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Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis.
Yin, Xiu-Yun; Chen, Huan-Xin; Chen, Zhuo; Yang, Qin; Han, Jun; He, Guo-Wei.
Afiliação
  • Yin XY; The Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin 300457, China.
  • Chen HX; School of Pharmacy, Drug Research & Development Center, Wannan Medical College, Wuhu 241002, China.
  • Chen Z; The Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin 300457, China.
  • Yang Q; The Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin 300457, China.
  • Han J; School of Pharmacy, Drug Research & Development Center, Wannan Medical College, Wuhu 241002, China.
  • He GW; The Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin 300457, China.
Biomolecules ; 13(2)2023 02 13.
Article em En | MEDLINE | ID: mdl-36830727
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Cardiopatias Congênitas Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tetralogia de Fallot / Cardiopatias Congênitas Idioma: En Ano de publicação: 2023 Tipo de documento: Article