Pages that link to "Q33716960"
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The following pages link to Differential expression of iron-, carbon-, and oxygen-responsive mycobacterial genes in the lungs of chronically infected mice and tuberculosis patients (Q33716960):
Displayed 50 items.
- A multi-level multi-scale approach to study essential genes in Mycobacterium tuberculosis (Q21202770) (← links)
- Pathogen roid rage: cholesterol utilization by Mycobacterium tuberculosis (Q22305694) (← links)
- Mycobacterium tuberculosis isocitrate lyases 1 and 2 are jointly required for in vivo growth and virulence (Q24544255) (← links)
- Dissecting transcription regulatory pathways through a new bacterial one-hybrid reporter system (Q24654994) (← links)
- Controlling gene expression in mycobacteria with anhydrotetracycline and Tet repressor (Q24802513) (← links)
- The enduring hypoxic response of Mycobacterium tuberculosis (Q27302134) (← links)
- Glycolytic and Non-glycolytic Functions of Mycobacterium tuberculosis Fructose-1,6-bisphosphate Aldolase, an Essential Enzyme Produced by Replicating and Non-replicating Bacilli (Q27674487) (← links)
- Structure-Guided Discovery of Phenyl-diketo Acids as Potent Inhibitors of M. tuberculosis Malate Synthase (Q27675581) (← links)
- Bisubstrate Adenylation Inhibitors of Biotin Protein Ligase from Mycobacterium tuberculosis (Q27675807) (← links)
- Mycobacterial genes essential for the pathogen's survival in the host (Q28083739) (← links)
- New insights into TB physiology suggest untapped therapeutic opportunities (Q28388477) (← links)
- Cytological and transcript analyses reveal fat and lazy persister-like bacilli in tuberculous sputum (Q28472502) (← links)
- A novel in vitro multiple-stress dormancy model for Mycobacterium tuberculosis generates a lipid-loaded, drug-tolerant, dormant pathogen (Q28475648) (← links)
- Portrait of a pathogen: the Mycobacterium tuberculosis proteome in vivo (Q28476108) (← links)
- Hypoxia induces an immunodominant target of tuberculosis specific T cells absent from common BCG vaccines (Q28476626) (← links)
- DosT and DevS are oxygen-switched kinases in Mycobacterium tuberculosis (Q28486387) (← links)
- Identification of an ABC transporter required for iron acquisition and virulence in Mycobacterium tuberculosis (Q28486535) (← links)
- Role of the transcriptional regulator RamB (Rv0465c) in the control of the glyoxylate cycle in Mycobacterium tuberculosis (Q28486545) (← links)
- A partner for the resuscitation-promoting factors of Mycobacterium tuberculosis (Q28486559) (← links)
- Regulation of central metabolism genes of Mycobacterium tuberculosis by parallel feed-forward loops controlled by sigma factor E (σ(E)) (Q28486675) (← links)
- Cyclic AMP intoxication of macrophages by a Mycobacterium tuberculosis adenylate cyclase (Q28487194) (← links)
- Role of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular growth, and virulence (Q28487215) (← links)
- A novel role of the PrpR as a transcription factor involved in the regulation of methylcitrate pathway in Mycobacterium tuberculosis (Q28487434) (← links)
- Dihydrolipoamide acyltransferase is critical for Mycobacterium tuberculosis pathogenesis (Q28487554) (← links)
- The spectrum of latent tuberculosis: rethinking the biology and intervention strategies (Q29619404) (← links)
- A philosophy of anti-infectives as a guide in the search for new drugs for tuberculosis. (Q30371769) (← links)
- Metabolic Perspectives on Persistence (Q30398195) (← links)
- Delayed bactericidal response of Mycobacterium tuberculosis to bedaquiline involves remodelling of bacterial metabolism. (Q30573771) (← links)
- Host cell-induced components of the sulfate assimilation pathway are major protective antigens of Mycobacterium tuberculosis (Q30580895) (← links)
- Iron Homeostasis in Mycobacterium tuberculosis: Mechanistic Insights into Siderophore-Mediated Iron Uptake (Q30804236) (← links)
- ICAT-based comparative proteomic analysis of non-replicating persistent Mycobacterium tuberculosis (Q33230269) (← links)
- Brucella suis urease encoded by ure1 but not ure2 is necessary for intestinal infection of BALB/c mice (Q33288192) (← links)
- Transcriptional analysis of Mycobacterium fortuitum cultures upon hydrogen peroxide treatment using the novel standard rrnA-P1. (Q33345023) (← links)
- Replication dynamics of Mycobacterium tuberculosis in chronically infected mice (Q33557117) (← links)
- New Insights in to the Intrinsic and Acquired Drug Resistance Mechanisms in Mycobacteria (Q33600161) (← links)
- Sputum Mycobacterium tuberculosis mRNA as a marker of bacteriologic clearance in response to antituberculosis therapy (Q33614197) (← links)
- S-nitroso proteome of Mycobacterium tuberculosis: Enzymes of intermediary metabolism and antioxidant defense (Q33722881) (← links)
- Escherichia coli global gene expression in urine from women with urinary tract infection (Q33750030) (← links)
- Development and analysis of an in vivo-compatible metabolic network of Mycobacterium tuberculosis (Q33752240) (← links)
- responses of mycobacterium tuberculosis to growth in the mouse lung (Q33788098) (← links)
- Probing bacterial pathogenesis with genetics, genomics, and chemical biology: past, present, and future approaches (Q33798373) (← links)
- Glucose 6-phosphate accumulation in mycobacteria: implications for a novel F420-dependent anti-oxidant defense system (Q33911251) (← links)
- A high-throughput screening fluorescence polarization assay for fatty acid adenylating enzymes in Mycobacterium tuberculosis (Q33965669) (← links)
- Gluconeogenic carbon flow of tricarboxylic acid cycle intermediates is critical for Mycobacterium tuberculosis to establish and maintain infection (Q34006776) (← links)
- The Mycobacterium avium ssp. paratuberculosis specific mptD gene is required for maintenance of the metabolic homeostasis necessary for full virulence in mouse infections (Q34042952) (← links)
- Function of the cytochrome bc1-aa3 branch of the respiratory network in mycobacteria and network adaptation occurring in response to its disruption (Q34048408) (← links)
- LipC (Rv0220) is an immunogenic cell surface esterase of Mycobacterium tuberculosis. (Q34061944) (← links)
- Slow growth of Mycobacterium tuberculosis at acidic pH is regulated by phoPR and host-associated carbon sources (Q34255665) (← links)
- Inferring carbon sources from gene expression profiles using metabolic flux models (Q34273782) (← links)
- Linking the transcriptional profiles and the physiological states of Mycobacterium tuberculosis during an extended intracellular infection (Q34318215) (← links)