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See detailLa Celestina en el siglo XIX, ¿mito de la españolidad?
Francois, Jeromine ULg

Conference (2016, May 21)

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See detailLa Celestina interroga el código teatral: Tragedia fantástica de la gitana Celestina (1978) de Alfonso Sastre
Francois, Jeromine ULg

in Revista de Literatura (2016), LXXVIII(156), 525-541

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See detailCelestina, del personaje reubicado al mito
Francois, Jeromine ULg

Conference (2016, October 10)

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See detailCelestina, mediadora espacial en Terra Nostra de Carlos Fuentes
Francois, Jeromine ULg

Conference (2016, April)

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See detailLa Célestine : des lectures contemporaines aux polémiques ultérieures
Francois, Jeromine ULg

Conference (2016, May 04)

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See detailLa Célestine versus Lazarillo: un cas de crossover littéraire
Francois, Jeromine ULg

Conference (2017)

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See detail« La Célestine, médiatrice temporelle de ses réécritures »
Francois, Jeromine ULg

Conference (2015)

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See detailCELINE : CELestial Infrared Nulling Experiment
Hanot, Charles ULg

Scientific conference (2010, February)

The small angular distance (<100 mas) and the huge flux ratio (10^7) between an Earth-like exoplanet in the so-called habitable zone and its host star makes it very difficult to direct image such systems ... [more ▼]

The small angular distance (<100 mas) and the huge flux ratio (10^7) between an Earth-like exoplanet in the so-called habitable zone and its host star makes it very difficult to direct image such systems. Nulling interferometry consists of a very powerful technique that combines destructively the light from two or more collectors to dim the starlight and to reveal faint companions in its vicinity. We have developed a new nulling experiment based on the fiber nuller principle (Serabyn et al. 2006 , Martin et al. 2008). This fully symmetric reflective nulling bench aims at testing broadband nulling in both H and K bands as well as characterizing photonic fibers for modal filtering. We present in this paper the design, the development as well as preliminary results of the experiment. [less ▲]

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See detailCell "circadian" cycle: new role for mammalian core clock genes.
Borgs, Laurence ULg; Beukelaers, Pierre ULg; Vandenbosch, Renaud ULg et al

in Cell Cycle (Georgetown, Tex.) (2009), 8(6), 832-7

In mammals, 24 hours rhythms are organized as a biochemical network of molecular clocks that are operative in all tissues, with the master clock residing in the hypothalamic suprachiasmatic nucleus (SCN ... [more ▼]

In mammals, 24 hours rhythms are organized as a biochemical network of molecular clocks that are operative in all tissues, with the master clock residing in the hypothalamic suprachiasmatic nucleus (SCN). The core pacemakers of these clocks consist of auto-regulatory transcriptional/post-transcriptional feedback loops. Several lines of evidence suggest the existence of a crosstalk between molecules that are responsible for the generation of circadian rhythms and molecules that control the cell cycle progression. In addition, highly specialized cell cycle checkpoints involved in DNA repair after damage seem also, at least in part, mediated by clock proteins. Recent studies have also highlighted a putative connection between clock protein dysfunction and cancer progression. This review discusses the intimate relation that exists between cell cycle progression and components of the circadian machinery. [less ▲]

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See detailCell based advanced therapeutic medicinal products for bone repair: Keep it simple?
Leijten, J.; Chai, Y. C.; Papantoniou, I. et al

in Advanced drug delivery reviews (2015), 84

The development of cell based advanced therapeutic medicinal products (ATMPs) for bone repair has been expected to revolutionize the health care system for the clinical treatment of bone defects. Despite ... [more ▼]

The development of cell based advanced therapeutic medicinal products (ATMPs) for bone repair has been expected to revolutionize the health care system for the clinical treatment of bone defects. Despite this great promise, the clinical outcomes of the few cell based ATMPs that have been translated into clinical treatments have been far from impressive. In part, the clinical outcomes have been hampered because of the simplicity of the first wave of products. In response the field has set-out and amassed a plethora of complexities to alleviate the simplicity induced limitations. Many of these potential second wave products have remained "stuck" in the development pipeline. This is due to a number of reasons including the lack of a regulatory framework that has been evolving in the last years and the shortage of enabling technologies for industrial manufacturing to deal with these novel complexities. In this review, we reflect on the current ATMPs and give special attention to novel approaches that are able to provide complexity to ATMPs in a straightforward manner. Moreover, we discuss the potential tools able to produce or predict 'goldilocks' ATMPs, which are neither too simple nor too complex. [less ▲]

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See detailA cell based modelling framework for skeletal tissue engineering applications
Geris, Liesbet ULg; Van Liedekerke, Paul; Smeets, Bart et al

in Journal of Biomechanics (2010), 43(5), 887-892

In this study, a cell based lattice free modelling framework is proposed to study cell aggregate behaviour in bone tissue engineering applications. The model encompasses cell-to-cell and cell environment ... [more ▼]

In this study, a cell based lattice free modelling framework is proposed to study cell aggregate behaviour in bone tissue engineering applications. The model encompasses cell-to-cell and cell environment interactions such as adhesion, repulsion and drag forces. Oxygen, nutrients, waste products, growth factors and inhibitors are explicitly represented in the model influencing cellular behaviour. Furthermore, a model for cell metabolism is incorporated representing the basic enzymic reactions of glycolysis and the Krebs cycle. Various types of cell death such as necrosis, apoptosis and anoikis are implemented. Finally, an explicit model of the cell cycle controls the proliferation process, taking into account the presence or absence of various metabolites, sufficient space and mechanical stress. Several examples are presented demonstrating the potential of the modelling framework. The behaviour of a synchronised cell aggregate under ideal circumstances is simulated, clearly showing the different stages of the cell cycle and the resulting growth of the aggregate. Also the difference in aggregate development under ideal (normoxic) and hypoxic conditions is simulated, showing hypoxia induced necrosis mainly in the centre of the aggregate grown under hypoxic conditions. The next step in this research will be the application of this modelling framework to specific experimental set-ups for bone tissue engineering applications. (C) 2009 Elsevier Ltd. All rights reserved. [less ▲]

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See detailCell cholesterol modulates metalloproteinase-dependent shedding of low-density lipoprotein receptor-related protein-1 (LRP-1) and clearance function.
Selvais, C.; D'Auria, L.; Tyteca, D. et al

in FASEB Journal (2011), 25(8), 2770-2781

Low-density lipoprotein receptor-related protein-1 (LRP-1) is a plasma membrane scavenger and signaling receptor, composed of a large ligand-binding subunit (515-kDa α-chain) linked to a shorter ... [more ▼]

Low-density lipoprotein receptor-related protein-1 (LRP-1) is a plasma membrane scavenger and signaling receptor, composed of a large ligand-binding subunit (515-kDa α-chain) linked to a shorter transmembrane subunit (85-kDa β-chain). LRP-1 cell-surface level and function are controlled by proteolytic shedding of its ectodomain. Here, we identified ectodomain sheddases in human HT1080 cells and demonstrated regulation of the cleavage by cholesterol by comparing the classical fibroblastoid type with a spontaneous epithelioid variant, enriched ∼2-fold in cholesterol. Two membrane-associated metalloproteinases were involved in LRP-1 shedding: a disintegrin and metalloproteinase-12 (ADAM-12) and membrane-type 1 matrix metalloproteinase (MT1-MMP). Although both variants expressed similar levels of LRP-1, ADAM-12, MT1-MMP, and specific tissue inhibitor of metalloproteinases-2 (TIMP-2), LRP-1 shedding from epithelioid cells was ∼4-fold lower than from fibroblastoid cells. Release of the ectodomain was triggered by cholesterol depletion in epithelioid cells and impaired by cholesterol overload in fibroblastoid cells. Modulation of LRP-1 shedding on clearance was reflected by accumulation of gelatinases (MMP-2 and MMP-9) in the medium. We conclude that cholesterol exerts an important control on LRP-1 levels and function at the plasma membrane by modulating shedding of its ectodomain, and therefore represents a novel regulator of extracellular proteolytic activities.-Selvais, C., D'Auria, L., Tyteca, D., Perrot, G, Lemoine, P., Troeberg, L., Dedieu, S., Noël, A., Nagase, H., Henriet, P., Courtoy, P. J., Marbaix, E., Emonard, H. Cell cholesterol modulates metalloproteinase-dependent shedding of low-density lipoprotein receptor-related protein-1 (LRP-1) and clearance function. [less ▲]

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See detailCell cultivation in chitosan alginate hydrogel beads
Henrotin, Yves ULg; Kesteloot, Frédéric; Sanchez, Christelle ULg

Patent (2014)

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See detailCell cultivation in chitosan alginate hydrogel beads
Henrotin, Yves ULg; Kesteloot, Frédéric; Sanchez, Christelle ULg

Patent (2011)

The present invention relates to a method of producing a hydrogel matrix comprising cartilage-forming cells wherein alginate, chitosan and cartilage-forming cells are mixed and subsequently polymerised ... [more ▼]

The present invention relates to a method of producing a hydrogel matrix comprising cartilage-forming cells wherein alginate, chitosan and cartilage-forming cells are mixed and subsequently polymerised into beads. [less ▲]

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See detailCELL CULTIVATION IN CHITOSAN ALGINATE HYDROGEL BEADS
Henrotin, Yves ULg; Kesteloot, Frédéric; Sanchez, Christelle ULg

Patent (2011)

The present invention relates to a method of producing a hydrogel matrix comprising cartilage-forming cells wherein alginate, chitosan and cartilage- forming cells are mixed and subsequently polymerised ... [more ▼]

The present invention relates to a method of producing a hydrogel matrix comprising cartilage-forming cells wherein alginate, chitosan and cartilage- forming cells are mixed and subsequently polymerised into beads. [less ▲]

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See detailCell cycle activation of hematopoietic progenitor cells increases very late antigen-5-mediated adhesion to fibronectin.
Giet, Olivier ULg; Huygen, Sandra; Beguin, Yves ULg et al

in Experimental hematology (2001), 29(4), 515-24

Recent studies suggested that trafficking of hematopoietic progenitor cells is related to cell cycle status. We studied whether adhesion of progenitor cells to extracellular matrix proteins was modulated ... [more ▼]

Recent studies suggested that trafficking of hematopoietic progenitor cells is related to cell cycle status. We studied whether adhesion of progenitor cells to extracellular matrix proteins was modulated by cell cycle transit.Mobilized peripheral blood CD34+ cells were stimulated ex vivo for 48 hours with stem cell factor, flt-3 ligand, and thrombopoietin and fractionated by adhesion to fibronectin or vascular cell adhesion molecule-1 (VCAM-1). Adherent and nonadherent cells were assayed for cell cycle status, long-term culture-initiating cell frequency, and integrin function. Binding to fibronectin, but not to VCAM-1, displayed a cell cycle selectivity as the adherent fraction to fibronectin was enriched in cycling CD34+ cells and in cycling long-term culture-initiating cells compared to the nonadherent fraction. Combined cell cycle and phenotypic analysis showed that the expression of VLA-5 was upregulated during S/G2+M but that of VLA-4 remained constant. The selective binding of cycling CD34+ cells to fibronectin was reverted by anti-VLA-5 but not by anti-VLA-4 blocking antibodies. Also, cycling CD34+ cells preferentially adhered to the VLA-5 binding domain but not to the VLA-4 binding domain of fibronectin. Adhesion of cycling CD34+ cells to fibronectin was a reversible process modulated by cell cycle progression, because adherent cells could exit the cell cycle and return to a nonadhesive state within an additional 48-hour culture period.The results indicate that the enhanced binding capacity of cycling progenitor cells to fibronectin is mediated by VLA-5. [less ▲]

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