about
Construction and evaluation of an ORFeome-based Brucella whole-genome DNA microarrayThe genes for erythritol catabolism are organized as an inducible operon in Brucella abortusEvolutionary diversification and characterization of the eubacterial gene family encoding DXR type II, an alternative isoprenoid biosynthetic enzymeGeneration of the Brucella melitensis ORFeome version 1.1.Brucella abortus ure2 region contains an acid-activated urea transporter and a nickel transport system.A new family of enzymes catalyzing the first committed step of the methylerythritol 4-phosphate (MEP) pathway for isoprenoid biosynthesis in bacteria.Mycobacterium avium interaction with macrophages and intestinal epithelial cells.Mycobacterium avium infection of epithelial cells results in inhibition or delay in the release of interleukin-8 and RANTESMycobacterium avium invades the intestinal mucosa primarily by interacting with enterocytesIdentification of a new virulence factor, BvfA, in Brucella suis.Cellular and molecular mechanisms of internalization of mycobacteria by host cells.Evaluation of the effects of erythritol on gene expression in Brucella abortus.Transfer of R388 derivatives by a pathogenesis-associated type IV secretion system into both bacteria and human cells.Characterization of the urease operon of Brucella abortus and assessment of its role in virulence of the bacterium.The efficiency of the translocation of Mycobacterium tuberculosis across a bilayer of epithelial and endothelial cells as a model of the alveolar wall is a consequence of transport within mononuclear phagocytes and invasion of alveolar epithelial cefecB, a gene potentially involved in iron transport in Mycobacterium avium, is not induced within macrophages.Characterization and expression of secA in Mycobacterium avium.Brucella abortus strain 2308 produces brucebactin, a highly efficient catecholic siderophore.Mycobacterium avium enters intestinal epithelial cells through the apical membrane, but not by the basolateral surface, activates small GTPase Rho and, once within epithelial cells, expresses an invasive phenotype.Ultrastructural study of Mycobacterium avium infection of HT-29 human intestinal epithelial cells.Molecular basis of Brucella pathogenicity: an update.Characterization of IS666, a newly described insertion element of Mycobacterium avium.Green fluorescent protein in the measurement of bacteria-host interactions.Identification of Brucella abortus B19 vaccine strain by the detection of DNA polymorphism at the ery locus.Mutagenesis of Brucella abortus: comparative efficiency of three transposon delivery systems.Functional interactions between type IV secretion systems involved in DNA transfer and virulenceImprovement of the Brucella abortus B19 vaccine by its preparation in a glycerol based medium
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-3298-6076
@en
name
Félix J Sangari
@ast
Félix J Sangari
@en
Félix J Sangari
@nl
type
label
Félix J Sangari
@ast
Félix J Sangari
@en
Félix J Sangari
@nl
prefLabel
Félix J Sangari
@ast
Félix J Sangari
@en
Félix J Sangari
@nl
P106
P31
P496
0000-0002-3298-6076