Control of PTH secretion by the TRPC1 ion channel

Familial hypocalciuric hypercalcemia (FHH) is a genetic condition associated with hypocalciuria, hypercalcemia, and, in some cases, inappropriately high levels of circulating parathyroid hormone (PTH). FHH is associated with inactivating mutations in the gene encoding the Ca(2+)-sensing receptor (Ca...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:JCI Insight
Prif Awduron: Onopiuk, Marta, Eby, Bonnie, Nesin, Vasyl, Ngo, Peter, Lerner, Megan, Gorvin, Caroline M., Stokes, Victoria J., Thakker, Rajesh V., Brandi, Maria Luisa, Chang, Wenhan, Humphrey, Mary Beth, Tsiokas, Leonidas, Lau, Kai
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Clinical Investigation 2020
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7205425/
https://ncbi.nlm.nih.gov/pubmed/32213715
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.132496
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