Molecular and functional characterization of urine‐derived podocytes from patients with Alport syndrome

Alport syndrome (AS) is a genetic disorder involving mutations in the genes encoding collagen IV α3, α4 or α5 chains, resulting in the impairment of glomerular basement membrane. Podocytes are responsible for production and correct assembly of collagen IV isoforms; however, data on the phenotypic ch...

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Detalhes bibliográficos
Publicado no:J Pathol
Main Authors: Iampietro, Corinne, Bellucci, Linda, Arcolino, Fanny O, Arigoni, Maddalena, Alessandri, Luca, Gomez, Yonathan, Papadimitriou, Elli, Calogero, Raffaele A, Cocchi, Enrico, Van Den Heuvel, Lambertus, Levtchenko, Elena, Bussolati, Benedetta
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2020
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Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7589231/
https://ncbi.nlm.nih.gov/pubmed/32652570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/path.5496
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