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PreviewIssue DateTitleAuthor(s)
2011Defining the substrate specificity determinants recognized by the active site of C-terminal Src kinase-homologous kinase (CHK) and identification of β-synuclein as a potential CHK physiological substrateIa, K.; Jeschke, G.; Deng, Y.; Kamaruddin, M.; Williamson, N.; Scanlon, D.; Culvenor, J.; Hossain, M.; Purcell, A.; Liu, S.; Zhu, H.; Turk, B.; Catimel, B.; Cheng, H.
2011An MD2 hot-spot-mimicking peptide that suppresses TLR4-mediated inflammatory response in vitro and in vivoLiu, L.; Ghosh, N.; Slivka, P.; Fiorini, Z.; Hutchinson, M.; Watkins, L.; Yin, H.
2011Histidine-containing host-defence skin peptides of anurans bind Cu²⁺. An electrospray ionisation mass spectrometry and computational modelling studyWang, T.; Andreazza, H.; Pukala, T.; Sherman, P.; Calabrese, A.; Bowie, J.
2011Molecular modeling: A search for a calpain inhibitor as a new treatment for cataractogenesisStuart, B.; Coxon, J.; Morton, J.; Abell, A.; McDonald, D.; Aitken, S.; Jones, M.; Bickerstaffe, R.
2011Gaucher disease in sheepKarageorgos, L.; Lancaster, M.; Nimmo, J.; Hopwood, J.
2011Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaKhan, K.; Rudkin, A.; Parry, D.; Burdon, K.; McKibbin, M.; Logan, C.; Abdelhamed, Z.; Muecke, J.; Fernandez-Fuentes, N.; Laurie, K.; Shires, M.; Fogarty, R.; Carr, I.; Poulter, J.; Morgan, J.; Mohamed, M.; Jafri, H.; Raashid, Y.; Meng, N.; Piseth, H.; et al.
2011Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicryJoron, M.; Frezal, L.; Jones, R.; Chamberlain, N.; Lee, S.; Haag, C.; Whibley, A.; Becuwe, M.; Baxter, S.; Ferguson, L.; Wilkinson, P.; Salazar, C.; Davidson, C.; Clark, R.; Quail, M.; Beasley, H.; Glithero, R.; Lloyd, C.; Sims, S.; Jones, M.; et al.
2011Species-specific responses of Late Quaternary megafauna to climate and humansCooper, A.
2011A biochemical-biophysical study of hemoglobins from woolly mammoth, asian elephant, and humansYuan, Y.; Shen, T.; Gupta, P.; Ho, N.; Simplaceanu, V.; Tam, T.; Hofreiter, M.; Cooper, A.; Campbell, K.; Ho, C.
2011Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaHahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.