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G C Tsay

Showing results (1-10 of 15) with videos related to

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Analytical Biochemistry|April 1, 1977
A sensitive spectrophotometric method for detection of L-fucoseG C Tsay, G Dawson
Birth Defects Original Article Series|January 1, 1976
Chemical diagnosis of inborn lysosomal storage disorders involving the eyeG Dawson, G C Tsay
Biochemical and Biophysical Research Communications|April 7, 1975
Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolismG C Tsay, G Dawson
Journal of Neurochemistry|September 1, 1976
Oligosaccharide storage in brains from patients with fucosidosis, GM1-gangliosidosis and GM2-gangliosidosis (Sandhoff's disease)G C Tsay, G Dawson
Advances in Experimental Medicine and Biology|January 1, 1976
FucosidosisG Dawson, G C Tsay
Biochemical and Biophysical Research Communications|June 8, 1973
Structure of the "keratosulfate-like" material in liver from a patient with G M1 -gangliosidosis ( -D-galactosidase deficiency)G C Tsay, G Dawson
Archives of Biochemistry and Biophysics|September 1, 1974
Enzymatic transfer of mannose from guanosine diphosphate mannose to yeast mannan-protein complexesR K Bretthauer, G C Tsay
Infection and Immunity|July 1, 1984
Preparation and characterization of a nontoxic polysaccharide-protein conjugate that induces active immunity and passively protective antibody against Pseudomonas aeruginosa immunotype 1 in miceG C Tsay, M S Collins
The Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R Matalon
The Journal of Pediatrics|June 1, 1974
Excretion of mannose-rich complex carbohydrates by a patient with alpha-mannosidase deficiency (mannosidosis)G C Tsay, G Dawson, R Matalon
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Analytical Biochemistry|April 1, 1977
A sensitive spectrophotometric method for detection of L-fucoseG C Tsay, G Dawson
Birth Defects Original Article Series|January 1, 1976
Chemical diagnosis of inborn lysosomal storage disorders involving the eyeG Dawson, G C Tsay
Biochemical and Biophysical Research Communications|April 7, 1975
Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolismG C Tsay, G Dawson
Journal of Neurochemistry|September 1, 1976
Oligosaccharide storage in brains from patients with fucosidosis, GM1-gangliosidosis and GM2-gangliosidosis (Sandhoff's disease)G C Tsay, G Dawson
Advances in Experimental Medicine and Biology|January 1, 1976
FucosidosisG Dawson, G C Tsay
Biochemical and Biophysical Research Communications|June 8, 1973
Structure of the "keratosulfate-like" material in liver from a patient with G M1 -gangliosidosis ( -D-galactosidase deficiency)G C Tsay, G Dawson
Archives of Biochemistry and Biophysics|September 1, 1974
Enzymatic transfer of mannose from guanosine diphosphate mannose to yeast mannan-protein complexesR K Bretthauer, G C Tsay
Infection and Immunity|July 1, 1984
Preparation and characterization of a nontoxic polysaccharide-protein conjugate that induces active immunity and passively protective antibody against Pseudomonas aeruginosa immunotype 1 in miceG C Tsay, M S Collins
The Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R Matalon
The Journal of Pediatrics|June 1, 1974
Excretion of mannose-rich complex carbohydrates by a patient with alpha-mannosidase deficiency (mannosidosis)G C Tsay, G Dawson, R Matalon
Pageof 2