Results 131 to 140 of about 2,732 (148)
Cell-Penetrating Peptide Enhances Tafazzin Gene Therapy in Mouse Model of Barth Syndrome [PDF]
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
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Role of Tafazzin in Mitochondrial Function, Development and Disease
Journal of Developmental Biology, 2020Simon J. Conway, Michael T Chin
exaly
Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria
Mitochondrion, 2009Riekelt H Houtkooper +2 more
exaly
Cardiolipin remodeling and the function of tafazzin
Biochimica Et Biophysica Acta - Molecular and Cell Biology of Lipids, 2013Michael Schlame
exaly

