References of "Tabart, J"
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See detailFeline polymorphonuclear neutrophils produce pro-inflammatory cytokines following exposure to Microsporum canis
Cambier, Ludivine ULg; Mathy, A; Baldo, A et al

in Veterinary Microbiology (2013), 162(2-4), 800-805

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See detailRôle des cellules Th17 dans les maladies infectieuses et auto-immunes
Cambier, Ludivine ULg; Defaweux, Valérie ULg; Baldo, Aline ULg et al

in Annales de Médecine Vétérinaire (2011), 154

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See detailSecreted subtilisin Sub3 from Microsporum canis is required for adherence to but not for invasion of the epidermis
Baldo, Aline ULg; Mathy, Anne ULg; Tabart, J. et al

in British Journal of Dermatology (2010), 162(5), 990-997

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See detailInvolvement of the secreted serine protease Sub3 of Microsporum canis in adherence to feline epidermis
Mathy, Anne ULg; Tabart, J.; Vermout, S. et al

Conference (2009)

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See detailImmunization and dermatophytes
Baldo, Aline ULg; Tabart, J.; Mathy, Anne ULg et al

Conference (2009)

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See detailRNA silencing in the dermatophyte Microsporum canis
Vermout, S.; Tabart, J.; Baldo, Aline ULg et al

in FEMS Microbiology Letters (2007), 275(1), 38-45

Dermatomycoses caused by Microsporum canis are frequent in domestic animals and easily transmissible to humans. Several proteases secreted by this fungus were identified as potential virulence factors ... [more ▼]

Dermatomycoses caused by Microsporum canis are frequent in domestic animals and easily transmissible to humans. Several proteases secreted by this fungus were identified as potential virulence factors, but the construction of deficient strains is required to investigate their role in the pathogenesis of the disease. Using target genes encoding two of these proteases, a first evaluation of the utility of RNA-mediated silencing as a reverse genetic tool in dermatophytes was carried out. SUB3 and DPPIV, respectively coding for a subtilisin and a dipeptidyl peptidase, were both down-regulated, by means of two plasmid constructs designed to express an RNA hairpin that corresponds to part of their respective sequence. The degree of attenuation was evaluated by enzymatic assay of the transformants culture supernatants, and by real-time reverse transcriptase-polymerase chain reaction. Enzymatic activities and expression levels varied from less than 5% to 100% of that of control transformants obtained with plasmid without hairpin inserts. Inhibition was globally more efficient for SUB3 than for DPPIV. These results show that RNA silencing can be used for functional genomics in M. canis, and particularly to circumvent the limits and technical difficulties of conventional disruption methods. [less ▲]

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See detailLes mécanismes d'adhérence des champignons responsables de mycoses superficielles
Baldo, Aline ULg; Mathy, Anne ULg; Vermout, S. et al

in Annales de Médecine Vétérinaire (2007), 151

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See detailReconstructed interfollicular feline epidermis as a model for the screening of drugs against Microsporum canis
Mignon, Bernard ULg; Tabart, J.; Baldo, Aline ULg et al

in Veterinary Dermatology (2007), 18

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See detailKinetics of Microsporum canis adherence using an in vitro model of reconstituted feline epidermis
Baldo, Aline ULg; Tabart, J.; Vermout, S. et al

Conference (2006)

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See detailRecent findings on the pathogenesis of dermatophytoses in dogs and cats
Mignon, Bernard ULg; Vermout, S.; Tabart, J. et al

in Revista Scientia Parasitologica (2006), 7(3/4), 7-15

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