Cardiolipin remodelling in mitochondrial therapeutics: translational evidence chains from elamipretide to emerging strategies. [PDF]
Di K, Hu Y, Sun H, Meng T, Han T, Qie R.
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Barth syndrome (BTHS) is a rare X-linked genetic disease classically characterized by cardiomyopathy, skeletal myopathy, and neutropenia. It is caused by mutations in the TAFAZZIN gene, which codes for the protein tafazzin (Taz), and this results in alterations in the level and molecular composition of the mitochondrial phospholipid cardiolipin with ...
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Cross-species evidence for cardiolipin remodeling in neonatal hypoxic-ischemic encephalopathy. [PDF]
Emaus KJ +9 more
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Saturated cardiolipins are potent disruptors of inner mitochondrial membrane structure and function. [PDF]
Venkatraman K +10 more
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Metabolic cardiomyopathies: untangling clinical heterogeneity with human stem-cell derived models. [PDF]
Passadouro AS +6 more
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Lard Intake Reduced Tetralinoleoyl Cardiolipin and Attenuated the Cardioprotective Effects of Exercise in Mice With Pressure Overload-Induced Heart Failure. [PDF]
Kitamura A +10 more
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Understanding the role of MLCL AT-1 and tafazzin in mitochondrial function
Cardiolipin (CL) is a phospholipid found exclusively in mitochondria and is required for normal mitochondrial function. CL biosynthesis requires a crucial remodelling step that incorporates specific acyl chains onto its molecular structure. The enzyme primarily responsible for CL remodelling is Tafazzin (TAZ), a mitochondrial protein encoded by the TAZ
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Insights into Neutrophil Dysfunction in Inherited Metabolic Disorders. [PDF]
Wolf A +8 more
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