A glycine substitution in the collagenous domain of Col4a3 in mice recapitulates late onset Alport syndrome

Alport syndrome (AS) is a severe inherited glomerulopathy caused by mutations in the genes encoding the α-chains of type-IV collagen, the most abundant component of the extracellular glomerular basement membrane (GBM). Currently most AS mouse models are knockout models for one of the collagen-IV gen...

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Опубликовано в: :Matrix Biol Plus
Главные авторы: Odiatis, Christoforos, Savva, Isavella, Pieri, Myrtani, Ioannou, Pavlos, Petrou, Petros, Papagregoriou, Gregory, Antoniadou, Kyriaki, Makrides, Neoklis, Stefanou, Charalambos, Ljubanović, Danica Galešić, Nikolaou, Georgios, Borza, Dorin-Bogdan, Stylianou, Kostas, Gross, Oliver, Deltas, Constantinos
Формат: Artigo
Язык:Inglês
Опубликовано: Elsevier 2020
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7930875/
https://ncbi.nlm.nih.gov/pubmed/33718859
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mbplus.2020.100053
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