scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Andrea Gioffré | |
Fabiana Bigi | |||
María de la Paz Santangelo | |||
Hector R Morbidoni | |||
Marina A Forrellad | |||
Angel A Cataldi | |||
Laura I Klepp | |||
Julia Sabio y García | |||
P2860 | cites work | The specialized secretory apparatus ESX-1 is essential for DNA transfer in Mycobacterium smegmatis. | Q41859091 |
Rapid and spontaneous loss of phthiocerol dimycocerosate (PDIM) from Mycobacterium tuberculosis grown in vitro: implications for virulence studies | Q41909471 | ||
Identification of two Mycobacterium smegmatis lipoproteins exported by a SecA2-dependent pathway | Q42412477 | ||
Convergence of Ser/Thr and two-component signaling to coordinate expression of the dormancy regulon in Mycobacterium tuberculosis | Q42427984 | ||
The Mycobacterium tuberculosis sigma factor sigmaB is required for full response to cell envelope stress and hypoxia in vitro, but it is dispensable for in vivo growth | Q42545993 | ||
The Mycobacterium tuberculosis SecA2 system subverts phagosome maturation to promote growth in macrophages. | Q42600002 | ||
Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis | Q21131582 | ||
Massive gene decay in the leprosy bacillus | Q22122381 | ||
Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence | Q22122411 | ||
Inhibition of SRC tyrosine kinases suppresses activation of nuclear factor-kappa B, and serine and tyrosine phosphorylation of Ikappa B-alpha in lipopolysaccharide-stimulated RAW 264.7 macrophages | Q23914895 | ||
The 19-kDa Mycobacterium tuberculosis protein induces macrophage apoptosis through Toll-like receptor-2 | Q24295054 | ||
Mycobacterium tuberculosis virulence is mediated by PtpA dephosphorylation of human vacuolar protein sorting 33B | Q24311987 | ||
Execution of macrophage apoptosis by PE_PGRS33 of Mycobacterium tuberculosis is mediated by Toll-like receptor 2-dependent release of tumor necrosis factor-alpha | Q24313360 | ||
The mycobacterial 38-kilodalton glycolipoprotein antigen activates the mitogen-activated protein kinase pathway and release of proinflammatory cytokines through Toll-like receptors 2 and 4 in human monocytes | Q24318584 | ||
A new evolutionary scenario for the Mycobacterium tuberculosis complex | Q24531514 | ||
Mycobacterium tuberculosis isocitrate lyases 1 and 2 are jointly required for in vivo growth and virulence | Q24544255 | ||
The embAB genes of Mycobacterium avium encode an arabinosyl transferase involved in cell wall arabinan biosynthesis that is the target for the antimycobacterial drug ethambutol | Q24603359 | ||
Biochemical differentiation of Mycobacterium tuberculosis grown in vivo and in vitro | Q24618059 | ||
A membrane protein preserves intrabacterial pH in intraphagosomal Mycobacterium tuberculosis | Q24650149 | ||
Mycolic acid synthesis: a target for ethionamide in mycobacteria? | Q24682672 | ||
Mycosin-1, a subtilisin-like serine protease of Mycobacterium tuberculosis, is cell wall-associated and expressed during infection of macrophages. | Q24793519 | ||
Mycobacterial mutants with defective control of phagosomal acidification | Q24811622 | ||
Functional analysis of molybdopterin biosynthesis in mycobacteria identifies a fused molybdopterin synthase in Mycobacterium tuberculosis | Q28486812 | ||
A stationary-phase stress-response sigma factor from Mycobacterium tuberculosis | Q28486820 | ||
Global analysis of the Mycobacterium tuberculosis Zur (FurB) regulon | Q28486821 | ||
An ABC transporter containing a forkhead-associated domain interacts with a serine-threonine protein kinase and is required for growth of Mycobacterium tuberculosis in mice | Q28486845 | ||
Individual RD1-region genes are required for export of ESAT-6/CFP-10 and for virulence of Mycobacterium tuberculosis | Q28486852 | ||
Inactivation of the antigen 85C gene profoundly affects the mycolate content and alters the permeability of the Mycobacterium tuberculosis cell envelope | Q28486853 | ||
A non-RD1 gene cluster is required for Snm secretion in Mycobacterium tuberculosis | Q28486855 | ||
Mechanism of phagolysosome biogenesis block by viable Mycobacterium tuberculosis | Q28486859 | ||
EmbR, a regulatory protein with ATPase activity, is a substrate of multiple serine/threonine kinases and phosphatase in Mycobacterium tuberculosis | Q28486867 | ||
High content phenotypic cell-based visual screen identifies Mycobacterium tuberculosis acyltrehalose-containing glycolipids involved in phagosome remodeling | Q28486868 | ||
ideR, An essential gene in mycobacterium tuberculosis: role of IdeR in iron-dependent gene expression, iron metabolism, and oxidative stress response | Q28486874 | ||
Posttranslational regulation of Mycobacterium tuberculosis extracytoplasmic-function sigma factor sigma L and roles in virulence and in global regulation of gene expression | Q28486877 | ||
Lipoprotein processing is required for virulence of Mycobacterium tuberculosis | Q28486879 | ||
The Mycobacterium tuberculosis pks2 gene encodes the synthase for the hepta- and octamethyl-branched fatty acids required for sulfolipid synthesis | Q28486880 | ||
LppX is a lipoprotein required for the translocation of phthiocerol dimycocerosates to the surface of Mycobacterium tuberculosis | Q28486885 | ||
Cloning and characterization of secretory tyrosine phosphatases of Mycobacterium tuberculosis | Q28486897 | ||
Genome-wide requirements for Mycobacterium tuberculosis adaptation and survival in macrophages | Q28486898 | ||
Multiple thioredoxin-mediated routes to detoxify hydroperoxides in Mycobacterium tuberculosis | Q28486909 | ||
Mce3R, a TetR-type transcriptional repressor, controls the expression of a regulon involved in lipid metabolism in Mycobacterium tuberculosis | Q28486926 | ||
Characterization of a Mycobacterium tuberculosis H37Rv transposon library reveals insertions in 351 ORFs and mutants with altered virulence | Q28486929 | ||
Virulence attenuation of two Mas-like polyketide synthase mutants of Mycobacterium tuberculosis | Q28486935 | ||
Protein kinase E of Mycobacterium tuberculosis has a role in the nitric oxide stress response and apoptosis in a human macrophage model of infection | Q28486937 | ||
Oxidative stress response genes in Mycobacterium tuberculosis: role of ahpC in resistance to peroxynitrite and stage-specific survival in macrophages | Q28486957 | ||
Mutation of the principal sigma factor causes loss of virulence in a strain of the Mycobacterium tuberculosis complex | Q28486968 | ||
Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase | Q28486974 | ||
A unique Mycobacterium ESX-1 protein co-secretes with CFP-10/ESAT-6 and is necessary for inhibiting phagosome maturation | Q28486984 | ||
Forkhead-associated domain-containing protein Rv0019c and polyketide-associated protein PapA5, from substrates of serine/threonine protein kinase PknB to interacting proteins of Mycobacterium tuberculosis | Q28487000 | ||
The extra cytoplasmic function sigma factor sigma(E) is essential for Mycobacterium tuberculosis virulence in mice | Q28487009 | ||
Functional analysis of the Mycobacterium tuberculosis MprAB two-component signal transduction system | Q28487011 | ||
Secreted Mycobacterium tuberculosis Rv3654c and Rv3655c proteins participate in the suppression of macrophage apoptosis | Q28487022 | ||
Serine/threonine protein kinases PknF and PknG of Mycobacterium tuberculosis: characterization and localization | Q28487028 | ||
Dissection of the heat-shock response in Mycobacterium tuberculosis using mutants and microarrays | Q28487046 | ||
Deletion of the Mycobacterium tuberculosis alpha-crystallin-like hspX gene causes increased bacterial growth in vivo | Q28487051 | ||
Secreted transcription factor controls Mycobacterium tuberculosis virulence | Q28487057 | ||
Rv3133c/dosR is a transcription factor that mediates the hypoxic response of Mycobacterium tuberculosis | Q28487067 | ||
Mycobacterial persistence requires the utilization of host cholesterol | Q28487070 | ||
Three different putative phosphate transport receptors are encoded by the Mycobacterium tuberculosis genome and are present at the surface of Mycobacterium bovis BCG | Q28487100 | ||
Mycobacterium tuberculosis WhiB3 responds to O2 and nitric oxide via its [4Fe-4S] cluster and is essential for nutrient starvation survival | Q28487104 | ||
Attenuation of Mycobacterium tuberculosis by disruption of a mas-like gene or a chalcone synthase-like gene, which causes deficiency in dimycocerosyl phthiocerol synthesis | Q28487105 | ||
Functional genomics reveals extended roles of the Mycobacterium tuberculosis stress response factor sigmaH | Q28487106 | ||
Genome-wide identification of Mycobacterium tuberculosis exported proteins with roles in intracellular growth | Q28487110 | ||
The Mycobacterium tuberculosis protein kinase K modulates activation of transcription from the promoter of mycobacterial monooxygenase operon through phosphorylation of the transcriptional regulator VirS | Q28487114 | ||
Complex lipid determines tissue-specific replication of Mycobacterium tuberculosis in mice | Q28487125 | ||
CtpV: a putative copper exporter required for full virulence of Mycobacterium tuberculosis | Q28487128 | ||
Differential expression of sigE by Mycobacterium tuberculosis during intracellular growth | Q28487158 | ||
Identification, function and structure of the mycobacterial sulfotransferase that initiates sulfolipid-1 biosynthesis | Q28487164 | ||
Phosphate starvation enhances expression of the immunodominant 38-kilodalton protein antigen of Mycobacterium tuberculosis: demonstration by immunogold electron microscopy | Q28487165 | ||
Mycobacterium tuberculosis functional network analysis by global subcellular protein profiling | Q28487173 | ||
Role of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular growth, and virulence | Q28487215 | ||
Interactions of anti-sigma factor antagonists of Mycobacterium tuberculosis in the yeast two-hybrid system | Q28487216 | ||
A mycobacterium ESX-1-secreted virulence factor with unique requirements for export | Q28487220 | ||
EmbA is an essential arabinosyltransferase in Mycobacterium tuberculosis | Q28487222 | ||
A novel mycolic acid cyclopropane synthetase is required for cording, persistence, and virulence of Mycobacterium tuberculosis | Q28487225 | ||
Deletion of kasB in Mycobacterium tuberculosis causes loss of acid-fastness and subclinical latent tuberculosis in immunocompetent mice | Q28487228 | ||
SecA2 functions in the secretion of superoxide dismutase A and in the virulence of Mycobacterium tuberculosis | Q28487244 | ||
Intra- and intermolecular domain interactions among novel two-component system proteins coded by Rv0600c, Rv0601c and Rv0602c of Mycobacterium tuberculosis | Q28487253 | ||
The functions of OmpATb, a pore-forming protein of Mycobacterium tuberculosis | Q28487254 | ||
Characterization of the Mycobacterium tuberculosis sigma factor SigM by assessment of virulence and identification of SigM-dependent genes | Q28487255 | ||
A mycobacterial extracytoplasmic function sigma factor involved in survival following stress | Q28487263 | ||
The Mycobacterium tuberculosis extracytoplasmic-function sigma factor SigL regulates polyketide synthases and secreted or membrane proteins and is required for virulence | Q28487267 | ||
Functional and structural characterization of a thiol peroxidase from Mycobacterium tuberculosis | Q28487269 | ||
Identification of a virulence gene cluster of Mycobacterium tuberculosis by signature-tagged transposon mutagenesis | Q28487304 | ||
Identification of Mycobacterium tuberculosis H37Rv integral membrane proteins by one-dimensional gel electrophoresis and liquid chromatography electrospray ionization tandem mass spectrometry | Q28487306 | ||
Cu,Zn superoxide dismutase of Mycobacterium tuberculosis contributes to survival in activated macrophages that are generating an oxidative burst | Q28487322 | ||
Transcriptional Adaptation of Mycobacterium tuberculosis within Macrophages: Insights into the Phagosomal Environment | Q28487339 | ||
The Ser/Thr protein kinase PknB is essential for sustaining mycobacterial growth | Q28487361 | ||
The mycosins of Mycobacterium tuberculosis H37Rv: a family of subtilisin-like serine proteases | Q28487363 | ||
The role of MmpL8 in sulfatide biogenesis and virulence of Mycobacterium tuberculosis | Q28487367 | ||
Evidence that mycobacterial PE_PGRS proteins are cell surface constituents that influence interactions with other cells | Q28487378 | ||
Proteomic definition of the cell wall of Mycobacterium tuberculosis | Q28487383 | ||
Mutually dependent secretion of proteins required for mycobacterial virulence. | Q28487400 | ||
C-terminal signal sequence promotes virulence factor secretion in Mycobacterium tuberculosis | Q28487404 | ||
The Mycobacterium tuberculosis protein serine/threonine kinase PknG is linked to cellular glutamate/glutamine levels and is important for growth in vivo | Q28487432 | ||
Construction and characterization of a Mycobacterium tuberculosis mutant lacking the alternate sigma factor gene, sigF. | Q28487440 | ||
The proteasome of Mycobacterium tuberculosis is required for resistance to nitric oxide | Q28487442 | ||
Mycobacterium tuberculosis Rv2224c modulates innate immune responses | Q28487461 | ||
Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling | Q28487482 | ||
Survival of pathogenic mycobacteria in macrophages is mediated through autophosphorylation of protein kinase G | Q28487492 | ||
The knockout of the lprG-Rv1410 operon produces strong attenuation of Mycobacterium tuberculosis | Q28487506 | ||
Mycobacterium tuberculosis WhiB3 maintains redox homeostasis by regulating virulence lipid anabolism to modulate macrophage response | Q28487513 | ||
Role of Mycobacterium tuberculosis Ser/Thr kinase PknF: implications in glucose transport and cell division | Q28487514 | ||
PhoY2 but not PhoY1 is the PhoU homologue involved in persisters in Mycobacterium tuberculosis | Q28487517 | ||
A two-component signal transduction system with a PAS domain-containing sensor is required for virulence of Mycobacterium tuberculosis in mice | Q28487520 | ||
Characterization of a Mycobacterium tuberculosis proteasomal ATPase homologue | Q28487523 | ||
Regulation of the Mycobacterium tuberculosis hypoxic response gene encoding α-crystallin | Q28487527 | ||
Analysis of the phthiocerol dimycocerosate locus of Mycobacterium tuberculosis. Evidence that this lipid is involved in the cell wall permeability barrier | Q28487534 | ||
MmpL8 is required for sulfolipid-1 biosynthesis and Mycobacterium tuberculosis virulence | Q28487543 | ||
The alternative sigma factor SigH regulates major components of oxidative and heat stress responses in Mycobacterium tuberculosis | Q28487558 | ||
LspA inactivation in Mycobacterium tuberculosis results in attenuation without affecting phagosome maturation arrest | Q28487560 | ||
ESAT-6 secretion-independent impact of ESX-1 genes espF and espG1 on virulence of Mycobacterium tuberculosis | Q28487574 | ||
Mycobacterium tuberculosis WhiB3 interacts with RpoV to affect host survival but is dispensable for in vivo growth. | Q28487575 | ||
Role of the major antigen of Mycobacterium tuberculosis in cell wall biogenesis | Q28487576 | ||
M. tuberculosis Ser/Thr protein kinase D phosphorylates an anti-anti-sigma factor homolog | Q28487585 | ||
MprAB is a stress-responsive two-component system that directly regulates expression of sigma factors SigB and SigE in Mycobacterium tuberculosis | Q28487587 | ||
Unique features of the sodC-encoded superoxide dismutase from Mycobacterium tuberculosis, a fully functional copper-containing enzyme lacking zinc in the active site | Q28487595 | ||
The SecA2 secretion factor of Mycobacterium tuberculosis promotes growth in macrophages and inhibits the host immune response | Q28487596 | ||
The serine/threonine protein kinase PknI controls the growth of Mycobacterium tuberculosis upon infection | Q28487604 | ||
Expression of a gene for a porin-like protein of the OmpA family from Mycobacterium tuberculosis H37Rv | Q28487606 | ||
Control of CydB and GltA1 expression by the SenX3 RegX3 two component regulatory system of Mycobacterium tuberculosis | Q28743557 | ||
Acute infection and macrophage subversion by Mycobacterium tuberculosis require a specialized secretion system | Q28941163 | ||
The enduring hypoxic response of Mycobacterium tuberculosis | Q27302134 | ||
Crystal structure of the secreted form of antigen 85C reveals potential targets for mycobacterial drugs and vaccines | Q27621188 | ||
Structure and function of the virulence-associated high-temperature requirement A of Mycobacterium tuberculosis | Q27650603 | ||
Structural Insight into the Heme-based Redox Sensing by DosS from Mycobacterium tuberculosis | Q27654057 | ||
The Mycobacterium tuberculosis Ser/Thr Kinase Substrate Rv2175c Is a DNA-binding Protein Regulated by Phosphorylation | Q27655549 | ||
Mycobacterium tuberculosis lipoprotein LprG (Rv1411c) binds triacylated glycolipid agonists of Toll-like receptor 2 | Q27663955 | ||
Structural Insight into Serine Protease Rv3671c that Protects M. tuberculosis from Oxidative and Acidic Stress | Q27665041 | ||
Genes required for mycobacterial growth defined by high density mutagenesis | Q27976512 | ||
The capsule of Mycobacterium tuberculosis and its implications for pathogenicity | Q28143892 | ||
Elevation of Mycobacterium tuberculosis subsp. caprae Aranaz et al. 1999 to species rank as Mycobacterium caprae comb. nov., sp. nov | Q28189341 | ||
Tuberculosis in seals caused by a novel member of the Mycobacterium tuberculosis complex: Mycobacterium pinnipedii sp. nov | Q28209511 | ||
Direct extracellular interaction between the early secreted antigen ESAT-6 of Mycobacterium tuberculosis and TLR2 inhibits TLR signaling in macrophages | Q28301043 | ||
The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages | Q28343891 | ||
Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl-acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis | Q28344391 | ||
Characterization of the Mycobacterium tuberculosis H37Rv alkyl hydroperoxidase AhpC points to the importance of ionic interactions in oligomerization and activity | Q28348191 | ||
Lipid modification of the Cu,Zn superoxide dismutase from Mycobacterium tuberculosis | Q28354773 | ||
Mycobacterium tuberculosis nuoG is a virulence gene that inhibits apoptosis of infected host cells | Q28469257 | ||
Mechanistic insights into a novel exporter-importer system of Mycobacterium tuberculosis unravel its role in trafficking of iron | Q28472648 | ||
Understanding the role of PknJ in Mycobacterium tuberculosis: biochemical characterization and identification of novel substrate pyruvate kinase A | Q28474053 | ||
Mycobacterium tuberculosis ClpP1 and ClpP2 function together in protein degradation and are required for viability in vitro and during infection | Q28480875 | ||
Phthiocerol dimycocerosates of M. tuberculosis participate in macrophage invasion by inducing changes in the organization of plasma membrane lipids | Q28486207 | ||
Gene knockout reveals a novel gene cluster for the synthesis of a class of cell wall lipids unique to pathogenic mycobacteria | Q28486208 | ||
The senX3-regX3 two-component regulatory system of Mycobacterium tuberculosis is required for virulence | Q28486347 | ||
Trehalose-recycling ABC transporter LpqY-SugA-SugB-SugC is essential for virulence of Mycobacterium tuberculosis | Q28486356 | ||
Identification of a heparin-binding hemagglutinin present in mycobacteria | Q28486374 | ||
mymA operon of Mycobacterium tuberculosis: its regulation and importance in the cell envelope | Q28486399 | ||
Accelerated immunopathological response of mice infected with Mycobacterium tuberculosis disrupted in the mce1 operon negative transcriptional regulator | Q28486402 | ||
Mycobacterium tuberculosis ECF sigma factor sigC is required for lethality in mice and for the conditional expression of a defined gene set | Q28486413 | ||
Role of Mycobacterium tuberculosis copper-zinc superoxide dismutase | Q28486437 | ||
Phospholipases C are involved in the virulence of Mycobacterium tuberculosis | Q28486439 | ||
Identification of genes encoding exported Mycobacterium tuberculosis proteins using a Tn552'phoA in vitro transposition system | Q28486448 | ||
Disruption of the genes encoding antigen 85A and antigen 85B of Mycobacterium tuberculosis H37Rv: effect on growth in culture and in macrophages | Q28486461 | ||
The principal sigma factor sigA mediates enhanced growth of Mycobacterium tuberculosis in vivo | Q28486462 | ||
Mycobacteria release active membrane vesicles that modulate immune responses in a TLR2-dependent manner in mice | Q28486466 | ||
Hypervirulent mutant of Mycobacterium tuberculosis resulting from disruption of the mce1 operon | Q28486470 | ||
Differential expression of 10 sigma factor genes in Mycobacterium tuberculosis | Q28486484 | ||
Mycobacterium tuberculosis controls host innate immune activation through cyclopropane modification of a glycolipid effector molecule | Q28486490 | ||
Iron-cofactored superoxide dismutase inhibits host responses to Mycobacterium tuberculosis | Q28486531 | ||
Identification of an ABC transporter required for iron acquisition and virulence in Mycobacterium tuberculosis | Q28486535 | ||
Cloning, expression, and immunological evaluation of two putative secreted serine protease antigens of Mycobacterium tuberculosis | Q28486541 | ||
The Mycobacterium tuberculosis PhoPR two-component system regulates genes essential for virulence and complex lipid biosynthesis | Q28486552 | ||
Regulation of the alpha-crystallin gene acr2 by the MprAB two-component system of Mycobacterium tuberculosis | Q28486554 | ||
The AhpC and AhpD antioxidant defense system of Mycobacterium tuberculosis | Q28486560 | ||
Identification of a Mycobacterium tuberculosis putative classical nitroreductase gene whose expression is coregulated with that of the acr aene within macrophages, in standing versus shaking cultures, and under low oxygen conditions. | Q28486565 | ||
The stress-responsive chaperone alpha-crystallin 2 is required for pathogenesis of Mycobacterium tuberculosis | Q28486576 | ||
Cholesterol oxidase is required for virulence of Mycobacterium tuberculosis | Q28486607 | ||
Mycobacterium tuberculosis Rv1395 is a class III transcriptional regulator of the AraC family involved in cytochrome P450 regulation | Q28486629 | ||
The OtsAB pathway is essential for trehalose biosynthesis in Mycobacterium tuberculosis | Q28486637 | ||
The critical role of embC in Mycobacterium tuberculosis | Q28486638 | ||
The Mycobacterium tuberculosis ECF sigma factor sigmaE: role in global gene expression and survival in macrophages | Q28486647 | ||
The Mycobacterium tuberculosis SigD sigma factor controls the expression of ribosome-associated gene products in stationary phase and is required for full virulence | Q28486649 | ||
Expression and localization of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA | Q28486659 | ||
Molecular characterization of the mycobacterial heparin-binding hemagglutinin, a mycobacterial adhesin | Q28486660 | ||
Characterization of P55, a multidrug efflux pump in Mycobacterium bovis and Mycobacterium tuberculosis | Q28486661 | ||
PepD participates in the mycobacterial stress response mediated through MprAB and SigE | Q28486663 | ||
Identification of outer membrane proteins of Mycobacterium tuberculosis | Q28486665 | ||
Mycobacterium tuberculosis MycP1 protease plays a dual role in regulation of ESX-1 secretion and virulence | Q28486671 | ||
Regulation of central metabolism genes of Mycobacterium tuberculosis by parallel feed-forward loops controlled by sigma factor E (σ(E)) | Q28486675 | ||
Phosphorylation of the Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein reductase MabA regulates mycolic acid biosynthesis | Q28486676 | ||
Characterization of the proteasome accessory factor (paf) operon in Mycobacterium tuberculosis | Q28486680 | ||
The Mycobacterium tuberculosis sigJ gene controls sensitivity of the bacterium to hydrogen peroxide | Q28486699 | ||
Acute and persistent Mycobacterium tuberculosis infections depend on the thiol peroxidase TpX | Q28486700 | ||
ClgR regulation of chaperone and protease systems is essential for Mycobacterium tuberculosis parasitism of the macrophage | Q28486713 | ||
The Mycobacterium tuberculosis high-affinity iron importer, IrtA, contains an FAD-binding domain | Q28486714 | ||
Evidence that protein antigen b of Mycobacterium tuberculosis is involved in phosphate metabolism | Q28486720 | ||
The allele encoding the mycobacterial Erp protein affects lung disease in mice | Q28486728 | ||
The AraC family transcriptional regulator Rv1931c plays a role in the virulence of Mycobacterium tuberculosis | Q28486737 | ||
Characterization of a novel Mycobacterium bovis secreted antigen containing PGLTS repeats | Q35422779 | ||
Effects of overexpression of the alkyl hydroperoxide reductase AhpC on the virulence and isoniazid resistance of Mycobacterium tuberculosis. | Q35545605 | ||
Induction of a type 1 immune response to a recombinant antigen from Mycobacterium tuberculosis expressed in Mycobacterium vaccae | Q35547040 | ||
Mycobacterial p(1)-type ATPases mediate resistance to zinc poisoning in human macrophages | Q35564117 | ||
Attenuation of Mycobacterium tuberculosis functionally disrupted in a fatty acyl-coenzyme A synthetase gene fadD5. | Q35575740 | ||
Mycobacterium tuberculosis protein tyrosine phosphatase (PtpA) excludes host vacuolar-H+-ATPase to inhibit phagosome acidification | Q35585768 | ||
Mce2 operon mutant strain of Mycobacterium tuberculosis is attenuated in C57BL/6 mice | Q35587058 | ||
Adaptation to environmental stimuli within the host: two-component signal transduction systems of Mycobacterium tuberculosis | Q35598334 | ||
Sigma factors and global gene regulation in Mycobacterium tuberculosis | Q35648489 | ||
The antigen 85 complex: a major secretion product of Mycobacterium tuberculosis | Q35655414 | ||
Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS) | Q35656072 | ||
Persistent and dormant tubercle bacilli and latent tuberculosis | Q35672664 | ||
Mycobacterium tuberculosis inhibits neutrophil apoptosis, leading to delayed activation of naive CD4 T cells | Q35697504 | ||
EspD is critical for the virulence-mediating ESX-1 secretion system in Mycobacterium tuberculosis. | Q35739146 | ||
The Mycobacterium tuberculosis stress response factor SigH is required for bacterial burden as well as immunopathology in primate lungs. | Q35842269 | ||
Mycobacterium tuberculosis SigF regulates genes encoding cell wall-associated proteins and directly regulates the transcriptional regulatory gene phoY1. | Q35879330 | ||
The extracytoplasmic function sigma factors: role in bacterial pathogenesis | Q35890602 | ||
Enhanced priming of adaptive immunity by a proapoptotic mutant of Mycobacterium tuberculosis | Q35916152 | ||
Mutations in katG, inhA, and ahpC genes of Brazilian isoniazid-resistant isolates of Mycobacterium tuberculosis | Q35922173 | ||
Lipoproteins of Mycobacterium tuberculosis: an abundant and functionally diverse class of cell envelope components. | Q35946170 | ||
On the nature of Mycobacterium tuberculosis-latent bacilli | Q35968192 | ||
Mycobacterium tuberculosis lacking all mycolic acid cyclopropanation is viable but highly attenuated and hyperinflammatory in mice | Q36018138 | ||
Disruption of the SapM locus in Mycobacterium bovis BCG improves its protective efficacy as a vaccine against M. tuberculosis | Q36038717 | ||
Function prediction and analysis of mycobacterium tuberculosis hypothetical proteins | Q36096977 | ||
The sigma 70 family: sequence conservation and evolutionary relationships | Q36112378 | ||
Structure and function of HtrA family proteins, the key players in protein quality control | Q36155965 | ||
Functional analyses of mycobacterial lipoprotein diacylglyceryl transferase and comparative secretome analysis of a mycobacterial lgt mutant. | Q36156186 | ||
A mutant of Mycobacterium tuberculosis lacking the 19-kDa lipoprotein Rv3763 is highly attenuated in vivo but retains potent vaccinogenic properties | Q36334430 | ||
Structure/function studies of Ser/Thr and Tyr protein phosphorylation in Mycobacterium tuberculosis | Q36369654 | ||
Mycobacterium marinum Escapes from Phagosomes and Is Propelled by Actin-based Motility | Q36371846 | ||
Self-compartmentalized bacterial proteases and pathogenesis | Q36455856 | ||
Function of a mycobacterial major facilitator superfamily pump requires a membrane-associated lipoprotein | Q36483194 | ||
Site-2 proteases in prokaryotes: regulated intramembrane proteolysis expands to microbial pathogenesis | Q36491119 | ||
Disclosure of the mycobacterial outer membrane: cryo-electron tomography and vitreous sections reveal the lipid bilayer structure. | Q36499160 | ||
Mechanisms of action of isoniazid | Q29026436 | ||
Genetic requirements for mycobacterial survival during infection | Q29547599 | ||
Superoxide radical and superoxide dismutases | Q29614204 | ||
Inhibition of respiration by nitric oxide induces a Mycobacterium tuberculosis dormancy program | Q29615311 | ||
Mycobacterium tuberculosis: here today, and here tomorrow | Q29619735 | ||
Mycobacterium tuberculosis phagosome maturation arrest: selective targeting of PI3P-dependent membrane trafficking. | Q30333276 | ||
Survival mechanisms of pathogenic Mycobacterium tuberculosis H37Rv | Q30390376 | ||
Mycobacterial PE/PPE proteins at the host-pathogen interface | Q30399629 | ||
Direct visualization of the outer membrane of mycobacteria and corynebacteria in their native state | Q30483173 | ||
Virulence factors of Mycobacterium bovis | Q30690491 | ||
Staphylococcus aureus nuclease is a useful secretion reporter for mycobacteria | Q30807347 | ||
A peptide permease mutant of Mycobacterium bovis BCG resistant to the toxic peptides glutathione and S-nitrosoglutathione | Q30833352 | ||
Virulent Mycobacterium tuberculosis strains evade apoptosis of infected alveolar macrophages. | Q30836327 | ||
Cloning of the gene encoding a 22-kilodalton cell surface antigen of Mycobacterium bovis BCG and analysis of its potential for DNA vaccination against tuberculosis | Q30839888 | ||
A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT-6 secretion | Q31108583 | ||
The largest open reading frame (pks12) in the Mycobacterium tuberculosis genome is involved in pathogenesis and dimycocerosyl phthiocerol synthesis | Q31147222 | ||
Response of cultured macrophages to Mycobacterium tuberculosis, with observations on fusion of lysosomes with phagosomes | Q31154479 | ||
A Mycobacterium avium PPE gene is associated with the ability of the bacterium to grow in macrophages and virulence in mice | Q33212752 | ||
A phylogenomic analysis of the Actinomycetales mce operons | Q33275639 | ||
Impact of Mycobacterium ulcerans biofilm on transmissibility to ecological niches and Buruli ulcer pathogenesis | Q33283728 | ||
The Delta fbpA mutant derived from Mycobacterium tuberculosis H37Rv has an enhanced susceptibility to intracellular antimicrobial oxidative mechanisms, undergoes limited phagosome maturation and activates macrophages and dendritic cells | Q33318121 | ||
PhoP: a missing piece in the intricate puzzle of Mycobacterium tuberculosis virulence | Q33346189 | ||
Altered cellular infiltration and cytokine levels during early Mycobacterium tuberculosis sigC mutant infection are associated with late-stage disease attenuation and milder immunopathology in mice | Q33370232 | ||
Polar localization of virulence-related Esx-1 secretion in mycobacteria | Q33404091 | ||
mosR, a novel transcriptional regulator of hypoxia and virulence in Mycobacterium tuberculosis | Q33489282 | ||
Systematic genetic nomenclature for type VII secretion systems. | Q33513967 | ||
Mycobacterial nucleoside diphosphate kinase blocks phagosome maturation in murine RAW 264.7 macrophages | Q33526364 | ||
Proteasomes and other self-compartmentalizing proteases in prokaryotes | Q33542295 | ||
The type I NADH dehydrogenase of Mycobacterium tuberculosis counters phagosomal NOX2 activity to inhibit TNF-alpha-mediated host cell apoptosis | Q33565446 | ||
Definition of novel cell envelope associated proteins in Triton X-114 extracts of Mycobacterium tuberculosis H37Rv | Q33568121 | ||
Contrasting transcriptional responses of a virulent and an attenuated strain of Mycobacterium tuberculosis infecting macrophages | Q33604711 | ||
Mycobacterium tuberculosis modulates its cell surface via an oligopeptide permease (Opp) transport system | Q33613246 | ||
Iron acquisition and metabolism by mycobacteria | Q33635173 | ||
Virulence and immunomodulatory roles of bacterial outer membrane vesicles | Q33704480 | ||
Interactions of attenuated Mycobacterium tuberculosis phoP mutant with human macrophages | Q33707510 | ||
Exploring drug-induced alterations in gene expression in Mycobacterium tuberculosis by microarray hybridization | Q36558993 | ||
Attenuation of late-stage disease in mice infected by the Mycobacterium tuberculosis mutant lacking the SigF alternate sigma factor and identification of SigF-dependent genes by microarray analysis | Q36576348 | ||
Lipoprotein synthesis in mycobacteria | Q36745186 | ||
Mycobacterium tuberculosis prevents inflammasome activation | Q36854168 | ||
Regulation of the SigH stress response regulon by an essential protein kinase in Mycobacterium tuberculosis | Q36861908 | ||
Comparative genomics of mycobacterial proteases | Q36870333 | ||
A novel 27 kDa lipoprotein antigen from Mycobacterium bovis | Q36893922 | ||
A novel mycobacterial antigen relevant to cellular immunity belongs to a family of secreted lipoproteins | Q36894662 | ||
Mycobacterium tuberculosis and the environment within the phagosome | Q36938592 | ||
Lipid mediators in innate immunity against tuberculosis: opposing roles of PGE2 and LXA4 in the induction of macrophage death | Q36979981 | ||
Effect of Mycobacterium tuberculosis-derived sulfolipid I on human phagocytic cells | Q37000678 | ||
Acid-susceptible mutants of Mycobacterium tuberculosis share hypersusceptibility to cell wall and oxidative stress and to the host environment | Q37051339 | ||
Role of the dosR-dosS two-component regulatory system in Mycobacterium tuberculosis virulence in three animal models. | Q37099497 | ||
Protection of Mycobacterium tuberculosis from reactive oxygen species conferred by the mel2 locus impacts persistence and dissemination | Q37204436 | ||
Living on the edge: inhibition of host cell apoptosis by Mycobacterium tuberculosis | Q37225668 | ||
The DosR regulon of M. tuberculosis and antibacterial tolerance | Q37283561 | ||
igr Genes and Mycobacterium tuberculosis cholesterol metabolism | Q37302014 | ||
Mycobacterium tuberculosis evades macrophage defenses by inhibiting plasma membrane repair | Q37314284 | ||
The temporal expression profile of Mycobacterium tuberculosis infection in mice. | Q37358252 | ||
ESX/type VII secretion systems and their role in host-pathogen interaction | Q37372996 | ||
Immunoendocrine alterations during human tuberculosis as an integrated view of disease pathology | Q37391198 | ||
Macrophage apoptosis in tuberculosis | Q37405951 | ||
Functional and evolutionary genomics of Mycobacterium tuberculosis: insights from genomic deletions in 100 strains | Q37415303 | ||
Transcription regulation by the Mycobacterium tuberculosis alternative sigma factor SigD and its role in virulence | Q37513666 | ||
Role of cholesterol in Mycobacterium tuberculosis infection. | Q37563338 | ||
The sigma factors of Mycobacterium tuberculosis: regulation of the regulators. | Q37642079 | ||
Mycobacterium tuberculosis blocks crosslinking of annexin-1 and apoptotic envelope formation on infected macrophages to maintain virulence | Q37701841 | ||
Carbon metabolism of intracellular bacterial pathogens and possible links to virulence | Q37746934 | ||
Manipulation of host cell death pathways during microbial infections | Q37773686 | ||
Recent advances in deciphering the contribution of Mycobacterium tuberculosis lipids to pathogenesis | Q37844310 | ||
Mycobacterium bovis lipids: virulence and vaccines | Q37855174 | ||
The PE and PPE proteins of Mycobacterium tuberculosis. | Q37869959 | ||
The PE/PPE multigene family codes for virulence factors and is a possible source of mycobacterial antigenic variation: perhaps more? | Q37946648 | ||
The structural basis of mode of activation and functional diversity: a case study with HtrA family of serine proteases | Q37949440 | ||
Mycobacterium tuberculosis proteases and implications for new antibiotics against tuberculosis | Q37969797 | ||
The ins and outs of Mycobacterium tuberculosis protein export | Q37970858 | ||
Escape from the Phagosome: The Explanation for MHC-I Processing of Mycobacterial Antigens? | Q38008357 | ||
The sensor kinase MprB is required for Rhodococcus equi virulence | Q38342393 | ||
Cytotoxic activity of nucleoside diphosphate kinase secreted from Mycobacterium tuberculosis | Q38357800 | ||
The live Mycobacterium tuberculosis phoP mutant strain is more attenuated than BCG and confers protective immunity against tuberculosis in mice and guinea pigs | Q38444585 | ||
Deletion of two-component regulatory systems increases the virulence of Mycobacterium tuberculosis | Q39338589 | ||
Mycobacterial secretion systems ESX-1 and ESX-5 play distinct roles in host cell death and inflammasome activation | Q39466150 | ||
pknE, a serine/threonine kinase of Mycobacterium tuberculosis modulates multiple apoptotic paradigms | Q39468597 | ||
Functional domains present in the mycobacterial hemagglutinin, HBHA | Q39498129 | ||
Two nonredundant SecA homologues function in mycobacteria. | Q39505468 | ||
Knockout mutation of p27-p55 operon severely reduces replication of Mycobacterium bovis in a macrophagic cell line and survival in a mouse model of infection | Q39547879 | ||
Infection biology of a novel alpha-crystallin of Mycobacterium tuberculosis: Acr2. | Q39594119 | ||
Mycobacterium tuberculosis Rv0198c, a putative matrix metalloprotease is involved in pathogenicity | Q39610458 | ||
Effective generation of reactive oxygen species in the mycobacterial phagosome requires K+ efflux from the bacterium | Q39724194 | ||
Incorporation of Mycobacterium tuberculosis lipoarabinomannan into macrophage membrane rafts is a prerequisite for the phagosomal maturation block. | Q39758435 | ||
The heat shock response of Mycobacterium tuberculosis: linking gene expression, immunology and pathogenesis. | Q39804317 | ||
Role of stress response sigma factor SigG in Mycobacterium tuberculosis | Q40044447 | ||
The ESAT6 protein of Mycobacterium tuberculosis induces apoptosis of macrophages by activating caspase expression | Q40171434 | ||
Examination of Mycobacterium tuberculosis sigma factor mutants using low-dose aerosol infection of guinea pigs suggests a role for SigC in pathogenesis. | Q40273626 | ||
The heparin-binding haemagglutinin of M. tuberculosis is required for extrapulmonary dissemination. | Q40793082 | ||
Relationships between EEA1 binding partners and their role in endosome fusion. | Q40809294 | ||
Human T cell responses to the ESAT-6 antigen from Mycobacterium tuberculosis. | Q40825071 | ||
Oxygenated mycolic acids are necessary for virulence of Mycobacterium tuberculosis in mice | Q40875190 | ||
Protection from oxidative inactivation of the 20S proteasome by heat-shock protein 90. | Q41027019 | ||
Polar assembly and scaffolding proteins of the virulence-associated ESX-1 secretory apparatus in mycobacteria | Q41048900 | ||
Differential induction of apoptosis by virulent Mycobacterium tuberculosis in resistant and susceptible murine macrophages: role of nitric oxide and mycobacterial products | Q41098203 | ||
M. tuberculosis intramembrane protease Rip1 controls transcription through three anti-sigma factor substrates | Q41430032 | ||
An essential role for phoP in Mycobacterium tuberculosis virulence | Q41475513 | ||
Biochemistry and molecular genetics of cell-wall lipid biosynthesis in mycobacteria | Q41477575 | ||
A parallel intraphagosomal survival strategy shared by mycobacterium tuberculosis and Salmonella enterica | Q41729653 | ||
aprABC: a Mycobacterium tuberculosis complex-specific locus that modulates pH-driven adaptation to the macrophage phagosome | Q41839590 | ||
MPB70 and MPB83 as indicators of protein localization in mycobacterial cells | Q33748708 | ||
Strains of the East Asian (W/Beijing) lineage of Mycobacterium tuberculosis are DosS/DosT-DosR two-component regulatory system natural mutants | Q33769184 | ||
Contribution of the Mycobacterium tuberculosis MmpL protein family to virulence and drug resistance | Q33788015 | ||
AhpC, oxidative stress and drug resistance in Mycobacterium tuberculosis. | Q33803305 | ||
Requirement of the mymA operon for appropriate cell wall ultrastructure and persistence of Mycobacterium tuberculosis in the spleens of guinea pigs. | Q33855579 | ||
Mycobacterium tuberculosis acg gene is required for growth and virulence in vivo | Q33936614 | ||
Role of protein kinase G in growth and glutamine metabolism of Mycobacterium bovis BCG. | Q33937532 | ||
Mycobacterium tuberculosis signal transduction system required for persistent infections | Q33948032 | ||
Vaccination of mice and cattle with plasmid DNA encoding the Mycobacterium bovis antigen MPB83. | Q33956274 | ||
Role of P27 -P55 operon from Mycobacterium tuberculosis in the resistance to toxic compounds | Q33962631 | ||
Differentiation among members of the Mycobacterium tuberculosis complex by molecular and biochemical features: evidence for two pyrazinamide-susceptible subtypes of M. bovis. | Q33964915 | ||
ESAT-6 proteins: protective antigens and virulence factors? | Q33982392 | ||
The transcriptional regulatory network of Mycobacterium tuberculosis | Q33983129 | ||
Episomal expression of specific sense and antisense mRNAs in Leishmania amazonensis: modulation of gp63 level in promastigotes and their infection of macrophages in vitro | Q34002959 | ||
ESAT-6 subunit vaccination against Mycobacterium tuberculosis | Q34003301 | ||
MTSA-10, the product of the Rv3874 gene of Mycobacterium tuberculosis, elicits tuberculosis-specific, delayed-type hypersensitivity in guinea pigs | Q34003410 | ||
Comparative immune response to PE and PE_PGRS antigens of Mycobacterium tuberculosis. | Q34008969 | ||
The ATP binding cassette (ABC) transport systems of Mycobacterium tuberculosis | Q34025966 | ||
Reduced immunopathology and mortality despite tissue persistence in a Mycobacterium tuberculosis mutant lacking alternative sigma factor, SigH | Q34032570 | ||
Posttreatment reactivation of tuberculosis in mice caused by Mycobacterium tuberculosis disrupted in mce1R. | Q34047894 | ||
Functional dissection of the PE domain responsible for translocation of PE_PGRS33 across the mycobacterial cell wall | Q34081754 | ||
The stress-response factor SigH modulates the interaction between Mycobacterium tuberculosis and host phagocytes | Q34123517 | ||
Role of Mycobacterium tuberculosis pknD in the pathogenesis of central nervous system tuberculosis | Q34127301 | ||
Re-annotation of the genome sequence of Mycobacterium tuberculosis H37Rv | Q34153293 | ||
Molecular Koch's postulates applied to microbial pathogenicity | Q34164339 | ||
Mycobacterium tuberculosis pathogenesis and molecular determinants of virulence | Q34213787 | ||
Interpreting cell wall 'virulence factors' of Mycobacterium tuberculosis | Q34241218 | ||
Elucidation and chemical modulation of sulfolipid-1 biosynthesis in Mycobacterium tuberculosis | Q34242596 | ||
Identification of novel Mycobacterium tuberculosis antigens with potential as diagnostic reagents or subunit vaccine candidates by comparative genomics. | Q34257884 | ||
The secreted lipoprotein, MPT83, of Mycobacterium tuberculosis is recognized during human tuberculosis and stimulates protective immunity in mice | Q34261521 | ||
Mycobacterial lipoprotein activates autophagy via TLR2/1/CD14 and a functional vitamin D receptor signalling | Q34268455 | ||
Regulation of virulence genes in Mycobacterium tuberculosis | Q34299076 | ||
Mycobacterium bovis BCG response regulator essential for hypoxic dormancy | Q34321220 | ||
Phosphorylation of enoyl-acyl carrier protein reductase InhA impacts mycobacterial growth and survival | Q34333844 | ||
Proteasome inhibitors: from research tools to drug candidates | Q34341985 | ||
Recombinant modified vaccinia virus Ankara expressing antigen 85A boosts BCG-primed and naturally acquired antimycobacterial immunity in humans | Q34361636 | ||
Expression of Th1-mediated immunity in mouse lungs induces a Mycobacterium tuberculosis transcription pattern characteristic of nonreplicating persistence | Q34467579 | ||
Region of Difference 2 Contributes to Virulence ofMycobacterium tuberculosis | Q34484770 | ||
SigG does not control gene expression in response to DNA damage in Mycobacterium tuberculosis H37Rv. | Q34528612 | ||
In vivo persistence and protective efficacy of the bacille Calmette Guerin vaccine overexpressing the HspX latency antigen | Q34558242 | ||
Deletion of RD1 from Mycobacterium tuberculosis mimics bacille Calmette-Guérin attenuation | Q34595265 | ||
Reactive nitrogen and oxygen intermediates and bacterial defenses: unusual adaptations in Mycobacterium tuberculosis | Q34611241 | ||
The PE multigene family: a 'molecular mantra' for mycobacteria | Q34612597 | ||
Protective immunity against tuberculosis induced by vaccination with major extracellular proteins of Mycobacterium tuberculosis | Q34629227 | ||
Lipids of pathogenic Mycobacteria: contributions to virulence and host immune suppression | Q34658621 | ||
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 | Q34681342 | ||
Bacterial alkaline proteases: molecular approaches and industrial applications. | Q34694673 | ||
The HtrA-like serine protease PepD interacts with and modulates the Mycobacterium tuberculosis 35-kDa antigen outer envelope protein | Q34708329 | ||
Cholesterol is not an essential source of nutrition for Mycobacterium tuberculosis during infection | Q34740636 | ||
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 | Q34747029 | ||
Regulation of Mycobacterium tuberculosis cell envelope composition and virulence by intramembrane proteolysis | Q34770334 | ||
Rv3615c is a highly immunodominant RD1 (Region of Difference 1)-dependent secreted antigen specific for Mycobacterium tuberculosis infection. | Q34804956 | ||
Deletion of Mycobacterium tuberculosis sigma factor E results in delayed time to death with bacterial persistence in the lungs of aerosol-infected mice | Q34944794 | ||
Characterization of mycobacterial virulence genes through genetic interaction mapping | Q34984552 | ||
Oxidative stress-mediated regulation of proteasome complexes | Q34994401 | ||
The Mycobacterium tuberculosis recombinant 27-kilodalton lipoprotein induces a strong Th1-type immune response deleterious to protection | Q35011298 | ||
Prevention of phagosome-lysosome fusion in cultured macrophages by sulfatides of Mycobacterium tuberculosis | Q35012546 | ||
Lipids, apoptosis, and cross-presentation: links in the chain of host defense against Mycobacterium tuberculosis. | Q35089558 | ||
Characterization of a novel heat shock protein (Hsp22.5) involved in the pathogenesis of Mycobacterium tuberculosis | Q35096474 | ||
Structure and mapping of antigenic domains of protein antigen b, a 38,000-molecular-weight protein of Mycobacterium tuberculosis | Q35100568 | ||
Protein tyrosine phosphatase PtpA is not required for Mycobacterium tuberculosis growth in mice | Q35111162 | ||
Apoptosis is an innate defense function of macrophages against Mycobacterium tuberculosis | Q35163164 | ||
Sulfolipid deficiency does not affect the virulence of Mycobacterium tuberculosis H37Rv in mice and guinea pigs | Q35164892 | ||
Mycobacterial survival strategies in the phagosome: defence against host stresses | Q35205535 | ||
Regulation of Mycobacterium tuberculosis whiB3 in the mouse lung and macrophages. | Q35217486 | ||
The 16-kDa alpha-crystallin (Acr) protein of Mycobacterium tuberculosis is required for growth in macrophages | Q28486738 | ||
EspA acts as a critical mediator of ESX1-dependent virulence in Mycobacterium tuberculosis by affecting bacterial cell wall integrity | Q28486742 | ||
Deletion of the Mycobacterium tuberculosis pknH gene confers a higher bacillary load during the chronic phase of infection in BALB/c mice | Q28486752 | ||
Study of the role of Mce3R on the transcription of mce genes of Mycobacterium tuberculosis | Q28486755 | ||
Mycobacterium tuberculosis with disruption in genes encoding the phosphate binding proteins PstS1 and PstS2 is deficient in phosphate uptake and demonstrates reduced in vivo virulence | Q28486756 | ||
Characterization of a novel cell wall-anchored protein with carboxylesterase activity required for virulence in Mycobacterium tuberculosis | Q28486765 | ||
Attenuation of virulence by disruption of the Mycobacterium tuberculosis erp gene | Q28486769 | ||
The acid-induced operon Rv3083-Rv3089 is required for growth of Mycobacterium tuberculosis in macrophages | Q28486782 | ||
The serine/threonine kinase PknB of Mycobacterium tuberculosis phosphorylates PBPA, a penicillin-binding protein required for cell division | Q28486785 | ||
The transcriptional regulator Rv0485 modulates the expression of a pe and ppe gene pair and is required for Mycobacterium tuberculosis virulence | Q28486800 | ||
Ability of PknA, a mycobacterial eukaryotic-type serine/threonine kinase, to transphosphorylate MurD, a ligase involved in the process of peptidoglycan biosynthesis | Q28486801 | ||
PE_PGRS30 is required for the full virulence of Mycobacterium tuberculosis | Q58453157 | ||
Detection of bovine tuberculosis in herds with different disease prevalence and influence of paratuberculosis infection on PPDB and ESAT-6/CFP10 specificity | Q58827793 | ||
Protection of macaques against Mycobacterium tuberculosis infection by a subunit vaccine based on a fusion protein of antigen 85B and ESAT-6 | Q58827826 | ||
A glycolipid of hypervirulent tuberculosis strains that inhibits the innate immune response | Q59057817 | ||
M. tuberculosis and M. leprae Translocate from the Phagolysosome to the Cytosol in Myeloid Cells | Q59498046 | ||
Identification of genetic markers forMycobacterium pinnipediithrough genome analysis | Q59755056 | ||
A mechanism for the specific immunogenicity of heat shock protein-chaperoned peptides | Q60307732 | ||
Mycobacterium tuberculosis transporter MmpL7 is a potential substrate for kinase PknD | Q60315834 | ||
Transcriptional regulation of lipid homeostasis in mycobacteria | Q60336018 | ||
PPE and PE_PGRS proteins ofMycobacterium marinumare transported via the type VII secretion system ESX-5 | Q61400121 | ||
Deletion of the 19kDa antigen does not alter the protective efficacy of BCG | Q62796607 | ||
Lipoprotein antigens of Mycobacterium tuberculosis | Q67992293 | ||
A 38-kD Mycobacterium tuberculosis antigen associated with infection. Its isolation and serologic evaluation | Q69108564 | ||
An esat6 knockout mutant of Mycobacterium bovis produced by homologous recombination will contribute to the development of a live tuberculosis vaccine | Q73127165 | ||
Alternate class I MHC antigen processing is inhibited by Toll-like receptor signaling pathogen-associated molecular patterns: Mycobacterium tuberculosis 19-kDa lipoprotein, CpG DNA, and lipopolysaccharide | Q73696475 | ||
The gene encoding P27 lipoprotein and a putative antibiotic-resistance gene form an operon in Mycobacterium tuberculosis and Mycobacterium bovis | Q73718237 | ||
Granuloma-specific expression of Mycobacterium virulence proteins from the glycine-rich PE-PGRS family | Q73827310 | ||
Vaccination with the T cell antigen Mtb 8.4 protects against challenge with Mycobacterium tuberculosis | Q73850568 | ||
Pathogenic Mycobacterium tuberculosis evades apoptosis of host macrophages by release of TNF-R2, resulting in inactivation of TNF-alpha | Q77186410 | ||
Deletion of a Mycobacterium tuberculosis proteasomal ATPase homologue gene produces a slow-growing strain that persists in host tissues | Q79242686 | ||
Aggravated infection in mice co-administered with Mycobacterium tuberculosis and the 27-kDa lipoprotein | Q79825911 | ||
Evidence for complex interactions of stress-associated regulons in an mprAB deletion mutant of Mycobacterium tuberculosis | Q80019159 | ||
Gene expression profiling of human macrophages at late time of infection with Mycobacterium tuberculosis | Q80076080 | ||
Mutation in mce operons attenuates Mycobacterium tuberculosis virulence | Q81603799 | ||
Mycobacterium tuberculosis sigma factor E regulon modulates the host inflammatory response | Q81702361 | ||
A novel vaccine strategy to induce mycobacterial antigen-specific Th1 responses by utilizing the C-terminal domain of heat shock protein 70 | Q83124189 | ||
Lack of production of the 19-kDa glycolipoprotein in certain strains of Mycobacterium tuberculosis | Q42636739 | ||
PE is a functional domain responsible for protein translocation and localization on mycobacterial cell wall | Q42637560 | ||
Identification of novel intergenic repetitive units in a mycobacterial two-component system operon | Q42670475 | ||
The ESAT-6/WXG100 superfamily -- and a new Gram-positive secretion system? | Q42675010 | ||
Generation of attenuated Mycobacterium bovis strains by signature-tagged mutagenesis for discovery of novel vaccine candidates | Q42727323 | ||
PhoU is a persistence switch involved in persister formation and tolerance to multiple antibiotics and stresses in Escherichia coli | Q42748156 | ||
Identification of four novel DC-SIGN ligands on Mycobacterium bovis BCG. | Q42762312 | ||
Mycobacterial FurA is a negative regulator of catalase-peroxidase gene katG. | Q43544105 | ||
Role of KatG catalase-peroxidase in mycobacterial pathogenesis: countering the phagocyte oxidative burst | Q43597705 | ||
Mycobacterium tuberculosis 19-kDa lipoprotein promotes neutrophil activation | Q43683662 | ||
Erp, an extracellular protein family specific to mycobacteria | Q43701766 | ||
Expression of katG in Mycobacterium tuberculosis is associated with its growth and persistence in mice and guinea pigs | Q43891804 | ||
Development and application of unstable GFP variants to kinetic studies of mycobacterial gene expression | Q44462871 | ||
pckA-deficient Mycobacterium bovis BCG shows attenuated virulence in mice and in macrophages | Q44509820 | ||
Mycobacterium tuberculosis infection causes different levels of apoptosis and necrosis in human macrophages and alveolar epithelial cells. | Q44553442 | ||
Different susceptibility of two animal species infected with isogenic mutants of Mycobacterium bovis identifies phoT as having roles in tuberculosis virulence and phosphate transport | Q44643967 | ||
Delay of phagosome maturation by a mycobacterial lipid is reversed by nitric oxide | Q44676853 | ||
Mutation in the P36 gene of Mycobacterium bovis provokes attenuation of the bacillus in a mouse model | Q44678369 | ||
The Mycobacterium tuberculosis dosRS two-component system is induced by multiple stresses. | Q44944731 | ||
Production of phthiocerol dimycocerosates protects Mycobacterium tuberculosis from the cidal activity of reactive nitrogen intermediates produced by macrophages and modulates the early immune response to infection | Q45263947 | ||
Mycobacterium tuberculosis glycoproteomics based on ConA-lectin affinity capture of mannosylated proteins | Q46131996 | ||
Deciphering the genes involved in pathogenesis of Mycobacterium tuberculosis | Q46196471 | ||
Mycobacterium tuberculosis strains disrupted in mce3 and mce4 operons are attenuated in mice | Q46304350 | ||
Structure and mechanism of the alkyl hydroperoxidase AhpC, a key element of the Mycobacterium tuberculosis defense system against oxidative stress | Q46484181 | ||
Sulfolipid accumulation in Mycobacterium tuberculosis disrupted in the mce2 operon | Q46499310 | ||
The 19-kDa antigen of Mycobacterium tuberculosis is a major adhesin that binds the mannose receptor of THP-1 monocytic cells and promotes phagocytosis of mycobacteria. | Q46648912 | ||
Microbial lipopeptides stimulate dendritic cell maturation via Toll-like receptor 2. | Q46685036 | ||
Antisense RNA to ahpC, an oxidative stress defence gene involved in isoniazid resistance, indicates that AhpC of Mycobacterium bovis has virulence properties | Q46765538 | ||
Disruption of the ESX-5 system of Mycobacterium tuberculosis causes loss of PPE protein secretion, reduction of cell wall integrity and strong attenuation | Q46837987 | ||
A 12.7 kb fragment of the Mycobacterium tuberculosis genome is not present in Mycobacterium bovis | Q47969253 | ||
Disruption of response regulator gene, devR, leads to attenuation in virulence of Mycobacterium tuberculosis | Q48029780 | ||
Cloning of an M. tuberculosis DNA fragment associated with entry and survival inside cells | Q48102004 | ||
Type VII secretion--mycobacteria show the way. | Q48689947 | ||
Virulence of selected Mycobacterium tuberculosis clinical isolates in the rabbit model of meningitis is dependent on phenolic glycolipid produced by the bacilli | Q48864122 | ||
Identification, isolation and partial characterization of Mycobacterium tuberculosis glycoprotein antigens | Q50886423 | ||
Serine threonine protein kinases of mycobacterial genus: phylogeny to function. | Q52000012 | ||
Granuloma formation is required to contain bacillus growth and delay mortality in mice chronically infected with Mycobacterium tuberculosis. | Q52537202 | ||
Involvement of the fadD33 gene in the growth of Mycobacterium tuberculosis in the liver of BALB/c mice. | Q52548604 | ||
Mutation in the transcriptional regulator PhoP contributes to avirulence of Mycobacterium tuberculosis H37Ra strain. | Q52919936 | ||
Apoptosis facilitates antigen presentation to T lymphocytes through MHC-I and CD1 in tuberculosis. | Q52950441 | ||
Effect of inhA and katG on isoniazid resistance and virulence of Mycobacterium bovis. | Q54179390 | ||
Mucosal administration of Ag85B-ESAT-6 protects against infection with Mycobacterium tuberculosis and boosts prior bacillus Calmette-Guerin immunity. | Q54453283 | ||
Profiling of Mycobacterium tuberculosis gene expression during human macrophage infection: upregulation of the alternative sigma factor G, a group of transcriptional regulators, and proteins with unknown function. | Q54617450 | ||
Molecular Koch's Postulates Applied to Microbial Pathogenicity | Q55933786 | ||
Non-clinical efficacy and safety of HyVac4:IC31 vaccine administered in a BCG prime-boost regimen | Q57100109 | ||
Mycobacterial PE, PPE and ESX clusters: novel insights into the secretion of these most unusual protein families | Q57984673 | ||
Recombinant BCG exporting ESAT-6 confers enhanced protection against tuberculosis | Q57984777 | ||
The M. tuberculosis antigen 85 complex and mycolyltransferase activity | Q58040682 | ||
Overexpression of heat-shock proteins reduces survival of Mycobacterium tuberculosis in the chronic phase of infection | Q58231674 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
P433 | issue | 1 | |
P921 | main subject | Mycobacterium tuberculosis | Q130971 |
virulence factor | Q1623405 | ||
bacteria | Q10876 | ||
P304 | page(s) | 3-66 | |
P577 | publication date | 2012-10-17 | |
2013-01-01 | |||
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Virulence | Q18712614 |
P1476 | title | Virulence factors of the Mycobacterium tuberculosis complex | |
P478 | volume | 4 |
Q89494857 | A Human Lung-Associated Streptomyces sp. TR1341 Produces Various Secondary Metabolites Responsible for Virulence, Cytotoxicity and Modulation of Immune Response |
Q42146154 | A Nonsynonymous SNP Catalog of Mycobacterium tuberculosis Virulence Genes and Its Use for Detecting New Potentially Virulent Sublineages |
Q28551471 | A Web-Based Platform for Designing Vaccines against Existing and Emerging Strains of Mycobacterium tuberculosis |
Q43462665 | A general protein O-glycosylation system within the Burkholderia cepacia complex is involved in motility and virulence. |
Q36814846 | A putative nitroreductase from the DosR regulon of Mycobacterium tuberculosis induces pro-inflammatory cytokine expression via TLR2 signaling pathway |
Q41672250 | A standardized production pipeline for high profile targets from Mycobacterium tuberculosis. |
Q64068073 | Accurate Phylogenetic Relationships Among Mycobacterium bovis Strains Circulating in France Based on Whole Genome Sequencing and Single Nucleotide Polymorphism Analysis |
Q35930689 | Alleles of HLA-DRB1*04 Associated with Pulmonary Tuberculosis in Amazon Brazilian Population |
Q96128937 | Alveolar lipids in pulmonary disease. A review |
Q64097921 | Ample glycosylation in membrane and cell envelope proteins may explain the phenotypic diversity and virulence in the Mycobacterium tuberculosis complex |
Q37267515 | An orphaned Mce-associated membrane protein of Mycobacterium tuberculosis is a virulence factor that stabilizes Mce transporters. |
Q91413392 | Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles |
Q36296764 | Analysis of the complete genome sequence of Nocardia seriolae UTF1, the causative agent of fish nocardiosis: The first reference genome sequence of the fish pathogenic Nocardia species |
Q36314805 | Antibody response against PhoP efficiently discriminates among healthy individuals, tuberculosis patients and their contacts |
Q57179042 | Antituberculous drugs modulate bacterial phagolysosome avoidance and autophagy in Mycobacterium tuberculosis-infected macrophages |
Q93080919 | Application of Transcriptomics to Enhance Early Diagnostics of Mycobacterial Infections, with an Emphasis on Mycobacterium avium ssp. paratuberculosis |
Q37571095 | Assessment of Mycobacterium bovis deleted in p27-p55 virulence operon as candidate vaccine against tuberculosis in animal models. |
Q39114153 | Bacterial Virulence Factors: Secreted for Survival. |
Q37833917 | Bacterial genome sequencing in clinical microbiology: a pathogen-oriented review |
Q46269762 | Benefits of Genomic Insights and CRISPR-Cas Signatures to Monitor Potential Pathogens across Drinking Water Production and Distribution Systems |
Q38700240 | Biochemical Investigation of Rv3404c from Mycobacterium tuberculosis |
Q50107983 | Biological and Epidemiological Consequences of MTBC Diversity |
Q92647920 | Cell wall peptidoglycan in Mycobacterium tuberculosis: An Achilles' heel for the TB-causing pathogen |
Q36411324 | Characterization of Mycobacterium smegmatis sigF mutant and its regulon: overexpression of SigF antagonist (MSMEG_1803) in M. smegmatis mimics sigF mutant phenotype, loss of pigmentation, and sensitivity to oxidative stress |
Q63493275 | Characterization of Two New Multidrug-Resistant Strains of : Tools for Routine In Vitro Screening of Novel Anti-Mycobacterial Agents |
Q90773622 | Characterization of the two component regulatory system PhoPR in Mycobacterium bovis |
Q37282173 | Chromosomal rearrangements and protein globularity changes in Mycobacterium tuberculosis isolates from cerebrospinal fluid |
Q47770288 | Clinical Mycobacterium abscessus strain inhibits autophagy flux and promotes its growth in murine macrophages |
Q59795745 | ClpC1 N-Terminal Domain Is Dispensable for Adaptor Protein-Dependent Allosteric Regulation |
Q42105004 | Comparative Genome and Network Centrality Analysis to Identify Drug Targets of Mycobacterium tuberculosis H37Rv |
Q34454941 | Comparative functional genomics and the bovine macrophage response to strains of the mycobacterium genus |
Q64064944 | Comparative genome sequencing and analyses of Mycobacterium cosmeticum reveal potential for biodesulfization of gasoline |
Q52684866 | Comparative lipidomics of drug sensitive and resistant Mycobacterium tuberculosis reveals altered lipid imprints. |
Q34981293 | Comparative phylogenomics of pathogenic and non-pathogenic mycobacterium |
Q89620810 | Computational Identification of the Proteins Associated With Quorum Sensing and Biofilm Formation in Mycobacterium tuberculosis |
Q28078686 | Contrasting Lifestyles Within the Host Cell |
Q35609343 | Correlates between models of virulence for Mycobacterium tuberculosis among isolates of the Central Asian lineage: a case for lysozyme resistance testing? |
Q99585076 | Correlation of Conservation of Sequence and Structures of Mycobacterial Hemerythrin-like Proteins with Evolutionary Relationship and Host Pathogenicity |
Q89699826 | CtpB is a plasma membrane copper (I) transporting P-type ATPase of Mycobacterium tuberculosis |
Q28087077 | Current efforts and future prospects in the development of live mycobacteria as vaccines |
Q33558525 | Cutaneous tuberculosis: epidemiologic, etiopathogenic and clinical aspects - part I. |
Q92139769 | Cytological diagnosis in a clinically unsuspected case of disseminated BCGosis: A case report |
Q89968223 | DMN-Tre Labeling for Detection and High-Content Screening of Compounds against Intracellular Mycobacteria |
Q97092975 | DNA vaccination with the Mycobacterium marinum MMAR_4110 antigen inhibits reactivation of a latent mycobacterial infection in the adult Zebrafish |
Q33982504 | Detection of Mycobacterium tuberculosis peptides in the exosomes of patients with active and latent M. tuberculosis infection using MRM-MS |
Q36315660 | Detection of a Putative TetR-Like Gene Related to Mycobacterium bovis BCG Growth in Cholesterol Using a gfp-Transposon Mutagenesis System. |
Q50045878 | Development of Potent Inhibitors of the Mycobacterium tuberculosis Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside Macrophages |
Q89582174 | Development of a Multidimensional Proteomic Approach to Detect Circulating Immune Complexes in Cattle Experimentally Infected With Mycobacterium bovis |
Q40189124 | Differential carriage of virulence-associated loci in the New Zealand Rangipo outbreak strain of Mycobacterium tuberculosis |
Q91772570 | Differential determinants of virulence in two Mycobacterium tuberculosis Colombian clinical isolates of the LAM09 family |
Q57789186 | Disseminated tuberculosis in a cow and a dromedary bull-camel in Zamfara State in Nigeria |
Q42673180 | Diversity and evolution of drug resistance mechanisms in Mycobacterium tuberculosis |
Q98243740 | Does Mycobacterium bovis persist in cattle in a non-replicative latent state as Mycobacterium tuberculosis in human beings? |
Q37719115 | Draft Genome Sequence of Chromobacterium subtsugae MWU12-2387 Isolated from a Wild Cranberry Bog in Truro, Massachusetts. |
Q35582974 | Draft Genome Sequence of Mycobacterium tuberculosis Strain E186hv of Beijing B0/W Lineage with Reduced Virulence. |
Q90279946 | Draft Genome Sequence of a Mycobacterium porcinum Strain Isolated from a Pet Cat with Atypical Mycobacterial Panniculitis |
Q91735195 | Draft Genome Sequences of Mycobacterium tuberculosis Clinical Isolates from the Ural Region of Russia That Carry the pks15/1 Gene |
Q92479384 | Dynamic Characterization of Protein and Posttranslational Modification Levels in Mycobacterial Cholesterol Catabolism |
Q93162612 | Dynamic Remodeling of the Host Cell Membrane by Virulent Mycobacterial Sulfoglycolipid-1 |
Q90384375 | Elucidating the Efficacy of the Bacille Calmette-Guérin Vaccination in Conjunction with First Line Antibiotics and Liposomal Glutathione |
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Q36199999 | Genomic epidemiology of Lineage 4 Mycobacterium tuberculosis subpopulations in New York City and New Jersey, 1999-2009. |
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Q38161475 | HIV-Mycobacterium tuberculosis co-infection: a 'danger-couple model' of disease pathogenesis |
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Q90053719 | Immune Response to Mycobacterium tuberculosis: A Narrative Review |
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Q40596457 | Mammalian cell entry (Mce) protein of Leptospira interrogans binds extracellular matrix components, plasminogen and β2 integrin. |
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Q91744044 | Morphology-based classification of mycobacteria-infected macrophages with convolutional neural network: reveal EsxA-induced morphologic changes indistinguishable by naked eyes |
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Q54952694 | Mycobacterium tuberculosis: An Adaptable Pathogen Associated With Multiple Human Diseases. |
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