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Pascal Reynier

Showing results (181-190 of 245) with videos related to

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International Journal of Molecular Sciences|April 30, 2020
Increased Protein <i>S</i>-Glutathionylation in Leber's Hereditary Optic Neuropathy (LHON)Lei Zhou, James Chun Yip Chan, Stephanie Chupin, et al.
Human Molecular Genetics|January 13, 2021
A plasma metabolomic signature of Leber hereditary optic neuropathy showing taurine and nicotinamide deficienciesCinzia Bocca, Victor Le Paih, Juan Manuel Chao de la Barca, et al.
Frontiers in Genetics|January 31, 2020
Data-Mining Approach on Transcriptomics and Methylomics Placental Analysis Highlights Genes in Fetal Growth RestrictionFloris Chabrun, Noémie Huetz, Xavier Dieu, et al.
Human Molecular Genetics|June 5, 2016
Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophyEmmanuelle Sarzi, Marie Seveno, Claire Angebault, et al.
Survey of Ophthalmology|April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of viewRaoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Scientific Reports|May 7, 2020
Sexual Dimorphism of Metabolomic Profile in Arterial HypertensionYaya Goïta, Juan Manuel Chao de la Barca, Asmaou Keïta, et al.
Molecular Vision|March 13, 2018
Obesity-induced metabolic disturbance drives oxidative stress and complement activation in the retinal environmentRiccardo Natoli, Nilisha Fernando, Tess Dahlenburg, et al.
Endocrine-Related Cancer|January 18, 2019
Metabolomics signatures of a subset of RET variants according to their oncogenic risk levelCharlotte Veyrat-Durebex, Nathalie Bouzamondo, Morgane Le Mao, et al.
Scientific Data|May 7, 2026
A dataset of patients with isolated and syndromic optic neuropathies linked to RTN4IP1 genetic variantsAude Rocatcher, Xavier Dieu, Valérie Desquiret-Dumas, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
Pageof 25

Showing results (181-190 of 245) with videos related to

Sort By:
Pageof 25
International Journal of Molecular Sciences|April 30, 2020
Increased Protein <i>S</i>-Glutathionylation in Leber's Hereditary Optic Neuropathy (LHON)Lei Zhou, James Chun Yip Chan, Stephanie Chupin, et al.
Human Molecular Genetics|January 13, 2021
A plasma metabolomic signature of Leber hereditary optic neuropathy showing taurine and nicotinamide deficienciesCinzia Bocca, Victor Le Paih, Juan Manuel Chao de la Barca, et al.
Frontiers in Genetics|January 31, 2020
Data-Mining Approach on Transcriptomics and Methylomics Placental Analysis Highlights Genes in Fetal Growth RestrictionFloris Chabrun, Noémie Huetz, Xavier Dieu, et al.
Human Molecular Genetics|June 5, 2016
Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophyEmmanuelle Sarzi, Marie Seveno, Claire Angebault, et al.
Survey of Ophthalmology|April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of viewRaoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Scientific Reports|May 7, 2020
Sexual Dimorphism of Metabolomic Profile in Arterial HypertensionYaya Goïta, Juan Manuel Chao de la Barca, Asmaou Keïta, et al.
Molecular Vision|March 13, 2018
Obesity-induced metabolic disturbance drives oxidative stress and complement activation in the retinal environmentRiccardo Natoli, Nilisha Fernando, Tess Dahlenburg, et al.
Endocrine-Related Cancer|January 18, 2019
Metabolomics signatures of a subset of RET variants according to their oncogenic risk levelCharlotte Veyrat-Durebex, Nathalie Bouzamondo, Morgane Le Mao, et al.
Scientific Data|May 7, 2026
A dataset of patients with isolated and syndromic optic neuropathies linked to RTN4IP1 genetic variantsAude Rocatcher, Xavier Dieu, Valérie Desquiret-Dumas, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
Pageof 25