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

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CISD1 codifies a mitochondrial protein upregulated by the CFTR channel von Taminelli, Guillermo L., Sotomayor, Verónica, Valdivieso, Ángel G., Teiber, María L., Marín, María C., Santa-Coloma, Tomás A.

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The Mitochondrial Complex I Activity Is Reduced in Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator von 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

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Ophthalmo-acromelic syndrome: Report of a case with vertebral anomalies von Teiber, Maria L., Garrido, Jeniffer A., Barreiro, Cristina Z.

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Novel Paraoxonase 2-Dependent Mechanism Mediating the Biological Effects of the Pseudomonas aeruginosa Quorum-Sensing Molecule N-(3-Oxo-Dodecanoyl)-L-Homoserine Lactone von Horke, Sven, Xiao, Junhui, Schütz, Eva-Maria, Kramer, Gerald L, Wilgenbus, Petra, Witte, Ines, Selbach, Moritz, Teiber, John F

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The expression of the mitochondrial gene MT-ND4 is downregulated in cystic fibrosis von Valdivieso, Ángel G., Marcucci, Florencia, Taminelli, Guillermo, Guerrico, Anatilde González, Álvarez, Sergio, Teiber, María Luz, Dankert, Marcelo A., Santa-Coloma, Tomás A.

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