ITABASHI Toshitaka 板橋俊隆

Researcher Number	20372295
External Links
Affiliation (based on the past Project Information) *help	2005 – 2006: 東北大学, 病院・助手 2004 – 2005: 東北大学, 病院, 助手
Review Section/Research Field	Principal Investigator Ophthalmology Except Principal Investigator Ophthalmology
Keywords	Principal Investigator 遺伝子変異 / コロイデレミア / 錐体棹体ジストロフィ / 網膜色素変性 / 遺伝子変異解析 / 遺伝性網膜変性疾患 Except Principal Investigator Peripherin / POMS / 網膜色素変性 / tetramer … More / rds gene / Rom1 gene / retinal degeneration / モデル動物 / モデル重物 / 遺伝子異常 / 四量体 / rds遺伝子 / Roml遺伝子 / 網膜変性 / Leber's congenital amaurosis / epidemiology / genetic analysis / retinitis pigmentosa / スクリーニング / 遺伝的異質性 / 表現型 / 遺伝子変異解析 / Leber先天盲 / 疫学検査 / 遺伝子解析 Less

Molecular mechanism of dominant retinal degeneration in mice resulted from a point mutation in the Rom1 gene.
- Principal Investigator
  
  SATO Hajime
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  TOHOKU UNIVERSITY
Molecular genetic analysis for inherited retinal degeneration and epidemiology
- Principal Investigator
  
  WADA Yuko
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  TOHOKU UNIVERSITY
遺伝性網膜変性疾患の分子遺伝学的研究Principal Investigator
- Principal Investigator
  
  板橋俊隆
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Ophthalmology
- Research Institution
  Tohoku University

All 2006 2005 2004

All Journal Article

[Journal Article] Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa2006
- Author(s)
  Tada A, Wada Y, Sato H, Itabashi T, Kawamura M, Tamai M, Nishida K
- Journal Title
  
  Mol Vision 12
  
  Pages: 441-444
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591817
[Journal Article] Screening of the MERTKgene for mutations in Japanese patients with autosomal recessiveretinitis pigmentosa2006
- Author(s)
  Tada A, Wada Y, Sato H, Itabashi T, Tamai M
- Journal Title
  
  Molecular Vision (印刷中)
- Data Source
  KAKENHI-PROJECT-17591817
[Journal Article] Screening of the MERTK gene for mutations in Japanese patients with autosomal retinitis pigmentosa.2006
- Author(s)
  Tada A, Wada Y, Sato H, Itabashi T, Kawamura M, Tamai M, Nishida K
- Journal Title
  
  Mol Vision 12
  
  Pages: 441-444
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591817
[Journal Article] Screen for the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa2005
- Author(s)
  Wada Y, Tada A, Itabashi T, Kawamura M, Hsato H, Tamai M.
- Journal Title
  
  American Journal of Ophthalmology 140
  
  Pages: 163-165
- Data Source
  KAKENHI-PROJECT-17591817
[Journal Article] Screening for Mutations in CYP4V2 Gene in Japanese Patients With Bietti's Crystalline Corneoretinal Dystrophy2005
- Author(s)
  Wada Y, Itabashi T, Sato H, Kawamura M, Tada A, Tamai M.
- Journal Title
  
  American Journal of Ophthalmology 139
  
  Pages: 894-899
- Data Source
  KAKENHI-PROJECT-17591817
[Journal Article] Clinical features of Japanese families with a 402delT or a 555-556delAG mutation in choroideremia gene.2004
- Author(s)
  Itabashi T, et al.
- Journal Title
  
  Retina 24(6)
  
  Pages: 940-945
- Data Source
  KAKENHI-PROJECT-16791041
[Journal Article] Novel 615delC mutation in the CRX gene in a Japanese family with cone-roddystrophy2004
- Author(s)
  Itabashi T, et al.
- Journal Title
  
  Am J Ophthalmol 138(5)
  
  Pages: 876-877
- Data Source
  KAKENHI-PROJECT-16791041

1. WADA Yuko (70302130)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
2. SATO Hajime (10312571)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
3. TSUJI Ichirou (20171994)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. WAKANA Shigeru (90192434)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

ITABASHI Toshitaka 板橋 俊隆

Research Projects

Research Products

Co-Researchers

Molecular mechanism of dominant retinal degeneration in mice resulted from a point mutation in the Rom1 gene.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular genetic analysis for inherited retinal degeneration and epidemiology

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

遺伝性網膜変性疾患の分子遺伝学的研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa2006

Author(s)

Journal Title

Description

Data Source

[Journal Article] Screening of the MERTKgene for mutations in Japanese patients with autosomal recessiveretinitis pigmentosa2006

Author(s)

Journal Title

Data Source

[Journal Article] Screening of the MERTK gene for mutations in Japanese patients with autosomal retinitis pigmentosa.2006

Author(s)

Journal Title

Description

Data Source

[Journal Article] Screen for the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa2005

Author(s)

Journal Title

Data Source

[Journal Article] Screening for Mutations in CYP4V2 Gene in Japanese Patients With Bietti's Crystalline Corneoretinal Dystrophy2005

Author(s)

Journal Title

Data Source

[Journal Article] Clinical features of Japanese families with a 402delT or a 555-556delAG mutation in choroideremia gene.2004

Author(s)

Journal Title

Data Source

[Journal Article] Novel 615delC mutation in the CRX gene in a Japanese family with cone-roddystrophy2004

Author(s)

Journal Title

Data Source

ITABASHI Toshitaka 板橋俊隆