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American Journal of Human Genetics|December 31, 2005
Mutational spectrum of D-bifunctional protein deficiency and structure-based genotype-phenotype analysisSacha Ferdinandusse, Mari S Ylianttila, Jolein Gloerich, et al.The EMBO Journal|August 1, 1996
The ABC transporter proteins Pat1 and Pat2 are required for import of long-chain fatty acids into peroxisomes of Saccharomyces cerevisiaeE H Hettema, C W van Roermund, B Distel, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 2, 2008
The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA estersCarlo W T van Roermund, Wouter F Visser, Lodewijk Ijlst, et al.Nucleic Acids Research|December 1, 2006
PeroxisomeDB: a database for the peroxisomal proteome, functional genomics and diseaseAgatha Schlüter, Stéphane Fourcade, Enric Domènech-Estévez, et al.Nederlands Tijdschrift Voor Geneeskunde|August 22, 2008
[Short-chain acyl-CoA dehydrogenase deficiency (SCADD): relatively high prevalence in the Netherlands and strongly variable fenotype; neonatal screening not indicated]B T van Maldegem, M Duran, R J A Wanders, et al.The Journal of Clinical Investigation|July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzymeJ C Heikoop, C W van Roermund, W W Just, et al.Journal of Inherited Metabolic Disease|August 3, 2020
Increased protein propionylation contributes to mitochondrial dysfunction in liver cells and fibroblasts, but not in myotubesBart Lagerwaard, Olga Pougovkina, Anna F Bekebrede, et al.Biochemical and Biophysical Research Communications|June 16, 1988
Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acidsR J Wanders, C W van Roermund, M J van Wijland, et al.The Journal of Pediatrics|November 1, 2002
Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblastsFredoen Valianpour, Ronald J A Wanders, Henk Overmars, et al.Nederlands Tijdschrift Voor Geneeskunde|May 9, 2000
[Identification of the gene for hyper-IgD syndrome: a model of modern genetics]J P Drenth, H R Waterham, W Kuis, et al.Pageof 133