An in vitro model for sequential study of shiftdown of Mycobacterium tuberculosis through two stages of nonreplicating persistence
about
Multiple M. tuberculosis phenotypes in mouse and guinea pig lung tissue revealed by a dual-staining approachComprehensive functional analysis of Mycobacterium tuberculosis toxin-antitoxin systems: implications for pathogenesis, stress responses, and evolutionCharacterization of phosphofructokinase activity in Mycobacterium tuberculosis reveals that a functional glycolytic carbon flow is necessary to limit the accumulation of toxic metabolic intermediates under hypoxiaThe role of the novel exopolyphosphatase MT0516 in Mycobacterium tuberculosis drug tolerance and persistenceMycobacterium tuberculosis septum site determining protein, Ssd encoded by rv3660c, promotes filamentation and elicits an alternative metabolic and dormancy stress responseThe combination of sulfamethoxazole, trimethoprim, and isoniazid or rifampin is bactericidal and prevents the emergence of drug resistance in Mycobacterium tuberculosisImmunotherapy for tuberculosis: future prospectsDormancy models for Mycobacterium tuberculosis: A minireviewHeterogeneity in tuberculosis pathology, microenvironments and therapeutic responsesTranslating basic science insight into public health action for multidrug- and extensively drug-resistant tuberculosisMycobacterium tuberculosis: success through dormancyA medicinal chemists' guide to the unique difficulties of lead optimization for tuberculosisRedox homeostasis in mycobacteria: the key to tuberculosis control?Innovative Strategies to Identify M. tuberculosis Antigens and Epitopes Using Genome-Wide AnalysesThe enduring hypoxic response of Mycobacterium tuberculosisGenomic and transcriptomic analysis of the streptomycin-dependent Mycobacterium tuberculosis strain 18b.Crystal structure of Mycobacterium tuberculosis LrpA, a leucine-responsive global regulator associated with starvation responseMeropenem-Clavulanate Is Effective Against Extensively Drug-Resistant Mycobacterium tuberculosisThe structure of the yeast NADH dehydrogenase (Ndi1) reveals overlapping binding sites for water- and lipid-soluble substratesGlycolytic and Non-glycolytic Functions of Mycobacterium tuberculosis Fructose-1,6-bisphosphate Aldolase, an Essential Enzyme Produced by Replicating and Non-replicating BacilliIdentification of a small molecule with activity against drug-resistant and persistent tuberculosisMycobacterium tuberculosis Transcription Machinery: Ready To Respond to Host AttacksGranulomas and Inflammation: Host-Directed Therapies for Tuberculosis.Uptake of carbon monoxide and hydrogen at environmentally relevant concentrations by mycobacteriaTuberculosis: latency and reactivationMetronidazole therapy in mice infected with tuberculosisCytological and transcript analyses reveal fat and lazy persister-like bacilli in tuberculous sputumSensitive detection of gene expression in mycobacteria under replicating and non-replicating conditions using optimized far-red reportersMycobacterium tuberculosis transcriptional adaptation, growth arrest and dormancy phenotype development is triggered by vitamin CA novel in vitro multiple-stress dormancy model for Mycobacterium tuberculosis generates a lipid-loaded, drug-tolerant, dormant pathogenInterpreting expression data with metabolic flux models: predicting Mycobacterium tuberculosis mycolic acid productionPolyphosphate kinase from M. tuberculosis: an interconnect between the genetic and biochemical roleLocation of intra- and extracellular M. tuberculosis populations in lungs of mice and guinea pigs during disease progression and after drug treatmentMetabolic regulation of mycobacterial growth and antibiotic sensitivityMycobacterium tuberculosis uses host triacylglycerol to accumulate lipid droplets and acquires a dormancy-like phenotype in lipid-loaded macrophagesDifferential producibility analysis (DPA) of transcriptomic data with metabolic networks: deconstructing the metabolic response of M. tuberculosis¹³C metabolic flux analysis identifies an unusual route for pyruvate dissimilation in mycobacteria which requires isocitrate lyase and carbon dioxide fixationDevS oxy complex stability identifies this heme protein as a gas sensor in Mycobacterium tuberculosis dormancyThe peptidoglycan of stationary-phase Mycobacterium tuberculosis predominantly contains cross-links generated by L,D-transpeptidationDosT and DevS are oxygen-switched kinases in Mycobacterium tuberculosis
P2860
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P2860
An in vitro model for sequential study of shiftdown of Mycobacterium tuberculosis through two stages of nonreplicating persistence
description
1996 nî lūn-bûn
@nan
1996 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
An in vitro model for sequenti ...... of nonreplicating persistence
@ast
An in vitro model for sequenti ...... of nonreplicating persistence
@en
An in vitro model for sequenti ...... of nonreplicating persistence
@nl
type
label
An in vitro model for sequenti ...... of nonreplicating persistence
@ast
An in vitro model for sequenti ...... of nonreplicating persistence
@en
An in vitro model for sequenti ...... of nonreplicating persistence
@nl
prefLabel
An in vitro model for sequenti ...... of nonreplicating persistence
@ast
An in vitro model for sequenti ...... of nonreplicating persistence
@en
An in vitro model for sequenti ...... of nonreplicating persistence
@nl
P2860
P3181
P1476
An in vitro model for sequenti ...... of nonreplicating persistence
@en
P2093
P2860
P304
P3181
P407
P577
1996-06-01T00:00:00Z