Axial stretch-dependent cation entry in dystrophic cardiomyopathy: Involvement of several TRPs channels

In Duchenne muscular dystrophy (DMD), deficiency of the cytoskeletal protein dystrophin leads to well-described defects in skeletal muscle but also to dilated cardiomyopathy (DCM). In cardiac cells, the subsarcolemmal localization of dystrophin is thought to protect the membrane from mechanical stre...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Cell Calcium
Asıl Yazarlar: Aguettaz, E., Lopez, J.J., Krzesiak, A., Lipskaia, L., Adnot, S., Hajjar, R.J., Cognard, C., Constantin, B., Sebille, S.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2016
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4844790/
https://ncbi.nlm.nih.gov/pubmed/26803937
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ceca.2016.01.001
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller