Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6

Nephronophthisis (NPH) is an autosomal recessive disorder characterized by renal fibrosis, tubular basement membrane disruption and corticomedullary cyst formation leading to end-stage renal failure. The disease is caused by mutations in NPHP1-9 genes, which encode the nephrocystins, proteins locali...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Delous, Marion, Hellman, Nathan E., Gaudé, Helori-Maël, Silbermann, Flora, Le Bivic, André, Salomon, Rémi, Antignac, Corinne, Saunier, Sophie
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2009
Teme:
Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2778369/
https://ncbi.nlm.nih.gov/pubmed/19755384
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp434
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki