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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Autors principals: Dennis, Jameel, Meehan, Daniel T., Delimont, Duane, Zallocchi, Marisa, Perry, Greg A., O'Brien, Stacie, Tu, Hongmin, Pihlajaniemi, Taina, Cosgrove, Dominic
Format: Artigo
Idioma:Inglês
Publicat: American Society for Investigative Pathology 2010
Matèries:
Regular Articles
Accés en línia: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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