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Ciba Foundation Symposium|January 1, 1992
Why are secondary metabolites biosynthesized? Sophistication in the inhibition of cell wall biosynthesis by vancomycin group antibioticsD H Williams, R A MaplestoneAnalytical Biochemistry|December 10, 1999
Kinetic analysis of antibody-antigen interactions at a supported lipid monolayerM A Cooper, D H WilliamsChemistry & Biology|September 1, 1996
Weak interactions and lessons from crystallizationD H Williams, M S WestwellBiochemistry|October 6, 1992
Why water-soluble, compact, globular proteins have similar specific enthalpies of unfolding at 110 degrees CA J Doig, D H WilliamsControlled Clinical Trials|August 1, 1994
Reporting of assignment methods in clinical trialsD H Williams, C E DavisJournal of the American Chemical Society|June 28, 2001
An enthalpic component in cooperativity: the relationship between enthalpy, entropy, and noncovalent structure in weak associationsC T Calderone, D H WilliamsMinerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|June 15, 2004
Current concepts in urinary tract infectionsD H Williams, A J SchaefferFEBS Letters|November 14, 1994
Specific amino acid substitutions in human collagenase cause decreased autoproteolysis and reveal a requirement for a second zinc atom for catalytic activityD H Williams, E J MurrayJournal of Molecular Biology|January 20, 1991
Is the hydrophobic effect stabilizing or destabilizing in proteins? The contribution of disulphide bonds to protein stabilityA J Doig, D H WilliamsCiba Foundation Symposium|January 1, 1991
The natural design of vancomycin family antibiotics to bind their target peptidesJ P Waltho, D H WilliamsPageof 17