Mycobacterium tuberculosis WhiB3 interacts with RpoV to affect host survival but is dispensable for in vivo growth.
about
The individual and common repertoire of DNA-binding transcriptional regulators of Corynebacterium glutamicum, Corynebacterium efficiens, Corynebacterium diphtheriae and Corynebacterium jeikeium deduced from the complete genome sequences.Dissecting transcription regulatory pathways through a new bacterial one-hybrid reporter systemGenome plasticity of BCG and impact on vaccine efficacyGenomics of Actinobacteria: tracing the evolutionary history of an ancient phylumThe emerging role of gasotransmitters in the pathogenesis of tuberculosisRedox homeostasis in mycobacteria: the key to tuberculosis control?Bacterial iron-sulfur cluster sensors in mammalian pathogensDissecting virulence pathways of Mycobacterium tuberculosis through protein-protein association.Mycobacterium tuberculosis Transcription Machinery: Ready To Respond to Host AttacksTranscriptional regulation of bacterial virulence gene expression by molecular oxygen and nitric oxideAncestral antibiotic resistance in Mycobacterium tuberculosisA partner for the resuscitation-promoting factors of Mycobacterium tuberculosisMolecular function of WhiB4/Rv3681c of Mycobacterium tuberculosis H37Rv: a [4Fe-4S] cluster co-ordinating protein disulphide reductaseMycobacterium tuberculosis Rv1395 is a class III transcriptional regulator of the AraC family involved in cytochrome P450 regulationTrans-cyclopropanation of mycolic acids on trehalose dimycolate suppresses Mycobacterium tuberculosis -induced inflammation and virulenceMycobacterium tuberculosis MycP1 protease plays a dual role in regulation of ESX-1 secretion and virulenceThe AraC family transcriptional regulator Rv1931c plays a role in the virulence of Mycobacterium tuberculosisRedox biology of Mycobacterium tuberculosis H37Rv: protein-protein interaction between GlgB and WhiB1 involves exchange of thiol-disulfideThe transcriptional regulator Rv0485 modulates the expression of a pe and ppe gene pair and is required for Mycobacterium tuberculosis virulenceActivation of the eis gene in a W-Beijing strain of Mycobacterium tuberculosis correlates with increased SigA levels and enhanced intracellular growthDeletion of the Mycobacterium tuberculosis alpha-crystallin-like hspX gene causes increased bacterial growth in vivoMycobacterium tuberculosis WhiB3 responds to O2 and nitric oxide via its [4Fe-4S] cluster and is essential for nutrient starvation survivalMycobacterium tuberculosis WhiB1 is an essential DNA-binding protein with a nitric oxide-sensitive iron-sulfur clusterMycobacterium tuberculosis WhiB3 maintains redox homeostasis by regulating virulence lipid anabolism to modulate macrophage responsePriming with a recombinant pantothenate auxotroph of Mycobacterium bovis BCG and boosting with MVA elicits HIV-1 Gag specific CD8+ T cellsComputational analysis of the ESX-1 region of Mycobacterium tuberculosis: insights into the mechanism of type VII secretion systemAcute infection and macrophage subversion by Mycobacterium tuberculosis require a specialized secretion systemThe mycobacterial antibiotic resistance determinant WhiB7 acts as a transcriptional activator by binding the primary sigma factor SigA (RpoV).Characterization of [4Fe-4S]-containing and cluster-free forms of Streptomyces WhiD.The lta4h locus modulates susceptibility to mycobacterial infection in zebrafish and humansNovel genome polymorphisms in BCG vaccine strains and impact on efficacy.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.Mycobacterium tuberculosis modulates its cell surface via an oligopeptide permease (Opp) transport system.Interaction and modulation of two antagonistic cell wall enzymes of mycobacteria.Mycobacterium tuberculosis arrests host cycle at the G1/S transition to establish long term infectionDesigner arrays for defined mutant analysis to detect genes essential for survival of Mycobacterium tuberculosis in mouse lungsresponses of mycobacterium tuberculosis to growth in the mouse lungRole of protein kinase G in growth and glutamine metabolism of Mycobacterium bovis BCG.Reduced immunopathology and mortality despite tissue persistence in a Mycobacterium tuberculosis mutant lacking alternative sigma factor, SigHMycobacterium tuberculosis pathogenesis and molecular determinants of virulence
P2860
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P2860
Mycobacterium tuberculosis WhiB3 interacts with RpoV to affect host survival but is dispensable for in vivo growth.
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Mycobacterium tuberculosis Whi ...... dispensable for in vivo growth
@nl
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@ast
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@en
type
label
Mycobacterium tuberculosis Whi ...... dispensable for in vivo growth
@nl
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@ast
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@en
prefLabel
Mycobacterium tuberculosis Whi ...... dispensable for in vivo growth
@nl
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@ast
Mycobacterium tuberculosis Whi ...... ispensable for in vivo growth.
@en
P2093
P2860
P356
P1476
Mycobacterium tuberculosis Whi ...... dispensable for in vivo growth
@en
P2093
Barry R Bloom
Desmond M Collins
Mary K Hondalus
R Pamela Kawakami
P2860
P304
P356
10.1073/PNAS.052705399
P407
P577
2002-03-01T00:00:00Z