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Methods of isolation and purification of outer membrane vesicles from gram-negative bacteriaComparative proteome analysis of cellular proteins extracted from highly virulent Francisella tularensis ssp. tularensis and less virulent F. tularensis ssp. holarctica and F. tularensis ssp. mediaasiatica.Proteomic analysis of anti-Francisella tularensis LVS antibody response in murine model of tularemia.Francisella tularensis live vaccine strain: proteomic analysis of membrane proteins enriched fraction.Coxiella burnetii whole cell lysate protein identification by mass spectrometry and tandem mass spectrometry.Identification of immunoreactive antigens in membrane proteins enriched fraction from Francisella tularensis LVS.Proteomic analysis of wheat proteins recognized by IgE antibodies of allergic patients.iTRAQ quantitative analysis of Francisella tularensis ssp. holarctica live vaccine strain and Francisella tularensis ssp. tularensis SCHU S4 response to different temperatures and stationary phases of growth.Identification of a putative chaperone involved in stress resistance and virulence in Francisella tularensisCharacterization of tetratricopeptide repeat-like proteins in Francisella tularensis and identification of a novel locus required for virulenceSystems-level effects of ectopic galectin-7 reconstitution in cervical cancer and its microenvironment.Vascular Endothelial Growth Factor Is Associated with the Morphologic and Functional Parameters in Patients with Hypertrophic CardiomyopathyBacterial protein complexes investigation using blue native PAGE.Tetratricopeptide repeat motifs in the world of bacterial pathogens: role in virulence mechanisms.Serving the new masters - dendritic cells as hosts for stealth intracellular bacteria.Proteomic investigation of embryonic rat heart-derived H9c2 cell line sheds new light on the molecular phenotype of the popular cell model.Tularemia vaccines.Quantitative proteomics analysis of macrophage-derived lipid rafts reveals induction of autophagy pathway at the early time of Francisella tularensis LVS infection.Comparative proteome profiling of host-pathogen interactions: insights into the adaptation mechanisms of Francisella tularensis in the host cell environment.Activation of B cell apoptotic pathways in the course of Francisella tularensis infection.Capillary immunotyping electrophoresis and high resolution two-dimensional electrophoresis for the detection of mu-heavy chain disease.Francisella tularensis strain LVS resides in MHC II-positive autophagic vacuoles in macrophages.The role of MAPK signal pathways during Francisella tularensis LVS infection-induced apoptosis in murine macrophages.Cooperation of both, the FKBP_N-like and the DSBA-like, domains is necessary for the correct function of FTS_1067 protein involved in Francisella tularensis virulence and pathogenesis.Francisella tularensis subsp. holarctica DsbA homologue: a thioredoxin-like protein with chaperone function.Use of magnetic hydrazide-modified polymer microspheres for enrichment of Francisella tularensis glycoproteins.Proteomics analysis of the Francisella tularensis LVS response to iron restriction: induction of the F. tularensis pathogenicity island proteins IglABC.Application of SILAC labeling to primary bone marrow-derived dendritic cells reveals extensive GM-CSF-dependent arginine metabolism.Comparative proteomic profiling of culture filtrate proteins of less and highly virulent Francisella tularensis strains.Changes in proteome of the Δhfq strain derived from Francisella tularensis LVS correspond with its attenuated phenotype.Inactivation of Francisella tularensis Gene Encoding Putative ABC Transporter Has a Pleiotropic Effect upon Production of Various Glycoconjugates.Francisella tularensis type VI secretion system comes of age.Plasma concentration of fibronectin is decreased in patients with hypertrophic cardiomyopathy.Francisella tularensis membrane complexome by blue native/SDS-PAGE.Identification of two substrates of FTS_1067 protein - An essential virulence factor of Francisella tularensis.Proteomic insights into chronic anthracycline cardiotoxicity.The heat-shock protein ClpB of Francisella tularensis is involved in stress tolerance and is required for multiplication in target organs of infected mice.Corrigendum to: "Proteomic investigation of embryonic rat heart-derived H9c2 cell line sheds new light on the molecular phenotype of the popular cell model" [Exp. Cell Res. 339 2 (2015) 174-186].Plasma glycogen phosphorylase BB is associated with pulmonary artery wedge pressure and left ventricle mass index in patients with hypertrophic cardiomyopathy.Identification of new celiac disease autoantigens using proteomic analysis
P50
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P50
description
hulumtues
@sq
researcher
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wetenschapper
@nl
հետազոտող
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name
Jiri Stulik
@ast
Jiri Stulik
@en
Jiri Stulik
@es
Jiri Stulik
@nl
Jiri Stulik
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Jiří Stulík
@cs
type
label
Jiri Stulik
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Jiri Stulik
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Jiri Stulik
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Jiri Stulik
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Jiri Stulik
@sl
Jiří Stulík
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prefLabel
Jiri Stulik
@ast
Jiri Stulik
@en
Jiri Stulik
@es
Jiri Stulik
@nl
Jiri Stulik
@sl
Jiří Stulík
@cs
P106
P1153
7006061632
P21
P2798
P31
P496
0000-0002-4790-2365