Results 121 to 130 of about 663 (143)
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Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes
American Journal of Physiology-Heart and Circulatory Physiology, 2010Mutation of the mitochondrial protein tafazzin causes dilated cardiomyopathy in Barth syndrome. We employed an adenovirus as a vector to transfer tafazzin small hairpin RNA (shRNA) into neonatal ventricular myocytes (NVMs) to investigate the effects of tafazzin knockdown. The tafazzin shRNA adenovirus consistently knocked down tafazzin mRNA and lowered
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Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene
Prenatal DiagnosisABSTRACT Objective To report a case of a fetus with multiple congenital anomalies and suspected Barth syndrome, highlighting potential phenotypic expansion of the syndrome. Methods A 32‐year‐old G4P2011 patient was ...
Cordelia R. Muir +3 more
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The role of cardiolipin in molecular assemblies of tafazzin
Mitochondrion, 2011Ashim Malhotra⁎ +3 more
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THE ROLE OF MACROPHAGE TAFAZZIN IN ATHEROSCLEROSIS
AtherosclerosisMatthew Batty +6 more
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Role of Tafazzin in Mitochondrial Function, Development and Disease
Journal of Developmental Biology, 2020Simon J. Conway, Michael T Chin
exaly
201 The role of macrophage tafazzin in atherosclerosis
Basic ScienceMatthew Batty +6 more
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