scholarly article | Q13442814 |
P50 | author | Carl F. Nathan | Q1037710 |
P2093 | author name string | North RJ | |
MacMicking JD | |||
Shah SK | |||
Mudgett JS | |||
LaCourse R | |||
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P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | tuberculosis | Q12204 |
P304 | page(s) | 5243-8 | |
P577 | publication date | 1997-05-13 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Identification of nitric oxide synthase as a protective locus against tuberculosis | |
P478 | volume | 94 |
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Q43266126 | Inhibitory effect of phytoglycoprotein (115 kDa) on the expression of TNF-alpha and interleukin-1beta via inhibition of MAP kinase in primary cultured mouse thymocytes |
Q26751060 | Innate Immunity Holding the Flanks until Reinforced by Adaptive Immunity against Mycobacterium tuberculosis Infection |
Q27000486 | Innate immune gene polymorphisms in tuberculosis |
Q37950226 | Inside or outside the phagosome? The controversy of the intracellular localization of Mycobacterium tuberculosis. |
Q36806048 | Insufficient Generation of Mycobactericidal Mediators and Inadequate Level of Phagosomal Maturation Are Related with Susceptibility to Virulent Mycobacterium tuberculosis Infection in Mouse Macrophages |
Q40882568 | Interaction of antimycobacterial drugs with the anti-Mycobacterium avium complex effects of antimicrobial effectors, reactive oxygen intermediates, reactive nitrogen intermediates, and free fatty acids produced by macrophages |
Q35563221 | Interactions between naïve and infected macrophages reduce Mycobacterium tuberculosis viability |
Q36380807 | Interferon (IFN)-alpha activation of human blood mononuclear cells in vitro and in vivo for nitric oxide synthase (NOS) type 2 mRNA and protein expression: possible relationship of induced NOS2 to the anti-hepatitis C effects of IFN-alpha in vivo. |
Q28478015 | Interferon gamma activated macrophages kill mycobacteria by nitric oxide induced apoptosis |
Q28395075 | Interferon-alphabeta mediates partial control of early pulmonary Mycobacterium bovis bacillus Calmette-Guérin infection |
Q40806985 | Interferon-gamma- and lipopolysaccharide-induced tumor necrosis factor-alpha is required for nitric oxide production: tumor necrosis factor-alpha and nitric oxide are independently involved in the killing of Mycobacterium microti in interferon-gamma |
Q33596687 | Interferon-gamma-responsive nonhematopoietic cells regulate the immune response to Mycobacterium tuberculosis |
Q90135468 | Interleukin 10 knock-down in bovine monocyte-derived macrophages has distinct effects during infection with two divergent strains of Mycobacterium bovis |
Q37309538 | Interleukin-10 promotes Mycobacterium tuberculosis disease progression in CBA/J mice |
Q61313267 | Interleukin-12p40 overexpression promotes interleukin-12p70 and interleukin-23 formation but does not affect bacille Calmette-Guérin and Mycobacterium tuberculosis clearance |
Q40634545 | Intracellular expression of Mycobacterium tuberculosis-specific 10-kDa antigen down-regulates macrophage B7.1 expression and nitric oxide release. |
Q44163367 | Investigation of chromosome 17 candidate genes in susceptibility to TB in a South African population |
Q38055958 | In vitro infection of human cells with Mycobacterium tuberculosis. |
Q92163260 | Iron Supplementation Therapy, A Friend and Foe of Mycobacterial Infections? |
Q37778480 | Is Mycobacterium tuberculosis stressed out? A critical assessment of the genetic evidence |
Q54976471 | Is Receptor-Interacting Protein Kinase 3 a Viable Therapeutic Target for Mycobacterium tuberculosis Infection? |
Q56469515 | Is Total Serum Nitrite and Nitrate (NOx) Level in Dengue Patients a Potential Prognostic Marker of Dengue Hemorrhagic Fever? |
Q34463493 | Is nitric oxide overproduction the target of choice for the management of septic shock? |
Q38756763 | Lack of IL-1 Receptor-Associated Kinase-4 Leads to Defective Th1 Cell Responses and Renders Mice Susceptible to Mycobacterial Infection |
Q45733743 | Lack of nitric oxide synthase type 2 (NOS2) results in reduced neuronal apoptosis and mortality following mouse hepatitis virus infection of the central nervous system |
Q40065379 | Lactoferricin Peptides Increase Macrophages' Capacity To Kill Mycobacterium avium. |
Q34297816 | Latent tuberculosis infection: myths, models, and molecular mechanisms |
Q35211295 | Latent tuberculosis: mechanisms of host and bacillus that contribute to persistent infection |
Q37421310 | Lazy, dynamic or minimally recrudescent? On the elusive nature and location of the mycobacterium responsible for latent tuberculosis |
Q73002017 | Lethal Mycobacterium bovis Bacillus Calmette Guérin infection in nitric oxide synthase 2-deficient mice: cell-mediated immunity requires nitric oxide synthase 2 |
Q36703585 | Life and death in the granuloma: immunopathology of tuberculosis |
Q79243126 | Life on the inside for Mycobacterium tuberculosis |
Q48165177 | Lipid droplet formation in Mycobacterium tuberculosis infected macrophages requires IFN-γ/HIF-1α signaling and supports host defense |
Q28140459 | Lipoarabinomannan from Mycobacterium tuberculosis promotes macrophage survival by phosphorylating Bad through a phosphatidylinositol 3-kinase/Akt pathway |
Q53908549 | Lung cell responses to M. tuberculosis in genetically susceptible and resistant mice following intratracheal challenge. |
Q35605917 | M. tuberculosis persistence, latency, and drug tolerance |
Q34280835 | Macrophage arginase-1 controls bacterial growth and pathology in hypoxic tuberculosis granulomas |
Q38363796 | Macrophage defense mechanisms against intracellular bacteria. |
Q35039679 | Macrophage immunoregulatory pathways in tuberculosis |
Q38497801 | Macrophage takeover and the host-bacilli interplay during tuberculosis. |
Q36959378 | Macrophage-mediated inflammatory response decreases mycobacterial survival in mouse MSCs by augmenting NO production |
Q37856707 | Macrophages and control of granulomatous inflammation in tuberculosis |
Q27319471 | Mechanism of inducible nitric oxide synthase exclusion from mycobacterial phagosomes |
Q37118101 | Mechanisms and consequences of persistence of intracellular pathogens: leishmaniasis as an example. |
Q30398195 | Metabolic Perspectives on Persistence |
Q28590692 | Mice lacking inducible nitric oxide synthase demonstrate impaired killing of Porphyromonas gingivalis |
Q37103066 | Microenvironments in tuberculous granulomas are delineated by distinct populations of macrophage subsets and expression of nitric oxide synthase and arginase isoforms |
Q28362977 | Modulation of Mycobacterium bovis-specific responses of bovine peripheral blood mononuclear cells by 1,25-dihydroxyvitamin D(3) |
Q80818732 | Modulation of immune responses in mice to recombinant antigens from PE and PPE families of proteins of Mycobacterium tuberculosis by the Ribi adjuvant |
Q45829514 | Molecular Mechanisms Modulating the Phenotype of Macrophages and Microglia |
Q36688480 | Molecular immunologic correlates of spontaneous latency in a rabbit model of pulmonary tuberculosis |
Q35622988 | Molecular mechanisms of host-pathogen interaction: entry and survival of mycobacteria in macrophages. |
Q91904779 | Mucosal-associated invariant T cells and disease |
Q28540070 | Mycobacteria counteract a TLR-mediated nitrosative defense mechanism in a zebrafish infection model |
Q37426403 | Mycobacteria inhibit nitric oxide synthase recruitment to phagosomes during macrophage infection |
Q54520033 | Mycobacteria-induced granuloma necrosis depends on IRF-1. |
Q28552338 | Mycobacterial Metabolic Syndrome: LprG and Rv1410 Regulate Triacylglyceride Levels, Growth Rate and Virulence in Mycobacterium tuberculosis |
Q28083739 | Mycobacterial genes essential for the pathogen's survival in the host |
Q35671416 | Mycobacterial glycolipids di-O-acylated trehalose and tri-O-acylated trehalose downregulate inducible nitric oxide synthase and nitric oxide production in macrophages |
Q34426515 | Mycobacterium marinum causes a latent infection that can be reactivated by gamma irradiation in adult zebrafish |
Q35598609 | Mycobacterium smegmatis RoxY is a repressor of oxyS and contributes to resistance to oxidative stress and bactericidal ubiquitin-derived peptides |
Q39655566 | Mycobacterium tuberculosis CDC1551 is resistant to reactive nitrogen and oxygen intermediates in vitro |
Q28486511 | Mycobacterium tuberculosis DosS is a redox sensor and DosT is a hypoxia sensor |
Q93220808 | Mycobacterium tuberculosis Requires Regulation of ESX-5 Secretion for Virulence in Irgm1-Deficient Mice |
Q91720786 | Mycobacterium tuberculosis Rv2700 Contributes to Cell Envelope Integrity and Virulence |
Q28552573 | Mycobacterium tuberculosis Thioredoxin Reductase Is Essential for Thiol Redox Homeostasis but Plays a Minor Role in Antioxidant Defense |
Q52722200 | Mycobacterium tuberculosis Transfer RNA Induces IL-12p70 via Synergistic Activation of Pattern Recognition Receptors within a Cell Network. |
Q89997913 | Mycobacterium tuberculosis WhiB3 maintains redox homeostasis and survival in response to reactive oxygen and nitrogen species |
Q36223232 | Mycobacterium tuberculosis WhiB4 regulates oxidative stress response to modulate survival and dissemination in vivo. |
Q36938592 | Mycobacterium tuberculosis and the environment within the phagosome |
Q35216595 | Mycobacterium tuberculosis and the intimate discourse of a chronic infection |
Q64964405 | Mycobacterium tuberculosis carrying a rifampicin drug resistance mutation reprograms macrophage metabolism through cell wall lipid changes. |
Q28486947 | Mycobacterium tuberculosis conserved hypothetical protein rRv2626c modulates macrophage effector functions |
Q28486777 | Mycobacterium tuberculosis expresses methionine sulphoxide reductases A and B that protect from killing by nitrite and hypochlorite |
Q34945420 | Mycobacterium tuberculosis growth at the cavity surface: a microenvironment with failed immunity |
Q41374063 | Mycobacterium tuberculosis has diminished capacity to counteract redox stress induced by elevated levels of endogenous superoxide. |
Q27633806 | Mycobacterium tuberculosis hemoglobin N displays a protein tunnel suited for O2 diffusion to the heme |
Q45000171 | Mycobacterium tuberculosis induces high production of nitric oxide in coordination with production of tumour necrosis factor-alpha in patients with fresh active tuberculosis but not in MDR tuberculosis |
Q34213787 | Mycobacterium tuberculosis pathogenesis and molecular determinants of virulence |
Q33982151 | Mycobacterium tuberculosis persistence mutants identified by screening in isoniazid-treated mice |
Q28486412 | Mycobacterium tuberculosis prcBA genes encode a gated proteasome with broad oligopeptide specificity |
Q34747029 | Mycobacterium tuberculosis protein kinase K confers survival advantage during early infection in mice and regulates growth in culture and during persistent infection: implications for immune modulation |
Q36506132 | Mycobacterium tuberculosis requires phosphate-responsive gene regulation to resist host immunity. |
Q38268279 | Mycobacterium tuberculosis response to stress from reactive oxygen and nitrogen species |
Q34089860 | Mycobacterium tuberculosis wears what it eats |
Q29619735 | Mycobacterium tuberculosis: here today, and here tomorrow |
Q38686660 | Mycobacterium tuberculosis: what is the role of PPE2 during infection? |
Q91321395 | Mycoplasma bovis delay in apoptosis of macrophages is accompanied by increased expression of anti-apoptotic genes, reduced cytochrome C translocation and inhibition of DNA fragmentation |
Q61755441 | Mycothiol-dependent mycobacterial response to oxidative stress |
Q90674170 | Myeloid HIF-1α regulates pulmonary inflammation during experimental Mycobacterium tuberculosis infection |
Q41969521 | N,C-Capped dipeptides with selectivity for mycobacterial proteasome over human proteasomes: role of S3 and S1 binding pockets |
Q38937950 | NOD-2 and TLR-4 Signaling Reinforces the Efficacy of Dendritic Cells and Reduces the Dose of TB Drugs against Mycobacterium tuberculosis. |
Q40087530 | NOS2-deficient mice with hypoxic necrotizing lung lesions predict outcomes of tuberculosis chemotherapy in humans |
Q44558306 | NOS2-derived nitric oxide regulates the size, quantity and quality of granuloma formation in Mycobacterium avium-infected mice without affecting bacterial loads |
Q39304314 | NOS2A promoter (CCTTT)n association with TB lacks independent functional correlation amongst Indians |
Q33896845 | NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans |
Q34460946 | Natural transmission of Plasmodium berghei exacerbates chronic tuberculosis in an experimental co-infection model |
Q40868823 | Naturally produced opsonizing antibodies restrict the survival of Mycobacterium tuberculosis in human macrophages by augmenting phagosome maturation |
Q48138531 | Necroptotic signaling is primed in Mycobacterium tuberculosis-infected macrophages, but its pathophysiological consequence in disease is restricted |
Q42908536 | Neuroinflammation, Oxidative Stress and the Pathogenesis of Parkinson's Disease |
Q28388477 | New insights into TB physiology suggest untapped therapeutic opportunities |
Q35095367 | New targets and inhibitors of mycobacterial sulfur metabolism. |
Q90468452 | Nitric Oxide Engages an Anti-inflammatory Feedback Loop Mediated by Peroxiredoxin 5 in Phagocytes |
Q40115065 | Nitric Oxide Modulates Macrophage Responses to Mycobacterium tuberculosis Infection through Activation of HIF-1α and Repression of NF-κB. |
Q33734476 | Nitric oxide and infectious diseases |
Q29617591 | Nitric oxide and the immune response |
Q27485884 | Nitric oxide and virus infection |
Q34941147 | Nitric oxide as an inflammatory mediator in autoimmune MRL-lpr/lpr mice |
Q37040409 | Nitric oxide controls the immunopathology of tuberculosis by inhibiting NLRP3 inflammasome-dependent processing of IL-1β. |
Q37400186 | Nitric oxide in dengue and dengue haemorrhagic fever: necessity or nuisance? |
Q77802828 | Nitric oxide in the failing myocardium |
Q34984498 | Nitric oxide inhibits exocytosis of cytolytic granules from lymphokine-activated killer cells |
Q36875493 | Nitric oxide inhibits the accumulation of CD4+CD44hiTbet+CD69lo T cells in mycobacterial infection |
Q48022256 | Nitric oxide participation in granulomatous response induced by Paracoccidioides brasiliensis infection in mice |
Q34932787 | Nitric oxide protects bacteria from aminoglycosides by blocking the energy-dependent phases of drug uptake |
Q28486473 | Nitric oxide scavenging and detoxification by the Mycobacterium tuberculosis haemoglobin, HbN in Escherichia coli |
Q35061791 | Nitric oxide synthase activity has limited influence on the control of Coccidioides infection in mice |
Q35558464 | Nitric oxide, inflammation and acute burn injury |
Q48379508 | Nitric oxide: from a mysterious labile factor to the molecule of the Nobel Prize. Recent progress in nitric oxide research |
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 |
Q34381833 | Nitrosylation. the prototypic redox-based signaling mechanism. |
Q58846273 | No evidence for association of the inducible nitric oxide synthase promoter polymorphism with Trypanosoma cruzi infection |
Q36342789 | Nonsteroidal anti-inflammatory drug sensitizes Mycobacterium tuberculosis to endogenous and exogenous antimicrobials |
Q37101494 | Novel Cephalosporins Selectively Active on Nonreplicating Mycobacterium tuberculosis |
Q27757495 | Novel non-heme iron center of nitrile hydratase with a claw setting of oxygen atoms |
Q47136699 | Nucleotide-Binding Oligomerization Domain 2 Contributes to Limiting Growth of Mycobacterium abscessus in the Lung of Mice by Regulating Cytokines and Nitric Oxide Production |
Q43985483 | On the killing of mycobacteria by macrophages |
Q36580383 | One Episode of Self-Resolving Plasmodium yoelii Infection Transiently Exacerbates Chronic Mycobacterium tuberculosis Infection |
Q38672958 | Oxidative Phosphorylation as a Target Space for Tuberculosis: Success, Caution, and Future Directions |
Q39567733 | Oxidative stress response and characterization of the oxyR-ahpC and furA-katG loci in Mycobacterium marinum. |
Q34543665 | Oxygen binding and NO scavenging properties of truncated hemoglobin, HbN, of Mycobacterium smegmatis |
Q24654913 | PA-824 kills nonreplicating Mycobacterium tuberculosis by intracellular NO release |
Q38085418 | PPE2 protein of Mycobacterium tuberculosis may inhibit nitric oxide in activated macrophages |
Q35150831 | Patients with tuberculosis disease have Mycobacterium tuberculosis-specific CD8 T cells with a pro-apoptotic phenotype and impaired proliferative capacity, which is not restored following treatment |
Q40548422 | Peroxiredoxin 1 Contributes to Host Defenses against Mycobacterium tuberculosis. |
Q35889600 | Persistent bacterial infections: the interface of the pathogen and the host immune system |
Q37368468 | Perspectives series: host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity |
Q37945715 | Pharmacogenetics of the lipodystrophy syndrome associated with HIV infection and combination antiretroviral therapy. |
Q33793673 | Pharmacological modulation of nitric oxide synthesis by mechanism-based inactivators and related inhibitors |
Q45274479 | Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase. |
Q36914816 | Phthiocerol dimycocerosate transport is required for resisting interferon-gamma-independent immunity |
Q38484210 | Phylogenomics of Mycobacterium Nitrate Reductase Operon |
Q36163097 | Polyclonal mucosa-associated invariant T cells have unique innate functions in bacterial infection |
Q35208353 | Preexisting helminth infection induces inhibition of innate pulmonary anti-tuberculosis defense by engaging the IL-4 receptor pathway |
Q58553806 | Presence of Infected Gr-1CD11bCD11c Monocytic Myeloid Derived Suppressor Cells Subverts T Cell Response and Is Associated With Impaired Dendritic Cell Function in -Infected Mice |
Q37282737 | Progress and new directions in genetics of tuberculosis: an NHLBI working group report |
Q39076238 | Prokaryotic expression and functional analysis of the Mb1514 gene in Mycobacterium bovis |
Q37502693 | Prokaryotic ubiquitin-like protein (Pup), proteasomes and pathogenesis |
Q28487570 | Proteasomal control of cytokinin synthesis protects Mycobacterium tuberculosis against nitric oxide |
Q37204436 | Protection of Mycobacterium tuberculosis from reactive oxygen species conferred by the mel2 locus impacts persistence and dissemination |
Q38247209 | Protective immune responses to fungal infections |
Q37033735 | Protective role of membrane tumour necrosis factor in the host's resistance to mycobacterial infection |
Q33751428 | Protective role of nitric oxide in Staphylococcus aureus infection in mice |
Q91966785 | Protein-protein interaction of Rv0148 with Htdy and its predicted role towards drug resistance in Mycobacterium tuberculosis |
Q38321484 | Pulmonary Mycobacterium tuberculosis infection in leptin-deficient ob/ob mice |
Q36404225 | Rapid interferon gamma-dependent clearance of influenza A virus and protection from consolidating pneumonitis in nitric oxide synthase 2-deficient mice |
Q43245570 | Rapid, Semiquantitative Assay To Discriminate among Compounds with Activity against Replicating or Nonreplicating Mycobacterium tuberculosis. |
Q37190166 | Reaction of Mycobacterium tuberculosis cytochrome P450 enzymes with nitric oxide |
Q34001719 | Reactivation of latent tuberculosis: variations on the Cornell murine model |
Q33840580 | Reactive nitrogen intermediates and the pathogenesis of Salmonella and mycobacteria |
Q39664494 | Reactive nitrogen intermediates have a bacteriostatic effect on Mycobacterium tuberculosis in vitro |
Q24630289 | Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens |
Q33840513 | Reactive oxygen and reactive nitrogen intermediates in innate and specific immunity |
Q34851055 | Recombinant gamma interferon stimulates signal transduction and gene expression in alveolar macrophages in vitro and in tuberculosis patients |
Q27012879 | Redox homeostasis in mycobacteria: the key to tuberculosis control? |
Q35356550 | Reduced oxidative and nitrosative damage in murine experimental colitis in the absence of inducible nitric oxide synthase |
Q40136119 | Reduced susceptibility of clinical strains of Mycobacterium tuberculosis to reactive nitrogen species promotes survival in activated macrophages |
Q28539327 | Reengineering redox sensitive GFP to measure mycothiol redox potential of Mycobacterium tuberculosis during infection |
Q58461876 | Regulation of granuloma fibrosis by nitric oxide during Mycobacterium avium experimental infection |
Q36040945 | Regulation of innate immunity by NADPH oxidase |
Q60300625 | Regulation of mycobacterial infection by macrophage Gch1 and tetrahydrobiopterin |
Q35441389 | Regulation of neutrophils by interferon-γ limits lung inflammation during tuberculosis infection |
Q28487527 | Regulation of the Mycobacterium tuberculosis hypoxic response gene encoding α-crystallin |
Q34445693 | Regulation of the ahpC gene encoding alkyl hydroperoxide reductase in Mycobacterium smegmatis |
Q50319373 | Reinforcing the Functionality of Mononuclear Phagocyte System to Control Tuberculosis |
Q36669873 | Relationship of bovine NOS2 gene polymorphisms to the risk of bovine tuberculosis in Holstein cattle. |
Q33943840 | Replication of Yersinia pestis in interferon gamma-activated macrophages requires ripA, a gene encoded in the pigmentation locus |
Q36369581 | Reprogramming of the macrophage transcriptome in response to interferon-gamma and Mycobacterium tuberculosis: signaling roles of nitric oxide synthase-2 and phagocyte oxidase |
Q28487034 | Response to reactive nitrogen intermediates in Mycobacterium tuberculosis: induction of the 16-kilodalton alpha-crystallin homolog by exposure to nitric oxide donors |
Q38003929 | Revisiting the role of the granuloma in tuberculosis |
Q62488588 | Rifampicin and dexamethasone have similar effects on macrophage phagocytosis of zymosan, but differ in their effects on nitrite and TNF-α production |
Q42237169 | Rifampin augments cytokine-induced nitric oxide production in human alveolar epithelial cells |
Q35627704 | Role for NOD2 in Mycobacterium tuberculosis-induced iNOS expression and NO production in human macrophages |
Q41946149 | Role for nucleotide excision repair in virulence of Mycobacterium tuberculosis |
Q28486437 | Role of Mycobacterium tuberculosis copper-zinc superoxide dismutase |
Q43126200 | Role of Pre-A motif in nitric oxide scavenging by truncated hemoglobin, HbN, of Mycobacterium tuberculosis. |
Q34191797 | Role of free radicals in viral pathogenesis and mutation |
Q33600697 | Role of inducible nitric oxide synthase in resistance to Mycobacterium leprae in mice |
Q34418998 | Role of nitric oxide in inflammation |
Q34714207 | Role of the NF-kappaB signaling pathway and kappaB cis-regulatory elements on the IRF-1 and iNOS promoter regions in mycobacterial lipoarabinomannan induction of nitric oxide |
Q37099497 | Role of the dosR-dosS two-component regulatory system in Mycobacterium tuberculosis virulence in three animal models. |
Q24546207 | S-Nitrosogluthathione reductase activity of amphioxus ADH3: insights into the nitric oxide metabolism |
Q33722881 | S-nitroso proteome of Mycobacterium tuberculosis: Enzymes of intermediary metabolism and antioxidant defense |
Q35119656 | S-nitrosylation in health and disease |
Q52728434 | S-nitrosylation of NADPH oxidase regulates cell death in plant immunity. |
Q57471957 | S-nitrosylation of the zinc finger protein SRG1 regulates plant immunity |
Q40623428 | STAT3 Represses Nitric Oxide Synthesis in Human Macrophages upon Mycobacterium tuberculosis Infection |
Q90521129 | Salmonella Persist in Activated Macrophages in T Cell-Sparse Granulomas but Are Contained by Surrounding CXCR3 Ligand-Positioned Th1 Cells |
Q28505858 | Serine protease activity contributes to control of Mycobacterium tuberculosis in hypoxic lung granulomas in mice |
Q34009146 | Silencing of oxidative stress response in Mycobacterium tuberculosis: expression patterns of ahpC in virulent and avirulent strains and effect of ahpC inactivation |
Q64097469 | Spatial and temporal localization of immune transcripts defines hallmarks and diversity in the tuberculosis granuloma |
Q58889002 | Species-Specific Transcriptional Regulation of Genes Involved in Nitric Oxide Production and Arginine Metabolism in Macrophages |
Q27694770 | Spotlights on immunological effects of reactive nitrogen species: When inflammation says nitric oxide |
Q39437320 | Striking the right immunological balance prevents progression of tuberculosis |
Q47259350 | Structure of a Wbl protein and implications for NO sensing by M. tuberculosis. |
Q45066836 | Study on myeloperoxidase role in antituberculous defense in the context of cytokine activation |
Q45952650 | Suppression of IFNgamma+mycobacterial lipoarabinomannan-induced NO by IL-4 is due to decreased IRF-1 expression. |
Q28397253 | Suppression of the NF-κB pathway by diesel exhaust particles impairs human antimycobacterial immunity |
Q47109680 | Suppressor of Cytokine Signaling 3 in Macrophages Prevents Exacerbated Interleukin-6-Dependent Arginase-1 Activity and Early Permissiveness to Experimental Tuberculosis. |
Q51655159 | Surfactant protein A enhances Mycobacterium avium ingestion but not killing by rat macrophages. |
Q33842618 | Surfactant protein A suppresses reactive nitrogen intermediates by alveolar macrophages in response to Mycobacterium tuberculosis |
Q33876178 | Survival of Mycobacterium avium and Mycobacterium tuberculosis in acidified vacuoles of murine macrophages |
Q51984727 | Susceptibility and resistance to monocytic ehrlichiosis in the mouse. |
Q53854589 | Susceptibility of brushtail possums (Trichosurus vulpecula) infected with Mycobacterium bovis is associated with a transient macrophage activation profile. |
Q98224728 | Susceptibility to Intracellular Infections: Contributions of TNF to Immune Defense |
Q36241272 | Sustained generation of nitric oxide and control of mycobacterial infection requires argininosuccinate synthase 1. |
Q38742184 | T Cell-Derived IL-10 Impairs Host Resistance to Mycobacterium tuberculosis Infection |
Q33536568 | T cell mediated immunity to Mycobacterium tuberculosis |
Q45948289 | T-cell release of granulysin contributes to host defense in leprosy. |
Q28083600 | TB drug development: immunology at the table |
Q38166990 | TB or not TB: that is no longer the question |
Q37435926 | TB vaccines: current status and future perspectives |
Q36666348 | TGF beta 1 and TNF alpha potentiate nitric oxide production in astrocyte cultures by recruiting distinct subpopulations of cells to express NOS-2. |
Q40178443 | TLR2 but not TLR4 signalling is critically involved in the inhibition of IFN-gamma-induced killing of mycobacteria by murine macrophages |
Q36403076 | TLR9 regulates Th1 responses and cooperates with TLR2 in mediating optimal resistance to Mycobacterium tuberculosis. |
Q41816750 | TNF dually mediates resistance and susceptibility to mycobacteria via mitochondrial reactive oxygen species |
Q55287141 | TNF-α blockade impairs in vitro tuberculous granuloma formation and down modulate Th1, Th17 and Treg cytokines. |
Q37891774 | Taking Out TB-Lysosomal Trafficking and Mycobactericidal Ubiquitin-Derived Peptides |
Q39149038 | Targeting Phenotypically Tolerant Mycobacterium tuberculosis |
Q24644997 | Targeting of the GTPase Irgm1 to the phagosomal membrane via PtdIns(3,4)P(2) and PtdIns(3,4,5)P(3) promotes immunity to mycobacteria |
Q52692190 | Targeting the Proteostasis Network for Mycobacterial Drug Discovery. |
Q26774207 | Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers |
Q49900955 | Th1 cytokines, true functional signatures for protective immunity against TB? |
Q38314435 | The BER necessities: the repair of DNA damage in human-adapted bacterial pathogens. |
Q39727290 | The CFP-10/ESAT-6 complex of Mycobacterium tuberculosis potentiates the activation of murine macrophages involvement of IFN-gamma signaling |
Q43082287 | The IL-13/IL-4Rα axis is involved in tuberculosis-associated pathology |
Q37594360 | The Minimal Unit of Infection: Mycobacterium tuberculosis in the Macrophage |
Q35628763 | The Mycobacterium marinum mel2 locus displays similarity to bacterial bioluminescence systems and plays a role in defense against reactive oxygen and nitrogen species |
Q42600002 | The Mycobacterium tuberculosis SecA2 system subverts phagosome maturation to promote growth in macrophages. |
Q33658714 | The Mycobacterium tuberculosis proteasome active site threonine is essential for persistence yet dispensable for replication and resistance to nitric oxide |
Q37578057 | The Mycobacterium tuberculosis proteasome: more than just a barrel-shaped protease |
Q54286145 | The Mycobacterium tuberculosis recombinant LprN protein of mce4 operon induces Th-1 type response deleterious to protection in mice. |
Q27702517 | The N-terminal pre-A region of Mycobacterium tuberculosis 2/2HbN promotes NO-dioxygenase activity |
Q26825089 | The Pup-Proteasome System of Mycobacteria |
Q27490787 | The Role of Nitric Oxide in Mycobacterial Infections |
Q34026690 | The SPRY domain-containing SOCS box protein SPSB2 targets iNOS for proteasomal degradation |
Q34888988 | The Sculpting of the Mycobacterium tuberculosis Genome by Host Cell-Derived Pressures |
Q28487596 | The SecA2 secretion factor of Mycobacterium tuberculosis promotes growth in macrophages and inhibits the host immune response |
Q30402360 | The Tyrosine Kinase Inhibitor Gefitinib Restricts Mycobacterium tuberculosis Growth through Increased Lysosomal Biogenesis and Modulation of Cytokine Signaling. |
Q39613066 | The capsule supports survival but not traversal of Escherichia coli K1 across the blood-brain barrier. |
Q26744038 | The emerging role of gasotransmitters in the pathogenesis of tuberculosis |
Q34595822 | The endothelin system has a significant role in the pathogenesis and progression of Mycobacterium tuberculosis infection. |
Q38872142 | The fibroblast growth factor-2 arrests Mycobacterium avium sp. paratuberculosis growth and immunomodulates host response in macrophages |
Q55653568 | The functional interplay of low molecular weight thiols in Mycobacterium tuberculosis. |
Q41727902 | The host immune response to tuberculosis |
Q35676581 | The immunological aspects of latency in tuberculosis |
Q33777367 | The immunology of tuberculosis: from bench to bedside |
Q34009836 | The inducible nitric oxide synthase locus confers protection against aerogenic challenge of both clinical and laboratory strains of Mycobacterium tuberculosis in mice |
Q37123814 | The intracellular environment of human macrophages that produce nitric oxide promotes growth of mycobacteria. |
Q36838527 | The iron export protein ferroportin 1 is differentially expressed in mouse macrophage populations and is present in the mycobacterial-containing phagosome. |
Q37419579 | The macrophage marches on its phagosome: dynamic assays of phagosome function. |
Q34266438 | The many faces of host responses to tuberculosis |
Q28487623 | The multifunctional histone-like protein Lsr2 protects mycobacteria against reactive oxygen intermediates |
Q36075177 | The pathogenesis of tuberculosis: the first one hundred (and twenty-three) years |
Q36376221 | The relative importance of T cell subsets in immunity and immunopathology of airborne Mycobacterium tuberculosis infection in mice |
Q37859621 | The role of IL-10 in immune regulation during M. tuberculosis infection |
Q37374958 | The role of cytokines in the initiation, expansion, and control of cellular immunity to tuberculosis |
Q34265039 | The role of gamma interferon in antimicrobial immunity |
Q44891712 | The role of nitric oxide in lung innate immunity: modulation by surfactant protein-A. |
Q47286732 | The role of nitric oxide in metabolic regulation of Dendritic cell immune function |
Q26863204 | The role of pro-resolution lipid mediators in infectious disease |
Q41965764 | The toll-like receptor 2/6 ligand MALP-2 reduces the viability of Mycobacterium tuberculosis in murine macrophages |
Q58746346 | Tolerating the Unwelcome Guest; How the Host Withstands Persistent |
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 |
Q40104128 | Toll-like receptor genes are differentially expressed at the sites of infection during the progression of Johne's disease in outbred sheep. |
Q34049969 | Toll-like receptors: molecular mechanisms of the mammalian immune response |
Q37228738 | Toll-like receptors: their roles in bacterial recognition and respiratory infections |
Q96435430 | Topologically correct synthetic reconstruction of pathogen social behavior found during Yersinia growth in deep tissue sites |
Q35117081 | Trans-species communication in the Mycobacterium tuberculosis-infected macrophage |
Q37248992 | Transcriptional characterization of the antioxidant response of Mycobacterium tuberculosis in vivo and during adaptation to hypoxia in vitro |
Q54224374 | Transcriptional landscape of Mycobacterium tuberculosis infection in macrophages. |
Q41570545 | Transcriptome changes upon in vitro challenge with Mycobacterium bovis in monocyte-derived macrophages from bovine tuberculosis-infected and healthy cows |
Q28593510 | Transient loss of resistance to pulmonary tuberculosis in p47(phox-/-) mice |
Q27658975 | Triazaspirodimethoxybenzoyls as Selective Inhibitors of Mycobacterial Lipoamide Dehydrogenase, |
Q36970544 | Triggering through NOD-2 Differentiates Bone Marrow Precursors to Dendritic Cells with Potent Bactericidal activity |
Q28486863 | Truncated hemoglobin HbN protects Mycobacterium bovis from nitric oxide |
Q35988766 | Tuberculosis - metabolism and respiration in the absence of growth |
Q47720001 | Tuberculosis Infectiousness and Host Susceptibility |
Q37270954 | Tuberculosis Susceptibility and Vaccine Protection Are Independently Controlled by Host Genotype |
Q21131403 | Tuberculosis and HIV co-infection |
Q34974987 | Tuberculosis chemotherapy: the influence of bacillary stress and damage response pathways on drug efficacy |
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