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9. Structural studies of MUC1 core related peptides

13. Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death

18. Novel small molecules that increase the susceptibility of Neisseria gonorrhoeae to cationic antimicrobial peptides by inhibiting lipid A phosphoethanolamine transferase

22. Selective Binding of Small Molecules to Vibrio cholerae DsbA Offers a Starting Point for the Design of Novel Antibacterials

27. Fatty acid binding proteins shape the cellular response to activation of the glucocorticoid receptor

28. Elaboration of a benzofuran scaffold and evaluation of binding affinity and inhibition of Escherichia coli DsbA: A fragment-based drug design approach to novel antivirulence compounds

32. Fragment screening libraries for the identification of protein hot spots and their minimal binding pharmacophoresElectronic supplementary information (ESI) available: Organic solvent and MicroFrag library SMILES, library design details, affinity characterisation, and crystallography statistics. See DOI: https://doi.org/10.1039/d2md00253a

35. Rapid Elaboration of Fragments into Leads by X-ray Crystallographic Screening of Parallel Chemical Libraries (REFiLX)

38. Solution structure of BSTI: a new trypsin inhibitor from skin secretions of Bombina bombina

39. Rapid Elaboration of Fragments into Leads by X-ray Crystallographic Screening of Parallel Chemical Libraries (REFiLX)

42. NMR solution structure of the RNA-binding peptide from human immunodeficiency virus (type 1) Rev

43. Three-dimensional structure of a cysteine-rich repeat from the low-density lipoprotein receptor

44. Three-dimensional structure in solution of the polypeptide cardiac stimulant anthopleurin-A

46. A ligand-induced structural change in fatty acid–binding protein 1 is associated with potentiation of peroxisome proliferator–activated receptor α agonists

47. Identification of the Binding Site of Apical Membrane Antigen 1 (AMA1) Inhibitors Using a Paramagnetic Probe

49. Fragment-based discovery of inhibitors of the bacterial DnaG-SSB interaction

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