MORI Asami 森麻美

… Alternative Names

森麻美モリアサミ

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Researcher Number	70437151
Affiliation (Current)	2025: 滋賀医科大学, 医学部, 非常勤講師
Affiliation (based on the past Project Information) *help	2012 – 2013: 滋賀医科大学, 医学部, 非常勤講師
Review Section/Research Field	Except Principal Investigator Pediatrics
Keywords	Except Principal Investigator 小児内分泌学 / DUOX2 / Dual oxidase 2 / 次世代シーケンサー / 先天性甲状腺機能低下症

The exhaustive analysis for congenital hypothyroidism using the next generation sequencer
- Principal Investigator
  
  MARUO YOSHIHIRO
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Shiga University of Medical Science

All 2014 2013 2012 2011 Other

All Journal Article Presentation

[Journal Article] Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients.2014
- Author(s)
  Kawakita R, Hosokawa Y, Fujimaru R, Tamagawa N, Urakami T, Takasawa K, Moriya K, Mizuno H, Maruo Y, Takuwa M, Nagasaka H, Nishi Y, Yamamoto Y, Aizu K, Yorifuji T.
- Journal Title
  
  Diabet Med
  
  Volume: mar Issue: 11 Pages: 17-17
- DOI
  10.1111/dme.12487
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24659495, KAKENHI-PROJECT-26461535
[Journal Article] Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice.2014
- Author(s)
  Maruo Y, Morioka Y, Fujito H, Nakahara S, Yanagi T, Matsui K, Mori A, Sato H, Tukey RH, Takeuchi Y.
- Journal Title
  
  J Pediatr
  
  Volume: may Issue: 1 Pages: 7-7
- DOI
  10.1016/j.jpeds.2014.01.060
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659495, KAKENHI-PROJECT-26670497
[Journal Article] UDP-グルクロン酸転移酵素1型ファミリー共通エクソン変異(p.P364L)の薬物代謝に及ぼす影響2012
- Author(s)
  三村由卯、丸尾良浩、森岡依子、佐藤浩、竹内義博
- Journal Title
  
  日本小児臨床薬理学会雑誌
  
  Volume: 25巻 Pages: 129-134
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Compound heterozygote of a novel missense mutation (p.K402T) and a double missense mutation (p.[G71R;Y486D]) in type II Crigler-Najjar syndrome2011
- Author(s)
  Maruo Y, Ozgenc F, Mimura Y, Ota Y, Matsui K, Takahashi H, Mori A, Taga T, Takano T, Sato H, Takeuchi Y.
- Journal Title
  
  J Pediatr Gastroenterol Nutr
  
  Volume: 52(3) Pages: 362-5
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Dual oxidase 2(DUOX2)の両アレル変異による一過性甲状腺機能低下症の8例2011
- Author(s)
  丸尾良浩、三村由卯、森岡依子、松井克之、森麻美、佐藤浩、竹内義博
- Journal Title
  
  ホルモンと臨床
  
  Volume: 59巻 Pages: 1057-1062
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuria
- Author(s)
  Maruo Y, Suzaki M, Matui K, Mimura Y, Mori A, Shintaku H, Takeuchi Y.
- Journal Title
  
  World J Pediatr
  
  Volume: (in press)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明 23例の解析より2014
- Author(s)
  丸尾良浩、長崎啓祐、森麻美、松井克之、三村由卯、深見真紀、竹内義博
- Organizer
  第117回日本小児科学会学術集会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明23例の解析より2014
- Author(s)
  丸尾良浩、長崎啓祐、森麻美、松井克之、三村由卯、深見真紀、竹内義博
- Organizer
  第117回日本小児科学会学術集会
- Place of Presentation
  名古屋市(口演・一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の2家系2013
- Author(s)
  丸尾良浩、森宗孝夫、國津智彬、松井克之、森麻美、三村由卯、竹内義博
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京(ポスター・一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の２家系2013
- Author(s)
  丸尾良浩、森宗孝夫、國津智彬、松井克之、森麻美、三村由卯、竹内義博
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Hutcinson-Gilford-Progeria Syndromeに認められた甲状腺機能低下症の検討2012
- Author(s)
  丸尾良浩、川北理恵、松井克之、森麻美、森岡依子、西尾友宏、岡本暢之、宮下文、西澤嘉四郎、竹内義博
- Organizer
  第115回日本小児科学会学術集会
- Place of Presentation
  福岡市(ポスター、一般)
- Data Source
  KAKENHI-PROJECT-24659495

1. MARUO YOSHIHIRO (80314160)

# of Collaborated Projects: 1 results

# of Collaborated Products: 11 results
2. MATSUI Katsuyuki (60595924)

# of Collaborated Projects: 1 results

# of Collaborated Products: 8 results

MORI Asami 森 麻美

森 麻美 モリ アサミ

Research Projects

Research Products

Co-Researchers

The exhaustive analysis for congenital hypothyroidism using the next generation sequencer

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients.2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice.2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] UDP-グルクロン酸転移酵素1型ファミリー共通エクソン変異(p.P364L)の薬物代謝に及ぼす影響2012

Author(s)

Journal Title

Data Source

[Journal Article] Compound heterozygote of a novel missense mutation (p.K402T) and a double missense mutation (p.[G71R;Y486D]) in type II Crigler-Najjar syndrome2011

Author(s)

Journal Title

Data Source

[Journal Article] Dual oxidase 2(DUOX2)の両アレル変異による一過性甲状腺機能低下症の8例2011

Author(s)

Journal Title

Data Source

[Journal Article] A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuria

Author(s)

Journal Title

Data Source

[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明 23例の解析より2014

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明23例の解析より2014

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の2家系2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の２家系2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Hutcinson-Gilford-Progeria Syndromeに認められた甲状腺機能低下症の検討2012

Author(s)

Organizer

Place of Presentation

Data Source

MORI Asami 森麻美

森麻美モリアサミ