A carregar...

α1β1 Integrin/Rac1-Dependent Mesangial Invasion of Glomerular Capillaries in Alport Syndrome

Alport syndrome, hereditary glomerulonephritis with hearing loss, results from mutations in type IV collagen COL4A3, COL4A4, or COL4A5 genes. The mechanism for delayed glomerular disease onset is unknown. Comparative analysis of Alport mice and CD151 knockout mice revealed progressive accumulation o...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Zallocchi, Marisa, Johnson, Brianna M., Meehan, Daniel T., Delimont, Duane, Cosgrove, Dominic
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3791686/
https://ncbi.nlm.nih.gov/pubmed/23911822
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2013.06.015
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!