Kitamura Katsumasa 北村勝誠

Researcher Number	40724381
Affiliation (based on the past Project Information) *help	2016: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, 客員研究員 2015: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, その他 2014: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, 流動研究員
Review Section/Research Field	Principal Investigator Pediatrics
Keywords	Principal Investigator 赤芽球系分化 / 巨核球系分化 / 赤芽球分化 / 巨核球分化 / 転写因子 / 巨大血小板 / 先天性血小板減少症

Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia.Principal Investigator
- Principal Investigator
  
  Kitamura Katsumasa
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Hospital Organization Nagoya Medical Center

All 2016 2015 2014 Other

All Journal Article Presentation

[Journal Article] Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia2016
- Author(s)
  Kitamura K, Okuno Y, Yoshida K, Sanada M, Shiraishi Y, Muramatsu H, Kobayashi R, Furukawa K, Miyano S, Kojima S, Ogawa S, Kunishima S
- Journal Title
  
  J Thromb Haemost
  
  Volume: 14 Issue: 7 Pages: 1462-9
- DOI
  10.1111/jth.13350
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Journal Article] Diagnostic biomarker for ACTN1 macrothrombocytopenia.2016
- Author(s)
  Kunishima S, Kitamura K, Yasutomi M, Kobayashi R.
- Journal Title
  
  Blood
  
  Volume: 126 Issue: 22 Pages: 2525-6
- DOI
  10.1182/blood-2015-08-666180
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Journal Article] The first two cases of MYH9 disorders in Thailand: an international collaborative study2015
- Author(s)
  Sirachainan N, Komwilaisak P, Kitamura K, Hongeng S, Sekine T, Kunishima S
- Journal Title
  
  Ann Hematol
  
  Volume: 94 Issue: 4 Pages: 707-709
- DOI
  10.1007/s00277-014-2234-6
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840, KAKENHI-PROJECT-15H04880
[Journal Article] Somatic mosaicism in MYH9 disorders : the need to carefully evaluate apparently healthy parents2014
- Author(s)
  Kunishima S, Kitamura K, Matsumo T, Sekine T, Saito H
- Journal Title
  
  British Journal of Haematology
  
  Volume: 165 Issue: 6 Pages: 885-887
- DOI
  10.1111/bjh.12797
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591586, KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Presentation] Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia2015
- Author(s)
  Katsumasa Kitamura, Yusuke Okuno, Kenichi Yoshida, Masashi Sanada, Yuichi Shiraishi, Hideki Muramatsu, Ryoji Kobayashi, Satoru Miyano, Seiji Kojima, Seishi Ogawa, Shinji Kunishima
- Organizer
  第57回米国血液学会
- Place of Presentation
  米国、オーランド
- Year and Date
  2015-12-05
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26860840
[Presentation] MYH9異常症の体細胞モザイク
- Author(s)
  國島伸治　北村勝誠　松本多絵　関根孝司
- Organizer
  第15回日本検査血液学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2014-07-20 – 2014-07-21
- Data Source
  KAKENHI-PROJECT-26860840
[Presentation] 巨核球特異的β1-tubulin異常は微小管構成阻害により胞体突起形成不全を来す
- Author(s)
  國島伸治　北村勝誠　西村智　鈴木英紀　今泉益栄　齋藤英彦
- Organizer
  第36回日本血栓止血学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2014-05-29 – 2014-05-31
- Data Source
  KAKENHI-PROJECT-26860840

1. 國島伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 4 results
2. 関根孝司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kitamura Katsumasa 北村 勝誠

Research Projects

Research Products

Co-Researchers

Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia.Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Diagnostic biomarker for ACTN1 macrothrombocytopenia.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] The first two cases of MYH9 disorders in Thailand: an international collaborative study2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Somatic mosaicism in MYH9 disorders : the need to carefully evaluate apparently healthy parents2014

Author(s)

Journal Title

DOI

Data Source

[Presentation] Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] MYH9異常症の体細胞モザイク

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] 巨核球特異的β1-tubulin異常は微小管構成阻害により胞体突起形成不全を来す

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

Kitamura Katsumasa 北村勝誠