Rifampin Resistance Mutations Are Associated with Broad Chemical Remodeling of Mycobacterium tuberculosis. - Wikidata - wikimedia - TriplyDB

Rifampin Resistance Mutations Are Associated with Broad Chemical Remodeling of Mycobacterium tuberculosis.

Rifampin Resistance Mutations Are Associated with Broad Chemical Remodeling of Mycobacterium tuberculosis.

http://www.wikidata.org/entity/Q37065759

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Emerging Approaches to Tuberculosis Drug Development: At Home in the Metabolome.In vitro and in vivo fitness costs associated with Mycobacterium tuberculosis RpoB mutation H526D.The role of metabolomics in tuberculosis treatment research.Characterization of the impact of rpoB mutations on the in vitro and in vivo competitive fitness of Clostridium difficile and susceptibility to fidaxomicin.Strain Diversity and the Evolution of Antibiotic Resistance.Comparative lipidomics of drug sensitive and resistant Mycobacterium tuberculosis reveals altered lipid imprints.Altered Mycobacterium tuberculosis Cell Wall Metabolism and Physiology Associated With RpoB Mutation H526D.

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Rifampin Resistance Mutations Are Associated with Broad Chemical Remodeling of Mycobacterium tuberculosis.

http://www.wikidata.org/entity/Q37065759

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 10 May 2016

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@en

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@nl

type

label

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@en

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@nl

prefLabel

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@en

Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@nl

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JBC.M116.716704

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Journal of Biological Chemistry

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Rifampin Resistance Mutations ...... of Mycobacterium tuberculosis.

@en

P2093

Chris Ford

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

David Young

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Emilie Layre

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Megan B Murray

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Nivedita Lahiri

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Rupal R Shah

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Sarah M Fortune

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P2860

Few amino acid positions in rpoB are associated with most of the rifampin resistance in Mycobacterium tuberculosis

Lipidomic profiling of model organisms and the world's major pathogens

Structural mechanism for rifampicin inhibition of bacterial rna polymerase

Structural basis for substrate loading in bacterial RNA polymerase

The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages

Identification of a Mycobacterium tuberculosis gene cluster encoding the biosynthetic enzymes for assembly of the virulence-conferring siderophore mycobactin

The role of MmpL8 in sulfatide biogenesis and virulence of Mycobacterium tuberculosis

Analysis of the phthiocerol dimycocerosate locus of Mycobacterium tuberculosis. Evidence that this lipid is involved in the cell wall permeability barrier

MmpL8 is required for sulfolipid-1 biosynthesis and Mycobacterium tuberculosis virulence

The Mycobacterium tuberculosis IdeR is a dual functional regulator that controls transcription of genes involved in iron acquisition, iron storage and survival in macrophages

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scholarly article

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10.1074/JBC.M116.716704

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David Branch Moody

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2016-05-10T00:00:00Z

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27226566

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Mycobacterium tuberculosis

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4933180

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