Nakamura Kazuhiro 中村和洋

… Alternative Names

中村和洋ナカムラカズヒロ

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Researcher Number	70363059
Affiliation (based on the past Project Information) *help	2015: 広島大学, 大学院医歯薬保健学研究院, 准教授 2013: 広島大学, 医歯薬保健学研究院, 准教授
Review Section/Research Field	Except Principal Investigator Pediatrics
Keywords	Except Principal Investigator TALEN / 遺伝子修復 / 人工ヌクレアーゼ / 遺伝子編集 / iPS細胞 / 先天性好中球減少症

Gene editing of iPS cells derived from patients with congenital phagocytic disorders
- Principal Investigator
  
  Kobayashi Masao
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Hiroshima University

All 2013 2012 Other

All Journal Article Presentation

[Journal Article] Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia-derived pluipotent stem cells with heterozygous ELANE mutation.2013
- Author(s)
  Hiramoto T
- Journal Title
  
  Proc Natl Acad Sci USA
  
  Volume: 110 Issue: 8 Pages: 3023-3028
- DOI
  10.1073/pnas.1217039110
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591161, KAKENHI-PROJECT-23310137, KAKENHI-PROJECT-23650150, KAKENHI-PROJECT-23790126, KAKENHI-PROJECT-24390257, KAKENHI-PROJECT-24390272, KAKENHI-PROJECT-24659489, KAKENHI-PROJECT-25293231, KAKENHI-PLANNED-23106004
[Journal Article] Heterozygosity for the Y701C STAT1 mutation in a multiplex kindred with multifocal osteomyelitis2013
- Author(s)
  Hirata, O.
- Journal Title
  
  Haematologica
  
  Volume: 98 Issue: 10 Pages: 1641-1649
- DOI
  10.3324/haematol.2013.083741
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25118717, KAKENHI-PROJECT-25293231, KAKENHI-PROJECT-25670477, KAKENHI-PROJECT-25713039, KAKENHI-PROJECT-25870468
[Journal Article] Identification of the integrin B3 L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis2012
- Author(s)
  Kobayashi Y
- Journal Title
  
  British Journal of Haematology
  
  Volume: 31 Issue: 4 Pages: 762-772
- DOI
  10.1111/bjh.12160
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591161, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-25293231
[Presentation] Genetic characteristic of patients with severe congenital neutropenia in Japan.2013
- Author(s)
  Masao Kobayashi, Yoko Mizoguchi, Shuhei Karakawa, Satoshi Okada, Hiroshi Kawaguchi, Kazuhiro Nakamura
- Organizer
  27th International Congress of Pediatrics
- Place of Presentation
  Melbourne, Australia
- Data Source
  KAKENHI-PROJECT-25293231
[Presentation] Excessive Nitric Oxide production of CGD neutrophils induces the down-regulation of NOS3 and EDN1 expression in human endothelial cells.
- Author(s)
  Akari N. Utsunomiya, Miyuki Tsumura, Norioki Ohno, Mizuka Miki, Hiroshi Kawaguchi, Kazuhiro Nakamura and Masao Kobayashi
- Organizer
  The 56th American Society of Hematology Annual Meeting and Exposition
- Place of Presentation
  San Francisco, CA, USA
- Year and Date
  2014-12-06 – 2014-12-09
- Data Source
  KAKENHI-PROJECT-25293231
[Presentation] Early elimination of Factor VIII inhibitor by ITI with high dose immunoglobulin in hemophilia A children.
- Author(s)
  Yoko Mizoguchi, Aya Furue, Ikue Chijimatsu, Mizuka Miki, Keita Tomioka, Nakao Konishi, Atsushi Ono, Hiroshi Kawaguchi, Kazuhiro Nakamura and Masao Kobayashi
- Organizer
  WORLD FEDERATION OF HEMOPHILIA, 2014 World Congress
- Place of Presentation
  Melbourne, Australia
- Year and Date
  2014-05-11 – 2014-05-15
- Data Source
  KAKENHI-PROJECT-25293231

1. Kobayashi Masao (00162016)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
2. Tsumura Miyuki (80646274)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
3. Okada Satoshi (80457241)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. Yamamoto Takashi (90244102)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

Nakamura Kazuhiro 中村 和洋

中村 和洋 ナカムラ カズヒロ

Research Projects

Research Products

Co-Researchers

Gene editing of iPS cells derived from patients with congenital phagocytic disorders

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia-derived pluipotent stem cells with heterozygous ELANE mutation.2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Heterozygosity for the Y701C STAT1 mutation in a multiplex kindred with multifocal osteomyelitis2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Identification of the integrin B3 L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis2012

Author(s)

Journal Title

DOI

Data Source

[Presentation] Genetic characteristic of patients with severe congenital neutropenia in Japan.2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Excessive Nitric Oxide production of CGD neutrophils induces the down-regulation of NOS3 and EDN1 expression in human endothelial cells.

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] Early elimination of Factor VIII inhibitor by ITI with high dose immunoglobulin in hemophilia A children.

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

Nakamura Kazuhiro 中村和洋

中村和洋ナカムラカズヒロ