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...

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Detalles Bibliográficos
Autores principales: Delous, Marion, Hellman, Nathan E., Gaudé, Helori-Maël, Silbermann, Flora, Le Bivic, André, Salomon, Rémi, Antignac, Corinne, Saunier, Sophie
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778369/
https://www.ncbi.nlm.nih.gov/pubmed/19755384
http://dx.doi.org/10.1093/hmg/ddp434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778369/
https://www.ncbi.nlm.nih.gov/pubmed/19755384
http://dx.doi.org/10.1093/hmg/ddp434

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