Ciliary Ion Channels in Polycystic Kidney Disease

Polycystic kidney disease (PKD) is the most common hereditary disorder that disrupts renal function and frequently progresses to end-stage renal disease. Recent advances have elucidated the critical role of primary cilia and ciliary ion channels, including transient receptor potential (TRP) channels...

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Bibliographic Details
Main Authors: Lubna A. Alshriem, Raghad Buqaileh, Qasim Alorjani, Wissam AbouAlaiwi
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/14/6/459
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