Mitochondrial transporters of the SLC25 family and associated diseases: a review.
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The human SLC25A33 and SLC25A36 genes of solute carrier family 25 encode two mitochondrial pyrimidine nucleotide transportersNutritional and Hormonal Regulation of Citrate and Carnitine/Acylcarnitine Transporters: Two Mitochondrial Carriers Involved in Fatty Acid MetabolismRecurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy NumberCalcium-induced conformational changes in the regulatory domain of the human mitochondrial ATP-Mg/Pi carrier.Lipid-Loving ANTs: Molecular Simulations of Cardiolipin Interactions and the Organization of the Adenine Nucleotide Translocase in Model Mitochondrial Membranes.Inhibition of the Mitochondrial Glutamate Carrier SLC25A22 in Astrocytes Leads to Intracellular Glutamate Accumulation.Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetrance.Fe-S cluster biogenesis in isolated mammalian mitochondria: coordinated use of persulfide sulfur and iron and requirements for GTP, NADH, and ATP.The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.Misfolding of mutant adenine nucleotide translocase in yeast supports a novel mechanism of Ant1-induced muscle diseases.Subcellular Distribution of NAD+ between Cytosol and Mitochondria Determines the Metabolic Profile of Human Cells.Bovine and murine models highlight novel roles for SLC25A46 in mitochondrial dynamics and metabolism, with implications for human and animal health.Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiaeFoxO1 Deacetylation Decreases Fatty Acid Oxidation in β-Cells and Sustains Insulin Secretion in Diabetes.Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.Mitochondrial iron overload: causes and consequences.IDH1 deficiency attenuates gluconeogenesis in mouse liver by impairing amino acid utilization.Mitochondrial transporters for ornithine and related amino acids: a review.Targeting mitochondrial metal dyshomeostasis for the treatment of neurodegeneration.SLC25A26 overexpression impairs cell function via mtDNA hypermethylation and rewiring of methyl metabolism.Asymmetric dimethylarginine is transported by the mitochondrial carrier SLC25A2.Diabetogenic milieus induce specific changes in mitochondrial transcriptome and differentiation of human pancreatic islets.Lipid synthesis and membrane contact sites: a crossroads for cellular physiology.When β-cells fail: lessons from dedifferentiation.Mitochondrial purine and pyrimidine metabolism and beyond.UCP1: A transporter for H+ and fatty acid anions.Action of Thyroid Hormones, T3 and T2, on Hepatic Fatty Acids: Differences in Metabolic Effects and Molecular Mechanisms.Functional Properties of the Mitochondrial Carrier System.Ornithine and Homocitrulline Impair Mitochondrial Function, Decrease Antioxidant Defenses and Induce Cell Death in Menadione-Stressed Rat Cortical Astrocytes: Potential Mechanisms of Neurological Dysfunction in HHH Syndrome.SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome.Expanding the Clinical Spectrum of Mitochondrial Citrate Carrier (SLC25A1) Deficiency: Facial Dysmorphism in Siblings with Epileptic Encephalopathy and Combined D,L-2-Hydroxyglutaric Aciduria.Molecular diagnosis of citrin deficiency in an infant with intrahepatic cholestasis: identification of a 21.7kb gross deletion that completely silences the transcriptional and translational expression of the affected SLC25A13 allele.An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants.Conservation/Mutation in the Splice Sites of Mitochondrial Solute Carrier Genes of Vertebrates.Analysis of islet beta cell functions and their correlations with liver dysfunction in patients with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.Mitochondrial network responses in oxidative physiology and disease.Uncoupling proteins 1 and 2 (UCP1 and UCP2) from Arabidopsis thaliana are mitochondrial transporters of aspartate, glutamate and dicarboxylates.Filling the mitochondrial copper pool.
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Mitochondrial transporters of the SLC25 family and associated diseases: a review.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Mitochondrial transporters of the SLC25 family and associated diseases: a review.
@en
type
label
Mitochondrial transporters of the SLC25 family and associated diseases: a review.
@en
prefLabel
Mitochondrial transporters of the SLC25 family and associated diseases: a review.
@en
P2860
P1476
Mitochondrial transporters of the SLC25 family and associated diseases: a review.
@en
P2093
Ferdinando Palmieri
P2860
P2888
P304
P356
10.1007/S10545-014-9708-5
P577
2014-05-06T00:00:00Z
P6179
1038106165