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1 Department of Chemistry and Chemical Biology, Northeastern University, Boston, Massachusetts, U.S.A. 2 Barnett Institute of Chemical and Biological Analysis, Northeastern University, Boston, Massachusetts, U.S.A (1)
Barnett Institute of Chemical and Biological Analysis, Department of Chemistry and Chemical Biology, Northeastern University (1)
Barnett Institute of Chemical and Biological Analysis, Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Ave., Boston, Massachusetts 02115, United States (1)
Dame Kate Campbell Fellow Department of Surgery| Melbourne Medical School Department of Anatomy and Physiology| School of Biomedical Sciences Faculty of Medicine, Dentistry and Health Sciences Medical Building (#181), Grattan Street The University of Melbourne, Victoria 3010 Australia P: +61 3 9035 5464 E: apebay@unimelb.edu.au W: https://medicine.unimelb.edu.au/school-structure/surgery W: https://biomedicalsciences.unimelb.edu.au/departments/anatomy-and-physiology (1)
Department of Chemistry and Chemical Biology, Barnett Institute of Chemical & Biological Analysis, Northeastern University, Boston, MA, United States (1)
Departments of Bioengineering, Biology, Chemistry, and Chemical Biology, Single Cell Proteomics Center, and Barnett Institute, Northeastern University (1)
Institute of Microbiology, The Czech Academy of Sciences, Třeboň, Czech Republic (1)
Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, L69 3BX, United Kingdom (1)
Max-Delbrück-Centre for Molecular Medicine in the Helmholtz Association (1)
Max-Planck-Institute for Biology of Ageing Department of Mitochondrial Proteostasis Joseph-Stelzmann-Str. 9b (1)
Netherlands Cancer Institute, Amsterdam, Netherlands. (1)
Oncode Institute, Hubrecht Institute-KNAW & University Medical Center Utrecht, Uppsalalaan 8, Utrecht, 3584 CT, The Netherlands (1)
School of Clinical Medicine, Ningxia Medical University, Yinchuan, Ningxia Hui Autonomous Region, China, 750004. Ningxia Human Stem Cell Institute, General Hospital of Ningxia Medical University, Yinchuan, Ningxia Hui Autonomous Region, China, 750004. (1)
University of Melbourne, Melbourne, Australia (1)
Wellcome Trust/ MRC Cambridge Stem Cell Institute & Department of Haematology, Univeristy of Cambridge, Cambridge, UK. (1)

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Expression data from wildtype Sinorhizobium meliloti Rm1021 and an hfq mutant

The RNA-binding protein Hfq is a global regulator, which controls diverse cellular processes in bacteria. To begin understanding the role of Hfq in the Sinorhizobium meliloti-Medicago truncatula nitrogen-fixing symbiosis, we defined free-living and symbiotic phenotypes of an hfq mutant. Over 500 tra...

ORGANISM(S): Sinorhizobium meliloti

2010-06-01 | E-GEOD-19346 | biostudies-arrayexpress

Dual RpoH sigma factors in Sinorhizobium meliloti

Sinorhizobium meliloti can live as a soil saprophyte, and can engage in a nitrogen fixing symbiosis with plant roots. To succeed in such diverse environments, the bacteria must continually adjust gene expression. Transcriptional plasticity in eubacteria is often mediated by alternative sigma facto...

ORGANISM(S): Sinorhizobium meliloti

2012-10-02 | E-GEOD-36186 | biostudies-arrayexpress

The Sinorhizobium meliloti SyrM regulon: effects on global gene expression are mediated by syrA and nodD3 (SyrA)

We characterized transcriptomes of a strain overexpressing syrA. Our work shows that the syrA transcriptome shares similar gene expression changes to the syrM and nodD3 transcriptomes and that nodD3 and syrA may be the only targets directly activated by SyrM. We propose that most of the gene expre...

ORGANISM(S): Sinorhizobium meliloti

2015-03-31 | E-GEOD-61524 | biostudies-arrayexpress

The Sinorhizobium meliloti SyrM regulon: effects on global gene expression are mediated by syrA and nodD3 (SyrM)

We characterized transcriptomes of a strain overexpressing syrM. Our work shows that the syrM transcriptome shares similar gene expression changes to the syrA and nodD3 transcriptomes and that nodD3 and syrA may be the only targets directly activated by SyrM. We propose that most of the gene expre...

ORGANISM(S): Sinorhizobium meliloti

2015-03-31 | E-GEOD-61525 | biostudies-arrayexpress

Nontargeted analysis of DNA adducts by mass-tag MS: reaction of p-benzoquinone with DNA.

Not available

S-EPMC3527073 | biostudies-literature

The Sinorhizobium meliloti SyrM regulon: effects on global gene expression are mediated by syrA and nodD3

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

ORGANISM(S): Sinorhizobium meliloti

2015-03-31 | E-GEOD-61526 | biostudies-arrayexpress

Identification of RpoE2 target genes in Sinorhizobium meliloti

Sinorhizobium meliloti lives as a soil saprophyte, and engages in a nitrogen fixing symbiosis with plant roots. To succeed in such diverse environments, the bacteria must continually adjust gene expression. Transcriptional plasticity in eubacteria is often mediated by alternative sigma factors int...

ORGANISM(S): Sinorhizobium meliloti

2013-07-22 | E-GEOD-40391 | biostudies-arrayexpress

The Conserved Polarity Factor PodJ1 Impacts Multiple Cell Envelope-Associated Functions in Sinorhizobium meliloti

Although diminutive in size, bacteria possess highly diverse and spatially confined cellular structures. Two related alpha-proteobacteria, Sinorhizobium meliloti and Caulobacter crescentus, serve as models for investigating the genetic basis of morphologic variations. S. meliloti, a symbiont of le...

ORGANISM(S): Sinorhizobium meliloti

2012-08-09 | E-GEOD-31325 | biostudies-arrayexpress

Genetic determinants of P wave duration and PR segment.

Not available

S-EPMC4141024 | biostudies-literature

Analytic P-value calculation for the higher criticism test in finite d problems.

Not available

S-EPMC4350786 | biostudies-literature