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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....

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Detalles Bibliográficos
Autores principales: Granados-Riveron, Javier T., Brook, J. David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
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