Pages that link to "Q50794086"
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The following pages link to Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected children. (Q50794086):
Displaying 24 items.
- Physiological and pathological roles of mitochondrial SLC25 carriers (Q28297551) (← links)
- miR-141 as a regulator of the mitochondrial phosphate carrier (Slc25a3) in the type 1 diabetic heart (Q28392445) (← links)
- Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic Acidosis (Q30371716) (← links)
- Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathy (Q30583137) (← links)
- Genetic manipulation of the cardiac mitochondrial phosphate carrier does not affect permeability transition (Q33840454) (← links)
- The mitochondrial phosphate transporters modulate plant responses to salt stress via affecting ATP and gibberellin metabolism in Arabidopsis thaliana (Q34399212) (← links)
- Infant with cardiomyopathy: When to suspect inborn errors of metabolism? (Q34574024) (← links)
- Kassiopeia: a database and web application for the analysis of mutually exclusive exomes of eukaryotes (Q35089205) (← links)
- Thermal manipulation of the chicken embryo triggers differential gene expression in response to a later heat challenge (Q36007969) (← links)
- Physiological and pathological roles of the mitochondrial permeability transition pore in the heart (Q36193286) (← links)
- Intrinsic aerobic capacity correlates with greater inherent mitochondrial oxidative and H2O2 emission capacities without major shifts in myosin heavy chain isoform (Q36473653) (← links)
- Mitochondrial transporters of the SLC25 family and associated diseases: a review (Q38209474) (← links)
- Role and convergent evolution of competing RNA secondary structures in mutually exclusive splicing (Q38917777) (← links)
- Tissue-specific expression and silencing phenotypes of mitochondrial phosphate carrier paralogues in several insect species (Q41987792) (← links)
- Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION. (Q46356615) (← links)
- The landscape of human mutually exclusive splicing. (Q47152826) (← links)
- The mammalian phosphate carrier SLC25A3 is a mitochondrial copper transporter required for cytochrome c oxidase biogenesis. (Q47296599) (← links)
- Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease (Q51764886) (← links)
- Expansion of the mutually exclusive spliced exome in Drosophila. (Q52760269) (← links)
- Emerging Roles in the Biogenesis of Cytochrome Oxidase for Members of the Mitochondrial Carrier Family (Q61805012) (← links)
- Unusual structure and splicing pattern of the vertebrate mitochondrial solute carrier SLC25A3 gene (Q88391287) (← links)
- Molecular regulation of MCU: Implications in physiology and disease (Q89446590) (← links)
- Slc20a1/Pit1 and Slc20a2/Pit2 are essential for normal skeletal myofiber function and survival (Q89810553) (← links)
- Role of phosphate sensing in bone and mineral metabolism (Q91458078) (← links)