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A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.
Ashraf, Hassan; Pradhan, Lagnajeet; Chang, Eileen I; Terada, Ryota; Ryan, Nicole J; Briggs, Laura E; Chowdhury, Rajib; Zárate, Miguel A; Sugi, Yukiko; Nam, Hyun-Joo; Benson, D Woodrow; Anderson, Robert H; Kasahara, Hideko.
Afiliação
  • Ashraf H; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Pradhan L; Department of Bioengineering, University of Texas at Dallas, TX 75080.
  • Chang EI; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Terada R; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Ryan NJ; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Briggs LE; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Chowdhury R; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Zárate MA; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
  • Sugi Y; Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29425.
  • Nam HJ; Department of Bioengineering, University of Texas at Dallas, TX 75080.
  • Benson DW; Department of Pediatrics, Herma Heart Center, Medical College of Wisconsin, Milwaukee, WI 53226.
  • Anderson RH; Institute of Genetic Medicine, Newcastle University, Newcastle, UK.
  • Kasahara H; Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610.
Circ Cardiovasc Genet ; 7(4): 423-433, 2014 Aug.
Article em En | MEDLINE | ID: mdl-25028484
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Cardiopatias Congênitas Tipo de estudo: Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Circ Cardiovasc Genet Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Homeodomínio / Cardiopatias Congênitas Tipo de estudo: Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Circ Cardiovasc Genet Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article