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European Journal of Biochemistry|September 17, 1998
Carboxymethylated phosphatidylethanolamine in mitochondrial membranes of mammals--evidence for intracellular lipid glycoxidationR Pamplona, J R Requena, M Portero-Otín, et al.
The Journal of Biological Chemistry|May 25, 1987
Effect of phosphate on the kinetics and specificity of glycation of proteinN G Watkins, C I Neglia-Fisher, D G Dyer, et al.
The Journal of Biological Chemistry|June 15, 1993
Formation of o-tyrosine and dityrosine in proteins during radiolytic and metal-catalyzed oxidationT G Huggins, M C Wells-Knecht, N A Detorie, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian familiesS Laradi, T Tukel, M Erazo, et al.
Molecular Genetics and Metabolism|December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patientsS Laradi, T Tukel, S Khediri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2001
Acute intermittent porphyria: novel missense mutations in the human hydroxymethylbilane synthase geneR B Ramdall, L Cunha, K H Astrin, et al.
Archives of Neurology|March 14, 2000
Myoclonus from selective dentate nucleus degeneration in type 3 Gaucher diseaseJ Verghese, R F Goldberg, R J Desnick, et al.
The Journal of Biological Chemistry|June 15, 1986
Identification of fibroblasts as a major site of albumin catabolism in peripheral tissuesJ L Strobel, S G Cady, T K Borg, et al.
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