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Items: 15

1.

Correction to: Evaluation of cell binding to collagen and gelatin: a study of the effect of 2D and 3D architecture and surface chemistry.

Davidenko N, Schuster CF, Bax DV, Farndale RW, Hamaia S, Best SM, Cameron RE.

J Mater Sci Mater Med. 2018 Mar 21;29(4):39. doi: 10.1007/s10856-018-6047-3.

PMID:
29564650
2.

Cyclic di-adenosine monophosphate (c-di-AMP) is required for osmotic regulation in Staphylococcus aureus but dispensable for viability in anaerobic conditions.

Zeden MS, Schuster CF, Bowman L, Zhong Q, Williams HD, Gründling A.

J Biol Chem. 2018 Mar 2;293(9):3180-3200. doi: 10.1074/jbc.M117.818716. Epub 2018 Jan 11.

3.

Selecting the correct cellular model for assessing of the biological response of collagen-based biomaterials.

Davidenko N, Hamaia S, Bax DV, Malcor JD, Schuster CF, Gullberg D, Farndale RW, Best SM, Cameron RE.

Acta Biomater. 2018 Jan;65:88-101. doi: 10.1016/j.actbio.2017.10.035. Epub 2017 Oct 26.

4.

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.

Bowman L, Zeden MS, Schuster CF, Kaever V, Gründling A.

J Biol Chem. 2016 Dec 30;291(53):26970-26986. doi: 10.1074/jbc.M116.747709. Epub 2016 Nov 10.

5.

Evaluation of cell binding to collagen and gelatin: a study of the effect of 2D and 3D architecture and surface chemistry.

Davidenko N, Schuster CF, Bax DV, Farndale RW, Hamaia S, Best SM, Cameron RE.

J Mater Sci Mater Med. 2016 Oct;27(10):148. doi: 10.1007/s10856-016-5763-9. Epub 2016 Aug 31. Erratum in: J Mater Sci Mater Med. 2018 Mar 21;29(4):39.

6.

The second messenger c-di-AMP inhibits the osmolyte uptake system OpuC in Staphylococcus aureus.

Schuster CF, Bellows LE, Tosi T, Campeotto I, Corrigan RM, Freemont P, Gründling A.

Sci Signal. 2016 Aug 16;9(441):ra81. doi: 10.1126/scisignal.aaf7279.

7.

Toxin-Antitoxin Systems of Staphylococcus aureus.

Schuster CF, Bertram R.

Toxins (Basel). 2016 May 5;8(5). pii: E140. doi: 10.3390/toxins8050140. Review.

8.

Optimisation of UV irradiation as a binding site conserving method for crosslinking collagen-based scaffolds.

Davidenko N, Bax DV, Schuster CF, Farndale RW, Hamaia SW, Best SM, Cameron RE.

J Mater Sci Mater Med. 2016 Jan;27(1):14. doi: 10.1007/s10856-015-5627-8. Epub 2015 Dec 16.

9.

Control of crosslinking for tailoring collagen-based scaffolds stability and mechanics.

Davidenko N, Schuster CF, Bax DV, Raynal N, Farndale RW, Best SM, Cameron RE.

Acta Biomater. 2015 Oct;25:131-42. doi: 10.1016/j.actbio.2015.07.034. Epub 2015 Jul 26.

10.

The MazEF Toxin-Antitoxin System Alters the β-Lactam Susceptibility of Staphylococcus aureus.

Schuster CF, Mechler L, Nolle N, Krismer B, Zelder ME, Götz F, Bertram R.

PLoS One. 2015 May 12;10(5):e0126118. doi: 10.1371/journal.pone.0126118. eCollection 2015.

11.
12.

Post-transcriptional regulation of gene expression in bacterial pathogens by toxin-antitoxin systems.

Bertram R, Schuster CF.

Front Cell Infect Microbiol. 2014 Jan 29;4:6. doi: 10.3389/fcimb.2014.00006. eCollection 2014. Review.

13.

Two paralogous yefM-yoeB loci from Staphylococcus equorum encode functional toxin-antitoxin systems.

Nolle N, Schuster CF, Bertram R.

Microbiology. 2013 Aug;159(Pt 8):1575-85. doi: 10.1099/mic.0.068049-0. Epub 2013 Jul 7.

PMID:
23832005
14.

Toxin-antitoxin systems are ubiquitous and versatile modulators of prokaryotic cell fate.

Schuster CF, Bertram R.

FEMS Microbiol Lett. 2013 Mar;340(2):73-85. doi: 10.1111/1574-6968.12074. Epub 2013 Jan 24. Review.

15.

Characterization of a mazEF toxin-antitoxin homologue from Staphylococcus equorum.

Schuster CF, Park JH, Prax M, Herbig A, Nieselt K, Rosenstein R, Inouye M, Bertram R.

J Bacteriol. 2013 Jan;195(1):115-25. doi: 10.1128/JB.00400-12. Epub 2012 Oct 26.

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