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Inward Ca(2+) current through the polycystin-2-dependent channels of renal primary cilia
In 15% of cases, autosomal dominant polycystic kidney disease arises from defects in polycystin-2 (PC2). PC2 is a member of the polycystin transient receptor potential subfamily of cation-conducting channels and is expressed in the endoplasmic reticulum and primary cilium of renal epithelial cells....
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| Publicado en: | Am J Physiol Renal Physiol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Physiological Society
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8285651/ https://ncbi.nlm.nih.gov/pubmed/33969696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00062.2021 |
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