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Role of PKD2 in the endoplasmic reticulum calcium homeostasis
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 a Ca(2+)-permeable channel located on the membrane...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399649/ https://www.ncbi.nlm.nih.gov/pubmed/36035467 http://dx.doi.org/10.3389/fphys.2022.962571 |