SHIMOKAWA Osamu 霜川修

Researcher Number	50513321
Other IDs	https://orcid.org/0000-0002-5750-3130
External Links
Affiliation (based on the past Project Information) *help	2010: Nagasaki University, 大学院・医歯薬学総合研究科, 客員研究員 2009: 長崎大, 医歯(薬)学総合研究科, 研究員 2009: Nagasaki University, 長崎大学・大学院・医歯薬学総合研究科, 客員研究員 2008: Nagasaki University, 医歯薬学総合研究科, 客員研究員
Review Section/Research Field	Principal Investigator Obstetrics and gynecology / Risk sciences of radiation/Chemicals
Keywords	Principal Investigator Gene Chip解析 / real time PCR / コピー数変化 / 習慣性不育症 / 習慣性流産 / 定量化 / 変異 / 放射線 / ゲノム不安定性

Identification of the genes for abortus habirualisPrincipal Investigator
- Principal Investigator
  
  SHIMOKAWA Osamu
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Nagasaki University
ゲノム変化を指標とした放射線影響の定量化Principal Investigator
- Principal Investigator
  
  霜川修
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (Start-up)
- Research Field
  
  Risk sciences of radiation/Chemicals
- Research Institution
  Nagasaki University

All 2011 2010 2009 2008

All Journal Article Presentation

[Journal Article] Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)2010
- Author(s)
  Horikoshi T, Kikuchi A, Tamaru S, Ono K, Kita M, Takagi K, Miyashita S, Kawame H, Shimokawa O, Harada N
- Journal Title
  
  Vol.36(3)
  
  Pages: 671-675
- NAID
  10031121675
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome.2010
- Author(s)
  Sasaki K, Okamoto N, Kosaki K, Shimokawa O., et al.
- Journal Title
  
  Clinical genetics
  
  Volume: 20 Pages: 1399-1404
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1).2010
- Author(s)
  Horikoshi T, Kikuchi A, Tamaru S, Ono K, Shimokawa O., et al.
- Journal Title
  
  Journal of obstetrics and gynaecology research
  
  Volume: 36(3) Pages: 671-675
- NAID
  10031121675
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome2010
- Author(s)
  Sasaki K, Okamoto N, Kosaki K, Yorifuji T, Shimokawa O, Mishima H, Yoshiura K, Harada N
- Journal Title
  
  Clinical genetics Vol.20
  
  Pages: 1399-1404
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D.2009
- Author(s)
  Kuniba H, Pooh Rk, Sasaki K, Shimokawa O., et al.
- Journal Title
  
  American Journal of Medical Genetics Part A. 149(A)
  
  Pages: 785-787
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D2009
- Author(s)
  Kuniba H, Pooh RK, Sasaki K, Shimokawa O, Harada N, Kondoh T, Egashira M, Moriuchi H, Yoshiura K, Niikawa N
- Journal Title
  
  American Journal of Medical Genetics Part A Vol.149(A)
  
  Pages: 785-787
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791565
[Journal Article] A girl with Down syndrome and partial trisomy for 21 pter-q22.13 : a clue to narrow the Down syndrome critical region.2008
- Author(s)
  Sato D, Kawara H, Shimokawa O, Harada N, Tonoki H, Takahashi N, lmai Y, Kimura H, Matsumoto N, Ariga T, Niikawa N, Yoshiura K.
- Journal Title
  
  American Journal of Medical Genetics 146A
  
  Pages: 124-127
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810020
[Journal Article] Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia.2008
- Author(s)
  Mizuguchi T, Hashimoto R, ltokawa M, Sano A, Shimokawa O. Yoshimura Y, Harada N, Miyake N, Nishimura A, Saitsu H, Sosonkina N, Niikawa N, Kunugi H, Matsumoto N.
- Journal Title
  
  Journal of Human Genetics 53
  
  Pages: 914-919
- NAID
  10022603067
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20810020
[Presentation] ・9q13-q21領域の重複バリアントの報告・染色体片親ダイソミーより発症した常染色体劣性遺伝性疾患の2例2011
- Author(s)
  霜川修
- Organizer
  第8回中国四国出生前医学研究会
- Place of Presentation
  愛媛県県民文化会館3階
- Year and Date
  2011-01-29
- Data Source
  KAKENHI-PROJECT-21791565
[Presentation] ・9q13-q21領域の重複バリアントの報告・染色体片親ダイソミーより発症した常染色体劣性遺伝性疾患の2例2010
- Author(s)
  霜川修
- Organizer
  第11回北海道出生前診断研究会
- Place of Presentation
  札幌医科大学記念ホール
- Year and Date
  2010-12-04
- Data Source
  KAKENHI-PROJECT-21791565
[Presentation] アレイ染色体検査のための健常人CNVデータベース構築の試み2009
- Author(s)
  松井健, 霜川修, その他
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  グランドプリンスホテル高輪,東京
- Data Source
  KAKENHI-PROJECT-21791565
[Presentation] マイクロアレイを使用した全ゲノムコピー数解析による染色体検査の有用性と問題点Availability and problem of whole genomic copy number analysis with microarray2008
- Author(s)
  霜川修, 佐々木健作, 冨土山龍伊, 近藤達郎, 松本直通, 吉浦孝一郎, 新川詔夫, 原田直樹
- Organizer
  日本遺伝子診療学会15回大会
- Place of Presentation
  仙台市戦災復興記念館
- Year and Date
  2008-08-02
- Data Source
  KAKENHI-PROJECT-20810020
[Presentation] 全ゲノムコピー数解析による染色体検査(Molecular karyotyping)の有用性2008
- Author(s)
  霜川修, 佐々木健作, 近藤達郎, 松本直通, 吉浦孝一郎, 新川詔夫, 原田直樹
- Organizer
  第10回甲信越・北陸出生前診断研究会
- Place of Presentation
  KKR甲府ニュー芙蓉
- Year and Date
  2008-10-04
- Data Source
  KAKENHI-PROJECT-20810020
[Presentation] 全ゲノムコピー数解析による染色体検査(Molecular karyotyping)の有用性2008
- Author(s)
  霜川修, 佐々木健作, 近藤達郎, 松本直通, 吉浦孝一郎, 新川詔夫, 原田直樹
- Organizer
  第11回北海道出生前診断研究会
- Place of Presentation
  札幌医科大学臨床教育研究棟IF 大講堂
- Year and Date
  2008-11-22
- Data Source
  KAKENHI-PROJECT-20810020
[Presentation] 羊水検査で検出した稀な9q近位部重複異形を有する3家系2008
- Author(s)
  霜川修, 佐々木健作, 坂井和裕, 長田久夫, 佐久本薫, 近藤達郎, 松本直通, 吉浦孝一郎, 新川詔夫, 原田直樹
- Organizer
  日本人類遺伝学会第53回大会
- Place of Presentation
  パシフィコ横浜会議センター
- Year and Date
  2008-09-27
- Data Source
  KAKENHI-PROJECT-20810020

1. YOSHIURA KOichiro (00304931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results

SHIMOKAWA Osamu 霜川 修

Research Projects

Research Products

Co-Researchers

Identification of the genes for abortus habirualisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

ゲノム変化を指標とした放射線影響の定量化Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)2010

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome.2010

Author(s)

Journal Title

Data Source

[Journal Article] Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1).2010

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome2010

Author(s)

Journal Title

Data Source

[Journal Article] Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D.2009

Author(s)

Journal Title

Data Source

[Journal Article] Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D2009

Author(s)

Journal Title

Data Source

[Journal Article] A girl with Down syndrome and partial trisomy for 21 pter-q22.13 : a clue to narrow the Down syndrome critical region.2008

Author(s)

Journal Title

Data Source

[Journal Article] Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia.2008

Author(s)

Journal Title

NAID

Data Source

[Presentation] ・9q13-q21領域の重複バリアントの報告・染色体片親ダイソミーより発症した常染色体劣性遺伝性疾患の2例2011

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] ・9q13-q21領域の重複バリアントの報告・染色体片親ダイソミーより発症した常染色体劣性遺伝性疾患の2例2010

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] アレイ染色体検査のための健常人CNVデータベース構築の試み2009

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] マイクロアレイを使用した全ゲノムコピー数解析による染色体検査の有用性と問題点Availability and problem of whole genomic copy number analysis with microarray2008

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] 全ゲノムコピー数解析による染色体検査(Molecular karyotyping)の有用性2008

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

SHIMOKAWA Osamu 霜川修