Your browser doesn't support javascript.
loading
Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-ß/SMAD3 signaling pathway.
Peng, Qian; Deng, Yan; Yang, Xiling; Leng, Xiangyou; Yang, Yuan; Liu, Hanmin.
Afiliação
  • Peng Q; Department of Pediatric Cardiology, West China Second University Hospital/West China Women's and Children's Hospital, West China School of Medicine, Sichuan University, Chengdu, 610041, China.
  • Deng Y; Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, 610041, China.
  • Yang X; Department of Pediatrics, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, 610072, China.
  • Leng X; Department of Cardiovascular Ultrasound and Non-invasive Cardiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, 610072, China.
  • Yang Y; Department of Medical Genetics, West China Hospital, West China School of Medicine, Sichuan University, Chengdu, 610041, China.
  • Liu H; Department of Medical Genetics, West China Hospital, West China School of Medicine, Sichuan University, Chengdu, 610041, China.
Eur J Pediatr ; 175(5): 705-13, 2016 May.
Article em En | MEDLINE | ID: mdl-26833052

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Fator de Crescimento Transformador beta / Vasos Coronários / Polimorfismo de Nucleotídeo Único / Proteína Smad3 / Proteína ADAM17 / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Fator de Crescimento Transformador beta / Vasos Coronários / Polimorfismo de Nucleotídeo Único / Proteína Smad3 / Proteína ADAM17 / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China