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P R Clements

Showing results (21-30 of 33) with videos related to

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Acta Crystallographica. Section D, Biological Crystallography|November 1, 1995
Crystallization and preliminary characterization of human recombinant N-acetylgalactosamine-4-sulfataseS 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 studiesP 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 carboxylaseA 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 valuesG 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 studiesS 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 therapyL 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 patientsL 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 DNAP 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 therapyG 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 expressionH S Scott, D S Anson, A M Orsborn, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Acta Crystallographica. Section D, Biological Crystallography|November 1, 1995
Crystallization and preliminary characterization of human recombinant N-acetylgalactosamine-4-sulfataseS 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 studiesP 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 carboxylaseA 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 valuesG 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 studiesS 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 therapyL 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 patientsL 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 DNAP 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 therapyG 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 expressionH S Scott, D S Anson, A M Orsborn, et al.
Pageof 4