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PreviewIssue DateTitleAuthor(s)
2009Identification of sequence elements regulating promoter activity and replication of a monopartite begomovirus-associated DNA β satelliteEini Gandomani, O.; Akbar Behjatnia, S.; Dogra, S.; Dry, I.; Randles, J.; Rezaian, M.
2009Thioredoxin reductase is essential for protection of neisseria gonorrhoeae against killing by nitric oxide and for bacterial growth during interaction with cervical epithelial cellsPotter, A.; Kidd, S.; Edwards, J.; Falsetta, M.; Apicella, M.; Jennings, M.; McEwan, A.
2009Prevalence and molecular characterization of Cryptosporidium spp. in dairy calves from 11 farms in Prince Edward Island, CanadaCoklin, T.; Uehlinger, F.; Farber, J.; Barkema, H.; O'Handley, R.; Dixon, B.
2009Carbapenem Resistance among Pseudomonas aeruginosa Strains from India: Evidence for Nationwide Endemicity of Multiple Metallo-beta-Lactamase Clones (VIM-2,-5,-6, and-11 and the Newly Characterized VIM-18)Castanheira, M.; Bell, J.; Turnidge, J.; Mathai, D.; Jones, R.
2009Cloning and characterization of an intracellular esterase from the wine-associated lactic acid bacterium Oenococcus oeniSumby, K.; Matthews, A.; Grbin, P.; Jiranek, V.
2009Rapid detection of ERG11 gene mutations in clinical Candida albicans isolates with reduced susceptibility to fluconazole by rolling circle amplification and DNA sequencingWang, H.; Kong, F.; Sorrell, T.; Wang, B.; McNicholas, P.; Pantarat, N.; Ellis, D.; Xiao, M.; Widmer, F.; Chen, S.
2009SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeSpurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.
2009Instability of Plastid DNA in the Nuclear GenomeSheppard, A.; Timmis, J.; Copenhaver, G.P.
2009A Novel Bocavirus Associated with Acute Gastroenteritis in Australian ChildrenArthur, J.; Higgins, G.; Davidson, G.; Givney, R.; Ratcliff, R.; Münger, K.
2009Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune PhenotypeHubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.

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