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Antoni L Andreu

Showing results (61-70 of 77) with videos related to

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Antioxidants & Redox Signaling|April 2, 2011
Oxidative damage compromises energy metabolism in the axonal degeneration mouse model of X-adrenoleukodystrophyJorge Galino, Montserrat Ruiz, Stéphane Fourcade, et al.
Brain : a Journal of Neurology|April 2, 2013
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 geneMaria J Melià, Akatsuki Kubota, Saida Ortolano, et al.
Psychoneuroendocrinology|June 7, 2011
Chronic psychosocial stress induces reversible mitochondrial damage and corticotropin-releasing factor receptor type-1 upregulation in the rat intestine and IBS-like gut dysfunctionMaría Vicario, Carmen Alonso, Mar Guilarte, et al.
International Journal of Molecular Sciences|May 14, 2022
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome AnalysisInés García-Consuegra, Sara Asensio-Peña, Rocío Garrido-Moraga, et al.
Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine|July 11, 2007
Favorable responses to acute and chronic exercise in McArdle patientsJosé L Maté-Muñoz, Maria Moran, Margarita Pérez, et al.
Human Mutation|July 17, 2018
Missense mutations have unexpected consequences: The McArdle disease paradigmInés García-Consuegra, Sara Asensio-Peña, Alfonsina Ballester-Lopez, et al.
Age (Dordrecht, Netherlands)|January 29, 2011
Are mitochondrial haplogroups associated with extreme longevity? A study on a Spanish cohortTomàs Pinós, Gisela Nogales-Gadea, Jonatan R Ruiz, et al.
Disease Models & Mechanisms|December 19, 2019
Absence of p.R50X <i>Pygm</i> read-through in McArdle disease cellular modelsGuillermo Tarrasó, Alberto Real-Martinez, Marta Parés, et al.
Nature Communications|May 10, 2012
The Eutherian Armcx genes regulate mitochondrial trafficking in neurons and interact with Miro and Trak2Guillermo López-Doménech, Román Serrat, Serena Mirra, et al.
Mitochondrion|March 16, 2010
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archHenry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Antioxidants & Redox Signaling|April 2, 2011
Oxidative damage compromises energy metabolism in the axonal degeneration mouse model of X-adrenoleukodystrophyJorge Galino, Montserrat Ruiz, Stéphane Fourcade, et al.
Brain : a Journal of Neurology|April 2, 2013
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 geneMaria J Melià, Akatsuki Kubota, Saida Ortolano, et al.
Psychoneuroendocrinology|June 7, 2011
Chronic psychosocial stress induces reversible mitochondrial damage and corticotropin-releasing factor receptor type-1 upregulation in the rat intestine and IBS-like gut dysfunctionMaría Vicario, Carmen Alonso, Mar Guilarte, et al.
International Journal of Molecular Sciences|May 14, 2022
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome AnalysisInés García-Consuegra, Sara Asensio-Peña, Rocío Garrido-Moraga, et al.
Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine|July 11, 2007
Favorable responses to acute and chronic exercise in McArdle patientsJosé L Maté-Muñoz, Maria Moran, Margarita Pérez, et al.
Human Mutation|July 17, 2018
Missense mutations have unexpected consequences: The McArdle disease paradigmInés García-Consuegra, Sara Asensio-Peña, Alfonsina Ballester-Lopez, et al.
Age (Dordrecht, Netherlands)|January 29, 2011
Are mitochondrial haplogroups associated with extreme longevity? A study on a Spanish cohortTomàs Pinós, Gisela Nogales-Gadea, Jonatan R Ruiz, et al.
Disease Models & Mechanisms|December 19, 2019
Absence of p.R50X <i>Pygm</i> read-through in McArdle disease cellular modelsGuillermo Tarrasó, Alberto Real-Martinez, Marta Parés, et al.
Nature Communications|May 10, 2012
The Eutherian Armcx genes regulate mitochondrial trafficking in neurons and interact with Miro and Trak2Guillermo López-Doménech, Román Serrat, Serena Mirra, et al.
Mitochondrion|March 16, 2010
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archHenry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, et al.
Pageof 8