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Journal of Enzyme Inhibition and Medicinal Chemistry|November 27, 2007
Characterisation of recombinant human fatty aldehyde dehydrogenase: implications for Sjögren-Larsson syndromeMatthew D Lloyd, Kieren D E Boardman, Andrew Smith, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old manS E Olpin, R J Pollitt, J McMenamin, et al.
Orphanet Journal of Rare Diseases|August 15, 2012
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and managementMarc Engelen, Stephan Kemp, Marianne de Visser, et al.
The Journal of Biological Chemistry|March 17, 2005
Developmental changes of bile acid composition and conjugation in L- and D-bifunctional protein single and double knockout miceSacha Ferdinandusse, Simone Denis, Henk Overmars, et al.
Human Genetics|April 10, 2002
Structure of the human argininosuccinate synthetase gene and an improved system for molecular diagnostics in patients with classical and mild citrullinemiaJ Häberle, S Pauli, M Linnebank, et al.
Annals of Human Genetics|August 14, 2003
Smith-Lemli-Opitz syndrome and the DHCR7 geneP E Jira, H R Waterham, R J A Wanders, et al.
The Journal of Biological Chemistry|April 12, 2012
Peroxisomal fatty acid uptake mechanism in Saccharomyces cerevisiaeCarlo W T van Roermund, Lodewijk Ijlst, Wiktor Majczak, et al.
Free Radical Biology & Medicine|June 24, 2023
Human peroxisomal NAD<sup>+</sup>/NADH homeostasis is regulated by two independent NAD(H) shuttle systemsSerhii Chornyi, Cláudio F Costa, Lodewijk IJlst, et al.
Journal of Lipid Research|April 18, 2012
Studying fatty aldehyde metabolism in living cells with pyrene-labeled compoundsMarkus A Keller, Katrin Watschinger, Karsten Lange, et al.
Molecular Genetics and Metabolism|July 12, 2003
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometryFredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, et al.
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