All Stories

  1. Cytochrome c Oxidase Subunit 4 Isoform Exchange Results in Modulation of Oxygen Affinity
  2. Biochemical thresholds for pathological presentation of ATP synthase deficiencies
  3. Mitochondrial targets of metformin—Are they physiologically relevant?
  4. Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production
  5. Mitochondrial Targeting of Metformin Enhances Its Activity against Pancreatic Cancer
  6. Pharmacological inhibition of fatty-acid oxidation synergistically enhances the effect of l-asparaginase in childhood ALL cells
  7. Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry
  8. ROS production in brown adipose tissue mitochondria: The question of UCP1-dependence
  9. Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology
  10. Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy
  11. Mitochondrially Targeted α-Tocopheryl Succinate Is Antiangiogenic: Potential Benefit Against Tumor Angiogenesis but Caution Against Wound Healing
  12. Evaluation of basic mitochondrial functions using rat tissue homogenates
  13. Phosphomimetic Substitution of CytochromecTyrosine 48 Decreases Respiration and Binding to Cardiolipin and Abolishes Ability to Trigger Downstream Caspase Activation
  14. Impaired mitochondrial energetic in patients harbouring SURF1 mutations is caused by uncoupling of cytochrome c oxidase
  15. Increased oxidative stress in fibroblasts from patients with ATP synthase deficiency
  16. Regulation of mitochondrial respiration and apoptosis through phosphorylation of cytochrome c
  17. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1   subunit
  18. A suggested role for mitochondria in Noonan syndrome
  19. Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy
  20. Chapter 11 Isolation of Regulatory‐Competent, Phosphorylated Cytochrome c Oxidase
  21. High efficiency of ROS production by glycerophosphate dehydrogenase in mammalian mitochondria
  22. Regulation of oxidative phosphorylation, the mitochondrial membrane potential, and their role in human disease
  23. HIF and reactive oxygen species regulate oxidative phosphorylation in cancer
  24. Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains
  25. Respiratory chain components involved in the glycerophosphate dehydrogenase-dependent ROS production by brown adipose tissue mitochondria
  26. Mitochondrial complex I inhibition in cerebral cortex of immature rats following homocysteic acid-induced seizures
  27. Mitochondrial diseases and genetic defects of ATP synthase
  28. Two components in pathogenic mechanism of mitochondrial ATPase deficiency: Energy deprivation and ROS production
  29. Evaluation of mitochondrial membrane potential using a computerized device with a tetraphenylphosphonium-selective electrode
  30. Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride
  31. Flow-cytometric monitoring of mitochondrial depolarisation: from fluorescence intensities to millivolts
  32. Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochromecoxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206
  33. A new role for the von Hippel-Lindau tumor suppressor protein: stimulation of mitochondrial oxidative phosphorylation complex biogenesis
  34. Mitochondrial diseases and ATPase defects of nuclear origin
  35. GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene
  36. Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase
  37. Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome