Role of PKD2 in the endoplasmic reticulum calcium homeostasis
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DOI: 10.3389/fphys.2022.962571
Abstract: Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in the PKD1 or PKD2 gene which encodes membrane receptor PKD1 and cation channel PKD2, respectively. PKD2, also called transient receptor potential polycystin-2 (TRPP2), is… read more here.
Keywords: role pkd2; pkd2; endoplasmic reticulum; homeostasis ... See more keywords