Collagen XIII Induced in Vascular Endothelium Mediates α1β1 Integrin-Dependent Transmigration of Monocytes in Renal Fibrosis

Alport syndrome is a common hereditary basement membrane disorder caused by mutations in the collagen IV α3, α4, or α5 genes that results in progressive glomerular and interstitial renal disease. Interstitial monocytes that accumulate in the renal cortex from Alport mice are immunopositive for integ...

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Detalhes bibliográficos
Main Authors: Dennis, Jameel, Meehan, Daniel T., Delimont, Duane, Zallocchi, Marisa, Perry, Greg A., O'Brien, Stacie, Tu, Hongmin, Pihlajaniemi, Taina, Cosgrove, Dominic
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2010
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2966809/
https://ncbi.nlm.nih.gov/pubmed/20864678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2010.100017
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