Showing results (11-20 of 39) with videos related to
Sort By:
Pageof 4
The Journal of Biological Chemistry|June 30, 2001
Molecular and Biochemical Characterization of Rat epsilon -N-Trimethyllysine Hydroxylase, the First Enzyme of Carnitine BiosynthesisF M Vaz, R Ofman, K Westinga, et al.Clinical Genetics|February 9, 2016
When silence is noise: infantile-onset Barth syndrome caused by a synonymous substitution affecting TAZ gene transcriptionL Ferri, C Dionisi-Vici, R Taurisano, et al.Journal of Inherited Metabolic Disease|September 15, 2006
Prolonged moderate-intensity exercise without and with L-carnitine supplementation in patients with MCAD deficiencyH H Huidekoper, J Schneider, T Westphal, et al.Cell Death and Differentiation|January 23, 2016
Cardiolipin or MTCH2 can serve as tBID receptors during apoptosisE Raemy, S Montessuit, S Pierredon, et al.Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.Frontiers in Pediatrics|July 15, 2024
Glycodeoxycholic acid as alternative treatment in 3β-hydroxy-Δ5-C27-steroid-oxidoreductase: a case reportS Majait, F M Vaz, E Marleen Kemper, et al.Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.Journal of Inherited Metabolic Disease|November 1, 2002
Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiencyZ Rahbeeni, F M Vaz, K Al-Hussein, et al.Human Reproduction (Oxford, England)|November 25, 2024
The composition of commercially available human embryo culture mediaM S Zagers, M Laverde, M Goddijn, et al.Research in Veterinary Science|October 11, 2022
Anthelmintic intoxication in goats and sheep: A systematic reviewC C Oliveira, D F L Costa, C H Limeira, et al.Pageof 4