The genetic requirements for fast and slow growth in mycobacteria
about
Comprehensive functional analysis of Mycobacterium tuberculosis toxin-antitoxin systems: implications for pathogenesis, stress responses, and evolutionThe application of tetracyclineregulated gene expression systems in the validation of novel drug targets in Mycobacterium tuberculosisInterplay between gene expression noise and regulatory network architectureMycobacterium tuberculosisRpfE crystal structure reveals a positively charged catalytic cleftCrystal structure of hexanoyl-CoA bound to β-ketoacyl reductase FabG4 of Mycobacterium tuberculosis¹³C metabolic flux analysis identifies an unusual route for pyruvate dissimilation in mycobacteria which requires isocitrate lyase and carbon dioxide fixationThe essential mycobacterial genes, fabG1 and fabG4, encode 3-oxoacyl-thioester reductases that are functional in yeast mitochondrial fatty acid synthase type 2In vitro characterization of the anti-bacterial activity of SQ109 against Helicobacter pyloriSuccinate dehydrogenase is the regulator of respiration in Mycobacterium tuberculosisMycobacterium tuberculosis Is Resistant to Isoniazid at a Slow Growth Rate by Single Nucleotide Polymorphisms in katG Codon Ser315Mycobacterium tuberculosis Type II Toxin-Antitoxin Systems: Genetic Polymorphisms and Functional Properties and the Possibility of Their Use for GenotypingApplications of genome-scale metabolic reconstructions.Metabolic Perspectives on PersistenceA Hidden Markov Model for identifying essential and growth-defect regions in bacterial genomes from transposon insertion sequencing data.Unique flexibility in energy metabolism allows mycobacteria to combat starvation and hypoxia.Comparative genomics of cell envelope components in mycobacteria.Posttreatment reactivation of tuberculosis in mice caused by Mycobacterium tuberculosis disrupted in mce1R.A VapBC toxin-antitoxin module is a posttranscriptional regulator of metabolic flux in mycobacteria.Mycobacterium tuberculosis protein kinase K confers survival advantage during early infection in mice and regulates growth in culture and during persistent infection: implications for immune modulation.MazF6 toxin of Mycobacterium tuberculosis demonstrates antitoxin specificity and is coupled to regulation of cell growth by a Soj-like protein.Mycobacterium tuberculosis pellicles express unique proteins recognized by the host humoral response.Mycobacterium tuberculosis WhiB3: a novel iron-sulfur cluster protein that regulates redox homeostasis and virulence.Phylogenomic exploration of the relationships between strains of Mycobacterium avium subspecies paratuberculosisTwo enzymes with redundant fructose bisphosphatase activity sustain gluconeogenesis and virulence in Mycobacterium tuberculosis.The effect of growth rate on pyrazinamide activity in Mycobacterium tuberculosis - insights for early bactericidal activity?Genomic epidemiology of Lineage 4 Mycobacterium tuberculosis subpopulations in New York City and New Jersey, 1999-2009.A Flow Cytometry Method for Rapidly Assessing Mycobacterium tuberculosis Responses to Antibiotics with Different Modes of ActionCytosolic Proteome Profiling of Aminoglycosides Resistant Mycobacterium tuberculosis Clinical Isolates Using MALDI-TOF/MSDiverse drug-resistant subpopulations of Mycobacterium tuberculosis are sustained in continuous culture.Genomic reconnaissance of clinical isolates of emerging human pathogen Mycobacterium abscessus reveals high evolutionary potential.System-level strategies for studying the metabolism of Mycobacterium tuberculosis.In vitro and in vivo fitness costs associated with Mycobacterium tuberculosis RpoB mutation H526D.Assessing essentiality of transketolase in Mycobacterium tuberculosis using an inducible protein degradation system.Mycobacterium tuberculosis Mce1 protein complex initiates rapid induction of transcription of genes involved in substrate trafficking.Toxin-antitoxin systems of Mycobacterium smegmatis are essential for cell survival.Crystallization and preliminary X-ray diffraction analysis of the high molecular weight ketoacyl reductase FabG4 complexed with NADH.A rhodanine agent active against non-replicating intracellular Mycobacterium avium subspecies paratuberculosis.Design, synthesis and characterization of novel inhibitors against mycobacterial β-ketoacyl CoA reductase FabG4.Modelling of mycobacterial load reveals bedaquiline's exposure-response relationship in patients with drug-resistant TB.Application of Continuous Culture for Assessing Antibiotic Activity Against Mycobacterium tuberculosis.
P2860
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P2860
The genetic requirements for fast and slow growth in mycobacteria
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
The genetic requirements for fast and slow growth in mycobacteria
@ast
The genetic requirements for fast and slow growth in mycobacteria
@en
type
label
The genetic requirements for fast and slow growth in mycobacteria
@ast
The genetic requirements for fast and slow growth in mycobacteria
@en
prefLabel
The genetic requirements for fast and slow growth in mycobacteria
@ast
The genetic requirements for fast and slow growth in mycobacteria
@en
P2860
P50
P1433
P1476
The genetic requirements for fast and slow growth in mycobacteria
@en
P2093
Bhushan Bonde
Dany J V Beste
P2860
P356
10.1371/JOURNAL.PONE.0005349
P407
P577
2009-04-28T00:00:00Z