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Biological Chemistry|April 20, 2001
Congenital disorders of glycosylation: glycosylation defects in man and biological models for their studyT Marquardt, H FreezeBiochemical and Biophysical Research Communications|March 17, 1995
Enzymes involved in the synthesis of mannose-6-phosphate from glucose are normal in carbohydrate deficient glycoprotein syndrome fibroblastsK Panneerselvam, H H FreezeBiochimica Et Biophysica Acta|December 29, 2005
Applied glycoproteomics--approaches to study genetic-environmental collisions causing protein-losing enteropathyLars Bode, Hudson H FreezeSeminars in Cell & Developmental Biology|April 6, 2010
Metabolic manipulation of glycosylation disorders in humans and animal modelsHudson H Freeze, Vandana SharmaThe Journal of Biological Chemistry|January 29, 2011
Mannose efflux from the cells: a potential source of mannose in bloodVandana Sharma, Hudson H FreezeCurrent Protocols in Protein Science|November 25, 2010
Endoglycosidase and glycoamidase release of N-linked glycansHudson H Freeze, Christian KranzBiochimica Et Biophysica Acta|November 26, 1999
Molecular basis of carbohydrate-deficient glycoprotein syndromes type I with normal phosphomannomutase activityH H Freeze, M AebiCurrent Opinion in Structural Biology|September 13, 2005
Altered glycan structures: the molecular basis of congenital disorders of glycosylationHudson H Freeze, Markus AebiBiochimica Et Biophysica Acta|December 9, 2008
Glycosylation diseases: quo vadis?Harry Schachter, Hudson H FreezePageof 31