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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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Bibliografiske detaljer
Main Authors: 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.
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3504030/
https://ncbi.nlm.nih.gov/pubmed/23185247
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0048059
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