Goto Jun 後藤順

… Alternative Names

GOTO Jun 後藤順

後藤順ゴトウジュン

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Researcher Number	10211252
Other IDs
External Links
Affiliation (Current)	2025: 国際医療福祉大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2017 – 2018: 国際医療福祉大学, 医学部, 教授 2016: 東京大学, 医学部附属病院, 准教授 2015 – 2016: 国際医療福祉大学, 大学病院, 教授 2012 – 2014: 東京大学, 医学部附属病院, 准教授 2013: 東京大学, 医学部, 講師 … More 2003 – 2011: The University of Tokyo, Faculty of Medicine, Lecturer, 医学部附属病院, 講師 2007: The University of Tokyo, Faculty of Medicine, Neurology, Lecturer 2004: 東京大学, 医学部・附属病院, 講師 2001 – 2002: DEPARTMENT OF NEUROLOGY, RESEARCH ASSOCIATE, 医学部附属病院, 助手 1998 – 2001: 東京大学, 医学部・附属病院, 助手 2000: The University of Tokyo Hospital Assistant Professor, 医学院・附属病院, 助手 1996: The University of Tokyo Hospital assistant professor, 医学部・附属病院, 助手 1995 – 1996: 東京大学, 医学部, 助手 1994 – 1995: 東京大学, 医学部(病), 助手 1989: 東京大学, 医学部(病), 教務職員 Less
Review Section/Research Field	Principal Investigator Neurology / Neurology Except Principal Investigator Neurology / Neurology / Biological Sciences
Keywords	Principal Investigator siRNA / Machado-Joseph disease / SNP / Huntington's disease / Polyglutamine / CAG repeat / ハンチントン病 / ポリグルタミン / CAGリピート / マシャド・ジョセフ病 … More / DNA sequence / Genome / Chromosome 14 / Triplet repeat disease / 14番染色 / 一塩基置換多型(SNP) / 塩基配列 / ゲノム / 14番染色体 / トリプレット・リピート病 / Machado-Joseph病 / 縁どり空砲変性 / 縁どり空胞変性 / レーザーマイクロダイセクション / 発現プロファイリング / RNA-seq / 縁取り空胞変性 / 封入体筋炎 / 炎症性筋疾患 / 遺伝子同定 / 遺伝性疾患 / 一塩基多型(SNP) / 連鎖解析 / 遺伝性脊髄小脳変性症 / 3番染色体 / cDNA / 多系統変性症(萎縮症) / イミノジプロピオニトリル / インサイチュウハイブリダイゼーション / 免疫組織化学 / 突然変異 / スーパーオキシドジスムターゼ / 筋萎縮性側索硬化症 … More Except Principal Investigator DRPLA / 脊髄小脳変性症 / CAG repeat / DNA chip / DNA microarray / PCR / resequencing / DNA repair / spinocerebellar degeneration / ocular motor apraxia / aprataxin / パーキンソン病 / 神経細胞死 / CAGリピート病 / Rotary shadowing / 神経変性疾患 / 分子遺伝学 / 遺伝子 / ゲノム / 神経病理 / 分子病理 / ミトコンドリア機能 / shojitsuji-tky / 神経分子病態学 / ミトコンドリア / coenzyme Q10 / フラックスアナライザー / COQ2 / 多系統萎縮症 / 病態機序 / RNA発現解析 / 筋炎 / 皮膚筋炎 / 次世代シーケンサー / 生検筋 / 筋炎自己抗体 / 発現解析 / 炎症性筋疾患 / biotechnology / gene / nervous disease / genome / Microarray / バイオテクノロジー / 神経疾患 / 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 / cerebellum / liypoalbuminemia / single strand DNA break / hypoalbuminemia / hypoalbuminenia / DNA Repair / spinoxerebellar degeneration / 小脳 / 低アルブミン血症 / 眼球運動失行 / XRCC1 / アプラタキシン / 一本鎖DNA修復 / DNA修復 / CASPASE INHIBITORS / NEURONAL CELL DEATH / CAG REPEAT DISEASES / CASPASES / 酵素活性阻害 / カテプシン / 蛋白質分解酵素 / カスパーゼ活性阻害 / カスパーゼ / dentatorubral-pallidoluysian atrophy / expression profiling / CREB-dependent transcriptional activation / cAMP-responsive gene / transcriptional dysregulation / nuclear accumulation / polyglutamine diseases / TAFII130 / 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 / Gene expression / CAG repeat disease / Machado-Joseph disease / Huntington disease / 多型 / 蛋白発現 / マシャド・ジョセフ病 / ハンチントン病 / immature fibers in cogenital myotonic dystrophy / abnormal splicing in BMD / revertant fibers in DMD / immunohistochemistry / Dystrophin / DMD / rotary shadowing / 免疫組織 / 単クロ-ン抗体 / DRP / congenital myotonic dystrophy / BMDのsplicing変化 / DMDのrevertant fiver / 組織化学 / ジストロフィン / NBCe1変異 / 尿細管性アシドーシス / NBC1 / 片頭痛 / IRBIT / NBCe1 / 連鎖解析 / 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 / AMPA受容体 / GluR2 / RNA編集 / 脊髄運動ニューロン / 筋萎縮性側索硬化症 / グルタミン酸受容体 / SCA1 / MJD / インシトウハイブリダイゼーション / 遺伝子性脊髄小脳変性症 Less

Gene expression profiling of inflammatory myopathy in correlation with autoantibodies
- Principal Investigator
  
  Shimizu Jun
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
Expression profiling of inclusion body myositis by massive parallel sequencingPrincipal Investigator
- Principal Investigator
  
  Goto Jun
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  International University of Health and Welfare
  The University of Tokyo
Elucidation of molecular mechanisms and development of surrogate markers for multiple system atrophy caused by COQ2 mutations
- Principal Investigator
  
  Tsuji Shoji
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
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 genes for hereditary neurological diseases by the high throughput SNP chip linkage systemPrincipal Investigator
- 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
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
Research for development of therapy of Machado-Joseph disease by siRNAPrincipal Investigator
- Principal Investigator
  
  GOTO Jun
- Project Period (FY)
  2003 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
Identified the causative gene for EAOH end elucidation the molecular mechanisms of neurodegeneration in EAOH
- Principal Investigator
  
  TSUJI Shoji
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
ALSモデル動物の単一運動ニューロンにおけるグルタミン酸受容体分子変化の検討
- Principal Investigator
  
  KWAK Shin
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (A)
- Review Section
  
  Biological Sciences
- 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
STRATEGIC RESEARCH FOR POSSIBLE SUPPRESSION OF NEURONAL DEATH BY CASPASE INHIBITORS
- Principal Investigator
  
  KANAZAWA Ichiro
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
The Complete Genomic Sequence of the Machado-Joseph Disease GenePrincipal Investigator
- Principal Investigator
  
  GOTO Jun
- Project Period (FY)
  1998 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
多系統変性症(MSA)において発現が増加している新奇遺伝子のクローニングPrincipal Investigator
- Principal Investigator
  
  後藤順
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
遺伝性脊髄小脳変性症の分子細胞病理学的研究
- Principal Investigator
  
  村山繁雄
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
筋萎縮性側索硬化症におけるスーパーオキシドジスムターゼの分子病理学的研究Principal Investigator
- Principal Investigator
  
  後藤順
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
Molecular cell biological research on CAG repeat disease
- Principal Investigator
  
  KANAZAWA Ichiro
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
歯状核・赤核・淡蒼球・ルイ体萎縮症の分子病理学的研究
- Principal Investigator
  
  MURAYAMA Shigeo
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  The University of Tokyo
Immunochemical analysis of DMD gene product dystrophin
- Principal Investigator
  
  SHIMIZU Teruo
- Project Period (FY)
  1989 – 1990
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Neurology
- Research Institution
  University of Tokyo

All 2017 2011 2010 2009 2008 2007 2006 2005 2004 2003 Other

All Journal Article Presentation

[Journal Article] Three-year follow-up of high-dose ubiquinol supplementation in a case of familial multiple system atrophy with compound heterozygous COQ2 mutations.2017
- Author(s)
  Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige S, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y and Tsuji S.
- Journal Title
  
  Cerebellum
  
  Volume: - Issue: 3 Pages: 1-9
- DOI
  10.1007/s12311-017-0846-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26253054, KAKENHI-PROJECT-26350915, KAKENHI-PROJECT-17H06159, KAKENHI-PROJECT-15H04270, KAKENHI-PROJECT-15K09334
[Journal Article] Partial duplication of DHH causes minifascicular neuropathy2017
- Author(s)
  Sato Naoko Saito、Maekawa Risa、Ishiura Hiroyuki、Mitsui Jun、Naruse Hiroya、Tokushige Shin-ichi、Sugie Kazuma、Tate Genshu、Shimizu Jun、Goto Jun、Tsuji Shoji、Shiio Yasushi
- Journal Title
  
  Ann Clin Transl Neurol
  
  Volume: 4 Issue: 6 Pages: 415-421
- DOI
  10.1002/acn3.417
- Data Source
  KAKENHI-PROJECT-15K09347
[Journal Article] Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology2017
- Author(s)
  Ikenaga C, Kubota A, Kadoya M, Taira K, Uchio N, Hida A, Maeda MH, Nagashima Y, Ishiura H, Kaida K, Goto J, Tsuji S, Shimizu J
- Journal Title
  
  Neurology
  
  Volume: 5;89(10) Issue: 10 Pages: 1060-1068
- DOI
  10.1212/wnl.0000000000004333
- Data Source
  KAKENHI-PROJECT-15K09347
[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] Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1.2011
- Author(s)
  Ishiura H, (6名略), Goto J, Sakai T, Tsuji S.
- Journal Title
  
  Neurogenetics
  
  Volume: (In press)
- 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] TDP-43 M337V mutation in familial amyotrophic lateral sclerosis in Japan.2010
- Author(s)
  Tamaoka A, 10名略, Goto J, Tsuji S, Akiyama H.
- Journal Title
  
  Intern Med. 49
  
  Pages: 331-334
- NAID
  130000152618
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590989
[Journal Article] A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operation.2010
- Author(s)
  Shirota Y, (3名略), Goto J, et al.
- Journal Title
  
  Intern Med.
  
  Volume: 49 Pages: 1627-1631
- NAID
  130000299592
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590989
[Journal Article] A mutation database for amyotrophic lateral sclerosis.2010
- Author(s)
  Yoshida M, (3名略), Goto J, Tsuji S
- Journal Title
  
  Hum Mutat
  
  Volume: 31 Pages: 1003-1010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590989
[Journal Article] TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan.2010
- Author(s)
  Hara K, 6名略, Goto J, Nishizawa M, Kuzuhara S, Tsuji S.
- Journal Title
  
  Am J Med Genet B Neuropsychiatr Genet. 153B
  
  Pages: 310-313
- 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, 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, 3名略, Goto J, 5名略, Ranum LP
- Journal Title
  
  PLoS One. 4
- 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] Mutations for Gaucher disease confer high susceptibility to Parkinson disease.2009
- Author(s)
  Mitsui J, 4名略, Goto J, 7名略, Tsuji S
- Journal Title
  
  Arch Neurol 66
  
  Pages: 571-576
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590989
[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] Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.2008
- Author(s)
  Hara K, (7名略), Goto J. Ikeuchi T, Tsuji S, Nishizawa M, Onodera O
- Journal Title
  
  Neurology 71
  
  Pages: 547-551
- 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] 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] 傍腫瘍性小脳変性症および筋無力症候群を呈した肺小細胞癌の1例2006
- Author(s)
  関尚美, 三井純, 星野将隆, 明城正博, 宇川義一, 後藤順, 辻省次
- Journal Title
  
  脳と神経 58・1
  
  Pages: 68-73
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] 脳神経病の遺伝子解析2005
- Author(s)
  後藤順, 辻省次
- Journal Title
  
  実験医学 23・4(Suppl)
  
  Pages: 485-489
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] 慢性GVHD経過中にみとめられた左右非対称性の脱髄性末梢神経障害の1例2005
- Author(s)
  松本英之, 関尚美, 山本知孝, 大島久美, 浅井隆司, 本倉徹, 宇川義一, 後藤順, 辻省次
- Journal Title
  
  臨床神経学 45・10
  
  Pages: 748-753
- NAID
  10016787357
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] ニコチン性アセチルコリン受容体と神経疾患2005
- Author(s)
  尾方克久, 後藤順
- Journal Title
  
  別冊・医学のあゆみイオンチャネル最前線update
  
  Pages: 237-242
- Data Source
  KAKENHI-PROJECT-15590880
[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・16
  
  Pages: 2115-2121
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Japanese SCA families with an autosomal phenotype linked toa locus overlapping with SCA15 locus.2004
- Author(s)
  Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S
- Journal Title
  
  Neurology 62
  
  Pages: 648-651
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Japanese SCA families with a distinct phenotype linked to a locus overlapping with SCA15 locus2004
- Author(s)
  Hara, K, Fukushima, T, Suzuki, T, Shimohata, T, Oyake, M, Ishiguro, H, Hirota, K, Miyashita, A, Kuwano, R, Kurisaki, H, Yomono, H, Goto, J, Kanazawa, I, Tsuji, S
- Journal Title
  
  Neurol. 62
  
  Pages: 648-651
- Data Source
  KAKENHI-PROJECT-16209028
[Journal Article] Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B52004
- Author(s)
  Ohtake H, Shimohata, T., Terajima, K., Kimura, T., Jo, R., Kaseda, R., Iizuka, O., Takano, M., Akaiwa, Y., Goto, H., Kobayashi, H., Sugai, T., Muratake, T., Hosoki, T., Shioiri, T., Okamoto, K., Onodera, O., Tanaka, K., Someya, T., Nakada, T., Tsuji, S.
- Journal Title
  
  Neurology 62
  
  Pages: 1601-1603
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16209028
[Journal Article] Adult-onset leukocncephalopathy with vanishing whitte matter with a missense mutation in EIF2B5.2004
- Author(s)
  Ohtake H, Shimohata, T, Terajima, K, Kimura, T, Jo, R, Kaseda, R, Iizuka, O, Takano, M, Akaiwa, Y, Goto, H, Kobayashi, H, Sugai, T, Muratake, T, Hosoki, T, Shioiri, T, Okamoto, K, Onodera, O, Tanaka, K, Someya, T, Nakada, T, Tsuji, S
- Journal Title
  
  Neurology 62
  
  Pages: 1601-3
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16209028
[Journal Article] 神経系疾患の遺伝子病額学2004
- Author(s)
  後藤順, 百瀬義雄, 辻省次他
- Journal Title
  
  最新医学 50
  
  Pages: 2008-2108
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF 2B5.2004
- Author(s)
  Ohtake H, Shimohata, T., Terajima, K., Kimura, T., Jo, R., Kaseda, R., Iizuka, O., Takano, M., Akaiwa, Y., Goto, H., Kobayashi, H., Sugai, T., Muratake, T., Hosoki, T., Shioiri T., Okamoto, K., Onodera, O., Tanaka, K., Someya, T., Nakada, T., Tsuji, S.
- Journal Title
  
  Neurology 62
  
  Pages: 1601-1603
- Data Source
  KAKENHI-PROJECT-16209028
[Journal Article] Japanese SCA families with an autosomal phenotype linked to a locus overlapping with SCA15 locus.2004
- Author(s)
  Hara K, (10名略), Goto J, (2名略)
- Journal Title
  
  Neurology 62
  
  Pages: 648-651
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] 遺伝子発現プロファイリングによる神経疾患分子病態へのアプローチ2004
- Author(s)
  後藤順, 周家毅, 佐藤俊哉
- Journal Title
  
  神経進歩 48・5
  
  Pages: 685-692
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.2003
- Author(s)
  Li M, (4名略), Goto J, (7名略)
- Journal Title
  
  Journal of Human Genetics 48
  
  Pages: 111-118
- NAID
  50000769971
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Human skeltal muscle calcium channel alpha 1S is expressed in the basal ganglia : distinctive expression pattern among L-type Ca2+ channels..2003
- Author(s)
  Takahashi Y, Jeong SY, Ogata K, Goto J, Hashida H, Isahara K, Uchiyama Y, Kanazawa I
- Journal Title
  
  Neuroscience Research 45
  
  Pages: 129-137
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Specific inhibition of Huntington' s disease gene expression by siRNA in cultured cells.2003
- Author(s)
  Liu W, Goto J, (4名略)
- Journal Title
  
  Proceedings of Japan Academy 79(Ser.B)
  
  Pages: 293-298
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Specific inhibition of Huntington's disease gene expression by siRNA in cultured cells.2003
- Author(s)
  Liu W, Goto J, Wang YL, Murata M, Wada K, Kanazawa I
- Journal Title
  
  Proceedings of Japan Academy 79(Ser B)
  
  Pages: 293-298
- NAID
  130000093713
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan2003
- Author(s)
  Li M, Ishikawa K, Toru S, Tomimitsu H, Takashiam M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H
- Journal Title
  
  Jornal of Human Genetics 48
  
  Pages: 111-118
- NAID
  50000769971
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[Journal Article] Human skeletal muscle calcium channel alpha IS is expressed in basal ganglia : distinctive expression pattern among L-type Ca~<++> channels.2003
- Author(s)
  Takahashi Y, (2名略), Goto J, (4名略)
- Journal Title
  
  Neuroscience Research 45
  
  Pages: 129-137
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590880
[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] A Japanese family of nemaline myopathy which is caused by TPM2 mutation.2010
- Author(s)
  Goto J, (7名略)
- Organizer
  60^<th> Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  Washington, DC USA
- Data Source
  KAKENHI-PROJECT-20590989
[Presentation] Clinical features of spinocerebellar ataxia type 31 in Japanese population.2010
- Author(s)
  Ichikawa Y, (4名略), Goto J
- Organizer
  60^<th> Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  Washington, DC USA
- Data Source
  KAKENHI-PROJECT-20590989
[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] 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, (11名略), 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] 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] Adult-onset leuloencephalopathies with vanishing white matter with novel missense mutations in EIF2B2 and EIF2B5 and decreased eIF2B activity2009
- Author(s)
  Matsukawa T, 9名略, Goto J, Proud CG, 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] 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] Molecular epidemiology of spinocerebellar ataxias in Japanese population.2009
- Author(s)
  Ichikawa Y, Tsuji S, Goto J
- 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] 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] Multiplexed resequencing analysis to identify rare variants in pooled DNA of barcode-indexed DNAs2009
- Author(s)
  Mitsui J, 4名略, 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] 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] 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. TAKAHASHI Yuji (00372392)

# of Collaborated Projects: 7 results

# of Collaborated Products: 45 results
2. TSUJI Shoji (70150612)

# of Collaborated Projects: 6 results

# of Collaborated Products: 26 results
3. MURAYAMA Shigeo (50183653)

# of Collaborated Projects: 5 results

# of Collaborated Products: 0 results
4. KANAZAWA Ichiro (30110498)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
5. ONODERA Osamu (20303167)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
6. Shimizu Jun (40260492)

# of Collaborated Projects: 3 results

# of Collaborated Products: 2 results
7. KWAK Shin (40160981)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
8. ISHIURA Hiroyuki (40632849)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
9. OYAKE Mutsuo (70313559)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
10. MITSUI Jun (70579862)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
11. ICHIKAWA Yaeko (90341081)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
12. FUKUDA Yoko (60396744)

# of Collaborated Projects: 1 results

# of Collaborated Products: 12 results
13. YAMADA Hideomi (60396752)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. HORITA Shoko (20534895)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. SEKI George (30206619)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. TOKUNAGA Katsushi (40163977)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. SHIMIZU Teruo (00107666)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. NUKINA Nobuyuki (10134595)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. MURATA Miho (30282643)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 百瀬義雄 (30359624)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 成瀬聡 (70313541)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. IKENAGA Chiseko

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. TODA Tatsuhi

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. SUNADA Yoshihide

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. MASAYASU Hiroyuki

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. 橋田秀司

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. 砂田芳彦

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

Goto Jun 後藤 順

GOTO Jun 後藤 順

後藤 順 ゴトウ ジュン

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Expression profiling of inclusion body myositis by massive parallel sequencingPrincipal Investigator

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

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Research for development of therapy of Machado-Joseph disease by siRNAPrincipal Investigator

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The Complete Genomic Sequence of the Machado-Joseph Disease GenePrincipal Investigator

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Goto Jun 後藤順

GOTO Jun 後藤順

後藤順ゴトウジュン