Related references
Note: Only part of the references are listed.Cardiolipin remodeling and the function of tafazzin
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Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis
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Cardiolipin stabilizes respiratory chain supercomplexes
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Phospholipid abnormalities in children with Barth syndrome
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Choline head groups stabilize the matrix loop regions of the ATP/ADP carrier ScAAC2
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Gluing the respiratory chain together - Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane
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Cardiolipin prevents rate-dependent uncoupling and provides osmotic stability in yeast mitochondria
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Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
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Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function
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The cytochrome bc1 and cytochrome c oxidase complexes associate to form a single supracomplex in yeast mitochondria
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Oxidative phosphorylation in cardiolipin-lacking yeast mitochondria
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