about
Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular TransmissionMitochondrial metabolite transportLattices for ab initio protein structure prediction.Computational approaches for protein function prediction: a combined strategy from multiple sequence alignment to molecular docking-based virtual screening.Identification of new highly selective inhibitors of the human ADP/ATP carriers by molecular docking and in vitro transport assays.Evolution, structure and function of mitochondrial carriers: a review with new insights.Mitochondrial glutamate carriers from Drosophila melanogaster: biochemical, evolutionary and modeling studies.Molecular modeling of antibodies for the treatment of TNFα-related immunological diseases.AGC1/2, the mitochondrial aspartate-glutamate carriers.Sirtuin 3 interacts with Lon protease and regulates its acetylation status.Dataset of the AAC2 conformations in the c-, intermediate- and m-states obtained from free-energy simulations.Structural-dynamical properties of the transmembrane segment VI of the mitochondrial oxoglutarate carrier studied by site directed spin-labeling.Characterization of mitochondrial dicarboxylate/tricarboxylate transporters from grape berries.Novel hydroxycinnamoyl-coenzyme A quinate transferase genes from artichoke are involved in the synthesis of chlorogenic acid.Single-nucleotide evolution quantifies the importance of each site along the structure of mitochondrial carriers.Prediction of high- and low-affinity quinol-analogue-binding sites in the aa3 and bo3 terminal oxidases from Bacillus subtilis and Escherichia coli1.AGC1 deficiency associated with global cerebral hypomyelination.Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster.SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency.A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.Isolation and characterization of novel variants of BBI coding genes from the legume Lathyrus sativus.Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter.Distance-dependent hydrophobic-hydrophobic contacts in protein folding simulations.New insights about the structural rearrangements required for substrate translocation in the bovine mitochondrial oxoglutarate carrier.Nitro-substituted tetrahydroindolizines and homologs: Design, kinetics, and mechanism of α-glucosidase inhibition.Effect of cariporide on ram sperm pH regulation and motility: possible role of NHE1.Isolated truncus arteriosus associated with a mutation in the plexin-D1 gene.Acetylation of human mitochondrial citrate carrier modulates mitochondrial citrate/malate exchange activity to sustain NADPH production during macrophage activationRiboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2The Bacterial Protein CNF1 as a Potential Therapeutic Strategy against Mitochondrial Diseases: A Pilot StudyTruncating Mutation in the Nitric Oxide Synthase 1 Gene Is Associated With Infantile AchalasiaBeyond the Big Five: Investigating Myostatin Structure, Polymorphism and Expression in Camelus dromedarius.The peroxisomal NAD+ carrier of Arabidopsis thaliana transports coenzyme A and its derivativesA new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): a clinical, molecular, and functional studyPathogenic potential of SLC25A15 mutations assessed by transport assays and complementation of Saccharomyces cerevisiae ORT1 null mutantThe switching mechanism of the mitochondrial ADP/ATP carrier explored by free-energy landscapesMetabolic Routes in Inflammation: The Citrate Pathway and its Potential as Therapeutic TargetA novel variant m.641A>T in the mitochondrial MT-TF gene is associated with epileptic encephalopathy in adolescentHeterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to ThriveFAD/NADH Dependent Oxidoreductases: From Different Amino Acid Sequences to Similar Protein Shapes for Playing an Ancient Function
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ciro Leonardo Pierri
@ast
Ciro Leonardo Pierri
@en
Ciro Leonardo Pierri
@es
Ciro Leonardo Pierri
@nl
type
label
Ciro Leonardo Pierri
@ast
Ciro Leonardo Pierri
@en
Ciro Leonardo Pierri
@es
Ciro Leonardo Pierri
@nl
prefLabel
Ciro Leonardo Pierri
@ast
Ciro Leonardo Pierri
@en
Ciro Leonardo Pierri
@es
Ciro Leonardo Pierri
@nl
P106
P1153
24076659700
P21
P31
P496
0000-0003-1816-548X