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Items: 1 to 20 of 29

1.
Cell-density-dependent killing of Myxococcus xanthus by autocide AMV.
I Gelvan, M Varon, E Rosenberg
J Bacteriol. 1987 Feb; 169(2): 844–848. doi: 10.1128/jb.169.2.844-848.1987
PMCID:
PMC211856
SummaryPage BrowsePDF–986K
2.
Myxococcus xanthus autocide AMI.
M Varon, A Tietz, E Rosenberg
J Bacteriol. 1986 Jul; 167(1): 356–361. doi: 10.1128/jb.167.1.356-361.1986
PMCID:
PMC212883
SummaryPage BrowsePDF–1.2M
3.
Role of autocide AMI in development of Myxococcus xanthus.
A Rosenbluh, E Rosenberg
J Bacteriol. 1990 Aug; 172(8): 4307–4314. doi: 10.1128/jb.172.8.4307-4314.1990
PMCID:
PMC213255
SummaryPage BrowsePDF–1.4M
4.
Autocide AMI rescues development in dsg mutants of Myxococcus xanthus.
A Rosenbluh, E Rosenberg
J Bacteriol. 1989 Mar; 171(3): 1513–1518. doi: 10.1128/jb.171.3.1513-1518.1989
PMCID:
PMC209774
SummaryPage BrowsePDF–1.3M
5.
Effects of glucosamine on lysis, glycerol formation, and sporulation in Myxococcus xanthus.
C Mueller, M Dworkin
J Bacteriol. 1991 Nov; 173(22): 7164–7175. doi: 10.1128/jb.173.22.7164-7175.1991
PMCID:
PMC209222
SummaryPage BrowsePDF–2.8M
6.
Autocides produced by Myxococcus xanthus.
M Varon, S Cohen, E Rosenberg
J Bacteriol. 1984 Dec; 160(3): 1146–1150. doi: 10.1128/jb.160.3.1146-1150.1984
PMCID:
PMC215832
SummaryPage BrowsePDF–919K
7.
Propionyl coenzyme A carboxylase is required for development of Myxococcus xanthus.
Y Kimura, R Sato, K Mimura, M Sato
J Bacteriol. 1997 Nov; 179(22): 7098–7102. doi: 10.1128/jb.179.22.7098-7102.1997
PMCID:
PMC179652
SummaryPDF–787K
8.
Role of a modified ovitrap in the control of Aedes aegypti in Houston, Texas, USA
Min-Lee Cheng, Beng-Chuan Ho, R. E. Bartnett, N. Goodwin
Bull World Health Organ. 1982; 60(2): 291–296.
PMCID:
PMC2535964
SummaryPage BrowsePDF–839K
9.
The Part-time Prosector: A Personal Experience of Medico-Legal Autopsies
H. E. Emson
Can Med Assoc J. 1971 Jan 9; 104(1): 37–43.
PMCID:
PMC1930830
SummaryPage BrowsePDF–1.5M
10.
Recent advances in the social and developmental biology of the myxobacteria.
M Dworkin
Microbiol Rev. 1996 Mar; 60(1): 70–102. doi: 10.1128/mr.60.1.70-102.1996
PMCID:
PMC239419
SummaryPDF–4.7M
11.
Nutrient-Regulated Proteolysis of MrpC Halts Expression of Genes Important for Commitment to Sporulation during Myxococcus xanthus Development
Ramya Rajagopalan, Lee Kroos
J Bacteriol. 2014 Aug; 196(15): 2736–2747. doi: 10.1128/JB.01692-14
PMCID:
PMC4135671
ArticlePDF–1.6M
12.
Myxobacteria: Moving, Killing, Feeding, and Surviving Together
José Muñoz-Dorado, Francisco J. Marcos-Torres, Elena García-Bravo, Aurelio Moraleda-Muñoz, Juana Pérez
Front Microbiol. 2016; 7: 781. Published online 2016 May 26. doi: 10.3389/fmicb.2016.00781
PMCID:
PMC4880591
ArticlePDF–1.0M
13.
The control of death and lysis in staphylococcal biofilms: a coordination of physiological signals
Marat R. Sadykov, Kenneth W. Bayles
Curr Opin Microbiol. Author manuscript; available in PMC 2013 Apr 1.
Published in final edited form as: Curr Opin Microbiol. 2012 Apr; 15(2): 211–215. Published online 2012 Jan 3. doi: 10.1016/j.mib.2011.12.010
PMCID:
PMC3320683
ArticlePDF–418K
14.
Characterization of the major autolysin (AtlC) of Staphylococcus carnosus
Maximilian Merz, Carolin J. Schiffer, Andreas Klingl, Matthias A. Ehrmann
BMC Microbiol. 2024; 24: 77. Published online 2024 Mar 8. doi: 10.1186/s12866-024-03231-6
PMCID:
PMC10921637
ArticlePDF–1.8M
15.
Social and developmental biology of the myxobacteria.
L J Shimkets
Microbiol Rev. 1990 Dec; 54(4): 473–501. doi: 10.1128/mr.54.4.473-501.1990
PMCID:
PMC372790
SummaryPage BrowsePDF–9.6M
16.
Résumés des articles
Bull World Health Organ. 1964; 31(4): 595–603.
PMCID:
PMC2555040
SummaryPage BrowsePDF–1.3M
17.
Cell-density-dependent lysis and sporulation of Myxococcus xanthus in agarose microbeads.
A Rosenbluh, R Nir, E Sahar, E Rosenberg
J Bacteriol. 1989 Sep; 171(9): 4923–4929. doi: 10.1128/jb.171.9.4923-4929.1989
PMCID:
PMC210298
SummaryPage BrowsePDF–2.7M
18.
Developmental Aggregation of Myxococcus xanthus Requires frgA, an frz-Related Gene
Kyungyun Cho, Anke Treuner-Lange, Kathleen A. O'Connor, David R. Zusman
J Bacteriol. 2000 Dec; 182(23): 6614–6621. doi: 10.1128/jb.182.23.6614-6621.2000
PMCID:
PMC111401
ArticlePDF–2.4M
19.
Cell Death in Pseudomonas aeruginosa Biofilm Development
Jeremy S. Webb, Lyndal S. Thompson, Sally James, Tim Charlton, Tim Tolker-Nielsen, Birgit Koch, Michael Givskov, Staffan Kjelleberg
J Bacteriol. 2003 Aug; 185(15): 4585–4592. doi: 10.1128/JB.185.15.4585-4592.2003
PMCID:
PMC165772
ArticlePDF–2.1M
20.
Defining futile life-prolonging treatments through Neo-Socratic Dialogue
Kuniko Aizawa, Atsushi Asai, Seiji Bito
BMC Med Ethics. 2013; 14: 51. Published online 2013 Dec 9. doi: 10.1186/1472-6939-14-51
PMCID:
PMC3883517
ArticlePDF–261K

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