Renal Cystic Disease: The Role of the Primary Cilium/Centrosome Complex in Pathogenesis
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference23 articles.
1. Polycystic kidney disease;Wilson;N Engl J Med,2004
2. Genetics and pathogenesis of polycystic kidney disease;Igarashi;J Am Soc Nephrol,2002
3. Molecular pathogenesis of ADPKD;Ong;Kidney Int,2005
4. Autosomal recessive polycystic kidney disease;Guay-Woodford;Pediatrics,2003
5. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats;Onuchic;Am J Hum Genet,2002
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1. Polycystin-2 (TRPP2) regulates primary cilium length in LLC-PK1 renal epithelial cells;Frontiers in Physiology;2022-10-04
2. Hyperglycemia in the absence of cilia accelerates cystogenesis and induces renal damage;American Journal of Physiology-Renal Physiology;2015-07-01
3. Activation of the intrarenal renin-angiotensin-system in murine polycystic kidney disease;Physiological Reports;2015-05
4. Centrosomal Abnormalities Characterize Human and Rodent Cystic Cholangiocytes and Are Associated with Cdc25A Overexpression;The American Journal of Pathology;2014-01
5. TRPV4 Dysfunction Promotes Renal Cystogenesis in Autosomal Recessive Polycystic Kidney Disease;Journal of the American Society of Nephrology;2013-02-14
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