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] ゲノム編集技術を用いた突然変異高感度検出系の改良2023

    • Author(s)
      明道友希、谷本早紀、長島明輝、坂本裕貴、坪田一希、宮本達雄、松浦伸也、田内 広
    • Organizer
      日本放射線影響学会第66回大会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] ゲノム編集技術を用いた突然変異高感度検出系の改良2023

    • Author(s)
      明道 友希, 谷本 早紀, 長島 明輝, 坂本 裕貴, 坪田 一希, 宮本 達雄, 松浦 伸也, 田内 広
    • Organizer
      第66回日本放射線影響学会大会
    • Data Source
      KAKENHI-PROJECT-21H02718
  • [Presentation] 放射線感受性の遺伝的背景2023

    • Author(s)
      松浦伸也
    • Organizer
      JASTRO第13回放射線生物セミナー
    • Invited
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] 異数性症候群におけるiPSCリプログラミングを介したトリソミー補正を追跡するモデル細胞系の開発2023

    • Author(s)
      阿久津シルビア夏子、松村梨紗、浅野孝基、松浦伸也
    • Organizer
      第7回放射線災害・医科学研究拠点カンファランス
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] 放射線高感受性を示すと考えられる新規原発性免疫不全症2023

    • Author(s)
      浅野孝基、松村梨紗、阿久津シルビア夏子、松浦伸也
    • Organizer
      中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] Generation of a model cell system to track trisomy correction during reprogramming in aneuploidy syndromes2023

    • Author(s)
      Silvia Natsuko Akutsu, Risa Matsumura, Takaki Asano, Shinya Matsuura
    • Organizer
      日本人類遺伝学会第68回大会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in the major autosomal trisomy syndromes2022

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, Keita Tomioka, Hiroshi Ochiai, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      日本人類遺伝学会第67回大会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] Reprogramming can induce chromosome self-correction2022

    • Author(s)
      Silvia Natsuko AKUTSU, Risa MATSUMURA, Shinya MATSUURA
    • Organizer
      第46回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] iPSC reprogramming-mediated aneuploid rescue in the major autosomal trisomy syndromes2022

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, Keita Tomioka, Hiroshi Ochiai, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      第45回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] iPSC reprogramming-mediated random trisomy correction in aneuploidy syndromes2022

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, Keita Tomioka, Hiroshi Ochiai, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 6th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 細胞初期化で誘導される染色体自己修正機構について2022

    • Author(s)
      阿久津シルビア夏子、松村梨紗、松浦伸也
    • Organizer
      日本放射線影響学会第65回大会
    • Data Source
      KAKENHI-PROJECT-23K24996
  • [Presentation] ゲノム編集法を用いた放射線感受性細胞の作製と解析2022

    • Author(s)
      松浦伸也
    • Organizer
      第3回放射線災害・医科学研究拠点ワークショップ
    • Invited
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] iPSC reprogramming-mediated random trisomy correction in aneuploidy syndromes2022

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, Keita Tomioka, Hiroshi Ochiai, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 6th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] ゲノム編集法を用いた放射線感受性細胞の作製と解析2022

    • Author(s)
      松浦伸也
    • Organizer
      第3回放射線災害・医科学研究拠点ワークショップ
    • Invited
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] ペルオキシソームを介した繊毛へのコレステロール輸送機構2021

    • Author(s)
      宮本達雄, 細羽康介, 板橋岳志, 岩根敦子, 阿久津シルビア夏子, 落合博, 斎藤裕見子, 山本卓, 松浦伸也
    • Organizer
      第94回日本生化学会大会
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] トリソミー症候群の細胞初期化で誘導されるトリソミーレスキュー2021

    • Author(s)
      阿久津シルビア夏子、宮本達雄、冨岡啓太、大場大樹、大橋博文、松浦伸也
    • Organizer
      第5回放射線災害・医科学研究拠点カンファランス
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2021

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 5th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] ペルオキシソーム欠損による繊毛シグナル伝達障害の分子機構2021

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合 博、斎藤裕見子、山本 卓、松浦伸也
    • Organizer
      第44回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] トリソミー症候群の細胞初期化で誘導されるトリソミーレスキュー2021

    • Author(s)
      阿久津シルビア夏子、宮本達雄、冨岡啓太、大場大樹、大橋博文、松浦伸也
    • Organizer
      第5回放射線災害・医科学研究拠点カンファランス
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] ペルオキシソームを介した繊毛へのコレステロール輸送機構2021

    • Author(s)
      宮本達雄, 細羽康介, 板橋岳志, 岩根敦子, 阿久津シルビア夏子, 落合博, 斎藤裕見子, 山本卓, 松浦伸也
    • Organizer
      第94回日本生化学会大会
    • Data Source
      KAKENHI-PROJECT-21H02718
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2021

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      第64回日本放射線影響学会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] ペルオキシソーム欠損による繊毛シグナル伝達障害の分子機構2021

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合 博、斎藤裕見子、山本 卓、松浦伸也
    • Organizer
      第44回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2021

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 5th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2021

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      第64回日本放射線影響学会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 繊毛病としてのペルオキシソーム形成不全症・Zellweger症候群2020

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合 博、斎藤裕見子、山本 卓、松浦伸也
    • Organizer
      第65回日本人類遺伝学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 機能ゲノミックスを用いた放射線感受性個人差を規定する遺伝素因の探索2020

    • Author(s)
      宮本達雄, 冨岡啓太, 藤田和将, 阿久津シルビア夏子, 工藤美樹, 小林正夫, 岡田賢, 田内広, 松浦伸也
    • Organizer
      第63回日本放射線影響学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] Peroxisomes ensure to supply cholesterol into the ciliary membrane : a lesson from a peroxisome-biogenesis disorder Zellweger syndrome2020

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Takeshi Itabashi, Atsuko H. Iwane, Silvia Natsuko Akutsu, Hiroshi Ochiai, Yumiko Saito, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      第43回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Peroxisomes ensure to supply cholesterol into the ciliary membrane: a lesson from a peroxisome-biogenesis disorder Zellweger syndrome2020

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Takeshi Itabashi, Atsuko H. Iwane, Silvia Natsuko Akutsu, Hiroshi Ochiai, Yumiko Saito, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      第43回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 染色体分配異常を伴う新規早老症患者におけるCDC20遺伝子変異の同定と分子病態の解析2020

    • Author(s)
      藤田 春美、佐々木 貴史、宮本 達雄、阿久津 シルビア 夏子、佐藤 尚武、森 毅彦、中林 一彦、秦 健一郎、鈴木 寿人、小崎 健次郎、松浦 伸也、松原 洋一、天谷 雅行、久保 亮治
    • Organizer
      第65回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] NBS1 I171V多型による放射線感受性個人差の定量的評価2020

    • Author(s)
      冨岡啓太、Silvia Natsuko Akutsu、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、藤田和将、宮本達雄、松浦伸也
    • Organizer
      第45回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 繊毛病としてのペルオキシソーム形成不全症・Zellweger症候群2020

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合博、斎藤裕見子、山本卓、松浦伸也
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2020

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 5th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] NBS1 I171V多型による放射線感受性個人差の定量的評価2020

    • Author(s)
      冨岡啓太、Silvia Natsuko Akutsu、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、藤田和将、宮本達雄、松浦伸也
    • Organizer
      第45回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 染色体分配異常を伴う新規早老症患者におけるCDC20遺伝子変異の同定と分子病態の解析2020

    • Author(s)
      藤田 春美、佐々木 貴史、宮本 達雄、阿久津シルビア夏子、佐藤 尚武、 森 毅彦、中林 一彦、秦 健一郎、鈴木 寿人、小崎 健次郎、松浦 伸也、 松原 洋一、天谷 雅行、久保 亮治
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes2020

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita Tomioka, Daiju Oba, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      The 5th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 繊毛病としてのペルオキシソーム形成不全症・Zellweger症候群2020

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合博、斎藤裕見子、山本卓、松浦伸也
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Quantitative evaluation of the NBS1 I171V variant on radiosensitivity2020

    • Author(s)
      Tomioka K, Fujita K, Akutsu SN, Tauchi H, Yamamoto T, Kobayashi M, Kudo Y, Miyamoto T, Matsuura S.
    • Organizer
      The 4th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] 先天異常症候群集団外来:モザイク型ダウン症候群外来の報告2020

    • Author(s)
      井坂美帆、大場大樹、小林美和、阿久津シルビア夏子、宮本達雄、松浦伸也、大橋博文
    • Organizer
      第65回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 機能ゲノミックスを用いた放射線感受性個人差を規定する遺伝素因の探索2020

    • Author(s)
      宮本達雄, 冨岡啓太, 藤田和将, 阿久津シルビア夏子, 工藤美樹, 小林正夫, 岡田賢, 田内広, 松浦伸也
    • Organizer
      日本放射線影響学会第63回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] 機能ゲノミックスを用いた放射線感受性個人差を規定する遺伝素因の探索2020

    • Author(s)
      宮本達雄, 冨岡啓太, 藤田和将, 阿久津シルビア夏子, 工藤美樹, 小林正夫, 岡田賢, 田内広, 松浦伸也
    • Organizer
      第63回日本放射線影響学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] Peroxisomes ensure to supply cholesterol into the ciliary membrane : a lesson from a peroxisome-biogenesis disorder Zellweger syndrome2020

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Takeshi Itabashi, Atsuko H. Iwane, Silvia Natsuko Akutsu, Hiroshi Ochiai, Yumiko Saito, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      第43回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] Quantitative evaluation of the NBS1 I171V variant on radiosensitivity2020

    • Author(s)
      Tomika K, Fujita K, Akutsu SN, Tauchi H, Yamamoto T, Kobayashi M, Kudo Y, Miyamoto T, Matsuura S
    • Organizer
      The 4th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science (Hiroshima)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 先天異常症候群集団外来:モザイク型ダウン症候群外来の報告2020

    • Author(s)
      井坂美帆、大場大樹、小林美和、阿久津シルビア夏子、宮本達雄、松浦伸也、大橋博文
    • Organizer
      第65回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] NBS1 I171V多型による放射線感受性個人差の定量的評価2020

    • Author(s)
      冨岡啓太、Silvia Natsuko Akutsu、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、藤田和将、宮本達雄、松浦伸也
    • Organizer
      第45回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-20K12165
  • [Presentation] 染色体分配異常を伴う新規早老症患者におけるCDC20遺伝子変異の同定と分子病態の解析2020

    • Author(s)
      藤田 春美、佐々木 貴史、宮本 達雄、阿久津シルビア夏子、佐藤 尚武、 森 毅彦、中林 一彦、秦 健一郎、鈴木 寿人、小崎 健次郎、松浦 伸也、 松原 洋一、天谷 雅行、久保 亮治
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] Peroxisomes ensure to supply cholesterol into the ciliary membrane: a lesson from a peroxisome-biogenesis disorder Zellweger syndrome2020

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Takeshi Itabashi, Atsuko H. Iwane, Silvia Natsuko Akutsu, Hiroshi Ochiai, Yumiko Saito, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      第43回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 染色体分配異常を伴う新規早老症患者におけるCDC20遺伝子変異の同定と分子病態の解析2020

    • Author(s)
      藤田 春美、佐々木 貴史、宮本 達雄、阿久津 シルビア 夏子、佐藤 尚武、森 毅彦、中林 一彦、秦 健一郎、鈴木 寿人、小崎 健次郎、松浦 伸也、松原 洋一、天谷 雅行、久保 亮治
    • Organizer
      第65回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 機能ゲノミックスを用いた放射線感受性個人差を規定する遺伝素因の探索2020

    • Author(s)
      宮本達雄, 冨岡啓太, 藤田和将, 阿久津シルビア夏子, 工藤美樹, 小林正夫, 岡田賢, 田内広, 松浦伸也
    • Organizer
      日本放射線影響学会第63回大会
    • Data Source
      KAKENHI-PROJECT-20K21845
  • [Presentation] Quantitative evaluation of the NBS1 I171V variant on radiosensitivity.2020

    • Author(s)
      Tomika K, Fujita K, Akutsu SN, Tauchi H, Yamamoto T, Kobayashi M, Kudo Y, Miyamoto T, Matsuura S
    • Organizer
      The 4th International Symposium of the Network-type Joint Usage/Research Center for Radiation Disaster Medical Science (Hiroshima)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 繊毛病としてのペルオキシソーム形成不全症・Zellweger症候群2020

    • Author(s)
      宮本達雄、細羽康介、板橋岳志、岩根敦子、阿久津シルビア夏子、落合 博、斎藤裕見子、山本 卓、松浦伸也
    • Organizer
      第65回日本人類遺伝学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] NBS1遺伝子I171V多型の放射線感受性に対する定量的評価2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内広、山本卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      日本放射線影響学会第62回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] DNA二重鎖切断修復を標的とした放射線治療薬の取り組み2019

    • Author(s)
      田内広、海野昌喜、松浦伸也、宮本達雄、鈴木啓司
    • Organizer
      日本放射線影響学会第62回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] 新規ATLD変異細胞を用いたMRN複合体形成タンパク質の発現制御メカニズムの解析2019

    • Author(s)
      河村香寿美、松浦伸也、小松賢志、小林純也、鈴木啓司
    • Organizer
      第42回日本分子生物学会年会(福岡)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] NBS1遺伝子I171V多型の放射線感受性に対する定量的評価2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の逆遺伝学的解析2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第42回日本分子生物学会年会(福岡)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] CRISPR-ObLiGaRe法を用いたiPS細胞における蛍光核標識によるモザイク・トリソミー21のモデル細胞系の開発2019

    • Author(s)
      Silvia Natsuko Akutsu、落合博、山本卓、大橋博文、宮本達雄、松浦伸也
    • Organizer
      日本ゲノム編集学会第4回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] CRISPR-ObLiGaRe法を用いたiPS細胞における蛍光核標識によるモザイク・トリソミー21のモデル細胞系の開発2019

    • Author(s)
      阿久津シルビア夏子、落合 博、山本 卓、大橋博文、宮本達雄、松浦伸也
    • Organizer
      第4回日本ゲノム編集学会(東京)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 放射線感受性個人差を規定する遺伝素因の探索とリスク定量2019

    • Author(s)
      宮本達雄、冨岡啓太、阿久津シルビア夏子、小林正夫、工藤美樹、松浦伸也
    • Organizer
      第4回放射線災害・医科学研究拠点カンファランス(広島)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 放射線に対する強さ・弱さの個人差を決める遺伝子変化の探索2019

    • Author(s)
      宮本達雄、冨岡啓太、阿久津シルビア夏子、松浦伸也
    • Organizer
      ふくしま県民公開大学
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] The generation of mosaic trisomy 21 model cells using cells from a patient with full trisomy 21 by trisomy rescue during cell reprogramming and their modification with fluorescent nuclear markers by genome editing technique.2019

    • Author(s)
      Akutsu SN, Ochiai H, Yamamoto T, Ohashi H, Miyamoto T, Matsuura S
    • Organizer
      The 65th Brazilian Congress of Genetics (Sao Paulo)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の逆遺伝学的解析2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第42回日本分子生物学会年会(福岡)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子 I171V多型の定量的評価2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原敬見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      原子爆弾後障害研究会(広島)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] Generation of Down Syndrome iPS cells targeted with fluoresence marker in chromosome 21 using genome editing technology2019

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Keita tomioka, Hiroshi Ochiai, Takashi Yamamoto, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      日本人類遺伝学会第64回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] ATLD細胞におけるMRN複合体形成タンパク質の発現制御メカニズム2019

    • Author(s)
      河村香寿美、松浦伸也、小松賢志、小林純也、鈴木啓司
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] ATLD細胞におけるMRN複合体形成タンパク質の発現制御メカニズム2019

    • Author(s)
      河村香寿美、松浦伸也、小松賢志、小林純也、鈴木啓司
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] DNA二重鎖切断修復を標的とした放射線治療創薬の取り組み2019

    • Author(s)
      田内 広、海野昌喜、松浦伸也、宮本達雄、鈴木啓司
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子 I171V多型の定量的評価2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原敬見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      原子爆弾後障害研究会(広島)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] DNA二重鎖切断修復を標的とした放射線治療創薬の取り組み2019

    • Author(s)
      田内 広、海野昌喜、松浦伸也、宮本達雄、鈴木啓司
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の定量2019

    • Author(s)
      冨岡啓太、Silivia Natsuko Akutsu、柳原啓見、田内広、山本卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第60回原子爆弾後障害研究会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] BUB1Bの生殖細胞系列の両アレルバリアントによる家族性横紋筋肉腫2019

    • Author(s)
      Yoshida K, Yamaoka S, Yoshida M, Nakabayashi K, Shirai R, Osumi T, Kiyotani C, Akutsu SN, Miyamoto T, Hata K, Kiyokawa N, Yuza Y, Matsumoto K, Matsuura S, Kato M
    • Organizer
      第61回小児血液・がん学会学術集会(広島)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] NBS1遺伝子I171V多型の放射線感受性に対する定量的評価2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内 広、山本 卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第62回日本放射線影響学会(京都)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 放射線感受性の遺伝的個人差を規定する候補素因としてのNBS1遺伝子I171V多型の逆遺伝学的解析2019

    • Author(s)
      冨岡啓太、阿久津シルビア夏子、柳原啓見、田内広、山本卓、小林正夫、工藤美樹、宮本達雄、松浦伸也
    • Organizer
      第42回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] The generation of mosaic trisomy 21 model cells using cells from a patient with full trisomy 21 by trisomy rescue during cell reprogramming and their modification with fluorescent nuclear markers by genome editing technique.2019

    • Author(s)
      Akutsu SN, Ochiai H, Yamamoto T, Ohashi H, Miyamoto T, Matsuura S
    • Organizer
      The 65th Brazilian Congress of Genetics (Sao Paulo)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] BUB1Bの生殖細胞系列の両アレルバリアントによる家族性横紋筋肉腫2019

    • Author(s)
      Yoshida K, Yamaoka S, Yoshida M, Nakabayashi K, Shirai R, Osumi T, Kiyotani C, Akutsu SN, Miyamoto T, Hata K, Kiyokawa N, Yuza Y, Matsumoto K, Matsuura S, Kato M
    • Organizer
      第61回小児血液・がん学会学術集会(広島)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 新規ATLD変異細胞を用いたMRN複合体形成タンパク質の発現制御メカニズムの解析2019

    • Author(s)
      河村香寿美、松浦伸也、小松賢志、小林純也、鈴木啓司
    • Organizer
      第42回日本分子生物学会年会(福岡)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] 放射線感受性個人差を規定する遺伝素因の探索とリスク定量2019

    • Author(s)
      宮本達雄、冨岡啓太、阿久津シルビア夏子、小林正夫、工藤美樹、松浦伸也
    • Organizer
      第4回放射線災害・医科学研究拠点カンファランス(広島)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] Generation of Down syndrome iPS cells tagged with fluorescence marker in chromosome 21 using genome editing technology.2019

    • Author(s)
      Akutsu SN, Miyamoto T, Tomioka K, Ochiai H, Yamamoto T, Ohashi H, Matsuura S
    • Organizer
      第64回日本人類遺伝学会(長崎)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] Generation of NBS1 I171V knock-in mice using genome editing technology2019

    • Author(s)
      Tatsuo Miyamoto, Keita Tomioka, Silvia Natsuko Akutsu, Hiroshi Tauchi, Shinya Matsuura
    • Organizer
      The 3rd International Symposium of the Next network-type Joint Usage / Research Center for Radiation Disaster Medical Science
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Generation of Down syndrome iPS cells tagged with fluorescence marker in chromosome 21 using genome editing technology2019

    • Author(s)
      Akutsu SN, Miyamoto T, Tomioka K, Ochiai H, Yamamoto T, Ohashi H, Matsuura S
    • Organizer
      第64回日本人類遺伝学会(長崎)
    • Data Source
      KAKENHI-PROJECT-19K22515
  • [Presentation] CRISPR-ObLiGaRe法を用いたiPS細胞における蛍光核標識によるモザイク・トリソミー21のモデル細胞系の開発2019

    • Author(s)
      阿久津シルビア夏子、落合 博、山本 卓、大橋博文、宮本達雄、松浦伸也
    • Organizer
      第4回日本ゲノム編集学会(東京)
    • Data Source
      KAKENHI-PROJECT-19H04270
  • [Presentation] A combined approch of exome sequencing and genome editing identified WDR62/MCPH2 mutations in the Japanese patients with primary microcephaly2018

    • Author(s)
      Tatsuo Miyamoto, Silvia Natsuko Akutsu, Akihiro Fukumitsu, Yoshinori Masatsuna, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Kenji Shimizu, Hirofumi Ohashi, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      The 9th Takeda Science Foundation Symposium on PharmaSciences Genome Editing towards medical applications
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 一塩基編集技術を用いた遺伝性小頭症の病因・病態解明2018

    • Author(s)
      宮本達雄, Silvia Natsuko Akutsu, 松浦伸也
    • Organizer
      日本生化学第91回大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] ゲノム編集技術を用いたNBS1 I171Vノックインマウスの作製2018

    • Author(s)
      宮本達雄、Silvia Natsuko Akutsu、田内広、松浦伸也
    • Organizer
      日本放射線影響学会第61回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Synthesis-Dependent-Strand Annealingに依存したssODNノックインの可能性:ssODN導入マウス作製からの知見2018

    • Author(s)
      宮本達雄, Silvia Natsuko Akutsu,田中貴雄, 山本卓, 松浦伸也
    • Organizer
      第3回日本ゲノム編集学会年会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Experimental strategies for the chromosome therapy in Down Syndrome cell2018

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      日本放射線影響学会第61回大会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] ゲノム編集技術を用いたナイミーヘン症候群原因遺伝子NBS1 I171V多型ノックインマウスの作製2018

    • Author(s)
      宮本達雄、冨岡啓太、阿久津シルビア夏子、山本卓、田内広、松浦伸也
    • Organizer
      第41回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] ヒト培養細胞におけるゲノム編集を用いた遺伝性小頭症の病因・病態解明2018

    • Author(s)
      宮本達雄, Silvia Natsuko Akutsu, 松浦伸也
    • Organizer
      日本人類遺伝学会 第63回大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Unravelling the pathological mechanisms of structure-chromosomal instability post IR in PCS(MVA) syndrome2018

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      The 7th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] Exprimental trials for the chromosome aneuploidy correction in Down syndrome cell lines2018

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Hrofumi Ohashi, Shinya Matsuura
    • Organizer
      第43回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-18H02624
  • [Presentation] Unravelling the pathological mechanisms of structure-chromosomal instability post IR in PCS(MVA) syndrome.2018

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      The 7th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 真性小頭症原因遺伝子産物WDR62による星状体微小管重合を介した細胞分裂軸制御2017

    • Author(s)
      宮本達雄、福満啓博、Silvia Natsuko Akutsu、政綱宜規、細羽康介、山本卓、松浦伸也
    • Organizer
      第40回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Evaluation of individual differences of radiosensitivity using genome editing2017

    • Author(s)
      Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Kosuke Hosoba, Yoshiki Kudo, Satoshi Tashiro,Shinya Matsuura,
    • Organizer
      The 1st International Symposium of the network-type Joint Usage/Research Center for Radiation Disaster Medical Sciences
    • Place of Presentation
      広島
    • Year and Date
      2017-02-21
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Trial for correction of trisomy 21 in a Down syndrome patient-derived induced pluripotent stem cells (iPSc)2017

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Hiroshi Ochiai, Kenichi Suzuki, Akira Shimamoto, Takashi Yamamoto and Shinya Matsuura
    • Organizer
      日本人類遺伝学会第62回大会
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] 真性小頭症原因遺伝子産物WDR62による星状体微小管重合を介した細胞分裂軸制御2017

    • Author(s)
      宮本達雄、福満啓博、Silvia Natsuko Akutsu、政綱宜規、細羽康介、山本卓、松浦伸也
    • Organizer
      第40回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] 分裂期キナーゼPLK1による遺伝性小頭症原因遺伝子産物WDR62のリン酸化を介した細胞分裂軸安定化機構2017

    • Author(s)
      宮本達雄、細羽康介、Silvia Natsuko Akutsu、福満啓博、政綱宣規、森野豊之、川上秀史、山本卓、清水健司、大橋博文、松浦伸也
    • Organizer
      第60回日本放射線影響学会
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] 日本人AT-LD患者におけるMRE11変異部位とDNA損傷応答異常との関係2017

    • Author(s)
      河村香寿、Qi Fei、加藤竹雄、松浦伸也、小松賢志、小林純也
    • Organizer
      日本放射線影響学会第60回大会
    • Data Source
      KAKENHI-PROJECT-26241013
  • [Presentation] Identification of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing technology2017

    • Author(s)
      Tatsuo Miyamoto, Ekaterina Royba, Silvia Natsuko Akutsu, Kosuke Hosoba, Hiroshi Tauchi, Yoshiki Kudo, Satoshi Tashiro, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      日本人類遺伝学会第62回大会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Trial for correction of trisomy 21 in a Down syndrome patient-derived induced pluripotent stem cells (iPSc)2017

    • Author(s)
      Silvia Natsuko Akutsu, Tatsuo Miyamoto, Hiroshi Ochiai, Kenichi Suzuki, Akira Shimamoto, Takashi Yamamoto, Shinya Matsuura
    • Organizer
      日本人類遺伝学会第62回大会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells2017

    • Author(s)
      Ekaterina Royba、宮本達雄、Silvia Natsuko Akutsu、細羽康介、工藤美樹、田代聡、山本卓、松浦伸也
    • Organizer
      第42回中国地区放射線影響研究会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Evaluation of individual differences of radiosensitivity using genome editing2017

    • Author(s)
      Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Kosuke Hosoba, Yoshiki Kudo, Satoshi Tashiro, Shinya Matsuura
    • Organizer
      The 1st International Symposium of the network-type Joint Usage/Research Center for Radiation Disaster Medical Science
    • Place of Presentation
      広島
    • Year and Date
      2017-02-21
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Genome editing technique as a useful tool for analysing individual differences of radiosensitivity2017

    • Author(s)
      Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Kosuke Hosoba, Yoshiki Kudo, Satoshi Tashiro, Shinya Matsuura;
    • Organizer
      The 6th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] 放射線感受性個人差を規定する遺伝素因の定量的評価としてのヒト培養細胞株におけるゲノム編集2017

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、細羽康介、田内 広、山本 卓、工藤美樹、田代 聡、松浦伸也
    • Organizer
      第58回原子爆弾後障害研究会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] PLK1-mediated phosphorylation of WDR62/MCPH2 is required for proper mitotic spindle orientation2017

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Silvia Natsuko Akutsu, Hiroyuki Morino, Akihiro Fukumitsu, Yoshinori Masatsuna, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      第75回日本癌学会学術総会
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] Identification of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing technolog2017

    • Author(s)
      Tatsuo Miyamoto, Ekaterina Royba, Silvia Natsuko Akutsu, Kosuke Hosoba, Hiroshi Tauchi, Yoshiki Kudo, Satoshi Tashiro, Takashi Yamamoto and Shinya Matsuura
    • Organizer
      日本人類遺伝学会第62回大会
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] PLK1-mediated phosphorylation of WDR62/MCPH2 is required for proper mitotic spindle orientation2017

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Silvia Natsuko Akutsu, Hiroyuki Morino, Akihiro Fukumitsu, Yoshinori Masatsuna, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      第75回日本癌学会学術総会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Genetic characterization of a patient with a progeroid phenotype and mosaic variegated aneuploidy.2017

    • Author(s)
      Harumi Fujita, Takashi Sasaki, Tatsuo Miyamoto, Takehiko Mori, Kazuhiko Nakabayashi, Kenichiro Hata, Shinya Matsuura, Yoichi Matsubara, Masayuki Amagai, Akiharu Kubo
    • Organizer
      KEYSTONE SYMPOSIA MEETING, Aging and Mechanism of Aging-Related Disease
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Genome editing technique as a useful tool for analysing individual differences of radiosensitivity2017

    • Author(s)
      Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Kosuke Hosoba, Yoshiki Kudo, Satoshi Tashiro, Shinya Matsuura
    • Organizer
      The 6th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2017-02-11
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] 分裂期キナーゼPLK1による遺伝性小頭症原因遺伝子産物WDR62のリン酸化を介した細胞分裂軸安定化機構2017

    • Author(s)
      宮本達雄、細羽康介、Silvia Natsuko Akutsu、福満啓博、政綱宣規、森野豊之、川上秀史、山本卓、清水健司、大橋博文、松浦伸也
    • Organizer
      第60回日本放射線影響学会年会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ヒト培養細胞におけるCRISPR-ObLiGaRe法を用いた放射線発がんリスクの個人差を規定する遺伝素因の探索2017

    • Author(s)
      宮本達雄, Ekaterina Royba, Silvia Natsuko Akutsu, 田代聡, 山本卓, 松浦伸也
    • Organizer
      第2回日本ゲノム編集学会年会
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Current research of low dose radiation effects in Hiroshima2016

    • Author(s)
      Shinya Matsuura
    • Organizer
      GAP related meeting between Hiroshima University and the University of Texas DM Anderson Cancer Center
    • Place of Presentation
      広島
    • Year and Date
      2016-06-22
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] ATM heterozygous mutations underlying individual differences in radiosensitivity in human populations2016

    • Author(s)
      Shinya Matsuura, Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Takashi Yamamoto, Yoshiki Kudo, Satoshi Tashiro
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] Impact of mutations in ATM gene on individual radiosensitivity in Ataxia-Telangiectasia family members.2016

    • Author(s)
      Royba E, Akutsu SN,Yanagihara H,Ochiai H,Kudo Y,Tashiro S,Miyamoto T,Matsuura S
    • Organizer
      The 5th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      東広島
    • Year and Date
      2016-02-14
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 全エクソーム解析とゲノム編集を用いた遺伝性小頭症の発症機構の解析2016

    • Author(s)
      宮本達雄、政綱宜規、細羽康介、森野豊之、川上秀史、山本卓、清水健司、大橋博文、松浦伸也
    • Organizer
      第57回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Year and Date
      2016-06-05
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of PCS (MVA) syndrome mutation knock-in mice using CRISPR/Cas9-mediated genome editing technology2016

    • Author(s)
      Kosuke Hosoba, Takao Tanaka, Akihiro Fukumitsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of PCS (MVA) syndrome mutation knock-in mice using CRISPR/Cas9-mediated genome editing technology2016

    • Author(s)
      Kosuke Hosoba, Tatsuo Miyamoto and Shinya Matsuura
    • Organizer
      ASHG2016
    • Place of Presentation
      Vancouver (Canada)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ゲノム編集技術を用いた放射線発がんリスクの個人差を規定する遺伝素因としてのATMヘテロ遺伝子変異の同定2016

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、田代 聡、山本 卓、松浦伸也
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] A combined approach of exome sequencing and genome editing identified WDR62/MCPH2 mutations in patients with primary microcephaly2016

    • Author(s)
      Tatsuo Miyamoto, Yoshinori Masatsuna, Akihiro Fukumitsu, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      ASHG2016
    • Place of Presentation
      Vancouver (Canada)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] CRISPR/Cas9システムとssODNを用いた遺伝性小頭症モデル細胞の樹立2016

    • Author(s)
      宮本達雄、福満啓博、政綱宜規、森野豊之、川上秀史、山本卓、清水健司、大橋博文、松浦伸也
    • Organizer
      日本ゲノム編集学会第1回大会
    • Place of Presentation
      広島
    • Year and Date
      2016-09-06
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of PCS (MVA) syndrome mutation knock-in mice using CRISPR/Cas9-mediated genome editing technology2016

    • Author(s)
      Kosuke Hosoba, Tatsuo Miyamoto and Shinya Matsuura
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Insufficiency of BubR1 gene increases structure-chromosomal instability postionizing radiation.2016

    • Author(s)
      Akutsu SN, Royba E, Hosoba K, Miyamoto T, Matsuura S
    • Organizer
      The 5th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster.
    • Place of Presentation
      東広島
    • Year and Date
      2016-02-14
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ATM heterozygous mutations underlying individual differences in radiosensitivity in human populations2016

    • Author(s)
      Shinya Matsuura, Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Takashi Yamamoto, Yoshiki Kudo, Satoshi Tashiro
    • Organizer
      ASHG2016
    • Place of Presentation
      Vancouver (Canada)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 低線量率放射線照射による細胞内ROS上昇とDNA損傷応答との関係2016

    • Author(s)
      小林純也、河村香寿美、斎藤裕一朗、周 慧、松浦伸也、小松賢志
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] ATMヘテロ遺伝子変異は放射線感受性個人差に寄与する2016

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、工藤美樹、田代聡、松浦伸也
    • Organizer
      日本放射線影響学会第59回大会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Effect of ATM heterozygous mutations on individual differences of radiosensitivity in human populations2016

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、工藤美樹、田代聡、松浦伸也
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] A combined approach of exome sequencing and genome editing identified WDR62/MCPH2 mutations in patients with primary microcephaly2016

    • Author(s)
      Tatsuo Miyamoto, Yoshinori Masatsuna, Akihiro Fukumitsu, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Oxidative stress and DNA damage responses under low dose rate irradiation2016

    • Author(s)
      Kobayashi J, Saito Y, Kato A, Oliveira DV, Yanagihara H, Matsuura S, Komatsu K.
    • Organizer
      The 2nd KU RBC-CEA Joint Workshop
    • Place of Presentation
      Kyoto.
    • Year and Date
      2016-04-11
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26241013
  • [Presentation] ATM heterozygous mutations underlying individual differences in radiosensitivity in human populations2016

    • Author(s)
      Shinya Matsuura, Ekaterina Royba, Tatsuo Miyamoto, Silvia Natsuko Akutsu, Takashi Yamamoto, Yoshiki Kudo, Satoshi Tashiro
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] 日本人AT-LD患者におけるMRE11変異部位とDNA損傷応答異常との関係2016

    • Author(s)
      河村香寿美、加藤竹雄、松浦伸也、小松賢志、小林純也
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] CRISPR/Cas9システムとssODNを用いた遺伝性小頭症モデル細胞の樹立2016

    • Author(s)
      宮本達雄、福満啓博、政綱宜規、森野豊之、川上秀史、清水健司、大橋博文、山本 卓、松浦伸也
    • Organizer
      第1回日本ゲノム編集学会
    • Place of Presentation
      広島
    • Year and Date
      2016-09-06
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Application of genome editing technology into radiation biology for understanding individual difference of radiosensitivity.2016

    • Author(s)
      Royba E, Akutsu SN,Yanagihara H,Hosoba K,Ochiai H,Kudo Y,Tashiro S, Miyamoto T,Matsuura S
    • Organizer
      The 5th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster.
    • Place of Presentation
      東広島
    • Year and Date
      2016-02-14
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of PCS(MVA) syndrome-mutation knock-in mice using CRISPR/Cas9 system and ssODN mediated genome editing technology2016

    • Author(s)
      Kosuke Hosoba, Takao Tanaka, Akihiro Fukumitsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] 遺伝性小頭症の原因遺伝子WDR62による細胞分裂軸制御機構2016

    • Author(s)
      福満啓博、政綱宣規、阿久津シルビア夏子、細羽康介、森野豊之、川上秀史、山本 卓、清水健司、大橋博文、宮本達雄、松浦伸也
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Molecular basis of human BUBR1 deficiency, a central protein of the spindle assembly checkpoint2016

    • Author(s)
      Shinya Matsuura, Tatsuo Miyamoto, Kosuke Hosoba, Hiroshi Ochiai, Takashi Yamamoto, Makoto Furutani-Seiki
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] ゲノム編集技術を用いた放射線発がんリスクの個人差を規定する遺伝素因としてのATMヘテロ遺伝子変異の同定2016

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、田代聡、山本卓、松浦伸也
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Inflammatory response in primary human endothelial cells subjected to gamma irradiation at different dose rates2016

    • Author(s)
      Zaharieva Elena、河合秀彦、稲葉俊哉、松浦伸也、神谷研二
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Effect of ATM heterozygous mutations on individual differences of radiosensitivity in human populations2016

    • Author(s)
      Tatsuo Miyamoto, Ekaterina Royba, Silvia Natsuko Akutsu, Yoshiki Kudo, Satoshi Tashiro, Shinya Matsuura
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] WDR62/MCPH2 mutations identified in patients with primary microcephaly by a combined approach of exome sequencing and genome editing technology2016

    • Author(s)
      Yoshinori Masatsuna, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Oohashi, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      ICHG2016
    • Place of Presentation
      Kyoto
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of PCS (MVA) syndrome mutation knock-in mice using CRISPR/Cas9-mediated genome editing technology2016

    • Author(s)
      Kosuke Hosoba, Tatsuo Miyamoto and Shinya Matsuura
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] ゲノム編集法を用いたNBS1 SNP導入細胞の作製と放射線感受性の評価2016

    • Author(s)
      柳原啓見、宮本達雄、Royba Ekaterina、Akutsu Silvia Natsuko、山本 卓、松浦伸也
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] 分裂期キナーゼPLK1による真性小頭症原因遺伝子産物WDR62のリン酸化を介した細胞分裂軸制御機構2016

    • Author(s)
      福満啓博、政綱宣規、Silvia Nastuko Akutsu、細羽康介、山本 卓、宮本達雄、松浦伸也
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] 遺伝性小頭症の原因遺伝子WDR62による細胞分裂軸制御機構2016

    • Author(s)
      福満啓博、政綱宜規、Silvia Natsuko Akutsu、細羽康介、森野豊之、川上秀史、山本卓、清水健司、大橋博文、宮本達雄、松浦伸也
    • Organizer
      日本放射線影響学会第59回大会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Molecular basis of human BUBR1 deficiency, a central protein of the spindle assembly checkpoint2016

    • Author(s)
      松浦伸也、宮本達雄、細羽康介、落合博、山本卓、古谷-清木誠
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ATMヘテロ遺伝子変異は放射線感受性個人差に寄与する2016

    • Author(s)
      宮本達雄、ロイバエカテリーナ、阿久津シルビア夏子、山本 卓、工藤美樹、田代 聡、松浦伸也
    • Organizer
      第59回日本放射線影響学会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15082
  • [Presentation] Molecular basis of human BUBR1 deficiency, a central protein of the spindle assembly checkpoint2016

    • Author(s)
      Shinya Matsuura, Tatsuo Miyamoto, Kosuke Hosoba, Hiroshi Ochiai, Takashi Yamamoto, Makoto Furutani-Seiki
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-06
    • Invited
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] WDR62/MCPH2 mutations identified in patients with primary microcephaly by a combined approach of exome sequencing and genome editing technology2016

    • Author(s)
      Nobunori Masatsuna, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Oohashi, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      ICHG2016 (Kyoto)
    • Place of Presentation
      Kyoto
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] A combined approach of exome sequencing and genome editing identified WDR62/MCPH2 mutations in patients with primary microcephaly2016

    • Author(s)
      Tatsuo Miyamoto, Yoshinori Masatsuna, Akihiro Fukumitsu, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Ohashi, Shinya Matsuura
    • Organizer
      ASHG2016 (Vancouver)
    • Place of Presentation
      Vancouver(カナダ)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04321
  • [Presentation] PLK1-dependent phosphorylation of WDR62, a causative gene product for primary microcephaly, maintains mitotic spindle orientation2016

    • Author(s)
      Tatsuo Miyamoto, Kosuke Hosoba, Yoshinori Masatsuna, Akihiro Fkumitsu, Silvia Natsuko Akustu, Kosuke Hosoba, Hiroyuki Morino, Hideshi Kawakami, Takashi Yamamoto, Kenji Shimizu, Hirofumi Oohashi, Shinya Matsuura
    • Organizer
      The 28th CDB meeting Cilia and Centrosomes
    • Place of Presentation
      神戸
    • Year and Date
      2016-11-27
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 分裂期キナーゼPLK1による真性小頭症原因遺伝子産物WDR62のリン酸化を介した細胞分裂軸制御機構2016

    • Author(s)
      福満啓博、政綱宜規、Silvia Natsuko Akutsu、細羽康介、山本卓、宮本達雄、松浦伸也
    • Organizer
      第39回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2016-11-30
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ゲノム編集法を用いたNBS1-SNP導入細胞の作製と放射線感受性の評価2016

    • Author(s)
      柳原啓見、宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、山本卓、松浦伸也
    • Organizer
      日本放射線影響学会第59回大会
    • Place of Presentation
      広島
    • Year and Date
      2016-10-26
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Introduction of SNPs in human cultured cellsusing single-base-pair editing technique.2015

    • Author(s)
      Miyamoto T, Ochiai H, Yamamoto T, Shinya Matsuura
    • Organizer
      Conference on Transposition and Genome Engineering 2015
    • Place of Presentation
      奈良
    • Year and Date
      2015-11-17
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ゲノム編集法を用いた放射線感受性の個人差を規定する遺伝的素因の同定2015

    • Author(s)
      宮本達雄、Ekaterina Royba、Silvia Natsuko Akutsu、柳原啓見、落合博、工藤美樹、田代聡、山本卓、松浦伸也
    • Organizer
      第40回中国地区放射線影響研究会
    • Place of Presentation
      東広島
    • Year and Date
      2015-07-17
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Custom-made system for estimation individual difference of radiosensitivity.2015

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura S
    • Organizer
      The 74th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      名古屋
    • Year and Date
      2015-10-08
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] 真性小頭症で同定されたWDR62/MCPH2遺伝子変異とゲノム編集技術を利用した疾患モデル細胞の作製2015

    • Author(s)
      宮本達雄、政綱宜規、Silvia Natsuko Akutsu、森野豊之、川上秀史、山本卓、清水健司、大橋博文、松浦伸也
    • 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-15K15017
  • [Presentation] 真性小頭症で同定されたWDR62/MCPH2遺伝子変異による細胞分裂軸制御不全2015

    • Author(s)
      政綱宜規、Silvia Natsuko Akutsu、細羽康介、森野豊之、川上秀史、山本卓、清水健司、大橋博文、宮本達雄、松浦伸也
    • Organizer
      第38回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Year and Date
      2015-12-01
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Generation of SNP-knock-in Cells Using CRISPR/Cas9 System for Elucidation of the Effect on Radiation Sensitivity.2015

    • Author(s)
      Yanagihara H, Miyamoto T, Royba E, Akutsu SN, Matsuura S
    • Organizer
      The 15th International Congress of Radiation Research
    • Place of Presentation
      Kyoto
    • Year and Date
      2015-05-25
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] ヒト培養細胞における1本鎖DNAを用いた簡便な放射線感受性候補SNP導入法の開発2015

    • Author(s)
      宮本達雄、柳原啓見、落合博、山本卓、松浦伸也
    • Organizer
      第56回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2015-06-07
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Inducible Cas9/CRISPR System as a Tool to Study DNA Damage Response.2015

    • Author(s)
      Miyamoto T, Oka T, Nakano S, Matsuura S
    • Organizer
      The 15th International Congress of Radiation Research
    • Place of Presentation
      Kyoto
    • Year and Date
      2015-05-25
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15017
  • [Presentation] Regulation of various DNA damage responses through complex formations of NBS1.2015

    • Author(s)
      Kobayashi J, Saito Y, Kato A, Oliveira DV, Yanagihara H, Matsuura S, Komatsu K.
    • Organizer
      16th Ataxia-Telangiectasia Workshop
    • Place of Presentation
      Beijing
    • Year and Date
      2015-10-11
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26241013
  • [Presentation] 放射線感受性SNPの定量的評価系構築のためのヒト培養細胞における一塩基編集法の開発2014

    • Author(s)
      宮本達雄、落合 博、Ekaterina Royba、Silvia Natsuko Akutsu、松浦伸也
    • Organizer
      第55回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Year and Date
      2014-06-01
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Individual difference of radiosensitivity detected by cytokinesis-block micronucleus assay2014

    • Author(s)
      Ekaterina Royba, Silvia Natsuko Akutsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      The third international symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      Hiroshima
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 放射線感受性SNPの定量的評価系構築のためのヒト培養細胞における一塩基編集法の開発2014

    • Author(s)
      宮本達雄、落合 博、Ekaterina Royba、Silvia Natsuko Akutsu、松浦伸也
    • Organizer
      第55回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Year and Date
      2014-06-01
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Functional evaluation system of single nucleotide polymorphisms linked to radiosensitivity using genomic editing technology2014

    • Author(s)
      atsuo Miyamoto, Hiroshi Ochiai, Ekaterina Royba, Shinya Matsuura
    • Organizer
      The fourth international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      Hiroshima
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 紫外線損傷応答における放射線修復因子NBS1の機能とマウスモデルの作製 第57回日本放射線影響学会2014

    • Author(s)
      柳原啓見、加藤晃弘、斎藤裕一朗、小林純也、松浦伸也、小松賢志
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Functional evaluation system of single nucleotide polymorphisms linked to radiosensitivity using genomic editing technology2014

    • Author(s)
      Tatsuo Miyamoto, Hiroshi Ochiai, Ekaterina Royba, Shinya Matsuura
    • Organizer
      The fourth international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      Hiroshima
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Individual difference of radiosensitivity detected by cytokinesis-block micronucleus assay2014

    • Author(s)
      Ekaterina Royba, Silvia Natsuko Akutsu, Tatsuo Miyamoto, Shinya Matsuura
    • Organizer
      The third international symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      Hiroshima
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 放射線感受性SNPの定量的評価系構築のためのヒト培養細胞における一塩基編集法の開発2014

    • Author(s)
      宮本達雄、落合 博、Ekaterina Royba、Silvia Natsuko Akutsu、松浦伸也
    • Organizer
      第55回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Year and Date
      2014-06-01
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 分裂期キネシンKIF2Aを介した細胞増殖に共役した繊毛退縮機構2013

    • Author(s)
      宮本 達雄、細羽 康介、落合 博、佐久間 哲史、山本 卓、松浦 伸也
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Kinetics of radiation-induced DNA double strand break rejoining in DNA repair deficient cells2013

    • Author(s)
      Ohara, M., Sakamoto, Y., Fukasaku, J., Komatsu, K., Matsuura, S., Tauchi, H.
    • Organizer
      The 3rd international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 酸化ストレスによるATMキナーゼの活性制御2013

    • Author(s)
      小林純也、藤本浩子、奥井理予、加藤竹雄、Lavin Martin、松浦伸也、小松賢志
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 人工ヌクレアーゼによる一塩基編集法を利用したPCS (MVA)症候群の遺伝子間領域変異の同定2013

    • Author(s)
      松浦伸也、落合 博、宮本達雄、金井昭教、 細羽康介、佐久間哲史、浅見 恵子、小川 淳、渡辺 輝浩、梶井 正、山本 卓
    • Organizer
      第58回日本人類遺伝学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Identification of an extragenic mutation of BUB1B gene for PCS (MVA) syndrome and functional analysis using TAL effector nucleases2013

    • Author(s)
      H Ochiai, A Kanai, K Hosoba, S Kume, T Sakuma, T Kajii, T Yamamoto, S Matsuura
    • Organizer
      63rd annual meeting of American Society of Human Genetics
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 細胞増殖シグナル依存的な一次繊毛抑制過程におけるPLK1-KIF2A経路の役割2013

    • Author(s)
      宮本達雄、細羽康介、落合博、佐久間哲史、山本卓、松浦伸也
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 細胞増殖に連動した分裂期キネシン分子KIF2Aによる繊毛退縮機構2013

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第54回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] PCS(MVA)症候群の遺伝子外変異の同定と人工ヌクレアーゼを用いた機能解析2013

    • Author(s)
      松浦伸也、落合博、宮本達雄、金井昭教、細羽康介、佐久間哲史、野路澄晴、山本卓
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Artificial nuclease-based targeted DSB introduction and its application2013

    • Author(s)
      Ochiai, H., Miyamoto, T., Kanai, A., Hosoba, K., Sakuma, T., Yamamoto, T., Matsuura, S.
    • Organizer
      The 3rd international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 細胞増殖に連動した分裂期キネシン分子KIF2Aによる繊毛退縮機構2013

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第54回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト培養細胞における一塩基編集技術:放射線感受性SNPの定量的評価系確立への試み2013

    • Author(s)
      宮本達雄、落合博、久米悟士、佐久間哲史、山本卓、松浦伸也
    • Organizer
      第38回中国地区放射線影響研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] PCS(MVA)症候群の遺伝子外変異の同定と人工ヌクレアーゼを用いた機能解析2013

    • Author(s)
      松浦伸也、落合博、宮本達雄、金井昭教、細羽康介、佐久間哲史、野路澄晴、山本卓
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Artificial nuclease-based targeted DSB introduction and its application2013

    • Author(s)
      Ochiai, H., Miyamoto, T., Kanai, A., Hosoba, K., Sakuma, T., Yamamoto, T., Matsuura, S.
    • Organizer
      The 3rd international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 人工ヌクレアーゼを用いたヒト培養細胞での一塩基編集:放射線感受性SNPの評価系構築への試み2013

    • Author(s)
      宮本 達雄、落合 博、金井昭教、久米悟士、佐久間 哲史、山本 卓、松浦 伸也
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] ヒト培養細胞における一塩基編集技術:放射線感受性SNPの定量的評価系確立への試み2013

    • Author(s)
      宮本達雄、落合博、久米悟士、佐久間哲史、山本卓、松浦伸也
    • Organizer
      第38回中国地区放射線影響研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Kinetics of radiation-induced DNA double strand break rejoining in DNA repair deficient cells2013

    • Author(s)
      Ohara, M., Sakamoto, Y., Fukasaku, J., Komatsu, K., Matsuura, S., Tauchi, H.
    • Organizer
      The 3rd international symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 分裂期キネシンKIF2Aを介した細胞増殖に共役した繊毛退縮機構2013

    • Author(s)
      宮本 達雄、細羽 康介、落合 博、佐久間 哲史、山本 卓、松浦 伸也
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト分裂期チェックポイント欠損症における繊毛形成異常2013

    • Author(s)
      宮本 達雄、細羽 康介、落合 博、松浦 伸也
    • Organizer
      2013年生体運動研究合同班会議
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 人工ヌクレアーゼを用いたヒト培養細胞での一塩基編集:放射線感受性SNPの評価系構築への試み2013

    • Author(s)
      宮本 達雄、落合 博、金井昭教、久米悟士、佐久間 哲史、山本 卓、松浦 伸也
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト培養細胞における一塩基編集技術:放射線感受性SNPの定量的評価系確立への試み2013

    • Author(s)
      宮本達雄、落合 博、久米悟士、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第38回中国地区放射線影響研究会
    • Place of Presentation
      広島
    • Year and Date
      2013-07-26
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Identification of an extragenic mutation of BUB1B gene for PCS (MVA) syndrome and functional analysis using TAL effector nucleases2013

    • Author(s)
      H Ochiai, A Kanai, K Hosoba, S Kume, T Sakuma, T Kajii, T Yamamoto, S Matsuura
    • Organizer
      63rd annual meeting of American Society of Human Genetics
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 細胞増殖シグナル依存的な一次繊毛抑制過程におけるPLK1-KIF2A経路の役割2013

    • Author(s)
      宮本達雄、細羽康介、落合博、佐久間哲史、山本卓、松浦伸也
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 酸化ストレスによるATMキナーゼの活性制御2013

    • Author(s)
      小林純也、藤本浩子、奥井理予、加藤竹雄、Lavin Martin、松浦伸也、小松賢志
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 人工ヌクレアーゼによる一塩基編集法を利用したPCS (MVA)症候群の遺伝子間領域変異の同定2013

    • Author(s)
      松浦伸也、落合 博、宮本達雄、金井昭教、 細羽康介、佐久間哲史、浅見 恵子、小川 淳、渡辺 輝浩、梶井 正、山本 卓
    • Organizer
      第58回日本人類遺伝学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 細胞増殖に連動した分裂期キネシン分子KIF2Aによる繊毛退縮機構2013

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第54回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2013-06-02
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] ヒト分裂期チェックポイント欠損症における繊毛形成異常2013

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      2013年生体運動研究合同班会議
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] KIF2A phosphorylation by PLK1 regulates primary cilia disassembly2013

    • Author(s)
      Hosoba, K., Miyamoto, T., Ochiai, H., Matsuura, S.
    • Organizer
      The 2nd international symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] KIF2A phosphorylation by PLK1 regulates primary cilia disassembly2013

    • Author(s)
      Hosoba, K., Miyamoto, T., Ochiai, H., Matsuura, S.
    • Organizer
      The 2nd international symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Role of MRE11/RAD50/NBS1 complex in regulation of ATM activation2012

    • Author(s)
      Kobayashi, J., Fujimoto, H., Okui, M., Kato, T., Matsuura, S., Komatsu, K.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Ciliary disassembly by the mitotic kinase PLK1 in a spindle assembly checkpoint-deficiency syndrome2012

    • Author(s)
      Miyamoto, T., Hosoba K., Ochiai, H., Matsuura, S.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Invited
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] TALENの効率的作製法および評価法の確立と改良型ヌクレアーゼの開発2012

    • Author(s)
      佐久間哲史、細井紗弥佳、落合博、宮本達雄、松浦伸也、坂本尚昭、野地澄晴、山本卓
    • Organizer
      第1回ゲノム編集研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] ゲノム安定性を司る紡錘体チェックポイント因子BUBR1の間期中心体における機能2012

    • Author(s)
      宮本 達雄、細羽 康介、落合 博、松浦 伸也
    • Organizer
      第53回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト遺伝性疾患の病因変異と考えられる遺伝子間領域に存在する一塩基多型(SNP)のZFNを利用した機能解析2012

    • Author(s)
      落合博、宮本達雄、細羽康介、山本卓、松浦伸也
    • Organizer
      第1回ゲノム編集研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] ゲノム安定性を司る紡錘体チェックポイント因子BUBR1の間期中心体における2012

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第53回原子爆弾後障害研究会
    • Place of Presentation
      長崎
    • Year and Date
      2012-06-03
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 人工ヌクレアーゼTALENを利用したDSB導入とその応用72012

    • Author(s)
      落合博、宮本達雄、細羽康介、佐久間哲史、野地澄睛、山本卓、松浦伸也
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Functional link between Nbs1 and Ku70 protein in cellular response to DNA damage induced by ionizing radiation2012

    • Author(s)
      Tauchi, H., Ohara, M., Abe, H., Matsuura, S., Komatsu, K.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes a ciliopathy with chromosomal instability2012

    • Author(s)
      Miyamoto, T., Kikuchi, A., Furutani-Seiki, M., Matsuura, S.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] 人工ヌクレアーゼを利用した一塩基置換の導入2012

    • Author(s)
      落合博、宮本達雄、細羽康介、佐久間哲史、野地澄晴、山本卓、松浦伸也
    • Organizer
      第2回ゲノム編集研究会
    • Place of Presentation
      岡崎
    • Year and Date
      2012-09-20
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 分裂期キネシンを標的とした単極性紡錘体形成の誘導法の探索二2012

    • Author(s)
      宮本達雄、細羽康介、落合博、松浦伸也
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Establishment of human disease model cell lines by introduction of intergenic single nucleotide mutation using artificial nucleases2012

    • Author(s)
      Ochiai, H., Miyamoto, T., Kanai, A., Hosoba, K., Sakuma, T., Noji, S., Yamamoto, T., Matsuura, S.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Invited
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Role of Histone modification in radiation-induced cellular response following low dose-rate irradiation2012

    • Author(s)
      KobayashiJ, FujimotoH, MatsuuraS
    • Organizer
      International symposium 50^th anniversary of RIRBM
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Targeted genome editing using transcription activator-like effector nucleases (TALENs)2012

    • Author(s)
      Sakuma, T., Hosoi, S., Ochiai, H., Miyamoto, T., Matsuura, S., Sakamoto, N., Yamamoto, T.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Targeted genome editing using transcription activator-like effector nucleases (TALENs)2012

    • Author(s)
      Sakuma, T., Hosoi, S., Ochiai, H., Miyamoto, T., Matsuura, S., Sakamoto, N., Yamamoto, T.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Role of Histone modification in radiation-induced cellular response following low dose-rate irradiation2012

    • Author(s)
      Kobayashi, J., Fujimoto, H., Matsuura, S.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Role of Histone modification in radiation-induced cellular response following low dose-rate irradiation2012

    • Author(s)
      Kobayashi, J., Fujimoto, H., Matsuura, S.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 低線量率放射線細胞応答おけるヒストン修飾の役割2012

    • Author(s)
      小林純也_1、藤本浩子、松浦伸也、小松賢志
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes a ciliopathy with chromosomalinstability2012

    • Author(s)
      MiyamotoT, KikuchiA, Furutani-SeikiM, MatsuuraS
    • Organizer
      International symposium 50^th anniversary of RIRBM
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 低線量率放射線細胞応答おけるヒストン修飾の役割2012

    • Author(s)
      小林 純也、藤本 浩子、松浦 伸也、小松 賢志
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] TALENの効率的作製法および評価法の確立と改良型ヌクレアーゼの開発2012

    • Author(s)
      佐久間哲史、細井紗弥佳、落合博、宮本達雄、松浦伸也、坂本尚昭、野地澄晴、山本卓
    • Organizer
      第1回ゲノム編集研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Functional link between Nbs1 and Ku70 protein in cellular response to DNA damage induced by ionizing radiation2012

    • Author(s)
      Tauchi, H., Ohara, M., Abe, H., Matsuura, S., Komatsu, K.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Functional link between Nbs1 and Ku70 protein in cellular response to DNA damage induced by ionizing radiation2012

    • Author(s)
      TauchiH, OharaM, AbeH, MatsuuraS, KomatsuK
    • Organizer
      International symposium 50th anniversary of RIRBM
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 分裂期キネシンを標的とした単極性紡錘体形成の誘導法の探索2012

    • Author(s)
      宮本 達雄、細羽 康介、落合 博、松浦 伸也
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Role of MRE11/RAD50/NBS1 complex in regulation of ATM activation2012

    • Author(s)
      Kobayashi, J., Fujimoto, H., Okui, M., Kato, T., Matsuura, S., Komatsu, K.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 人工ヌクレアーゼを利用した一塩基置換の導入2012

    • Author(s)
      落合 博、宮本 達雄、細羽 康介、 佐久間 哲史、野地 澄晴、山本 卓、松浦 伸也
    • Organizer
      第2回ゲノム編集研究会
    • Place of Presentation
      岡崎
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Establishment of human disease model cell lines by introduction of intergenic single nucleotide mutation using artificial nucleases2012

    • Author(s)
      Ochiai, H., Miyamoto, T., Kanai, A., Hosoba, K., Sakuma, T., Noji, S., Yamamoto, T., Matsuura, S.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡(招待講演)
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] ヒト遺伝性疾患の病因変異と考えられる遺伝子間領域に存在する一塩基多型(SNP)のZFNを利用した機能解析2012

    • Author(s)
      落合博、宮本達雄、細羽康介、山本卓、松浦伸也
    • Organizer
      第1回ゲノム編集研究会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Ciliary disassembly by the* mitotic kinase PLKl in a spindle assembly checkpoint-deficiency syndrome2012

    • Author(s)
      Miyamoto, T., Hosoba K., Ochiai, H., Matsuura, S.
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡(招待講演)
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 人工ヌクレアーゼTALENを利用したDSB導入とその応用2012

    • Author(s)
      落合 博、宮本 達雄、細羽 康介、 佐久間 哲史、野地 澄晴、山本 卓、松浦 伸也
    • Organizer
      第55回日本放射線影響学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes a ciliopathy with chromosomal instability2012

    • Author(s)
      Miyamoto, T., Kikuchi, A., Furutani-Seiki, M., Matsuura, S.
    • Organizer
      International symposium 50th anniversary of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Targeted genome editing using transcription activator-like effector nucleases(TALENs)2012

    • Author(s)
      SakumaT, HosoiS, OchiaiH, MiyamotoT, MatsuuraS, SakamotoN, YamamotoT
    • Organizer
      International symposium 50^th anniversary of RIRBM
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Zinc-finger nuclease-mediated targeted transgene integration enables quantitative imaging of endogenous gene expression in living sea urchin embryo2011

    • Author(s)
      chiai, H., Jujita, K., Nishikawa, M., Suzuki, K., Matsuura, S., Miyamoto, T., Sakuma, T., Sakamoto, N., Shibata, T., Yamamoto, T
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] TALEヌクレアーゼ作製法の確立2011

    • Author(s)
      落合博、佐久間哲史、宮本達雄、野地澄晴、松浦伸也、山本卓
    • Organizer
      自然科学研究機構・基礎生物学研究所共同利用共同研究・研究会
    • Place of Presentation
      岡崎
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Mole cularpa thogenesiso fanove lMRE11Amutatio nintwo patients with Nijmegen breakagesyndro me-likesevere microce phaly2011

    • Author(s)
      MiyamotoT, MatsumotoY, SakamotoH, NakazawaY, OgiT, MatsuuraS
    • Organizer
      The First RIRMB Internatio nalSympo sium
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 産業医活動における放射能の知識2011

    • Author(s)
      松浦伸也
    • Organizer
      平成23年度第2回日医認定産業医研修会
    • Place of Presentation
      広島
    • Year and Date
      2011-09-15
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 紡錘体チェックポイント分子BUBR1はG0期において繊毛形成を制御する2011

    • Author(s)
      宮本達雄、菊池章、古谷-清木誠、松浦伸也
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 紡錘体チェックポイント分子BUBR1はG0期において繊毛形成を制御する2011

    • Author(s)
      宮本達雄、菊池章、古谷-清木誠、松浦伸也
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] BUBR, a mitotic spindle checkpoint regulator, plays a role of ciliogenesis in G0 phase2011

    • Author(s)
      MiyamotoT, PorazinskiS, HuijiaW, ShimizuA, KajiiT, KikuchiA, Furutani-SeikiM, MatsuuraS
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 繊毛病としての染色分体早期解離(PCS)症候群2011

    • Author(s)
      宮本達雄、古谷-清木誠、松浦伸也
    • Organizer
      第56回日本人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] TALEヌクレアーゼ作製法の確立2011

    • Author(s)
      落合博、佐久間哲史、宮本達雄、野地澄晴、松浦伸也、山本卓
    • Organizer
      自然科学研究機構・基礎生物学研究所共同利用共同研究・研究会
    • Place of Presentation
      岡崎
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] BUBR1, a mitotic spindle checkpoint regulator, plays a role of ciliogenesis in G0 phase2011

    • Author(s)
      Miyamoto, T., Porazinski, S., Huijia, W., Shimizu, A., Kajii, T., Kikuchi, A., Furutani-Seiki M., Matsuura, S.
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 分裂期チェックポイント分子BUBR1は脊椎動物における繊毛形成を制御する2011

    • Author(s)
      宮本達雄、PORAZINSKI Sean、WANG Huijia、清水厚志、梶井正、菊池章、古谷-清木誠、松浦伸也
    • Organizer
      第54回日本放射線影響学会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 分裂期チェックポイント分子BUBR1欠損による高発がん性と繊毛病2011

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      第52回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2011-06-05
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 分裂期チェックポイント分子BUBR1は脊椎動物における繊毛形成を制御する2011

    • Author(s)
      宮本達雄、PORAZINSKI Sean、WANG Huijia、清水厚志、梶井正、菊池章、古谷-清木誠、松浦伸也
    • Organizer
      第54回日本放射線影響学会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] Molecular pathogenesis of a novel MRE11A mutation in two patients with Nijmegen breakage syndrome-like severe microcephaly.2011

    • Author(s)
      T Miyamoto, Y Matsumoto, H Sakamoto, Y Nakazawa, T Ogi, S Matsuura
    • Organizer
      The First RIRMB International Symposium
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 繊毛病としての染色分体早期解離(PCS)症候群2011

    • Author(s)
      宮本達雄、古谷-清木誠、松浦伸也
    • Organizer
      第56回日本人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] TALEヌクレアーゼ作製法の確立2011

    • Author(s)
      落合博、佐久間哲史、宮本達雄、野地澄晴、松浦伸也、山本卓
    • Organizer
      自然科学研究機構・基礎生物学研究所共同利用共同研究・研究会「遺伝子機能解析の最先端
    • Place of Presentation
      岡崎
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] DNA修復障害・染色体不安定に起因するヒト遺伝病2011

    • Author(s)
      松浦伸也
    • Organizer
      第146回染色体研究会
    • Place of Presentation
      東京(招待講演)
    • Year and Date
      2011-06-11
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] 分裂期チェックポイント分子BUBR1欠損による高発がん性と繊毛病2011

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      第52回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2011-06-05
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] DNA修復障害・染色体不安定に起因するヒト遺伝病2011

    • Author(s)
      松浦伸也
    • Organizer
      第146回染色体研究会
    • Place of Presentation
      東京(招待講演)
    • Year and Date
      2011-06-11
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] BUBR1, a mitotic spindle checkpoint regulator, plays a role of ciliogenesis in G0 phase2011

    • Author(s)
      Miyamoto, T., Porazinski, S., Huijia, W., Shimizu, A., Kajii, T., Kikuchi, A., Furutani-Seiki M., Matsuura, S.
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PUBLICLY-22019026
  • [Presentation] DNA修復障害・染色体不安定に起因するヒト遺伝病2011

    • Author(s)
      松浦伸也
    • Organizer
      第146回染色体研究会
    • Place of Presentation
      東京
    • Year and Date
      2011-06-11
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Zinc-finger nuclease-mediated targeted transgene integration enables quantitative imaging of endogenous gene expression in living sea urchin embryo2011

    • Author(s)
      chiai, H., Jujita, K., Nishikawa, M., Suzuki, K., Matsuura, S., Miyamoto, T., Sakuma, T., Sakamoto, N., Shibata, T., Yamamoto, T
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] MRE11遺伝子変異を原因とする重度小頭症におけるATM依存性アポトーシスの充進2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、松浦伸也
    • Organizer
      日本放射線影響学会第53回大会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Mre11遺伝子変異を原因とする重度小頭症の分子病理2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、松浦伸也
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 地域と連携したHBOC遺伝子検査の導入に向けた活動報告2010

    • Author(s)
      音部玲子、加瀬佳寿江、家護谷五月、兵頭麻希、大原正裕、村上茂、横山恭之、檜山桂子、丸山博文、檜山英三、松浦伸也、小林正夫
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 筋萎縮性側索硬化症の原因遺伝子Optineurinの同定2010

    • Author(s)
      丸山博文、森野豊之、伊東秀文、和泉唯信、鎌田正紀、松浦伸也、阿部康二、青木正志、萩原弘一、川上秀史
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Mre11遺伝子変異を原因とする重度小頭症におけるATM依存性アポトーシスの亢進2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、松浦伸也
    • Organizer
      日本放射線影響学会第53回大会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 筋萎縮性側索硬化症の原因遺伝子Optineurinの同定2010

    • Author(s)
      丸山博文、森野豊之、伊東秀文、和泉唯信、鎌田正紀、松浦伸也、阿部康二、青木正志、萩原弘一、川上秀史
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] ナイミーヘン症候群に類似した2症例で同定したMRE11A遺伝子変異とその機能解析2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、泉秀樹、松浦伸也
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 地域と連携したHBOC遺伝子検査の導入に向けた活動報告2010

    • Author(s)
      音部玲子、加瀬佳寿江、家護谷五月、兵頭麻希、大原正裕、村上茂,横山恭之、檜山桂子、丸山博文、檜山英三、松浦伸也、小林正夫
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Mosaic Variegated Aneuploidy(Premature Chromatid Separation) Syndrome2010

    • Author(s)
      Matsuura S
    • Organizer
      Joint Egyptian-Japanese Scientific Workshop “A New Era of Genetic Diseases”
    • Place of Presentation
      Cairo, Egypt
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] Geneand functio ninmicro cephaly2010

    • Author(s)
      Matsuura S
    • Organizer
      Joint Egyptian-Japanese Scientific Workshop"A New Eraof Genetic Diseases"
    • Place of Presentation
      Cairo, Egypt
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] ナイミーヘン症候群に類似した2症例で同定したMRE11A遺伝子変異とその機能解析2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、泉秀樹、松浦伸也
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 紡錘体チェソクポイント欠損症における細胞分裂軸異常の解析2010

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] MRE11遺伝子変異を原因とする重度小頭症の分子病理2010

    • Author(s)
      宮本達雄、松本祥幸、坂本裕美、松浦伸也
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      埼玉
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 紡錘体チェックポイント欠損症における細胞分裂軸異常の解析2010

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-22651018
  • [Presentation] 遺伝性小頭症MOPDIIで同定されたPericentrin遺伝子変異と細胞周期異常2009

    • Author(s)
      坂本裕美、宮本達雄、松本祥幸、小沢浩、長谷川奉延、松浦伸也
    • Organizer
      日本人類遺伝学会第54回大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] NBS1修飾によるDNA損傷誘発アポトーシスの制御2009

    • Author(s)
      田内広、小林純也、松浦伸也、小松賢志
    • Organizer
      第68回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 中心体構成分子Pericentrin変異による遺伝性小頭症に見られる多様な細胞周期異常2009

    • Author(s)
      宮本達雄、坂本裕美、松本祥幸、松浦伸也
    • Organizer
      日本放射線影響学会第52回大会
    • Place of Presentation
      広島
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] PCS (MVA) syndrome and dual roles of BubR12009

    • Author(s)
      Matsuura, S.
    • Organizer
      The 25^<th> Radiation Biology Center International Symposium
    • Place of Presentation
      Kyoto
    • Year and Date
      2009-12-01
    • Data Source
      KAKENHI-PROJECT-20012036
  • [Presentation] 染色分体早期解離(PCS)症候群の臨床症状の分子病態2009

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Pericentrin変異を原因とする遺伝性小頭症の患者はG2/M期とG1期の細胞周期制御に異常を示す2009

    • Author(s)
      坂本裕美、宮本達雄、松本祥幸、松浦伸也
    • Organizer
      第50回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2009-06-07
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 染色分体早期解離(PCS)症候群に見られる一次繊毛機能不全の分子病態2009

    • Author(s)
      宮本達雄、松浦伸也
    • Organizer
      日本人類遺伝学会第54回大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] AT様疾患におけるDNA損傷応答の解析2009

    • Author(s)
      小林純也、松浦伸也、小松賢志
    • Organizer
      第68回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] PCS (MVA) syndrome and dual roles of BubR12009

    • Author(s)
      Matsuura, S.
    • Organizer
      The 25^<th> Radiation Biology Center International Symposium
    • Place of Presentation
      Kyoto
    • Year and Date
      2009-12-18
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 中心体タンパク質Pericentrinによる細胞周期制御機構の解析2009

    • Author(s)
      坂本裕美、宮本達雄、松本祥幸、松浦伸也
    • Organizer
      第34回中国地区放射線影響研究会
    • Place of Presentation
      広島
    • Year and Date
      2009-07-29
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 中心体タンパク質Pericentrin欠損によって生じる遺伝性小頭症MOPDHに見られる細胞周期異常2009

    • Author(s)
      坂本裕美、宮本達雄、松本祥幸、松浦伸也
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] NBS1が制御する新規のDNA損傷誘発アポトーシス経路2008

    • Author(s)
      田内広、小林純也、坂本修一、松浦伸也、小松賢志
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] 高発がん性遺伝病による染色体恒常性メカニズムの解明2008

    • Author(s)
      松浦伸也
    • Organizer
      第12回癌の分子細胞生物学懇話会
    • Place of Presentation
      横浜
    • Year and Date
      2008-02-19
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] セッケル症候群患者で同定した変異型MRE11の機能解析2008

    • Author(s)
      松本祥幸、坂本裕美、泉秀樹、宮本達雄、松浦伸也
    • Organizer
      第31回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] New role of BubR1 : BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells2008

    • Author(s)
      Hideki Izumi, Yoshiyuki Matsumoto, Tatsuro Ikeuchi, Saya Hideyuki, Tadashi Kajii, Shinya Matsuura
    • Organizer
      The Fifth International Symposium
    • Place of Presentation
      Radiation and Cancer, Hiroshima
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1が制御する新規のDNA損傷誘発アポトーシス経路2008

    • Author(s)
      田内広、小林純也、坂本修一、松浦伸也、小松賢志
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] MRE11遺伝子変異を原因とするセツケル症候群の2例2008

    • Author(s)
      松浦伸也
    • Organizer
      第53回日本人類遺伝学会
    • Place of Presentation
      横浜市
    • Year and Date
      2008-09-29
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Regulation of bipolar spindle formation by Polo-like kinase1 (Plk1)2008

    • Author(s)
      泉秀樹、松本祥幸、松浦伸也
    • Organizer
      第31回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] MRE11遺伝子変異を原因とするセッケル症候群の2家系2008

    • Author(s)
      松浦伸也、松本祥幸、泉秀樹、坂本裕美
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1のアルキル化剤によるDNA損傷修復における役割2008

    • Author(s)
      藤本浩子、小林純也、松浦伸也、小松賢志
    • Organizer
      日本放射線影響学会第51回大会
    • Place of Presentation
      北九州
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] MRE11遺伝子はセッケル症候群の発症に関与している2008

    • Author(s)
      松本祥幸、坂本裕美、泉秀樹、宮本達雄、松浦伸也
    • Organizer
      日本放射線影響学会第5回大会
    • Place of Presentation
      北九州
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] MRE11遺伝子変異を原因とするセッケル症候群の2例2008

    • Author(s)
      松浦伸也、松本祥幸、坂本裕美、泉秀樹、奥章三、平元東、椎木俊秀、藤沢由樹、大橋博文、酒見好弘
    • Organizer
      日本人類遺伝学会第53回大会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] MRE11遺伝子はセッケル症候群の発症に関与している2008

    • Author(s)
      松本祥幸、坂本裕美、泉秀樹、宮本達雄、松浦伸也
    • Organizer
      日本放射線影響学会第51回大会
    • Place of Presentation
      北九州
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] MRE11遺伝子変異を原因とするセソケル症候群の2家系2008

    • Author(s)
      松浦伸也、松本祥幸、泉秀樹、坂本裕美
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Plk1による両極性紡錘体形成の制御機構2008

    • Author(s)
      泉秀樹、松本祥幸、松浦伸也
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1のアルキル化剤によるDNA損傷修復における役割2008

    • Author(s)
      藤本浩子、小林純也、松浦伸也、小松賢志
    • Organizer
      日本放射線影響学会第51回大会
    • Place of Presentation
      北九州
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Plk1による両極性紡錘体形成の制御機構2008

    • Author(s)
      泉秀樹、松本祥幸、松浦伸也
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-20390100
  • [Presentation] Regulation of bipolar spindle formation by Polo-like kinase1 (Plk1)2008

    • Author(s)
      泉秀樹、松本祥幸、松浦伸也
    • Organizer
      第31回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] MRE11遺伝子変異を原因とするセッケル症候群の2例2008

    • Author(s)
      松浦伸也、松本祥幸、坂本裕美、泉秀樹、奥章三、平元東、椎木俊秀、藤沢由樹、大橋博文、酒見好弘
    • Organizer
      日本人類遺伝学会第53回大会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] セッケル症候群患者で同定した変異型Mre11の機能解析2008

    • Author(s)
      松本祥幸、坂本裕美、泉秀樹、宮本達雄、松浦伸也
    • Organizer
      第31回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubR1 deficiency causes centrosome amplification in PCS (MVA) syndrome2007

    • Author(s)
      Shinya Matsuura, Hideki Izumi, Yoshiyuki Matsumoto, Tatsuro Ikeuchi, Hideyuki Saya, Tadashi Kajii
    • Organizer
      57th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      San Diego U.S.A(concurrent platform sessions)
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] Dual roles of BubR1-the underlying protein for cancer-prone PCS syndrome-in chromosome segregation2007

    • Author(s)
      Shinya Matsuura, Hideki Izumi, Yoshiyuki Matsumoto, Tatsuro Ikeuchi, Hideyuki Saya, Tadashi Kajii
    • Organizer
      66th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      Yokohama(invited)
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1 is required for DNA damage-induced apoptosis2007

    • Author(s)
      Hiroshi Tauchi, Junya Kobayashi, Shuichi Sakamoto, Shinya Matsuura, Kenshi Komatsu
    • Organizer
      66^<th> Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      Yokohama
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1によるBax活性化を通じたDNA損傷誘発アポトーシスの制御2007

    • Author(s)
      飯島健太、村中千寿子、小林純也、坂本修一、小松賢志、松浦伸也、田内広
    • Organizer
      第30回日本分子生物学会年会・第80回日本生化学会大会合同大会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubRl deficiency causes centrosome amplification in PCS (MVA) syndrome.2007

    • Author(s)
      Shinya Matsuura, et. al.
    • Organizer
      57th Annual Meeting of the American Society of HumanGenetics
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-18012034
  • [Presentation] DNA二重鎖切断修復におけるNBS1、ATMの役割2007

    • Author(s)
      小林純也、坂本修一、森島賢一、飯島健太、松浦伸也、田内広、小松賢志
    • Organizer
      第30回日本分子生物学会年会・第80回日本生化学会大会合同大会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] Domain analysis of the Nbs1 gene in murine cells2007

    • Author(s)
      Ahikiro Kato, Hiromi Yanagihara, Shinya Matsuura, Tstsuo Noda, Kenshi Komatsu
    • Organizer
      66^<th> Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      Yokohama
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubR1は間期の中心体に局在し、Polo-like kinase 1(Plk1)の活性を制御して中心体の過剰複製を抑制する2007

    • Author(s)
      泉秀樹、松本祥幸、池内達郎、梶井正、松浦伸也
    • Organizer
      第48回原子爆弾後障害研究会
    • Place of Presentation
      広島
    • Year and Date
      2007-06-03
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] 紫外線損傷応答におけるNBS1の機能解析2007

    • Author(s)
      柳原啓見、鎚田謙、小林純也、森俊雄、松浦伸也、小松賢志
    • Organizer
      日本放射線影響学会第50回大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS1のアルキル化剤によるDNA損傷修復における役割2007

    • Author(s)
      岡本優紀、藤本浩子、小林純也、松浦伸也、小松賢志
    • Organizer
      日本放射線影響学会第50回大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] NBS患者細胞とNbs1欠損マウス細胞の解析2007

    • Author(s)
      初村裕英、加藤晃弘、松浦伸也、小松賢志
    • Organizer
      日本放射線影響学会第50回大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubR1は間期の中心体に局在し、Polo-like kinase 1(Plk1)の活性を制御して中心体の過剰複製を抑制する2007

    • Author(s)
      泉秀樹、松本祥幸、池内達郎、佐谷秀行、梶井正、松浦伸也
    • Organizer
      日本人類遺伝学会第52回大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] Variegated translocation mosaicismを呈する染色体不安定症候群の1例2007

    • Author(s)
      松本浩、松本祥幸、森島賢一、松浦伸也
    • Organizer
      2007年秋季ヘリカーゼ研究会
    • Place of Presentation
      加賀
    • Year and Date
      2007-11-24
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] DNA二重鎖切断損傷におけるNBS1とヒストンH2AXの役割2007

    • Author(s)
      小林純也、坂本修一、飯島健太、森島賢一、中村恭介、松浦伸也、田内広、小松賢志
    • Organizer
      日本放射線影響学会第50回大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubR1 localizes to centrosomes and suppresses centrosomes amplification via regulating Plk1 activity in interphase cells2007

    • Author(s)
      Hideki Izumi, Yoshiyuki Matsumoto, Tatsuro Ikeuchi, Hideuki Saya, Tadashi Kajii, Shinya Matsuura
    • Organizer
      66th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      Yokohama
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] DNA二重鎖切断修復におけるNBS1とATMの役割2007

    • Author(s)
      中村恭介、坂本修一、飯島健太、望月大輔、勅使河原計介、小林純也、松浦伸也、田内広、小松賢志
    • Organizer
      日本放射線影響学会第50回大会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] BubR1は間期の中心体に局在し、Polo-like kinase 1(Plk1)の活性を制御して中心体の過剰複製を抑制する2007

    • Author(s)
      泉秀樹、松本祥幸、池内達郎、佐谷秀行、梶井正、松浦伸也
    • Organizer
      第30回日本分子生物学会年会・第80回日本生化学会大会合同大会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-19590334
  • [Presentation] Chromosomal analysis in myelodysplastic syndrome and acute myeloid leukemia cell lines through the cytokinesis block micronucleus assay (CBMA) and cytogenetic study

    • Author(s)
      Akutsu SN, Royba E, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] NBS1 initiates UV damage tolerance

    • Author(s)
      Yanagihara H, Kato A, Matsuura S, Kobayashi J, Komatsu K
    • Organizer
      The 30th RBC-NIRS International symposium
    • Place of Presentation
      京都
    • Year and Date
      2015-02-20 – 2015-02-21
    • Invited
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Identification of an extragenic mutation of BUB1B gene for PCS (MVA) syndrome and functional analysis using TAL effector nucleases

    • Author(s)
      Miyamoto T,Ochiai H, Kanai A, Hosoba K, Kume S, Sakuma T, Kajii T, Yamamoto T, Matsuura S
    • Organizer
      The 63rd annual meeting of American Society of Human Genetics
    • Place of Presentation
      ボストン, USA
    • Year and Date
      2013-10-22 – 2013-10-24
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 紫外線損傷応答における放射線修復因子NBS1の機能とマウスモデルの作製 第57回日本放射線影響学会

    • Author(s)
      柳原啓見、加藤晃弘、斎藤裕一朗、小林純也、松浦伸也、小松賢志
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Constitutive activation of cell proliferation coupled-ciliary disassembly in a spindle assembly checkpoint-deficiency syndrome

    • Author(s)
      Miyamoto T, Hosoba K, Ochiai H, Royba E, Matsuura S
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト紡錘体チェックポイント欠損症における細胞増殖に共役した一次繊毛退縮制御の破綻による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、Ekaterina Royba、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Constitutive activation of cell proliferation coupled-ciliary disassembly in a spindle assembly checkpoint-deficiency syndrome

    • Author(s)
      Miyamoto T, Hosoba K, Ochiai H, Royba E, Matsuura S
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 次世代シーケンサーとゲノム編集法を用いた非コード領域の原因変異の解析

    • Author(s)
      松浦伸也、宮本達雄、落合 博、浅見恵子、小川 淳、渡辺輝浩、梶井 正、山本 卓
    • Organizer
      第59回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Invited
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura M
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura M
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 横紋筋肉腫治療終了後、長期寛解を維持している染色分体早期解離(PCS)症候群の姉弟例

    • Author(s)
      角田治美、沖本由理、種山雄一、古舘和季、岩井潤、東本恭幸、四本克己、菱木知郎、小松秀吾、堀江弘、宮本達雄、松浦伸也
    • Organizer
      第56回日本小児血液・がん学会
    • Place of Presentation
      岡山
    • Year and Date
      2014-11-28 – 2014-11-30
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Chromosomal analysis in myelodysplastic syndrome and acute myeloid leukemia cell lines through the cytokinesis block micronucleus assay (CBMA) and cytogenetic study

    • Author(s)
      Akutsu SN, Royba E, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 酸化ストレスによるATMキナーゼの活性制御

    • Author(s)
      小林純也、藤本浩子、奥井理予、加藤竹雄、Lavin Martin、松浦伸也、小松賢志
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Year and Date
      2013-10-18 – 2013-10-20
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 次世代シーケンサーとゲノム編集法を用いた非コード領域の原因変異の解析

    • Author(s)
      松浦伸也、宮本達雄、落合 博、浅見恵子、小川 淳、渡辺輝浩、梶井 正、山本 卓
    • Organizer
      第59回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Invited
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 次世代シーケンサーとゲノム編集法を用いた非コード領域の原因変異の解析

    • Author(s)
      松浦伸也、宮本達雄、落合 博、浅見恵子、小川 淳、渡辺輝浩、梶井 正、山本 卓
    • Organizer
      第59回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Invited
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Constitutive activation of cell proliferation coupled-ciliary disassembly in a spindle assembly checkpoint-deficiency syndrome

    • Author(s)
      Miyamoto T, Hosoba K, Ochiai H, Royba E, Matsuura S
    • Organizer
      The 5th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2015-03-02 – 2015-03-03
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Chromosomal analysis in myelodysplastic syndrome and acute myeloid leukemia cell lines through the cytokinesis block micronucleus assay (CBMA) and cytogenetic study

    • Author(s)
      Akutsu SN, Royba E, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] ヒト分裂期チェックポイント欠損症におけるPLK1-KIF2A経路の亢進による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] ヒト紡錘体チェックポイント欠損症における細胞増殖に共役した一次繊毛退縮制御の破綻による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、Ekaterina Royba、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] ヒト分裂期チェックポイント欠損症におけるPLK1-KIF2A経路の亢進による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 人工ヌクレアーゼによる一塩基編集法を利用したPCS (MVA)症候群の遺伝子間領域変異の同定

    • Author(s)
      松浦伸也、落合 博、宮本達雄、金井昭教、細羽康介、佐久間哲史、浅見恵子、小川 淳、渡辺輝浩、梶井 正、山本 卓
    • Organizer
      第58回日本人類遺伝学会
    • Place of Presentation
      仙台
    • Year and Date
      2013-11-20 – 2013-11-23
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 人工ヌクレアーゼを用いたヒト培養細胞での一塩基編集:放射線感受性SNPの評価系構築への試み

    • Author(s)
      宮本達雄、落合 博、金井昭教、久米悟士、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第56回日本放射線影響学会
    • Place of Presentation
      青森
    • Year and Date
      2013-10-18 – 2013-10-20
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] PCS(MVA)症候群の遺伝子外変異の同定と人工ヌクレアーゼを用いた機能解析

    • Author(s)
      松浦伸也、落合博、宮本達雄、金井昭教、細羽康介、佐久間哲史、野路澄晴、山本卓
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2013-10-03 – 2013-10-05
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Functional evaluation system of single nucleotide polymorphisms linked to radiosensitivity using genomic editing technology

    • Author(s)
      Miyamoto T, Ochiai H, Royba R, Matsuura S
    • Organizer
      The 4th International symposium of RIRBM, Hiroshima University
    • Place of Presentation
      広島
    • Year and Date
      2014-02-13 – 2014-02-14
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 横紋筋肉腫治療終了後、長期寛解を維持している染色分体早期解離(PCS)症候群の姉弟例

    • Author(s)
      角田治美、沖本由理、種山雄一、古舘和季、岩井潤、東本恭幸、四本克己、菱木知郎、小松秀吾、堀江弘、宮本達雄、松浦伸也
    • Organizer
      第56回日本小児血液・がん学会
    • Place of Presentation
      岡山
    • Year and Date
      2014-11-28 – 2014-11-30
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] NBS1 initiates UV damage tolerance

    • Author(s)
      Yanagihara H, Kato A, Matsuura S, Kobayashi J, Komatsu K
    • Organizer
      The 30th RBC-NIRS International symposium
    • Place of Presentation
      京都
    • Year and Date
      2015-02-20 – 2015-02-21
    • Invited
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] ヒト紡錘体チェックポイント欠損症における細胞増殖に共役した一次繊毛退縮制御の破綻による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、Ekaterina Royba、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] Individual difference of radiosensitivity evaluated by semi-automatic cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Yanagihara H, Ochiai H, Kudo Y, Tashiro S, Miyamoto T, Matsuura M
    • Organizer
      The 4th International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2015-02-14 – 2015-02-15
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] Individual difference of radiosensitivity detected by cytokinesis-block micronucleus assay

    • Author(s)
      Royba E, Akutsu SN, Miyamoto T, Matsuura M
    • Organizer
      The 3rd International symposium of Phoenix Leader Education Program for Renaissance from Radiation Disaster
    • Place of Presentation
      広島
    • Year and Date
      2014-02-13 – 2014-02-14
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] NBS1 initiates UV damage tolerance

    • Author(s)
      Yanagihara H, Kato A, Matsuura S, Kobayashi J, Komatsu K
    • Organizer
      The 30th RBC-NIRS International symposium
    • Place of Presentation
      京都
    • Year and Date
      2015-02-20 – 2015-02-21
    • Invited
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 分裂期キネシンKIF2Aを介した細胞増殖に共役した繊毛退縮機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Year and Date
      2013-12-03 – 2013-12-06
    • Data Source
      KAKENHI-PUBLICLY-25113521
  • [Presentation] 横紋筋肉腫治療終了後、長期寛解を維持している染色分体早期解離(PCS)症候群の姉弟例

    • Author(s)
      角田治美、沖本由理、種山雄一、古舘和季、岩井潤、東本恭幸、四本克己、菱木知郎、小松秀吾、堀江弘、宮本達雄、松浦伸也
    • Organizer
      第56回日本小児血液・がん学会
    • Place of Presentation
      岡山
    • Year and Date
      2014-11-28 – 2014-11-30
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] ヒト分裂期チェックポイント欠損症におけるPLK1-KIF2A経路の亢進による繊毛病発症機構

    • Author(s)
      宮本達雄、細羽康介、落合 博、松浦伸也
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Data Source
      KAKENHI-PROJECT-24651222
  • [Presentation] 紫外線損傷応答における放射線修復因子NBS1の機能とマウスモデルの作製

    • Author(s)
      柳原啓見、加藤晃弘、斎藤裕一朗、小林純也、松浦伸也、小松賢志
    • Organizer
      第57回日本放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Data Source
      KAKENHI-PROJECT-24310043
  • [Presentation] 細胞増殖シグナル依存的な一次繊毛抑制過程におけるPLK1-KIF2A経路の役割

    • Author(s)
      宮本達雄、細羽康介、落合 博、佐久間哲史、山本 卓、松浦伸也
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2013-10-03 – 2013-10-05
    • Data Source
      KAKENHI-PUBLICLY-25113521
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