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HAYASHI Kenshi  林 健志

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… Alternative Names

林 建志  ハヤシ ケンシ

林健 志  ハヤシケン シ

北川 知行  キタカ゛ワ トモユキ

林 健志  ハヤシ ケンシ

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Researcher Number 00019671
Other IDs
Affiliation (based on the past Project Information) *help 2013: 九州大学, 生体防御医学研究所, 名誉教授
2012: 九州大学, 生体防御医学研究所, 特任教授
2009: 九州大学, 生体防御医学研究所, 教授
2008 – 2009: 九州大学, 生体防御医学研究所, 特任教授
2007 – 2009: 九州大学, 生体防御医学研究所, 学術研究員 … More
2001 – 2007: 九州大学, 生体防御医学研究所, 教授
2006: 生態防御医学研究所附属遺伝子情報実験センター, 教授
2004: 九州大学, 生体防御医学研究科, 教授
2003: 九州大学, 生態防御医学研究所, 教授
2000: Faculty of Med., KYUSHU UNIVERSITY, Prof., 遺伝実験情報施設, 教授
1993 – 2000: 九州大学, 遺伝情報実験施設, 教授
1997 – 1998: 九州大学, 遺伝子情報実験施設, 教授
1990: (財)癌研究会癌研究所, 病理, 副所長
1989: 国立がんセンター研究所, 室長
1989: 国立がんセンター研究所, 腫瘍遺伝子研究部, 研究員
1987 – 1988: 国立がんセンター研究所, 腫瘍遺伝子研究部, 室長
1987: 国立がんセンター研究所, 腫瘍遺伝子研究部 室長
1986: 国立がんセ, その他, その他
1986: 国立がんセンター研究所, 生化学部, 室長
1985: 国立がんセンター, その他, その他 Less
Review Section/Research Field
Except Principal Investigator
Biological Sciences / Ophthalmology / 基礎ゲノム科学 / Human pathology / Genetics/Genome dynamics / Cerebral neurosurgery / Psychiatric science
Keywords
Principal Investigator
プロモーター / c-myc / 肝がん / アフラトキシン【B_1】 / がん遺伝子c-erbB-2 / がん抑制遺伝子WT1 / △FosB / がん遺伝子EVI-1 / 軟部悪性腫瘍 / 蛍光標識PCR-SSCP法 … More / Gフリーカセット / 無細胞転写系 / 再生肝 / 転写制御 / 合成オリゴヌクレオチド / G-freeカセット / in vitro転写実験 / ポリA付加シグナル / C-myc mRNA / C-myc遺伝子 / FeLV / アデノウイルスE4 / ニワトリcーfos / マウス赤白血病細胞 / ヌタロチオネインプロモーター / mRNAの半減期 / ラット肝がん細胞 / ラウス肉腫ウィルス / アデノウィルスE1A / ヒトメタロチオネインプロモーター / mRNAの代謝回転 / 遺伝子増殖 / 発がんプロモーター / 転写活性化 / シクロヘキシミド / 塩基配列 / 胃がん / 増幅 / C-myc / ATM / 癌抑制遺伝子 / PLACE-SSCP法 / LOH / SNP / 蛍光PCR-SSCP法 / 転写因子YB-1 / 平滑筋肉腫 / 尿路腫瘍 / p53 / Kid / EVI-1 / hMTH1 / Zink finger … More
Except Principal Investigator
SSCP / 遺伝子診断 / がん / 遺伝子解析 / PCR / キャピラリー電気泳動 / 家族性滲出性硝子体網膜症 / SNP / 遺伝子 / ゲノム / 一塩基多型 / ハプロタイプ / アポトーシス / 全身性エリテマトーデス / レーザー蛍光検出 / キャピラリーアレイ電気泳動 / DNA複製 / 突然変異 / がん遺伝子 / B10 / 網膜疾患 / TSPAN12 / 網膜剥離 / WNTシグナル / 未熟児網膜症 / がん抑制遺伝子 / PLACE-SSCP / 一塩基多型(SNP) / SLE / マイクロチップ / 細胞周期 / 前癌病変 / familial optic atrophy / retinitis pigmentosa / familial exudative vitreoretinopathy / autosomal recessive / microsatellite marker / genetic diagnosis / human genome / retinal disease / 常染色体劣性遺伝 / 家族性視神経萎縮 / 網膜色素変性症 / 常染色体劣性 / マイクロサテライトマーカ / ヒトゲノム / natural selection / polymorphism / 自然選択 / 多型 / Diabetes / high blood pressure / circulatory organ / A genome / Allergic asthma / DNAチップ / リュウマチ / 多因子疾患 / 喘息 / アレルギー / 高血圧 / 糖尿病 / 循環器・高血圧 / アレルギー喘息 / growth factor / molecular biology / pathology / tumor progression / metastasis / sarcoma / soft tissue / bone / 骨軟部肉腫 / 増殖因子 / 癌関連遺伝子 / MDM2 / P53 / 平滑筋肉腫 / C-MET / HGF / ABI PRISM 7700 / APC遺伝子 / cyclin D1 / β-catenin / 軟部デスモイド腫瘍 / 滑膜肉腫 / 成長因子 / 分子生物学 / 病理 / 腫瘍進展 / 転移 / 肉腫 / 骨軟部腫瘍 / SCAN method / Endometrial Cancer / Early onset ataxia / Hereditary defness DFNB8 / Whole Sequence / Chromosome 11 / Chromosome 22 / Chromosome 21 / 改良型SSCP法 / 福山型筋ジストロフィー / SCA2遺伝子 / HLA遺伝子群 / 免疫グロブリン遺伝子 / ダウン症必須領域 / 11番染色体物理地図 / 高速大規模プラスミド調整機 / 変異検出法 / 福山型先天性ジストロフィー / 自己免疫疾患APECED / MHCクラスI領域 / シークエンス地図 / 11q13領域 / Transcriptional sequencing / SKY法の改良 / HLAクラス1遺伝子群 / シークエンス解析 / S番染色体特異的BACクローン / ヒト11q22-23領域 / SKY法 / Bardet-Biedl症候群 / TGFβ1遺伝子 / 進行性骨異形症 / ヒト21番染色体 / 11q23 / Sotos症候群 / 遺伝性聾DFNB8・B10 / ドラフトシーケンス / 染色体カラーバンディング法 / 子宮体癌 / 遺伝性脊髄小脳変性症 / 遺伝性聾DFNB8 / 全塩基配列 / 11番染色体 / 22番染色体 / 21番染色体 / テレオシジンの合成発癌遺伝子 / テレオシジンB / テレオシジンA / 発癌プロモーター / 遺伝子多様性 / ヒトゲノム構造多様性 / Norrie病 / 血管内皮成長因子 / 網膜 / 小児 / VEGF / 血管内皮増殖因子 / NDP遺伝子 / Coats病 / SuperTopflash / PAX3 / Stickler症候群 / 新生血管 / ノリエ病 / 遺伝子発現 / 10番染色体 / LOH / SNPs / グリオーマ / 全身性エリテマトーデス(SLE) / ゲノムワイドな関連解析 / ゲノムワイドな確定ハプロタイプ / 胞状奇胎 / ソフトウェア「QSNP lite」 / 高精度アレル頻度決定 / SSCP解析 / CpGアイランド / DHaploDB / 日本人確定ハプロタイプ / プールDNAによるゲノムワイド関連解析 / QSNPlite / 全胞状奇胎 / 確定ハプロタイプ / 関連解析 / データベース / 自己免疫疾患 / 疾患関連解析 / ゲノムインフォーマティックス / 遺伝医学 / 生命倫理 / ゲノムインフォーマティック / 病原微生物 / 有用微生物 / 多型解析 / 分子遺伝学 / 社会医学 / 微生物 / 臨床 / 産業微生物ゲノム / 微生物ゲノム / メディカルインフォマティクス / ヒトゲノム配列再解析 / ゲノムワイド関連解析 / 疾患関連遺伝子 / ハプロタイプ解析 / 遺伝解析 / 中枢神経系 / 細胞内情報伝達 / セカンドメッセンジャー系 / 精神分裂病 / ゲノタイピング / 相関解析 / セカンドメッセンジャーシステム / 細胞内情報伝達システム / 統合失調症 / caspase-8 / 慢性関節リウマチ / 遺伝病 / 遺伝的不安定性 / 自然突然変異 / DNAポリメラーゼ / DNA組換え / DNA / 酸素ラジカル / ノックアウトマウス / 繰り返し配列 / フレームシフト / DNA修復 / 酵素ラジカル / ミスマッチ修復 / 複製エラー / 非放射化SSCP / レーザー蛍光検出装置 / DNA付加体 / イニシエ-タ- / イニシエ-ション / DNA付加体形成 / イニシエーター / イニシエーション / 遺伝子導入 / マウス赤白血病細胞 / cーmyb / cーmyc / 癌遺伝子 / 分化の決定 / 細胞分化 / タンパク質工学 / 遺伝子発現制御機構 / 遺伝子クローニング / グルタチオンSートランスフェラーゼ / 酵素変異 / 前がん病変 / 肝発がん Less
  • Research Projects

    (40 results)
  • Research Products

    (85 results)
  • Co-Researchers

    (89 People)
  •  Elucidation of structural variations in Japanese genome by massively parallel sequencing of haploid genome

    • Principal Investigator
      TAHIRA Tomoko
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Genetics/Genome dynamics
    • Research Institution
      Kyushu University
  •  Pathogenesisof Coats disease: establishing a concept of pediatric retinal detachment

    • Principal Investigator
      KONDO Hiroyuki
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Ophthalmology
    • Research Institution
      University of Occupational and Environmental Health, Japan
  •  Genetic study for diseases of insufficient development of retinal vessels

    • Principal Investigator
      KONDO Hiroyuki
    • Project Period (FY)
      2007 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Ophthalmology
    • Research Institution
      Fukuoka University
  •  Analysis of allele-specific expression and its correlation with haplotypes

    • Principal Investigator
      TAHIRA Tomoko
    • Project Period (FY)
      2006 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      基礎ゲノム科学
    • Research Institution
      Kyushu University
  •  DEVELOPMENT OF QUANTITATIVE METHODS FOR SINGLE NUCLEOTIDE POLYMORPHISMS ANALYSIS AND ITS APPLICATION IN MEDICAL GENETICSPrincipal Investigator

    • Principal Investigator
      TAHIRA Tomoko, 林 健志
    • Project Period (FY)
      2005 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  一塩基多型を用いた10番染色体の解析-新規がん抑制遺伝子同定への試み-

    • Principal Investigator
      溝口 昌弘
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Cerebral neurosurgery
    • Research Institution
      Kyushu University
  •  (DNAプール)PLACE‐SSCP法による自己免疫疾患の病因遺伝子の網羅的探索

    • Principal Investigator
      堀内 孝彦
    • Project Period (FY)
      2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  Applied Genomics

    • Principal Investigator
      TSUJI Shoji
    • Project Period (FY)
      2004 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      The University of Tokyo
  •  (DNAプール)PLACE-SSCP法による自己免疫疾患の病因遺伝子の網羅的探索

    • Principal Investigator
      堀内 孝彦
    • Project Period (FY)
      2003
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  Detection of natural selection in Japanese population by analyzing distribution of polymorphisms

    • Principal Investigator
      TAHIRA Tomoko
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      基礎ゲノム科学
    • Research Institution
      KYUSHU UNIVERSITY
  •  Development of a comprehensive system of linkage analysis for identification of hereditary retinal disease genes using genomic information

    • Principal Investigator
      KONDO Hiroyuki
    • Project Period (FY)
      2003 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Ophthalmology
    • Research Institution
      Fukuoka University
  •  (DNAプール)PLACE-SSCP法による自己免疫疾患の病因遺伝子の網羅的探索

    • Principal Investigator
      堀内 孝彦
    • Project Period (FY)
      2002
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  精神分裂病における新しい細胞内セカンドメッセンジャー標的遺伝子群の遺伝解析

    • Principal Investigator
      川嵜 弘詔
    • Project Period (FY)
      2002 – 2004
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Psychiatric science
    • Research Institution
      Kyushu University
  •  新しい遺伝子多型検出システムを用いた免疫・アレルギー疾患の病因遺伝子の探索

    • Principal Investigator
      堀内 孝彦
    • Project Period (FY)
      2001
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  がん化におけるcaspase-8機能異常の解析

    • Principal Investigator
      堀内 孝彦
    • Project Period (FY)
      2001
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  新しい遺伝子多型検出システムによる免疫・アレルギー性疾患の病因遺伝子の解析

    • Principal Investigator
      HORIUCHI Takahiko
    • Project Period (FY)
      2000
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Kyushu University
  •  Genomic analysis on genetic factors of human diseases and elucidation of their molecular mechanisms

    • Principal Investigator
      SUGANO Sumio
    • Project Period (FY)
      2000 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      The University of Tokyo
  •  マイクロチップ化キャピラリー電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1998
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      The University of Tokushima
  •  一塩基多型を利用した癌抑制遺伝子異常のDNA診断Principal Investigator

    • Principal Investigator
      林 建志
    • Project Period (FY)
      1998
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Kyushu University
  •  マイクロチップ化キャピラリー電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1997
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      The University of Tokushima
  •  Molecular and pathologic analysis of growth factors on the proliferating activities and metastases in bone and soft tissue sarcomas

    • Principal Investigator
      TSUNEYOSHI Masazumi
    • Project Period (FY)
      1997 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      Human pathology
    • Research Institution
      KYUSHU UNIVERSITY
  •  転写制御遺伝子群の発癌への関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kyushu University
  •  キャピラリーアレイ電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe Pharmaceutical University
  •  突然変異の分子病態

    • Principal Investigator
      真木 寿治
    • Project Period (FY)
      1996 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Nara Institute of Science and Technology
  •  Human Genome Analysis

    • Principal Investigator
      OHKI Misao
    • Project Period (FY)
      1996 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      National Cancer Center Research Institute
  •  転写制御遺伝子群の発癌への関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kyushu University
  •  キャピラリーアレイ電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe Pharmaceutical University
  •  転写制御遺伝子群の発癌への関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kyushu University
  •  キャピラリーアレイ電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe Pharmaceutical University
  •  キャピラリー電気泳動によるがんの高性能遺伝子診断システムの開発

    • Principal Investigator
      馬場 嘉信
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Kobe Pharmaceutical University
  •  化学発癌におけるイニシエ-ション機構の解析

    • Principal Investigator
      石川 隆俊
    • Project Period (FY)
      1990
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      The University of Tokyo
  •  肝化学発癌過程の前癌細胞における遺伝子および遺伝子発現の異常の解析

    • Principal Investigator
      佐藤 清美
    • Project Period (FY)
      1989
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Hirosaki University
  •  細胞分化のプログラミングと癌遺伝子

    • Principal Investigator
      帯刀 益夫
    • Project Period (FY)
      1989
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Tohoku University
  •  化学発癌におけるイニシエーション機構の解析

    • Principal Investigator
      石川 隆俊
    • Project Period (FY)
      1988 – 1990
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      The University of Tokyo
  •  c-myc遺伝子の転写制御機構Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1988
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East
  •  化学発がん過程におけるCーmyc遺伝子活性化の関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East
  •  C-myc遺伝子の転写制御Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East
  •  化学発癌におけるc-myc遺伝子活性化の関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1985
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East
  •  化学発がん過程におけるc-myc遺伝子活性化の関与Principal Investigator

    • Principal Investigator
      林 健志
    • Project Period (FY)
      1985 – 1987
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East
  •  発癌プロモーターによって誘導される遺伝的・非可逆的変化について

    • Principal Investigator
      藤木 博太
    • Project Period (FY)
      1984 – 1986
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      National Cancer Center Research Institute and Research Center for Innovative Oncology, National Cancer Center Hospital East

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  • [Book] SNP ゲノタイピング(総論) 「DNAチップ/マイクロアレイ臨床応用の実際」(油谷浩幸編)2008

    • Author(s)
      久木田洋児, 林健志
    • Publisher
      メディカルATゥ
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Book] メンデルからDNAを経てゲノムへ バイオ研究マスターシリーズ「遺伝子工学集中マスター」2006

    • Author(s)
      林健志
    • Publisher
      羊土社
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] A definitive haplotype map of structural variation determined by microarray analysis of duplicated haploid genomes2014

    • Author(s)
      Tahira T, Yahara K, Kukita Y, Higasa K, Kato K, Wake N, Hayashi K.
    • Journal Title

      Genomics Data

      Volume: 印刷中 Pages: 55-59

    • DOI

      10.1016/j.gdata.2014.04.006

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24657005
  • [Journal Article] 重症未熟児網膜症に対しベバシズマブ硝子体内投与を行った症例の検討2011

    • Author(s)
      有田直子、林英之、内尾英一、近藤寛之
    • Journal Title

      臨床眼科

      Volume: (65) Pages: 1225-1229

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591956
  • [Journal Article] 成人と小児における増殖硝子体網膜症の手術成績2010

    • Author(s)
      小山田剛、近藤寛之、林英之、内尾英一
    • Journal Title

      臨眼

      Volume: (64) Pages: 543-546

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591956
  • [Journal Article] A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy number variation events.2010

    • Author(s)
      Kukita Y, Yahara K, Tahira T, Higasa K, Sonoda M, Yamamoto K, Kato K, Wake N, Hayashi K.
    • Journal Title

      Am.J.Hum.Genet. 86(6)

      Pages: 918-928

    • NAID

      120002239171

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] 成人と小児における増殖硝子体網膜症の手術成績2010

    • Author(s)
      小山田剛、近藤寛之、林英之、内尾英一
    • Journal Title

      臨床眼科

      Volume: 64 Pages: 543-546

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591956
  • [Journal Article] 壮年期発症の眼底所見が軽微な錐体杆体ジストロフィの1例2009

    • Author(s)
      原潤、近藤寛之、林英之、内尾英一、藤原恵理子、林研
    • Journal Title

      臨眼 63

      Pages: 1155-1158

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Aggressive posterior retinopathy of prematurityの臨床経過と治療成績2009

    • Author(s)
      有田直子、近藤寛之、林英之、内尾英一
    • Journal Title

      臨眼 63

      Pages: 1081-1085

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Evaluation of haplotype inference using definitive haplotype data obtained from complete hydatidiform moles, and its significance for the analyses of positively selected regions.2009

    • Author(s)
      Higasa K, Kukita Y, Kato K, Wake N, Tahira T, Hayashi K.
    • Journal Title

      PLoS Genetics 5(5)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity2009

    • Author(s)
      Kondo H, Arita N, Osato M, Hayashi H, et al.
    • Journal Title

      Am J Ophthalmol 147

      Pages: 661-666

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity.2009

    • Author(s)
      Kondo H, Arita N, Ohsato M, Hayashi H, Uchio E, Oshima K
    • Journal Title

      Am J Ophthalmol 147

      Pages: 661-666

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Novel mutation in PAX3 gene in Waardenburg syndrome accompanied by unilateral macular degeneration.2009

    • Author(s)
      Kozawa M, Kondo H, Tahira T, Hayashi K, Uchio E
    • Journal Title

      Eye 23

      Pages: 1619-1621

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Estimation of SNP allele frequencies by SSCP analysis of poolepooleolepooleleNA.2009

    • Author(s)
      Tahira T, Kukita Y, Higasa K, Okazaki Y, Yoshinaga A, Hayashi K.
    • Journal Title

      Methods in Molecular Biology 578

      Pages: 193-207

    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.2008

    • Author(s)
      Qin M, Kondo H, Tahira T, Hayashi K.
    • Journal Title

      Human Genetics 122(6)

      Pages: 615-623

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus.2008

    • Author(s)
      Miyagawa H, Yamai M, Sakaguchi D, Kiyohara C, Tsukamoto H, Kimoto Y, Nakamura T, Lee J-H, Tsai C-Y, Chiang B-L, Nagasawa K, Harada M, Tahira T, Hayashi K, Horiuchi T.
    • Journal Title

      Rheumatology 47(2)

      Pages: 158-164

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy2008

    • Author(s)
      Qin M, Kondo H, Tahira T, Hayashi K
    • Journal Title

      Hum Genet 122

      Pages: 615-623

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.2008

    • Author(s)
      Qin M, Kondo H, Tahira T, Hayashi K
    • Journal Title

      Hum Genet 122

      Pages: 615-623

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Prevalence of copy number neutral LOH in glioblastomas revealed by genome-wide analysis of laser- microdissected tissues.2008

    • Author(s)
      Kuga D, Mizoguchi M, Guan Y, Hata N, Yoshimoto K, Shono T, Suzuki SO, Kukita Y, Tahira T, Nagata S, Sasaki T, Hayashi K.
    • Journal Title

      Neuro Oncol 10(6)

      Pages: 995-1003

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] 遺伝子診断を行ったノリエ病2家系の臨床像2008

    • Author(s)
      宮河あやこ, 近藤寛之, 林英之, 他
    • Journal Title

      眼科臨床紀要 1

      Pages: 453-456

    • NAID

      10024295594

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Narrowing the regions of allelic losses of chromosome 1p36 in meningioma tissues by an improved SSCP analysis.2008

    • Author(s)
      Guan Y, Hata N, Kuga D, Yoshimoto K, Mizoguchi M, Shono T, Suzuki S, Tahira T, Kukita Y, Higasa K, Yokoyama N, Nagata S, Iwaki T, Sasaki T, Hayashi K.
    • Journal Title

      Int.J.Cancer 122(8)

      Pages: 1820-1826

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus2008

    • Author(s)
      Miyagawa, H, Yamai, M, Sakaguchi, D, Kiyohara, C, Tsukamoto, H, Kimoto, Y, Nakamura, T, Lee, J-H, Tsai, C-Y, Chiang, B-L, Nagasawa, K, Harada, M, Tahira, T, Hayashi, K, and Horiuchi, T.
    • Journal Title

      Rheumatology 47

      Pages: 158-164

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] D-HaploDB : a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples.2007

    • Author(s)
      Higasa K, Miyatake K, Kukita Y, Tahira T, Hayashi K.
    • Journal Title

      Nucleic Acids Res. 35

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] 生後4週目に光凝固を行った色素失調症の1例2007

    • Author(s)
      淵上 あき, 近藤 寛之, 林 英之, 内尾 英一
    • Journal Title

      眼科臨床医報 101

      Pages: 529-531

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.2007

    • Author(s)
      Kondo H, Qin M, Kusaka S, Tahira T, Hasebe H, Hayashi H, Uchio E, Hayashi K.
    • Journal Title

      Invest.Ophthalmol.Vis.Sci 48(3)

      Pages: 1276-1282

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] D-HaploDB : a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples2007

    • Author(s)
      Higasa, K, Miyatake, K, Kukita, Y, Tahira, T, and Hayashi, K.
    • Journal Title

      Nucleic Acids Res. 35

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene.2007

    • Author(s)
      Kondo H, Qin M, Tahira T, Hayashi K.
    • Journal Title

      Ophthalmic Genetics 28(4)

      Pages: 220-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy2007

    • Author(s)
      Qin, M, Kondo, H, Uno, H, Tahira, T, and Hayashi, K
    • Journal Title

      Human Genetics 122

      Pages: 615-623

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] Severe Form of Familial Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene.2007

    • Author(s)
      Kondo H, Qin M, Tahira T, Uchio E, Hayashi K
    • Journal Title

      Ophthalmic Genet 28

      Pages: 220-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] D-HaploDB : a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples.2007

    • Author(s)
      Higasa, K., Miyatake K., Kukita, Y., Tahira, T., Hayashi, K.
    • Journal Title

      Nucleic Acids Res. 35 (Database issue)

    • Data Source
      KAKENHI-PROJECT-16065101
  • [Journal Article] Severe Form of Famital Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene2007

    • Author(s)
      Kondo H, Qin M, Tahira T, Uchio E, Hayashi K
    • Journal Title

      Ophthalmic Genet 28

      Pages: 220-223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Journal Article] Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy2006

    • Author(s)
      M.Qin, H.Kondo, H.Uno, E.Fujiwara, E.Uchio T.Tahira, K.Hayashi
    • Journal Title

      Mol Vis 12

      Pages: 485-491

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Optimization of capillary array electrophoresis single strand conformation polymorphism analysis for routine molecular diagnostics.2006

    • Author(s)
      Jespersgaard C, Larsen LA, Baba S, Kukita Y, Tahira T, Christiansen M, Vuust J, Hayashi K, Andersen PS.
    • Journal Title

      Electrophoresis 27(19)

      Pages: 3816-3822

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy.2006

    • Author(s)
      Qin M, Kondo H, Uno H, Fujiwara E, Uchino E, Tahira T, Hayashi K.
    • Journal Title

      Molecular Vision 12

      Pages: 485-491

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Novel OPA1 Mutations Identified in Japanese Pedigrees with Optic Atrophy2006

    • Author(s)
      Qin M, Kondo H, Uno H, Hayashi K, Fujiwara E, Uchio E, Tahira T, Hayashi K
    • Journal Title

      Mol Vis 12

      Pages: 485-491

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] QSNPlite, a software system for quantitative analysis of SNPs based on capillary array SSCP analysis.2006

    • Author(s)
      Tahira T, Okazaki Y, Miura K, Yoshinaga A, Masumoto K, Higasa K, Kukita Y, Hayashi K.
    • Journal Title

      Electrophoresis 27(19)

      Pages: 3869-3878

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] LRP5遺伝子変異による常染色体劣性家族性滲出性硝子体網膜症2006

    • Author(s)
      井上 浩利, 近藤 寛之, 宇野 英明, 秦 明輝, 林 健志
    • Journal Title

      日本学科紀要 57

      Pages: 139-142

    • NAID

      10018327732

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Periodicity of SNP distribution around transcription start sites.2006

    • Author(s)
      Higasa K, Hayashi K.
    • Journal Title

      BMC Genomics 7

      Pages: 66-66

    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Periodicity of SNP distribution around transcription start sites.2006

    • Author(s)
      Higasa K, Hayashi K
    • Journal Title

      BMC Genomics 7

      Pages: 66-66

    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Autosomal-recessive familial exudative vitreoretinopahty associated with LRP5 gene mutations2006

    • Author(s)
      T.Inoue, H.Kondo, H.Uno, M.Qin, K.Hayashi
    • Journal Title

      Folia Ophthalmol Jpn 57-2

      Pages: 139-142

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Genotype-phenotype correlation in familial exudative vitreoretinopathy or Norrie disease with mutations in the Norrie disease gene2006

    • Author(s)
      Hondo H, Qin M, Hayashi H, Uchio E, Tahira T, Hayashi K
    • Journal Title

      Invest Ophthalmol Vis Sci 47

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Allelic Losses of Chromosome 10 in Glioma Tissues Detected by Quantitative Single-Strand Conformation Polymorphism Analysis.2006

    • Author(s)
      Hata N, Yoshimoto K, Yokoyama N, Mizoguchi M, Shono T, Guan Y, Tahira T, Kukita Y, Higasa K, Nagata S, Iwaki T, Sasaki T, Hayashi K.
    • Journal Title

      Clin.Chem 52(3)

      Pages: 370-378

    • NAID

      120000986935

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] QSNPlite, a software system for quantitative analysis of SNPs based on capillary array SSCP analysis2006

    • Author(s)
      Tahira, T, Okazaki, Y, Miura, K, Yoshinaga, A, Masumoto, K, Higasa, K, Kukita, Y, and Hayashi, K.
    • Journal Title

      Electrophoresis 27

      Pages: 3869-3878

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] Genotype-phenotype correlation in familial exudative vitreoretinopathy or Norrie disease with mutations in the Norrie disease gen2006

    • Author(s)
      H.Kondo, M.Qin, H.Hayashi, E.Uchio, T.Tahira, K.Hayashi
    • Journal Title

      Invest Ophthalmol Vis Sci 47-E-4606

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics.2006

    • Author(s)
      Jespersgaard, C, Larsen, LA, Baba, S, Kukita, Y, Tahira, T, Christiansen, M, Vuust, J, Hayashi, K, and Andersen, PS.
    • Journal Title

      Electrophoresis 27

      Pages: 3816-3822

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005

    • Author(s)
      Kondo H, Qin M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Hum Mutal 26

      Pages: 104-112

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.2005

    • Author(s)
      Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H.
    • Journal Title

      Human Mutation 26(2)

      Pages: 104-112

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] FZD4 and/or LRP5 Gene Mutations in 14 Japanese Families With Familial Exudative Vitreoretinopathy2005

    • Author(s)
      H.Kondo, M.Qin, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
    • Journal Title

      Invest Ophthalmol Vis Sci 46-E-1797

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] FZD4 and/or LRP5 Gene Mutations in 14 Jaoanese Families With Familial Exudative Vitreoretinopathy2005

    • Author(s)
      Kondo H, Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Invest Ophthalmol Vis Sci 46

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] dbQSNP : a database of SNPs in human promoter regions with allele frequency information determined by single-strand conformation polymorphism- based method.2005

    • Author(s)
      Tahira T, Baba S, Higasa K, Kukita Y, Suzuki Y, Sugano S, Hayashi K.
    • Journal Title

      Human Mutation 26(2)

      Pages: 69-77

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] A Case of Incontinentia Pigmenti in Japan : Clinical Manifestations and Genetic Examination2005

    • Author(s)
      J.Y.Huang, H.Kondo, H.Hayashi, K.Oshima
    • Journal Title

      Invest Ophthalmol Vis Sci 46-E-1799

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Genome-wide detinitive haplotypes determined using a collection of complete hydatidirorm moles.2005

    • Author(s)
      Kukita, Y., Miyatake, K., Stokowski, R., Hinds, D.Higasa, K., Wake, N., Hirakawa, T., Kato, H., Matsuda, T., Pant, K., Cox, D., Taira, T., Hayashi, K.
    • Journal Title

      Genome Res 15

      Pages: 1511-1518

    • Data Source
      KAKENHI-PROJECT-16065101
  • [Journal Article] A Case of Incontinentia Pigmenti in Japan : Clinical Manifestations and Genetic Examination2005

    • Author(s)
      Huang JY, Kondo H, Hayashi H, Oshima K
    • Journal Title

      Invest Ophthalmol Vis Sci 46

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles.2005

    • Author(s)
      Kukita Y, Miyatake K, Stokowski R, Hinds D, Higasa K, Wake N, Hirakawa T, Kato H, Matsuda T, Pant K, Cox D, Tahira T, Hayashi K.
    • Journal Title

      Genome Res. 15(11)

      Pages: 1511-1518

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005

    • Author(s)
      M.Qin, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi, H.Kondo
    • Journal Title

      Hum Mutat 26-2

      Pages: 104-112

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Complexity of the phenotype-genotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005

    • Author(s)
      Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo
    • Journal Title

      Hum Mutat 26・2

      Pages: 104-112

    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Association of MBL gene polymorphisms with major bacterial infection in patients treated with high-dose chemotherapy and autologous PBSCT.2005

    • Author(s)
      Horiuchi T, Gondo H, Miyagawa H, Otsuka J, Inaba S, Nagafuji K, Takase K, Tsukamoto H, Koyama T, Mitoma H, Tamimoto Y, Miyagi Y, Tahira T, Hayashi K, Hashimura C, Okamura S, Harada M.
    • Journal Title

      Gene Immun 6(2)

      Pages: 162-166

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Journal Article] Search for mulations in patients with autosomal recessive retinitis pigmentosa using homozygosity-based screening with multiple locus?specific microsatellite markers2004

    • Author(s)
      Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Invest Ophthalmol Vis Sci 45

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers2004

    • Author(s)
      Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, et al.
    • Journal Title

      Invest Ophthalmol Vis Sci 45

      Pages: 4433-4439

    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Search for mutations in patients with autosomal recessive retinitis pigmentosa using homozygosity-based screening with multiple locus-specific micro satellite markers2004

    • Author(s)
      H.Kondo, M.Qin, A.Mizota, M.Kondo, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
    • Journal Title

      Invest Ophthalmol Vis Sci 45-E-5091

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa using mirosatellite markers2004

    • Author(s)
      H.Kondo, M.Qin, A.Mizota, M.Kondo, H.Hayashi, K.Hayashi, K.Oshima, T.Tahira, K.Hayashi
    • Journal Title

      Invest Ophthalmol Vis Sci 45-12

      Pages: 4433-4439

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentose using microsatellite markers2004

    • Author(s)
      Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Invest Ophthalmol Vis Sci 45

      Pages: 4433-4439

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Homozygosity-based screening with multiple locus-specific microsatellite markers toward the diagnosis of autosomal recessive retinitis pigmentosa2003

    • Author(s)
      H.Kondo, T.Tahira, A.Mizota, M.Kondo, H.Hayashi, K.Hayashi
    • Journal Title

      Am J Hum Genet 73(suppl)-s578

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Frizzled 4 gene(FZD4)mutations in patients with familial exudative vitreoretinopathy with variable expressivity2003

    • Author(s)
      H.Kondo, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
    • Journal Title

      Br J Ophthalmol 87-10

      Pages: 1291-1295

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Homozygosity-based screening with multiple locus-specific microsatellite markerstoward the diagnosis of autosomal recessive retinitis pigmentose2003

    • Author(s)
      Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Am J Hum Genet 73

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity2003

    • Author(s)
      Kondo H, Hayashi H, Oshima K, Tahira T, Hayashi K
    • Journal Title

      Br J Ophthalmol 87

      Pages: 1291-1295

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Estimation of SNP allele frequencies by SSCP analysis of pooled DNA

    • Author(s)
      Tahira T, Kukita Y, Higasa K, Okazaki Y, Yoshinaga A, Hayashi K.
    • Journal Title

      Methods in Molecular Biology (in press)

    • Data Source
      KAKENHI-PROJECT-18310131
  • [Journal Article] Novel OPAl mutations identified in Japanese pedigrees with optic atrophy

    • Author(s)
      Qin M, Kondo H, Uno H, Fujiwara E, Uchio E, Tahira T, Hayashi K
    • Journal Title

      Mol Vis (in press)

    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Complexity of the phenotype-genotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes

    • Author(s)
      Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H
    • Journal Title

      Hum Mutat (in press)

    • Data Source
      KAKENHI-PROJECT-15591883
  • [Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or ZD4 genes.

    • Author(s)
      Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H.
    • Journal Title

      Human Mutation (in press)

    • Data Source
      KAKENHI-PROJECT-16065101
  • [Presentation] Structural variations of pharmacogenetic genes detected in haploid genomes of Japanese population2013

    • Author(s)
      田平知子, 久木田洋児, 加藤聖子, 和氣徳夫, 林健志
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2013-10-05
    • Data Source
      KAKENHI-PROJECT-24657005
  • [Presentation] 日本人ハプロイド試料のゲノムワイド解析により同定された構造多型の機能予測2013

    • Author(s)
      田平知子, 久木田洋児, 矢原耕史, 山本健, 加藤聖子, 和氣徳夫, 林健志
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Year and Date
      2013-12-05
    • Data Source
      KAKENHI-PROJECT-24657005
  • [Presentation] 日本人ハプロイド試料のゲノムワイド解析により同定された構造多型の機能予測2013

    • Author(s)
      田平知子, 久木田洋児, 矢原耕史, 山本健, 加藤聖子, 和氣徳夫, 林健志
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-24657005
  • [Presentation] 日本人集団の確定的ハプロタイプ決定とゲノム薬理学への応用2013

    • Author(s)
      田平知子, 久木田洋児, 矢原耕史, 山本健, 加藤聖子, 和気徳夫, 林健志
    • Organizer
      日本薬学会第133年会
    • Place of Presentation
      横浜
    • Year and Date
      2013-03-28
    • Data Source
      KAKENHI-PROJECT-24657005
  • [Presentation] わが国の常染色体優性家族性滲出性硝子体網膜症の遺伝子診断に基づいた浸透率.2009

    • Author(s)
      近藤寛之、林健志, 他
    • Organizer
      第63回日本臨床眼科学会
    • Place of Presentation
      福岡
    • Year and Date
      2009-10-10
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] Definitive SNP/CNV haplotyping of Asian genomes using DNAs derived from complete hydatidiform moles.2009

    • Author(s)
      Hayashi K, et al.
    • Organizer
      58th Annual Meeting of American Society of Human Genetics.
    • Place of Presentation
      Honolulu, U.S.A.
    • Year and Date
      2009-10-23
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Presentation] Genetic heterogeneity in familial exudative vitreoretinopathy with reduced bone mineral density2009

    • Author(s)
      Kondo H, Nakamori G, Qin M, Tahira T, Uchio E, Hayashi K
    • Organizer
      ARVO Annual Meeting
    • Place of Presentation
      Fort Lauderdale
    • Year and Date
      2009-01-31
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] Definitive SNP/CNV haplotyping of Asian genomes using DNAs derived from complete hydatidiform moles.2009

    • Author(s)
      Hayashi K, et al.
    • Organizer
      59th Annual Meeting of the American Society of Human Genetic
    • Place of Presentation
      Honolulu, USA
    • Year and Date
      2009-10-23
    • Data Source
      KAKENHI-PROJECT-17019051
  • [Presentation] Aggressive posterior ROPの臨床経過と治療成績2008

    • Author(s)
      有田直子, 近藤寛之, 林英之, 内尾英一
    • Organizer
      第62回臨床眼科学会
    • Place of Presentation
      東京
    • Year and Date
      2008-10-25
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] Genetic heterogeneityin familial exudative vitreoretinopathywith reduced bone mineral density2008

    • Author(s)
      Kondo H, Nakamori G, Qin M, Tahira T, Uchio E, Hayashi K
    • Organizer
      ARVO Annual Meeting
    • Place of Presentation
      Fort Lauderdale
    • Year and Date
      2008-04-29
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] 常染色体優性遺伝性の前眼部形成異常を伴う小眼球症に対する遺伝子解析2007

    • Author(s)
      近藤 寛之, 秦明 輝, 田平 知子, 中森 玄司, 内尾 英一, 林健 志
    • Organizer
      第61回日本臨床眼科学会
    • Place of Presentation
      京都
    • Year and Date
      2007-10-12
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] 家族性滲出性硝子体網膜症の遺伝子変異とWNTシグナル古典的経路の転写活性の変化2007

    • Author(s)
      近藤 寛之, 秦明 輝, 田平 知子, 内尾 英一, 林健 志
    • Organizer
      第111回日本眼科学会総会
    • Place of Presentation
      大阪
    • Year and Date
      2007-04-19
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] Clinical and Genetic Characteristics of a Japanese Family with Bilateral Microphathalmia, Cataract and the Absence of Pupil Formation2007

    • Author(s)
      Kondo H, Qin M, Tahira T、 Uchio E, Hayashi K
    • Organizer
      ARVO Annual Meeting
    • Place of Presentation
      Fort Lauderdale
    • Year and Date
      2007-05-07
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] 家族性滲出性硝子体網膜症の遺伝子変異とwntシグナル古典的経路の転写活性の変化.2007

    • Author(s)
      近藤寛之, 秦明輝, 田平知子, 内尾英一, 林健志
    • Organizer
      第111回日本眼科学会総会
    • Place of Presentation
      大阪
    • Year and Date
      2007-04-19
    • Data Source
      KAKENHI-PROJECT-19592047
  • [Presentation] D-haplo : a genome-wide definitive haplotype determined using complete hydatidiform moles.2006

    • Author(s)
      Hayashi K.
    • Organizer
      The 8th international meeting on human genome variation and complex genome analysis (HGV2006)
    • Place of Presentation
      Hong Kong, SAR, China(招待講演)
    • Year and Date
      2006-09-14
    • Data Source
      KAKENHI-PROJECT-17019051
  • 1.  HORIUCHI Takahiko (90219212)
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