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Identification of Polycystin-1 interacting proteins after transfection of PC1 in HEK cells
ORGANISM(S): Homo sapiens (Human) 
2024-11-12 | PXD056889 | Pride
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the formation of multiple fluid-filled cysts that destroy the kidney architecture resulting in end-stage renal failure. Mutations in the ADPKD genes PKD1 and PKD2 account for nearly all the cases of ADPKD. Increased cell prolif...
ORGANISM(S): Rattus norvegicus 
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common hereditary cause of kidney failure, resulting from germline mutations in PKD1 and PKD2 in over 90% of cases. Polycystin-1 (PC-1), a cell surface receptor linked to focal adhesion proteins, plays a critical role in regulating cel...
ORGANISM(S): Homo sapiens 
The goal of this microarray study was to determine genes whose transcriptional profile was altered in the absence of polycystin-1 expression. Placentas from knockout and wild-type littermates were compared at the latest viable timepoints (14.5d and 15.5dpc) and genes with a fold change > 1.5 were i...
ORGANISM(S): Mus musculus 
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