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Alteration of cardiolipin-dependent mitochondrial coupling in muscle protects against obesity

https://doi.org/10.1101/715953
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Large-scale gene function analysis with the PANTHER classification system
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Mitochondrial proton and electron leaks
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ELOVL1 production of C24 acyl-CoAs is linked to C24 sphingolipid synthesis
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Molecular structural diversity of mitochondrial cardiolipins
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Evidence for conduction of protons along the interface between water and a polar lipid monolayer.
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The 3-hydroxyacyl-CoA dehydratases HACD1 and HACD2 exhibit functional redundancy and are active in a wide range of fatty acid elongation pathways
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Cardiolipin Is Essential for Organization of Complexes III and IV into a Supercomplex in Intact Yeast Mitochondria
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Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit
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Congenital myopathy is caused by mutation of HACD1
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Loss of LRPPRC causes ATP synthase deficiency
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Impaired Epidermal Permeability Barrier in Mice Lacking Elovl1 , the Gene Responsible for Very-Long-Chain Fatty Acid Production
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The Yeast Split-Ubiquitin Membrane Protein Two-Hybrid Screen Identifies BAP31 as a Regulator of the Turnover of Endoplasmic Reticulum-Associated Protein Tyrosine Phosphatase-Like B
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Calorie restriction increases fatty acid synthesis and whole body fat oxidation rates
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Electrophoretic separation of rat skeletal muscle myosin heavy-chain isoforms
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Exercise, GLUT4, and Skeletal Muscle Glucose Uptake
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Myocardial Alterations in Senescent Mice and Effect of Exercise Training
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Membrane Deformation under Local pH Gradient: Mimicking Mitochondrial Cristae Dynamics
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Brown Fat and Browning for the Treatment of Obesity and Related Metabolic Disorders
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