TORU Shuta 融衆太

Researcher Number	50376711
Other IDs
External Links
Affiliation (based on the past Project Information) *help	2006: Tokyo Medical and Dental University, Neurology, Part-time Lecturer, 医学部, 非常勤講師 2005: 東京医科歯科大学, 医学部附属病院, 助手
Review Section/Research Field	Principal Investigator Neurology Except Principal Investigator Neurology
Keywords	Principal Investigator Spinocerebeller ataxia / Neuroscience / Central nervous system disease / 原因遺伝子 / 16q-ADCA typeIII / 細胞骨格蛋白 / two-hybrid system法 / puratrophin-1 / 優性遺伝性小脳変性症 / 第16番染色体長腕 / 脊髄小脳変性症 / 脳神経科学 / 脳神経疾患 … More Except Principal Investigator … More SCA6 / P / splicing / neurodegeneration / gene therapy / Q type calcium channel / polyglutamine disease / 培養細胞 / 動物モデル / RNAi / Caチャンネル / 脊髄小脳変性症6型 / スプライス / 神経変性 / 遺伝子治療 / Q型カルシウムチャネル / 脊髓小脳変性症 / ポリグルタミン病 Less

Elucidation of pathomechanism and development of treatment of spinocerebellar ataxia type 6
- Principal Investigator
  
  MIZUSAWA Hidehiro
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
The functional analysis of !6q-linled autosomal dominant cerabeller ataxia associated gene.Principal Investigator
- Principal Investigator
  
  TORU Shuta
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University

All 2008 2007 2006 2005

All Journal Article Presentation

[Journal Article] Direct and accurate measurement of CAG repeat configuration in the ataxin-l(ATXN-I)gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"2008
- Author(s)
  Lin JX, Ishikawa K, Sakamoto M, Tsunemi T, Ishiguro T, Amino T, Toru S, Kondo 1, Mizusawa H.
- Journal Title
  
  Journal of Human Genetics 53
  
  Pages: 287-295
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.2007
- Author(s)
  Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H.
- Journal Title
  
  Journal of Human Genetics 52
  
  Pages: 643-649
- NAID
  10019812756
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2006
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, et al.
- Journal Title
  
  Am J Hum Genet 77(2)
  
  Pages: 280-296
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] 脊髄小脳萎縮症の新しい病型と病態2006
- Author(s)
  融衆太, 水澤英洋
- Journal Title
  
  Annual Review神経 2007
  
  Pages: 183-193
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] 【脊髄小脳変性症研究の最近の進歩】常染色体優性遺伝性脊髄小脳変性症第16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症2006
- Author(s)
  石川欽也, 融衆太, 水澤英洋
- Journal Title
  
  神経研究の進歩 50巻3号
  
  Pages: 355-362
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotidesubstitution in the 5 untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H.
- Journal Title
  
  Am J Hum Genet. 77(2)
  
  Pages: 280-296
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, et al.
- Journal Title
  
  Am J Hum Genet 77(2)
  
  Pages: 280-296
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, et al.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, et al.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] Somatosensory-evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis.2005
- Author(s)
  Toru S, Yokota T, Tomimitsu H, Kanouchi T, Yamada M, Mizusawa H.
- Journal Title
  
  Eur J Neurol. 12(3)
  
  Pages: 233-234
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] Somatosensory-evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis.2005
- Author(s)
  Toru S, Yokota T, Tomimitsu H, et al.
- Journal Title
  
  Eur J Neurol 12(3)
  
  Pages: 233-234
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5'untranslated region of the gene encoding a protein with spectrin repeat and rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Mizusawa H et al.
- Journal Title
  
  Am.J.Hum.Genet 77
  
  Pages: 280-296
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Mizusawa H et al.
- Journal Title
  
  Neurology 65
  
  Pages: 629-632
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA typeIII.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Kitayama K, Kondo I, Noguchi E, Arinami T, Mizusawa H.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Data Source
  KAKENHI-PROJECT-17590866
[Presentation] 16番染色体長腕連鎖型優性遺伝性脊髄小脳変性症の原因遺伝子座の解析.2007
- Author(s)
  網野猛志, 佐藤望, 石黒太郎, 常深泰司, 融衆太, 戸田達史, 水澤英洋, 石川欽也.
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-17
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 第16番染色体長腕連鎖型優性遺伝性小脳皮質萎縮症床的特徴.2005
- Author(s)
  融衆太, 他
- Organizer
  第46回日本神経学会総会
- Place of Presentation
  鹿児島
- Year and Date
  2005-05-25
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031

1. ISHIKAWA Kinya (30313240)

# of Collaborated Projects: 2 results

# of Collaborated Products: 12 results
2. MIZUSAWA Hidehiro (30144091)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
3. YOKOTA Takanori (90231688)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. WATASE Kei (30376800)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 常深泰司 (50401344)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results

TORU Shuta 融 衆太

Research Projects

Research Products

Co-Researchers

Elucidation of pathomechanism and development of treatment of spinocerebellar ataxia type 6

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The functional analysis of !6q-linled autosomal dominant cerabeller ataxia associated gene.Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Direct and accurate measurement of CAG repeat configuration in the ataxin-l(ATXN-I)gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"2008

Author(s)

Journal Title

Data Source

[Journal Article] Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.2007

Author(s)

Journal Title

NAID

Data Source

[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2006

Author(s)

Journal Title

Description

Data Source

[Journal Article] 脊髄小脳萎縮症の新しい病型と病態2006

Author(s)

Journal Title

Data Source

[Journal Article] 【脊髄小脳変性症研究の最近の進歩】 常染色体優性遺伝性脊髄小脳変性症 第16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症2006

Author(s)

Journal Title

Data Source

[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotidesubstitution in the 5 untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005

Author(s)

Journal Title

Data Source

[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005

Author(s)

Journal Title

Description

Data Source

[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005

Author(s)

Journal Title

Description

Data Source

[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III2005

Author(s)

Journal Title

Description

Data Source

[Journal Article] Somatosensory-evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis.2005

Author(s)

Journal Title

Data Source

[Journal Article] Somatosensory-evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis.2005

Author(s)

Journal Title

Description

Data Source

[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5'untranslated region of the gene encoding a protein with spectrin repeat and rho guanine-nucleotide exchange-factor domains.2005

Author(s)

Journal Title

Data Source

[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005

Author(s)

Journal Title

Data Source

[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA typeIII.2005

Author(s)

Journal Title

Data Source

[Presentation] 16番染色体長腕連鎖型優性遺伝性脊髄小脳変性症の原因遺伝子座の解析.2007

Author(s)

TORU Shuta 融衆太

[Journal Article] 【脊髄小脳変性症研究の最近の進歩】常染色体優性遺伝性脊髄小脳変性症第16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症2006