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Mycobacterial ESX-1 secretion system mediates host cell lysis through bacterium contact-dependent gross membrane disruptions

https://doi.org/10.1073/pnas.1620133114
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1873-3468.12072openalex-snapshot
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inferredcites →https://doi.org/10.1007/978-1-60327-360-2_13openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cell.2007.05.059openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cell.2014.11.024openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.celrep.2012.06.008openalex-snapshot
An In Vivo Platform for Rapid High-Throughput Antitubercular Drug Discovery
inferredcites →https://doi.org/10.1016/j.chom.2015.05.003openalex-snapshot
Mycobacterium tuberculosis Differentially Activates cGAS- and Inflammasome-Dependent Intracellular Immune Responses through ESX-1
inferredcites →https://doi.org/10.1016/j.chom.2016.07.007openalex-snapshot
Mycobacterial Acid Tolerance Enables Phagolysosomal Survival and Establishment of Tuberculous Infection In Vivo
inferredcites →https://doi.org/10.1016/j.jmii.2014.06.002openalex-snapshot
Additive effect of recombinant Mycobacterium tuberculosis ESAT-6 protein and ESAT-6/CFP-10 fusion protein in adhesion of macrophages through fibronectin receptors
inferredcites →https://doi.org/10.1016/j.tim.2004.09.007openalex-snapshot
ESAT-6 proteins: protective antigens and virulence factors?
inferredcites →https://doi.org/10.1016/j.toxicon.2015.10.003openalex-snapshot
Mechanism of ESAT-6 membrane interaction and its roles in pathogenesis of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.tube.2004.02.002openalex-snapshot
The Mycobacterium tuberculosis complex transcriptome of attenuation
inferredcites →https://doi.org/10.1016/s0769-2609(86)80033-3openalex-snapshot
Plasmid-mediated contact haemolytic activity in Shigella species: Correlation with penetration into HeLa cells
inferredcites →https://doi.org/10.1017/s002217240001158xopenalex-snapshot
The estimation of the bactericidal power of the blood
inferredcites →https://doi.org/10.1021/pr500484wopenalex-snapshot
Correlation of Phenotypic Profiles Using Targeted Proteomics Identifies Mycobacterial Esx-1 Substrates
inferredcites →https://doi.org/10.1038/cddis.2014.394openalex-snapshot
Mycobacterium tuberculosis ESAT-6 is a leukocidin causing Ca2+ influx, necrosis and neutrophil extracellular trap formation
inferredcites →https://doi.org/10.1038/nm.3813openalex-snapshot
A bacterial cyclic dinucleotide activates the cytosolic surveillance pathway and mediates innate resistance to tuberculosis
inferredcites →https://doi.org/10.1038/nm859openalex-snapshot
Recombinant BCG exporting ESAT-6 confers enhanced protection against tuberculosis
inferredcites →https://doi.org/10.1038/nprot.2013.068openalex-snapshot
Evaluation of the pathogenesis and treatment of Mycobacterium marinum infection in zebrafish
inferredcites →https://doi.org/10.1038/nrmicro.2016.131openalex-snapshot
ESX secretion systems: mycobacterial evolution to counter host immunity
inferredcites →https://doi.org/10.1038/sj.emboj.7600732openalex-snapshot
Structure and function of the complex formed by the tuberculosis virulence factors CFP‐10 and ESAT‐6
inferredcites →https://doi.org/10.1038/sj.icb.7100117openalex-snapshot
Mycobacterium tuberculosis secretory proteins CFP‐10, ESAT‐6 and the CFP10:ESAT6 complex inhibit lipopolysaccharide‐induced NF‐κB transactivation by downregulation of reactive oxidative species (ROS) production
inferredcites →https://doi.org/10.1038/srep14352openalex-snapshot
Crystal structure of Streptococcus pneumoniae pneumolysin provides key insights into early steps of pore formation
inferredcites →https://doi.org/10.1038/srep16918openalex-snapshot
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inferredcites →https://doi.org/10.1038/srep23089openalex-snapshot
Mycobacterial escape from macrophage phagosomes to the cytoplasm represents an alternate adaptation mechanism
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.6031978.xopenalex-snapshot
Specific phosphatidylethanolamine dependence of Serratia marcescens cytotoxin activity
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03237.xopenalex-snapshot
Loss of RD1 contributed to the attenuation of the live tuberculosis vaccines Mycobacterium bovis BCG and Mycobacterium microti
inferredcites →https://doi.org/10.1046/j.1462-5822.2001.00105.xopenalex-snapshot
EspA filament-mediated protein translocation into red blood cells
inferredcites →https://doi.org/10.1054/tuld.1999.0220openalex-snapshot
Analysis of the proteome of Mycobacterium tuberculosis in silico
inferredcites →https://doi.org/10.1054/tuld.2000.0244openalex-snapshot
An esat6 knockout mutant of Mycobacterium bovis produced by homologous recombination will contribute to the development of a live tuberculosis vaccine
inferredcites →https://doi.org/10.1073/pnas.0504922102openalex-snapshot
Mutually dependent secretion of proteins required for mycobacterial virulence
inferredcites →https://doi.org/10.1073/pnas.071065798openalex-snapshot
Polymerization of a single protein of the pathogen Yersinia enterocolitica into needles punctures eukaryotic cells
inferredcites →https://doi.org/10.1073/pnas.1635213100openalex-snapshot
The primary mechanism of attenuation of bacillus Calmette–Guérin is a loss of secreted lytic function required for invasion of lung interstitial tissue
inferredcites →https://doi.org/10.1074/jbc.m112.420869openalex-snapshot
Mycobacterium tuberculosis ESAT-6 Exhibits a Unique Membrane-interacting Activity That Is Not Found in Its Ortholog from Non-pathogenic Mycobacterium smegmatis
inferredcites →https://doi.org/10.1074/jbc.m114.622076openalex-snapshot
Characterization of Mycobacterium tuberculosis EsxA Membrane Insertion
inferredcites →https://doi.org/10.1074/jbc.m503515200openalex-snapshot
Functional Analysis of Early Secreted Antigenic Target-6, the Dominant T-cell Antigen of Mycobacterium tuberculosis, Reveals Key Residues Involved in Secretion, Complex Formation, Virulence, and Immunogenicity
inferredcites →https://doi.org/10.1086/314640openalex-snapshot
Human T Cell Responses to the ESAT‐6 Antigen fromMycobacterium tuberculosis
inferredcites →https://doi.org/10.1086/345862openalex-snapshot
Deletion of RD1 fromMycobacterium tuberculosisMimics Bacille Calmette‐Guérin Attenuation
inferredcites →https://doi.org/10.1099/00221287-144-11-3195openalex-snapshot
A Mycobacterium tuberculosis operon encoding ESAT=6 and a novel low-molecular-mass culture filtrate protein (CFP-10)
inferredcites →https://doi.org/10.1111/febs.13408openalex-snapshot
Two distinct conformational states of Mycobacterium tuberculosis virulent factor early secreted antigenic target 6 kD a are behind the discrepancy around its biological functions
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04261.xopenalex-snapshot
A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT‐6 secretion
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06959.xopenalex-snapshot
Potential role for ESAT6 in dissemination ofM. tuberculosisvia human lung epithelial cells
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.00892.xopenalex-snapshot
The ESAT6 protein of Mycobacterium tuberculosis induces apoptosis of macrophages by activating caspase expression
inferredcites →https://doi.org/10.1111/j.1462-5822.2012.01799.xopenalex-snapshot
ESX‐1‐mediated translocation to the cytosol controls virulence of mycobacteria
inferredcites →https://doi.org/10.1111/mmi.13073openalex-snapshot
Surface hydrolysis of sphingomyelin by the outer membrane protein R v0888 supports replication of M ycobacterium tuberculosis in macrophages
inferredcites →https://doi.org/10.1111/mmi.13575openalex-snapshot
E sp C forms a filamentous structure in the cell envelope of M ycobacterium tuberculosis and impacts ESX ‐1 secretion
inferredcites →https://doi.org/10.1111/mmi.13579openalex-snapshot
D iscovery of the type VII ESX‐1 secretion needle?
inferredcites →https://doi.org/10.1126/science.1179663openalex-snapshot
Tuberculous Granuloma Induction via Interaction of a Bacterial Secreted Protein with Host Epithelium
inferredcites →https://doi.org/10.1126/science.284.5419.1520openalex-snapshot
Comparative Genomics of BCG Vaccines by Whole-Genome DNA Microarray
inferredcites →https://doi.org/10.1128/iai.00115-09openalex-snapshot
Anti-Alpha-Hemolysin Monoclonal Antibodies Mediate Protection againstStaphylococcus aureusPneumonia
inferredcites →https://doi.org/10.1128/iai.00614-08openalex-snapshot
Evidence for Pore Formation in Host Cell Membranes by ESX-1-Secreted ESAT-6 and Its Role in Mycobacterium marinum Escape from the Vacuole
inferredcites →https://doi.org/10.1128/iai.00887-06openalex-snapshot
Mycobacterium marinum Infection of Adult Zebrafish Causes Caseating Granulomatous Tuberculosis and Is Moderated by Adaptive Immunity
inferredcites →https://doi.org/10.1128/iai.59.6.1905-1910.1991openalex-snapshot
Proteins released from Mycobacterium tuberculosis during growth
inferredcites →https://doi.org/10.1128/iai.61.6.2708-2712.1993openalex-snapshot
Expression of contact-dependent cytolytic activity by Mycobacterium tuberculosis and isolation of the genomic locus that encodes the activity
inferredcites →https://doi.org/10.1128/iai.62.8.3222-3229.1994openalex-snapshot
Mycobacterium marinum persists in cultured mammalian cells in a temperature-restricted fashion
inferredcites →https://doi.org/10.1128/iai.66.7.3454-3456.1998openalex-snapshot
Delayed-Type Hypersensitivity Responses to ESAT-6 and MPT64 fromMycobacterium tuberculosisin the Guinea Pig
inferredcites →https://doi.org/10.1128/iai.74.1.88-98.2006openalex-snapshot
Dissection of ESAT-6 System 1 of Mycobacterium tuberculosis and Impact on Immunogenicity and Virulence
inferredcites →https://doi.org/10.1128/jb.00469-07openalex-snapshot
ESAT-6 from Mycobacterium tuberculosis Dissociates from Its Putative Chaperone CFP-10 under Acidic Conditions and Exhibits Membrane-Lysing Activity
inferredcites →https://doi.org/10.1128/jb.178.5.1274-1282.1996openalex-snapshot
Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis
inferredcites →https://doi.org/10.1128/jb.186.8.2487-2491.2004openalex-snapshot
Protein-Protein Interactions of Proteins from the ESAT-6 Family of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1128/jb.95.3.1153-1168.1968openalex-snapshot
Interaction of Staphylococcal α-Toxin with Artificial and Natural Membranes
inferredcites →https://doi.org/10.1165/rcmb.2016-0162ocopenalex-snapshot
Early Secretory Antigenic Target-6 Drives Matrix Metalloproteinase-10 Gene Expression and Secretion in Tuberculosis
inferredcites →https://doi.org/10.1371/journal.pbio.0020367openalex-snapshot
Tuberculous Granuloma Formation Is Enhanced by a Mycobacterium Virulence Determinant
inferredcites →https://doi.org/10.1371/journal.pone.0038488openalex-snapshot
Networked T Cell Death following Macrophage Infection by Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.ppat.0040033openalex-snapshot
Control of M. tuberculosis ESAT-6 Secretion and Specific T Cell Recognition by PhoP
inferredcites →https://doi.org/10.1371/journal.ppat.1002378openalex-snapshot
Early Secreted Antigen ESAT-6 of Mycobacterium tuberculosis Promotes Protective T Helper 17 Cell Responses in a Toll-Like Receptor-2-dependent Manner
inferredcites →https://doi.org/10.1371/journal.ppat.1002507openalex-snapshot
Phagosomal Rupture by Mycobacterium tuberculosis Results in Toxicity and Host Cell Death
inferredcites →https://doi.org/10.1590/s1517-83822013000100042openalex-snapshot
Measuring of Mycobacterium tuberculosis growth: a correlation of the optical measurements with colony forming units
inferredcites →https://doi.org/10.3389/fcimb.2012.00012openalex-snapshot
Staphylococcus aureus Hemolysins, bi-component Leukocidins, and Cytolytic Peptides: A Redundant Arsenal of Membrane-Damaging Virulence Factors?
inferredcites →https://doi.org/10.3390/toxins6031049openalex-snapshot
Identification of a Key Residue for Oligomerisation and Pore-Formation of Clostridium perfringens NetB
inferredcites →https://doi.org/10.3791/50116openalex-snapshot
Single Cell Measurements of Vacuolar Rupture Caused by Intracellular Pathogens
inferredcites →https://doi.org/10.3791/50116-vopenalex-snapshot
Single Cell Measurements of Vacuolar Rupture Caused by Intracellular Pathogens
inferredcites →https://doi.org/10.3791/51649openalex-snapshot
Establishment and Optimization of a High Throughput Setup to Study Staphylococcus epidermidis and Mycobacterium marinum Infection as a Model for Drug Discovery
inferredcites →https://doi.org/10.4049/jimmunol.0803579openalex-snapshot
ESAT-6 Inhibits Production of IFN-γ by Mycobacterium tuberculosis- Responsive Human T Cells
inferredcites →https://doi.org/10.4049/jimmunol.154.7.3359openalex-snapshot
Recall of long-lived immunity to Mycobacterium tuberculosis infection in mice.
inferredcites →https://doi.org/10.4049/jimmunol.169.8.4488openalex-snapshot
Coxiella burnetii Survival in THP-1 Monocytes Involves the Impairment of Phagosome Maturation: IFN-γ Mediates its Restoration and Bacterial Killing
inferredcites →https://doi.org/10.4269/ajtmh.2001.65.936openalex-snapshot
Rickettsial phospholipase A2 as a pathogenic mechanism in a model of cell injury by typhus and spotted fever group rickettsiae.

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4160714openalex-extracted
inferred← citeshttps://doi.org/10.1002/cyto.a.23129openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlb.3ce0520-104ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-33308-9_26openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-56905-1_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-19-3995-2_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00203-018-1519-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11024-018-9356-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11908-018-0611-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12223-018-0591-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00105-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-819985-5.00011-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-822368-0.00017-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-36518-8.00021-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.pmbts.2025.06.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119787openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bej.2019.107419openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2022.08.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2022.10.019openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2023.09.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2017.02.057openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115328openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116653openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116661openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chom.2017.09.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.coi.2023.102366openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.crstbi.2021.06.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijmm.2021.151495openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.imbio.2022.152224openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.intimp.2019.04.056openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115211openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2021.103585openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2026.116745openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102761openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jmb.2018.08.027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.meegid.2018.12.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mib.2020.01.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2018.10.030openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2022.105826openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108528openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108749openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108766openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micres.2024.128039openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2019.11.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tim.2020.01.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tube.2019.04.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tube.2019.07.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tube.2020.101959openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tube.2025.102690openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.vaccine.2021.08.030openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.vetmic.2018.06.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.yjsbx.2020.100029openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.analchem.5c08046openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.biomac.1c00554openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41396-019-0572-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41420-021-00716-5openalex-snapshot
Gasdermin D mediates host cell death but not interleukin-1β secretion in Mycobacterium tuberculosis-infected macrophages
inferred← citeshttps://doi.org/10.1038/s41467-020-16143-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41467-020-20533-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41541-025-01150-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41564-023-01354-6openalex-snapshot
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Plant roots temporarily leak iron to promote colonization by beneficial rhizobacterium
inferred← citeshttps://doi.org/10.1038/s41579-019-0273-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41579-021-00560-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-020-59932-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-020-71653-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s44319-026-00836-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/srep46666openalex-snapshot
An attenuated Mycobacterium tuberculosis clinical strain with a defect in ESX-1 secretion induces minimal host immune responses and pathology
inferred← citeshttps://doi.org/10.1073/pnas.1710167114openalex-snapshot
WhiB6 regulation of ESX-1 gene expression is controlled by a negative feedback loop in Mycobacterium marinum
inferred← citeshttps://doi.org/10.1073/pnas.1911646117openalex-snapshot
The Mycobacterium marinum ESX-1 system mediates phagosomal permeabilization and type I interferon production via separable mechanisms
inferred← citeshttps://doi.org/10.1073/pnas.2122161119openalex-snapshot
The C terminus of the mycobacterium ESX-1 secretion system substrate ESAT-6 is required for phagosomal membrane damage and virulence
inferred← citeshttps://doi.org/10.1073/pnas.2123100119openalex-snapshot
Proteo-genetic analysis reveals clear hierarchy of ESX-1 secretion in Mycobacterium marinum
inferred← citeshttps://doi.org/10.1074/jbc.ra119.012497openalex-snapshot
Nα-Acetylation of the virulence factor EsxA is required for mycobacterial cytosolic translocation and virulence
inferred← citeshttps://doi.org/10.1080/02648725.2022.2076031openalex-snapshot
The chamber of secretome in Mycobacterium tuberculosis as a potential therapeutic target
inferred← citeshttps://doi.org/10.1080/07391102.2023.2175257openalex-snapshot
A systematic computational analysis of Mycobacterium tuberculosis H37Rv and human CD34+ genomic expression reveals crucial molecular entities involved in infection progression
inferred← citeshttps://doi.org/10.1080/08830185.2025.2531828openalex-snapshot
Phagosomal escape and sabotage: The role of ESX-1 and PDIMs in Mycobacterium tuberculosis pathogenesis
inferred← citeshttps://doi.org/10.1080/10409238.2024.2411264openalex-snapshot
Mechanisms of immune evasion by Mycobacterium tuberculosis : the impact of T7SS and cell wall lipids on host defenses
inferred← citeshttps://doi.org/10.1080/19490976.2021.1959841openalex-snapshot
Molecular trafficking between bacteria determines the shape of gut microbial community
inferred← citeshttps://doi.org/10.1080/21505594.2020.1867438openalex-snapshot
Post-translational knockdown and post-secretional modification of EsxA determine contribution of EsxA membrane permeabilizing activity for mycobacterial intracellular survival
inferred← citeshttps://doi.org/10.1080/22221751.2020.1861913openalex-snapshot
Mycobacterium tuberculosis ESX-1-secreted substrate protein EspC promotes mycobacterial survival through endoplasmic reticulum stress-mediated apoptosis
inferred← citeshttps://doi.org/10.1093/femsml/uqae013openalex-snapshot
Multiple variants of the type VII secretion system in Gram-positive bacteria
inferred← citeshttps://doi.org/10.1093/femspd/ftac032openalex-snapshot
Mycobacterial response to an acidic environment: protective mechanisms
inferred← citeshttps://doi.org/10.1093/femspd/fty008openalex-snapshot
Cyclic di-AMP-mediated interaction between Mycobacterium tuberculosis ΔcnpB and macrophages implicates a novel strategy for improving BCG vaccination
inferred← citeshttps://doi.org/10.1093/femspd/fty037openalex-snapshot
Tuberculosis and the art of macrophage manipulation
inferred← citeshttps://doi.org/10.1093/femsre/fuy013openalex-snapshot
Tiny architects: biogenesis of intracellular replicative niches by bacterial pathogens
inferred← citeshttps://doi.org/10.1093/femsre/fuz006openalex-snapshot
Mycobacterium tuberculosis infection of host cells in space and time
inferred← citeshttps://doi.org/10.1093/gbe/evy145openalex-snapshot
Unexpected Genomic and Phenotypic Diversity of Mycobacterium africanum Lineage 5 Affects Drug Resistance, Protein Secretion, and Immunogenicity
inferred← citeshttps://doi.org/10.1099/mgen.0.000664openalex-snapshot
The open pan-genome architecture and virulence landscape of Mycobacterium bovis
inferred← citeshttps://doi.org/10.1099/mic.0.000896openalex-snapshot
Characterization of the hemolytic activity of Riemerella anatipestifer
inferred← citeshttps://doi.org/10.1099/mic.0.001054openalex-snapshot
Conserved and specialized functions of Type VII secretion systems in non-tuberculous mycobacteria
inferred← citeshttps://doi.org/10.1099/mic.0.001420openalex-snapshot
Interbacterial competition mediated by the type VIIb secretion system
inferred← citeshttps://doi.org/10.1101/2020.04.09.035238openalex-snapshot
Membrane Insertion of Mycobacterium tuberculosis EsxA in Cultured Lung Epithelial Cells
inferred← citeshttps://doi.org/10.1101/2020.10.13.337667openalex-snapshot
Mycobacterial surface-associated ESX-1 virulence factors play a role in mycobacterial adherence and invasion into lung epithelial cells
inferred← citeshttps://doi.org/10.1101/2021.08.01.454677openalex-snapshot
The beneficial rhizobacterium Bacillus velezensis acquires iron from roots via a type VII secretion system for colonization
inferred← citeshttps://doi.org/10.1101/2023.01.11.523669openalex-snapshot
Uptake-independent killing of macrophages by extracellular aggregates of Mycobacterium tuberculosis is ESX-1 and PDIM-dependent
inferred← citeshttps://doi.org/10.1101/2023.02.15.528779openalex-snapshot
The EspN transcription factor is an infection-dependent regulator of the ESX-1 system in M. marinum
inferred← citeshttps://doi.org/10.1101/2023.03.14.532585openalex-snapshot
An N-acetyltransferase required for EsxA N-terminal protein acetylation and virulence in Mycobacterium marinum.
inferred← citeshttps://doi.org/10.1101/2023.03.22.533734openalex-snapshot
Temporal genome-wide fitness analysis of Mycobacterium marinum during infection reveals genetic requirement for virulence and survival in amoebae and microglial cells
inferred← citeshttps://doi.org/10.1101/2023.08.16.553641openalex-snapshot
ESAT-6 undergoes self-association at phagosomal pH and an ESAT-6 specific nanobody restricts M. tuberculosis growth in macrophages
inferred← citeshttps://doi.org/10.1101/2024.01.05.574391openalex-snapshot
Macrophages drive the earliest anti-tumoral response to BCG therapy by directly killing bladder cancer through TNF signaling
inferred← citeshttps://doi.org/10.1101/2024.04.19.590309openalex-snapshot
Real-time visualization reveals Mycobacterium tuberculosis ESAT-6 disrupts phagosome via fibril-mediated vesiculation
inferred← citeshttps://doi.org/10.1101/2024.09.04.611260openalex-snapshot
Mycobacterial load and direct contact primes spacious to compact phagosome switching for egress
inferred← citeshttps://doi.org/10.1101/2025.11.04.685750openalex-snapshot
NINJ1 mediates necrosis of Mycobacterium tuberculosis infected human macrophages
inferred← citeshttps://doi.org/10.1101/2025.11.07.687260openalex-snapshot
Higher-order organization of bacterial cords and an amyloid-like matrix define the Mycobacterium tuberculosis biofilm
inferred← citeshttps://doi.org/10.1101/365411openalex-snapshot
BCG overexpressing an endogenous STING agonist provides enhanced protection against pulmonary tuberculosis
inferred← citeshttps://doi.org/10.1101/402099openalex-snapshot
Screening Mycobacterium tuberculosis secreted proteins identifies Mpt64 as eukaryotic membrane-binding virulence factor
inferred← citeshttps://doi.org/10.1101/828574openalex-snapshot
Ebselen attenuates mycobacterial virulence through inhibition of ESX-1 secretion
inferred← citeshttps://doi.org/10.1111/cmi.12726openalex-snapshot
ESX-1 and phthiocerol dimycocerosates of Mycobacterium tuberculosis act in concert to cause phagosomal rupture and host cell apoptosis
inferred← citeshttps://doi.org/10.1111/cmi.13008openalex-snapshot
Distinct Mycobacterium marinum phosphatases determine pathogen vacuole phosphoinositide pattern, phagosome maturation, and escape to the cytosol
inferred← citeshttps://doi.org/10.1111/cmi.13344openalex-snapshot
Breaching the phagosome, the case of the tuberculosis agent
inferred← citeshttps://doi.org/10.1111/febs.70084openalex-snapshot
Countering the effector functions of ESAT ‐6 protein in Mycobacterium tuberculosis: strategies for developing antimycobacterial therapeutics
inferred← citeshttps://doi.org/10.1111/imr.12902openalex-snapshot
NOD1 and NOD2 in inflammatory and infectious diseases
inferred← citeshttps://doi.org/10.1111/mmi.14680openalex-snapshot
Bacterial type VII secretion: An important player in host‐microbe and microbe‐microbe interactions
inferred← citeshttps://doi.org/10.1111/omi.12222openalex-snapshot
Whole genome sequence and phenotypic characterization of a Cbm+ serotype e strain of Streptococcus mutans
inferred← citeshttps://doi.org/10.1126/sciadv.aaz1767openalex-snapshot
A systematic approach to simultaneously evaluate safety, immunogenicity, and efficacy of novel tuberculosis vaccination strategies
inferred← citeshttps://doi.org/10.1126/sciadv.adq8158openalex-snapshot
Single-cell analysis reveals Mycobacterium tuberculosis ESX-1–mediated accumulation of permissive macrophages in infected mouse lungs
inferred← citeshttps://doi.org/10.1126/sciadv.adr6166openalex-snapshot
VPS18 contributes to phagosome membrane integrity in Mycobacterium tuberculosis –infected macrophages
inferred← citeshttps://doi.org/10.1126/scitranslmed.adw9184openalex-snapshot
Immunopeptidomics can inform the design of mRNA vaccines for the delivery of Mycobacterium tuberculosis MHC class II antigens
inferred← citeshttps://doi.org/10.1128/9781683670131.ch64openalex-snapshot
Immunology ofMycobacterium tuberculosisInfections
inferred← citeshttps://doi.org/10.1128/9781683670131.ch68openalex-snapshot
Protein Export into and across the Atypical Diderm Cell Envelope of Mycobacteria
inferred← citeshttps://doi.org/10.1128/9781683670261.ch8openalex-snapshot
Infect and Inject
inferred← citeshttps://doi.org/10.1128/aac.01310-24openalex-snapshot
Emergence of antibiotic-specific Mycobacterium tuberculosis phenotypes during prolonged treatment of mice
inferred← citeshttps://doi.org/10.1128/iai.00088-20openalex-snapshot
The ESX-1 Virulence Factors Downregulate miR-147-3p in Mycobacterium marinum-Infected Macrophages
inferred← citeshttps://doi.org/10.1128/iai.00155-23openalex-snapshot
Transcriptomic Analysis of Mycobacterial Infected Macrophages Reveals a High MOI Specific Type I IFN Signaling
inferred← citeshttps://doi.org/10.1128/iai.00289-20openalex-snapshot
Conserved ESX-1 Substrates EspE and EspF Are Virulence Factors That Regulate Gene Expression
inferred← citeshttps://doi.org/10.1128/iai.00457-19openalex-snapshot
Stenotrophomonas maltophilia Encodes a VirB/VirD4 Type IV Secretion System That Modulates Apoptosis in Human Cells and Promotes Competition against Heterologous Bacteria, Including Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/iai.00687-20openalex-snapshot
Mitochondria: Powering the Innate Immune Response to Mycobacterium tuberculosis Infection
inferred← citeshttps://doi.org/10.1128/iai.00803-18openalex-snapshot
Retention of EsxA in the Capsule-Like Layer of Mycobacterium tuberculosis Is Associated with Cytotoxicity and Is Counteracted by Lung Surfactant
inferred← citeshttps://doi.org/10.1128/jb.00047-25openalex-snapshot
Mycobacterium marinum as a model for understanding principles of mycobacterial pathogenesis
inferred← citeshttps://doi.org/10.1128/jb.00131-17openalex-snapshot
Esx Systems and the Mycobacterial Cell Envelope: What's the Connection?
inferred← citeshttps://doi.org/10.1128/jb.00271-24openalex-snapshot
The regulatory functions of ESX-1 substrates, EspE and EspF, are separable from secretion
inferred← citeshttps://doi.org/10.1128/jb.00662-19openalex-snapshot
Polarly Localized EccE 1 Is Required for ESX-1 Function and Stabilization of ESX-1 Membrane Proteins in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1128/jb.00726-17openalex-snapshot
Esx Paralogs Are Functionally Equivalent to ESX-1 Proteins but Are Dispensable for Virulence in Mycobacterium marinum
inferred← citeshttps://doi.org/10.1128/jb.00760-18openalex-snapshot
A New ESX-1 Substrate in Mycobacterium marinum That Is Required for Hemolysis but Not Host Cell Lysis
inferred← citeshttps://doi.org/10.1128/mbio.00987-23openalex-snapshot
An N-acetyltransferase required for ESAT-6 N-terminal acetylation and virulence in Mycobacterium marinum
inferred← citeshttps://doi.org/10.1128/mbio.01232-23openalex-snapshot
Phosphorylation of CFP10 modulates Mycobacterium tuberculosis virulence
inferred← citeshttps://doi.org/10.1128/mbio.01332-22openalex-snapshot
Bacterial Strain–Dependent Dissociation of Cell Recruitment and Cell-to-Cell Spread in Early M. tuberculosis Infection
inferred← citeshttps://doi.org/10.1128/mbio.01765-18openalex-snapshot
Mycobacterium tuberculosis Type VII Secretion System Effectors Differentially Impact the ESCRT Endomembrane Damage Response
inferred← citeshttps://doi.org/10.1128/mbio.02807-19openalex-snapshot
EspM Is a Conserved Transcription Factor That Regulates Gene Expression in Response to the ESX-1 System
inferred← citeshttps://doi.org/10.1128/mbio.02819-22openalex-snapshot
The ESX-1 Substrate PPE68 Has a Key Function in ESX-1-Mediated Secretion in Mycobacterium marinum
inferred← citeshttps://doi.org/10.1128/mbio.02983-20openalex-snapshot
Mycobacterium tuberculosis Toxin CpnT Is an ESX-5 Substrate and Requires Three Type VII Secretion Systems for Intracellular Secretion
inferred← citeshttps://doi.org/10.1128/mbio.03357-23openalex-snapshot
The antagonistic transcription factors, EspM and EspN, regulate the ESX-1 secretion system in M. marinum
inferred← citeshttps://doi.org/10.1128/mbio.03865-21openalex-snapshot
Augmentation of the Riboflavin-Biosynthetic Pathway Enhances Mucosa-Associated Invariant T (MAIT) Cell Activation and Diminishes Mycobacterium tuberculosis Virulence
inferred← citeshttps://doi.org/10.1128/microbiolspec.bai-0024-2019openalex-snapshot
Infect and Inject: How Mycobacterium tuberculosis Exploits Its Major Virulence-Associated Type VII Secretion System, ESX-1
inferred← citeshttps://doi.org/10.1128/microbiolspec.gpp3-0022-2018openalex-snapshot
Immunology of Mycobacterium tuberculosis Infections
inferred← citeshttps://doi.org/10.1128/microbiolspec.gpp3-0043-2018openalex-snapshot
Protein Export into and across the Atypical Diderm Cell Envelope of Mycobacteria
inferred← citeshttps://doi.org/10.1128/mmbr.00082-19openalex-snapshot
Modeling Tubercular ESX-1 Secretion Using Mycobacterium marinum
inferred← citeshttps://doi.org/10.1128/mra.00155-21openalex-snapshot
Genome Sequence of Mycobacterium abscessus Phage phiT45-1
inferred← citeshttps://doi.org/10.1128/mra.01421-20openalex-snapshot
Genome Sequence of Mycobacterium abscessus Phage phiT46-1
inferred← citeshttps://doi.org/10.1128/msphere.00354-19openalex-snapshot
Screening Mycobacterium tuberculosis Secreted Proteins Identifies Mpt64 as a Eukaryotic Membrane-Binding Bacterial Effector
inferred← citeshttps://doi.org/10.1128/msystems.01326-23openalex-snapshot
Temporal genome-wide fitness analysis of Mycobacterium marinum during infection reveals the genetic requirement for virulence and survival in amoebae and microglial cells
inferred← citeshttps://doi.org/10.1128/spectrum.00915-26openalex-snapshot
Deletion of ppe27 in Mycobacterium bovis BCG augments macrophage immune responses during infection
inferred← citeshttps://doi.org/10.1128/spectrum.03816-23openalex-snapshot
Single nucleotide variation catalog from clinical isolates mapped on tertiary and quaternary structures of ESX-1-related proteins reveals critical regions as putative Mtb therapeutic targets
inferred← citeshttps://doi.org/10.1134/s0006297925603302openalex-snapshot
Interaction of Mycobacterium tuberculosis with the Host from the Pathogen’s Perspective
inferred← citeshttps://doi.org/10.1146/annurev-micro-012420-081657openalex-snapshot
Structure and Function of the Mycobacterial Type VII Secretion Systems
inferred← citeshttps://doi.org/10.1146/annurev-pathol-042120-032916openalex-snapshot
Perspectives and Advances in the Understanding of Tuberculosis
inferred← citeshttps://doi.org/10.1152/ajpcell.00246.2022openalex-snapshot
Different modalities of host cell death and their impact on Mycobacterium tuberculosis infection
inferred← citeshttps://doi.org/10.1183/2312508x.10026118openalex-snapshot
What next? Basic research, new treatments and a patient-centred approach in controlling tuberculosis
inferred← citeshttps://doi.org/10.1186/s13567-022-01089-yopenalex-snapshot
Delineating transcriptional crosstalk between Mycobacterium avium subsp. paratuberculosis and human THP-1 cells at the early stage of infection via dual RNA-seq analysis
inferred← citeshttps://doi.org/10.1242/dmm.050693openalex-snapshot
Macrophages directly kill bladder cancer cells through TNF signaling as an early response to BCG therapy
inferred← citeshttps://doi.org/10.1242/dmm.050698openalex-snapshot
Exploring host–pathogen interactions in the Dictyostelium discoideum–Mycobacterium marinum infection model of tuberculosis
inferred← citeshttps://doi.org/10.12688/f1000research.20572.1openalex-snapshot
Mycobacterial virulence: impact on immunogenicity and vaccine research
inferred← citeshttps://doi.org/10.13028/m27m3nopenalex-snapshot
Antigen Specific CD4+ and CD8+ T Cell Recognition During Mycobacterium Tuberculosis Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0233252openalex-snapshot
Mycobacterium marinum phthiocerol dimycocerosates enhance macrophage phagosomal permeabilization and membrane damage
inferred← citeshttps://doi.org/10.1371/journal.pone.0281769openalex-snapshot
Unusual prophages in Mycobacterium abscessus genomes and strain variations in phage susceptibilities
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006363openalex-snapshot
Systematic, multiparametric analysis of Mycobacterium tuberculosis intracellular infection offers insight into coordinated virulence
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007247openalex-snapshot
EspH is a hypervirulence factor for Mycobacterium marinum and essential for the secretion of the ESX-1 substrates EspE and EspF
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007501openalex-snapshot
The ESCRT and autophagy machineries cooperate to repair ESX-1-dependent damage at the Mycobacterium-containing vacuole but have opposite impact on containing the infection
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009186openalex-snapshot
Mycobacterial infection-induced miR-206 inhibits protective neutrophil recruitment via the CXCL12/CXCR4 signalling axis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010121openalex-snapshot
A type VII secretion system in Group B Streptococcus mediates cytotoxicity and virulence
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010610openalex-snapshot
Bacterial secretion systems: Networks of pathogenic regulation and adaptation in mycobacteria and beyond
inferred← citeshttps://doi.org/10.1371/journal.ppat.1011192openalex-snapshot
Tirap controls Mycobacterium tuberculosis phagosomal acidification
inferred← citeshttps://doi.org/10.1371/journal.ppat.1011559openalex-snapshot
Druggable redox pathways against Mycobacterium abscessus in cystic fibrosis patient-derived airway organoids
inferred← citeshttps://doi.org/10.1515/hsz-2022-0350openalex-snapshot
Mycobacterial type VII secretion systems
inferred← citeshttps://doi.org/10.15252/embj.2023113490openalex-snapshot
Uptake‐independent killing of macrophages by extracellular Mycobacterium tuberculosis aggregates
inferred← citeshttps://doi.org/10.18174/464871openalex-snapshot
Semantic systems biology of prokaryotes : heterogeneous data integration to understand bacterial metabolism
inferred← citeshttps://doi.org/10.26508/lsa.202201476openalex-snapshot
OXSR1 inhibits inflammasome activation by limiting potassium efflux during mycobacterial infection
inferred← citeshttps://doi.org/10.29011/2575-789x.000144openalex-snapshot
Rv3615c-Specific CD4+ T Cells Express IL-21 To Help B Cells Produce Immunoglobulins in Tuberculosis Pleurisy
inferred← citeshttps://doi.org/10.32657/10356/180359openalex-snapshot
Use of the zebrafish model for target identification for host-directed therapies against tuberculosis
inferred← citeshttps://doi.org/10.33564/ijeast.2021.v06i06.047openalex-snapshot
A COMPREHENSIVE REVIEW ABOUT THE PATHOGENESIS AND VIRULENCE OF DIFFERENT PATHOGENS
inferred← citeshttps://doi.org/10.3389/978-2-88945-446-4openalex-snapshot
Reassessing Twenty Years of Vaccine Development Against Tuberculosis
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00529openalex-snapshot
When Dicty Met Myco, a (Not So) Romantic Story about One Amoeba and Its Intracellular Pathogen
inferred← citeshttps://doi.org/10.3389/fcimb.2020.00122openalex-snapshot
Comparative Genomic and Transcriptomic Analyses of Mycobacterium kansasii Subtypes Provide New Insights Into Their Pathogenicity and Taxonomy
inferred← citeshttps://doi.org/10.3389/fcimb.2020.00420openalex-snapshot
Phthiocerol Dimycocerosates From Mycobacterium tuberculosis Increase the Membrane Activity of Bacterial Effectors and Host Receptors
inferred← citeshttps://doi.org/10.3389/fcimb.2020.595029openalex-snapshot
Host Cell Targets of Released Lipid and Secreted Protein Effectors of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3389/fcimb.2021.629836openalex-snapshot
Mycobacterium PPE31 Contributes to Host Cell Death
inferred← citeshttps://doi.org/10.3389/fcimb.2022.862582openalex-snapshot
Mycobacterium tuberculosis Induces Irg1 in Murine Macrophages by a Pathway Involving Both TLR-2 and STING/IFNAR Signaling and Requiring Bacterial Phagocytosis
inferred← citeshttps://doi.org/10.3389/fcimb.2022.956607openalex-snapshot
Phenotypic adaptation of Mycobacterium tuberculosis to host-associated stressors that induce persister formation
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1146571openalex-snapshot
Mechanisms of lung damage in tuberculosis: implications for chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.3389/fcimb.2026.1797994openalex-snapshot
Functional analysis of type VII secretion system links to host immune evasion mechanism in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01147openalex-snapshot
The Recombinant Bacille Calmette–Guérin Vaccine VPM1002: Ready for Clinical Efficacy Testing
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01633openalex-snapshot
Type I Interferons in the Pathogenesis of Tuberculosis: Molecular Drivers and Immunological Consequences
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00806openalex-snapshot
Type I Interferons, Autophagy and Host Metabolism in Leprosy
inferred← citeshttps://doi.org/10.3389/fimmu.2018.01490openalex-snapshot
Necrosis Driven Triglyceride Synthesis Primes Macrophages for Inflammation During Mycobacterium tuberculosis Infection
inferred← citeshttps://doi.org/10.3389/fimmu.2019.00528openalex-snapshot
Mycobacterial Evolution Intersects With Host Tolerance
inferred← citeshttps://doi.org/10.3389/fimmu.2021.668060openalex-snapshot
Integrative Analysis of Human Macrophage Inflammatory Response Related to Mycobacterium tuberculosis Virulence
inferred← citeshttps://doi.org/10.3389/fimmu.2021.814709openalex-snapshot
The cGAS-STING Pathway in Bacterial Infection and Bacterial Immunity
inferred← citeshttps://doi.org/10.3389/fimmu.2022.747799openalex-snapshot
Macrophage: A Cell With Many Faces and Functions in Tuberculosis
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