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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 31, 1983
HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage disease
P M Strasberg, I Warren, M A Skomorowski, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1982
Evidence for two dissimilar polypeptide chains in the beta 2 subunit of hexosaminidase
D J Mahuran, F Tsui, R A Gravel, et al.
Canadian Medical Association Journal
|
August 3, 1974
Screening for carriers of Tay-Sachs disease: A community project
J A Lowden, S Zuker, A J Wilensky, et al.
Journal of Lipid Research
|
July 1, 1979
Preparation of radiolabeled GM2 and GA2 gangliosides
A Novak, J A Lowden, Y L Gravel, et al.
Experimental Cell Research
|
April 1, 1979
Lectin-mediated uptake of lysosomal hydrolases by genetically deficient human fibroblasts
R L Juliano, M R Moore, J W Callahan, et al.
Biochimica Et Biophysica Acta
|
November 2, 1978
Concanavalin A promotes the uptake of lysosomal hydrolases by human fibroblasts
R L Juliano, M R Moore, J W Callahan, et al.
The Journal of Clinical Investigation
|
April 1, 1983
Characterization of polypeptides serologically and structurally related to hexosaminidase in cultured fibroblasts
F Tsui, D J Mahuran, J A Lowden, et al.
The New England Journal of Medicine
|
February 1, 1973
Prenatal diagnosis of G M1 -gangliosidosis
J A Lowden, E Cutz, P E Conen, et al.
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire
|
March 1, 1985
A statistical comparison of parameter estimation for the Michaelis-Menten kinetics of human placental hexosaminidase
R Tommasini, L Endrenyi, P A Taylor, et al.
Archives of Neurology
|
September 1, 1974
Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase components
J A Lowden, J W Callahan, M G Norman, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 8
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 31, 1983
HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage disease
P M Strasberg, I Warren, M A Skomorowski, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1982
Evidence for two dissimilar polypeptide chains in the beta 2 subunit of hexosaminidase
D J Mahuran, F Tsui, R A Gravel, et al.
Canadian Medical Association Journal
|
August 3, 1974
Screening for carriers of Tay-Sachs disease: A community project
J A Lowden, S Zuker, A J Wilensky, et al.
Journal of Lipid Research
|
July 1, 1979
Preparation of radiolabeled GM2 and GA2 gangliosides
A Novak, J A Lowden, Y L Gravel, et al.
Experimental Cell Research
|
April 1, 1979
Lectin-mediated uptake of lysosomal hydrolases by genetically deficient human fibroblasts
R L Juliano, M R Moore, J W Callahan, et al.
Biochimica Et Biophysica Acta
|
November 2, 1978
Concanavalin A promotes the uptake of lysosomal hydrolases by human fibroblasts
R L Juliano, M R Moore, J W Callahan, et al.
The Journal of Clinical Investigation
|
April 1, 1983
Characterization of polypeptides serologically and structurally related to hexosaminidase in cultured fibroblasts
F Tsui, D J Mahuran, J A Lowden, et al.
The New England Journal of Medicine
|
February 1, 1973
Prenatal diagnosis of G M1 -gangliosidosis
J A Lowden, E Cutz, P E Conen, et al.
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire
|
March 1, 1985
A statistical comparison of parameter estimation for the Michaelis-Menten kinetics of human placental hexosaminidase
R Tommasini, L Endrenyi, P A Taylor, et al.
Archives of Neurology
|
September 1, 1974
Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase components
J A Lowden, J W Callahan, M G Norman, et al.
Page
of 8