review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1462-5822.2009.01335.X |
P8608 | Fatcat ID | release_ox2a5kxgzbh5rgj3xgvllff3x4 |
P932 | PMC publication ID | 3170014 |
P698 | PubMed publication ID | 19438516 |
P5875 | ResearchGate publication ID | 24423771 |
P50 | author | Sabine Ehrt | Q61189875 |
Dirk Schnappinger | Q88475126 | ||
P2860 | cites work | Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence | Q22122411 |
Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens | Q24630289 | ||
Biosynthesis and functions of mycothiol, the unique protective thiol of Actinobacteria | Q24646505 | ||
A membrane protein preserves intrabacterial pH in intraphagosomal Mycobacterium tuberculosis | Q24650149 | ||
Comparative roles of free fatty acids with reactive nitrogen intermediates and reactive oxygen intermediates in expression of the anti-microbial activity of macrophages against Mycobacterium tuberculosis | Q74129598 | ||
Cytokine activation leads to acidification and increases maturation of Mycobacterium avium-containing phagosomes in murine macrophages | Q74506194 | ||
Comparison of the roles of reactive oxygen and nitrogen intermediates in the host response to Mycobacterium tuberculosis using transgenic mice | Q77344847 | ||
Methionine residues as endogenous antioxidants in proteins | Q24658367 | ||
A conserved mechanism for sulfonucleotide reduction | Q24811125 | ||
Metabolic enzymes of mycobacteria linked to antioxidant defense by a thioredoxin-like protein | Q27637390 | ||
The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology | Q27860991 | ||
The curious characteristics of pyrazinamide: a review | Q28191713 | ||
Transcriptional regulation of multi-drug tolerance and antibiotic-induced responses by the histone-like protein Lsr2 in M. tuberculosis | Q28469237 | ||
Role of Mycobacterium tuberculosis copper-zinc superoxide dismutase | Q28486437 | ||
Iron-cofactored superoxide dismutase inhibits host responses to Mycobacterium tuberculosis | Q28486531 | ||
Peroxynitrite reductase activity of bacterial peroxiredoxins | Q28486648 | ||
Mycobacterium tuberculosis expresses methionine sulphoxide reductases A and B that protect from killing by nitrite and hypochlorite | Q28486777 | ||
A genetic screen for Mycobacterium tuberculosis mutants defective for phagosome maturation arrest identifies components of the ESX-1 secretion system | Q28486783 | ||
pH-dependent pore-forming activity of OmpATb from Mycobacterium tuberculosis and characterization of the channel by peptidic dissection | Q28486819 | ||
Mycobacterium tuberculosis appears to lack alpha-ketoglutarate dehydrogenase and encodes pyruvate dehydrogenase in widely separated genes | Q28486842 | ||
Identification and subcellular localization of a novel Cu,Zn superoxide dismutase of Mycobacterium tuberculosis | Q28486918 | ||
SecA2 functions in the secretion of superoxide dismutase A and in the virulence of Mycobacterium tuberculosis | Q28487244 | ||
The functions of OmpATb, a pore-forming protein of Mycobacterium tuberculosis | Q28487254 | ||
A mycothiol synthase mutant of Mycobacterium tuberculosis has an altered thiol-disulfide content and limited tolerance to stress | Q28487293 | ||
Cu,Zn superoxide dismutase of Mycobacterium tuberculosis contributes to survival in activated macrophages that are generating an oxidative burst | Q28487322 | ||
Peptide methionine sulfoxide reductase from Escherichia coli and Mycobacterium tuberculosis protects bacteria against oxidative damage from reactive nitrogen intermediates | Q28487325 | ||
Mycothiol biosynthesis is essential for ethionamide susceptibility in Mycobacterium tuberculosis | Q28487401 | ||
The proteasome of Mycobacterium tuberculosis is required for resistance to nitric oxide | Q28487442 | ||
Isolation of Mycobacterium tuberculosis mutants defective in the arrest of phagosome maturation | Q28487528 | ||
Dihydrolipoamide acyltransferase is critical for Mycobacterium tuberculosis pathogenesis | Q28487554 | ||
The SecA2 secretion factor of Mycobacterium tuberculosis promotes growth in macrophages and inhibits the host immune response | Q28487596 | ||
The multifunctional histone-like protein Lsr2 protects mycobacteria against reactive oxygen intermediates | Q28487623 | ||
Transient loss of resistance to pulmonary tuberculosis in p47(phox-/-) mice | Q28593510 | ||
In vivo gene silencing identifies the Mycobacterium tuberculosis proteasome as essential for the bacteria to persist in mice | Q28909142 | ||
Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide | Q29547245 | ||
Genetic requirements for mycobacterial survival during infection | Q29547599 | ||
Lack of acidification in Mycobacterium phagosomes produced by exclusion of the vesicular proton-ATPase | Q29617355 | ||
The bacA gene of Escherichia coli encodes an undecaprenyl pyrophosphate phosphatase activity | Q31060474 | ||
Response of cultured macrophages to Mycobacterium tuberculosis, with observations on fusion of lysosomes with phagosomes | Q31154479 | ||
Methionine sulfoxide reductase A (MsrA) deficiency affects the survival of Mycobacterium smegmatis within macrophages | Q33203022 | ||
When protons attack: microbial strategies of acid adaptation | Q33632480 | ||
Multiple methionine sulfoxide reductase genes in Staphylococcus aureus: expression of activity and roles in tolerance of oxidative stress | Q33972924 | ||
The enzymology and biochemistry of methionine sulfoxide reductases | Q33984676 | ||
Superoxide dismutase-deficient mutants of Helicobacter pylori are hypersensitive to oxidative stress and defective in host colonization | Q34008070 | ||
DnaE2 polymerase contributes to in vivo survival and the emergence of drug resistance in Mycobacterium tuberculosis | Q34191816 | ||
Immune Control of Tuberculosis by IFN-γ-Inducible LRG-47 | Q34272123 | ||
Peptide methionine sulfoxide reductase: structure, mechanism of action, and biological function | Q34497879 | ||
Genetic dissection of immunity to mycobacteria: the human model | Q34542276 | ||
The MgtC virulence factor of Salmonella enterica serovar Typhimurium activates Na(+),K(+)-ATPase | Q34976659 | ||
Surviving the acid test: responses of gram-positive bacteria to low pH. | Q35215950 | ||
Interplay between mycobacteria and host signalling pathways | Q35745231 | ||
Lysosomal killing of Mycobacterium mediated by ubiquitin-derived peptides is enhanced by autophagy | Q35749637 | ||
Escherichia coli acid resistance: tales of an amateur acidophile | Q35923268 | ||
Virulent but not avirulent Mycobacterium tuberculosis can evade the growth inhibitory action of a T helper 1-dependent, nitric oxide Synthase 2-independent defense in mice | Q36371162 | ||
Virulent Salmonella typhimurium has two periplasmic Cu, Zn-superoxide dismutases | Q36398159 | ||
Self-compartmentalized bacterial proteases and pathogenesis | Q36455856 | ||
The many faces of glutathione in bacteria | Q36505576 | ||
Mycobacterial truncated hemoglobins: from genes to functions | Q36833081 | ||
Acid-susceptible mutants of Mycobacterium tuberculosis share hypersusceptibility to cell wall and oxidative stress and to the host environment | Q37051339 | ||
Conversion of NO2 to NO by reduced coenzyme F420 protects mycobacteria from nitrosative damage | Q37159082 | ||
A new twist on an old pathway--accessory Sec [corrected] systems | Q37187834 | ||
Mycobacterial manipulation of vacuolar sorting | Q37265579 | ||
Selective killing of nonreplicating mycobacteria | Q39038658 | ||
Virulence and Resistance to Superoxide, Low pH and Hydrogen Peroxide among Strains of Mycobacterium tuberculosis | Q39182715 | ||
Rational live oral carrier vaccine design by mutating virulence-associated genes of Yersinia enterocolitica | Q39512451 | ||
Magnesium and the role of MgtC in growth of Salmonella typhimurium. | Q39572347 | ||
Regulation of cytoplasmic pH in bacteria | Q39840875 | ||
Variation in Resistance of Mycobacterium paratuberculosis to Acid Environments as a Function of Culture Medium | Q40171903 | ||
Effects of cytokines on mycobacterial phagosome maturation | Q41043022 | ||
Mycobacterium avium resists exposure to the acidic conditions of the stomach | Q41710897 | ||
A parallel intraphagosomal survival strategy shared by mycobacterium tuberculosis and Salmonella enterica | Q41729653 | ||
Role for nucleotide excision repair in virulence of Mycobacterium tuberculosis | Q41946149 | ||
Cytosolic phospholipase A2 enzymes are not required by mouse bone marrow-derived macrophages for the control of Mycobacterium tuberculosis in vitro | Q42016478 | ||
Role of Pre-A motif in nitric oxide scavenging by truncated hemoglobin, HbN, of Mycobacterium tuberculosis. | Q43126200 | ||
Role of KatG catalase-peroxidase in mycobacterial pathogenesis: countering the phagocyte oxidative burst | Q43597705 | ||
The mshA gene encoding the glycosyltransferase of mycothiol biosynthesis is essential in Mycobacterium tuberculosis Erdman | Q44878839 | ||
Methionine sulphoxide reductase is an important antioxidant enzyme in the gastric pathogen Helicobacter pylori | Q45074875 | ||
5'-Adenosinephosphosulphate reductase (CysH) protects Mycobacterium tuberculosis against free radicals during chronic infection phase in mice. | Q46037070 | ||
Proteome analysis of Streptomyces coelicolor mutants affected in the proteasome system reveals changes in stress-responsive proteins. | Q51009947 | ||
BCG-osis and tuberculosis in a child with chronic granulomatous disease | Q56940502 | ||
Mycobacterium tuberculosis Invasion of Macrophages: Linking Bacterial Gene Expression to Environmental Cues | Q60343829 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1170-1178 | |
P577 | publication date | 2009-05-06 | |
P1433 | published in | Cellular Microbiology | Q1921948 |
P1476 | title | Mycobacterial survival strategies in the phagosome: defence against host stresses | |
P478 | volume | 11 |
Q98566962 | A Fluorogenic Trehalose Probe for Tracking Phagocytosed Mycobacterium tuberculosis |
Q27657658 | A Mycobacterial Cyclic AMP Phosphodiesterase That Moonlights as a Modifier of Cell Wall Permeability |
Q47112934 | A Novel TetR-Like Transcriptional Regulator Is Induced in Acid-Nitrosative Stress and Controls Expression of an Efflux Pump in Mycobacteria |
Q42552716 | A Role for Sigma Factor σ(E) in Corynebacterium pseudotuberculosis Resistance to Nitric Oxide/Peroxide Stress |
Q36595025 | A novel F(420) -dependent anti-oxidant mechanism protects Mycobacterium tuberculosis against oxidative stress and bactericidal agents |
Q34059004 | A specific polymorphism in Mycobacterium tuberculosis H37Rv causes differential ESAT-6 expression and identifies WhiB6 as a novel ESX-1 component |
Q40986049 | AhpC of the mycobacterial antioxidant defense system and its interaction with its reducing partner Thioredoxin-C. |
Q89966117 | Alveolar Macrophage Chromatin Is Modified to Orchestrate Host Response to Mycobacterium bovis Infection |
Q39171381 | Amino acid capture and utilization within the Mycobacterium tuberculosis phagosome |
Q49849006 | Antimycobacterial effect of IFNG (interferon gamma)-induced autophagy is dependent on the HMOX1 (heme oxygenase 1)-mediated increase in the intracellular calcium levels and modulation of PPP3/calcineurin-TFEB (transcription factor EB) axis. |
Q57179042 | Antituberculous drugs modulate bacterial phagolysosome avoidance and autophagy in Mycobacterium tuberculosis-infected macrophages |
Q33573490 | Apurinic/apyrimidinic endonucleases of Mycobacterium tuberculosis protect against DNA damage but are dispensable for the growth of the pathogen in guinea pigs |
Q91890852 | Autophagy-activating strategies to promote innate defense against mycobacteria |
Q37901961 | Base excision and nucleotide excision repair pathways in mycobacteria |
Q39797576 | Biochemical properties of MutT2 proteins from Mycobacterium tuberculosis and M. smegmatis and their contrasting antimutator roles in Escherichia coli |
Q27014743 | Biology of IL-27 and its role in the host immunity against Mycobacterium tuberculosis |
Q54652832 | Bystander inhibition of dendritic cell differentiation by Mycobacterium tuberculosis-induced IL-10. |
Q38911752 | C-type lectin receptors in tuberculosis: what we know |
Q43599511 | CCL20 is overexpressed in Mycobacterium tuberculosis-infected monocytes and inhibits the production of reactive oxygen species (ROS). |
Q35890491 | Calcium and Superoxide-Mediated Pathways Converge to Induce Nitric Oxide-Dependent Apoptosis in Mycobacterium fortuitum-Infected Fish Macrophages |
Q36927203 | Cell-Envelope Remodeling as a Determinant of Phenotypic Antibacterial Tolerance in Mycobacterium tuberculosis |
Q53124028 | Changes in activity of free radical oxidation processes in the early stages of BCG granulomatosis. |
Q27700391 | Chemical probing suggests redox-regulation of the carbonic anhydrase activity of mycobacterial Rv1284 |
Q35213214 | ClpR protein-like regulator specifically recognizes RecA protein-independent promoter motif and broadly regulates expression of DNA damage-inducible genes in mycobacteria |
Q34454941 | Comparative functional genomics and the bovine macrophage response to strains of the mycobacterium genus |
Q97519324 | Conditional DnaB Protein Splicing Is Reversibly Inhibited by Zinc in Mycobacteria |
Q33654036 | Contrasting persistence strategies in Salmonella and Mycobacterium |
Q89113667 | Cyclic nucleotide signaling in Mycobacterium tuberculosis: an expanding repertoire |
Q37451149 | Differential roles for the Co(2+) /Ni(2+) transporting ATPases, CtpD and CtpJ, in Mycobacterium tuberculosis virulence. |
Q37716173 | Disruption of immune regulation by microbial pathogens and resulting chronic inflammation. |
Q89208544 | Drug permeation and metabolism in Mycobacterium tuberculosis: Prioritising local exposure as essential criterion in new TB drug development |
Q39360723 | ESX-1-mediated translocation to the cytosol controls virulence of mycobacteria |
Q37566056 | Effects of conserved residues and naturally occurring mutations on Mycobacterium tuberculosis RecG helicase activity. |
Q37739076 | Endogenous and Exogenous KdpF Peptide Increases Susceptibility of Mycobacterium bovis BCG to Nitrosative Stress and Reduces Intramacrophage Replication |
Q35611656 | Endoplasmic reticulum stress pathway-mediated apoptosis in macrophages contributes to the survival of Mycobacterium tuberculosis |
Q46241400 | Enhancement of the antimycobacterial activity of macrophages by ajoene. |
Q91841958 | Evaluation of in silico designed inhibitors targeting MelF (Rv1936) against Mycobacterium marinum within macrophages |
Q34312082 | Exposure to a cutinase-like serine esterase triggers rapid lysis of multiple mycobacterial species |
Q28486644 | Expression of the ompATb operon accelerates ammonia secretion and adaptation of Mycobacterium tuberculosis to acidic environments |
Q64128191 | Genome-Wide Transcriptional Responses of to Antibiotics |
Q34550747 | Glucose phosphorylation is required for Mycobacterium tuberculosis persistence in mice |
Q49417693 | Harnessing the mTOR Pathway for Tuberculosis Treatment |
Q34548268 | High throughput phenotypic selection of Mycobacterium tuberculosis mutants with impaired resistance to reactive oxygen species identifies genes important for intracellular growth |
Q38168037 | Host-directed therapeutics for tuberculosis: can we harness the host? |
Q55022151 | Host-pathogen redox dynamics modulate Mycobacterium tuberculosis pathogenesis. |
Q40159927 | IFNγ-producing CD4+ T lymphocytes: the double-edged swords in tuberculosis |
Q37549335 | Identification of genes preferentially expressed by highly virulent piscine Streptococcus agalactiae upon interaction with macrophages |
Q89983441 | Identification of serum biomarkers for active pulmonary tuberculosis using a targeted metabolomics approach |
Q34132379 | Identifying co-targets to fight drug resistance based on a random walk model |
Q91820033 | Immunology of Mycobacterium tuberculosis Infections |
Q38202063 | Immunomagnetic isolation of pathogen-containing phagosomes and apoptotic blebs from primary phagocytes |
Q36018335 | Important role for Mycobacterium tuberculosis UvrD1 in pathogenesis and persistence apart from its function in nucleotide excision repair. |
Q39325554 | Interaction of Corynebacterium pseudotuberculosis with ovine cells in vitro. |
Q35378010 | InvA protein is a Nudix hydrolase required for infection by pathogenic Leptospira in cell lines and animals |
Q90093039 | Isoniazid and host immune system interactions: A proposal for a novel comprehensive mode of action |
Q35946350 | Keap1 regulates inflammatory signaling in Mycobacterium avium-infected human macrophages |
Q37400207 | KefB inhibits phagosomal acidification but its role is unrelated to M. tuberculosis survival in host. |
Q40062766 | LAG-3 potentiates the survival of Mycobacterium tuberculosis in host phagocytes by modulating mitochondrial signaling in an in-vitro granuloma model |
Q34891768 | Label-free proteomic analysis to confirm the predicted proteome of Corynebacterium pseudotuberculosis under nitrosative stress mediated by nitric oxide |
Q42728855 | Latent Tuberculosis: Models, Computational Efforts and the Pathogen's Regulatory Mechanisms during Dormancy |
Q35588375 | Lipid metabolism and Type VII secretion systems dominate the genome scale virulence profile of Mycobacterium tuberculosis in human dendritic cells |
Q33999220 | Macrophage control of phagocytosed mycobacteria is increased by factors secreted by alveolar epithelial cells through nitric oxide independent mechanisms |
Q38363796 | Macrophage defense mechanisms against intracellular bacteria. |
Q102054047 | Macrophage metabolic reprogramming during chronic lung disease |
Q38009240 | Macrophage-related diseases of the gut: a pathologist's perspective |
Q54228837 | Metabolic principles of persistence and pathogenicity in Mycobacterium tuberculosis. |
Q37687656 | Methylcitrate cycle defines the bactericidal essentiality of isocitrate lyase for survival of Mycobacterium tuberculosis on fatty acids |
Q38994235 | MicroRNA in innate immunity and autophagy during mycobacterial infection |
Q64064017 | MmpL Proteins in Physiology and Pathogenesis of |
Q26740514 | Modulation of Host miRNAs by Intracellular Bacterial Pathogens |
Q54278115 | Modulation of phagolysosome maturation by bacterial tlyA gene product. |
Q36782015 | Multifunctional essentiality of succinate metabolism in adaptation to hypoxia in Mycobacterium tuberculosis |
Q38144839 | Mutation rate and the emergence of drug resistance in Mycobacterium tuberculosis. |
Q37998504 | Mycobacteria and the intraphagosomal environment: take it with a pinch of salt(s)! |
Q28540070 | Mycobacteria counteract a TLR-mediated nitrosative defense mechanism in a zebrafish infection model |
Q35907046 | Mycobacteria, metals, and the macrophage |
Q28487369 | Mycobacterial MazG is a novel NTP pyrophosphohydrolase involved in oxidative stress response |
Q38786048 | Mycobacterial escape from macrophage phagosomes to the cytoplasm represents an alternate adaptation mechanism |
Q28083739 | Mycobacterial genes essential for the pathogen's survival in the host |
Q50134131 | Mycobacterium abscessus Smooth And Rough Morpohotypes Form Antimicrobial-Tolerant Biofilm Phenotypes But Are Killed by Acetic Acid |
Q34489588 | Mycobacterium smegmatis DinB2 misincorporates deoxyribonucleotides and ribonucleotides during templated synthesis and lesion bypass |
Q27678837 | Mycobacterium tuberculosis Eis protein initiates suppression of host immune responses by acetylation of DUSP16/MKP-7 |
Q40086916 | Mycobacterium tuberculosis EsxO (Rv2346c) promotes bacillary survival by inducing oxidative stress mediated genomic instability in macrophages |
Q47407316 | Mycobacterium tuberculosis GroEL2 modulates dendritic cell responses |
Q35598079 | Mycobacterium tuberculosis Hip1 dampens macrophage proinflammatory responses by limiting toll-like receptor 2 activation |
Q28538895 | Mycobacterium tuberculosis Hip1 modulates macrophage responses through proteolysis of GroEL2 |
Q35774201 | Mycobacterium tuberculosis Is a Natural Ornithine Aminotransferase (rocD) Mutant and Depends on Rv2323c for Growth on Arginine |
Q39958783 | Mycobacterium tuberculosis MutT1 (Rv2985) and ADPRase (Rv1700) proteins constitute a two-stage mechanism of 8-oxo-dGTP and 8-oxo-GTP detoxification and adenosine to cytidine mutation avoidance. |
Q35959194 | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Also Exhibit Chaperone like Activity In-Vitro and In-Vivo |
Q37643055 | Mycobacterium tuberculosis Peptidyl-Prolyl Isomerases Are Immunogenic, Alter Cytokine Profile and Aid in Intracellular Survival |
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 |
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Q41352384 | Mycobacterium tuberculosis TlyA Protein Negatively Regulates T Helper (Th) 1 and Th17 Differentiation and Promotes Tuberculosis Pathogenesis. |
Q38265532 | Mycobacterium tuberculosis WhiB3 Responds to Vacuolar pH-induced Changes in Mycothiol Redox Potential to Modulate Phagosomal Maturation and Virulence |
Q52661262 | Mycobacterium tuberculosis class II apurinic/apyrimidinic-endonuclease/3'-5' exonuclease III exhibits DNA regulated modes of interaction with the sliding DNA β-clamp. |
Q92857480 | Mycobacterium tuberculosis cysteine biosynthesis genes mec+-cysO-cysM confer resistance to clofazimine |
Q28539963 | Mycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infection |
Q41374063 | Mycobacterium tuberculosis has diminished capacity to counteract redox stress induced by elevated levels of endogenous superoxide. |
Q37716941 | Mycobacterium tuberculosis impairs dendritic cell functions through the serine hydrolase Hip1. |
Q36506132 | Mycobacterium tuberculosis requires phosphate-responsive gene regulation to resist host immunity. |
Q54952694 | Mycobacterium tuberculosis: An Adaptable Pathogen Associated With Multiple Human Diseases. |
Q26852023 | Mycobacterium tuberculosis: success through dormancy |
Q27682237 | Mycoredoxin-1 is one of the missing links in the oxidative stress defence mechanism of Mycobacteria |
Q91720654 | NU-6027 Inhibits Growth of Mycobacterium tuberculosis by Targeting Protein Kinase D and Protein Kinase G |
Q44852605 | Nitric Oxide in the Pathogenesis and Treatment of Tuberculosis |
Q37318269 | Nitrite produced by Mycobacterium tuberculosis in human macrophages in physiologic oxygen impacts bacterial ATP consumption and gene expression |
Q38253107 | Nitrogen metabolism in Mycobacterium tuberculosis physiology and virulence |
Q28727945 | Non-coding RNA and its potential role in Mycobacterium tuberculosis pathogenesis |
Q40079297 | OsmC proteins of Mycobacterium tuberculosis and Mycobacterium smegmatis protect against organic hydroperoxide stress |
Q40548422 | Peroxiredoxin 1 Contributes to Host Defenses against Mycobacterium tuberculosis. |
Q65002704 | Peroxisomes and Oxidative Stress: Their Implications in the Modulation of Cellular Immunity During Mycobacterial Infection. |
Q37009017 | Persistent bacterial infections, antibiotic tolerance, and the oxidative stress response |
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Q34423996 | Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections |
Q35728994 | Phagosomal rupture by Mycobacterium tuberculosis results in toxicity and host cell death |
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Q35045290 | Potent antimycobacterial activity of the pyridoxal isonicotinoyl hydrazone analog 2-pyridylcarboxaldehyde isonicotinoyl hydrazone: a lipophilic transport vehicle for isonicotinic acid hydrazide. |
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Q92451979 | Reactive oxygen species-mediated endoplasmic reticulum stress response induces apoptosis of Mycobacterium avium-infected macrophages by activating regulated IRE1-dependent decay pathway |
Q28487142 | RecA-independent DNA damage induction of Mycobacterium tuberculosis ruvC despite an appropriately located SOS box |
Q37493185 | Reconstitution of a Mycobacterium tuberculosis proteostasis network highlights essential cofactor interactions with chaperone DnaK. |
Q58784985 | Redox-dependent condensation of the mycobacterial nucleoid by WhiB4 |
Q28539327 | Reengineering redox sensitive GFP to measure mycothiol redox potential of Mycobacterium tuberculosis during infection |
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Q40460259 | Role of DnaK in HspR-HAIR interaction of Mycobacterium tuberculosis. |
Q39438318 | Role of Interferons in the Development of Diagnostics, Vaccines, and Therapy for Tuberculosis. |
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Q40968419 | Role of mitochondrial oxidative stress on lymphocyte homeostasis in patients diagnosed with extra-pulmonary tuberculosis |
Q92854305 | Roles of Toll-Like Receptors in Nitroxidative Stress in Mammals |
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Q27001010 | Striking the Right Balance Determines TB or Not TB |
Q40277109 | Structure Determination of Mycobacterium tuberculosis Serine Protease Hip1 (Rv2224c). |
Q34336211 | Structure-function relationships of the Mycobacterium tuberculosis transcription factor WhiB1 |
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Q35989779 | SufB intein of Mycobacterium tuberculosis as a sensor for oxidative and nitrosative stresses |
Q36241272 | Sustained generation of nitric oxide and control of mycobacterial infection requires argininosuccinate synthase 1. |
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Q49637506 | The Macrophage: A Disputed Fortress in the Battle against Mycobacterium tuberculosis |
Q27673424 | The Oxidation-sensing Regulator (MosR) Is a New Redox-dependent Transcription Factor in Mycobacterium tuberculosis |
Q55431830 | The PGRS Domain of Mycobacterium tuberculosis PE_PGRS Protein Rv0297 Is Involved in Endoplasmic Reticulum Stress-Mediated Apoptosis through Toll-Like Receptor 4. |
Q37198725 | The Role of Prostate Apoptosis Response-4 (Par-4) in Mycobacterium tuberculosis Infected Macrophages. |
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Q37683485 | The impact of drug resistance on Mycobacterium tuberculosis physiology: what can we learn from rifampicin? |
Q37123814 | The intracellular environment of human macrophages that produce nitric oxide promotes growth of mycobacteria. |
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Q33834159 | Thioredoxin 80-activated-monocytes (TAMs) inhibit the replication of intracellular pathogens |
Q37199876 | Transcriptional Profiling of Mycobacterium tuberculosis Exposed to In Vitro Lysosomal Stress |
Q37515820 | Tryptophan biosynthesis protects mycobacteria from CD4 T-cell-mediated killing |
Q54211356 | Tuberculosis and the art of macrophage manipulation. |
Q38006467 | Understanding delayed T-cell priming, lung recruitment, and airway luminal T-cell responses in host defense against pulmonary tuberculosis |
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Q33955336 | VapC toxins from Mycobacterium tuberculosis are ribonucleases that differentially inhibit growth and are neutralized by cognate VapB antitoxins |
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