Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Arnaud Chevrollier

Showing results (31-40 of 79) with videos related to

Pageof 8
Sort By:
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.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Brain : a Journal of Neurology|October 7, 2023
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondriaArnaud Chevrollier, Adeline Alice Bonnard, Lyse Ruaud, 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.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesionsPhilippe Codron, Julien Cassereau, Patrick Vourc'h, 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.
Frontiers in Neurology|October 10, 2022
Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel <i>de novo</i> heterozygous <i>DNM1L</i> variantCharlène Lhuissier, Bart E Wagner, Amy Vincent, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, 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.
Frontiers in Endocrinology|June 7, 2024
Ketogenic diet enhances the anti-cancer effects of PD-L1 blockade in renal cell carcinomaJeremy Richard, Céline Beauvillain, Maxime Benoit, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
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.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Brain : a Journal of Neurology|October 7, 2023
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondriaArnaud Chevrollier, Adeline Alice Bonnard, Lyse Ruaud, 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.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesionsPhilippe Codron, Julien Cassereau, Patrick Vourc'h, 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.
Frontiers in Neurology|October 10, 2022
Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel <i>de novo</i> heterozygous <i>DNM1L</i> variantCharlène Lhuissier, Bart E Wagner, Amy Vincent, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, 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.
Frontiers in Endocrinology|June 7, 2024
Ketogenic diet enhances the anti-cancer effects of PD-L1 blockade in renal cell carcinomaJeremy Richard, Céline Beauvillain, Maxime Benoit, et al.
Pageof 8