Showing results (391-400 of 1,319) with videos related to

Sort By:
Pageof 132
Molecular Genetics and Metabolism|August 29, 2006
An improved enzyme assay for carnitine palmitoyl transferase I in fibroblasts using tandem mass spectrometryNaomi van Vlies, Jos P N Ruiter, Mirjam Doolaard, et al.
Biochemical and Biophysical Research Communications|November 18, 2005
OCTN3 is a mammalian peroxisomal membrane carnitine transporterAnne-Marie Lamhonwah, Cameron A Ackerley, Aina Tilups, et al.
Developmental Medicine and Child Neurology|September 6, 2000
Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency)L Sztriha, L I Al-Gazali, R J Wanders, et al.
Oncology (Williston Park, N.Y.)|August 12, 1999
UFT and oral calcium folinate as first-line chemotherapy for metastatic gastric cancerA Ravaud, M Borner, J H Schellens, et al.
Applied and Environmental Microbiology|June 29, 2002
Genotypic and phenotypic diversity within species of purple nonsulfur bacteria isolated from aquatic sedimentsYasuhiro Oda, Wouter Wanders, Louis A Huisman, et al.
Journal of Inherited Metabolic Disease|January 11, 2024
Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylateSander F Garrelfs, Serhii Chornyi, Heleen Te Brinke, et al.
Nature Communications|November 1, 2019
Moving from drought hazard to impact forecastsSamuel J Sutanto, Melati van der Weert, Niko Wanders, et al.
Frontiers in Cell and Developmental Biology|February 7, 2022
Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD TransportersCarlo W T van Roermund, Lodewijk IJlst, Nicole Linka, et al.
Biochimica Et Biophysica Acta|November 29, 1994
2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Pageof 132