The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
about
Rapid impact of effective treatment on transmission of multidrug-resistant tuberculosisThe Oxidation-sensing Regulator (MosR) Is a New Redox-dependent Transcription Factor in Mycobacterium tuberculosisBiochemical and Structural Studies of the Mycobacterium tuberculosis O6-Methylguanine Methyltransferase and Mutated VariantsResistance to first-line anti-TB drugs is associated with reduced nitric oxide susceptibility in Mycobacterium tuberculosisMycobacterium tuberculosis Lsr2 is a global transcriptional regulator required for adaptation to changing oxygen levels and virulenceMycobacteria counteract a TLR-mediated nitrosative defense mechanism in a zebrafish infection modelCysK2 from Mycobacterium tuberculosis is an O-phospho-L-serine-dependent S-sulfocysteine synthaseTuberQ: a Mycobacterium tuberculosis protein druggability databaseMycobacterial Cultures Contain Cell Size and Density Specific Sub-populations of Cells with Significant Differential Susceptibility to Antibiotics, Oxidative and Nitrite StressAn outer membrane channel protein of Mycobacterium tuberculosis with exotoxin activity.Detection of Mycobacterium tuberculosis peptides in the exosomes of patients with active and latent M. tuberculosis infection using MRM-MSGene expression profiling of Mycobacterium avium subsp. paratuberculosis in simulated multi-stress conditions and within THP-1 cells reveals a new kind of interactive intramacrophage behaviour.Comparative analysis of mycobacterial truncated hemoglobin promoters and the groEL2 promoter in free-living and intracellular mycobacteria.Structure-function relationships of the Mycobacterium tuberculosis transcription factor WhiB1Mycobacterium tuberculosis cholesterol catabolism requires a new class of acyl coenzyme A dehydrogenase.Phagocyte NADPH oxidase, chronic granulomatous disease and mycobacterial infections.Mycobacterium smegmatis DinB2 misincorporates deoxyribonucleotides and ribonucleotides during templated synthesis and lesion bypassHigh throughput phenotypic selection of Mycobacterium tuberculosis mutants with impaired resistance to reactive oxygen species identifies genes important for intracellular growth.DNA methylation impacts gene expression and ensures hypoxic survival of Mycobacterium tuberculosis.Label-free proteomic analysis to confirm the predicted proteome of Corynebacterium pseudotuberculosis under nitrosative stress mediated by nitric oxide.Lymphangiogenesis is induced by mycobacterial granulomas via vascular endothelial growth factor receptor-3 and supports systemic T-cell responses against mycobacterial antigen.Trans-species communication in the Mycobacterium tuberculosis-infected macrophageDistinct Responses of Mycobacterium smegmatis to Exposure to Low and High Levels of Hydrogen PeroxideMetabolic modeling predicts metabolite changes in Mycobacterium tuberculosis.Strain specific transcriptional response in Mycobacterium tuberculosis infected macrophages.Comparative Genomic Analysis Reveals a Possible Novel Non-Tuberculous Mycobacterium Species with High Pathogenic Potential.SufB intein of Mycobacterium tuberculosis as a sensor for oxidative and nitrosative stresses.Functional characterization of the Mycobacterium abscessus genome coupled with condition specific transcriptomics reveals conserved molecular strategies for host adaptation and persistenceThe Mycobacterium tuberculosis transcriptional landscape under genotoxic stress.Environmental heme-based sensor proteins: implications for understanding bacterial pathogenesis.Transcriptome analysis of mycobacteria in sputum samples of pulmonary tuberculosis patientsPE11, a PE/PPE family protein of Mycobacterium tuberculosis is involved in cell wall remodeling and virulenceMycobacterium tuberculosis Zinc Metalloprotease-1 Elicits Tuberculosis-Specific Humoral Immune Response Independent of Mycobacterial Load in Pulmonary and Extra-Pulmonary Tuberculosis Patients.Insufficient Generation of Mycobactericidal Mediators and Inadequate Level of Phagosomal Maturation Are Related with Susceptibility to Virulent Mycobacterium tuberculosis Infection in Mouse Macrophages.Immune activation of the host cell induces drug tolerance in Mycobacterium tuberculosis both in vitro and in vivo.MRA_1571 is required for isoleucine biosynthesis and improves Mycobacterium tuberculosis H37Ra survival under stress.The intracellular environment of human macrophages that produce nitric oxide promotes growth of mycobacteria.Perturbation of cytochrome c maturation reveals adaptability of the respiratory chain in Mycobacterium tuberculosis.Nitrite reductase NirBD is induced and plays an important role during in vitro dormancy of Mycobacterium tuberculosisNitrite produced by Mycobacterium tuberculosis in human macrophages in physiologic oxygen impacts bacterial ATP consumption and gene expression.
P2860
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P2860
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@en
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@nl
type
label
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@en
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@nl
prefLabel
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@en
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@nl
P2093
P2860
P356
P1476
The response of mycobacterium tuberculosis to reactive oxygen and nitrogen species
@en
P2093
Gary K Schoolnik
Iona L Bartek
Kevin Visconti
Martin I Voskuil
P2860
P356
10.3389/FMICB.2011.00105
P577
2011-05-13T00:00:00Z