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1. Discovery of a highly potent, selective, orally bioavailable inhibitor of KAT6A/B histone acetyltransferases with efficacy against KAT6A-high ER+ breast cancer

2. Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth

9. Crystal structures of human ENPP1 in apo and bound forms

14. Fragment screening for a protein-protein interaction inhibitor to WDR5

16. 8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase

17. Structure-Based Design and Development of Functionalized Mercaptoguanine Derivatives as Inhibitors of the Folate Biosynthesis Pathway Enzyme 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinase from Staphylococcus aureus

18. Kinetic Characterization of a Panel of High-Affinity Monoclonal Antibodies Targeting Ricin and Recombinant Re-Formatting for Biosensor Applications

25. Selection and affinity maturation of IgNAR variable domains targeting Plasmodium falciparum AMA1

27. Structure-Based Design andDevelopment of FunctionalizedMercaptoguanine Derivatives as Inhibitors of the Folate BiosynthesisPathway Enzyme 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinasefrom Staphylococcus aureus.

29. Utilization of the Streptoalloteichus hindustanusResistance Determinant ShBle as a Protein Framework: Effect of Mutation upon ShBle Dimerization and Interaction of C-Terminal Displayed Peptide Epitopes

30. 8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.

31. Single-chain Fv multimers of the anti-neuraminidase antibody NC10: the residue at position 15 in the V(L) domain of the scFv-0 (V(L)-V(H)) molecule is primarily responsible for formation of a tetramer-trimer equilibrium.

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