Výsledky vyhledávání - "María L Teiber"

Akademický článek

The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Autor: Angel G Valdivieso, Mariángeles Clauzure, María C Marín, Guillermo L Taminelli, María M Massip Copiz, Francisco Sánchez, Gustavo Schulman, María L Teiber, Tomás A Santa-Coloma

Publikováno v: PLoS ONE, Vol 7, Iss 11, p e48059 (2012)

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 a

Externí odkaz: https://doaj.org/article/30c5dfba9f9f4babbffaf3c44fc5646a

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

Autor: María L. Teiber, María C. Marín, G. Taminelli, Francisco Sánchez, Mariángeles Clauzure, María M. Massip Copiz, Tomás A. Santa-Coloma, Gustavo Schulman, Ángel G. Valdivieso

Publikováno v: PLoS ONE
PLoS ONE Vol. 7, N° 11, 2012
Repositorio Institucional (UCA)
Pontificia Universidad Católica Argentina
instacron:UCA
PLoS ONE, Vol 7, Iss 11, p e48059 (2012)

Fil: Valdivieso, Ángel Gabriel. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Biomédicas. Laboratorio de Biología Celular y Molecular; Argentina Fil: Valdivieso, Ángel Gabriel. Consejo Nac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::754ef1e431039867106c061b51398dc5
http://europepmc.org/articles/PMC3504030

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CISD1 codifies a mitochondrial protein upregulated by the CFTR channel

Autor: María L. Teiber, Ángel G. Valdivieso, María C. Marín, Verónica Sotomayor, G. Taminelli, Tomás A. Santa-Coloma

Publikováno v: Biochemical and biophysical research communications. 365(4)

Cystic fibrosis (CF) is an autosomic recessive disease caused by mutations in the CFTR chloride channel, which indirectly affect the expression of a net of genes. Here we describe a new CFTR-dependent gene, CISD1, encoding for the first member of a f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c3369952c9f5261f6a200b473a1a0e2
https://pubmed.ncbi.nlm.nih.gov/18047834

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The expression of the mitochondrial gene MT-ND4 is downregulated in cystic fibrosis

Autor: Anatilde González Guerrico, María L. Teiber, Florencia Marcucci, Sergio Álvarez, Ángel G. Valdivieso, G. Taminelli, Tomás A. Santa-Coloma, Marcelo A. Dankert

Publikováno v: Biochemical and biophysical research communications. 356(3)

Cystic fibrosis (CF) is a disease produced by mutations in the CFTR channel. We have previously reported that the CFTR chloride transport activity indirectly regulates the differential expression of several genes, including SRC and MUC1. Here we repo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d802f15f690f45604775e413d57b15
https://pubmed.ncbi.nlm.nih.gov/17382898

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