IMOTO Kyoko 井本恭子

Researcher Number	80445064
Affiliation (based on the past Project Information) *help	2008 – 2010: Nara Medical University, 医学部, 助教
Review Section/Research Field	Principal Investigator Dermatology
Keywords	Principal Investigator 遺伝子 / 毛髪 / 光線過敏症

Research Projects
(1 results)
Research Products
(6 results)

Phemotype-genotype correlation of Japanese TrichothiodystrophyPrincipal Investigator
- Principal Investigator
  
  IMOTO Kyoko
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Dermatology
- Research Institution
  Nara Medical University

All 2010 2009 2008

All Journal Article Presentation

[Journal Article] XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients2010
- Author(s)
  Khan SG, Yamanegi K, Zheng ZM, Boyle J, Imoto K, et al
- Journal Title
  
  Human Mutation 31巻
  
  Pages: 167-75
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790813
[Journal Article] XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms2009
- Author(s)
  Khan SG, Oh KS, Emmert S, Imoto K, et al
- Journal Title
  
  DNA Repair (Amst) 8巻
  
  Pages: 114-25
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790813
[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009
- Author(s)
  Christen-Zaech S, Imoto K, et al
- Journal Title
  
  Arch Dermatol 145巻
  
  Pages: 12885-91
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790813
[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009
- Author(s)
  Christen-Zaech S and Imoto K, et.al.
- Journal Title
  
  Archives of Dermatology (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790813
[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009
- Author(s)
  Christen-Zaech S, Imoto K, et al.
- Journal Title
  
  Archives of Dermatology 145(11)
  
  Pages: 1285-91
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790813
[Presentation] Ancient origin of a Japanese xeroderma pigmentosum founder mutation2008
- Author(s)
  Kyoko Imoto, et al
- Organizer
  SID
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20790813

IMOTO Kyoko 井本 恭子

Research Projects

Research Products

Phemotype-genotype correlation of Japanese TrichothiodystrophyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients2010

Author(s)

Journal Title

Data Source

[Journal Article] XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms2009

Author(s)

Journal Title

Data Source

[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009

Author(s)

Journal Title

Data Source

[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009

Author(s)

Journal Title

Data Source

[Journal Article] Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew2009

Author(s)

Journal Title

Data Source

[Presentation] Ancient origin of a Japanese xeroderma pigmentosum founder mutation2008

Author(s)

Organizer

Place of Presentation

Data Source

IMOTO Kyoko 井本恭子