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L Andreu

Showing results (261-270 of 313) with videos related to

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Medicine and Science in Sports and Exercise|April 1, 2016
Muscle Signaling in Exercise Intolerance: Insights from the McArdle Mouse ModelCarmen Fiuza-Luces, Gisela Nogales-Gadea, Inés García-Consuegra, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
Neuromuscular Disorders : NMD|June 15, 2007
The 577X allele of the ACTN3 gene is associated with improved exercise capacity in women with McArdle's diseaseAlejandro Lucia, Félix Gómez-Gallego, Catalina Santiago, et al.
Scientific Reports|March 28, 2019
Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse modelAlberto Real-Martinez, Astrid Brull, Jordi Huerta, et al.
Molecular Genetics and Metabolism|April 11, 2006
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNAJordi P Guallar, Maya R Vilà, Ester López-Gallardo, et al.
Plos One|February 21, 2012
A transcriptomic approach to search for novel phenotypic regulators in McArdle diseaseGisela Nogales-Gadea, Inés Consuegra-García, Juan C Rubio, et al.
Mitochondrion|February 10, 2011
Quality assessment of human mitochondrial DNA quantification: MITONAUTS, an international multicentre surveyHélène C F Côté, Mariana Gerschenson, Ulrich A Walker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2012
Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registryAlejandro Lucia, Jonatan R Ruiz, Alfredo Santalla, et al.
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.
Pageof 32

Showing results (261-270 of 313) with videos related to

Sort By:
Pageof 32
Medicine and Science in Sports and Exercise|April 1, 2016
Muscle Signaling in Exercise Intolerance: Insights from the McArdle Mouse ModelCarmen Fiuza-Luces, Gisela Nogales-Gadea, Inés García-Consuegra, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
Neuromuscular Disorders : NMD|June 15, 2007
The 577X allele of the ACTN3 gene is associated with improved exercise capacity in women with McArdle's diseaseAlejandro Lucia, Félix Gómez-Gallego, Catalina Santiago, et al.
Scientific Reports|March 28, 2019
Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse modelAlberto Real-Martinez, Astrid Brull, Jordi Huerta, et al.
Molecular Genetics and Metabolism|April 11, 2006
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNAJordi P Guallar, Maya R Vilà, Ester López-Gallardo, et al.
Plos One|February 21, 2012
A transcriptomic approach to search for novel phenotypic regulators in McArdle diseaseGisela Nogales-Gadea, Inés Consuegra-García, Juan C Rubio, et al.
Mitochondrion|February 10, 2011
Quality assessment of human mitochondrial DNA quantification: MITONAUTS, an international multicentre surveyHélène C F Côté, Mariana Gerschenson, Ulrich A Walker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2012
Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registryAlejandro Lucia, Jonatan R Ruiz, Alfredo Santalla, et al.
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.
Pageof 32