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Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5.
Gao, Xiaobo; Zheng, Panpan; Yang, Liping; Luo, Haiyan; Zhang, Chen; Qiu, Yongqiang; Huang, Guoying; Sheng, Wei; Ma, Xu; Lu, Cailing.
Afiliação
  • Gao X; Department of Genetics, National Research Institute for Family Planning, Beijing, China.
  • Zheng P; Department of Genetics, National Research Institute for Family Planning, Beijing, China.
  • Yang L; Graduate School of Peking Union Medical College, Beijing, China.
  • Luo H; Department of Cardiovascular Surgery, Union Hospital, Fujian Medical University, Fuzhou, China.
  • Zhang C; Department of Genetics, National Research Institute for Family Planning, Beijing, China.
  • Qiu Y; Department of Genetics, National Research Institute for Family Planning, Beijing, China.
  • Huang G; Graduate School of Peking Union Medical College, Beijing, China.
  • Sheng W; Union Clinical Medical College of Research Institute of Fujian Medical University, Fuzhou, China.
  • Ma X; Children's Hospital of Fudan University, Shanghai, China.
  • Lu C; Children's Hospital of Fudan University, Shanghai, China Sheng4616@126.com lucailing@sina.com genetics66@sina.com.
Clin Sci (Lond) ; 133(12): 1281-1295, 2019 06 28.
Article em En | MEDLINE | ID: mdl-31171573

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Ativação Transcricional / Regiões Promotoras Genéticas / Polimorfismo de Nucleotídeo Único / Fator 1 de Diferenciação de Crescimento / Proteína Homeobox Nkx-2.5 / Cardiopatias Congênitas / Mutação Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transcrição Gênica / Ativação Transcricional / Regiões Promotoras Genéticas / Polimorfismo de Nucleotídeo Único / Fator 1 de Diferenciação de Crescimento / Proteína Homeobox Nkx-2.5 / Cardiopatias Congênitas / Mutação Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article