KATO Fumiko 加藤芙弥子

Researcher Number	10462798
Affiliation *help	2015 – 2016 : 浜松医科大学, 医学部, 特任研究員 2012 – 2013 : 浜松医科大学, 医学部, 研究員 2013 : 浜松医科大学, 小児科, 研究員 2012 : 浜松医科大学, 医学部, 特任研究員 2011 : 国立大学法人浜松医科大学, 医学部, 研究員 2007 : 国立研究開発法人国立成育医療研究センター, 分子内分泌研究部, 共同研究員
Review Section/Research Field	Principal Investigator Pediatrics / Embryonic/Neonatal medicine Except Principal Investigator Endocrinology
Keywords	Principal Investigator シルバーラッセル症候群 / エピ変異 / ICR2 / IMAGe症候群 / ICR1 / 遺伝学 Except Principal Investigator 先天疾患 / 小児内分泌学 / 遺伝子 / ホルモン / 性分化

シルバーラッセル症構群発症機序の解明と（エピ）遺伝子型―表現型解析Principal InvestigatorOngoing
- Principal Investigator
  
  加藤芙弥子
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
  Embryonic/Neonatal medicine
- Research Institution
  Hamamatsu University School of Medicine
Investigation for molecular basis of hypothalamo-pituitary-gonadal dysfunction
- Principal Investigator
  
  FUKAMI MAKI
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Endocrinology
- Research Institution
  National Research Institute for Child Health and Development

All 2013 2012

All Journal Article Presentation

[Journal Article] A 68-year-old phenotypically male patient with 21 -hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol2013
- Author(s)
  Hayashi M, Kataoka Y, Sugimura Y, Kato F, Fukami M, Ogata T, Homma K, Hasegawa T, Oiso Y, Sasano H, Tanaka H
- Journal Title
  
  Tohoku J Exp Med
  
  Volume : 231 (2) Pages : 75-84
- Data Source
  KAKENHI-PROJECT-23390249
[Journal Article] A 68-year-old phenotypically male patient with 21-hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol.2013
- Author(s)
  Hayashi M, Kataoka Y, Sugimura Y, Kato F, Fukami M, Ogata T, Homma K, Hasegawa T, Oiso Y, Sasano H, Tanaka H
- Journal Title
  
  Tohoku J Exp Med.
  
  Volume : 231
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390249
[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome.2012
- Author(s)
  Igarashi M, Kato F, Tsuji Y, Hasegawa Y, Ogata T, Fukami M.
- Organizer
  6th International Symposium on the Biology of Vertebrate Sex Determination
- Place of Presentation
  Kona, USA
- Data Source
  KAKENHI-PROJECT-23390249
[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome2012
- Author(s)
  Igarashi M, Kato F, Tsuji Y, Hasegawa Y, Ogata T, Fukami M
- Organizer
  6th International Symposium on the Biology of Vertebrate Sex Determination
- Place of Presentation
  USA
- Data Source
  KAKENHI-PROJECT-23390249

1. FUKAMI MAKI (40265872)

# of Collaborated Projects : 1results

# of Collaborated Products : 4results
2. SONEDA Shun (10367378)

# of Collaborated Projects : 1results

# of Collaborated Products : 0results

KATO Fumiko 加藤芙弥子

Research Projects

Research Products

Co-Researchers

シルバーラッセル症構群発症機序の解明と（エピ）遺伝子型―表現型解析Principal InvestigatorOngoing

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Investigation for molecular basis of hypothalamo-pituitary-gonadal dysfunction

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A 68-year-old phenotypically male patient with 21 -hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol2013

Author(s)

Journal Title

Data Source

[Journal Article] A 68-year-old phenotypically male patient with 21-hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol.2013

Author(s)

Journal Title

Data Source

[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome.2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome2012

Author(s)

Organizer

Place of Presentation

Data Source

KATO Fumiko 加藤 芙弥子

Research Projects

Research Products

Co-Researchers

シルバーラッセル症構群発症機序の解明と（エピ）遺伝子型―表現型解析Principal InvestigatorOngoing

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Investigation for molecular basis of hypothalamo-pituitary-gonadal dysfunction

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A 68-year-old phenotypically male patient with 21 -hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol2013

Author(s)

Journal Title

Data Source

[Journal Article] A 68-year-old phenotypically male patient with 21-hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol.2013

Author(s)

Journal Title

Data Source

[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome.2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome2012

Author(s)

Organizer

Place of Presentation

Data Source

KATO Fumiko 加藤芙弥子