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Acta Crystallographica. Section D, Biological Crystallography
|
November 1, 1995
Crystallization and preliminary characterization of human recombinant N-acetylgalactosamine-4-sulfatase
S J Ashby, P R Clements, J M Guss, et al.
The Biochemical Journal
|
November 1, 1982
Irreversible inhibition of fatty acid synthase from rat mammary gland with S-(4-bromo-2,3-dioxobutyl)-CoA. Effect on the partial reactions, protection by substrates and stoichiometry studies
P R Clements, R E Barden, P M Ahmad, et al.
The Biochemical Journal
|
June 15, 1991
Further studies on the localization of the reactive lysyl residue of pyruvate carboxylase
A Chapman-Smith, G W Booker, P R Clements, et al.
The Biochemical Journal
|
December 15, 1987
Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values
G J Gibson, G T Saccone, D A Brooks, et al.
Biochimica Et Biophysica Acta
|
September 28, 1998
Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies
S Bunge, P R Clements, S Byers, et al.
Human Mutation
|
February 20, 2004
Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy
L Karageorgos, P Harmatz, J Simon, et al.
American Journal of Human Genetics
|
April 1, 1992
Immunoquantification and enzyme kinetics of alpha-L-iduronidase in cultured fibroblasts from normal controls and mucopolysaccharidosis type I patients
L J Ashton, D A Brooks, P A McCourt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA
P J Wilson, C P Morris, D S Anson, et al.
Human Mutation
|
August 10, 2004
Identification and molecular characterization of alpha-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy
G Yogalingam, X-H Guo, V J Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expression
H S Scott, D S Anson, A M Orsborn, et al.
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of 4
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Showing results (21-30 of 33) with videos related to
Sort By:
Page
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Acta Crystallographica. Section D, Biological Crystallography
|
November 1, 1995
Crystallization and preliminary characterization of human recombinant N-acetylgalactosamine-4-sulfatase
S J Ashby, P R Clements, J M Guss, et al.
The Biochemical Journal
|
November 1, 1982
Irreversible inhibition of fatty acid synthase from rat mammary gland with S-(4-bromo-2,3-dioxobutyl)-CoA. Effect on the partial reactions, protection by substrates and stoichiometry studies
P R Clements, R E Barden, P M Ahmad, et al.
The Biochemical Journal
|
June 15, 1991
Further studies on the localization of the reactive lysyl residue of pyruvate carboxylase
A Chapman-Smith, G W Booker, P R Clements, et al.
The Biochemical Journal
|
December 15, 1987
Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values
G J Gibson, G T Saccone, D A Brooks, et al.
Biochimica Et Biophysica Acta
|
September 28, 1998
Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies
S Bunge, P R Clements, S Byers, et al.
Human Mutation
|
February 20, 2004
Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy
L Karageorgos, P Harmatz, J Simon, et al.
American Journal of Human Genetics
|
April 1, 1992
Immunoquantification and enzyme kinetics of alpha-L-iduronidase in cultured fibroblasts from normal controls and mucopolysaccharidosis type I patients
L J Ashton, D A Brooks, P A McCourt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA
P J Wilson, C P Morris, D S Anson, et al.
Human Mutation
|
August 10, 2004
Identification and molecular characterization of alpha-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy
G Yogalingam, X-H Guo, V J Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expression
H S Scott, D S Anson, A M Orsborn, et al.
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of 4