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Pascal Reynier

Showing results (201-210 of 245) with videos related to

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Plos One|March 25, 2021
DRP1 haploinsufficiency attenuates cardiac ischemia/reperfusion injuriesLaura Bouche, Rima Kamel, Sophie Tamareille, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 16, 2021
Protective role of the mitochondrial fusion protein OPA1 in hypertensionPauline Robert, Phuc Minh Chau Nguyen, Alexis Richard, et al.
Brain : a Journal of Neurology|February 7, 2013
Sensorineural hearing loss in OPA1-linked disordersStéphanie Leruez, Dan Milea, Sabine Defoort-Dhellemmes, et al.
Neurobiology of Disease|August 28, 2015
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiologyJuan Manuel Chao de la Barca, Delphine Prunier-Mirebeau, Patrizia Amati-Bonneau, et al.
Plos One|October 4, 2022
Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cellsMarie Deck, Gerben Van Hameren, Graham Campbell, et al.
Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
American Journal of Medical Genetics. Part A|December 4, 2019
Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorderMarine Tessarech, Magali Gorce, Françoise Boussion, et al.
Investigative Ophthalmology & Visual Science|January 18, 2018
A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related DisordersCinzia Bocca, Judith Kouassi Nzoughet, Stéphanie Leruez, et al.
Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Annals of Neurology|October 22, 2005
OPA1 R445H mutation in optic atrophy associated with sensorineural deafnessPatrizia Amati-Bonneau, Agnès Guichet, Aurélien Olichon, et al.
Pageof 25

Showing results (201-210 of 245) with videos related to

Sort By:
Pageof 25
Plos One|March 25, 2021
DRP1 haploinsufficiency attenuates cardiac ischemia/reperfusion injuriesLaura Bouche, Rima Kamel, Sophie Tamareille, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 16, 2021
Protective role of the mitochondrial fusion protein OPA1 in hypertensionPauline Robert, Phuc Minh Chau Nguyen, Alexis Richard, et al.
Brain : a Journal of Neurology|February 7, 2013
Sensorineural hearing loss in OPA1-linked disordersStéphanie Leruez, Dan Milea, Sabine Defoort-Dhellemmes, et al.
Neurobiology of Disease|August 28, 2015
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiologyJuan Manuel Chao de la Barca, Delphine Prunier-Mirebeau, Patrizia Amati-Bonneau, et al.
Plos One|October 4, 2022
Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cellsMarie Deck, Gerben Van Hameren, Graham Campbell, et al.
Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
American Journal of Medical Genetics. Part A|December 4, 2019
Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorderMarine Tessarech, Magali Gorce, Françoise Boussion, et al.
Investigative Ophthalmology & Visual Science|January 18, 2018
A Plasma Metabolomic Signature Involving Purine Metabolism in Human Optic Atrophy 1 (OPA1)-Related DisordersCinzia Bocca, Judith Kouassi Nzoughet, Stéphanie Leruez, et al.
Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Annals of Neurology|October 22, 2005
OPA1 R445H mutation in optic atrophy associated with sensorineural deafnessPatrizia Amati-Bonneau, Agnès Guichet, Aurélien Olichon, et al.
Pageof 25