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Vincent Procaccio

Showing results (61-70 of 197) with videos related to

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Mitochondrion|July 1, 2009
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b geneKonstantina Fragaki, Vincent Procaccio, Sylvie Bannwarth, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Nucleic Acids Research|December 21, 2006
An enhanced MITOMAP with a global mtDNA mutational phylogenyEduardo Ruiz-Pesini, Marie T Lott, Vincent Procaccio, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Neuro-Oncology Advances|February 4, 2022
Mitochondrial DNA copy number as a prognostic marker is age-dependent in adult glioblastomaBaptiste Sourty, Laure-Marie Dardaud, Céline Bris, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
Human Reproduction Update|August 27, 2016
Ovarian ageing: the role of mitochondria in oocytes and folliclesPascale May-Panloup, Lisa Boucret, Juan-Manuel Chao de la Barca, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
Pageof 20

Showing results (61-70 of 197) with videos related to

Sort By:
Pageof 20
Mitochondrion|July 1, 2009
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b geneKonstantina Fragaki, Vincent Procaccio, Sylvie Bannwarth, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Nucleic Acids Research|December 21, 2006
An enhanced MITOMAP with a global mtDNA mutational phylogenyEduardo Ruiz-Pesini, Marie T Lott, Vincent Procaccio, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Neuro-Oncology Advances|February 4, 2022
Mitochondrial DNA copy number as a prognostic marker is age-dependent in adult glioblastomaBaptiste Sourty, Laure-Marie Dardaud, Céline Bris, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
Human Reproduction Update|August 27, 2016
Ovarian ageing: the role of mitochondria in oocytes and folliclesPascale May-Panloup, Lisa Boucret, Juan-Manuel Chao de la Barca, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
Pageof 20