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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2020
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589231/
https://www.ncbi.nlm.nih.gov/pubmed/32652570
http://dx.doi.org/10.1002/path.5496

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589231/
https://www.ncbi.nlm.nih.gov/pubmed/32652570
http://dx.doi.org/10.1002/path.5496

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