Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
about
SigmaE-dependent small RNAs of Salmonella respond to membrane stress by accelerating global omp mRNA decayMechanism to control the cell lysis and the cell survival strategy in stationary phase under heat stressStress relief during host infection: The phage shock protein response supports bacterial virulence in various waysAnalysis of bacterial biofilms using NMR-based metabolomicsAn intimate link: two-component signal transduction systems and metal transport systems in bacteriaThe crystal structureEscherichia coliSpyStructural Basis for Two-component System Inhibition and Pilus Sensing by the Auxiliary CpxP ProteinThe crystal structure of the periplasmic domain ofVibrio parahaemolyticusCpxAThe cell membrane as a major site of damage during aerosolization of Escherichia coliSimilarities between exogenously- and endogenously-induced envelope stress: the effects of a new antibacterial molecule, TPI1609-10MexCD-OprJ multidrug efflux system of Pseudomonas aeruginosa: involvement in chlorhexidine resistance and induction by membrane-damaging agents dependent upon the AlgU stress response sigma factorInvestigation into the physiologies of Aeromonas veronii in vitro and inside the digestive tract of the medicinal leech using RNA-seqProtease homolog BepA (YfgC) promotes assembly and degradation of β-barrel membrane proteins in Escherichia coli.Chlamydia trachomatis responds to heat shock, penicillin induced persistence, and IFN-gamma persistence by altering levels of the extracytoplasmic stress response protease HtrA.Loss of FlhE in the flagellar Type III secretion system allows proton influx into Salmonella and Escherichia coli.A Tale of Transmission: Aeromonas veronii Activity within Leech-Exuded Mucus.The extracytoplasmic stress factor, sigmaE, is required to maintain cell envelope integrity in Escherichia coli.Global analysis of extracytoplasmic stress signaling in Escherichia coli.Tuning the properties of the bacterial membrane with aminoacylated phosphatidylglycerol.The transcriptome of the nosocomial pathogen Enterococcus faecalis V583 reveals adaptive responses to growth in blood.Comparative genomic analysis of pathogenic and probiotic Enterococcus faecalis isolates, and their transcriptional responses to growth in human urineThe Pseudomonas aeruginosa AlgZR two-component system coordinates multiple phenotypes.The Potential Link between Thermal Resistance and Virulence in Salmonella: A Review.Effect of NlpE overproduction on multidrug resistance in Escherichia coli.Characterization of UDP-glucose dehydrogenase and UDP-glucose pyrophosphorylase mutants of Proteus mirabilis: defectiveness in polymyxin B resistance, swarming, and virulence.From qualitative data to quantitative models: analysis of the phage shock protein stress response in Escherichia coli.Small heat-shock protein HspL is induced by VirB protein(s) and promotes VirB/D4-mediated DNA transfer in Agrobacterium tumefaciens.Novel inducers of the envelope stress response BaeSR in Salmonella Typhimurium: BaeR is critically required for tungstate waste disposalRegulation of the expression of the Vibrio parahaemolyticus peuA gene encoding an alternative ferric enterobactin receptorActivation of the CpxRA system by deletion of cpxA impairs the ability of Haemophilus ducreyi to infect humansProduction of outer membrane vesicles by the plague pathogen Yersinia pestisThe phage shock protein PspA facilitates divalent metal transport and is required for virulence of Salmonella enterica sv. Typhimurium.The AfaR small RNA controls expression of the AfaD-VIII invasin in pathogenic Escherichia coli strains.sigE facilitates the adaptation of Bordetella bronchiseptica to stress conditions and lethal infection in immunocompromised miceInteractions of the CpxA sensor kinase and cognate CpxR response regulator from Yersinia pseudotuberculosis.Insights into the extracytoplasmic stress response of Xanthomonas campestris pv. campestris: role and regulation of {sigma}E-dependent activity.A linkage between SmeIJK efflux pump, cell envelope integrity, and σE-mediated envelope stress response in Stenotrophomonas maltophilia.Genome-scale identification of resistance functions in Pseudomonas aeruginosa using Tn-seq.The Bacillus subtilis sigma(M) regulon and its contribution to cell envelope stress responsesThe evolution of the phage shock protein response system: interplay between protein function, genomic organization, and system function.
P2860
Q24669800-5B8C3D91-02E9-4B43-851E-2816CC497E45Q26778679-EB399705-4241-47A4-B6F4-990EFFC9AE58Q26823890-5DA98521-2FCE-41B7-A222-D59EFCEF1FCFQ26851303-9426F0FB-DE3D-4431-9D59-1B7EA46037CAQ26859829-6DEBAAD6-D5E9-4188-93BE-EE8BFE3A5980Q27664199-5847CFAC-0017-4BE7-A491-9E8EF66A9C68Q27666591-A3C4AB95-5F11-4C03-9CB9-533AD5A616C3Q27670628-A32FDF75-8C46-4CB2-8EBF-25B285DED89FQ28385951-06C10B65-9308-40E9-AE79-67D8AD8359B4Q28484374-90FB1AE7-609E-41F4-B0E3-E207FE64BD0DQ28492463-EF20C875-B624-45A4-947D-1C5220B0A838Q28688452-D574CF99-0C84-4A60-AABB-4C42FCA991C1Q30153518-7FCC2837-DDA7-43E5-A32A-CBFE00BD49B4Q30484662-31862FCC-E757-4EC6-A7FA-A186F005059BQ30513626-FCB29EDD-DA34-487F-8539-C44F657D3AEEQ30744603-70F5EC4E-C6B4-468B-854A-2A925B3D565EQ33318472-69975AA8-D084-4C04-842A-7F1EE882E006Q33504535-5E1ECADE-01F6-4F4A-B4BB-56CD80D800DCQ33507347-E47DF45F-2D74-423B-98CA-366250E71B52Q33514863-1697B63E-3500-4013-AE32-46889F34C013Q33687310-1AE3021C-D233-49E9-B81B-0268AFFE166FQ33780971-3DF9DF4D-1CB5-49A0-A614-C8D2AB07AA49Q33794506-8B8B909A-C8FC-4405-AC5E-B7C5B8A538C1Q33826287-40CF094E-E9DA-4A93-BDDB-C4833FAB5C56Q33826394-7E2654D4-492E-46A3-B721-4B321C106E4DQ33898803-33C64635-C1F1-4457-966F-24906AC860E4Q33913149-796938EC-22C8-4C94-ACF7-E92542DDEB02Q34008904-6605B000-1078-4C9E-88AF-D9A286A02814Q34078721-684EF795-3A13-4AF1-8DB0-75F0DFC87AC5Q34119494-6035DABA-88B2-4315-A5E6-0202792CA519Q34149973-9476998C-4701-401D-A10F-57E2146D8595Q34238580-FFC1C0B6-F9AB-4F7C-9941-8D6ECA07CDBBQ34337618-0D61B28D-DBA1-476C-A6D6-F269AC202908Q34381822-0B8FFB6E-CB62-480E-952B-70BEDAB24836Q34421965-BF6EE554-3C1D-49FD-87BF-9CCBF763DE82Q34484930-29E9E151-FFC3-4B8D-BCCB-F9028DBB639FQ34497384-B3DF6840-A126-4F6D-BDEC-12C81319CC56Q34504913-3C94A907-193D-44A2-93F2-FEE4A79F08E1Q34514019-255589D4-8DC7-401D-9C3C-E957E4EF7091Q34585807-E14EDCA6-8BC7-42DF-82A7-7A57191BBAB5
P2860
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@ast
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@en
type
label
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@ast
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@en
prefLabel
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@ast
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@en
P2093
P2860
P356
P1476
Pushing the envelope: extracytoplasmic stress responses in bacterial pathogens.
@en
P2093
Gary Rowley
Mark Roberts
Michael Spector
P2860
P2888
P304
P356
10.1038/NRMICRO1394
P407
P50
P577
2006-05-01T00:00:00Z