MIWA Nobutomo 三輪晋智

… Alternative Names

三輪晋智ミワノブトモ

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Researcher Number	30419626
External Links
Affiliation (based on the past Project Information) *help	2009: 長崎大学, 大学院・医歯薬学総合研究科, 助教 2007: Nagasaki University, 大学院・医歯薬学総合研究科, 助教 2006: 長崎大学, 大学院医歯薬学総合研究科, 助手
Review Section/Research Field	Principal Investigator Applied pharmacology Except Principal Investigator Biological Sciences
Keywords	Principal Investigator 電子顕微鏡 / 免疫染色 / 耳垢 / Baculovirus / 薬剤耐性 / バキュロウィルス / アポクリン腺 / 薬剤感受性 / MRP8 / ABCC11 / 耳垢型 … More Except Principal Investigator … More 精神遅滞症 / Kabuki make-up症候群 / 家族性心房中隔欠損症 / 染色体構造異常 / 一過性運動誘発性コレオアテトーシス / 特発性手掌多汗症 / 遺伝子単離 / 歌舞伎症候群 / 合指症 / 多指趾症 / 染色体 / 因子疾患 / 疾患感受性遺伝子 / 関連解析 / 多因子疾患 / 単因子疾患 / 連鎖解析 / 疾患遺伝子 / 染色体異常 Less

耳垢型決定遺伝子が薬剤感受性に与える影響に関する研究Principal Investigator
- Principal Investigator
  
  三輪晋智
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Young Scientists (Start-up)
- Research Field
  
  Applied pharmacology
- Research Institution
  Nagasaki University
A family-analysis-based search for genes susceptible to mono-, oligo- and polygenic disorders
- Principal Investigator
  
  NIIKAWA Norio
- Project Period (FY)
  2005 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Health Sciences University of Hokkaido
  Nagasaki University

All 2009 2008 2007

All Journal Article Presentation

[Journal Article] A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene2009
- Author(s)
  Nakano M, Miwa N, Hirano A, Yoshiura K, Niikawa N
- Journal Title
  
  BMC Genet 10
  
  Pages: 42-44
- NAID
  120006983999
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019055
[Journal Article] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family2008
- Author(s)
  Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura K
- Journal Title
  
  J Hum Genet 53(1)
  
  Pages: 34-41
- NAID
  10021247449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019055
[Journal Article] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family2008
- Author(s)
  Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura K
- Journal Title
  
  J Hum Genet 53
  
  Pages: 34-41
- NAID
  10021247449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019055
[Journal Article] Congenital arhinia : Molecular-genetic analysis of five patients2007
- Author(s)
  Sato D, Shimokawa O, Harada N, OlsenOE, Hou J-W, Muhlbauer W, Blinkenberg E, Okamoto N, Kinoshita A, Matsumoto N, Kondo S, Kishino T, Miwa N, Niikawa N, Yoshiura K
- Journal Title
  
  American Journal of Medical Genetics (in press)
- Data Source
  KAKENHI-PROJECT-17019055
[Journal Article] Congenital arhinia: Molecular-genetic analysis of five patients2007
- Author(s)
  Sato D, Shimokawa O, Harada N, OlsenOE, Hou J-W, Muhlbauer W, Blinkenberg E, Okamoto N, Kinoshita A, Matsumoto N, Kondo S, Kishino T, Miwa N, Niikawa N, Yoshiura K
- Journal Title
  
  Am J Med Genet 143A
  
  Pages: 546-552
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019055
[Presentation] ABCC11の耳垢型決定多型による機能変化2007
- Author(s)
  三輪晋智
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  京王プラザホテル
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-18890142

1. NIIKAWA Norio (00111170)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
2. OHTA Tohru (10223835)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. KINOSHITA Akira (60372778)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
4. YOSHIURA Koh-Ichiro (00304931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results

MIWA Nobutomo 三輪 晋智

三輪 晋智 ミワ ノブトモ

Research Projects

Research Products

Co-Researchers

耳垢型決定遺伝子が薬剤感受性に与える影響に関する研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

A family-analysis-based search for genes susceptible to mono-, oligo- and polygenic disorders

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family2008

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family2008

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Congenital arhinia : Molecular-genetic analysis of five patients2007

Author(s)

Journal Title

Data Source

[Journal Article] Congenital arhinia: Molecular-genetic analysis of five patients2007

Author(s)

Journal Title

Data Source

[Presentation] ABCC11の耳垢型決定多型による機能変化2007

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

MIWA Nobutomo 三輪晋智

三輪晋智ミワノブトモ