about
A tissue-specific approach to the analysis of metabolic changes in Caenorhabditis elegansLoss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activitySuccinate dehydrogenase upregulation destabilize complex I and limits the lifespan of gas-1 mutantIntra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulationThe bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster.Adipose tissue mitochondrial dysfunction triggers a lipodystrophic syndrome with insulin resistance, hepatosteatosis, and cardiovascular complicationsMTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals.Drosophila melanogaster LRPPRC2 is involved in coordination of mitochondrial translationMitofusin 2 is required to maintain mitochondrial coenzyme Q levels.SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation.Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission.POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA.A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease.Changes of mitochondrial ultrastructure and function during ageing in mice and Drosophila.Bioenergetic roles of mitochondrial fusion.Loss of LRPPRC causes ATP synthase deficiencyCOX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation.Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly.MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture.Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAsActive proton leak in mitochondria: a new way to regulate substrate oxidation.Kinetic activation of yeast mitochondrial D-lactate dehydrogenase by carboxylic acids.Mitochondrial adaptations to steatohepatitis induced by a methionine- and choline-deficient diet.Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals.A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency.POLRMT does not transcribe nuclear genes.Dietary methionine deficiency affects oxidative status, mitochondrial integrity and mitophagy in the liver of rainbow trout (Oncorhynchus mykiss).Glycerol supports growth of the Trypanosoma brucei bloodstream forms in the absence of glucose: Analysis of metabolic adaptations on glycerol-rich conditionsHuman COX7A2L Regulates Complex III Biogenesis and Promotes Supercomplex Organization Remodeling without Affecting Mitochondrial BioenergeticsBase-excision repair deficiency alone or combined with increased oxidative stress does not increase mtDNA point mutations in miceMitochondrial fusion is required for regulation of mitochondrial DNA replication
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Arnaud Mourier
@ast
Arnaud Mourier
@en
Arnaud Mourier
@es
Arnaud Mourier
@nl
type
label
Arnaud Mourier
@ast
Arnaud Mourier
@en
Arnaud Mourier
@es
Arnaud Mourier
@nl
prefLabel
Arnaud Mourier
@ast
Arnaud Mourier
@en
Arnaud Mourier
@es
Arnaud Mourier
@nl
P106
P21
P31
P496
0000-0002-5413-611X