Takahashi Yuji 高橋祐二

… 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

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

Takahashi Yuji 高橋 祐二

高橋 祐二 タカハシ ユウジ

TAKAHASHI Yuji 高橋 祐二

Research Projects

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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

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A novel model animal recapitulating ALS pathophysiologyPrincipal Investigator

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Establishment of common mechanism and therapeutic base for amyotrophic lateral sclerosis based on a novel causative genePrincipal Investigator

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Molecular pathogenesis study for migraine through integrated genomics based on exome analysisPrincipal Investigator

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The mechanism of regulation to occur the migraine

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Identification of a causative gene for autosomal recessive familial amyotrophic lateral sclerosisPrincipal Investigator

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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

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Identification of genes for hereditary neurological diseases by the high throughput SNP chip linkage system

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Development of a comprehensive molecular diagnosis system for neurological diseases based on DNAmicroarrays.

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Elucidation of molecular mechanisms of neurological diseases based on genome analysis

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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

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Development of DNA microarray-based reseqeuncing system for neurological diseases.

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Molecular mechanisms of neurodegeneration

Principal Investigator

Takahashi Yuji 高橋祐二

高橋祐二タカハシユウジ

TAKAHASHI Yuji 高橋祐二