Ohsawa Ryosuke 大澤亮介

Researcher Number	20719356
Other IDs
Affiliation (Current)	2020: 広島大学, 原爆放射線医科学研究所, 助教
Affiliation (based on the past Project Information) *help	2014 – 2017: 広島大学, 原爆放射線医科学研究所, 助教
Review Section/Research Field	Principal Investigator Nerve anatomy/Neuropathology Except Principal Investigator Basic / Social brain science
Keywords	Principal Investigator 筋萎縮性側索硬化症 / 神経変性疾患 / ALS / Optineurin / オートファジー Except Principal Investigator 脊髄小脳変性症 / Ca チャンネル / 脳神経疾患 / 遺伝子 / 神経科学 / 遺伝性脊髄小脳変性症

Study of cerebellum disturbance by genetic approaches
- Principal Investigator
  
  Kawakami Hideshi
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Basic / Social brain science
- Research Institution
  Hiroshima University
Identification of molecular mechanism underlying ALS pathogenesis by Optineurin mutationPrincipal Investigator
- Principal Investigator
  
  Ohsawa Ryosuke
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Nerve anatomy/Neuropathology
- Research Institution
  Hiroshima University

All 2015 2014

All Journal Article

[Journal Article] A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia2015
- Author(s)
  Morino H., Matsuda Y., Muguruma K., Miyamoto R., Ohsawa R., Ohtake T., Otobe R., Watanabe M., Maruyama H., Hashimoto K., Kawakami H.
- Journal Title
  
  Mol Brain
  
  Volume: 8 Pages: 89-89
- DOI
  10.1186/s13041-015-0180-4
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K07089, KAKENHI-PROJECT-15K15083, KAKENHI-PLANNED-23111008, KAKENHI-PLANNED-25117006, KAKENHI-PROJECT-24220007, KAKENHI-PROJECT-26293211, KAKENHI-PROJECT-26242085
[Journal Article] Mutations in Twinkle Primase-Helicase causes Perrault Syndrome with neurological features2014
- Author(s)
  Morino H
- Journal Title
  
  Neurology
  
  Volume: 83 Pages: 2054-2061
- DOI
  10.1212/wnl.0000000000001036
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-23111008, KAKENHI-PROJECT-26242085, KAKENHI-PROJECT-26293211

1. Kawakami Hideshi (70253060)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
2. 森野豊之 (10397953)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
3. 福士雅也 (50313515)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 山本卓 (90244102)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 丸山博文 (90304443)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
6. 外丸祐介 (90309352)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 平木啓子 (10455397)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 六車恵子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
9. 橋本浩一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. 渡辺雅彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Ohsawa Ryosuke 大澤亮介

Research Projects

Research Products

Co-Researchers

Study of cerebellum disturbance by genetic approaches

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of molecular mechanism underlying ALS pathogenesis by Optineurin mutationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Mutations in Twinkle Primase-Helicase causes Perrault Syndrome with neurological features2014

Author(s)

Journal Title

DOI

Data Source

Ohsawa Ryosuke 大澤 亮介

Research Projects

Research Products

Co-Researchers

Study of cerebellum disturbance by genetic approaches

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of molecular mechanism underlying ALS pathogenesis by Optineurin mutationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Mutations in Twinkle Primase-Helicase causes Perrault Syndrome with neurological features2014

Author(s)

Journal Title

DOI

Data Source

Ohsawa Ryosuke 大澤亮介