Tada Yui 多田有似

Researcher Number	90881285
Other IDs
Affiliation (based on the past Project Information) *help	2023: 広島大学, ゲノム編集イノベーションセンター, 特任助教 2021 – 2022: 広島大学, 原爆放射線医科学研究所, 助教
Review Section/Research Field	Principal Investigator Basic Section 51030:Pathophysiologic neuroscience-related / Basic Section 52020:Neurology-related Except Principal Investigator Medium-sized Section 52:General internal medicine and related fields
Keywords	Principal Investigator 原因遺伝子 / 多系統萎縮症 / 神経変性疾患 / 次世代シーケンサー / 脊髄小脳変性症 Except Principal Investigator リピート / 眼咽頭遠位型ミオパチー / 原因遺伝子 / ロングリードシーケンサー / 筋萎縮性側索硬化症

多系統萎縮症の原因遺伝子探索と発症メカニズムの解明Principal Investigator
- Principal Investigator
  
  多田有似
- Project Period (FY)
  2023 – 2024
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 51030:Pathophysiologic neuroscience-related
- Research Institution
  Hiroshima University
Identifying the causative genes of multiple system atrophyPrincipal Investigator
- Principal Investigator
  
  Tada Yui
- Project Period (FY)
  2021 – 2022
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Hiroshima University
Identification and analysis of novel genes of amyotrophic lateral screlosis
- Principal Investigator
  
  川上秀史
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Hiroshima University

All 2022 2021

All Journal Article

[Journal Article] Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient2022
- Author(s)
  Saito Rie、Tada Yui、Oikawa Daisuke、Sato Yusuke、Seto Makiko、Satoh Akira、Kume Kodai、Ueki Nozomi、Nakashima Masahiro、Hayashi Shintaro、Toyoshima Yasuko、Tokunaga Fuminori、Kawakami Hideshi、Kakita Akiyoshi
- Journal Title
  
  Acta Neuropathologica Communications
  
  Volume: 10 Issue: 1 Pages: 177-177
- DOI
  10.1186/s40478-022-01486-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06873, KAKENHI-PROJECT-22K18385, KAKENHI-PROJECT-22H04922, KAKENHI-PROJECT-21H04818, KAKENHI-PROJECT-21H02418, KAKENHI-PROJECT-21H02688, KAKENHI-PROJECT-20K07424, KAKENHI-PROJECT-20K08886, KAKENHI-PUBLICLY-21H00283, KAKENHI-PUBLICLY-21H00291
[Journal Article] Comparison of two families with and without ataxia harboring novel variants in PRKCG2022
- Author(s)
  Tada Yui、Kume Kodai、Noguchi Soma、Sekiya Tomoko、Nishinaka Kazuto、Ishiguchi Hiroshi、Koh Jinsoo、Emori Seiji、Nakayama Yoshiaki、Kurashige Takashi、Izumi Yuishin、Ito Hidefumi、Sakai Norio、Kawakami Hideshi
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 67 Issue: 10 Pages: 595-599
- DOI
  10.1038/s10038-022-01057-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21H04818
[Journal Article] Novel monoallelic variant in ERLIN2 causes spastic paraplegia converted to amyotrophic lateral sclerosis2021
- Author(s)
  Kodai Kume, Masaki Kamada, Yoshimitsu Shimatani, Tadayuki Takata, Yuishin Izumi, Hideshi Kawakami
- Journal Title
  
  Journal of the Neurological Sciences
  
  Volume: 430 Pages: 119984-119984
- DOI
  10.1016/j.jns.2021.119984
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K16580, KAKENHI-PROJECT-21H04818

1. 川上秀史 (70253060)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
2. 六車恵子 (30209978)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 宮本達雄 (40452627)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 久米広大 (20592314)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. 倉重毅志 (20710627)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. 及川大輔

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Tada Yui 多田有似

Research Projects

Research Products

Co-Researchers

多系統萎縮症の原因遺伝子探索と発症メカニズムの解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identifying the causative genes of multiple system atrophyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identification and analysis of novel genes of amyotrophic lateral screlosis

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Comparison of two families with and without ataxia harboring novel variants in PRKCG2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel monoallelic variant in ERLIN2 causes spastic paraplegia converted to amyotrophic lateral sclerosis2021

Author(s)

Journal Title

DOI

Data Source

Tada Yui 多田 有似

Research Projects

Research Products

Co-Researchers

多系統萎縮症の原因遺伝子探索と発症メカニズムの解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identifying the causative genes of multiple system atrophyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identification and analysis of novel genes of amyotrophic lateral screlosis

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Comparison of two families with and without ataxia harboring novel variants in PRKCG2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel monoallelic variant in ERLIN2 causes spastic paraplegia converted to amyotrophic lateral sclerosis2021

Author(s)

Journal Title

DOI

Data Source

Tada Yui 多田有似