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Establishment of microRNA, transcript and protein regulatory networks in Alport syndrome induced pluripotent stem cells

Alport syndrome (AS) is an inherited progressive disease caused by mutations in genes encoding for the α3, α4 and α5 chains, which are an essential component of type IV collagen and are required for formation of the glomerular basement membrane. However, the underlying etiology of AS remains largely...

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Detalles Bibliográficos
Autores principales: Chen, Wenbiao, Tang, Donge, Dai, Yong, Diao, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297794/
https://www.ncbi.nlm.nih.gov/pubmed/30483741
http://dx.doi.org/10.3892/mmr.2018.9672