All Stories

  1. Mitochondrial Dysfunction in the Inflammatory Process of Neurodegenerative Diseases
  2. Metabolic Comparison of Mature and Immature Bovine Cumulus–Oocyte Complexes with Standardization of Bioenergetic Assessment
  3. Dextromethorphan Is a Novel Pharmacological Inhibitor of F 1 F O ‐ ...
  4. Mitochondrial Permeability Transition Pore: The Cardiovascular Disease’s Molecular Achilles Heel
  5. Reprogramming the Mitochondrion in Atherosclerosis: Targets for Vascular Protection
  6. Inflammatory mitochondrial signalling and viral mimicry in cancer
  7. Oxygen Deprivation and Brain Inflammation: The Mitochondrial Link to Alzheimer's Progression
  8. Mitochondrial bioenergetics analysis on SLC-selected boar spermatozoa during liquid storage
  9. Analysis of stallion spermatozoa metabolism using Agilent Seahorse XFp Technology
  10. Mitochondrial sirtuin 3 and role of natural compounds: the effect of post-translational modifications on cellular metabolism
  11. UCP2, a Member of the Mitochondrial Uncoupling Proteins: An Overview from Physiological to Pathological Roles
  12. H+‐slip correlated to rotor free‐wheeling as cause of F1FO‐ATPase dysfunction in primary mitochondrial disorders
  13. Selenite ameliorates the ATP hydrolysis of mitochondrial F1FO-ATPase by changing the redox state of thiol groups and impairs the ADP phosphorylation
  14. Understanding differential aspects of microdiffusion (channeling) in the Coenzyme Q and Cytochrome c regions of the mitochondrial respiratory system
  15. Mineralocorticoid Receptor Antagonism Prevents Type 2 Familial Partial Lipodystrophy Brown Adipocyte Dysfunction
  16. Proton leak through the UCPs and ANT carriers and beyond: A breath for the electron transport chain
  17. Inflammatory signaling in NASH driven by hepatocyte mitochondrial dysfunctions
  18. Cell bioenergetics and ATP production of boar spermatozoa
  19. Cell Metabolism Therapy by Small Natural Compounds
  20. Two separate pathways underlie NADH and succinate oxidation in swine heart mitochondria: Kinetic evidence on the mobile electron carriers
  21. Inflammation, Mitochondria and Natural Compounds Together in the Circle of Trust
  22. Novel Regioselective Synthesis of 1,3,4,5-Tetrasubstituted Pyrazoles and Biochemical Valuation on F1FO-ATPase and Mitochondrial Permeability Transition Pore Formation
  23. ‘Rotor free-wheeling’ in impaired F1FO-ATPase induces congenital hypermetabolism
  24. GPR35, ally of the anti-ischemic ATPIF1-ATP synthase interaction
  25. Effects of cryopreservation on the mitochondrial bioenergetics of bovine sperm
  26. The Impairment of Cell Metabolism by Cardiovascular Toxicity of Doxorubicin Is Reversed by Bergamot Polyphenolic Fraction Treatment in Endothelial Cells
  27. Cellular Metabolism and Bioenergetic Function in Human Fibroblasts and Preadipocytes of Type 2 Familial Partial Lipodystrophy
  28. What happens when the mitochondrial H+-translocating F1FO-ATP(hydrol)ase becomes a molecular target of calcium? The pore opens
  29. Protein folding and unfolding: proline cis‐trans isomerization at the c subunits of F1FO‐ATPase might open a high conductance ion channel
  30. Mitochondria Bioenergetic Functions and Cell Metabolism Are Modulated by the Bergamot Polyphenolic Fraction
  31. From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases
  32. From the Structural and (Dys)function of ATP Synthase to Deficiency in Age-Related Diseases
  33. Impaired Mitochondrial Bioenergetics under Pathological Conditions
  34. Protein folding and unfolding: proline cis - trans isomerization at the c subunits of F 1 F O -ATPase might open a high conductance ion channel
  35. Unraveling Energy Substrate Utilization in Sperm Cells
  36. Enjoy your journey: the bergamot polyphenols from the tree to the cell metabolism
  37. The mitochondrial F1FO-ATPase exploits the dithiol redox state to modulate the permeability transition pore
  38. SARS‐CoV‐2 first contact: Spike–ACE2 interactions in COVID‐19
  39. Sulfide affects the mitochondrial respiration, the Ca2+-activated F1FO-ATPase activity and the permeability transition pore but does not change the Mg2+-activated F1FO-ATPase activity in swine heart mitochondria
  40. Relationship between serum concentration, functional parameters and cell bioenergetics in IPEC-J2 cell line
  41. Molecular and Supramolecular Structure of the Mitochondrial Oxidative Phosphorylation System: Implications for Pathology
  42. Biological characteristics and metabolic profile of canine mesenchymal stem cells isolated from adipose tissue and umbilical cord matrix
  43. Ca2+ as cofactor of the mitochondrial H+‐translocating F1FO‐ATP(hydrol)ase
  44. Mitochondrial F1FO-ATPase and permeability transition pore response to sulfide in the midgut gland of Mytilus galloprovincialis
  45. Incoming news on the F-type ATPase structure and functions in mammalian mitochondria
  46. 1,5‐Disubstituted‐1,2,3‐triazoles as inhibitors of the mitochondrial Ca 2+ ‐activated F 1 F O ‐ATP(hydrol)ase and the permeability transition pore
  47. Effects of Hydrogen Sulfide Donor NaHS on Porcine Vascular Wall-Mesenchymal Stem Cells
  48. Mitochondrial F-type ATP synthase: multiple enzyme functions revealed by the membrane-embedded FO structure
  49. Nicotinamide Nucleotide Transhydrogenase as a Sensor of Mitochondrial Biology
  50. The mitochondrial permeability transition pore in cell death: A promising drug binding bioarchitecture
  51. Mitochondrial Ca 2+ ‐activated F 1 F O ‐ATPase hydrolyzes ATP and promotes the permeability transition pore
  52. Emerging Roles for the Mitochondrial ATP Synthase Supercomplexes
  53. A Therapeutic Role for the F1FO-ATP Synthase
  54. Characterization of metabolic profiles and lipopolysaccharide effects on porcine vascular wall mesenchymal stem cells
  55. Crucial aminoacids in the FO sector of the F1FO-ATP synthase address H+ across the inner mitochondrial membrane: molecular implications in mitochondrial dysfunctions
  56. Lipid-protein interactions in mitochondrial membranes from bivalve mollusks: molecular strategies in different species
  57. From the Ca 2+ -activated F 1 F O -ATPase to the mitochondrial permeability transition pore: an overview
  58. A Lethal Channel between the ATP Synthase Monomers
  59. New insight in a new entity: the mitochondrial permeability transition pore arises from the Ca 2+ -activated F 1 F O -ATPases
  60. The inhibition of the mitochondrial F1FO-ATPase activity when activated by Ca2+ opens new regulatory roles for NAD+
  61. Mitochondrial permeability transition, F 1 F O ‐ATPase and calcium: an enigmatic triangle
  62. Post-translational modifications of the mitochondrial F 1 F O -ATPase
  63. A preliminary study on a novel sea water disinfection process by a peroxy-acid compound to complement and improve the microbial depuration of clams ( Ruditapes philippinarum )
  64. Kinetic properties of the mitochondrial F 1 F O -ATPase activity elicited by Ca 2+ in replacement of Mg 2+
  65. Mitochondrial permeability transition, F 1 F O ‐ATPase and calcium: an enigmatic triangle
  66. Glucose and glutamine in the mitochondrial oxidative metabolism of stem cells
  67. Mercury and protein thiols: Stimulation of mitochondrial F1FO-ATPase and inhibition of respiration
  68. Preferential nitrite inhibition of the mitochondrial F1FO-ATPase activities when activated by Ca2+ in replacement of the natural cofactor Mg2+
  69. Lipid unsaturation per se does not explain the physical state of mitochondrial membranes in Mytilus galloprovincialis
  70. Thiol-Related Regulation of the Mitochondrial F1FO-ATPase Activity
  71. The c-Ring of the F1FO-ATP Synthase: Facts and Perspectives
  72. Opposite Rotation Directions in the Synthesis and Hydrolysis of ATP by the ATP Synthase: Hints from a Subunit Asymmetry
  73. Long-chain PUFA enrichment in microalgae and metabolic dynamics inTapes philippinarumlarvae
  74. The a subunit asymmetry dictates the two opposite rotation directions in the synthesis and hydrolysis of ATP by the mitochondrial ATP synthase
  75. Thiol oxidation of mitochondrial FO-c subunits: A way to switch off antimicrobial drug targets of the mitochondrial ATP synthase
  76. Thiol oxidation is crucial in the desensitization of the mitochondrial F1FO-ATPase to oligomycin and other macrolide antibiotics
  77. The mitochondrial F1FO-ATPase desensitization to oligomycin by tributyltin is due to thiol oxidation
  78. Modifiers of the oligomycin sensitivity of the mitochondrial F1F0-ATPase
  79. Mussel and mammalian ATP synthase share the same bioenergetic cost of ATP
  80. Toxicity of organotin compounds: Shared and unshared biochemical targets and mechanisms in animal cells
  81. Modulation of the F1FO-ATPase function by butyltin compounds
  82. Dietary Enhancement of Selected Fatty Acid Biosynthesis in the Digestive Gland of Mytilus galloprovincialis Lmk.
  83. Tri-n-butyltin binding to a low-affinity site decreases the F1FO-ATPase sensitivity to oligomycin in mussel mitochondria
  84. Organotin Effects in Different Phyla: Discrepancies and Similarities
  85. Tributyltin-driven enhancement of the DCCD insensitive Mg-ATPase activity in mussel digestive gland mitochondria
  86. Structural and functional changes in gill mitochondrial membranes from the Mediterranean mussel Mytilus galloprovincialis exposed to tri-n-butyltin
  87. Multi-site TBT binding skews the inhibition of oligomycin on the mitochondrial Mg–ATPase in Mytilus galloprovincialis
  88. Tributyltin (TBT) and mitochondrial respiration in mussel digestive gland
  89. Tributyltin (TBT) and dibutyltin (DBT) differently inhibit the mitochondrial Mg-ATPase activity in mussel digestive gland
  90. Tributyltin inhibits the oligomycin-sensitive Mg-ATPase activity in Mytilus galloprovincialis digestive gland mitochondria
  91. Tributyltin (TBT) inhibition of oligomycin-sensitive Mg-ATPase activity in mussel mitochondria