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Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling.
Xie, Yifang; Ma, Anyun; Wang, Boshi; Peng, Rui; Jing, Yingchun; Wang, Deqian; Finnell, Richard H; Qiao, Bin; Wang, Yongming; Wang, Hongyan; Zheng, Yufang.
Afiliação
  • Xie Y; Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.
  • Ma A; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai 200011, China.
  • Wang B; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai 200011, China.
  • Peng R; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai 200011, China.
  • Jing Y; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai 200011, China.
  • Wang D; Key Laboratory of Reproduction Regulation of NPFPC, Collaborative Innovation Center of Genetics and Development, Fudan University, Shanghai 200032, China.
  • Finnell RH; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai 200011, China.
  • Qiao B; Institute of Developmental Biology & Molecular Medicine, Fudan University, Shanghai 200433, China.
  • Wang Y; School of Life Sciences, Fudan University, Shanghai 200438, China.
  • Wang H; Departments of Molecular and Cellular Biology and Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Zheng Y; Collaborative Innovation Center for Genetics & Development, School of Life Sciences, Fudan University, Shanghai 200438, China.
Clin Sci (Lond) ; 133(2): 225-238, 2019 01 31.
Article em En | MEDLINE | ID: mdl-30610007
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Cardiomegalia / Mutação de Sentido Incorreto / Miócitos Cardíacos / Fator de Crescimento Semelhante a EGF de Ligação à Heparina / Células-Tronco Embrionárias Humanas / Proteína ADAM17 / Mutação com Perda de Função Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Sci (Lond) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Cardiomegalia / Mutação de Sentido Incorreto / Miócitos Cardíacos / Fator de Crescimento Semelhante a EGF de Ligação à Heparina / Células-Tronco Embrionárias Humanas / Proteína ADAM17 / Mutação com Perda de Função Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Sci (Lond) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido