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Infection and Immunity|January 6, 2016
Genomic Comparison of Two O111:H- Enterohemorrhagic Escherichia coli Isolates from a Historic Hemolytic-Uremic Syndrome Outbreak in AustraliaLauren J McAllister, Stephen J Bent, Nicola K Petty, et al.
NPJ Vaccines|November 6, 2018
A recombinant conjugated pneumococcal vaccine that protects against murine infections with a similar efficacy to Prevnar-13Mark Reglinski, Giuseppe Ercoli, Charlie Plumptre, et al.
American Journal of Epidemiology|November 1, 1996
Association of transient ischemic attack/stroke symptoms assessed by standardized questionnaire and algorithm with cerebrovascular risk factors and carotid artery wall thickness. The ARIC Study, 1987-1989L E Chambless, E Shahar, A R Sharrett, et al.
Frontiers in Immunology|January 9, 2019
Long Interleukin-22 Binding Protein Isoform-1 Is an Intracellular Activator of the Unfolded Protein ResponsePaloma Gómez-Fernández, Andoni Urtasun, Adrienne W Paton, et al.
Toxins|August 26, 2021
Combined Action of Shiga Toxin Type 2 and Subtilase Cytotoxin in the Pathogenesis of Hemolytic Uremic SyndromeRomina S Álvarez, Fernando D Gómez, Elsa Zotta, et al.
Infection and Immunity|January 13, 2016
The Variable Region of Pneumococcal Pathogenicity Island 1 Is Responsible for Unusually High Virulence of a Serotype 1 IsolateRichard M Harvey, Claudia Trappetti, Layla K Mahdi, et al.
BMC Biology|November 7, 2020
Modelling the Wolbachia incompatible insect technique: strategies for effective mosquito population eliminationD E Pagendam, B J Trewin, N Snoad, et al.
Scientific Reports|August 21, 2015
ZnuA and zinc homeostasis in Pseudomonas aeruginosaVictoria G Pederick, Bart A Eijkelkamp, Stephanie L Begg, et al.
Clinical Science (London, England : 1979)|February 3, 2016
Intranasal vaccination with γ-irradiated Streptococcus pneumoniae whole-cell vaccine provides serotype-independent protection mediated by B-cells and innate IL-17 responsesRachelle Babb, Austen Chen, Timothy R Hirst, et al.
The Journal of Biological Chemistry|February 15, 1992
Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common geneD Schnabel, M Schröder, W Fürst, et al.
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