864 research outputs found
Multimodal counter-argumentation in the workplace : the contribution of gesture and gaze to the expression of disagreement
This paper examines argumentative talk-in-interaction in the workplace. It focuses on counter-argumentative references, which consist of the various resources that the opponent uses to refer to the origin/source of his/her opposition, namely the confronted position and the person who expressed it. Particular attention is paid to the relationship - in terms of sequential positioning and referential extension - between reported speech, polyphony, pointing gestures and shifts in gaze direction. Data are taken from workplace management meetings that have been recorded in New Zealand by the Language in the Workplace Project
IMPACT : un dispositif de transcription et de commentaire de l'oral, pour l'enseignement et la recherche
Questionner le niveau méso-interactionnel comme lieu d'articulation entre langage et activité
Chemical analysis and aqueous solution properties of Charged Amphiphilic Block Copolymers PBA-b-PAA synthesized by MADIX
We have linked the structural and dynamic properties in aqueous solution of
amphiphilic charged diblock copolymers poly(butyl acrylate)-b-poly(acrylic
acid), PBA-b-PAA, synthesized by controlled radical polymerization, with the
physico-chemical characteristics of the samples. Despite product imperfections,
the samples self-assemble in melt and aqueous solutions as predicted by
monodisperse microphase separation theory. However, the PBA core are abnormally
large; the swelling of PBA cores is not due to AA (the Flory parameter
chiPBA/PAA, determined at 0.25, means strong segregation), but to h-PBA
homopolymers (content determined by Liquid Chromatography at the Point of
Exclusion and Adsorption Transition LC-PEAT). Beside the dominant population of
micelles detected by scattering experiments, capillary electrophoresis CE
analysis permitted detection of two other populations, one of h-PAA, and the
other of free PBA-b-PAA chains, that have very short PBA blocks and never
self-assemble. Despite the presence of these free unimers, the self-assembly in
solution was found out of equilibrium: the aggregation state is history
dependant and no unimer exchange between micelles occurs over months
(time-evolution SANS). The high PBA/water interfacial tension, measured at 20
mN/m, prohibits unimer exchange between micelles. PBA-b-PAA solution systems
are neither at thermal equilibrium nor completely frozen systems: internal
fractionation of individual aggregates can occur.Comment: 32 pages, 16 figures and 4 tables submitted to Journal of Interface
and Colloidal Scienc
Versatile control of Plasmodium falciparum gene expression with an inducible protein–RNA interaction
The available tools for conditional gene expression in Plasmodium falciparum are limited. Here, to enable reliable control of target gene expression, we build a system to efficiently modulate translation. We overcame several problems associated with other approaches for regulating gene expression in P. falciparum. Specifically, our system functions predictably across several native and engineered promoter contexts, and affords control over reporter and native parasite proteins irrespective of their subcellular compartmentalization. Induction and repression of gene expression are rapid, homogeneous and stable over prolonged periods. To demonstrate practical application of our system, we used it to reveal direct links between antimalarial drugs and their native parasite molecular target. This is an important outcome given the rapid spread of resistance, and intensified efforts to efficiently discover and optimize new antimalarial drugs. Overall, the studies presented highlight the utility of our system for broadly controlling gene expression and performing functional genetics in P. falciparum.National Institutes of Health (U.S.) (Health Director's New Innovator Award 1DP2OD007124)Bill & Melinda Gates Foundation (Grand Challenges Explorations Initiative OPP1069759)National Institute of Environmental Health Sciences (Predoctoral Training Grant 5-T32-ES007020)National Institute of General Medical Sciences (U.S.) (Biotechnology Training Grant 5-T32-GM08334)Thomas and Stacey Siebel FoundationMIT Start-up Fund
Field theoretic formulation of a mode-coupling equation for colloids
The only available quantitative description of the slowing down of the
dynamics upon approaching the glass transition has been, so far, the
mode-coupling theory, developed in the 80's by G\"otze and collaborators. The
standard derivation of this theory does not result from a systematic expansion.
We present a field theoretic formulation that arrives at very similar
mode-coupling equation but which is based on a variational principle and on a
controlled expansion in a small dimensioneless parameter. Our approach applies
to such physical systems as colloids interacting via a mildly repulsive
potential. It can in principle, with moderate efforts, be extended to higher
orders and to multipoint correlation functions
Schématisation et argumentation dans les allocutions des 11 et 16 mai 1968 de Georges Pompidou
Inducible Control of Subcellular RNA Localization Using a Synthetic Protein-RNA Aptamer Interaction
Evidence is accumulating in support of the functional importance of subcellular RNA localization in diverse biological contexts. In different cell types, distinct RNA localization patterns are frequently observed, and the available data indicate that this is achieved through a series of highly coordinated events. Classically, cis–elements within the RNA to be localized are recognized by RNA-binding proteins (RBPs), which then direct specific localization of a target RNA. Until now, the precise control of the spatiotemporal parameters inherent to regulating RNA localization has not been experimentally possible. Here, we demonstrate the development and use of a chemically–inducible RNA–protein interaction to regulate subcellular RNA localization. Our system is composed primarily of two parts: (i) the Tet Repressor protein (TetR) genetically fused to proteins natively involved in localizing endogenous transcripts; and (ii) a target transcript containing genetically encoded TetR–binding RNA aptamers. TetR–fusion protein binding to the target RNA and subsequent localization of the latter are directly regulated by doxycycline. Using this platform, we demonstrate that enhanced and controlled subcellular localization of engineered transcripts are achievable. We also analyze rules for forward engineering this RNA localization system in an effort to facilitate its straightforward application to studying RNA localization more generally.National Institutes of Health (U.S.) (Director’s New Innovator Award Program (grant number 1DP2OD007124 )
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