45 results on '"Schuster, Christopher F."'
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2. Histidine transport is essential for the growth of Staphylococcus aureus at low pH
3. Histidine and its uptake are essential for the growth of Staphylococcus aureus at low pH
4. Staphylococcus aureusColony Polymerase Chain Reaction
5. Allelic Exchange: Construction of an Unmarked In-Frame Deletion inStaphylococcus aureus
6. Construction of aStaphylococcus aureusGene-Deletion Allelic-Exchange Plasmid by Gibson Assembly and Recovery inEscherichia coli
7. Allelic-Exchange Procedure inStaphylococcus aureus
8. Preparation of ElectrocompetentStaphylococcus aureusCells and Plasmid Transformation
9. Additional file 1 of Recurrent bacteremia with a hypermucoviscous Escherichia coli isolated from a patient with perihilar cholangiocarcinoma: insights from a comprehensive genome-based analysis
10. High‐throughput transposon sequencing highlights the cell wall as an important barrier for osmotic stress in methicillin resistantStaphylococcus aureusand underlines a tailored response to different osmotic stressors
11. Complete Genome Sequences of Two Nosocomiicoccus ampullae Strains and a Growth-Adapted Mutant
12. Ultra-deep long-read sequencing detects IS-mediated gene duplications as a potential trigger to generate arrays of resistance genes and a mechanism to induce novel gene variants such as blaCTX-M-243
13. Status quo of tet regulation in bacteria
14. Mutations in the gdpP gene are a clinically relevant mechanism for β-lactam resistance in meticillin-resistant Staphylococcus aureus lacking mec determinants
15. Status quo of tet regulation in bacteria.
16. Ultra-deep long-read sequencing detects IS-mediated gene duplications as a potential trigger to generate arrays of resistance genes and a mechanism to induce novel gene variants such as blaCTX-M-243.
17. Identification of the main glutamine and glutamate transporters in Staphylococcus aureus and their impact on c‐di‐AMP production
18. Identification of the main glutamine and glutamate transporters inStaphylococcus aureusand their impact on c-di-AMP production
19. High-throughput transposon sequencing highlights the cell wall as an important barrier for osmotic stress in methicillin resistantStaphylococcus aureusand underlines a tailored response to different osmotic stressors
20. Use of the counter selectable marker PheS* for genome engineering in Staphylococcus aureus
21. Inactivation of the Monofunctional Peptidoglycan Glycosyltransferase SgtB Allows Staphylococcus aureus To Survive in the Absence of Lipoteichoic Acid
22. New Insights into the Cyclic di-Adenosine Monophosphate (c-di-AMP) Degradation Pathway and the Requirement of the Cyclic-Dinucleotide for Acid Stress Resistance in Staphylococcus aureus
23. High‐throughput transposon sequencing highlights the cell wall as an important barrier for osmotic stress in methicillin resistant Staphylococcus aureus and underlines a tailored response to different osmotic stressors.
24. Inactivation of the monofunctional peptidoglycan glycosyltransferase SgtB allowsStaphylococcus aureusto survive in the absence of lipoteichoic acid
25. Cyclic di-adenosine monophosphate (c-di-AMP) is required for osmotic regulation in Staphylococcus aureus but dispensable for viability in anaerobic conditions
26. Cyclic-di-adenosine monophosphate (c-di-AMP) is required for osmotic regulation inStaphylococcus aureusbut dispensable for viability in anaerobic conditions
27. New Insights into the Cyclic Di-adenosine Monophosphate (c-di-AMP) Degradation Pathway and the Requirement of the Cyclic Dinucleotide for Acid Stress Resistance in Staphylococcus aureus
28. The second messenger c-di-AMP inhibits the osmolyte uptake system OpuC in Staphylococcus aureus
29. The MazEF Toxin-Antitoxin System Alters the β-Lactam Susceptibility of Staphylococcus aureus
30. Fluorescence Based Primer Extension Technique to Determine Transcriptional Starting Points and Cleavage Sites of RNases In Vivo
31. Post-transcriptional regulation of gene expression in bacterial pathogens by toxin-antitoxin systems
32. Two paralogous yefM-yoeB loci from Staphylococcus equorum encode functional toxin–antitoxin systems
33. Toxin-antitoxin systems are ubiquitous and versatile modulators of prokaryotic cell fate
34. Characterization of a mazEF Toxin-Antitoxin Homologue from Staphylococcus equorum
35. Toxin-Antitoxin Systems of Staphylococcus aureus.
36. Allelic Exchange: Construction of an Unmarked In-Frame Deletion in Staphylococcus aureus
37. Allelic-Exchange Procedure in Staphylococcus aureus
38. Preparation of Electrocompetent Staphylococcus aureusCells and Plasmid Transformation
39. Construction of a Staphylococcus aureusGene-Deletion Allelic-Exchange Plasmid by Gibson Assembly and Recovery in Escherichia coli
40. The genes mgtE and spoVG are involved in zinc tolerance of Staphylococcus aureus.
41. New Insights into the Cyclic Di-adenosineMonophosphate (c-di-AMP) Degradation Pathway and the Requirement of the Cyclic Dinucleotide for Acid Stress Resistance in Staphylococcus aureus.
42. Staphylococcus aureus Colony Polymerase Chain Reaction.
43. Preparation of Electrocompetent Staphylococcus aureus Cells and Plasmid Transformation.
44. Construction of a Staphylococcus aureus Gene-Deletion Allelic-Exchange Plasmid by Gibson Assembly and Recovery in Escherichia coli .
45. Inactivation of the Monofunctional Peptidoglycan Glycosyltransferase SgtB Allows Staphylococcus aureus To Survive in the Absence of Lipoteichoic Acid.
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