316 research outputs found

    Sélectionner un entrepÎt thématique de confiance pour la diffusion des données de recherche :

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    L’ambition des politiques du ministĂšre de l’Enseignement supĂ©rieur et de la Recherche concernant les donnĂ©es de la recherche est de faire en sorte que ces donnĂ©es soient progressivement structurĂ©es en conformitĂ© avec les principes FAIR (Facile Ă  trouver, Accessible, InteropĂ©rable, RĂ©utilisable), prĂ©servĂ©es et partagĂ©es ou ouvertes par des entrepĂŽts de donnĂ©es de confiance. Afin de guider les Ă©quipes de recherche vers l’entrepĂŽt le plus adaptĂ© pour le partage et l’ouverture des donnĂ©es de leur domaine thĂ©matique, il est indispensable d’identifier les entrepĂŽts thĂ©matiques nationaux et internationaux de confiance, certifiĂ©s Core Trust Seal ou non. Dans ce cadre, le CollĂšge DonnĂ©es de la recherche a dĂ©fini une liste de critĂšres d’exclusion permettant de sĂ©lectionner les entrepĂŽts thĂ©matiques de confiance, qui pourront non seulement accepter les dĂ©pĂŽts et la publication des jeux de donnĂ©es, mais aussi concourir Ă  leur diffusion et leur rĂ©utilisation ultĂ©rieure parles communautĂ©s scientifiques

    Pyroséquençage pour le développement d'EST et de SNP aviaires

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    Le but du programme est de combler les dĂ©ficits en marqueurs observĂ©s pour trois espĂšces aviaires : la caille, le canard et la poule. La stratĂ©gie choisie est l'obtention, Ă  partir de plusieurs individus de lignĂ©es d'intĂ©rĂȘt, de SNP (Single Nucleotide Polymorphism, polymorphisme d'un nuclĂ©otide) par une nouvelle technologie de sĂ©quençage Ă  haut dĂ©bit (sĂ©quenceur 454 GS-FLX, Roche). Nous sĂ©quençons des reprĂ©sentations rĂ©duites du gĂ©nome, en sĂ©lectionnant d'une part des fragments de restriction d'ADN gĂ©nomique - les mĂȘmes chez tous les individus - et d'autre part les transcrits qui reprĂ©sentent globalement la partie du gĂ©nome correspondant aux gĂšnes exprimĂ©s. Ces expĂ©rimentations sont rĂ©alisĂ©es Ă  partir d'Ă©chantillons d'ADN ou d'ARN issus d'individus de lignĂ©es Ă  l'origine de croisements existants, pour chacune des trois espĂšces. Les donnĂ©es gĂ©nĂ©rĂ©es par plusieurs "runs" de sĂ©quence seront traitĂ©es in silico : contigage Ă  haut dĂ©bit, recherche de SNP, comparaison avec les banques de sĂ©quences connues...En plus de l'intĂ©rĂȘt que reprĂ©sente la production d'un trĂšs grand nombre de SNP nouveaux, cette technologie devrait permettre de mieux sĂ©quencer les rĂ©gions riches en (G+C) correspondant aux plus petits des microchromosomes pour lesquels il n'y a pas de sĂ©quence chez la poule. La comparaison des sĂ©quences des transcrits obtenues chez la caille et le canard avec la sĂ©quence du gĂ©nome de la poule permettra d'Ă©tablir une "cartographie virtuelle" des SNP obtenus, grĂące Ă  la grande conservation de syntĂ©nie existant entre ces trois espĂšces

    Ophthalmol Ther

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    The healthcare burden of cardiovascular diseases remains a major issue worldwide. Understanding the underlying mechanisms and improving identification of people with a higher risk profile of systemic vascular disease through noninvasive examinations is crucial. In ophthalmology, retinal vascular network imaging is simple and noninvasive and can provide in vivo information of the microstructure and vascular health. For more than 10 years, different research teams have been working on developing software to enable automatic analysis of the retinal vascular network from different imaging techniques (retinal fundus photographs, OCT angiography, adaptive optics, etc.) and to provide a description of the geometric characteristics of its arterial and venous components. Thus, the structure of retinal vessels could be considered a witness of the systemic vascular status. A new approach called "oculomics" using retinal image datasets and artificial intelligence algorithms recently increased the interest in retinal microvascular biomarkers. Despite the large volume of associated research, the role of retinal biomarkers in the screening, monitoring, or prediction of systemic vascular disease remains uncertain. A PubMed search was conducted until August 2022 and yielded relevant peer-reviewed articles based on a set of inclusion criteria. This literature review is intended to summarize the state of the art in oculomics and cardiovascular disease research

    Study on the representativeness o the social partner organisations in the professional football players sector

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    A portada: Université catholique de Louvain. Institut des sciences du travailResearch project conducted on behalf of the Employment and Social Affairs DG of the European CommissionThe aim of the report is to produce a study that sets out both brief descriptions of the way that social dialogue functions in the countries concerned, and descriptions of the various workers' and employers' organisations involved in social dialogue at sector level. This study may be seen as a tool to help understand these quantitative and qualitative factors. It will also make it possible to understand the various systems of industrial relations in different countries, and to introduce the actors involved in social dialogue

    Study on the representativeness of the social partner organisations in the extractive industry

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    Tipus de projecte: Projecte europeuA portada: Universite catholique de Louvain. Institut de sciences du travailResearch project conducted on behalf of the Employment and Social Affairs DG of the European Commissio

    Association of Systemic Medication Use with Glaucoma and Intraocular Pressure:The European Eye Epidemiology Consortium

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    Purpose: To investigate the association of commonly used systemic medications with glaucoma and intraocular pressure (IOP) in the European population. Design: Meta-analysis of 11 population-based cohort studies of the European Eye Epidemiology Consortium. Participants: The glaucoma analyses included 143 240 participants and the IOP analyses included 47 177 participants. Methods: We examined associations of 4 categories of systemic medications—antihypertensive medications (ÎČ-blockers, diuretics, calcium channel blockers [CCBs], α-agonists, angiotensin-converting enzyme inhibitors, and angiotensin II receptor blockers), lipid-lowering medications, antidepressants, and antidiabetic medications—with glaucoma prevalence and IOP. Glaucoma ascertainment and IOP measurement method were according to individual study protocols. Results of multivariable regression analyses of each study were pooled using random effects meta-analyses. Associations with antidiabetic medications were examined in participants with diabetes only. Main Outcome Measures: Glaucoma prevalence and IOP. Results: In the meta-analyses of our maximally adjusted multivariable models, use of CCBs was associated with a higher prevalence of glaucoma (odds ratio [OR], 1.23; 95% confidence interval [CI], 1.08 to 1.39). This association was stronger for monotherapy of CCBs with direct cardiac effects (OR, 1.96; 95% CI, 1.23 to 3.12). No other antihypertensive medications, lipid-lowering medications, antidepressants, or antidiabetic medications were associated with glaucoma. Use of systemic ÎČ-blockers was associated with a lower IOP (ÎČ coefficient, −0.33 mmHg; 95% CI, −0.57 to −0.08 mmHg). Monotherapy of both selective systemic ÎČ-blockers (ÎČ coefficient, −0.45 mmHg; 95% CI −0.74 to −0.16 mmHg) and nonselective systemic ÎČ-blockers (ÎČ coefficient, −0.54 mmHg; 95% CI, −0.94 to −0.15 mmHg) was associated with lower IOP. A suggestive association was found between use of high-ceiling diuretics and lower IOP (ÎČ coefficient, −0.30 mmHg; 95% CI, −0.47 to −0.14 mmHg) but not when used as monotherapy. No other antihypertensive medications, lipid-lowering medications, antidepressants, or antidiabetic medications were associated with IOP. Conclusions: We identified a potentially harmful association between use of CCBs and glaucoma prevalence. Additionally, we observed and quantified the association of lower IOP with systemic ÎČ-blocker use. Both findings potentially are important, given that patients with glaucoma frequently use systemic antihypertensive medications. Determining causality of the CCB association should be a research priority. Financial Disclosure(s): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</p

    Association of systemic medication use with glaucoma and intraocular pressure: the E3 Consortium

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    PURPOSE: To investigate the association of commonly used systemic medications with glaucoma and intraocular pressure (IOP) in the European population. DESIGN: Meta-analysis of eleven population-based cohort studies of the European Eye Epidemiology (E3) consortium. PARTICIPANTS: A total of 143240 participants were included in the glaucoma analyses and 47177 participants in the IOP analyses. METHODS: We examined associations of four categories of systemic medications (antihypertensive medications: beta-blockers, diuretics, calcium channel blockers [CCBs], alpha-agonists, angiotensin-converting-enzyme inhibitors, angiotensin II receptor blockers; lipid-lowering medications; antidepressants; antidiabetic medications) with glaucoma prevalence and IOP. Glaucoma ascertainment and IOP measurement method were according to individual study protocols. Multivariable regression analyses were carried out in each study and results were pooled using random effects meta-analyses. Associations with antidiabetic medications were examined in diabetic participants only. MAIN OUTCOME MEASURES: Glaucoma prevalence and IOP. RESULTS: In the meta-analyses of our maximally-adjusted multivariable models, use of CCBs was associated with a higher prevalence of glaucoma (odds ratio [OR] with corresponding 95% confidence interval [95% CI]: 1.23 [1.08 to 1.39]). This association was stronger for monotherapy of CCBs with direct cardiac effects (OR [95% CI]: 1.96 [1.23 to 3.12]). The use of other antihypertensive medications, lipid-lowering medications, antidepressants or antidiabetic medications were not clearly associated with glaucoma. Use of systemic beta-blockers was associated with a lower IOP (Beta [95% CI]: -0.33 [-0.57 to -0.08] mmHg). Monotherapy of both selective (Beta [95% CI]: -0.45 [-0.74 to -0.16] mmHg) and non-selective (Beta [95% CI]: -0.54 [-0.94 to -0.15] mmHg) systemic beta-blockers was associated with lower IOP. There was a suggestive association between use of high-ceiling diuretics and lower IOP (Beta [95% CI]: -0.30 [-0.47; -0.14] mmHg), but not when used as monotherapy. Use of other antihypertensive medications, lipid-lowering medications, antidepressants, or antidiabetic medications were not associated with IOP. CONCLUSIONS: We identified a potentially harmful association between use of CCBs and glaucoma prevalence. Additionally, we observed and quantified the association of lower IOP with systemic beta-blocker use. Both findings are potentially important given that glaucoma patients frequently use systemic antihypertensive medications. Determining whether the CCB association is causal should be a research priority

    A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers.

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    HER2-positive breast cancer has long proven to be a clinically distinct class of breast cancers for which several targeted therapies are now available. However, resistance to the treatment associated with specific gene expressions or mutations has been observed, revealing the underlying diversity of these cancers. Therefore, understanding the full extent of the HER2-positive disease heterogeneity still remains challenging. Here we carry out an in-depth genomic characterization of 64 HER2-positive breast tumour genomes that exhibit four subgroups, based on the expression data, with distinctive genomic features in terms of somatic mutations, copy-number changes or structural variations. The results suggest that, despite being clinically defined by a specific gene amplification, HER2-positive tumours melt into the whole luminal-basal breast cancer spectrum rather than standing apart. The results also lead to a refined ERBB2 amplicon of 106 kb and show that several cases of amplifications are compatible with a breakage-fusion-bridge mechanism
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