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V Procaccio

Showing results (1-10 of 33) with videos related to

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European Journal of Neurology|January 7, 2012
Correlation between genetic polymorphisms and stroke recovery: analysis of the GAIN Americas and GAIN International StudiesS C Cramer, V Procaccio, , et al.
Analytical Biochemistry|August 15, 1997
A nonradioactive double detection method for the assignment of spots in two-dimensional blotsM Chevallet, V Procaccio, T Rabilloud
American Journal of Human Genetics|June 1, 1997
Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscleN Monnier, V Procaccio, P Stieglitz, et al.
Gene|July 17, 1998
Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductaseR de Sury, P Martinez, V Procaccio, et al.
Neuromuscular Disorders : NMD|November 25, 2022
Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathiesM Masingue, B Rucheton, C Bris, et al.
Biochimica Et Biophysica Acta|March 20, 1997
cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex IV Procaccio, D Depetris, P Soularue, et al.
Revue Neurologique|May 7, 2014
Mitochondrial dysfunction affecting visual pathwaysS Leruez, P Amati-Bonneau, C Verny, et al.
Gene|December 29, 1995
Identification of five Rhodobacter capsulatus genes encoding the equivalent of ND subunits of the mitochondrial NADH-ubiquinone oxidoreductaseA Dupuis, A Peinnequin, M Chevallet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 28, 1998
Mapping to 1q23 of the human gene (NDUFS2) encoding the 49-kDa subunit of the mitochondrial respiratory Complex I and immunodetection of the mature protein in mitochondriaV Procaccio, R de Sury, P Martinez, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
European Journal of Neurology|January 7, 2012
Correlation between genetic polymorphisms and stroke recovery: analysis of the GAIN Americas and GAIN International StudiesS C Cramer, V Procaccio, , et al.
Analytical Biochemistry|August 15, 1997
A nonradioactive double detection method for the assignment of spots in two-dimensional blotsM Chevallet, V Procaccio, T Rabilloud
American Journal of Human Genetics|June 1, 1997
Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscleN Monnier, V Procaccio, P Stieglitz, et al.
Gene|July 17, 1998
Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductaseR de Sury, P Martinez, V Procaccio, et al.
Neuromuscular Disorders : NMD|November 25, 2022
Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathiesM Masingue, B Rucheton, C Bris, et al.
Biochimica Et Biophysica Acta|March 20, 1997
cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex IV Procaccio, D Depetris, P Soularue, et al.
Revue Neurologique|May 7, 2014
Mitochondrial dysfunction affecting visual pathwaysS Leruez, P Amati-Bonneau, C Verny, et al.
Gene|December 29, 1995
Identification of five Rhodobacter capsulatus genes encoding the equivalent of ND subunits of the mitochondrial NADH-ubiquinone oxidoreductaseA Dupuis, A Peinnequin, M Chevallet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 28, 1998
Mapping to 1q23 of the human gene (NDUFS2) encoding the 49-kDa subunit of the mitochondrial respiratory Complex I and immunodetection of the mature protein in mitochondriaV Procaccio, R de Sury, P Martinez, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Pageof 4