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Takahashi Yuji  高橋 祐二

ORCIDConnect your ORCID iD *help
… Alternative Names

高橋 祐二  タカハシ ユウジ

TAKAHASHI Yuji  高橋 祐二

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Researcher Number 00372392
Other IDs
Affiliation (Current) 2025: 国立研究開発法人国立精神・神経医療研究センター, 病院 脳神経内科診療部, 部長
Affiliation (based on the past Project Information) *help 2023: 国立研究開発法人国立精神・神経医療研究センター, 病院 脳神経内科診療部, 部長
2016 – 2021: 国立研究開発法人国立精神・神経医療研究センター, 病院, 部長
2015: 国立研究開発法人国立精神・神経医療研究センター, 病院, 医長
2013 – 2014: 独立行政法人国立精神・神経医療研究センター, 病院, 医長
2009 – 2012: 東京大学, 医学部附属病院, 助教 … More
2009: 東京大学, 医学部付属病院, 特任助教
2007: The University of Tokyo, Faculty of Medicine, Neurology, Research Associate
2006 – 2007: 東京大学, 医学部附属病院, 助教
2004 – 2006: The University of Tokyo, Faculty, Research Associate, 医学部附属病院, 助手
2004: 東京大学, 医学部・附属病院, 助手 Less
Review Section/Research Field
Principal Investigator
Neurology / Basic Section 52020:Neurology-related
Except Principal Investigator
Neurology / Biological Sciences / Nerve anatomy/Neuropathology
Keywords
Principal Investigator
筋萎縮性側索硬化症 / コンディショナルノックアウトマウス / ErbB4 / モデルマウス / 運動ニューロン / 運動神経細胞死 / 変異解析 / 遺伝子 / 脳神経疾患 / 核小体 … More / TDP-43 / 神経細胞死 / コンディショナルノックアウト / 神経科学 / ノックアウトマウス / 初代培養 / 神経細胞 / 突起伸長 / 細胞内局在 / 培養細胞 / モデル動物 / 軸索伸長 / イオントランスポーター / 電位依存性カルシウムチャネル / 網膜色素変性症 / エクソーム / 片麻痺性片頭痛 / ALS / ゲノム解析 / エクソーム解析 / 連鎖解析 / ゲノム / 家族性片麻痺型片頭痛 / 片頭痛 / チャネロパチー / DNAマイクロアレイ / 遺伝子診断 … More
Except Principal Investigator
連鎖解析 / DNA chip / DNA microarray / PCR / resequencing / CAG repeat / 神経疾患 / 遺伝子同定 / 脊髄小脳変性症 / 神経変性疾患 / 分子遺伝学 / 遺伝子 / ゲノム / biotechnology / gene / nervous disease / genome / Microarray / バイオテクノロジー / マイクロアレイ / molecular genetics / disease-associated genes / neurodegenerative diseases / Parkinson disease / DNA micro array / 疾患関連遺伝子 / 分子遺伝子 / 疾患関連 / DNAチップ / DNAマイクロアレイ / パーキンソン病 / dentatorubral-pallidoluysian atrophy / expression profiling / CREB-dependent transcriptional activation / cAMP-responsive gene / transcriptional dysregulation / nuclear accumulation / polyglutamine diseases / TAFII130 / 神経細胞死 / 転写因子 / 遺伝性神経変性疾患 / トランスジェニックマウス / c-fos / CREB-依存性転写活性化 / animal model / transcription / polyglutamine disease / molecular mechanism / neurodegeneration / 歯状核赤核・淡倉球ルイ体萎縮症 / CAGリピート / 歯状核赤核・淡蒼球ルイ体萎縮症 / 遺伝子発現プロファイリング / CREB依存性転写活性化 / cAMP依存性遺伝病 / 転写障害 / 核内集積 / ポリグルタミン病 / NBCe1変異 / 尿細管性アシドーシス / NBC1 / 片頭痛 / IRBIT / NBCe1 / iPS細胞 / SNP / 遺伝性疾患 / 一塩基多型(SNP) / 相関解析 / 連鎖漢籍 / 脳血管障害 / 多型解析 / 脳・神経 / 遺伝学 / 脳神経疾患 Less
  • Research Projects

    (13 results)
  • Research Products

    (83 results)
  • Co-Researchers

    (20 People)
  •  新規動物モデルを活用した筋萎縮性側索硬化症の分子病態解明と治療法開発Principal Investigator

    • Principal Investigator
      高橋 祐二
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      National Center of Neurology and Psychiatry
  •  A novel model animal recapitulating ALS pathophysiologyPrincipal Investigator

    • Principal Investigator
      Takahashi Yuji
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Establishment of common mechanism and therapeutic base for amyotrophic lateral sclerosis based on a novel causative genePrincipal Investigator

    • Principal Investigator
      Takahashi Yuji
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Molecular pathogenesis study for migraine through integrated genomics based on exome analysisPrincipal Investigator

    • Principal Investigator
      Takahashi Yuji
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  The mechanism of regulation to occur the migraine

    • Principal Investigator
      YAMADA Hideomi
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Identification of a causative gene for autosomal recessive familial amyotrophic lateral sclerosisPrincipal Investigator

    • Principal Investigator
      TAKAHASHI Yuji
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  iPS細胞分化による神経疾患の原因遺伝子同定手法の開発

    • Principal Investigator
      伊達 英俊, 福田 陽子
    • Project Period (FY)
      2009 – 2010
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Nerve anatomy/Neuropathology
    • Research Institution
      The University of Tokyo
  •  Identification of genes for hereditary neurological diseases by the high throughput SNP chip linkage system

    • Principal Investigator
      GOTO Jun
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Development of a comprehensive molecular diagnosis system for neurological diseases based on DNAmicroarrays.

    • Principal Investigator
      TSUJI Shoji
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Elucidation of molecular mechanisms of neurological diseases based on genome analysis

    • Principal Investigator
      TSUJI Shoji
    • Project Period (FY)
      2005 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      The University of Tokyo
  •  DNAマイクロアレイを応用したチャネロパチーのハイスループット遺伝子解析Principal Investigator

    • Principal Investigator
      高橋 祐二
    • Project Period (FY)
      2005 – 2007
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Development of DNA microarray-based reseqeuncing system for neurological diseases.

    • Principal Investigator
      TSUJI Shoji
    • Project Period (FY)
      2004 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Molecular mechanisms of neurodegeneration

    • Principal Investigator
      TSUJI Shoji
    • Project Period (FY)
      2000 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      The University of Tokyo
      Niigata University

All 2019 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation

  • [Journal Article] Altered immunoreactivity of ErbB4, a causative gene product for ALS19, in the spinal cord of patients with sporadic ALS2019

    • Author(s)
      Takahashi Yuji、Uchino Akiko、Shioya Ayako、Sano Terunori、Matsumoto Chihiro、Numata‐Uematsu Yurika、Nagano Seiichi、Araki Toshiyuki、Murayama Shigeo、Saito Yuko
    • Journal Title

      Neuropathology

      Volume: 39 Issue: 4 Pages: 268-278

    • DOI

      10.1111/neup.12558

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K08006, KAKENHI-PROJECT-19K16970, KAKENHI-PROJECT-16K09690, KAKENHI-PROJECT-16H06277
  • [Journal Article] Exploring the frequency and clinical background of the “zebra sign” in amyotrophic lateral sclerosis and multiple system atrophy2019

    • Author(s)
      Atsuhiko Sugiyama, Noriko Sato, Yukio Kimura, Yoko Shigemoto, Fumio Suzuki, Emiko Morimoto, Yuji Takahashi, Hiroshi Matsuda, Satoshi Kuwabara
    • Journal Title

      Journal of the Neurological Sciences

      Volume: 401 Pages: 90-94

    • DOI

      10.1016/j.jns.2019.04.032

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K10423, KAKENHI-PROJECT-19K08006
  • [Journal Article] Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.2014

    • Author(s)
      Doi K, Monjo T, Hoang PH, Yoshimura J, Yurino H, Mitsui J, Ishiura H, Takahashi Y, Ichikawa Y, Goto J, Tsuji S, Morishita S.
    • Journal Title

      Bioinformatics

      Volume: 30 Issue: 6 Pages: 815-822

    • DOI

      10.1093/bioinformatics/btt647

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-ORGANIZER-22129001, KAKENHI-PLANNED-22129002, KAKENHI-PLANNED-22129008, KAKENHI-PROJECT-25461270, KAKENHI-PROJECT-25860700, KAKENHI-PROJECT-221S0002
  • [Journal Article] Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines.2011

    • Author(s)
      Mitsui J, Takahashi Y, Goto J, et al.
    • Journal Title

      Am J Hum Genet

      Volume: 87 Pages: 75-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1.2011

    • Author(s)
      Ishiura H, Fukuda Y, Mitsui J, Nakahara Y, Ahsan B, Takahashi Y, Ichikawa Y, Goto J, Sakai T, Tsuji S
    • Journal Title

      Neurogenetics. 12(2)

      Pages: 117-21

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5.2011

    • Author(s)
      Matsukawa T, Wang X, Liu R, Wortham NC, Onuki Y, Kubota A, Hida A, Kowa H, Fukuda Y, Ishiura H, Mitsui J, Takahashi Y, Aoki S, Takizawa S, Shimizu J, Goto J, Proud CG, Tsuji S
    • Journal Title

      Neurogenetics. (Epub ahead of print)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.2011

    • Author(s)
      Matsukawa T, Asheuer M, Takahashi Y, Goto J, et al.
    • Journal Title

      Neurogenetics

      Volume: 12 Pages: 41-50

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] A mutation database for amyotrophic lateral sclerosis2010

    • Author(s)
      Yoshida, M.Takahashi, Y., et.al.
    • Journal Title

      Human Mutation

      Volume: 31 Pages: 1003-1010

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Journal Article] SNP HiTLink : a high-throughput linkage analysis system employing dense SNP data.2009

    • Author(s)
      Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, Miyashita A, Kuwano R, Adachi H, Nakamura E, Tsuji S
    • Journal Title

      BMC Bioinformatics. 10

      Pages: 121-121

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] SNP haplotype mapping in a small ALS family.2009

    • Author(s)
      Krueger KA, Tsuji S, Fukuda Y, Takahashi Y, Goto J, Mitsui J, Ishiura H, Dalton JC, Miller MB, Day JW, Ranum LP
    • Journal Title

      PLoS One. 4(5)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] SNP HiTLink : a high-throughput linkage analysis system employing dense SNP data.2009

    • Author(s)
      Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, 4名略, Tsuji S
    • Journal Title

      BMC Bioinformatics. 10

      Pages: 121-121

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Familial Ischemic Cerebral Small-Vessel Disease, Alopecia, and Spondylosis Caused by Mutations in the HTRA1 Gene2009

    • Author(s)
      Hara K, Shiga A, Fukutake T, Nozaki H, Miyashita A, Yokoseki A, Kawata H, Koyama A, Arima K, Takahashi T, Ikeda M, Shiota H, Tamura M, Shimoe Y, Hirayama M, Arisato T, Yanagawa S, Tanaka A, Nakano I, Ikeda S, Yoshida Y, Yamamoto T, Ikeuchi T, Kuwano R, Nishizawa M, Tsuji S, Onodera O.
    • Journal Title

      New Engl J Med 360

      Pages: 1729-1739

    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] SNP HiTLink: a high-throughput likage analysis system employing dense SNP data.2009

    • Author(s)
      Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, et al
    • Journal Title

      BMC Bioinformatics (In press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.2009

    • Author(s)
      Wang K, Takahashi Y, 3名略, Goto J, Lou JN, Tsuji S
    • Journal Title

      Neurogenetics 10

      Pages: 337-345

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] otal deletion and a missensemutation of ITPRl inJapanese SCA15 families2008

    • Author(s)
      348. Hara, K, Shiga, A, Nozaki, H, Mitsui, J, Takahashi, Y, Ishiguro, H, Yomono, H, Kurisaki, H, GotomJ, Ikeuchi, T, Tsuji, S, Nishizawa, M, and Onodera, O.
    • Journal Title

      Neurology

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Familial cases presenting very early onset autosomal dominant Alzheimer' s disease with D43T in presenilin-1 gene : Implication for genotype-phenotype correlation2008

    • Author(s)
      Arai , N, Kishino, A, Takahashi, Y, Ida, M., Goto, J, Tsuji, S.
    • Journal Title

      Neurogenetics 9

      Pages: 65-67

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: Implication for genotype-phenotype correlation.2008

    • Author(s)
      Arai, N, Kishino, A, Takahashi, Y, Morita1, D, Nakamura, K, Yokoyama, T, Watanabe, T, Ida, M., Goto, J, Tsuji, S.
    • Journal Title

      Neurogeneticcs 9

      Pages: 65-67

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Familial cases presenting very early onset autosomaldominant Aizheimer's disease with I143T in presenilin-1 gene: Implication for genotype-phenotype correlation2008

    • Author(s)
      Arai, N, Kishino, A, Takahashi, Y, Morital, D, Nakamura, K, Yokoyama, T, Watanabe, T, Ida, M., Goto, J, Tsuji, S.
    • Journal Title

      Neurogeneticcs

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Devcelopment of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.2008

    • Author(s)
      Takahashi Y, (13名略), Goto J, Tsuji S
    • Journal Title

      Archives of Neurology 65

      Pages: 1326-1332

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene : Implication for genotype-phenotype correlation2008

    • Author(s)
      Arai, N, Kishino, A, Takahashi, Y, Morital, D, Nakamura, K, Yokoyama, T, Watanabe, T, Ida, M., Goto, J, Tsuji, S.
    • Journal Title

      Neurogenetics 9

      Pages: 65-67

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Development of high-throughput microarray-based resequencing system for neurologica1 disorders and its application to molecular genetics of amyotrophic lateral sclerosis2008

    • Author(s)
      Takahashi, Y, Seki, N, Ishiura, H, Goto, J and Tsuji, S.
    • Journal Title

      Arch Neurol 65

      Pages: 1326-1332

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Development of high-throughput microarray-based resequencing system for neurological disorders and its app-lication to molecular genetics of amyotrophic lateral sclerosis2008

    • Author(s)
      347. Takahashi, Y, Seki, N, Ishiura, H, Mitsui, J, Matsukawa, T, Kishino, A, Onodera, O, Aoki, M, Shimozawa, M, Murayama, S, Itoyama, Y, Suzuki, Y, Sobue, S, Nishizawa, M, Goto, J
    • Journal Title

      Archives of Neurology

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] DNAマイクロアレイによるリシークエンシングを応用したハイスループット遺伝子解析システム2007

    • Author(s)
      高橋祐二, 後藤順, 辻省次
    • Journal Title

      実験医学 25巻2号

      Pages: 192-198

    • Data Source
      KAKENHI-PROJECT-17790571
  • [Journal Article] Multiplex families with multiple system atrophy.2007

    • Author(s)
      Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, Kakita A, Yamada M, Takahashi H, Hirasawa M, Mizuno Y, Ogata K, Goto J, Kanazawa I, Nishizawa M, Tsuji S
    • Journal Title

      Arch Neurol. 64(4)

      Pages: 545-551

    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Aprataxin, causative gene product for EAOH/AOAI, repairs DNA single-strand breaks with 3'-phosphate and 3'-phosphoglycolate ends2007

    • Author(s)
      Takahashi T, Tada M, Igarashi S, Koyama A, Date H, Yokoseki A, Shiga A, Yoshida Y, Tsuji S, Nishizawa M, Onodera O
    • Journal Title

      Nucleic Acids Res (in press)

    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Aprataxin, causative gene product, for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.2007

    • Author(s)
      Takahashi, T., Tada, M.,…Tsuji, S., Nishizawa, M., Onodera, O.
    • Journal Title

      Nucleic Acids Res 35

      Pages: 3797-3809

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Neuronal atrophy and synaptic alteration in a mouse model of dentatorubral-pallidoluyslan atrophy.2006

    • Author(s)
      SaKai K, Yamada M, Sato T, Yamada M, Tsuji S, Takahashi H
    • Journal Title

      Brain 129(PT9)

      Pages: 2353-2362

    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Polyglutamine represses cAMP-responsive-element-mediated transcription without aggregate formation.2005

    • Author(s)
      Takahashi T, Nozaki K, Tsuji S, S, Nishizawa M, Onodera O.
    • Journal Title

      Neuroreport 16(3)

      Pages: 295-299

    • Data Source
      KAKENHI-PROJECT-17019006
  • [Journal Article] Polyglutamine represses cAMP-responsive-element-mediated transcription without aggregate formation.2005

    • Author(s)
      Takahashi T, Nozaki K, Tsuji S, Nishizawa M, Onodera O.
    • Journal Title

      Neuroreport 16(3)

      Pages: 295-299

    • Data Source
      KAKENHI-PROJECT-16209028
  • [Journal Article] Polyglutamine represses cAMP-mediated transcription without aggregate formation.2005

    • Author(s)
      Takahashi T, Nozaki K, Tsuji S, Nishizawa M, Onodera O.
    • Journal Title

      Neuroreport 16(3)

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16209028
  • [Journal Article] O.Polyglutamine represses cAMP-responsive-element-mediated transcription without aggregate formation.2005

    • Author(s)
      Takahashi T, Nozaki K, Tsuji S, Nishizawa M, Onodera
    • Journal Title

      Neuroreport 16(3)

      Pages: 295-299

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16209028
  • [Journal Article] ゲノムから医学 DNAマイクロアレイの遺伝子診断への応用2005

    • Author(s)
      高橋祐二, 後藤順, 辻省次
    • Journal Title

      蛋白質・核酸・酵素 50巻16号

      Pages: 2115-2121

    • Data Source
      KAKENHI-PROJECT-17790571
  • [Journal Article] The FHA domain of aprataxin (APTX) interacts with The C terminal region of XRCC1.2004

    • Author(s)
      Date, H, Igarashi, S, Sano, Y, Takahashi, T, Takahashi, T, Takano, H, Tsuji, S, Nishizawa, S, Onodera, 0.
    • Journal Title

      Biochem.Biophys.Res.Commun. 325

      Pages: 1279-1285

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Aprataxin, the causative protein for early-onset ataxia with ocular motor apraxia and hypoalbuminemia, is a nuclear protein wi2004

    • Author(s)
      Sano, Y., Date, H, Igarashi, S, Onodera, O, Oyake, M, Takahashi, T, Hayashi, S, Morimatsu, M, Takahashi, H, Makifuchi, T, Fukuhara, N, Tsuji, S.
    • Journal Title

      Ann.Neurol. 55

      Pages: 241-249

    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Sharing of polyglutamine transport by the neuronal nucleus and cytoplasm in CAG-repeat diseases.2004

    • Author(s)
      Yamada, M, Tan, S-H, Inenaga, C, Tsuji, S, Takahashi, H
    • Journal Title

      Neuropathol. Appl. Neurobiol. 30

      Pages: 665-675

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.2004

    • Author(s)
      Zuchner S, Mersiyanova, I V., Muglia, M., Bissar-Tadmouri, N., Rochelle, J., Dadali, E L., Zappia, M., Nelis, E., Patitucci, A., Senderek, J., Parman, Y., Evgrafov, O., Jonghe, P D., Takahashi, Y., Tsuji, S., Pericak-Vance, M A., Quattrone, A., Battaloglu, E., Polyakov, AV., Timmerman, V., Schroder, J M., Vance, J M., Battologlu E.
    • Journal Title

      Nat Genet 36

      Pages: 449-451

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Aprataxin, the causative protein for early-onset ataxia with ocular motor apraxia and hypoalbuminemia, is a nuclear protein with a potential role as a nucleotide repair protein.2004

    • Author(s)
      Sano, Y., Date, H, Igarashi, S, Onodera, O, Oyake, M, Takahashi, T, Hayashi, S, Morimatsu, M, Takahashi, H, Makifuchi, T, Fukuhara, N, Tsuji, S.
    • Journal Title

      Ann.Neurol. 55

      Pages: 241-249

    • Data Source
      KAKENHI-PROJECT-16209028
  • [Journal Article] Aprataxin, the causative protein for early-onset ataxia with ocular motor apraxia and hypoalbuminemia, is a nuclear protein with a potential role as a nucleotide repair protein.2004

    • Author(s)
      Sano, Y., Date, H, Igarashi, S, Onodera, O, Oyake, M, Takahashi, T, Hayashi, S, Morimatsu, M, Takahashi, H, Makifuchi, T, Fukuhara, N, Tsuji, S
    • Journal Title

      Ann. Neurol. 55

      Pages: 241-249

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Mutations in the mitochondrial GTPase mito fusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.2004

    • Author(s)
      Zuchner S, Mersiyanova, I V.Muglia, M.Bissar-Tadmouri, N.Rochelle, J.Dadali, E L.Zappia, M.Nelis, E.Patitucci, A.Senderek, J.Parman, Y.Evgrafov, O.Jonghe, P D.Takahashi, Y.Tsuji, S.Pericak-Vance, M A.Quattrone, A.Battaloglu, E.Polyakov, A V.Timmerman, V.Schroder, J M.Vance, J M.Battologlu, E.
    • Journal Title

      Nat Genet 36

      Pages: 449-451

    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Aprataxin, the causative protein for early-onset ataxia with ocular motor apraxia and hypoalbuminemia, is a nuclear protein with a potential role as a nucleotide repair protein.2004

    • Author(s)
      Sano, Y., Date, H, Igarashi, S, Onodera, 0, Oyake, M, Takahashi, T, Hayashi, S, Morimatsu, M, Takahashi, H, Makifuchi, T, Fukuhara, N, Tsuji, S.
    • Journal Title

      Ann. Neurol 55

      Pages: 241-249

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.2004

    • Author(s)
      Zuchner S, Mersiyanova, I V.Muglia, M.Bissar-Tadmouri, N.Rochelle, J.Dadali, E L.Zappia, M.Nelis, E.Patitucci, A.Senderek, J.Parman, Y.Evgrafov, 0.Jonghe, P D.Takahashi, Y.Tsuji, S.Pericak-Vance, M A.Quattrone, A.Battaloglu, E.Polyakov, AV.Timmerman, V.Schroder, J M.Vance, J M.Battologlu, E.
    • Journal Title

      Nat Genet 36

      Pages: 449-451

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Sharing of polyglutamine transport by the neuronal nucleus and cytoplasm in CAG-repeat diseases.2004

    • Author(s)
      Yamada, M, Tan, S-H, Inenaga, C, Tsuji, S, Takahashi, H.
    • Journal Title

      Neuropathol.Appl.Neurobiol 30

      Pages: 665-675

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] The FHA domain of aprataxin (APTX) interacts with the C terminal region of XRCC1.2004

    • Author(s)
      Date, H, Igarashi, S, Sano, Y, Takahashi, T, Takahashi, T, Takano, H, Tsuji, S, Nishizawa, S, Onodera, O.
    • Journal Title

      Biochem.Biophys.Res.Commun. 325

      Pages: 1279-1285

    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Beta-synuclein gene alterations in dementia with Lewy bodies.2004

    • Author(s)
      Ohtake H, Limprasert, P., Fan, Y., Onodera, O., Kakita, A., Takahashi, H., Bonner, L T., Tsuang, D W., Murray, I V., Lee, V M., Trojanowski, JQ., Ishikawa, A., Idezuka, J., Murata, M., Toda, T., Bird, T D., Leverenz, J B., Tsuii, S.
    • Journal Title

      Neurology 63

      Pages: 805-811

    • Data Source
      KAKENHI-PROJECT-16209028
  • [Journal Article] The FHA domain of aprataxin (APTX) interacts with the C terminal region of XRCC1.2004

    • Author(s)
      Date, H, Igarashi, S, Sano, Y, Takahashi, T, Takahashi, T, Takano, H, Tsuji, S, Nishizawa, S, Onodera, O
    • Journal Title

      Biochem. Biophys. Res. Commun. 325

      Pages: 1279-1285

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Sharing of polyglutamine transport by the neuronal nucleus and cytoplasm in CAG-repeat diseases.2004

    • Author(s)
      Yamada, M, Tan, S-H, Inenaga, C, Tsuji, S, Takahashi, H.
    • Journal Title

      Neuropathol.Appl.Neurobiol. 30

      Pages: 665-675

    • Data Source
      KAKENHI-PROJECT-12210008
  • [Journal Article] Development of high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis

    • Author(s)
      Takahashi, Y, Seki, N, Ishiura, H, Mitsui, J, Matsukawa, T, Kishino, A, Onodera, O, Aoki, M, Shimozawa, M, Murayama, S, Itoyama, Y, Suzuki, Y, Sobue, S, Nishizawa, M, Goto, J., Tsuji, S.
    • Journal Title

      Archives of Neurology (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] 「研究成果報告書概要(欧文)」より

    • Author(s)
      Hara, K, Shiga, A, Nozaki, H, Mitsui, J, Takahashi, Y, Ishiguro, H, Yomono, H, Kurisaki, H, Gotom J, Ikeuchi, T, Tsuji, S, Nishizawa, M, Onodera, O.
    • Journal Title

      Neurology (in press)

    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Development of high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.

    • Author(s)
      Takahashi, Y, Seki, N, Ishiura, H, Mitsui, J, Matsukawa, T, Kishino, A, Onodera, O, Aoki, M, Shimozawa, M, Murayama, S, Itoyama, Y, Suzuki, Y, Sobue, S, Nishizawa, M, Goto, J
    • Journal Title

      Archives of Neurology (In press)

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Journal Article] Total deletion and a missense mutatio of ITPR1 in Japanese SCA15 families.

    • Author(s)
      Hara, K, Shiga, A, Nozaki, H, Mitsui, J, Takahashi, Y, Ishiguro, H, Yomono, H, Kurisaki, H, Gotom J, Ikeuchi, T, Tsuji, S, Nishizawa, M, and Onodera, O.
    • Journal Title

      Neurology (In press)

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Implication of rare variants in causative genes for Charcot-Marie-Tooth disease in patients clinically diagnosed as ALS2019

    • Author(s)
      Yuka Hama, Hidetoshi Date, Hiroyuki Ishiura, Jun Mitsui, Koichiro Doi, Jun Yoshimura, Shinichi Morishita, Shoji Tsuji, Hidehiro Mizusawa, Yuji Takahashi
    • Organizer
      30th International Symposium on ALS/MND
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08006
  • [Presentation] 網膜色素変性症を伴う家族性片麻痺性片頭痛における病因遺伝子探索.2015

    • Author(s)
      高橋 祐二,滝澤 歩武,古澤 嘉彦,石浦 浩之,三井 純,森下 真一,辻 省次,村田 美穂
    • Organizer
      第43回日本頭痛学会総会
    • Place of Presentation
      東京
    • Year and Date
      2015-11-13
    • Data Source
      KAKENHI-PROJECT-25461270
  • [Presentation] Genetic epidemiological study on migraine and episodic ataxia in the Japanese population2013

    • Author(s)
      Yuji Takahashi, Hiroyuki Ishiura, Jun Goto and Shoji Tsuji
    • Organizer
      American Society of Human Genetics 63rd Annual Meeting
    • Place of Presentation
      Boston Convention & Exhibition Center, Boston, MA, USA
    • Data Source
      KAKENHI-PROJECT-25461270
  • [Presentation] Exome analysis for early-onset amyotrophic lateral sclerosis with autosomal recessive mode of inheritance.2012

    • Author(s)
      Yuji Takahashi, Koichiro Higasa, Satoshi Takagi, Tadashi Kurita, Hiroyuki Ishiura, Jun Mitsui, Yoko Fukuda, Jun Yoshimura, Taro L. Saito, Shinichi Morishita, Jun Goto and Shoji Tsuji.
    • Organizer
      The 62nd American Society of Human Genetics Annual Meeting
    • Place of Presentation
      San Francisco, USA
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Presentation] Exome analysis for early-onset amyotrophic lateral sclerosis with autosomal recessive mode of inheritance.2012

    • Author(s)
      Yuji Takahashi, Koichiro Higasa, Satoshi Takagi, Tadashi Kurita, Hiroyuki Ishiura, Jun Mitsui, Yoko Fukuda, Jun Yoshimura, Taro L. Saito, Shinichi Morishita, Jun Goto and Shoji Tsuji
    • Organizer
      American Society of Human Genetics 62nd Annual Meeting
    • Place of Presentation
      San Francisco, Ca., USA.
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Presentation] Search for genetic risk factors and phenotypic modifiers for sporadic ALS based on extensive resequencing of causative genes for familial ALS2011

    • Author(s)
      Yuji Takahashi, Jun Goto, Shoji Tsuji
    • Organizer
      American Academy of Neurology 63rd Annual Meeting
    • Place of Presentation
      Hawaii Convention Center in Honolulu, Hawaii USA
    • Year and Date
      2011-04-13
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Presentation] Kesequencing-based case control study of SQSTM1 for sporadic amyotrophic lateral sclerosis based on common disease-multiple rare variant hypothesis2011

    • Author(s)
      Yuji Takahashi, Jun Goto, Shoji Tsuji
    • Organizer
      ASHG/ICHG 2011 Meeting
    • Place of Presentation
      Palais des Congres, Montreal Canada
    • Year and Date
      2011-10-04
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Presentation] Mutational analysis of optineurin (OPTN) in familial amyotrophic lateral sclerosis in the Japanese population.2010

    • Author(s)
      Naruse H, Takahashi Y, Goto J, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington, DC USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A case-control study focusing on rare variants obtained by comprehensive resequencing of the causative genes for familial amyotrophic lateral sclerosis (ALS) to identify disease-relevant alleles for sporadic ALS.2010

    • Author(s)
      Takahashi Y, Goto J, Toyoda A, Fujiyama A, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington, DC USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A Japanese family ofnemaline myopathy which is caused by TPM2 mutation.2010

    • Author(s)
      Goto J, Ishiura H, Fukuda Y, Nagashima Y, Shimizu J, Takahashi Y, Ichikawa Y, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington DC, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A case-control study focusing on rare variants obtained by comprehensive resequencing of the causative genes for familial amyotrophic lateral sclerosis(ALS)to identify disease-relevant alleles for sporadic ALS2010

    • Author(s)
      Y.Takahashi, J.Goto, A.Toyoda, A.Fujiyama, S.Tsuji
    • Organizer
      The American Society of Human Genetics 60^<th> Annual Meeting
    • Place of Presentation
      Washington, DC, USA
    • Year and Date
      2010-11-05
    • Data Source
      KAKENHI-PROJECT-22590923
  • [Presentation] Case-control association study of PARK2 exon rearrangements in Parkinson disease using an array comparative genomoic hybridization analysis.2010

    • Author(s)
      Mitsui J, Takahashi Y, Matsukawa T, Goto J.Saito Y, Murayama S, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington, DC USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Siblings of pathologically proven multiple system atrophy : an application of whole genome analysis toward finding strong genetic factors for sporadic diseases.2010

    • Author(s)
      Ishiura H, Ahsan B, Mitsui J, Takahashi Y, Fukuda Y, Ichikawa Y, Nakahara Y, Kara K, Takahashi T, Kakita A, Onodera O, Nishizawa M, Goto J, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington DC, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A variation database for amyotrophic lateral sclerosis.2009

    • Author(s)
      Yoshida M, Takahashi Y, Koike A, Fukuda Y, Goto J, Tsuji S
    • Organizer
      59th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Honolulu, Hawaii, USA
    • Year and Date
      2009-10-23
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Mutational analysis FUS/TLS in familial and sporadic amyotrophic lateral sclrerosis in the Japanese population.2009

    • Author(s)
      Takahashi Y, Goto J, Tsuji S
    • Organizer
      59th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Honolulu, Hawaii, USA
    • Year and Date
      2009-10-22
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A comprehensive diagnostic system for hereditary spastic paraplegia employing resequencing microarray, Snager sequencing and comparative genomic hybridization array allows efficient identification of various types of mutations in the causative genes.2009

    • Author(s)
      Ishiura H, Takahashi Y, Goto J, Tsuji S
    • Organizer
      59th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Honolulu, Hawaii, USA
    • Year and Date
      2009-10-21
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Adult-onset leukoencephalopathies with vanishing white matter with novel mussense mutations in EIF2B2 and EIF2B5, and decresed eIF2B activity.2009

    • Author(s)
      Matsukawa T, Wang X, Liu R, Hida A, Kubota A, Fukuda Y, Kowa H, Takahashi Y, Aoki S, Shimizu J, Goto J, Proud CG, Tsuji S
    • Organizer
      59^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Honolulu, Hawaii, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Development of high-throughput linkage analysis system and application for the linkage analysis of familial multiple system atrophy (MAS).2008

    • Author(s)
      Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, et al
    • Organizer
      The American Society of Human Genetics, 58th Annual Meeting
    • Place of Presentation
      Philadelphia
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Development of a high-throughput analysis system and application for the linkage analysis of familial multiple system atrophy (MSA).2008

    • Author(s)
      Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, Hara K, Nishizawa M, Nakamura E, Adachi H, Tsuji S
    • Organizer
      58^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Philadelphia, Pennsylvania, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Identification of novel heterozygous nonsynonymous variations of(ANG),VEGF and ALS2 in SporadicALS(SALS)patients and its imphcation in the genetic risks of SALS2007

    • Author(s)
      Y. Takahashi, J, Goto, S. Tsuji,
    • Organizer
      57th Annual Meeting of American Scoeity of Human Genetics
    • Place of Presentation
      San Diego,USA
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Genome-wide association studies on Multiple system atrophy (MSA).2007

    • Author(s)
      Y. Nakahara1, Y. Momose Y. Takahashi, J. Goto1, S. Tsuji
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] comprehensive mutational analysis system using resequencing microarray delineates molecular epidemiology of hereditary spastic paraplegias in the Japanese population2007

    • Author(s)
      H. Ishiura, Y. Takahashi, J. Goto, S. Tsuji. A.
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Genome-wide association stμdies on MUItiple system atrophy(MSA)2007

    • Author(s)
      Y. Nakaharal, Y. Momose Y. Takahashi, J. Gotol, S. Tsuji
    • Organizer
      57th Annual Meeting of American Scoeity of Human Genetics
    • Place of Presentation
      San Diego,USA
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Comprehensive analysis of breakpoints of PARK2 rearrangements in patients with autosomal recessive juvenile parkinsonism (AR-JP)employing a high-density tiling array-based comparative genomic hybridization (array-CGH) system.2007

    • Author(s)
      J. Mitsui, Y. Takahashi1, H. Tomiyama, H. Yoshino, J. Goto, Y. Mizuno, N. Hattori, S. Tsuji1.
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Japan A comprehensive mutational analysis sysbem using resequencing microarray dekmeates molecular epidemiology of hererhtary spastic paraplegias hl the Japanese population2007

    • Author(s)
      H. lshiura, Y. Takahashi, J. Goto, S. Tsuji
    • Organizer
      57th Annual Meeting of American Scoeity of Human Genetics
    • Place of Presentation
      San Diego,USA
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Identification of novel heterozygous nonsynonymous variations of (ANG), VEGF and ALS2 in sporadic ALS (SALS) patients and its implication in the genetic risks of SALS.2007

    • Author(s)
      Y. Takahashi, J. Goto, S. Tsuji.
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Comprehensive analysis of causative and related genes for ALS using a high throughput DNA microarray-based resequencing syste2007

    • Author(s)
      Yuji Takahashi
    • Organizer
      59th Annual Meeting of the American Academy of Neurology
    • Place of Presentation
      Boston, MA, USA
    • Year and Date
      2007-05-03
    • Data Source
      KAKENHI-PROJECT-17790571
  • [Presentation] Tsujil. Comprehensive analysis of breakpoints of PARK2 rearrangements in patients with autosomal recessive juvenile parkinsonism (AR-JP) employing a high-density tiling array-based comparative genomic hybridization (array-CGH) system2007

    • Author(s)
      J. Mitsui, Y. Takahashil, H. Tomiyama, H. Yoshino, J. Goto, Y. Mizuno, N. Hattori, S.
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Identification of novel heterozygous nonsynonymous variations of (ANG), VEGF and ALS2 in sporadic ALS (SALS) patients and its implication in the genetic risks of SALS2007

    • Author(s)
      Y. Takahashi, J. Goto, S. Tsuji
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] A comprehensive mutational analysis system using resequencing microarray delineates molecular epidemiology of hereditary spastic paraplegias in the Japanese population.2007

    • Author(s)
      H. Ishiura, Y. Takahashi, J. Goto, S. Tsuji.
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Identification of novel heterozygous nonsynonymous variations of ANG, VEGF and ALS2 in sporadic ALS(SALS) patients and its implication in the genetic risks of SALS2007

    • Author(s)
      Yuji Takahashi
    • Organizer
      57th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      San Diego, CA, USA
    • Year and Date
      2007-10-26
    • Data Source
      KAKENHI-PROJECT-17790571
  • [Presentation] Comprehensive analysis of breakpoints of PARK2 rearrangements in patients with autosomal recessive juvenile parkinsonism(AR-JP)employing a high-density tiling array-based comparative genomic hybri(lization(array-CGH)system2007

    • Author(s)
      J. Mitsui, Y. Takahashil, H. Tomiyama, H. Yoshino, J. Goto, Y. Mizuno, N. Hattori, S. Tsujil
    • Organizer
      57th Annual Meeting of American Scoeity of Human Genetics
    • Place of Presentation
      San Diego,USA
    • Data Source
      KAKENHI-PROJECT-18209032
  • [Presentation] Genome-wide association studies on Multiple system atrophy (MSA)2007

    • Author(s)
      Y. Nakaharal, Y. Momose Y. Takahashi, J. Gotol, S. Tsuji
    • Organizer
      57th Annual Meeting of American Society of Human Genetics
    • Place of Presentation
      San Diego, USA
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18209032
  • 1.  GOTO Jun (10211252)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 45 results
  • 2.  TSUJI Shoji (70150612)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 43 results
  • 3.  伊達 英俊 (30401037)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 0 results
  • 4.  ONODERA Osamu (20303167)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 11 results
  • 5.  FUKUDA Yoko (60396744)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 12 results
  • 6.  MURAYAMA Shigeo (50183653)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  ICHIKAWA Yaeko (90341081)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 8.  YAMADA Hideomi (60396752)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  HORITA Shoko (20534895)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  SEKI George (30206619)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  TOKUNAGA Katsushi (40163977)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  百瀬 義雄 (30359624)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  清水 潤 (40260492)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  小宅 睦郎 (70313559)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 15.  成瀬 聡 (70313541)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  Nagano Seiichi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  Saito Yuko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  Matsumoto Chihiro
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  MORISHITA Shinichi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 20.  木村 有喜男
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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