Showing results (1-10 of 117) with videos related to
Sort By:
Pageof 12
Molecular Genetics and Metabolism|August 5, 2000
Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation IcV Westphal, C Schottstädt, T Marquardt, et al.Molecular Genetics and Metabolism|May 15, 2001
Functional analysis of novel mutations in a congenital disorder of glycosylation Ia patient with mixed Asian ancestryV Westphal, G M Enns, M F McCracken, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 20, 2001
Two proteins modulating transendothelial migration of leukocytes recognize novel carboxylated glycans on endothelial cellsG Srikrishna, K Panneerselvam, V Westphal, et al.Molecular Genetics and Metabolism|May 15, 2001
Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementationV Westphal, S Kjaergaard, J A Davis, et al.The American Journal of Pathology|December 7, 2000
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylationV Westphal, S Murch, S Kim, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation IaV Westphal, S Peterson, M Patterson, et al.The Journal of Biological Chemistry|July 25, 1985
Interaction of Dictyostelium discoideum lysosomal enzymes with the mammalian phosphomannosyl receptor. The importance of oligosaccharides which contain phosphodiestersH H FreezeCurrent Protocols in Molecular Biology|February 12, 2008
Analysis of sulfate esters by solvolysis or hydrolysisH H FreezePageof 12