Silencing Mycobacterium smegmatis by using tetracycline repressors. - Wikidata - awgldk - TriplyDB

Silencing Mycobacterium smegmatis by using tetracycline repressors.

Silencing Mycobacterium smegmatis by using tetracycline repressors.

http://www.wikidata.org/entity/Q35879464

about

The application of tetracyclineregulated gene expression systems in the validation of novel drug targets in Mycobacterium tuberculosis Sensitive detection of gene expression in mycobacteria under replicating and non-replicating conditions using optimized far-red reporters Optimisation of bioluminescent reporters for use with mycobacteria Simultaneous analysis of multiple Mycobacterium tuberculosis knockdown mutants in vitro and in vivo MspA nanopores from subunit dimers CarD is an essential regulator of rRNA transcription required for Mycobacterium tuberculosis persistence Three Mycobacterium tuberculosis Rel toxin-antitoxin modules inhibit mycobacterial growth and are expressed in infected human macrophages Inhibition of mycolic acid transport across the Mycobacterium tuberculosis plasma membrane ATPase activity of Mycobacterium tuberculosis SecA1 and SecA2 proteins and its importance for SecA2 function in macrophages In vivo gene silencing identifies the Mycobacterium tuberculosis proteasome as essential for the bacteria to persist in mice Recombinant Mycobacterium bovis BCG as an HIV vaccine vector.To catch a killer. What can mycobacterial models teach us about Mycobacterium tuberculosis pathogenesis?Conditional gene expression in Mycobacterium abscessus.A new in vivo model to test anti-tuberculosis drugs using fluorescence imaging.Pathway-selective sensitization of Mycobacterium tuberculosis for target-based whole-cell screening Regulated Expression Systems for Mycobacteria and Their Applications The HtrA-like serine protease PepD interacts with and modulates the Mycobacterium tuberculosis 35-kDa antigen outer envelope protein.Protein inactivation in mycobacteria by controlled proteolysis and its application to deplete the beta subunit of RNA polymerase.Deficiency of the novel exopolyphosphatase Rv1026/PPX2 leads to metabolic downshift and altered cell wall permeability in Mycobacterium tuberculosis Benzoic Acid-Inducible Gene Expression in Mycobacteria.SecA: a potential antimicrobial target.Mycobacterium tuberculosis thymidylate synthase gene thyX is essential and potentially bifunctional, while thyA deletion confers resistance to p-aminosalicylic acid.Emerging themes in SecA2-mediated protein export.Expansion of the tetracycline-dependent regulation toolbox for Helicobacter pylori Systematic, multiparametric analysis of Mycobacterium tuberculosis intracellular infection offers insight into coordinated virulence Structural Similarities and Differences between Two Functionally Distinct SecA Proteins, Mycobacterium tuberculosis SecA1 and SecA2.Critical roles for lipomannan and lipoarabinomannan in cell wall integrity of mycobacteria and pathogenesis of tuberculosis Development of a new generation of vectors for gene expression, gene replacement, and protein-protein interaction studies in mycobacteria.Tools for functional postgenomic analysis of listeria monocytogenes.Rv2744c Is a PspA Ortholog That Regulates Lipid Droplet Homeostasis and Nonreplicating Persistence in Mycobacterium tuberculosis.Improved tetracycline repressors for gene silencing in mycobacteria A new twist on an old pathway--accessory Sec [corrected] systems The MprB extracytoplasmic domain negatively regulates activation of the Mycobacterium tuberculosis MprAB two-component system.Protein export systems of Mycobacterium tuberculosis: novel targets for drug development?Tuberculosis drugs: new candidates and how to find more.The ins and outs of Mycobacterium tuberculosis protein export.Updating and curating metabolic pathways of TB.Application of distributive conjugal DNA transfer in Mycobacterium smegmatis to establish a genome-wide synthetic genetic array.TetR-based gene regulation systems for Francisella tularensis.Biochemical characterization of L1 repressor mutants with altered operator DNA binding activity

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P2860

Silencing Mycobacterium smegmatis by using tetracycline repressors.

http://www.wikidata.org/entity/Q35879464

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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P1433

Journal of Bacteriology

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Silencing Mycobacterium smegmatis by using tetracycline repressors.

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P2093

Annette Kamionka

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Dirk Schnappinger

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Marcus Klotzsche

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Mercedes Monteleone

http://www.w3.org/2001/XMLSchema#string

Miriam Braunstein

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Sabine Ehrt

http://www.w3.org/2001/XMLSchema#string

Wolfgang Hillen

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Xinzheng V Guo

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P2860

Massive gene decay in the leprosy bacillus

Common themes in microbial pathogenicity revisited

Essential Bacillus subtilis genes

Controlling gene expression in mycobacteria with anhydrotetracycline and Tet repressor

Crystal structure of Mycobacterium tuberculosis SecA, a preprotein translocating ATPase

Genes required for mycobacterial growth defined by high density mutagenesis

Alkyl hydroperoxide reductase subunit C (AhpC) protects bacterial and human cells against reactive nitrogen intermediates

Individual RD1-region genes are required for export of ESAT-6/CFP-10 and for virulence of Mycobacterium tuberculosis

Inactivation of Rv2525c, a substrate of the twin arginine translocation (Tat) system of Mycobacterium tuberculosis, increases beta-lactam susceptibility and virulence

SecA2 functions in the secretion of superoxide dismutase A and in the virulence of Mycobacterium tuberculosis

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4614-4623

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10.1128/JB.00216-07

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13

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189

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6348616

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17483222

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1913471

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