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Biochemical and Biophysical Research Communications|August 31, 1992
Selective and potent inhibition of different hepatic UDP-glucuronosyltransferase activities by omega,omega,omega-triphenylalcohols and UDP derivativesM Said, D Noort, J Magdalou, et al.
Bioorganic & Medicinal Chemistry|October 26, 1999
Synthesis of heparin-like antithrombotics having perphosphorylated thrombin binding domainsR C Buijsman, J E Basten, C M Dreef-Tromp, et al.
Biochemical Pharmacology|September 29, 2000
Inhibitors of prenylation of Ras and other G-proteins and their application as therapeuticsL H Cohen, E Pieterman, R E van Leeuwen, et al.
Journal of Biomolecular Structure & Dynamics|April 1, 1986
On loop folding in nucleic acid hairpin-type structuresC A Haasnoot, C W Hilbers, G A van der Marel, et al.
European Journal of Biochemistry|March 10, 1990
Inhibition of UDP-glucuronosyltransferase activity by possible transition-state analogues in rat-liver microsomesD Noort, M W Coughtrie, B Burchell, et al.
Bioorganic & Medicinal Chemistry Letters|August 18, 1999
Design and synthesis of a novel synthetic NAPAP-penta-saccharide conjugate displaying a dual antithrombotic actionR C Buijsman, J E Basten, T G van Dinther, et al.
Gene|January 1, 1986
A dot-blot screening procedure for mutated ras oncogenes using synthetic oligodeoxynucleotidesM Verlaan-de Vries, M E Bogaard, H van den Elst, et al.
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