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Clinical and Translational Gastroenterology|April 1, 2022
AGPAT1 as a Novel Colonic Biomarker for Discriminating Between Ulcerative Colitis With and Without Primary Sclerosing CholangitisJohan Vessby, Jacek R Wisniewski, Cecilia Lindskog, et al.
Pediatric Research|November 25, 2003
Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorderJeannette Gootjes, Orly Elpeleg, François Eyskens, et al.
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.
European Journal of Pediatrics|March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcomeE Lopriore, R J Gemke, N M Verhoeven, et al.
Journal of Medicinal Chemistry|June 25, 2005
Peptoid-peptide hybrids as potent novel melanocortin receptor ligandsJohn A W Kruijtzer, Wouter A J Nijenhuis, Nienke Wanders, 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.
Journal of Lipid Research|July 1, 1985
Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndromeG Schrakamp, C F Roosenboom, R B Schutgens, et al.
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