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Arnaud Besse

Showing results (11-20 of 17) with videos related to

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Molecular and Cellular Biology|May 5, 2005
The human beta-globin locus control region can silence as well as activate gene expressionYong-Qing Feng, Renaud Warin, Taihao Li, et al.
Human Mutation|January 4, 2018
Loss-of-function mutations in ISCA2 disrupt 4Fe-4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletionJoseph T Alaimo, Arnaud Besse, Charlotte L Alston, et al.
Cell Metabolism|March 5, 2015
The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolismArnaud Besse, Ping Wu, Francesco Bruni, et al.
Journal of Inherited Metabolic Disease|October 4, 2016
Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduriaMonika Oláhová, Kyle Thompson, Steven A Hardy, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonismLionel Van Maldergem, Arnaud Besse, Boel De Paepe, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenancePenelope E Bonnen, John W Yarham, Arnaud Besse, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Molecular and Cellular Biology|May 5, 2005
The human beta-globin locus control region can silence as well as activate gene expressionYong-Qing Feng, Renaud Warin, Taihao Li, et al.
Human Mutation|January 4, 2018
Loss-of-function mutations in ISCA2 disrupt 4Fe-4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletionJoseph T Alaimo, Arnaud Besse, Charlotte L Alston, et al.
Cell Metabolism|March 5, 2015
The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolismArnaud Besse, Ping Wu, Francesco Bruni, et al.
Journal of Inherited Metabolic Disease|October 4, 2016
Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduriaMonika Oláhová, Kyle Thompson, Steven A Hardy, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonismLionel Van Maldergem, Arnaud Besse, Boel De Paepe, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenancePenelope E Bonnen, John W Yarham, Arnaud Besse, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Pageof 2