The 16-kDa alpha-crystallin (Acr) protein of Mycobacterium tuberculosis is required for growth in macrophages
about
Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogensDissecting transcription regulatory pathways through a new bacterial one-hybrid reporter systemThe emerging role of gasotransmitters in the pathogenesis of tuberculosisThe enduring hypoxic response of Mycobacterium tuberculosisCrystal Structure of Reduced MsAcg, a Putative Nitroreductase from Mycobacterium smegmatis and a Close Homologue of Mycobacterium tuberculosis AcgThe salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophagesMetabolic regulation of mycobacterial growth and antibiotic sensitivityThe effect of oxygenated mycolic acid composition on cell wall function and macrophage growth in Mycobacterium tuberculosisTwo sensor kinases contribute to the hypoxic response of Mycobacterium tuberculosisThe stringent response of Mycobacterium tuberculosis is required for long-term survivalDosS responds to a reduced electron transport system to induce the Mycobacterium tuberculosis DosR regulonIdentification 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.The Mycobacterium tuberculosis ECF sigma factor sigmaE: role in global gene expression and survival in macrophagesThe role of RelMtb-mediated adaptation to stationary phase in long-term persistence of Mycobacterium tuberculosis in miceFunctional similarities between the small heat shock proteins Mycobacterium tuberculosis HSP 16.3 and human alphaB-crystallinDeletion of the Mycobacterium tuberculosis alpha-crystallin-like hspX gene causes increased bacterial growth in vivoRv3133c/dosR is a transcription factor that mediates the hypoxic response of Mycobacterium tuberculosisHypoxic response of Mycobacterium tuberculosis studied by metabolic labeling and proteome analysis of cellular and extracellular proteinsMycobacterium tuberculosis genes induced during infection of human macrophagesAttenuation of and protection induced by a leucine auxotroph of Mycobacterium tuberculosisRegulation of the Mycobacterium tuberculosis hypoxic response gene encoding alpha -crystallinAn increase in expression of a Mycobacterium tuberculosis mycolyl transferase gene (fbpB) occurs early after infection of human monocytesThe Mycobacterium tuberculosis IdeR is a dual functional regulator that controls transcription of genes involved in iron acquisition, iron storage and survival in macrophagesExpression of the Mycobacterium tuberculosis acr-coregulated genes from the DevR (DosR) regulon is controlled by multiple levels of regulationDual-Reporter Mycobacteriophages (Φ2DRMs) Reveal Preexisting Mycobacterium tuberculosis Persistent Cells in Human SputumIntracellular Mycobacterium avium intersect transferrin in the Rab11(+) recycling endocytic pathway and avoid lipocalin 2 trafficking to the lysosomal pathway.Fumarate reductase activity maintains an energized membrane in anaerobic Mycobacterium tuberculosis.Whole genome identification of Mycobacterium tuberculosis vaccine candidates by comprehensive data mining and bioinformatic analysesAntagonists of Hsp16.3, a low-molecular-weight mycobacterial chaperone and virulence factor, derived from phage-displayed peptide librariesmosR, a novel transcriptional regulator of hypoxia and virulence in Mycobacterium tuberculosis.IFNgamma response to Mycobacterium tuberculosis, risk of infection and disease in household contacts of tuberculosis patients in Colombia.A blind deconvolution approach to high-resolution mapping of transcription factor binding sites from ChIP-seq data.Sputum Mycobacterium tuberculosis mRNA as a marker of bacteriologic clearance in response to antituberculosis therapy.The relA homolog of Mycobacterium smegmatis affects cell appearance, viability, and gene expressionDiametric Role of the Latency-Associated Protein Acr1 of Mycobacterium tuberculosis in Modulating the Functionality of Pre- and Post-maturational Stages of Dendritic Cells.The DosS-DosT/DosR Mycobacterial Sensor System.The development and biology of bradyzoites of Toxoplasma gondii.Mycobacterium tuberculosis acg gene is required for growth and virulence in vivo.Mycobacterium tuberculosis signal transduction system required for persistent infections.Lipid droplet-associated proteins are involved in the biosynthesis and hydrolysis of triacylglycerol in Mycobacterium bovis bacillus Calmette-Guerin.
P2860
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P2860
The 16-kDa alpha-crystallin (Acr) protein of Mycobacterium tuberculosis is required for growth in macrophages
description
1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1998
@ast
im August 1998 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1998/08/04)
@sk
vědecký článek publikovaný v roce 1998
@cs
wetenschappelijk artikel (gepubliceerd op 1998/08/04)
@nl
наукова стаття, опублікована в серпні 1998
@uk
name
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@ast
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@en
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@nl
type
label
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@ast
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@en
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@nl
prefLabel
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@ast
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@en
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@nl
P2093
P2860
P921
P3181
P356
P1476
The 16-kDa alpha-crystallin (A ...... ired for growth in macrophages
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.95.16.9578
P407
P577
1998-08-01T00:00:00Z