Results 151 to 156 of about 2,315 (156)

Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency

Biochimica Et Biophysica Acta - Molecular and Cell Biology of Lipids, 2018
Maik Hüttemann, Miriam Greenberg, Christian Reynolds   +2 more
exaly  

Mögliche Ursache einer fetalen Herzinsuffizienz: TAFAZZIN-Genvariante

Ultraschall in der Medizin - European Journal of Ultrasound
M. Rehn, E. Kunstmann, P. Paul, D. Schröder, A. Wöckel, U. Pecks   +5 more
openaire   +1 more source

Mis-sesnse mutations in Tafazzin (TAZ) that escort to mild clinical symptoms of Barth syndrome is owed to the minimal inhibitory effect of the mutations on the enzyme function: In-silico evidence

Interdisciplinary Sciences, Computational Life Sciences, 2014
Surajit Debnath
exaly  

MITOCHONDRIAL LOCALIZATION SIGNALS IN HUMAN TAFAZZIN AND USES THEREOF

2019
openaire   +2 more sources

Modified tafazzin proteins and methods of making and using the same

2017
CHIN MICHAEL T, CHIEN WEI-MING, DINCA ANA   +2 more
openaire   +1 more source

Barth syndorme, tafazzin and mitochondrial lyso-PC acyltransferase.

2006
openaire   +1 more source