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See detailEtude de la fatigue dans l'analyse de la marche
Maquet, Didier ULg; Chapelier, D.; Bouquegneau, Adeline ULg et al

in Julia, M.; Perrey, S.; Dupeyron, A. (Eds.) et al Fatigue musculaire (2010)

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See detailEtude de la fiabilité d'un nouvel analyseur de lactate portable chez le cheval
Meynie, J.; Art, Tatiana ULg; Olaerts, J. et al

in Pratique Vétérinaire Equine (1996), 28(1), 37-40

A new portable lactate analyzer has been tested for its accuracy and reproducibility. Venous blood has been sampled on 12 horses while they were performing a treadmill exercise. A total of 134 samples ... [more ▼]

A new portable lactate analyzer has been tested for its accuracy and reproducibility. Venous blood has been sampled on 12 horses while they were performing a treadmill exercise. A total of 134 samples were obtained and analyzed either with the portable analyzer or with a reference method. The packed cell volume has been also determined for each sample. The results obtained with both methods were compared : the correlation between the two sets of data was satisfactory ((R2 = 0,86) but higher when the PCV was lower or equal to 55 % (R2 = 0,88). It was concluded that the portable analyzer is reliable for lactate determination in horses [less ▲]

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See detailEtude de la fiabilité du SMA 12/60.
Vos, A.; Ers, P.; Albert, Adelin ULg et al

in Expansion scientifique française (1973)

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See detailEtude de la fibrose pulmonaire idiopathique canine: analyse du transcriptome, investigation des voies du TGF beta 1 et recherche de biomarqueurs
Krafft, Emilie ULg

Doctoral thesis (2014)

Canine idiopathic pulmonary fibrosis (cIPF) is a fibrotic disease of the pulmonary parenchyma, mainly seen in the West Highland white terrier. It is characterized by exercise intolerance and cough with a ... [more ▼]

Canine idiopathic pulmonary fibrosis (cIPF) is a fibrotic disease of the pulmonary parenchyma, mainly seen in the West Highland white terrier. It is characterized by exercise intolerance and cough with a progressive deterioration until death from respiratory insufficiency. Clinical, tomodensitometric and histological characteristics of cIPF have been described recently. However, this disease remains largely unknown and the clinicians are dealing with two major challenges: confirmation of the diagnosis, which requires many complementary exams, and absence of effective treatment. Identification of a targeted therapy is difficult without having a good understanding of the mechanisms leading to pulmonary parenchyma fibrosis. A similar disease, the idiopathic pulmonary fibrosis (IPF) is recognized in humans and cIPF might be interesting as a spontaneous model. This project in dogs was undertaken to answer, at least partly, to these challenges. The aims were to elucidate some mechanisms involved in cIPF pathogenesis and to identify biomarkers that could be used in the diagnosis process. The hypotheses were first that analysis of the transcriptome through microarray experiment would identify altered biological functions in cIPF, highlight specific molecules with an altered expression and identify potential biomarkers. Another hypothesis was the transforming growth factor beta 1 (TGFB1) pathways, considered central in the pathogenesis of IPF, would also be modified in cIPF. Finally, ET1, a known biomarker in human IPF, might also be an interesting biomarker in dogs. Gene expression analysis through microarray analysis, combined with the use of IPA, a data analysis program, identified altered biological functions in cIPF: cellular growth and proliferation, developmental processes, cellular movement, cell to cell signaling and interaction and antigen presentation. Some genes highlighted in the microarray experiment were then analyzed individually. Quantitative RT-PCR analysis confirmed an upregulation of the expression of CCL2, CCL7, CXCL14, IL8 and FAP (fibroblast activation protein) as well as a downregulation of the expression of PLUNC (palate, lung and nasal epithelium associated). We then complete the gene expression analysis with a search for potential biomarkers. Thirty-four potential biomarkers were identified with 32 biomarkers potentially measurable in blood (including CCL2, serum amyloid 1, IL8) and 2 biomarkers measurable only in the bronchoalveolar lavage fluid (BALF) (PLUNC and mesothelin). This approach was validated by measurement in serum of one of this biomarker: CCL2. CCL2 serum concentration was higher in affected WHWT compared to healthy WHWT and also higher in dogs with cIPF compared to dogs with chronic bronchitis (CB) or eosinophilic bronchopneumopathy (EBP). Based on serum CCL2 determination, cIPF was diagnosed with a sensibility of 92% and a specificity of 80%. We then studied TGFB1 and part of its storage, activation and signaling pathways. TGFB1 gene expression was not significantly different in the pulmonary parenchyma between affected and control dogs. However, in affected dogs, increased TGFB1 protein levels were seen by immunohistochemistry in fibrotic areas. High expression of bothTGFB1 type I receptor and phosphorylated Smad2/3, markers of an active intracellular TGFB1 signal, were seen in epithelial cells. No difference in expression for the storage proteins LTBP1 and LTBP2 was seen while expression of LTBP4 was significantly decreased in dogs with cIPF. Concerning the proteins involved in TGFB1 activation, gene expression was decreased for integrin subunit β8, increased for thrombospondin-1 and not modified for integrin subunit β6. Expression of Smad 7, involved in intracellular TGFB1 signal inhibition, was not modified. No difference for TGFB1 serum concentration was seen between WHWT with cIPF and healthy WHWT. A multivariate analysis performed on healthy dogs showed no age effect but a significant breed effect with higher levels in predisposed breeds. We evaluated part of the serotonin pathway, as one of its receptor (5HTR2B) was highlighted during the gene expression analysis. Serotonin has also been involved in the pathogenesis of human IPF and described to be of potential use as a biomarker in degenerative mitral valve disease in dogs. Expression of 2 serotonin receptors (5HTR2A and 5HTR2B), evaluated by quantitative RT-PCR in pulmonary tissue, was not different between dogs with cIPF and control dogs while expression of the serotonin transporter (5HTT) was significantly lower in affected dogs. No difference in serotonin serum level was seen between affected and healthy WHWT or between dogs with cIPF, CB or EBP. ET1 was evaluated as a biomarker in serum and BALF. ET1 serum concentration was not different between healthy WHWT and Beagles. Covariance analysis did not reveal any significant age effect. Serum levels were significantly higher in dogs with cIPF compared to dogs with CB or EBP. ROC curve analysis was then used to evaluate its diagnostic performances. The area under the curve was 0,818 with a sensitivity of 91.7% and a specificity of 87.5%. ET1 was also measured in the BALF in a small number of dogs. Its concentration was measurable in all dogs with cIPF while it was below the detection limit in all other dogs tested (healthy and with CB). Even though cIPF and human IPF are not completely identical from clinical, tomodensitometric or histological points of view, these results show that both canine and human diseases share molecular pathways, supporting the idea that cIPF might have an interest as spontaneous model. This work allowed a better understanding of cIPF pathogenesis. Gene expression analysis in the pulmonary parenchyma of affected dogs first identified several altered biological functions that should be analyzed in details in further studies. A more targeted analysis of some genes confirmed an upregulated expression of CCL2, CCL7, CXCL14, IL8 and FAP. Such a positive regulation of the expression of various inflammatory cytokines tends to suggest that inflammation might have a role in cIPF pathogenesis. Some of these cytokines also have profibrotic properties. PLUNC was one of the top down-regulated genes. Roles of the protein are still largely unknown; it might have a role in the inflammatory response and in the innate immunity. Developmental pathways were also altered in cIPF and quantitative RT-PCR confirmed an upregulation of FAP, a protein normally expressed in areas of tissue remodeling during fetal development and also positively regulated in human IPF. This study has shown that there is an active TGFB1 signal in the lungs of dogs with cIPF, especially at the level of the pathological epithelium. TGFB1 storage and activation pathways also seemed to be altered. Elevated TGFB1 circulating levels were found in predisposed breeds, which might explain at least partly their susceptibility for cIPF. Because of these results and its well-known profibrotic properties, we can suggest that TGFB1 is probably involved in cIPF pathogenesis and that modulation of its storage, activation or intracellular signaling might offer potential therapeutic targets. Our preliminary results are not in favor of a significant modification of the serotonin pathways in cIPF, although a decreased expression of 5HTT was seen in affected dogs and might have an impact on the amount of serotonin present locally. However, other studies are needed to conclude. Finally, several potential biomarkers have been identified and some of them were evaluated in details. While serum measurements performed for TGFB1 and serotonin indicated that these molecules have no interest as diagnostic biomarkers, ET1 and CCL2 were identified as interesting candidates with good diagnostic performances. However these results need to be confirmed in an independent validation cohort and the interest of combining both biomarkers should be evaluated. [less ▲]

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See detailEtude de la filière "pommes de terre" en Pologne
Gazinski, Benon; Burny, Philippe ULg

Report (1995)

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See detailEtude de la filière industrielle des énergirs renouvelables
Scheuren, Claude; Andre, Philippe ULg; Germani, David et al

Report (2010)

Rapport final du projet Firewal2, réalisé en collaboration avec l'asbl Energy Factor 4

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See detailEtude de la flore bactérienne de steacks tartares prélevés en boucherie, sandwicherie et restaurant par analyse métagénomique ciblée sur l’ADN ribosomial 16S.
Taminiau, Bernard ULg; Delhalle, Laurent ULg; Nezer, Carine et al

Poster (2012, May 24)

Etude de la flore bactérienne de steacks tartares prélevés en boucheries, sandwicheries et restaurants par analyse métagénomique ciblée sur l’ADN ribosomial 16S. Taminiau B.1, Delhalle L 2, Nezer C.2 ... [more ▼]

Etude de la flore bactérienne de steacks tartares prélevés en boucheries, sandwicheries et restaurants par analyse métagénomique ciblée sur l’ADN ribosomial 16S. Taminiau B.1, Delhalle L 2, Nezer C.2, Daube G 1 1 Université de Liège, Faculté de Médecine Vétérinaire, Département des Sciences des Denrées Alimentaires ; Sart Tilman B43 Bis, 4000 Liège, Belgique ; T+32 (0)4 366 40 29 / F+32 (0)4 366 40 44 2 Quality Partner sa, 62 Rue Hayeneux, 4040 Herstal, Belgique ; T+32 (0)4 240 75 00 / F+32 (0)4 240 75 10 Le steak tartare est une préparation à base de viande hachée de boeuf crue assaisonnée et souvent additionnée de condiments. Cette préparation est souvent accompagnée de frites ou étalée dans un sandwich. L’utilisation de viande crue et la composition de cet aliment rend cette préparation très sensible à l’altération d’origine bactérienne. Une meilleure compréhension de la flore bactérienne composant ce produit est indispensable pour contrôler et comprendre les phénomènes d'altération. L'analyse métagénomique ciblée a permis de caractériser les populations bactériennes de plusieurs échantillons de steak tartare achetés dans deux boucheries, deux sandwicheries et deux restaurants et analysés le jour-même. Une analyse classique microbiologique a été réalisée en parallèle. L'analyse métagénomique a été ciblée sur deux régions différentes de l'ADNr 16S bactérien (V&-V3 et V5-V6), afin de comparer l'efficacité d'identification des bactéries présentes. L’analyse métagénomique a permis de collecter un total de 60.500 séquences pour les 6 échantillons analysés par les deux approches et 356 espèces bactériennes différentes ont pu être identifiées via la région V1-V3. Lactobacillus algidus est la principale espèce présente (52% des séquences totales analysées), suivie par Pseudomonas sp. (8,43%) et Photobacterium phosphoreum (7,92%). L'analyse des résultats montre des différences remarquables entre les trois sources commerciales de steak tartare. Les échantillons provenant des deux boucheries et d’un restaurant étaient principalement composés de populations de Lactobacillus et, dans une moindre mesure, de contaminants environnementaux, comme Xanthomonas campestris. Les échantillons provenant de l'un des deux restaurants étaient fortement contaminés par des Leuconostocaceae comme Leuconostoc carnosum ou Weissella sp., ou avec des gamma-protéobactéries comme Pseudomonas sp. ou Psychrobacter sp. Ces derniers échantillons présentaient aussi des signes d’altérations (mauvaise odeur, aspect) qui peuvent ainsi être mis en relation avec la nature et le niveau des populations bactériennes identifiées. Les échantillons provenant des sandwicheries et probablement issues de filières de production industrielles étaient faiblement contaminés mais avec une grande variabilité dans les flores identifiées. Beaucoup d’entre elles ne sont pas classiquement décrites dans les viandes crues et doivent provenir des autres ingrédients. La combinaison du séquençage haut débit couplé à la bioinformatique est désormais un outil puissant pour l’analyse microbiologique des denrées alimentaires. Son application peut être étendue à pratiquement tous les aliments. Enfin, cette technologie ouvre de nouvelles perspectives aux industries agro alimentaires pour améliorer leurs procédés de fabrication, leurs recettes et leurs méthodes de conservation. [less ▲]

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See detailÉtude de la fonction Fc-récepteur du système mononucléé phagocytaire dans les affections immunes
Malaise, Michel ULg; Foidart, J.; Hoyoux, C. et al

in Bulletin et Mémoires de l'Académie Royale de Médecine de Belgique (1985), 140(10), 362-367

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See detailEtude de la fragmentation d'un paysage cas de la forêt de Uapaca Bojeri, Madagascar
de Haulleville, Thalès ULg; Bogaert, Jan ULg

Scientific conference (2012, October 16)

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