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Cell-Penetrating Peptide Enhances Tafazzin Gene Therapy in Mouse Model of Barth Syndrome [PDF]

open access: yesInternational Journal of Molecular Sciences
Barth Syndrome (BTHS) is an early onset, lethal X-linked disorder caused by a mutation in tafazzin (TAFAZZIN), a mitochondrial acyltransferase that remodels monolysocardiolipin (MLCL) to mature cardiolipin (CL) and is essential for normal mitochondrial ...
Rahul Raghav   +2 more
exaly   +4 more sources
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The lipid environment modulates cardiolipin and phospholipid constitution in wild type and tafazzin-deficient cells

Journal of Inherited Metabolic Disease, 2022
Yvonne Wohlfarter   +2 more
exaly  

Role of Tafazzin in Mitochondrial Function, Development and Disease

Journal of Developmental Biology, 2020
Simon J. Conway, Michael T Chin
exaly  

Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria

Mitochondrion, 2009
Riekelt H Houtkooper   +2 more
exaly  

Cardiolipin remodeling and the function of tafazzin

Biochimica Et Biophysica Acta - Molecular and Cell Biology of Lipids, 2013
Michael Schlame
exaly  

Mechanism for Remodeling of the Acyl Chain Composition of Cardiolipin Catalyzed by Saccharomyces cerevisiae Tafazzin*

Journal of Biological Chemistry, 2016
Masahide Oku   +2 more
exaly  

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