The L‐type Ca(2+) channel facilitates abnormal metabolic activity in the cTnI‐G203S mouse model of hypertrophic cardiomyopathy

KEY POINTS: Genetic mutations in cardiac troponin I (cTnI) are associated with development of hypertrophic cardiomyopathy characterized by myocyte remodelling, disorganization of cytoskeletal proteins and altered energy metabolism. The L‐type Ca(2+) channel is the main route for calcium influx and i...

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Detaylı Bibliyografya
Yayımlandı:J Physiol
Asıl Yazarlar: Viola, Helena, Johnstone, Victoria, Cserne Szappanos, Henrietta, Richman, Tara, Tsoutsman, Tatiana, Filipovska, Aleksandra, Semsarian, Christopher, Hool, Livia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2016
Konular:
Cardiovascular
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4945708/
https://ncbi.nlm.nih.gov/pubmed/27062056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP271681
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