responses of mycobacterium tuberculosis to growth in the mouse lung - Wikidata - awgldk - TriplyDB

responses of mycobacterium tuberculosis to growth in the mouse lung

responses of mycobacterium tuberculosis to growth in the mouse lung

http://www.wikidata.org/entity/Q33788098

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Pathogen roid rage: cholesterol utilization by Mycobacterium tuberculosis Identification of moaA3 gene in patient isolates of Mycobacterium tuberculosis in Kerala, which is absent in M. tuberculosis H37Rv and H37Ra Crystal structures ofMycobacterium tuberculosisS-adenosyl-L-homocysteine hydrolase in ternary complex with substrate and inhibitors Biochemical and structural characterization of CYP124: A methyl-branched lipid -hydroxylase from Mycobacterium tuberculosis Portrait of a pathogen: the Mycobacterium tuberculosis proteome in vivo Role of the transcriptional regulator RamB (Rv0465c) in the control of the glyoxylate cycle in Mycobacterium tuberculosis Molecular function of WhiB4/Rv3681c of Mycobacterium tuberculosis H37Rv: a [4Fe-4S] cluster co-ordinating protein disulphide reductase Role of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular growth, and virulence Cholesterol utilization in mycobacteria is controlled by two TetR-type transcriptional regulators: kstR and kstR2 Catabolism and biotechnological applications of cholesterol degrading bacteria.Whole genome identification of Mycobacterium tuberculosis vaccine candidates by comprehensive data mining and bioinformatic analyses Transcriptional analysis of Mycobacterium fortuitum cultures upon hydrogen peroxide treatment using the novel standard rrnA-P1.A thiolase of Mycobacterium tuberculosis is required for virulence and production of androstenedione and androstadienedione from cholesterol.The EXIT Strategy: an Approach for Identifying Bacterial Proteins Exported during Host Infection.The Mycobacterium tuberculosis cytochrome P450 system.Development and analysis of an in vivo-compatible metabolic network of Mycobacterium tuberculosis Analysis of intracellular expressed proteins of Mycobacterium tuberculosis clinical isolates.Identification of Mycobacterium avium genes expressed during in vivo infection and the role of the oligopeptide transporter OppA in virulence.Carbon flux rerouting during Mycobacterium tuberculosis growth arrest.New targets and inhibitors of mycobacterial sulfur metabolism.Comprehensive insights into transcriptional adaptation of intracellular mycobacteria by microbe-enriched dual RNA sequencing Attenuation of Mycobacterium tuberculosis functionally disrupted in a fatty acyl-coenzyme A synthetase gene fadD5.A recombinant Mycobacterium smegmatis induces potent bactericidal immunity against Mycobacterium tuberculosis.Lipidomics reveals control of Mycobacterium tuberculosis virulence lipids via metabolic coupling.The TB Structural Genomics Consortium: a decade of progress.Carbon metabolism of intracellular bacteria.Lipoprotein LprI of Mycobacterium tuberculosis Acts as a Lysozyme Inhibitor.Analysis of serum metabolic profile by ultra-performance liquid chromatography-mass spectrometry for biomarkers discovery: application in a pilot study to discriminate patients with tuberculosis.Microarray analysis of whole genome expression of intracellular Mycobacterium tuberculosis.Physiology of mycobacteria Adjusting to a new home: Mycobacterium tuberculosis gene expression in response to an intracellular lifestyle.Mycobacterium abscessus: a new antibiotic nightmare.Biochemical Investigation of Rv3404c from Mycobacterium tuberculosis.Molecular basis of mycobacterial survival in macrophages.A Physiologically Based Pharmacokinetic Model of Isoniazid and Its Application in Individualizing Tuberculosis Chemotherapy.Differential gene expression in response to exposure to antimycobacterial agents and other stress conditions among seven Mycobacterium tuberculosis whiB-like genes.Initial step in the catabolism of cholesterol by Mycobacterium smegmatis mc2 155.Effect of efflux pump inhibitors on the susceptibility of Mycobacterium tuberculosis to isoniazid.The Mycobacterium tuberculosis Complex has a Pathway for the Biosynthesis of 4-Formamido-4,6-Dideoxy-d-Glucose.

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P2860

responses of mycobacterium tuberculosis to growth in the mouse lung

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2005年の論文

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responses of mycobacterium tuberculosis to growth in the mouse lung

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responses of mycobacterium tuberculosis to growth in the mouse lung

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responses of mycobacterium tuberculosis to growth in the mouse lung

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responses of mycobacterium tuberculosis to growth in the mouse lung

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Infection and Immunity

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responses of mycobacterium tuberculosis to growth in the mouse lung

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Eugenie Dubnau

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Issar Smith

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John Chan

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P2860

Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence

Biochemical differentiation of Mycobacterium tuberculosis grown in vivo and in vitro

ideR, An essential gene in mycobacterium tuberculosis: role of IdeR in iron-dependent gene expression, iron metabolism, and oxidative stress response

Mutation of the principal sigma factor causes loss of virulence in a strain of the Mycobacterium tuberculosis complex

Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase

Mycobacterium tuberculosis genes induced during infection of human macrophages

Transcriptional Adaptation of Mycobacterium tuberculosis within Macrophages: Insights into the Phagosomal Environment

Mycobacterium tuberculosis WhiB3 interacts with RpoV to affect host survival but is dispensable for in vivo growth.

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

inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis

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Mycobacterium tuberculosis

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