Formation, Contraction, and Mechanotransduction of Myofribrils in Cardiac Development: Clues from Genetics

Congenital heart disease (CHD) is the most common birth defect in humans. It is a leading infant mortality factor worldwide, caused by defective cardiac development. Mutations in transcription factors, signalling and structural molecules have been shown to contribute to the genetic component of CHD....

Descripción completa

Detalles Bibliográficos
Autores principales: Granados-Riveron, Javier T., Brook, J. David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376475/
https://www.ncbi.nlm.nih.gov/pubmed/22720160
http://dx.doi.org/10.1155/2012/504906

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376475/
https://www.ncbi.nlm.nih.gov/pubmed/22720160
http://dx.doi.org/10.1155/2012/504906

Ejemplares similares