Quantitative proteomic profiling of host-pathogen interactions: the macrophage response to Mycobacterium tuberculosis lipids. - Wikidata - awgldk - TriplyDB

Quantitative proteomic profiling of host-pathogen interactions: the macrophage response to Mycobacterium tuberculosis lipids.

Quantitative proteomic profiling of host-pathogen interactions: the macrophage response to Mycobacterium tuberculosis lipids.

http://www.wikidata.org/entity/Q37127448

about

Phosphodiesterase-4 inhibition alters gene expression and improves isoniazid-mediated clearance of Mycobacterium tuberculosis in rabbit lungs Elucidating Host-Pathogen Interactions Based on Post-Translational Modifications Using Proteomics Approaches Metabolic Perspectives on Persistence Tuberculosis: global approaches to a global disease.Organelle membrane proteomics reveals differential influence of mycobacterial lipoglycans on macrophage phagosome maturation and autophagosome accumulation.Thematic Review Series: Proteomics. An integrated omics analysis of eicosanoid biology.Pulsed stable isotope labeling of amino acids in cell culture uncovers the dynamic interactions between HIV-1 and the monocyte-derived macrophage.Metabolic host responses to infection by intracellular bacterial pathogens Plasma Membrane Profiling Reveals Upregulation of ABCA1 by Infected Macrophages Leading to Restriction of Mycobacterial Growth.Comparative Proteomics Analysis of Human Macrophages Infected with Virulent Mycobacterium bovis Proteomics as a probe of microbial pathogenesis and its molecular boundaries.A proteomic view of mycobacteria.Monocyte/macrophage proteomics: recent findings and biomedical applications.Mycobacterial proteomics: analysis of expressed proteomes and post-translational modifications to identify candidate virulence factors.High-throughput proteomics and the fight against pathogens.Sample preparation of Mycobacterium tuberculosis extracts for nuclear magnetic resonance metabolomic studies.Proteomics of Mycobacterium Infection: Moving towards a Better Understanding of Pathogen-Driven Immunomodulation.Proteomics of Aspergillus fumigatus conidia-containing phagolysosomes identifies processes governing immune evasion.

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Quantitative proteomic profiling of host-pathogen interactions: the macrophage response to Mycobacterium tuberculosis lipids.

http://www.wikidata.org/entity/Q37127448

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on January 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@en

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@nl

type

label

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@en

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@nl

prefLabel

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@en

Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@nl

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Journal of Proteome Research

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Quantitative proteomic profili ...... bacterium tuberculosis lipids.

@en

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Jay D Keasling

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

Jun Liu

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

Leslie Sheu

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

Sarah A Gilmore

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

Wenqing Shui

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

P2860

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A proteomics strategy to elucidate functional protein-protein interactions applied to EGF signaling

Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens

Quantitative phosphotyrosine proteomics of EphB2 signaling by stable isotope labeling with amino acids in cell culture (SILAC)

Toll-like receptors

Quantitative analysis of complex protein mixtures using isotope-coded affinity tags

Macrophage migration inhibitory factor: a regulator of innate immunity

Identifying and quantifying in vivo methylation sites by heavy methyl SILAC

Time-resolved mass spectrometry of tyrosine phosphorylation sites in the epidermal growth factor receptor signaling network reveals dynamic modules

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282-289

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scholarly article

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10.1021/PR800422E

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1

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8

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Carolyn Bertozzi

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2009-01-01T00:00:00Z

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23568470

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19053526

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Mycobacterium tuberculosis

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2655317

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