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F Y Choy

Showing results (11-20 of 32) with videos related to

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Pediatric Research|December 1, 1978
Gaucher's disease. I. Solubilization and electrophoresis of beta-glucosidase from leukocytes and cultured fibroblastsF Y Choy, R G Davidson
American Journal of Human Genetics|September 1, 1980
Gaucher disease. III. Substrate specificity of glucocerebrosidase and the use of nonlabeled natural substrates for the investigation of patientsF Y Choy, R G Davidson
Progress in Clinical and Biological Research|January 1, 1982
Qualitative characteristics of the beta-glucosidase isozymesF Y Choy, R G Davidson
American Journal of Medical Genetics|October 26, 2000
Mutation analysis of Gaucher disease using dot-blood samples on FTA filter paperN C Devost, F Y Choy
Pediatric Research|January 1, 1980
Gaucher's disease II. Studies on the kinetics of beta-glucosidase and the effects of sodium taurocholate in normal and Gaucher tissuesF Y Choy, R G Davidson
Blood Cells, Molecules & Diseases|December 16, 1998
A novel complex allele and two new point mutations in type 2 (acute neuronopathic) Gaucher diseaseG Sinclair, F Y Choy, L Humphries
American Journal of Medical Genetics|October 28, 1996
Gaucher disease: functional expression of the normal glucocerebrosidase and Gaucher T1366G and G1604A alleles in Baculovirus-transfected Spodoptera frugiperda cellsF Y Choy, C Wei, D Levin
Molecular Genetics and Metabolism|November 16, 2001
Heterologous expression and characterization of a rare Gaucher disease mutation (c.481C > T) from a Canadian aboriginal population using archival tissue samplesG Sinclair, F Y Choy, P Ferreira
Biochimica Et Biophysica Acta|March 7, 1986
In situ radiation-inactivation size of fibroblast membrane-bound acid beta-glucosidase in Gaucher type 1, type 2 and type 3 diseaseF Y Choy, M Woo, M Potier
American Journal of Medical Genetics|June 9, 1999
Glucocerebrosidase mutations among Chinese neuronopathic and non-neuronopathic Gaucher disease patientsF Y Choy, K Wong, H P Shi
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Pediatric Research|December 1, 1978
Gaucher's disease. I. Solubilization and electrophoresis of beta-glucosidase from leukocytes and cultured fibroblastsF Y Choy, R G Davidson
American Journal of Human Genetics|September 1, 1980
Gaucher disease. III. Substrate specificity of glucocerebrosidase and the use of nonlabeled natural substrates for the investigation of patientsF Y Choy, R G Davidson
Progress in Clinical and Biological Research|January 1, 1982
Qualitative characteristics of the beta-glucosidase isozymesF Y Choy, R G Davidson
American Journal of Medical Genetics|October 26, 2000
Mutation analysis of Gaucher disease using dot-blood samples on FTA filter paperN C Devost, F Y Choy
Pediatric Research|January 1, 1980
Gaucher's disease II. Studies on the kinetics of beta-glucosidase and the effects of sodium taurocholate in normal and Gaucher tissuesF Y Choy, R G Davidson
Blood Cells, Molecules & Diseases|December 16, 1998
A novel complex allele and two new point mutations in type 2 (acute neuronopathic) Gaucher diseaseG Sinclair, F Y Choy, L Humphries
American Journal of Medical Genetics|October 28, 1996
Gaucher disease: functional expression of the normal glucocerebrosidase and Gaucher T1366G and G1604A alleles in Baculovirus-transfected Spodoptera frugiperda cellsF Y Choy, C Wei, D Levin
Molecular Genetics and Metabolism|November 16, 2001
Heterologous expression and characterization of a rare Gaucher disease mutation (c.481C > T) from a Canadian aboriginal population using archival tissue samplesG Sinclair, F Y Choy, P Ferreira
Biochimica Et Biophysica Acta|March 7, 1986
In situ radiation-inactivation size of fibroblast membrane-bound acid beta-glucosidase in Gaucher type 1, type 2 and type 3 diseaseF Y Choy, M Woo, M Potier
American Journal of Medical Genetics|June 9, 1999
Glucocerebrosidase mutations among Chinese neuronopathic and non-neuronopathic Gaucher disease patientsF Y Choy, K Wong, H P Shi
Pageof 4