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PreviewIssue DateTitleAuthor(s)
2015A second component of the SltA-dependent cation tolerance pathway in Aspergillus nidulansMellado, L.; Calcagno-Pizarelli, A.; Lockington, R.; Cortese, M.; Kelly, J.; Arst, H.; Espeso, E.
2016Predictability of phenotype in relation to common β-lactam resistance mechanisms in Escherichia coli and Klebsiella pneumoniaeAgyekum, A.; Fajardo-Lubián, A.; Ai, X.; Ginn, A.; Zong, Z.; Guo, X.; Turnidge, J.; Partridge, S.; Iredell, J.; Ledeboer, N.
2015Mutational analysis of the major periplasmic loops of Shigella flexneri Wzy; identification of the residues affecting O antigen modal chain length control, and Wzz dependent polymerisation activityNath, P.; Morona, R.
2013ER stress causes rapid loss of intestinal epithelial stemness through activation of the unfolded protein responseHeijmans, J.; van Lidth de Jeude, J.; Koo, B.; Rosekrans, S.; Wielenga, M.; van de Wetering, M.; Ferrante, M.; Lee, A.; Onderwater, J.; Paton, J.; Paton, A.; Mommaas, A.; Kodach, L.; Hardwick, J.; Hommes, D.; Clevers, H.; Muncan, V.; van den Brink, G.
2012Guanylate cyclase-C receptor activation: unexpected biologyBrierley, S.
2011A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaCorbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, S.
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2012BRCA1/2 mutations, fertility and the grandmother effectDa Silva, J.
2011Conservation of plastid sequences in the plant nuclear genome for millions of years facilitates endosymbiotic evolutionRousseau, M.; Ayliffe, M.; Timmis, J.
2011Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearingFasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.

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