Structure and function of polycystin channels in primary cilia
Author:
Funder
NIH NIDDK
NU GoKidney George M. O’Brien Kidney Research Core Center
Publisher
Elsevier BV
Subject
Cell Biology
Reference107 articles.
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2. Autosomal dominant polycystic kidney disease: core curriculum 2016;Chebib;Am. J. Kidney Dis.,2016
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4. Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesis;Brasier;J. Clin. Invest.,1997
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1. Editorial: Molecular mechanisms underlying polycystic kidney disease: from the smallest bricks to the big scenario;Frontiers in Molecular Biosciences;2024-05-21
2. Glis2 is an early effector of polycystin signaling and a target for therapy in polycystic kidney disease;Nature Communications;2024-05-01
3. Calcium signalling and transport in the kidney;Nature Reviews Nephrology;2024-04-19
4. A unique subset of pericystic endothelium associates with aberrant microvascular remodelling and impaired blood perfusion early in polycystic kidney disease;2024-03-06
5. Polycystin-2 Ion Channel Function and Pathogenesis in Autosomal Dominant Polycystic Kidney;PROG BIOCHEM BIOPHYS;2024
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