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Virginie Guillet

Showing results (1-10 of 15) with videos related to

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Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, 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.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Molecular Vision|March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defectYannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2026
COQ7-Related Neuropathy: Two New Cases and Review of the LiteratureJulian Theuriet, Shams Ribault, Fanny Fontaine, et al.
The International Journal of Biochemistry & Cell Biology|April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiologyPatrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
Brain Pathology (Zurich, Switzerland)|December 20, 2022
Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseasesIsabelle Journe-Mallet, Julien Gouju, Frédérique Etcharry-Bouyx, et al.
BMC Research Notes|December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respirationClaire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2024
Stochastic Optical Reconstruction Microscopy Imaging of Multiple System Atrophy Inclusions Suggests Stepwise α-Synuclein AggregationBenoît Vovard, Alexia Bodin, Julien Gouju, et al.
Annals of Neurology|April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A diseaseDominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, 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.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Molecular Vision|March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defectYannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2026
COQ7-Related Neuropathy: Two New Cases and Review of the LiteratureJulian Theuriet, Shams Ribault, Fanny Fontaine, et al.
The International Journal of Biochemistry & Cell Biology|April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiologyPatrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
Brain Pathology (Zurich, Switzerland)|December 20, 2022
Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseasesIsabelle Journe-Mallet, Julien Gouju, Frédérique Etcharry-Bouyx, et al.
BMC Research Notes|December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respirationClaire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2024
Stochastic Optical Reconstruction Microscopy Imaging of Multiple System Atrophy Inclusions Suggests Stepwise α-Synuclein AggregationBenoît Vovard, Alexia Bodin, Julien Gouju, et al.
Annals of Neurology|April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A diseaseDominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Pageof 2