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Christophe Rocher

Showing results (11-20 of 22) with videos related to

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BMC Medical Genetics|July 22, 2009
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA backgroundDenis Pierron, Marc Ferré, Christophe Rocher, et al.
The FEBS Journal|February 1, 2024
Mlg1, a yeast acyltransferase located in ER membranes associated with mitochondria (MAMs), is involved in de novo synthesis and remodelling of phospholipidsPatricia Laquel, Sophie Ayciriex, François Doignon, et al.
Plos One|July 9, 2011
Mutation rate switch inside Eurasian mitochondrial haplogroups: impact of selection and consequences for dating settlement in EuropeDenis Pierron, Ivan Chang, Amal Arachiche, et al.
Human Mutation|January 14, 2012
Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing lossNicolás Gutiérrez Cortés, Claire Pertuiset, Elodie Dumon, et al.
Science (New York, N.Y.)|February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutationsWeiwei Fan, Katrina G Waymire, Navneet Narula, et al.
Antioxidants & Redox Signaling|February 29, 2012
Adaptative capacity of mitochondrial biogenesis and of mitochondrial dynamics in response to pathogenic respiratory chain dysfunctionGiovanni Benard, Thomas Trian, Nadège Bellance, et al.
Human Molecular Genetics|February 4, 2020
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestationsNicolás Gutiérrez Cortés, Claire Pertuiset, Elodie Dumon, et al.
Molecular Nutrition & Food Research|August 1, 2017
Fast digestive, leucine-rich, soluble milk proteins improve muscle protein anabolism, and mitochondrial function in undernourished old ratsJérôme Salles, Audrey Chanet, Alexandre Berry, et al.
BMC Medical Genetics|May 9, 2008
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutationDenis Pierron, Christophe Rocher, Patricia Amati-Bonneau, et al.
Communications Biology|November 26, 2022
Vitamin D status modulates mitochondrial oxidative capacities in skeletal muscle: role in sarcopeniaJérôme Salles, Audrey Chanet, Christelle Guillet, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
BMC Medical Genetics|July 22, 2009
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA backgroundDenis Pierron, Marc Ferré, Christophe Rocher, et al.
The FEBS Journal|February 1, 2024
Mlg1, a yeast acyltransferase located in ER membranes associated with mitochondria (MAMs), is involved in de novo synthesis and remodelling of phospholipidsPatricia Laquel, Sophie Ayciriex, François Doignon, et al.
Plos One|July 9, 2011
Mutation rate switch inside Eurasian mitochondrial haplogroups: impact of selection and consequences for dating settlement in EuropeDenis Pierron, Ivan Chang, Amal Arachiche, et al.
Human Mutation|January 14, 2012
Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing lossNicolás Gutiérrez Cortés, Claire Pertuiset, Elodie Dumon, et al.
Science (New York, N.Y.)|February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutationsWeiwei Fan, Katrina G Waymire, Navneet Narula, et al.
Antioxidants & Redox Signaling|February 29, 2012
Adaptative capacity of mitochondrial biogenesis and of mitochondrial dynamics in response to pathogenic respiratory chain dysfunctionGiovanni Benard, Thomas Trian, Nadège Bellance, et al.
Human Molecular Genetics|February 4, 2020
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestationsNicolás Gutiérrez Cortés, Claire Pertuiset, Elodie Dumon, et al.
Molecular Nutrition & Food Research|August 1, 2017
Fast digestive, leucine-rich, soluble milk proteins improve muscle protein anabolism, and mitochondrial function in undernourished old ratsJérôme Salles, Audrey Chanet, Alexandre Berry, et al.
BMC Medical Genetics|May 9, 2008
New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutationDenis Pierron, Christophe Rocher, Patricia Amati-Bonneau, et al.
Communications Biology|November 26, 2022
Vitamin D status modulates mitochondrial oxidative capacities in skeletal muscle: role in sarcopeniaJérôme Salles, Audrey Chanet, Christelle Guillet, et al.
Pageof 3