WADA Yuka 和田友香

… Alternative Names

和田友香ワダユカ

Less

Researcher Number	80399485
Other IDs
Affiliation (Current)	2025: 国立研究開発法人国立成育医療研究センター, 周産期センター, 医師
Affiliation (based on the past Project Information) *help	2016 – 2017: 国立研究開発法人国立成育医療研究センター, 周産期センター, 医師 2015: 国立研究開発法人国立成育医療研究センター, その他部局等, その他 2013: 独立行政法人国立成育医療研究センター, 新生児科, 医員 2012 – 2013: 独立行政法人国立成育医療研究センター, その他部局等, その他 2010: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 研究員 … More 2010: 独立行政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 2010: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 研究員 2009: National Research Institute for Child Health and Development, 小児思春期発育研究部, 共同研究員 2008 – 2009: National Research Institute for Child Health and Development, 小児思春期発育研究部, 共同研究員 2008 – 2009: 国立成育医療センター研究所, 小児思春期発育研究部, 研究員 2007 – 2008: National Research Institute for Child Health and Development, 小児思春期発育研究部, 流動研究員 2005 – 2007: 国立成育医療センター(研究所), 小児思春期発育研究部, 研究員 2006: National Research Institute for Child Health and Development, Research Fellow, 研究員 Less
Review Section/Research Field	Principal Investigator Embryonic/Neonatal medicine / Endocrinology / Human genetics Except Principal Investigator Pediatrics / Embryonic/Neonatal medicine / Endocrinology
Keywords	Principal Investigator 分子遺伝学 / 授乳 / 薬剤 / 未熟児 / 薬物 / 母乳 / スプライシング / 尿道下裂 / 性分化異常症(DSD) / 停留精巣 … More Except Principal Investigator … More SHOX / MAMLD1 / 性分化 / 染色体構造異常 / メチル化異常 / インプリンティング異常症 / 染色体微細構造異常 / 筋緊張低下 / インプリンティング疾患 / 3' region / Enhancer / Full length cDNA / In silico analysis / Haploinsufficiency / Sex chromosomes / Regulatory seqiuence / in silico / 3'領域 / エンハンサー / 完全長cDNA / in silico解析 / 半量不全 / 性染色体 / 発現調節領域 / Notch / ステロイド / 性ホルモン / 生殖内分泌学 / テストステロン産生 / 精子形成障害 / 卵巣機能不全 / Metabglic syndrome / 性分化異常症 / Metabolic syndrome / ノックダウン / Notchシグナル / 尿道下裂 / CXorf6 / ノックアウトマウス / 臨床像 / 遺伝子機能 / 遺伝子変異 Less

The frequency of cases with imprinting disorders in hypotonic neonates and infants
- Principal Investigator
  
  Matsubara Keiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  National Center for Child Health and Development
Influence of the medicine through the breast milk in the premature infantPrincipal Investigator
- Principal Investigator
  
  WADA Yuka
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  National Research Institute for Child Health and Development
Splice site mutation of MAMLD1 in disorders of sex development patientsPrincipal Investigator
- Principal Investigator
  
  WADA Yuka
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Endocrinology
- Research Institution
  National Research Institute for Child Health and Development
Molecular mechanism leading to impaired sexual differentiation and reproductive failure in patients with MAMLD mutations
- Principal Investigator
  
  FUKAMI Maki
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Endocrinology
- Research Institution
  National Research Institute for Child Health and Development
Novel sex development gene CXorf6 : determination of clinical spectrum in mutation positive patients and clarification of underlying factors
- Principal Investigator
  
  OGATA Tsutomu
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Research Institute for Child Health and Development
Mutation and polymorphism analyses of INSL3, LGR8/GREAT and SF-1 in patients with cryptorchidismPrincipal Investigator
- Principal Investigator
  
  WADA Yuka
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  National Research Institute for Child Health and Development
Clarification of the genetic mechanisms underlying the regulation for the expression of SHOX, a causative gene for short stature and sdyschomndrosteosis
- Principal Investigator
  
  OGATA Tsutomu
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  National Research Institute for Child Health and Development

All 2014 2013 2012 2010 2009 2008 2007 Other

All Journal Article Presentation Book

[Book] 第9回医師のための母乳育児支援セミナー2013
- Author(s)
  和田　友香、瀬川雅史、本郷寛子、水井雅子、大山牧子、奥起久子、瀬尾智子、水野克己、田中奈美
- Total Pages
  15
- Publisher
  日本ラクテーションコンサルタント協会
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 母乳と薬剤2014
- Author(s)
  和田友香
- Journal Title
  
  東京小児科医会報
  
  Volume: 32(3) Pages: 20-25
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 新生児における先天性乳麋胸水に対するオクトレオチド投与療法2014
- Author(s)
  和田友香
- Journal Title
  
  薬局
  
  Volume: 65(1) Pages: 12-12
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 胆汁うっ滞性肝障害に対する待望の治療薬！魚油由来脂肪製剤Omegaven○R2014
- Author(s)
  和田　友香
- Journal Title
  
  薬局
  
  Volume: ６５（２） Pages: 9-9
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 胆汁うっ滞性肝障害に対する待望の治療薬! 魚油由来脂肪製剤Omegaven®2014
- Author(s)
  和田友香
- Journal Title
  
  薬局
  
  Volume: 65(2) Pages: 9-9
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 20世紀の新生児医療を変えたサーファクタント補充療法2013
- Author(s)
  和田友香
- Journal Title
  
  薬局
  
  Volume: 64(13) Pages: 7-7
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 小腸機能不全関連肝機能障害に対するFish oilの使用経験2013
- Author(s)
  渡辺稔彦、船山理恵、山田耕嗣、山田和歌、高橋正貴、石濱秀雄、武田憲子、藤野明浩、田中秀明、濱郁子、兼重昌夫、和田友香、淵本康史、伊藤玲子、中村知夫、伊藤裕司、新井勝大、金森豊
- Journal Title
  
  日本小児栄養消化器肝臓学会雑誌
  
  Volume: ２７（２） Pages: 143-147
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 小腸機能不全関連肝機能障害に対するFish oil の使用経験2013
- Author(s)
  渡辺稔彦, 船山理恵, 山田耕嗣, 山田和歌, 高橋正貴, 石濱秀雄, 武田憲子, 藤野明浩, 田中秀明, 濱郁子, 兼重昌夫, 和田友香, 淵本康史, 伊藤玲子, 中村知夫, 伊藤裕司, 新井勝大, 金森豊
- Journal Title
  
  日本小児栄養消化器肝臓学会雑誌
  
  Volume: 27(2) Pages: 143-147
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 新生児における先天性乳麋胸水に対するオクトレオチド投与療法.2013
- Author(s)
  和田　友香
- Journal Title
  
  薬局
  
  Volume: ６５（１） Pages: 12-12
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 母乳育児が結ぶ母と子の絆2012
- Author(s)
  和田友香
- Journal Title
  
  日本母乳哺育学会雑誌
  
  Volume: 6(suppl) Pages: 34-35
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 母乳育児が結ぶ母とこの絆2012
- Author(s)
  和田友香
- Journal Title
  
  日本母乳哺育学会雑誌
  
  Volume: 6(1) Pages: 30-34
- Data Source
  KAKENHI-PROJECT-24791127
[Journal Article] 小児内分泌学の進歩2009.性分化異常症発症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2010
- Author(s)
  深見真紀、和田友香、上松あゆ美、長谷川奉延、緒方勤
- Journal Title
  
  ホルモンと臨床 57(12)
  
  Pages: 1025-1029
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] 性分化異常症発症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2010
- Author(s)
  深見真紀、和田友香、上松あゆ美、長谷川奉延、緒方勤
- Journal Title
  
  ホルモンと臨床
  
  Volume: 57(12) Pages: 1025-1029
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Cytochrome P450 Oxidoreductase Deficiency : Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients.2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T.
- Journal Title
  
  J Clin Endocrinol Metab. 94(5)
  
  Pages: 1723-1731
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with Campomelic dysplasia or Acampomelic dysplasia2009
- Author(s)
  Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T.
- Journal Title
  
  Am J Med Genet. 149A(12)
  
  Pages: 2882-2885
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790899
[Journal Article] Mutation analysis of SOX9 and single copy number variantanalysis of the upstream region in eight patients with Campomelic dysplasia or Acampomelic dysplasia.2009
- Author(s)
  Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T.
- Journal Title
  
  Am J Med Genet. 149A(12)
  
  Pages: 2882-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790899
[Journal Article] Cytochrome P450 oxidoreductase deficiency : identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, TIshii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T
- Journal Title
  
  Journal of Clinical Endocrinology & Metabolism 94(5)
  
  Pages: 1723-1731
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] 性分化異常症発症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2009
- Author(s)
  深見真紀、和田友香, 他
- Journal Title
  
  ホルモンと臨床 (印刷中)
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T
- Journal Title
  
  Journal of Clinical Endocrinology & Metabolism 94(5)
  
  Pages: 1723-1731
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] 尿道下裂2009
- Author(s)
  深見真紀、和田友香、緒方勤
- Journal Title
  
  小児科 50(7)
  
  Pages: 939-945
- Data Source
  KAKENHI-PROJECT-21790899
[Journal Article] 日本人が発見にかかわった遣伝子:尿道下裂(CXorf6)2009
- Author(s)
  深見真紀、和田友香、緒方勤
- Journal Title
  
  小児科 50(7)
  
  Pages: 939-945
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia or acampomelic campomelic dysplasia.2009
- Author(s)
  Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T
- Journal Title
  
  American Journal of Medical Genetics A 149A(12)
  
  Pages: 2882-2885
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] MAMLD1 : a new gene for hypospadias.2008
- Author(s)
  和田友香, 深見真紀, 緒方勤
- Journal Title
  
  J Japan Soc Reproduct Endocrinol 13
  
  Pages: 37-42
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] MAMLD1 (CXorf6) : a new gene for hypospadias2008
- Author(s)
  Ogata T, Wada Y, Fukami M
- Journal Title
  
  Sexual Development 2
  
  Pages: 244-50
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with Campomelic dysplasia or Acampomelic dysplasia2008
- Author(s)
  Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T
- Journal Title
  
  Am J Med Genet (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] MAMLD1 : a new gene for hypospadias2008
- Author(s)
  Wada Y, Fukami M, Ogata T
- Journal Title
  
  Journal of Japan Society of Reproductive Endocrinology 13
  
  Pages: 37-42
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] MAMLD1 (CXorf6) is a new gene for hypospadias2008
- Author(s)
  Ogata T, Fukami M, Wada Y.
- Journal Title
  
  Clinical Pediatric Endocrinology 17
  
  Pages: 87-93
- NAID
  10031199580
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] MAMLD1(CXorf6)is a new genge for Hypospadias2008
- Author(s)
  Ogata T, Fukami M, Wada Y
- Journal Title
  
  Clin Pediatr Endocrinol 174
  
  Pages: 87-93
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] MAMLD1 (CXorf6) : a new gene for hypospadias.2008
- Author(s)
  緒方勤, 和田友香, 深見真紀
- Journal Title
  
  Sex Dev. 2(4-5)
  
  Pages: 244-250
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Mastermind-like domain-containing 1 (MAMLD1 or CXorf6) transactivates the Hes3 promoter, augments testosterone production, and contains the SF1 target sequence.2008
- Author(s)
  Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T
- Journal Title
  
  Journal of Biological Chemistry 283(9)
  
  Pages: 5525-5532
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] MAMLD1(CXorf6): A new gene for hypospadias2008
- Author(s)
  Wada Y, Fukami M, Ogata T
- Journal Title
  
  生殖内分泌学会雑誌 13
  
  Pages: 37-43
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] Mastermind-like domain-containing 1 (MAMLD1 or CXorf6) transactivates the Hes3 promoter, augments testosterone production, and contains the SF1 target sequence.2008
- Author(s)
  Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T.
- Journal Title
  
  J Biol Chem. 283(9)
  
  Pages: 5525-5532
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] MAMLD1 (CXorf6) is a new genge for Hypospadias2008
- Author(s)
  Ogata T, Fukami M, Wada Y
- Journal Title
  
  Clin Pediatr Endocrinol 17(4)
  
  Pages: 87-93
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] MAMLD1 (CXorf6) is a new gene for hypospadias.2008
- Author(s)
  Ogata T, Fukami M, Wada Y
- Journal Title
  
  Clinical Pediatric Endocrinology 17(4)
  
  Pages: 87-93
- NAID
  10031199580
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] Mastermind-like domain-containing 1 (MAMLD1 or CXorf6) transactivates the Hes3 promoter, augments testosterone production, and contains the SF1 target sequence2008
- Author(s)
  Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T
- Journal Title
  
  Journal of Biological Chemistry 283
  
  Pages: 5525-5532
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] MAMLD1 (CXorf6) is a new gene for hypospadias.2008
- Author(s)
  緒方勤, 深見真紀, 和田友香
- Journal Title
  
  Clin Pediatr Endocrinol. 17(4)
  
  Pages: 87-93
- NAID
  10031199580
- Data Source
  KAKENHI-PROJECT-20390265
[Journal Article] Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with Campomelic dysplasia or Acampomelic dysplasia2008
- Author(s)
  Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T.
- Journal Title
  
  Am J Med Genet. (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] MAMLD1 (CXorf6): a new gene for hypospadias.2008
- Author(s)
  Ogata T, Wada Y, Fukami M
- Journal Title
  
  Sexual Development 2(4-5)
  
  Pages: 244-250
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] CXorf6 (MAMR1 : mastermind-related 1) transactivates the Hes3 promoter, augments testosterone production, and contains the target sequence for SF-12008
- Author(s)
  Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T
- Journal Title
  
  Journal of Biological Chemistry 283(9)
  
  Pages: 5525-5532
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] CXorf6(MAMRI:mastermind-related1)trmsactivates the Hes3 promoter, augmentstestosterone production, and contains the target sequence fbr SF-12008
- Author(s)
  Fukami M, Wada Y, Okada M, K:ato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T
- Journal Title
  
  Jburnal of Biological Chemistry 283(9)
  
  Pages: 5525-5532
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390290
[Journal Article] MAMLD1(CXorf6): A new gene for hypospadias2008
- Author(s)
  Wada Y, Fukami M, Ogata T.
- Journal Title
  
  生殖内分泌学会雑誌 13
  
  Pages: 37-43
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790248
[Journal Article] Premature ovanan tallure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns
- Author(s)
  Sugawa F, Wada Y, Okada M, Maruyama T, Uchida H, Arase T, Hamada N, Ishizuka B, Ogata T
- Journal Title
  
  Fertility and Sterility in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] 母乳育児が結ぶ母と子の絆~最新のEBM から~2013
- Author(s)
  和田友香
- Organizer
  第27回日本助産学会学術集会プレコングレス, 第14回母乳育児支援を学ぶ北陸教室
- Place of Presentation
  金沢
- Year and Date
  2013-04-30
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 薬剤を内服中のお母さんと母乳育児2013
- Author(s)
  和田友香
- Organizer
  筑波大学地域と大学の連携による周産期医療人材育成事業教育セミナー58 第7回つくば母乳育児支援勉強会
- Place of Presentation
  つくば
- Year and Date
  2013-11-16
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 母乳育児最前線母乳育児が結ぶ母と子の絆2013
- Author(s)
  和田友香
- Organizer
  第10回IBCLC のための母乳育児カンファレンス
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 授乳と薬剤2013
- Author(s)
  和田友香
- Organizer
  第7回京浜新生児医療研究会~フレッシュマンセミナー~
- Place of Presentation
  東京
- Year and Date
  2013-05-11
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 赤ちゃんとお母さんの健康のための「母乳と薬剤」2013
- Author(s)
  和田友香
- Organizer
  第9回医師のための母乳育児支援セミナー
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] パネルディスカッション　「母乳研究最前線」母乳育児が結ぶ母と子の絆2012
- Author(s)
  和田　友香
- Organizer
  第27回日本母乳哺育学会・学術集会
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 薬剤と母乳育児~精神神経系の薬剤・Canada Motherisk program の取り組みを含めて~2012
- Author(s)
  和田友香
- Organizer
  第8回医師のための母乳育児支援セミナー
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 第8回　医師のための母乳育児支援セミナー2012
- Author(s)
  和田　友香
- Organizer
  薬剤と母乳育児　～精神神経系の薬剤・Canada Motherrisk programの取り組みを含めて～
- Place of Presentation
  名古屋
- Invited
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] パネルディスカッション母乳研究最前線母乳育児が結ぶ母と子の絆2012
- Author(s)
  和田友香
- Organizer
  第27回日本母乳哺乳学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 新生児低血糖における簡易血糖測定器2機種(StatStrip、メディセーフミニ)の比較と血糖干渉物質2010
- Author(s)
  和田友香、垣内五月、花井彩江、高橋重裕、藤永英志、難波由喜子、塚本桂子、伊藤裕司、中村知夫
- Organizer
  第46回日本周産期・新生児医学会学術総会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-21790899
[Presentation] MAMLD1 mutations and impaired testosterone production : phenotypic analysis of mutation-positive patients and knockout mice and in vitro functional assays.2010
- Author(s)
  Fukami M, Wada Y, Nakamura M, Miyado M, Ogata T.
- Organizer
  The 49th Annual Meeting of European Society for Paediatric Endocrinology
- Place of Presentation
  Prague
- Data Source
  KAKENHI-PROJECT-20390265
[Presentation] MAMLD1遺伝子におけるスプライス部位変異(IVS4-2A>G)の検討2009
- Author(s)
  和田友香, 深見真紀, 須川史啓, 宮戸真美, 緒方勤
- Organizer
  第112回日本小児科学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-20390265
[Presentation] Campomelic dysplasiaとAcampomelic campomelic dysplasia8症例におけるSOX9変異解析とCNV解析2009
- Author(s)
  和田友香
- Organizer
  第32回日本小児遺伝学会学術集会
- Place of Presentation
  奈良
- Year and Date
  2009-04-16
- Data Source
  KAKENHI-PROJECT-21790899
[Presentation] MAMLD1異常症:新規遺伝子変異の同定と変異陽性患者の表現型2009
- Author(s)
  加藤芙弥子, 深見真紀, 和田友香, マイラブランダオ, 中村美智子, 上松あゆみ, 長谷川奉延, 宮戸真美, 緒方勤
- Organizer
  第43回日本小児内分泌学会
- Place of Presentation
  宇都宮
- Data Source
  KAKENHI-PROJECT-20390265
[Presentation] MAMLD1遺伝子におけるスプライス部位変異(IVS4-2A>G)の検討2009
- Author(s)
  和田友香, 深見真紀, 須川史啓, 宮戸真美, 緒方勤
- Organizer
  第112回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] MAMLD1遺伝子におけるスプライス部位変異(IVS4-2A>G)の検討2009
- Author(s)
  和田友香
- Organizer
  日本小児科学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-21790899
[Presentation] MAMLD1遺伝子におけるスプライス部位変異(IVS4-2A>G)の検討2009
- Author(s)
  和田友香, 深見真紀, 緒方勤
- Organizer
  第54回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] MAMLDI遺伝子におけるスプライス部位変異(IVS4-2A>G)の検討2009
- Author(s)
  和田友香
- Organizer
  日本小児科学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-21790899
[Presentation] Cxorf6(MAMALD1)is a causative gene for hypospadias2008
- Author(s)
  和田友香、深見真紅、宮林加奈子、西野一三、長谷川奉延、山田源、諸橋憲一郎、緒方勤
- Organizer
  アンドロロジー学会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] Campomelic dysplasaiaとcampomelic campomelic dysplasia患者14例におけるSOX9変異の有無と臨床像の関連性2008
- Author(s)
  和田友香、山澤一樹、鏡雅代、吉形真由美、埴田卓志、宮河真一郎
- Organizer
  日本周産期学会
- Place of Presentation
  横浜
- Year and Date
  2008-07-14
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] Campomelic dysplasiaとacampomelic campomelic dysplasia8症例におけるSOX9変異解析とCNV解析2008
- Author(s)
  和田友香、澤井英明、吉形真由美、宮河真一郎、埴田卓志、佐藤清二、長谷川奉延、永井敏郎、山本俊平、西村玄、緒方勤
- Organizer
  日本人類遺伝学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] 性分化異常症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2008
- Author(s)
  深見真紀, 和田友香, 須川史啓, 宮戸真美, 上松あゆ美, 長谷川奉延, 緒方勤
- Organizer
  第53回日本人類遺伝学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20390265
[Presentation] Haplotype analysis of the estrogen receptor a gene in male genital and reproductive abnormalities2008
- Author(s)
  T, Fukami M, Wada Y, Yoshida R, Watanabe M
- Organizer
  In: The Royan International Twin Congress (The 9th Congress on Reproductive Biomedicine and The 4th Congress on Stem Cell Biology and Technology)
- Place of Presentation
  Tehran
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] 性分化異常症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2008
- Author(s)
  深見真紀, 和田友香, 須川史啓, 宮戸真美, 上松あゆ美, 長谷川奉延, 諸橋憲一郎, 緒方勤
- Organizer
  第31回日分子生物学会総会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] Haplotype analysis of the estrogen receptor a gene in male genital and reproductive abnormalities2008
- Author(s)
  Ogata T, Fukami M, Wada Y, Yoshida R, Watanabe M.
- Organizer
  The 9th Congress on Reproductive Biomedicine and The 4th Congress on Stem Cell Biology and Technology
- Place of Presentation
  テヘラン・イラン
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] Campomelic dysplasaiaとACampomelic campomelic dysplasia患者14例におけるSOX9変異の有無と臨床像の関連性2008
- Author(s)
  和田友香、山澤一樹、鏡雅代、吉形真由美、埴田卓志、宮河真一郎
- Organizer
  日本周産期学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] Cxorf6(MAMALD1) is a causative gene for hypospadias2008
- Author(s)
  和田友香、深見真紀、宮林加奈子、西野一三、長谷川奉延、山田源、諸橋憲一郎、緒方勤
- Organizer
  アンドロロジー学会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] 性分化異常症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2008
- Author(s)
  深見真紀, 和田友香, 須川史啓, 宮戸真美, 上松あゆ美, 長谷川奉延, 緒方勤
- Organizer
  第42回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] 性分化異常症責任遺伝子MAMLD1の臨床的および分子遺伝学的解析2008
- Author(s)
  深見真紀, 和田友香, 須川史啓, 宮戸真美, 上松あゆ美, 長谷川奉延, 緒方勤
- Organizer
  第53回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] Campomelic dysplasiaとacampomelic campomelic dysplasia 8症例におけるSOX9変異解析とCNV解析2008
- Author(s)
  和田友香、澤井英明、吉形真由美、宮河真一郎、埴田卓志、佐藤清二、長谷川奉延、永井敏郎、山本俊平、西村玄、緒方勤
- Organizer
  第53回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-19790248
[Presentation] 新規性分化異常症責任遺伝子の同定と機能解析2007
- Author(s)
  深見真紀, 和田友香, 岡田美智代, 宮林香奈子, 長谷川奉延, 山田源, 諸橋憲一郎, Jocelyn Laporte, 北川元生, 緒方勤
- Organizer
  第52回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] 新規性分化異常症責任遺伝子の同定と機能解析2007
- Author(s)
  深見真紀, 和田友香, 長谷川奉延, 山田源, 諸橋憲一郎, 緒方勤
- Organizer
  第80回内分泌学会学術総会:高得点演題
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] The novel hypospadias gene CXorf6 transactivates the promoter of a non-canonical Notch target gene Hes3 and contaills the target sequence for SF-12007
- Author(s)
  Fukami M, Morohashi K, Wada Y, Okada M, Laporte J, Kitagawa M, Ogata T
- Organizer
  The Endocrine Society's 89th Amual Meeting
- Place of Presentation
  トロント
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] The novel hypospadias gene CXorf6 transactivates the promoter of a non-canonical Notch target gene Hes3 and contains the target sequence for SF-1.2007
- Author(s)
  Fukami M, Morohashi K, Wada Y, Okada M, Laporte J, Kitagawa M, Ogata T
- Organizer
  The Endocrine Society's 89th Annual Meeting
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] CXorf6 (MAMLD1: mastermind-like domain containing 1) transactivates the promoter of Hes3 and contains the target sequence for SF-12007
- Author(s)
  深見真紀, 和田友香, 岡田美智代, 加藤芙美子, 勝又則行, 馬場崇, 諸橋憲一郎, Jocelyn Laporte, 北川元生, 緒方勤
- Organizer
  第11回小児分子内分泌研究会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] 新規性分化異常症責任遺伝子によるNotch標的遺伝子の活性化2007
- Author(s)
  深見真紀, 和田友香, 岡田美智代, 長谷川奉延, 山田源, 諸橋憲一郎, 北川元生, 緒方勤
- Organizer
  第30回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-19390290
[Presentation] 授乳と薬剤
- Author(s)
  和田　友香
- Organizer
  第７回京浜新生児医療研究会～フレッシュマンセミナー～
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 母乳育児が結ぶ母と子の絆　～最新のABMから～
- Author(s)
  和田　友香
- Organizer
  平成26年度妊産婦・新生児・乳幼児等支援者研修会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 母乳育児が結ぶ母と子の絆～最近のEBMから～
- Author(s)
  和田　友香
- Organizer
  第２７回日本助産学会学術集会
- Place of Presentation
  金沢
- Data Source
  KAKENHI-PROJECT-24791127
[Presentation] 薬剤を内服中のお母さんと母乳育児
- Author(s)
  和田　友香
- Organizer
  筑波大学　地域と大学の連携による周産期医療人材育成事業　教育セミナー58　第７回つくば母乳育児支援勉強会
- Place of Presentation
  つくば
- Data Source
  KAKENHI-PROJECT-24791127

1. OGATA Tsutomu (40169173)

# of Collaborated Projects: 3 results

# of Collaborated Products: 36 results
2. FUKAMI Maki (40265872)

# of Collaborated Projects: 3 results

# of Collaborated Products: 35 results
3. KAGAMI Masayo (70399484)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. Matsubara Keiko (90542952)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. Shibasaki Jun (30540471)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

WADA Yuka 和田 友香

和田 友香 ワダ ユカ

Research Projects

Research Products

Co-Researchers

The frequency of cases with imprinting disorders in hypotonic neonates and infants

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Influence of the medicine through the breast milk in the premature infantPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Splice site mutation of MAMLD1 in disorders of sex development patientsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular mechanism leading to impaired sexual differentiation and reproductive failure in patients with MAMLD mutations

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Novel sex development gene CXorf6 : determination of clinical spectrum in mutation positive patients and clarification of underlying factors

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Mutation and polymorphism analyses of INSL3, LGR8/GREAT and SF-1 in patients with cryptorchidismPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Clarification of the genetic mechanisms underlying the regulation for the expression of SHOX, a causative gene for short stature and sdyschomndrosteosis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 第9回 医師のための母乳育児支援セミナー2013

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] 母乳と薬剤2014

Author(s)

Journal Title

Data Source

[Journal Article] 新生児における先天性乳麋胸水に対するオクトレオチド投与療法2014

Author(s)

Journal Title

Data Source

[Journal Article] 胆汁うっ滞性肝障害に対する待望の治療薬！魚油由来脂肪製剤Omegaven○R2014

Author(s)

Journal Title

Data Source

[Journal Article] 胆汁うっ滞性肝障害に対する待望の治療薬! 魚油由来脂肪製剤Omegaven®2014

Author(s)

Journal Title

Data Source

[Journal Article] 20世紀の新生児医療を変えたサーファクタント補充療法2013

Author(s)

Journal Title

Data Source

[Journal Article] 小腸機能不全関連肝機能障害に対するFish oilの使用経験2013

Author(s)

Journal Title

Data Source

[Journal Article] 小腸機能不全関連肝機能障害に対するFish oil の使用経験2013

Author(s)

Journal Title

Data Source

WADA Yuka 和田友香

和田友香ワダユカ

[Book] 第9回医師のための母乳育児支援セミナー2013