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Animal and in silico models for the study of sarcomeric cardiomyopathies

Over the past decade, our understanding of cardiomyopathies has improved dramatically, due to improvements in screening and detection of gene defects in the human genome as well as a variety of novel animal models (mouse, zebrafish, and drosophila) and in silico computational models. These novel exp...

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Detalles Bibliográficos
Publicado en:Cardiovasc Res
Autores principales: Duncker, Dirk J., Bakkers, Jeroen, Brundel, Bianca J., Robbins, Jeff, Tardiff, Jil C., Carrier, Lucie
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4375391/
https://ncbi.nlm.nih.gov/pubmed/25600962
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvv006
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