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American Journal of Mental Retardation : AJMR|June 9, 2005
Etiology of mental retardation in children referred to a tertiary care center: a prospective studyClara D M van Karnebeek, Frederike Y Scheper, Nico G Abeling, et al.American Journal of Human Genetics|January 11, 2003
Identification of PEX7 as the second gene involved in Refsum diseaseDaan M van den Brink, Pedro Brites, Janet Haasjes, et al.Journal of Medical Genetics|November 2, 2016
ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolismSacha Ferdinandusse, Kim D Falkenberg, Janet Koster, et al.Biochimica Et Biophysica Acta|July 19, 2016
CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acidsCatherine E van Engen, Rob Ofman, Inge M E Dijkstra, et al.Journal of Lipid Research|April 5, 2005
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosisFredoen Valianpour, Voula Mitsakos, Dimitri Schlemmer, et al.Neurology|February 28, 2007
Phenotype of adult Refsum disease due to a defect in peroxin 7M A Horn, D M van den Brink, R J A Wanders, et al.Journal of Inherited Metabolic Disease|May 6, 2010
Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduriaChristina B Pedersen, Zarazuela Zolkipli, Søren Vang, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 31, 2009
Increased mitochondrial content rescues in vivo muscle oxidative capacity in long-term high-fat-diet-fed ratsN M A van den Broek, J Ciapaite, H M M L De Feyter, et al.Molecular Genetics and Metabolism Reports|April 19, 2021
Dietary restriction in the long-chain acyl-CoA dehydrogenase knockout mouseEugène F Diekman, Michel van Weeghel, Mayte Suárez-Fariñas, et al.Scientific Reports|July 21, 2019
Mutagenesis separates ATPase and thioesterase activities of the peroxisomal ABC transporter, ComatoseDavid J Carrier, Carlo W T van Roermund, Theresia A Schaedler, et al.Pageof 48