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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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Опубликовано в: :Cardiovasc Res
Главные авторы: Duncker, Dirk J., Bakkers, Jeroen, Brundel, Bianca J., Robbins, Jeff, Tardiff, Jil C., Carrier, Lucie
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2015
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Online-ссылка: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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