The Mitochondrial Complex I Activity Is Reduced in Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Function

Cystic fibrosis (CF) is a frequent and lethal autosomal recessive disease. It results from different possible mutations in the CFTR gene, which encodes the CFTR chloride channel. We have previously studied the differential expression of genes in CF and CF corrected cell lines, and found a reduced ex...

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Detalles Bibliográficos
Autores principales: Valdivieso, Angel G., Clauzure, Mariángeles, Marín, María C., Taminelli, Guillermo L., Massip Copiz, María M., Sánchez, Francisco, Schulman, Gustavo, Teiber, María L., Santa-Coloma, Tomás A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504030/
https://www.ncbi.nlm.nih.gov/pubmed/23185247
http://dx.doi.org/10.1371/journal.pone.0048059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504030/
https://www.ncbi.nlm.nih.gov/pubmed/23185247
http://dx.doi.org/10.1371/journal.pone.0048059

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