Browsing
     by title


0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:   
OK
Full Text
See detailMicroencapsulation, principes et applications
Grandfils, Christian ULg

Conference (2002, May 16)

Detailed reference viewed: 7 (0 ULg)
Peer Reviewed
See detailMicroenvironment and cell fate determination in MCF10A is mediated by ionizing radiation, TGF beta and the extracellular matrix
Fernandez-Garcia, Ignacio; Paupert, Jenny ULg; Barcellos-Hoff, Mary-Helen

Poster (2010)

Detailed reference viewed: 18 (0 ULg)
See detailMicroenvironmental Regulation of Vascular Homeostasis and Leakage
Sounni, Nor Eddine ULg

Conference (2007, May 22)

Detailed reference viewed: 5 (0 ULg)
See detailMicroenvironments during antigen stimulation
Heinen, Ernst ULg; Bosseloir, A.; Cormann, N. et al

in Molecular biology of B cells developements (1990)

Detailed reference viewed: 6 (0 ULg)
Peer Reviewed
See detailMicroenvironments for B cell production and stimulation
Heinen, Ernst ULg; Tsunoda, R.

in Immunology Today (1987), 8

Detailed reference viewed: 3 (0 ULg)
See detailMicroexplant cultures of the cerebellum
Rogister, Bernard ULg; Moonen, Gustave ULg

in Feoroff, Serguei; Richardson, Arleen (Eds.) Protocols for neural cell cultures (2001)

Detailed reference viewed: 6 (3 ULg)
See detailMicroexplant cultures of the cerebellum
Rogister, Bernard ULg; Moonen, Gustave ULg

in Fedoroff, Serguei; Richardson, Anne (Eds.) Protocols for Neural Cell Culture (1997)

Detailed reference viewed: 8 (1 ULg)
See detailMicroexplants cultures of the cerebellum
Rogister, Bernard ULg; Moonen, Gustave ULg

in Fedoroff, Serguei; Richardson, Anne (Eds.) Protocols for Neural cells Cultures (1992)

Detailed reference viewed: 4 (0 ULg)
Peer Reviewed
See detailMicrofabrication of gold wires for atom guides
Koukharenko, Elena; Moktadir, Zakaria; Bagnall, D. et al

in Eurosensors XVII, 17th European Conference on Solid-State Transducers (2003)

Detailed reference viewed: 5 (0 ULg)
Full Text
See detailLa microfibrillation du myocarde
Fredericq, Léon ULg

in Archives Internationales de Physiologie (1931), XXXXIV

Detailed reference viewed: 17 (0 ULg)
Full Text
Peer Reviewed
See detailMicrofinance et micro-assurance santé : réflexions sur des articulations possibles à partir de quelques expériences au Bénin et au Burkina Faso
Labie, Marc; Nyssens, Marthe; Wele Idrissou, Pascal ULg

in Mondes en Développement (2007), 139(3), 57-71

Detailed reference viewed: 21 (6 ULg)
See detailMicroflore anaérobie des décharges
Hiligsmann, Serge ULg; Thonart, Philippe ULg

in Actes de l'Atelier "La problématique des déchets solides dans les villes africaines" (1997, May)

Detailed reference viewed: 14 (4 ULg)
Full Text
See detailMicroflore des monticules frasniens "F2j" de Belgique
Mamet, B.; Boulvain, Frédéric ULg

in Revue de micropaléontologie (1992), 35(4), 283-302

Detailed reference viewed: 16 (3 ULg)
Full Text
Peer Reviewed
See detailMicrofluidic Enzymatic Biosensing Systems: a Review
Mross, Stefan; Pierrat, Sebastien; Zimmermann, Tom et al

in Biosensors & Bioelectronics (2015), 70

Microfluidic biosensing systems with enzyme-based detection have been extensively studied in the last years owing to features such as high specificity, a broad range of analytes and a high degree of ... [more ▼]

Microfluidic biosensing systems with enzyme-based detection have been extensively studied in the last years owing to features such as high specificity, a broad range of analytes and a high degree of automation. This review gives an overview of the most important factors associated with these systems. In the first part, frequently used immobilization protocols such as physisorption and covalent bonding and detection techniques such as amperometry and fluorescence measurements are discussed with respect to effort, lifetime and measurement range. The Michaelis–Menten model describing the kinetics of enzymatic reactions, the role of redox mediators and the limitations of the linear measurement range of enzymatic sensors are introduced. Several possibilities of extending the linear measurement range in microfluidic systems such as diffusion-limiting membranes and the flow injection setup are presented. Regarding the integration of enzymes into microfluidic systems during the fabrication process, the constraints imposed by the biomolecules due to the limited usage of high temperatures and solvents are addressed. In the second part, the most common forms of enzyme integration into microfluidic systems, i.e. in channels and on electrodes, on microparticles, on paper and thread and as injected enzyme solutions, are reviewed, focusing on fabrication, applications and performance. [less ▲]

Detailed reference viewed: 18 (0 ULg)
Full Text
See detailMicrofluidic on a wire
Terwagne, Denis ULg; Vandewalle, Nicolas ULg; Gilet, Tristan ULg

Poster (2009, November)

Detailed reference viewed: 18 (3 ULg)
Full Text
See detailMicrofluidic on optical fibers: Towards a new kind of fluorescent biosensor
Lismont, Marjorie ULg; Vandewalle, Nicolas ULg; Weyer, Floriane ULg et al

Poster (2014, February)

In recent works, the behavior of droplets moving along vertical treads due to gravity was studied. It appeared that the droplet can be stopped by encountering a horizontal fiber depending on droplet ... [more ▼]

In recent works, the behavior of droplets moving along vertical treads due to gravity was studied. It appeared that the droplet can be stopped by encountering a horizontal fiber depending on droplet volumes and fiber characteristics. On the basis of this behavior and by replacing treads by two crossed optical fibers, it is possible to combine fluidics and optics to develop a new kind of fluorescent sensor. In our work, the intersection between two crossed optical fibers is used as the basic unit of an original optofluidic biosensor. These two optical fibers are used as droplets carriers: one for probe molecules and the other one for target species. The fiber's junction catches the droplets and act as a reaction center. The main advantage of using optical fibers resides in their ability to propagate and collect light to and from the droplet localized at the fiber's crossing. This optical fiber configuration can therefore allow the study of biological interactions using fluorescent labels. This new and versatile detection scheme was validated on a calcium indicator where ions detection is accomplished by using a dye, Oregon green Bapta-2, that has a Ca 2+ recognition group as well as an entity exhibiting fluorescence. A FRET recognition event, between Rh-Con A and FITC-Dextran, was also investigated to detect glucose. Finally, a prototype of a multiplexing device, composed of several juxtaposed fibers' junctions, was developed. [less ▲]

Detailed reference viewed: 95 (21 ULg)