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Blood|August 1, 1987
Age-related deficiency of the synthesis of platelet activating factor by leukocytes from Zellweger patientsA Sturk, M C Schaap, A Prins, et al.Journal of Lipid Research|December 10, 1997
A two-base deletion in exon 6 of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene producing the skipping of exons 5 and 6 determines 3-hydroxy-3-methylglutaric aciduriaN Casals, J Pié, C H Casale, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 26, 2008
Increased intramyocellular lipid content but normal skeletal muscle mitochondrial oxidative capacity throughout the pathogenesis of type 2 diabetesHenk M De Feyter, Ellen Lenaers, Sander M Houten, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Carnitine supplementation induces long-chain acylcarnitine production--studies in the VLCAD-deficient mouseM Liebig, M Gyenes, G Brauers, et al.Molecular Genetics and Metabolism|April 20, 2006
High incidence of hyperoxaluria in generalized peroxisomal disordersChristiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.Biochimica Et Biophysica Acta|July 16, 2013
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficientSara Violante, Lodewijk Ijlst, Heleen Te Brinke, et al.Annals of Neurology|August 10, 2010
Mutations in PEX10 are a cause of autosomal recessive ataxiaLuc Régal, Merel S Ebberink, Nathalie Goemans, et al.The Journal of Cell Biology|October 1, 1995
Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1A Motley, M J Lumb, P B Oatey, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|July 1, 1994
A phase II trial with docetaxel (Taxotere) in second line treatment with chemotherapy for advanced breast cancer. A study of the EORTC Early Clinical Trials GroupW W ten Bokkel Huinink, A M Prove, M Piccart, et al.Clinical Case Reports|February 11, 2016
Mild phenotype in an adult male with X-linked adrenoleukodystrophy - case reportMorten A Horn, Karin B M Mikaelsen, Sacha Ferdinandusse, et al.Pageof 133