borna nurun nahar ヌルン・ナハールボルナ

Researcher Number	30849609
Other IDs	https://orcid.org/0000-0002-7891-2507
Affiliation (based on the past Project Information) *help	2022: 順天堂大学, 大学院医学研究科, 博士研究員 2019 – 2020: 順天堂大学, 医学(系)研究科(研究院), 博士研究員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / 0902:General internal medicine and related fields
Keywords	Principal Investigator NAD/NADH / ミトコンドリア病 / ミトコンドリア / Mitochondrial Disorders / ATP / OxPhos / Mitoribosome / Mitochondrial disease

Development of the therapy for mitochondrial diseasesPrincipal Investigator
- Principal Investigator
  
  ヌルン・ナハールボルナ
- Project Period (FY)
  2022 – 2023
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Juntendo University
Novel mitochondrial ribosomal genes are associated with mitochondrial disordersPrincipal Investigator
- Principal Investigator
  
  borna nurun nahar
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Review Section
  
  0902:General internal medicine and related fields
- Research Institution
  Juntendo University

All 2020

All Journal Article

[Journal Article] Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL2020
- Author(s)
  Borna Nurun Nahar、Kishita Yoshihito、Sakai Norio、Hamada Yusuke、Kamagata Koji、Kohda Masakazu、Ohtake Akira、Murayama Kei、Okazaki Yasushi
- Journal Title
  
  Genes
  
  Volume: 11 Issue: 11 Pages: 1325-1325
- DOI
  10.3390/genes11111325
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PUBLICLY-20H05519, KAKENHI-PROJECT-19K23954
[Journal Article] NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness2020
- Author(s)
  Borna Nurun Nahar、Kishita Yoshihito、Abe Jiro、Furukawa Takuro、Ogawa-Tominaga Minako、Fushimi Takuya、Imai-Okazaki Atsuko、Takeda Atsuhito、Ohtake Akira、Murayama Kei、Okazaki Yasushi
- Journal Title
  
  Brain
  
  Volume: 143 Issue: 7 Pages: e54-e54
- DOI
  10.1093/brain/awaa130
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K23954

1. 木下善仁

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

borna nurun nahar ヌルン・ナハールボルナ

Research Projects

Research Products

Co-Researchers

Development of the therapy for mitochondrial diseasesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Novel mitochondrial ribosomal genes are associated with mitochondrial disordersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness2020

Author(s)

Journal Title

DOI

Data Source

borna nurun nahar ヌルン・ナハール ボルナ

Research Projects

Research Products

Co-Researchers

Development of the therapy for mitochondrial diseasesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Novel mitochondrial ribosomal genes are associated with mitochondrial disordersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness2020

Author(s)

Journal Title

DOI

Data Source

borna nurun nahar ヌルン・ナハールボルナ