| human | Q5 |
| P496 | ORCID iD | 0000-0002-0991-8737 |
| P1053 | ResearcherID | B-1326-2013 |
| P69 | educated at | University of Texas at Dallas | Q1781394 |
| P108 | employer | University of Nebraska–Lincoln | Q1353679 |
| P735 | given name | Greg | Q18857387 |
| Greg | Q18857387 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q37105664 | A dysfunctional tricarboxylic acid cycle enhances fitness of Staphylococcus epidermidis during β-lactam stress |
| Q44294791 | An apoptosis-differentiation program in human polymorphonuclear leukocytes facilitates resolution of inflammation |
| Q37232546 | At the crossroads of bacterial metabolism and virulence factor synthesis in Staphylococci |
| Q37388861 | Catabolite control protein E (CcpE) is a LysR-type transcriptional regulator of tricarboxylic acid cycle activity in Staphylococcus aureus |
| Q91174272 | ClpC affects the intracellular survival capacity of Staphylococcus aureus in non-professional phagocytic cells |
| Q59944531 | Coordinated regulation of transcription by CcpA and the Staphylococcus aureus two-component system HptRS |
| Q34549733 | Cultivation conditions and the diffusion of oxygen into culture media: the rationale for the flask-to-medium ratio in microbiology. |
| Q43230013 | Cytolytic toxin production by Staphylococcus aureus is dependent upon the activity of the protoheme IX farnesyltransferase |
| Q33876899 | Direct targets of CodY in Staphylococcus aureus. |
| Q34514410 | Glycerol-3-phosphate acquisition in spirochetes: distribution and biological activity of glycerophosphodiester phosphodiesterase (GlpQ) among Borrelia species |
| Q86713134 | Growth and preparation of Staphylococcus epidermidis for NMR metabolomic analysis |
| Q37688562 | Identification of low-molecular-weight compounds inhibiting growth of corynebacteria: potential lead compounds for antibiotics |
| Q96353815 | Metabolic changes associated with adaptive resistance to daptomycin in Streptococcus mitis-oralis |
| Q35155421 | NMR analysis of a stress response metabolic signaling network |
| Q44559548 | Quorum-sensing control of biofilm factors in Staphylococcus epidermidis. |
| Q26799806 | Regulating the Intersection of Metabolism and Pathogenesis in Gram-positive Bacteria |
| Q36474392 | Rgg Coordinates Virulence Factor Synthesis and Metabolism inStreptococcus pyogenes |
| Q26991866 | Staphylococcal response to oxidative stress |
| Q46103989 | Staphylococcus aureus ClpC ATPase is a late growth phase effector of metabolism and persistence. |
| Q33855760 | Staphylococcus aureus ClpC is required for stress resistance, aconitase activity, growth recovery, and death |
| Q36540515 | Staphylococcus aureus CodY negatively regulates virulence gene expression. |
| Q35947342 | Staphylococcus aureus biofilm metabolism and the influence of arginine on polysaccharide intercellular adhesin synthesis, biofilm formation, and pathogenesis. |
| Q35746096 | Staphylococcus aureus metabolic adaptations during the transition from a daptomycin susceptibility phenotype to a daptomycin nonsusceptibility phenotype. |
| Q37052310 | Synthesis and deformylation of Staphylococcus aureus delta-toxin are linked to tricarboxylic acid cycle activity. |
| Q34396811 | The catabolite control protein E (CcpE) affects virulence determinant production and pathogenesis of Staphylococcus aureus |
| Q34299123 | Using NMR Metabolomics to Investigate Tricarboxylic Acid Cycle-dependent Signal Transduction in Staphylococcus epidermidis |
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