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G Winchester

Showing results (41-50 of 51) with videos related to

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Acta Neuropathologica|September 14, 2000
GM1-gangliosidosis in a cross-bred dog confirmed by detection of GM1-ganglioside using electrospray ionisation-tandem mass spectrometryP Whitfield, A W Johnson, K A Dunn, et al.
Clinical Chemistry|October 24, 2001
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technologyK Mills, P B Mills, P T Clayton, et al.
Pediatric Research|April 1, 1976
Enzyme replacement therapy--an experiment of nature in a chimeric mannosidosis calfR D Jolly, K G Thompson, C E Murphy, et al.
Human Genetics|December 6, 2001
Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutationsC E Beesley, C A Meaney, G Greenland, et al.
Molecular Genetics and Metabolism|January 21, 2009
Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometryClare E Beesley, Elisabeth P Young, Niamh Finnegan, et al.
The Biochemical Journal|December 1, 1978
Characterization of the mutant alpha-mannosidase in bovine mannosidosisL J Burditt, N C Phillips, D Robinson, et al.
The Biochemical Journal|July 1, 1990
The structural basis of the inhibition of human glycosidases by castanospermine analoguesB G Winchester, I Cenci di Bello, A C Richardson, et al.
Archives of Disease in Childhood|September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannoseC J Hendriksz, P McClean, M J Henderson, et al.
Biochimica Et Biophysica Acta|June 16, 2005
A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristicsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Journal of Inherited Metabolic Disease|April 24, 2009
Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substratesO P van Diggelen, L F Oemardien, N A M E van der Beek, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Acta Neuropathologica|September 14, 2000
GM1-gangliosidosis in a cross-bred dog confirmed by detection of GM1-ganglioside using electrospray ionisation-tandem mass spectrometryP Whitfield, A W Johnson, K A Dunn, et al.
Clinical Chemistry|October 24, 2001
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technologyK Mills, P B Mills, P T Clayton, et al.
Pediatric Research|April 1, 1976
Enzyme replacement therapy--an experiment of nature in a chimeric mannosidosis calfR D Jolly, K G Thompson, C E Murphy, et al.
Human Genetics|December 6, 2001
Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutationsC E Beesley, C A Meaney, G Greenland, et al.
Molecular Genetics and Metabolism|January 21, 2009
Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometryClare E Beesley, Elisabeth P Young, Niamh Finnegan, et al.
The Biochemical Journal|December 1, 1978
Characterization of the mutant alpha-mannosidase in bovine mannosidosisL J Burditt, N C Phillips, D Robinson, et al.
The Biochemical Journal|July 1, 1990
The structural basis of the inhibition of human glycosidases by castanospermine analoguesB G Winchester, I Cenci di Bello, A C Richardson, et al.
Archives of Disease in Childhood|September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannoseC J Hendriksz, P McClean, M J Henderson, et al.
Biochimica Et Biophysica Acta|June 16, 2005
A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristicsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Journal of Inherited Metabolic Disease|April 24, 2009
Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substratesO P van Diggelen, L F Oemardien, N A M E van der Beek, et al.
Pageof 6