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Garcia, E., Scanlon, M. and Naranjo, D. (1999) A Marine Snail Neurotoxin Shares with Scorpion Toxins a Convergent Mechanism of Blockade on the Pore of Voltage-gated K Channels. Journal of General Physiology, 114 1: 141-157. doi:10.1085/jgp.114.1.141 79   24 Cited 21 times in Scopus21 0
Reid, R. C., Abbenante, G., March, D. R., Scanlon, M. and Fairlie, D. P. (1997) A novel strategy for the design of potent peptidomimetic inhibitors of proteolytic enzymes: Application to HIV-1 protease.. Abstracts of Papers of The American Chemical Society, 214 177-MEDI. 73   0
Fairlie, D. P., Tyndall, J. D. A., Reid, R. C., Wong, A. K., Abbenante, G., Scanlon, M. J., March, D. R., Bergman, D. A., Chai, C. L. L. and Burkett, B. A. (2000) Conformational selection of inhibitors and substrates by proteolytic enzymes: Implications for drug design and polypeptide processing. Journal of Medicinal Chemistry, 43 7: 1271-1281. doi:10.1021/jm990315t 102   102 Cited 102 times in Scopus102 0
Sokolenko, N., Abbenante, G., Scanlon, M. J., Jones, A., Gahan, L. R., Hanson, G. R. and Fairlie, D. P. (1999) Cyclooligomerization of Thiazole-Containing Tetrapeptides. Symmetrical Macrocycles with up to 76 Amino Acids. Journal of the American Chemical Society, 121 11: 2603-2604. doi:10.1021/ja983354n 64   40 Cited 42 times in Scopus42 0
Meutermans, W., Bourne, G. T., Golding, S., Horton, D., Campitelli, M. R., Craik, D. J., Scanlon, M. J. and Smythe, M. L. (2003) Difficult macrocyclizations: New strategies for synthesizing highly strained cyclic tetrapeptides. Organic Letters, 5 15: 2711-2714. doi:10.1021/ol034907o 82   44 Cited 44 times in Scopus44 0
Heras, B, Shouldice, S. R., Totsika, M, Scanlon, M. J., Schembri, M. A. and Martin, J. L. (2009) DSB proteins and bacterial pathogenicity. Nature Reviews Microbiology, 7 3: 215-225. doi:10.1038/nrmicro2087 63   93 Cited 87 times in Scopus87 0
Hayman, W. A., Toth, I., Flinn, N., Scanlon, M. and Good, M. F. (2002) Enhancing the immunogenicity and modulating the fine epitope recognition of antisera to a helical group A streptococcal peptide vaccine candidate from the M protein using lipid-core peptide technology. Immunology And Cell Biology, 80 2: 178-187. doi:10.1046/j.1440-1711.2002.01067.x 56   28 Cited 29 times in Scopus29 0
Duprez, W., Lakshmanane, P., Kurth, F., Bachu, P., Halili, M., Cooper, M., Scanlon, M., Fairlie, D. P. and Martin, J. L. (2013). Inhibiting Virulence in E. coli: Screening of Peptidomimetics Ttargeting the DsbA Disulfide Bond Formation Machinery. In: Biopolymers. 23rd American Peptide Symposium, Waikoloa Hi, (302-302). Jun 22-27, 2013. 7   0
Craik, D. J. and Scanlon, M. J. (2000). Marine toxins as a starting point for drugs. In Luis M Botana (Ed.), Seafood and Freshwater Toxins Pharmacology, Physiology and Dection (pp. 715-740) New York: Marcel Dekker Inc. 67  
Craik, D. J. and Scanlon, M. J. (2000). Pharmaceutical Applications of NMR. In Webb and GA (Ed.), Annual Reports on NMR Spectroscopy (pp. 115-174) USA: Academic Press. 66  
Rosengren, K. J., Daly, N. L., Scanlon, M. J. and Craik, D. J. (2001) Solution structure of BSTI: A new trypsin inhibitor from skin secretions of Bombina bombina. Biochemistry, 40 15: 4601-4609. doi:10.1021/bi002623v 67   13 Cited 12 times in Scopus12 0
Vivian, J. P., Scoullar, J, Rimmer, K, Bushell, S. R., Beddoe, T, Wilce, M. C. J., Byres, E, Boyle, T. P., Doak, B, Simpson, J. S., Graham, B, Heras, B, Kahler, C. M., Rossjohn, J and Scanlon, M. J. (2009) Structure and Function of the Oxidoreductase DsbA1 from Neisseria meningitidis. Journal of Molecular Biology, 394 5: 931-943. doi:10.1016/j.jmb.2009.09.065 387   13 Cited 13 times in Scopus13 0
Schirra, H. J., Scanlon, M. J., Lee, M. C. S., Anderson, M. A. and Craik, D. J. (2001) The solution structure of C1-T1, a two-domain proteinase inhibitor derived from a circular precursor protein from Nicotiana alata. Journal of Molecular Biology, 306 1: 69-79. doi:10.1006/jmbi.2000.4318 58   15 Cited 16 times in Scopus16 0