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Molecular Genetics and Metabolism
|
October 6, 1998
Deficiency of biotinyl-AMP synthetase activity in fibroblasts of patients with holocarboxylase synthetase deficiency
J Morita, L P Thuy, L Sweetman
European Journal of Biochemistry
|
November 11, 1971
Effects of oxaloacetate and L-glutamate on glyceraldehyde 3-phosphate inhibition of aspartate aminotransferase isozymes as measured by a 2oxoglutarate dehydrogenase coupled assay
J S Nisselbaum, L Sweetman, L Kopelovich
Advances in Enzyme Regulation
|
January 1, 1972
Regulation of aspartate aminotransferase isozymes by glyceraldehyde-3-phosphate
J S Nisselbaum, L Sweetman, L Kopelovich
Neurology
|
March 1, 1975
Short-chain organic acidemia and Reye's syndrome
D A Trauner, W L Nyhan, L Sweetman
Antimicrobial Agents and Chemotherapy
|
December 1, 1978
Simple sensitive microbioassay for adenine arabinoside and hypoxanthine arabinoside in human plasma
Y J Bryson, L Sweetman, J D Connor
The Journal of Pediatrics
|
September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiency
S Packman, L Sweetman, H Baker, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Biotin holocarboxylase synthetase deficiency
L Sweetman, B J Burri, W L Nyhan
American Journal of Human Genetics
|
March 1, 1985
Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency
B J Burri, L Sweetman, W L Nyhan
Journal of Inherited Metabolic Disease
|
January 1, 1985
The role of lipid in the management of methylmalonic acidaemia: administration of linoleic acid does not increase excretion of methylmalonic acid
J A Wolff, L Sweetman, W L Nyhan
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1991
A new immunochemical assay for biotin
L P Thuy, L Sweetman, W L Nyhan
Page
of 18
Search research articles
Search
Showing results (31-40 of 175) with videos related to
Sort By:
Page
of 18
Molecular Genetics and Metabolism
|
October 6, 1998
Deficiency of biotinyl-AMP synthetase activity in fibroblasts of patients with holocarboxylase synthetase deficiency
J Morita, L P Thuy, L Sweetman
European Journal of Biochemistry
|
November 11, 1971
Effects of oxaloacetate and L-glutamate on glyceraldehyde 3-phosphate inhibition of aspartate aminotransferase isozymes as measured by a 2oxoglutarate dehydrogenase coupled assay
J S Nisselbaum, L Sweetman, L Kopelovich
Advances in Enzyme Regulation
|
January 1, 1972
Regulation of aspartate aminotransferase isozymes by glyceraldehyde-3-phosphate
J S Nisselbaum, L Sweetman, L Kopelovich
Neurology
|
March 1, 1975
Short-chain organic acidemia and Reye's syndrome
D A Trauner, W L Nyhan, L Sweetman
Antimicrobial Agents and Chemotherapy
|
December 1, 1978
Simple sensitive microbioassay for adenine arabinoside and hypoxanthine arabinoside in human plasma
Y J Bryson, L Sweetman, J D Connor
The Journal of Pediatrics
|
September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiency
S Packman, L Sweetman, H Baker, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Biotin holocarboxylase synthetase deficiency
L Sweetman, B J Burri, W L Nyhan
American Journal of Human Genetics
|
March 1, 1985
Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency
B J Burri, L Sweetman, W L Nyhan
Journal of Inherited Metabolic Disease
|
January 1, 1985
The role of lipid in the management of methylmalonic acidaemia: administration of linoleic acid does not increase excretion of methylmalonic acid
J A Wolff, L Sweetman, W L Nyhan
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1991
A new immunochemical assay for biotin
L P Thuy, L Sweetman, W L Nyhan
Page
of 18