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Identification of the mitochondrial GTP/GDP transporter in Saccharomyces cerevisiae.Identification and metabolic role of the mitochondrial aspartate-glutamate transporter in Saccharomyces cerevisiae.Identification of the yeast mitochondrial transporter for oxaloacetate and sulfate.Identification and functions of new transporters in yeast mitochondria.The biochemical properties of the mitochondrial thiamine pyrophosphate carrier from Drosophila melanogaster.Cytopathic effects of the cytomegalovirus-encoded apoptosis inhibitory protein vMIA.Identification of mitochondrial carriers in Saccharomyces cerevisiae by transport assay of reconstituted recombinant proteins.UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation.Transcription of the mitochondrial citrate carrier gene: identification of a silencer and its binding protein ZNF224.Yeast mitochondria lacking the phosphate carrier/p32 are blocked in phosphate transport but can import preproteins after regeneration of a membrane potential.Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster.Overexpression in E. coli and purification of the L. pneumophila Lpp2981 protein.Effect Of Diazoxide on Friedreich Ataxia Models.Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes.New insights about the structural rearrangements required for substrate translocation in the bovine mitochondrial oxoglutarate carrier.Molecular identification and functional characterization of a novel glutamate transporter in yeast and plant mitochondriaISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteinsRiboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2The mitochondrial dicarboxylate carrier is essential for the growth of Saccharomyces cerevisiae on ethanol or acetate as the sole carbon sourceA new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): a clinical, molecular, and functional studyFunctional characterization and organ distribution of three mitochondrial ATP-Mg/Pi carriers in Arabidopsis thalianaISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Angelo Vozza
@ast
Angelo Vozza
@en
Angelo Vozza
@es
Angelo Vozza
@nl
type
label
Angelo Vozza
@ast
Angelo Vozza
@en
Angelo Vozza
@es
Angelo Vozza
@nl
prefLabel
Angelo Vozza
@ast
Angelo Vozza
@en
Angelo Vozza
@es
Angelo Vozza
@nl
P106
P21
P31
P496
0000-0002-2433-465X