scholarly article | Q13442814 |
P50 | author | Carl F. Nathan | Q1037710 |
Sabine Ehrt | Q61189875 | ||
Philip Butcher | Q61996782 | ||
Dirk Schnappinger | Q88475126 | ||
Gary K Schoolnik | Q114419730 | ||
P2093 | author name string | Yang Liu | |
Gregory Dolganov | |||
Martin I Voskuil | |||
Irene M Monahan | |||
Joseph A Mangan | |||
Brad Efron | |||
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P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Mycobacterium tuberculosis | Q130971 |
macrophage | Q184204 | ||
P304 | page(s) | 693-704 | |
P577 | publication date | 2003-09-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | Transcriptional Adaptation of Mycobacterium tuberculosis within Macrophages: Insights into the Phagosomal Environment | |
P478 | volume | 198 |
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Q33632198 | Functional genetic diversity among Mycobacterium tuberculosis complex clinical isolates: delineation of conserved core and lineage-specific transcriptomes during intracellular survival |
Q28487106 | Functional genomics reveals extended roles of the Mycobacterium tuberculosis stress response factor sigmaH |
Q38085081 | Functional, biochemical and 3D studies of Mycobacterium tuberculosis protein peptides for an effective anti-tuberculosis vaccine. |
Q92953796 | Functioning of Mycobacterial Heat Shock Repressors Requires the Master Virulence Regulator PhoP |
Q30377994 | Gene expression in HIV-1/Mycobacterium tuberculosis co-infected macrophages is dominated by M. tuberculosis. |
Q34285993 | Gene expression profiling of Mycobacterium avium subsp. paratuberculosis in simulated multi-stress conditions and within THP-1 cells reveals a new kind of interactive intramacrophage behaviour. |
Q80076080 | Gene expression profiling of human macrophages at late time of infection with Mycobacterium tuberculosis |
Q37127810 | Generation of branched-chain fatty acids through lipoate-dependent metabolism facilitates intracellular growth of Listeria monocytogenes. |
Q24656263 | Genome sequence of the Fleming strain of Micrococcus luteus, a simple free-living actinobacterium |
Q28471684 | Genome sequence of the versatile fish pathogen Edwardsiella tarda provides insights into its adaptation to broad host ranges and intracellular niches |
Q34704997 | Genome wide analysis of the complete GlnR nitrogen-response regulon in Mycobacterium smegmatis |
Q64128191 | Genome-Wide Transcriptional Responses of to Antibiotics |
Q36939230 | Genome-Wide Transcriptome Profiling of Mycobacterium smegmatis MC² 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
Q56769021 | Genome-wide expression profiling of the response to linezolid in Mycobacterium tuberculosis |
Q28486898 | Genome-wide requirements for Mycobacterium tuberculosis adaptation and survival in macrophages |
Q38198853 | Genomic insights into tuberculosis |
Q55514836 | GlnR-Mediated Regulation of Short-Chain Fatty Acid Assimilation in Mycobacterium smegmatis. |
Q39859501 | Global adaptation to a lipid environment triggers the dormancy-related phenotype of Mycobacterium tuberculosis. |
Q42095032 | Global effects of inactivation of the pyruvate kinase gene in the Mycobacterium tuberculosis complex |
Q34119457 | Global gene expression profiling of Yersinia pestis replicating inside macrophages reveals the roles of a putative stress-induced operon in regulating type III secretion and intracellular cell division |
Q40037104 | Global transcriptional profile of Mycobacterium tuberculosis during THP-1 human macrophage infection |
Q40717512 | Gluconeogenesis, an essential metabolic pathway for pathogenic Francisella |
Q34006776 | Gluconeogenic carbon flow of tricarboxylic acid cycle intermediates is critical for Mycobacterium tuberculosis to establish and maintain infection |
Q34550747 | Glucose phosphorylation is required for Mycobacterium tuberculosis persistence in mice |
Q55031669 | Glutamate mediated metabolic neutralization mitigates propionate toxicity in intracellular Mycobacterium tuberculosis. |
Q28486803 | Glycine betaine uptake by the ProXVWZ ABC transporter contributes to the ability of Mycobacterium tuberculosis to initiate growth in human macrophages |
Q27674487 | Glycolytic and Non-glycolytic Functions of Mycobacterium tuberculosis Fructose-1,6-bisphosphate Aldolase, an Essential Enzyme Produced by Replicating and Non-replicating Bacilli |
Q40462971 | Growing and Handling of Mycobacterium tuberculosis for Macrophage Infection Assays. |
Q43133893 | HIV-Associated Tuberculosis: Does the Iron-Regulatory Hormone Hepcidin Connect Anemia With Poor Prognosis? |
Q37762509 | Haptoglobin polymorphism and infection |
Q36737557 | Heme oxygenase-1-derived carbon monoxide induces the Mycobacterium tuberculosis dormancy regulon |
Q28661723 | Hemoglobin: a nitric-oxide dioxygenase |
Q26823503 | Heterogeneity in tuberculosis pathology, microenvironments and therapeutic responses |
Q28471626 | High content screening identifies decaprenyl-phosphoribose 2' epimerase as a target for intracellular antimycobacterial inhibitors |
Q34548268 | High throughput phenotypic selection of Mycobacterium tuberculosis mutants with impaired resistance to reactive oxygen species identifies genes important for intracellular growth |
Q37548205 | Histoplasma capsulatum depends on de novo vitamin biosynthesis for intraphagosomal proliferation |
Q38559379 | Histoplasma capsulatum surmounts obstacles to intracellular pathogenesis. |
Q47702665 | Hit Generation in TB Drug Discovery: From Genome to Granuloma |
Q24656253 | Host cell-free growth of the Q fever bacterium Coxiella burnetii |
Q30580895 | Host cell-induced components of the sulfate assimilation pathway are major protective antigens of Mycobacterium tuberculosis |
Q35013546 | Host-Mycobacterium avium subsp. paratuberculosis interactome reveals a novel iron assimilation mechanism linked to nitric oxide stress during early infection |
Q37996091 | How Mycobacterium tuberculosis goes to sleep: the dormancy survival regulator DosR a decade later. |
Q34785626 | Human Mycobacterium tuberculosis CD8 T Cell Antigens/Epitopes Identified by a Proteomic Peptide Library |
Q92059250 | Hybridization-based capture of pathogen mRNA enables paired host-pathogen transcriptional analysis |
Q41203509 | Identification of FadAB Complexes Involved in Fatty Acid β-Oxidation in Streptomyces coelicolor and Construction of a Triacylglycerol Overproducing strain |
Q44446760 | Identification of Mycobacterium tuberculosis genes preferentially expressed during human infection |
Q28486406 | Identification of Rv3230c as the NADPH oxidoreductase of a two-protein DesA3 acyl-CoA desaturase in Mycobacterium tuberculosis H37Rv |
Q57491148 | Identification of Virulence Markers of Mycobacterium abscessus for Intracellular Replication in Phagocytes |
Q52375535 | Identification of a Mycothiol-Dependent Nitroreductase from Mycobacterium tuberculosis. |
Q28487141 | Identification of a copper-binding metallothionein in pathogenic mycobacteria |
Q28487402 | Identification of a diacylglycerol acyltransferase gene involved in accumulation of triacylglycerol in Mycobacterium tuberculosis under stress |
Q28486535 | Identification of an ABC transporter required for iron acquisition and virulence in Mycobacterium tuberculosis |
Q33291875 | Identification of gene targets against dormant phase Mycobacterium tuberculosis infections |
Q30662681 | Identification of idiosyncratic Mycobacterium tuberculosis ribosomal protein subunits with implications in extraribosomal function, persistence, and drug resistance based on transcriptome data |
Q42060168 | Identification of mycobacterial sigma factor binding sites by chromatin immunoprecipitation assays |
Q24651584 | Identification of small RNAs in Mycobacterium tuberculosis |
Q40439252 | Imaging the NADH:NAD(+) Homeostasis for Understanding the Metabolic Response of Mycobacterium to Physiologically Relevant Stresses. |
Q36863134 | Immune activation of the host cell induces drug tolerance in Mycobacterium tuberculosis both in vitro and in vivo. |
Q33627055 | Immune responses in cattle inoculated with Mycobacterium bovis, Mycobacterium tuberculosis, or Mycobacterium kansasii |
Q27334541 | Immune responses to the enduring hypoxic response antigen Rv0188 are preferentially detected in Mycobacterium bovis infected cattle with low pathology |
Q38168398 | Immunogenic potential of latency associated antigens against Mycobacterium tuberculosis |
Q34306108 | Immunogenicity of 60 novel latency-related antigens of Mycobacterium tuberculosis |
Q42913490 | Immunogenicity of eight dormancy regulon-encoded proteins of Mycobacterium tuberculosis in DNA-vaccinated and tuberculosis-infected mice |
Q37301865 | Immunogenicity of novel DosR regulon-encoded candidate antigens of Mycobacterium tuberculosis in three high-burden populations in Africa |
Q33220256 | Immunogenicity of the Mycobacterium tuberculosis PPE55 (Rv3347c) protein during incipient and clinical tuberculosis |
Q91820033 | Immunology of Mycobacterium tuberculosis Infections |
Q57598511 | Impfung gegen Tuberkulose |
Q52893287 | Improved long-term protection against Mycobacterium tuberculosis Beijing/W in mice after intra-dermal inoculation of recombinant BCG expressing latency associated antigens. |
Q34432461 | In silico identification and characterization of the ion transport specificity for P-type ATPases in the Mycobacterium tuberculosis complex |
Q36933802 | In vivo inactivation of the mycobacterial integral membrane stearoyl coenzyme A desaturase DesA3 by a C-terminus-specific degradation process |
Q35744854 | In-Vivo Gene Signatures of Mycobacterium tuberculosis in C3HeB/FeJ Mice |
Q30482598 | Inactivation of lsr2 results in a hypermotile phenotype in Mycobacterium smegmatis |
Q28487140 | Increased sulfate uptake by E. coli overexpressing the SLC26-related SulP protein Rv1739c from Mycobacterium tuberculosis |
Q34037486 | Individual Mycobacterium tuberculosis universal stress protein homologues are dispensable in vitro. |
Q28486396 | Induction of a novel class of diacylglycerol acyltransferases and triacylglycerol accumulation in Mycobacterium tuberculosis as it goes into a dormancy-like state in culture |
Q54998979 | Induction of the acid inducible lipF promoter is reversibly inhibited in pH ranges of pH 4.2-4.0. |
Q34681342 | Infection of human dendritic cells with a Mycobacterium tuberculosis sigE mutant stimulates production of high levels of interleukin-10 but low levels of CXCL10: impact on the T-cell response |
Q36314324 | Inferring biomarkers for Mycobacterium avium subsp. paratuberculosis infection and disease progression in cattle using experimental data |
Q34273782 | Inferring carbon sources from gene expression profiles using metabolic flux models |
Q29615311 | Inhibition of respiration by nitric oxide induces a Mycobacterium tuberculosis dormancy program |
Q42375941 | Inhibition of the DevSR Two-Component System by Overexpression of Mycobacterium tuberculosis PknB in Mycobacterium smegmatis |
Q39118449 | Inhibitory effect of citrinin on lipopolisaccharide-induced nitric oxide production by mouse macrophage cells |
Q27027110 | Innovative Strategies to Identify M. tuberculosis Antigens and Epitopes Using Genome-Wide Analyses |
Q37978561 | Ins and outs of Mycobacterium tuberculosis PPE family in pathogenesis and implications for novel measures against tuberculosis |
Q34344292 | Insight into human alveolar macrophage and M. tuberculosis interactions via metabolic reconstructions |
Q36087019 | Insights into host responses against pathogens from transcriptional profiling. |
Q37647932 | Insights into redox sensing metalloproteins in Mycobacterium tuberculosis |
Q54937099 | Integrated proteomics, genomics, metabolomics approaches reveal oxalic acid as pathogenicity factor in Tilletia indica inciting Karnal bunt disease of wheat. |
Q38620366 | Integrating knowledge of Mycobacterium tuberculosis pathogenesis for the design of better vaccines |
Q38606162 | Integration of Metabolomics and Transcriptomics Reveals a Complex Diet of Mycobacterium tuberculosis during Early Macrophage Infection |
Q22252359 | Interaction of pathogenic mycobacteria with the host immune system |
Q40237990 | Interference of Mycobacterium tuberculosis cell division by Rv2719c, a cell wall hydrolase |
Q35745231 | Interplay between mycobacteria and host signalling pathways |
Q28475985 | Interpreting expression data with metabolic flux models: predicting Mycobacterium tuberculosis mycolic acid production |
Q35835081 | Interpreting the host-pathogen dialogue through microarrays |
Q91877791 | Intracellular Mycobacterium tuberculosis Exploits Multiple Host Nitrogen Sources during Growth in Human Macrophages |
Q37353316 | Intracellular biology and virulence determinants of Francisella tularensis revealed by transcriptional profiling inside macrophages |
Q82599395 | Intranasal IFNgamma extends passive IgA antibody protection of mice against Mycobacterium tuberculosis lung infection |
Q42706554 | Involvement of an alternative oxidase in oxidative stress and mycelium-to-yeast differentiation in Paracoccidioides brasiliensis |
Q39601233 | Iron Acquisition in Mycobacterium avium subsp. paratuberculosis. |
Q30804236 | Iron Homeostasis in Mycobacterium tuberculosis: Mechanistic Insights into Siderophore-Mediated Iron Uptake |
Q33909430 | Iron at the interface of immunity and infection |
Q26860448 | Iron metabolism and the innate immune response to infection |
Q37655750 | Iron sulfur cluster proteins and microbial regulation: implications for understanding tuberculosis |
Q48053573 | Is RORγ a therapeutic target for treating Mycobacterium tuberculosis infections? |
Q35027753 | Isozyme-specific ligands for O-acetylserine sulfhydrylase, a novel antibiotic target |
Q36911402 | Key role for the alternative sigma factor, SigH, in the intracellular life of Mycobacterium avium subsp. paratuberculosis during macrophage stress. |
Q39431238 | Kunkel Lecture: Fundamental immunodeficiency and its correction |
Q35692102 | Label-free Quantitative Proteomics Reveals a Role for the Mycobacterium tuberculosis SecA2 Pathway in Exporting Solute Binding Proteins and Mce Transporters to the Cell Wall |
Q35913675 | Lack of immune responses to Mycobacterium tuberculosis DosR regulon proteins following Mycobacterium bovis BCG vaccination |
Q41682772 | Lack of mycothiol and ergothioneine induces different protective mechanisms in Mycobacterium smegmatis |
Q40108526 | Lactate oxidation facilitates growth of Mycobacterium tuberculosis in human macrophages |
Q42728855 | Latent Tuberculosis: Models, Computational Efforts and the Pathogen's Regulatory Mechanisms during Dormancy |
Q34297816 | Latent tuberculosis infection: myths, models, and molecular mechanisms |
Q38237997 | Latent tuberculosis infection: what we know about its genetic control? |
Q34632057 | Legionella pneumophila adaptation to intracellular life and the host response: clues from genomics and transcriptomics |
Q79243126 | Life on the inside for Mycobacterium tuberculosis |
Q34318215 | Linking the transcriptional profiles and the physiological states of Mycobacterium tuberculosis during an extended intracellular infection |
Q28486753 | Lipid composition and transcriptional response of Mycobacterium tuberculosis grown under iron-limitation in continuous culture: identification of a novel wax ester |
Q53129928 | Lipid-labeling facilitates a novel magnetic isolation procedure to characterize pathogen-containing phagosomes. |
Q28545076 | Lipidomic analysis links mycobactin synthase K to iron uptake and virulence in M. tuberculosis |
Q35709328 | Lipidomic discovery of deoxysiderophores reveals a revised mycobactin biosynthesis pathway in Mycobacterium tuberculosis |
Q35691083 | Lipidomics reveals control of Mycobacterium tuberculosis virulence lipids via metabolic coupling. |
Q24652935 | Liver X receptors contribute to the protective immune response against Mycobacterium tuberculosis in mice |
Q35942760 | Long-range transcriptional control of an operon necessary for virulence-critical ESX-1 secretion in Mycobacterium tuberculosis |
Q37573774 | Loops and networks in control of Francisella tularensis virulence |
Q34903137 | Low concentrations of hydrogen peroxide or nitrite induced of Paracoccidioides brasiliensis cell proliferation in a Ras-dependent manner |
Q53791894 | Lysine succinylation of Mycobacterium tuberculosis isocitrate lyase (ICL) fine-tunes the microbial resistance to antibiotics. |
Q39967017 | M. tuberculosis Gene Expression during Transition to the "Non-Culturable" State |
Q41430032 | M. tuberculosis intramembrane protease Rip1 controls transcription through three anti-sigma factor substrates |
Q38363796 | Macrophage defense mechanisms against intracellular bacteria. |
Q38497801 | Macrophage takeover and the host-bacilli interplay during tuberculosis. |
Q36554384 | Mammalian cell entry genes in Streptomyces may provide clues to the evolution of bacterial virulence |
Q26767547 | Mass Spectrometry Offers Insight into the Role of Ser/Thr/Tyr Phosphorylation in the Mycobacteria |
Q35778015 | Metabolic modeling predicts metabolite changes in Mycobacterium tuberculosis |
Q36238442 | Metabolic plasticity of central carbon metabolism protects mycobacteria. |
Q38244693 | Metabolomics: a window into the adaptive physiology of Mycobacterium tuberculosis |
Q33321061 | Microarray analysis of defined Mycobacterium tuberculosis populations using RNA amplification strategies. |
Q36822548 | Microarray analysis of whole genome expression of intracellular Mycobacterium tuberculosis |
Q80221973 | Microarrays for Mycobacterium tuberculosis |
Q42779053 | Mimicry of the pathogenic mycobacterium vacuole in vitro elicits the bacterial intracellular phenotype, including early-onset macrophage death |
Q64258716 | Modeling Host-Pathogen Interaction to Elucidate the Metabolic Drug Response of Intracellular |
Q92394080 | Modeling of Mycobacterium tuberculosis dormancy in bacterial cultures |
Q58801759 | Modeling the Metabolic State of Upon Infection |
Q39014492 | Molecular basis of mycobacterial survival in macrophages |
Q36163086 | MprA and DosR coregulate a Mycobacterium tuberculosis virulence operon encoding Rv1813c and Rv1812c. |
Q36506250 | MprAB regulates the espA operon in Mycobacterium tuberculosis and modulates ESX-1 function and host cytokine response. |
Q36410732 | Mucosal immunotherapy of tuberculosis: is there a value in passive IgA? |
Q48508433 | Multifaceted remodeling by vitamin C boosts sensitivity of Mycobacterium tuberculosis subpopulations to combination treatment by anti-tubercular drugs. |
Q36782015 | Multifunctional essentiality of succinate metabolism in adaptation to hypoxia in Mycobacterium tuberculosis |
Q21090008 | Multiple M. tuberculosis phenotypes in mouse and guinea pig lung tissue revealed by a dual-staining approach |
Q33849837 | Multiple Substrate Usage of Coxiella burnetii to Feed a Bipartite Metabolic Network |
Q28487200 | Mutations in Mycobacterium tuberculosis Rv0444c, the gene encoding anti-SigK, explain high level expression of MPB70 and MPB83 in Mycobacterium bovis |
Q37998504 | Mycobacteria and the intraphagosomal environment: take it with a pinch of salt(s)! |
Q37642050 | Mycobacterial Dormancy Systems and Host Responses in Tuberculosis |
Q28487139 | Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition |
Q28487369 | Mycobacterial MazG is a novel NTP pyrophosphohydrolase involved in oxidative stress response |
Q35879358 | Mycobacterial bacilli are metabolically active during chronic tuberculosis in murine lungs: insights from genome-wide transcriptional profiling |
Q24644318 | Mycobacterial cytochrome p450 125 (cyp125) catalyzes the terminal hydroxylation of c27 steroids |
Q28083739 | Mycobacterial genes essential for the pathogen's survival in the host |
Q24811622 | Mycobacterial mutants with defective control of phagosomal acidification |
Q22251442 | Mycobacterial outer membranes: in search of proteins |
Q44322701 | Mycobacterium bovis antigens for the differential diagnosis of vaccinated and infected cattle |
Q38051244 | Mycobacterium sulfur metabolism and implications for novel drug targets |
Q24603833 | Mycobacterium tuberculosis CYP125A1, a steroid C27 monooxygenase that detoxifies intracellularly generated cholest-4-en-3-one |
Q41089843 | Mycobacterium tuberculosis Complex Exhibits Lineage-Specific Variations Affecting Protein Ductility and Epitope Recognition |
Q46265783 | Mycobacterium tuberculosis Complex Members Adapted to Wild and Domestic Animals |
Q40140644 | Mycobacterium tuberculosis DosR Regulon Gene Rv2004c Encodes a Novel Antigen with Pro-inflammatory Functions and Potential Diagnostic Application for Detection of Latent Tuberculosis |
Q35247912 | Mycobacterium tuberculosis DosR is required for activity of the PmbtB and PmbtI promoters under hypoxia |
Q50058300 | Mycobacterium tuberculosis H37Rv infection regulates alternative splicing in Macrophages |
Q27728469 | Mycobacterium tuberculosis Malate Synthase Structures with Fragments Reveal a Portal for Substrate/Product Exchange |
Q48124372 | Mycobacterium tuberculosis Molecular Determinants of Infection, Survival Strategies, and Vulnerable Targets |
Q38238758 | Mycobacterium tuberculosis P-type ATPases: possible targets for drug or vaccine development |
Q37089946 | Mycobacterium tuberculosis PE_PGRS17 promotes the death of host cell and cytokines secretion via Erk kinase accompanying with enhanced survival of recombinant Mycobacterium smegmatis |
Q93189840 | Mycobacterium tuberculosis Primary Infection and Dissemination: A Critical Role for Alveolar Epithelial Cells |
Q35662000 | Mycobacterium tuberculosis RNA Expression Patterns in Sputum Bacteria Indicate Secreted Esx Factors Contributing to Growth are Highly Expressed in Active Disease |
Q36524017 | Mycobacterium tuberculosis RecG binds and unwinds model DNA substrates with a preference for Holliday junctions |
Q38297065 | Mycobacterium tuberculosis RecG protein but not RuvAB or RecA protein is efficient at remodeling the stalled replication forks: implications for multiple mechanisms of replication restart in mycobacteria |
Q41117369 | Mycobacterium tuberculosis Rv1265 promotes mycobacterial intracellular survival and alters cytokine profile of the infected macrophage. |
Q35145130 | Mycobacterium tuberculosis Rv3402c enhances mycobacterial survival within macrophages and modulates the host pro-inflammatory cytokines production via NF-kappa B/ERK/p38 signaling |
Q35220629 | Mycobacterium tuberculosis SigM positively regulates Esx secreted protein and nonribosomal peptide synthetase genes and down regulates virulence-associated surface lipid synthesis |
Q38265532 | Mycobacterium tuberculosis WhiB3 Responds to Vacuolar pH-induced Changes in Mycothiol Redox Potential to Modulate Phagosomal Maturation and Virulence |
Q36223232 | Mycobacterium tuberculosis WhiB4 regulates oxidative stress response to modulate survival and dissemination in vivo. |
Q33936614 | Mycobacterium tuberculosis acg gene is required for growth and virulence in vivo |
Q34275913 | Mycobacterium tuberculosis activates the DNA-dependent cytosolic surveillance pathway within macrophages |
Q36938592 | Mycobacterium tuberculosis and the environment within the phagosome |
Q35216595 | Mycobacterium tuberculosis and the intimate discourse of a chronic infection |
Q33758010 | Mycobacterium tuberculosis arrests host cycle at the G1/S transition to establish long term infection |
Q28486570 | Mycobacterium tuberculosis cAMP receptor protein (Rv3676) differs from the Escherichia coli paradigm in its cAMP binding and DNA binding properties and transcription activation properties |
Q40315233 | Mycobacterium tuberculosis cells growing in macrophages are filamentous and deficient in FtsZ rings |
Q38012197 | Mycobacterium tuberculosis cytochrome P450 enzymes: a cohort of novel TB drug targets |
Q28539963 | Mycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infection |
Q28486777 | Mycobacterium tuberculosis expresses methionine sulphoxide reductases A and B that protect from killing by nitrite and hypochlorite |
Q28486955 | Mycobacterium tuberculosis ftsH expression in response to stress and viability |
Q28486837 | Mycobacterium tuberculosis is able to accumulate and utilize cholesterol |
Q24544255 | Mycobacterium tuberculosis isocitrate lyases 1 and 2 are jointly required for in vivo growth and virulence |
Q36018138 | Mycobacterium tuberculosis lacking all mycolic acid cyclopropanation is viable but highly attenuated and hyperinflammatory in mice |
Q35245286 | Mycobacterium tuberculosis metabolism |
Q33613246 | Mycobacterium tuberculosis modulates its cell surface via an oligopeptide permease (Opp) transport system |
Q35221562 | Mycobacterium tuberculosis response regulators, DevR and NarL, interact in vivo and co-regulate gene expression during aerobic nitrate metabolism |
Q38268279 | Mycobacterium tuberculosis response to stress from reactive oxygen and nitrogen species |
Q40642475 | Mycobacterium tuberculosis senses host-derived carbon monoxide during macrophage infection. |
Q35960308 | Mycobacterium tuberculosis thymidylate synthase gene thyX is essential and potentially bifunctional, while thyA deletion confers resistance to p-aminosalicylic acid |
Q28474100 | Mycobacterium tuberculosis transcriptional adaptation, growth arrest and dormancy phenotype development is triggered by vitamin C |
Q28475519 | Mycobacterium tuberculosis universal stress protein Rv2623 regulates bacillary growth by ATP-Binding: requirement for establishing chronic persistent infection |
Q34089860 | Mycobacterium tuberculosis wears what it eats |
Q26852023 | Mycobacterium tuberculosis: success through dormancy |
Q40728049 | Mycobacterium-Host Cell Relationships in Granulomatous Lesions in a Mouse Model of Latent Tuberculous Infection. |
Q52596288 | NTM drug discovery: status, gaps and the way forward. |
Q37445202 | New Genome-Wide Algorithm Identifies Novel In-Vivo Expressed Mycobacterium Tuberculosis Antigens Inducing Human T-Cell Responses with Classical and Unconventional Cytokine Profiles |
Q28388477 | New insights into TB physiology suggest untapped therapeutic opportunities |
Q35095367 | New targets and inhibitors of mycobacterial sulfur metabolism. |
Q28486578 | Nitrate respiration protects hypoxic Mycobacterium tuberculosis against acid- and reactive nitrogen species stresses |
Q42754647 | Nitric oxide detoxification systems enhance survival of Neisseria meningitidis in human macrophages and in nasopharyngeal mucosa |
Q37318269 | Nitrite produced by Mycobacterium tuberculosis in human macrophages in physiologic oxygen impacts bacterial ATP consumption and gene expression |
Q37253014 | Nitrite reductase NirBD is induced and plays an important role during in vitro dormancy of Mycobacterium tuberculosis |
Q28727945 | Non-coding RNA and its potential role in Mycobacterium tuberculosis pathogenesis |
Q35091433 | Non-replicating Mycobacterium tuberculosis elicits a reduced infectivity profile with corresponding modifications to the cell wall and extracellular matrix |
Q36342789 | Nonsteroidal anti-inflammatory drug sensitizes Mycobacterium tuberculosis to endogenous and exogenous antimicrobials |
Q37309256 | Not to wake a sleeping giant: new insights into host-pathogen interactions identify new targets for vaccination against latent Mycobacterium tuberculosis infection |
Q37101494 | Novel Cephalosporins Selectively Active on Nonreplicating Mycobacterium tuberculosis |
Q28543551 | Novel inhibitors of cholesterol degradation in Mycobacterium tuberculosis reveal how the bacterium's metabolism is constrained by the intracellular environment |
Q41128029 | Novel mechanism of gene regulation: the protein Rv1222 of Mycobacterium tuberculosis inhibits transcription by anchoring the RNA polymerase onto DNA. |
Q37808854 | Novel targets in M. tuberculosis: search for new drugs |
Q37685973 | Novel vaccine potential of Rv3131, a DosR regulon-encoded putative nitroreductase, against hyper-virulent Mycobacterium tuberculosis strain K. |
Q44662188 | Nutritional risk factors for tuberculosis among adults in the United States, 1971-1992. |
Q89824505 | On a stake-out: Mycobacterial small RNA identification and regulation |
Q35117372 | Outcome correlation of smear-positivity but culture-negativity during standard anti-tuberculosis treatment in Taiwan |
Q57203102 | Overexpression of DosR in Mycobacterium tuberculosis does not affect aerobic replication in vitro or in murine macrophages |
Q36933343 | Oxadiazoles Have Butyrate-Specific Conditional Activity against Mycobacterium tuberculosis |
Q38672958 | Oxidative Phosphorylation as a Target Space for Tuberculosis: Success, Caution, and Future Directions |
Q36605885 | PE11, a PE/PPE family protein of Mycobacterium tuberculosis is involved in cell wall remodeling and virulence |
Q38919677 | PPAR-α Activation Mediates Innate Host Defense through Induction of TFEB and Lipid Catabolism |
Q93220831 | PPE37 Is Essential for Mycobacterium tuberculosis Heme-Iron Acquisition (HIA), and a Defective PPE37 in Mycobacterium bovis BCG Prevents HIA |
Q36822439 | PPE38 of Mycobacterium marinum triggers the cross-talk of multiple pathways involved in the host response, as revealed by subcellular quantitative proteomics |
Q64068874 | Path-seq identifies an essential mycolate remodeling program for mycobacterial host adaptation |
Q22305694 | Pathogen roid rage: cholesterol utilization by Mycobacterium tuberculosis |
Q50131423 | Pathogenesis of HIV-1 and Mycobacterium tuberculosis co-infection |
Q33511900 | Pathogenetic mechanisms of the intracellular parasite Mycobacterium ulcerans leading to Buruli ulcer |
Q37009017 | Persistent bacterial infections, antibiotic tolerance, and the oxidative stress response |
Q35889600 | Persistent bacterial infections: the interface of the pathogen and the host immune system |
Q40094485 | Persistent mycobacteria evade an antibacterial program mediated by phagolysosomal TLR7/8/MyD88 in human primary macrophages. |
Q33346189 | PhoP: a missing piece in the intricate puzzle of Mycobacterium tuberculosis virulence |
Q28477281 | Phosphodiesterase 4 inhibition reduces innate immunity and improves isoniazid clearance of Mycobacterium tuberculosis in the lungs of infected mice |
Q21089606 | Phosphodiesterase-4 inhibition alters gene expression and improves isoniazid-mediated clearance of Mycobacterium tuberculosis in rabbit lungs |
Q46894574 | Phylogenetic relationships and classification of thiolases and thiolase-like proteins of Mycobacterium tuberculosis and Mycobacterium smegmatis. |
Q37058451 | Physiology of mycobacteria |
Q47362810 | PknG supports mycobacterial adaptation in acidic environment |
Q91044969 | Plasticity of the Mycobacterium tuberculosis respiratory chain and its impact on tuberculosis drug development |
Q35855415 | Porins are required for uptake of phosphates by Mycobacterium smegmatis |
Q34461036 | Potassium availability triggers Mycobacterium tuberculosis transition to, and resuscitation from, non-culturable (dormant) states |
Q47223863 | Potential of DosR and Rpf antigens from Mycobacterium tuberculosis to discriminate between latent and active tuberculosis in a tuberculosis endemic population of Medellin Colombia |
Q34133162 | Potential of novel Mycobacterium tuberculosis infection phase-dependent antigens in the diagnosis of TB disease in a high burden setting |
Q42148676 | Powerful induction of divergent tgs1-Rv3131 genes in Mycobacterium tuberculosis is mediated by DevR interaction with a high-affinity site and an adjacent cryptic low-affinity site |
Q35515497 | Predicting growth conditions from internal metabolic fluxes in an in-silico model of E. coli |
Q27321660 | Preferential use of central metabolism in vivo reveals a nutritional basis for polymicrobial infection |
Q28469010 | Prioritizing genomic drug targets in pathogens: application to Mycobacterium tuberculosis |
Q33798373 | Probing bacterial pathogenesis with genetics, genomics, and chemical biology: past, present, and future approaches |
Q33312964 | Probing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages |
Q35983023 | Profiling persistent tubercule bacilli from patient sputa during therapy predicts early drug efficacy |
Q35956508 | Proline-proline-glutamic acid (PPE) protein Rv1168c of Mycobacterium tuberculosis augments transcription from HIV-1 long terminal repeat promoter. |
Q36399929 | Properties and protective value of the secondary versus primary T helper type 1 response to airborne Mycobacterium tuberculosis infection in mice |
Q45812839 | Protective and survival efficacies of Rv0160c protein in murine model of Mycobacterium tuberculosis |
Q90341634 | Protein kinase B controls Mycobacterium tuberculosis growth via phosphorylation of the transcriptional regulator Lsr2 at threonine 112 |
Q39147396 | Putative roles of a proline-glutamic acid-rich protein (PE3) in intracellular survival and as a candidate for subunit vaccine against Mycobacterium tuberculosis |
Q37000830 | Quantifying Limits on Replication, Death, and Quiescence of Mycobacterium tuberculosis in Mice |
Q34468343 | Quantitative mass spectrometry reveals plasticity of metabolic networks in Mycobacterium smegmatis |
Q42912797 | Quaternary structure and biochemical properties of mycobacterial RNase E/G. |
Q40637730 | RNA Purification from Intracellularly Grown Listeria monocytogenes in Macrophage Cells |
Q35083298 | RNA profiling in host-pathogen interactions |
Q36424616 | RUTI: a new chance to shorten the treatment of latent tuberculosis infection |
Q43245570 | Rapid, Semiquantitative Assay To Discriminate among Compounds with Activity against Replicating or Nonreplicating Mycobacterium tuberculosis. |
Q33700813 | RegA Plays a Key Role in Oxygen-Dependent Establishment of Persistence and in Isocitrate Lyase Activity, a Critical Determinant of In vivo Brucella suis Pathogenicity. |
Q34484770 | Region of Difference 2 Contributes to Virulence ofMycobacterium tuberculosis |
Q26799806 | Regulating the Intersection of Metabolism and Pathogenesis in Gram-positive Bacteria |
Q35217486 | Regulation of Mycobacterium tuberculosis whiB3 in the mouse lung and macrophages. |
Q47319382 | Regulation of the Mycobacterium tuberculosis PE/PPE genes |
Q34303211 | Regulation of the Mycobacterium tuberculosis mce1 operon |
Q28486554 | Regulation of the alpha-crystallin gene acr2 by the MprAB two-component system of Mycobacterium tuberculosis |
Q37081655 | Regulation of whole bacterial pathogen transcription within infected hosts |
Q36741503 | Regulators of bacterial responses to nitric oxide |
Q36646314 | Regulatory and structural differences in the Cu,Zn-superoxide dismutases of Salmonella enterica and their significance for virulence |
Q33855579 | Requirement of the mymA operon for appropriate cell wall ultrastructure and persistence of Mycobacterium tuberculosis in the spleens of guinea pigs. |
Q37197388 | Reversible acetylation regulates acetate and propionate metabolism in Mycobacterium smegmatis |
Q36316419 | Revisiting the role of phospholipases C in virulence and the lifecycle of Mycobacterium tuberculosis |
Q24653292 | Rhodococcus rhodochrous DSM 43269 3-ketosteroid 9alpha-hydroxylase, a two-component iron-sulfur-containing monooxygenase with subtle steroid substrate specificity |
Q35151635 | Role of TNF in the altered interaction of dormant Mycobacterium tuberculosis with host macrophages. |
Q40044447 | Role of stress response sigma factor SigG in Mycobacterium tuberculosis |
Q37099497 | Role of the dosR-dosS two-component regulatory system in Mycobacterium tuberculosis virulence in three animal models. |
Q28487215 | Role of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular growth, and virulence |
Q28486545 | Role of the transcriptional regulator RamB (Rv0465c) in the control of the glyoxylate cycle in Mycobacterium tuberculosis |
Q56984711 | Rv1460, a SufR homologue, is a repressor of the suf operon in Mycobacterium tuberculosis |
Q36768250 | Rv1894c is a novel hypoxia-induced nitronate monooxygenase required for Mycobacterium tuberculosis virulence |
Q28477960 | Rv2607 from Mycobacterium tuberculosis is a pyridoxine 5'-phosphate oxidase with unusual substrate specificity |
Q33842523 | Rv3723/LucA coordinates fatty acid and cholesterol uptake in Mycobacterium tuberculosis |
Q33722881 | S-nitroso proteome of Mycobacterium tuberculosis: Enzymes of intermediary metabolism and antioxidant defense |
Q43030693 | Sabine Ehrt: searching for mycobacterial stress points. Interview by Hema Bashyam |
Q41609686 | Sample preparation of Mycobacterium tuberculosis extracts for nuclear magnetic resonance metabolomic studies |
Q28487057 | Secreted transcription factor controls Mycobacterium tuberculosis virulence |
Q38443780 | Selection of novel TB vaccine candidates and their evaluation as DNA vaccines against aerosol challenge |
Q39038658 | Selective killing of nonreplicating mycobacteria |
Q28477804 | Sequence-based analysis uncovers an abundance of non-coding RNA in the total transcriptome of Mycobacterium tuberculosis |
Q35648489 | Sigma factors and global gene regulation in Mycobacterium tuberculosis |
Q35689125 | Signature-tagged transposon mutagenesis identifies novel Mycobacterium tuberculosis genes involved in the parasitism of human macrophages |
Q31152179 | Significance analysis of microarray for relative quantitation of LC/MS data in proteomics |
Q35063762 | Simultaneous transcriptional profiling of bacteria and their host cells |
Q28487166 | Siroheme- and [Fe4-S4]-dependent NirA from Mycobacterium tuberculosis is a sulfite reductase with a covalent Cys-Tyr bond in the active site |
Q47549354 | Skin microbiota-host interactions. |
Q41728120 | Small heat shock proteins (HSP12, HSP20 and HSP30) play a role in Ustilago maydis pathogenesis |
Q27648016 | Small-Molecule Scaffolds for CYP51 Inhibitors Identified by High-Throughput Screening and Defined by X-Ray Crystallography |
Q27661119 | Solution structure of Rv2377c-founding member of the MbtH-like protein family |
Q35328837 | Spontaneous phthiocerol dimycocerosate-deficient variants of Mycobacterium tuberculosis are susceptible to gamma interferon-mediated immunity. |
Q39017100 | Sputum is a surrogate for bronchoalveolar lavage for monitoring Mycobacterium tuberculosis transcriptional profiles in TB patients |
Q28487315 | Src homology 3-interacting domain of Rv1917c of Mycobacterium tuberculosis induces selective maturation of human dendritic cells by regulating PI3K-MAPK-NF-kappaB signaling and drives Th2 immune responses |
Q38730565 | Stationary phase gene expression of Mycobacterium tuberculosis following a progressive nutrient depletion: a model for persistent organisms? |
Q35865490 | Strain specific transcriptional response in Mycobacterium tuberculosis infected macrophages |
Q33769184 | Strains of the East Asian (W/Beijing) lineage of Mycobacterium tuberculosis are DosS/DosT-DosR two-component regulatory system natural mutants |
Q34033185 | Streptomycin-dependent exhibition of cytokine-inducing activity in streptomycin-dependent Mycobacterium tuberculosis strain 18b. |
Q36514519 | Stress wars: the direct role of host and bacterial molecular chaperones in bacterial infection |
Q37274903 | Strong antibody responses to Mycobacterium tuberculosis PE-PGRS62 protein are associated with latent and active tuberculosis. |
Q39661414 | Structural and functional analysis of the solute-binding protein UspC from Mycobacterium tuberculosis that is specific for amino sugars |
Q27645768 | Structural insights into catalysis and inhibition of O-acetylserine sulfhydrylase from Mycobacterium tuberculosis. Crystal structures of the enzyme alpha-aminoacrylate intermediate and an enzyme-inhibitor complex |
Q57454259 | Structural, functional and biological insights into the role of Mycobacterium tuberculosis VapBC11 toxin-antitoxin system: targeting a tRNase to tackle mycobacterial adaptation |
Q24531451 | Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6 |
Q27681341 | Structure of the Sensor Domain of Mycobacterium tuberculosis PknH Receptor Kinase Reveals a Conserved Binding Cleft |
Q27675581 | Structure-Guided Discovery of Phenyl-diketo Acids as Potent Inhibitors of M. tuberculosis Malate Synthase |
Q21131582 | Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis |
Q39251983 | Subunit Vaccines Consisting of Antigens from Dormant and Replicating Bacteria Show Promising Therapeutic Effect against Mycobacterium Bovis BCG Latent Infection. |
Q24671998 | Sulfite reduction in mycobacteria |
Q37611701 | Superoxide Generation and Its Involvement in the Growth of Mycobacterium smegmatis |
Q28486781 | Surface hydrolysis of sphingomyelin by the outer membrane protein Rv0888 supports replication of Mycobacterium tuberculosis in macrophages |
Q36594623 | Sustained axenic metabolic activity by the obligate intracellular bacterium Coxiella burnetii |
Q35893383 | Synthesis and anti-tubercular activity of N(2)-arylbenzo[g]isoquinoline-5,10-dione-3-iminium bromides |
Q54250514 | System-wide coordinates of higher order functions in host-pathogen environment upon Mycobacterium tuberculosis infection. |
Q37915093 | Systematic review and meta-analysis of antigen detection tests for the diagnosis of tuberculosis |
Q37808939 | Systems biology approaches to understanding mycobacterial survival mechanisms |
Q37184399 | Systems biology of persistent infection: tuberculosis as a case study |
Q35010150 | Systems-based approaches to probing metabolic variation within the Mycobacterium tuberculosis complex |
Q28083600 | TB drug development: immunology at the table |
Q36470057 | TB vaccine strategies--what is needed to solve a complex problem? |
Q37435926 | TB vaccines: current status and future perspectives |
Q39149038 | Targeting Phenotypically Tolerant Mycobacterium tuberculosis |
Q52692190 | Targeting the Proteostasis Network for Mycobacterial Drug Discovery. |
Q38202181 | The BCG replacement vaccine VPM1002: from drawing board to clinical trial |
Q37416335 | The Differential Gene Expression Pattern of Mycobacterium tuberculosis in Response to Capreomycin and PA-824 versus First-Line TB Drugs Reveals Stress- and PE/PPE-Related Drug Targets |
Q42460819 | The DosR dormancy regulator of Mycobacterium tuberculosis stimulates the Na(+)/K (+) and Ca (2+) ATPase activities in plasma membrane vesicles of mycobacteria |
Q37283561 | The DosR regulon of M. tuberculosis and antibacterial tolerance |
Q33848256 | The DosS-DosT/DosR Mycobacterial Sensor System |
Q33603832 | The EXIT Strategy: an Approach for Identifying Bacterial Proteins Exported during Host Infection |
Q39152237 | The LuxR family regulator Rv0195 modulates Mycobacterium tuberculosis dormancy and virulence. |
Q40265746 | The MarR family transcription factor Rv1404 coordinates adaptation of Mycobacterium tuberculosis to acid stress via controlled expression of Rv1405c, a virulence-associated methyltransferase |
Q37594360 | The Minimal Unit of Infection: Mycobacterium tuberculosis in the Macrophage |
Q34042952 | The Mycobacterium avium ssp. paratuberculosis specific mptD gene is required for maintenance of the metabolic homeostasis necessary for full virulence in mouse infections |
Q28487516 | The Mycobacterium tuberculosis DosR regulon assists in metabolic homeostasis and enables rapid recovery from nonrespiring dormancy |
Q28486552 | The Mycobacterium tuberculosis PhoPR two-component system regulates genes essential for virulence and complex lipid biosynthesis |
Q40723997 | The Mycobacterium tuberculosis TrcR response regulator represses transcription of the intracellularly expressed Rv1057 gene, encoding a seven-bladed beta-propeller. |
Q33615471 | The Mycobacterium tuberculosis cytochrome P450 system |
Q37855840 | The Mycobacterium tuberculosis cytochromes P450: physiology, biochemistry & molecular intervention |
Q28655962 | The Mycobacterium tuberculosis regulatory network and hypoxia |
Q36159650 | The Mycobacterium tuberculosis transcriptional landscape under genotoxic stress |
Q35563370 | The Mycobacterium tuberculosis β-oxidation genes echA5 and fadB3 are dispensable for growth in vitro and in vivo |
Q33834816 | The N-terminal domain of Mycobacterium tuberculosis PPE17 (Rv1168c) protein plays a dominant role in inducing antibody responses in active TB patients |
Q27673424 | The Oxidation-sensing Regulator (MosR) Is a New Redox-dependent Transcription Factor in Mycobacterium tuberculosis |
Q91588350 | The P-type ATPase CtpF is a plasma membrane transporter mediating calcium efflux in Mycobacterium tuberculosis cells |
Q37869959 | The PE and PPE proteins of Mycobacterium tuberculosis. |
Q34888988 | The Sculpting of the Mycobacterium tuberculosis Genome by Host Cell-Derived Pressures |
Q42869507 | The TetR‐type transcriptional regulator FasR of Corynebacterium glutamicum controls genes of lipid synthesis during growth on acetate |
Q92826528 | The Varied Role of Efflux Pumps of the MFS Family in the Interplay of Bacteria with Animal and Plant Cells |
Q35759546 | The W-Beijing lineage of Mycobacterium tuberculosis overproduces triglycerides and has the DosR dormancy regulon constitutively upregulated |
Q98564292 | The aceE involves in mycolic acid synthesis and biofilm formation in Mycobacterium smegmatis |
Q48269997 | The antibacterial prodrug activator Rv2466c is a mycothiol-dependent reductase in the oxidative stress response of Mycobacterium tuberculosis |
Q26795478 | The application of tetracyclineregulated gene expression systems in the validation of novel drug targets in Mycobacterium tuberculosis |
Q37679327 | The bacillary and macrophage response to hypoxia in tuberculosis and the consequences for T cell antigen recognition |
Q36256803 | The bacterial and host factors associated with extrapulmonary dissemination of Mycobacterium tuberculosis |
Q28486370 | The carbon starvation-inducible genes Rv2557 and Rv2558 of Mycobacterium tuberculosis are not required for long-term survival under carbon starvation and for virulence in SCID mice |
Q38047152 | The complex architecture of mycobacterial promoters. |
Q34889629 | The conserved hypothetical protein Rv0574c is required for cell wall integrity, stress tolerance, and virulence of Mycobacterium tuberculosis |
Q39199131 | The diverse family of MmpL transporters in mycobacteria: from regulation to antimicrobial developments. |
Q26744038 | The emerging role of gasotransmitters in the pathogenesis of tuberculosis |
Q27302134 | The enduring hypoxic response of Mycobacterium tuberculosis |
Q36088505 | The expanding role of microarrays in the investigation of macrophage responses to pathogens. |
Q28487009 | The extra cytoplasmic function sigma factor sigma(E) is essential for Mycobacterium tuberculosis virulence in mice |
Q81637351 | The genetic portrait of an outbreak strain |
Q61797368 | The genetic requirements of fatty acid import by within macrophages |
Q28486613 | The global responses of Mycobacterium tuberculosis to physiological levels of copper |
Q54545897 | The heat-shock protein ClpB of Francisella tularensis is involved in stress tolerance and is required for multiplication in target organs of infected mice. |
Q38449680 | The influence of reduced oxygen availability on pathogenicity and gene expression in Mycobacterium tuberculosis |
Q37123814 | The intracellular environment of human macrophages that produce nitric oxide promotes growth of mycobacteria. |
Q28486603 | The multifunctional PE_PGRS11 protein from Mycobacterium tuberculosis plays a role in regulating resistance to oxidative stress |
Q28487547 | The oxidative DNA glycosylases of Mycobacterium tuberculosis exhibit different substrate preferences from their Escherichia coli counterparts |
Q33271748 | The phagosome: compartment with a license to kill |
Q64276310 | The prominent alteration in transcriptome and metabolome of Mycobacterium bovis BCG str. Tokyo 172 induced by vitamin B |
Q28482080 | The promoter of Rv0560c is induced by salicylate and structurally-related compounds in Mycobacterium tuberculosis |
Q36954404 | The protonmotive force is required for maintaining ATP homeostasis and viability of hypoxic, nonreplicating Mycobacterium tuberculosis |
Q34496647 | The pupylation pathway and its role in mycobacteria. |
Q28479234 | The regulation of sulfur metabolism in Mycobacterium tuberculosis |
Q42766350 | The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species |
Q92461310 | The role of low molecular weight thiols in Mycobacterium tuberculosis |
Q38373062 | The role of transcriptional regulation in maintaining the availability of mycobacterial adenylate cyclases |
Q37642079 | The sigma factors of Mycobacterium tuberculosis: regulation of the regulators. |
Q29619404 | The spectrum of latent tuberculosis: rethinking the biology and intervention strategies |
Q79888520 | The survival kit of Mycobacterium tuberculosis |
Q37358252 | The temporal expression profile of Mycobacterium tuberculosis infection in mice. |
Q33648717 | The three RelE homologs of Mycobacterium tuberculosis have individual, drug-specific effects on bacterial antibiotic tolerance |
Q36826401 | The transcriptional response of Cryptococcus neoformans to ingestion by Acanthamoeba castellanii and macrophages provides insights into the evolutionary adaptation to the mammalian host. |
Q47215316 | The transcriptional responses of Mycobacterium tuberculosis to inhibitors of metabolism: novel insights into drug mechanisms of action |
Q35664209 | The tuberculosis drug discovery and development pipeline and emerging drug targets |
Q44944734 | The use of microarray analysis to determine the gene expression profiles of Mycobacterium tuberculosis in response to anti-bacterial compounds. |
Q35643173 | The β-propeller gene Rv1057 of Mycobacterium tuberculosis has a complex promoter directly regulated by both the MprAB and TrcRS two-component systems. |
Q38365541 | Thiol-based redox switches in prokaryotes |
Q35609316 | Toll-like receptor 2-dependent extracellular signal-regulated kinase signaling in Mycobacterium tuberculosis-infected macrophages drives anti-inflammatory responses and inhibits Th1 polarization of responding T cells |
Q34657537 | Toll-like receptor-induced arginase 1 in macrophages thwarts effective immunity against intracellular pathogens |
Q40813624 | Towards understanding the biological function of the unusual chaperonin Cpn60.1 (GroEL1) of Mycobacterium tuberculosis |
Q35117081 | Trans-species communication in the Mycobacterium tuberculosis-infected macrophage |
Q58693946 | Transcription factors Rv0081 and Rv3334 connect the early and the enduring hypoxic response of Mycobacterium tuberculosis |
Q37513666 | Transcription regulation by the Mycobacterium tuberculosis alternative sigma factor SigD and its role in virulence |
Q50097352 | Transcriptional Profiling Mycobacterium tuberculosis from Patient Sputa |
Q37199876 | Transcriptional Profiling of Mycobacterium tuberculosis Exposed to In Vitro Lysosomal Stress |
Q35923650 | Transcriptional Profiling of Mycobacterium tuberculosis Replicating in the Human Type II Alveolar Epithelial Cell Line, A549 |
Q37248992 | Transcriptional characterization of the antioxidant response of Mycobacterium tuberculosis in vivo and during adaptation to hypoxia in vitro |
Q38890697 | Transcriptional profile of Mycobacterium tuberculosis replicating in type II alveolar epithelial cells |
Q35154909 | Transcriptional profiling of Mycobacterium tuberculosis replicating ex vivo in blood from HIV- and HIV+ subjects |
Q42730857 | Transcriptional profiling of mycobacterium tuberculosis during infection: lessons learned |
Q33702509 | Transcriptional profiling reveals the expression of novel genes in response to various stimuli in the human dermatophyte Trichophyton rubrum. |
Q42015850 | Transcriptional regulation of fatty acid biosynthesis in mycobacteria. |
Q36304467 | Transcriptome analysis of mycobacteria in sputum samples of pulmonary tuberculosis patients |
Q42321297 | Transcriptome-Level Signatures in Gene Expression and Gene Expression Variability during Bacterial Adaptive Evolution |
Q42618762 | Transcriptomic analysis identifies growth rate modulation as a component of the adaptation of mycobacteria to survival inside the macrophage. |
Q27023437 | Translating genomics research into control of tuberculosis: lessons learned and future prospects |
Q28486356 | Trehalose-recycling ABC transporter LpqY-SugA-SugB-SugC is essential for virulence of Mycobacterium tuberculosis |
Q37714865 | Triosephosphate isomerase is dispensable in vitro yet essential for Mycobacterium tuberculosis to establish infection |
Q37226285 | Truncated hemoglobin, HbN, is post-translationally modified in Mycobacterium tuberculosis and modulates host-pathogen interactions during intracellular infection. |
Q35988766 | Tuberculosis - metabolism and respiration in the absence of growth |
Q34974987 | Tuberculosis chemotherapy: the influence of bacillary stress and damage response pathways on drug efficacy |
Q38219605 | Tuberculosis drug discovery and emerging targets |
Q37126922 | Tuberculosis genes expressed during persistence and reactivation in the resistant rabbit model |
Q36238724 | Tuberculosis: from genome to vaccine |
Q49446442 | Ultrastructural Analysis of Cell Envelope and Accumulation of Lipid Inclusions in Clinical Mycobacterium tuberculosis Isolates from Sputum, Oxidative Stress, and Iron Deficiency |
Q38639041 | Understanding HIV-Mycobacteria synergism through comparative proteomics of intra-phagosomal mycobacteria during mono- and HIV co-infection |
Q28731026 | Understanding communication signals during mycobacterial latency through predicted genome-wide protein interactions and boolean modeling |
Q36238015 | Understanding latent tuberculosis: the key to improved diagnostic and novel treatment strategies |
Q40259283 | Unique Regulation of the DosR Regulon in the Beijing Lineage of Mycobacterium tuberculosis. |
Q33523042 | Unique flexibility in energy metabolism allows mycobacteria to combat starvation and hypoxia |
Q34334118 | Unique transcriptome signature of Mycobacterium tuberculosis in pulmonary tuberculosis. |
Q59548522 | Unveiling the pathogen behind the vacuole |
Q35805849 | Uptake of sulfate but not phosphate by Mycobacterium tuberculosis is slower than that for Mycobacterium smegmatis |
Q36211121 | Urease activity represents an alternative pathway for Mycobacterium tuberculosis nitrogen metabolism |
Q33459176 | Using structural knowledge in the protein data bank to inform the search for potential host-microbe protein interactions in sequence space: application to Mycobacterium tuberculosis |
Q26992233 | Vaccines against tuberculosis: where are we and where do we need to go? |
Q28487497 | Variant tricarboxylic acid cycle in Mycobacterium tuberculosis: identification of alpha-ketoglutarate decarboxylase |
Q49791987 | Verapamil targets membrane energetics in Mycobacterium tuberculosis |
Q33899751 | Virulence and immunity orchestrated by the global gene regulator sigL in Mycobacterium avium subsp. paratuberculosis |
Q38053069 | Virulence factors of the Mycobacterium tuberculosis complex |
Q41907887 | Virulence of Mycobacterium tuberculosis depends on lipoamide dehydrogenase, a member of three multienzyme complexes |
Q94545324 | Vitamin B and Vitamin C Affect DNA Methylation and Amino Acid Metabolism in Mycobacterium bovis BCG |
Q49623828 | When Dicty Met Myco, a (Not So) Romantic Story about One Amoeba and Its Intracellular Pathogen |
Q31156691 | Whole genome identification of Mycobacterium tuberculosis vaccine candidates by comprehensive data mining and bioinformatic analyses |
Q50062010 | Why Might Bacterial Pathogens Have Small Genomes? |
Q37302014 | igr Genes and Mycobacterium tuberculosis cholesterol metabolism |
Q33489282 | mosR, a novel transcriptional regulator of hypoxia and virulence in Mycobacterium tuberculosis |
Q33788098 | responses of mycobacterium tuberculosis to growth in the mouse lung |
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