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Y Ben-Yoseph

Showing results (21-30 of 44) with videos related to

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European Journal of Biochemistry|August 1, 1975
Specific determination of N-acetyl-beta-D-hexosaminidase isozymes A and B by radioimmunoassay and radial immunodiffusionB Geiger, R Navon, Y Ben-Yoseph, et al.
Analytical Biochemistry|November 1, 1984
Radiometric assays of N-acetylglucosaminylphosphotransferase and alpha-N-acetylglucosaminyl phosphodiesterase with substrates labeled in the glucosamine moietyY Ben-Yoseph, M S Baylerian, H L Nadler
The Journal of Clinical Investigation|January 1, 1974
Enzymatically inactive red cell carbonic anhydrase B in a family with renal tubular acidosisE Shapira, Y Ben-Yoseph, F G Eyal, et al.
Biochimica Et Biophysica Acta|June 6, 1979
Multiple carbohydrate-cleaving specificities in human acidic and neutral glycosidasesY Ben-Yoseph, M B Fiddler, R Rousson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 1982
Km defect in neuraminidase of dysmorphic type sialidosis with and without beta-galactosidase deficiencyY Ben-Yoseph, T Momoi, M S Baylerian, et al.
Clinical Genetics|June 1, 1982
Catalytically defective ganglioside neuraminidase in mucolipidosis IVY Ben-Yoseph, T Momoi, L C Hahn, et al.
American Journal of Human Genetics|July 1, 1985
Diagnosis and carrier detection of Tay-Sachs disease: direct determination of hexosaminidase A using 4-methylumbelliferyl derivatives of beta-N-acetylglucosamine-6-sulfate and beta-N-acetylgalactosamine-6-sulfateY Ben-Yoseph, J E Reid, B Shapiro, et al.
The Biochemical Journal|June 15, 1979
Demonstration of altered acidic hydrolases in fibroblasts from patients with mucolipidosis II by lectin titrationR Rousson, Y Ben-Yoseph, M B Fiddler, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Thermal activation of hexosaminidase A in a genetic compound with Tay-Sachs diseaseY Ben-Yoseph, M S Baylerian, T Momoi, et al.
The Biochemical Journal|February 1, 1981
Deficient phosphorylation of mannose residues of mannan in fibroblasts of patients with mucolipidoses II and IIIY Ben-Yoseph, L C Hahn, C L DeFranco, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
European Journal of Biochemistry|August 1, 1975
Specific determination of N-acetyl-beta-D-hexosaminidase isozymes A and B by radioimmunoassay and radial immunodiffusionB Geiger, R Navon, Y Ben-Yoseph, et al.
Analytical Biochemistry|November 1, 1984
Radiometric assays of N-acetylglucosaminylphosphotransferase and alpha-N-acetylglucosaminyl phosphodiesterase with substrates labeled in the glucosamine moietyY Ben-Yoseph, M S Baylerian, H L Nadler
The Journal of Clinical Investigation|January 1, 1974
Enzymatically inactive red cell carbonic anhydrase B in a family with renal tubular acidosisE Shapira, Y Ben-Yoseph, F G Eyal, et al.
Biochimica Et Biophysica Acta|June 6, 1979
Multiple carbohydrate-cleaving specificities in human acidic and neutral glycosidasesY Ben-Yoseph, M B Fiddler, R Rousson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 1982
Km defect in neuraminidase of dysmorphic type sialidosis with and without beta-galactosidase deficiencyY Ben-Yoseph, T Momoi, M S Baylerian, et al.
Clinical Genetics|June 1, 1982
Catalytically defective ganglioside neuraminidase in mucolipidosis IVY Ben-Yoseph, T Momoi, L C Hahn, et al.
American Journal of Human Genetics|July 1, 1985
Diagnosis and carrier detection of Tay-Sachs disease: direct determination of hexosaminidase A using 4-methylumbelliferyl derivatives of beta-N-acetylglucosamine-6-sulfate and beta-N-acetylgalactosamine-6-sulfateY Ben-Yoseph, J E Reid, B Shapiro, et al.
The Biochemical Journal|June 15, 1979
Demonstration of altered acidic hydrolases in fibroblasts from patients with mucolipidosis II by lectin titrationR Rousson, Y Ben-Yoseph, M B Fiddler, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Thermal activation of hexosaminidase A in a genetic compound with Tay-Sachs diseaseY Ben-Yoseph, M S Baylerian, T Momoi, et al.
The Biochemical Journal|February 1, 1981
Deficient phosphorylation of mannose residues of mannan in fibroblasts of patients with mucolipidoses II and IIIY Ben-Yoseph, L C Hahn, C L DeFranco, et al.
Pageof 5