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Gender-Dependent Phenotype in Polycystic Kidney Disease Is Determined by Differential Intracellular Ca(2+) Signals

Autosomal dominant polycystic kidney disease (ADPKD) is caused by loss of function of PKD1 (polycystin 1) or PKD2 (polycystin 2). The Ca(2+)-activated Cl(−) channel TMEM16A has a central role in ADPKD. Expression and function of TMEM16A is upregulated in ADPKD which causes enhanced intracellular Ca(...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Talbi, Khaoula, Cabrita, Inês, Schreiber, Rainer, Kunzelmann, Karl
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8199720/
https://ncbi.nlm.nih.gov/pubmed/34199520
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22116019
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