TRPC6 Single Nucleotide Polymorphisms and Progression of Idiopathic Membranous Nephropathy

BACKGROUND: Activating mutations in the Transient Receptor Potential channel C6 (TRPC6) cause autosomal dominant focal segmental glomerular sclerosis (FSGS). TRPC6 expression is upregulated in renal biopsies of patients with idiopathic membranous glomerulopathy (iMN) and animal models thereof. In iM...

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Detalles Bibliográficos
Autores principales: Hofstra, Julia M., Coenen, Marieke J. H., Schijvenaars, Mascha M. V. A. P., Berden, Jo H. M., van der Vlag, Johan, Hoefsloot, Lies H., Knoers, Nine V. A. M., Wetzels, Jack F. M., Nijenhuis, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096511/
https://www.ncbi.nlm.nih.gov/pubmed/25019165
http://dx.doi.org/10.1371/journal.pone.0102065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096511/
https://www.ncbi.nlm.nih.gov/pubmed/25019165
http://dx.doi.org/10.1371/journal.pone.0102065

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