Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
about
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesAlternative isoform regulation in human tissue transcriptomesBiochemical diagnosis of mitochondrial disordersmiR-141 as a regulator of the mitochondrial phosphate carrier (Slc25a3) in the type 1 diabetic heartSpermidine promotes human hair growth and is a novel modulator of human epithelial stem cell functionsPathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic AcidosisCardiolipin, a critical determinant of mitochondrial carrier protein assembly and function.Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathyTissue-specific expression and regulatory networks of pig microRNAome.Identifying differential exon splicing using linear models and correlation coefficients.The in-depth evaluation of suspected mitochondrial diseaseGenetic manipulation of the cardiac mitochondrial phosphate carrier does not affect permeability transition.The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseasesLack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.The mitochondrial phosphate transporters modulate plant responses to salt stress via affecting ATP and gibberellin metabolism in Arabidopsis thalianaFunctional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells.Infant with cardiomyopathy: When to suspect inborn errors of metabolism?Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathwayOverexpression of Mitochondrial Phosphate Transporter 3 Severely Hampers Plant Development through Regulating Mitochondrial Function in Arabidopsis.Yeast mitochondrial interactosome model: metabolon membrane proteins complex involved in the channeling of ADP/ATPPhysiological and pathological roles of the mitochondrial permeability transition pore in the heart.Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiaeMicroarray analyses of genes regulated by isoflurane anesthesia in vivo: a novel approach to identifying potential preconditioning mechanisms.Impaired regulation of brain mitochondria by extramitochondrial Ca2+ in transgenic Huntington disease ratsApproaches to finding the molecular basis of mitochondrial oxidative phosphorylation disorders.Mechanisms of disease: hypertrophic cardiomyopathy.Mitochondrial transporters of the SLC25 family and associated diseases: a review.A sperm-specific proteome-scale metabolic network model identifies non-glycolytic genes for energy deficiency in asthenozoospermia.Functional Properties of the Mitochondrial Carrier System.Orchestration of dynamic copper navigation - new and missing pieces.Role of mitochondrial phosphate carrier in metabolism-secretion coupling in rat insulinoma cell line INS-1.Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation.Extraintestinal manifestations of celiac disease: 33-mer gliadin binding to glutamate receptor GRINA as a new explanation.Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy.Tissue-specific expression and silencing phenotypes of mitochondrial phosphate carrier paralogues in several insect species.Evaluation of the mitochondrial respiratory chain and oxidative phosphorylation system using yeast models of OXPHOS deficiencies.Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION.Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers.Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.The mammalian phosphate carrier SLC25A3 is a mitochondrial copper transporter required for cytochrome c oxidase biogenesis.
P2860
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P2860
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
description
2007 nî lūn-bûn
@nan
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@ast
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@en
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@nl
type
label
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@ast
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@en
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@nl
prefLabel
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@ast
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@en
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@nl
P2093
P2860
P50
P356
P1476
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation
@en
P2093
Boris R Gebhardt
Hansjosef Böhles
Johannes Koch
Michaela Jaksch
Peter Freisinger
Rita Horváth
Ulrike Fötschl
Wolfgang Sperl
P2860
P304
P356
10.1086/511788
P407
P577
2007-03-01T00:00:00Z