Matsunoshita Natsuki 松野下夏樹

Researcher Number	70622885
Affiliation (based on the past Project Information) *help	2016: 神戸大学, 医学研究科, 医学研究員 2015: 神戸大学, 医学(系)研究科(研究院), 研究員 2014: 神戸大学, 医学(系)研究科(研究院), 助教
Review Section/Research Field	Principal Investigator Pediatrics
Keywords	Principal Investigator マイクロRNA / podocyte障害 / 蛋白尿惹起因子 / 小児特発性ネフローゼ症候群 / 次世代シークエンサー / 網羅的診断体制 / podocyte / ネフローゼ症候群

The role of microRNA for pediatric idiopathic nephrotic syndromePrincipal Investigator
- Principal Investigator
  
  Matsunoshita Natsuki
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University

All 2016

All Journal Article

[Journal Article] Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics2016
- Author(s)
  Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K
- Journal Title
  
  Genetics in Medicine
  
  Volume: 18 Issue: 2 Pages: 180-188
- DOI
  10.1038/gim.2015.56
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09695
[Journal Article] Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.2016
- Author(s)
  Fu XJ, Nozu K, Kaito H, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Ohtsubo H, Matsunoshita N, Kamiyoshi N, Matsumura C, Takagi N, Maekawa K, Taniguchi-Ikeda M, Iijima K
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 24 Issue: 3 Pages: 387-391
- DOI
  10.1038/ejhg.2015.113
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09695
[Journal Article] Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.2016
- Author(s)
  Kamiyoshi N, Nozu K, Urahama Y, Matsunoshita N, Yamamura T, Minamikawa S, Ninchoji T, Morisada N, Nakanishi K, Kaito H, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20 Issue: 2 Pages: 253-257
- DOI
  10.1007/s10157-015-1160-9
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09261

1. YOSHIKAWA Norishige

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
2. NAKANISHI Koichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
3. 野津寛大

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
4. 庄野朱美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. 飯島一誠

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Matsunoshita Natsuki 松野下夏樹

Research Projects

Research Products

Co-Researchers

The role of microRNA for pediatric idiopathic nephrotic syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.2016

Author(s)

Journal Title

DOI

Data Source

Matsunoshita Natsuki 松野下 夏樹

Research Projects

Research Products

Co-Researchers

The role of microRNA for pediatric idiopathic nephrotic syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.2016

Author(s)

Journal Title

DOI

Data Source

Matsunoshita Natsuki 松野下夏樹