221 research outputs found
Status of Diamond Detector Development for Beam Halo Investigation at ATF2
Work supported by Chinese Scholarship Council - THPME092, ISBN 978-3-95450-132-8International audienceWe are developing a diamond detector for beam halo and Compton spectrum diagnostics after the interaction point (IP) of ATF2, a low energy (1.3 GeV) prototype of the final focus system for ILC and CLIC linear collider projects. Tests of a 500 ÎŒm thick sCVD diamond detector with a dimension of 4.5 mmĂ4.5 mm have been carried out with radioactive sources and with electron beam from PHIL low energy (<10 MeV) photo-injector at LAL. The tests at PHIL were done with different beam intensities in air, just after the exit window at the end of the beam line, to test the response of the diamond detector and the readout electronics. We have successfully detected signals from single electrons, using a 40 dB amplifier, and from an electron beam of 108 electrons, using a 24 dB attenuator. A diamond sensor with 4 strips has been designed and fabricated for installation in the vacuum chambers of ATF2 and PHIL, with the aim to scan both the beam halo (with 2 strips of 1.5 mmĂ4 mm) and the beam core (with 2 strips of 0.1 mmĂ4 mm) transverse distributions
PHIL photoinjector test line
LAL is now equiped with its own platform for photoinjectors tests and
Research and Developement, named PHIL (PHotoInjectors at LAL). This facility
has two main purposes: push the limits of the photoinjectors performances
working on both the design and the associated technology and provide a low
energy (MeV) short pulses (ps) electron beam for the interested users. Another
very important goal of this machine will be to provide an opportunity to form
accelerator physics students, working in a high technology environment. To
achieve this goal a test line was realised equipped with an RF source, magnets
and beam diagnostics. In this article we will desrcibe the PHIL beamline and
its characteristics together with the description of the first two
photoinjector realised in LAL and tested: the ALPHAX and the PHIN RF Guns
Low Energy Beam Measurements Using PHIL Accelerator at LAL, Comparison with PARMELA Simulations
http://accelconf.web.cern.ch/AccelConf/PAC2011/papers/wep210.pdfInternational audiencePHIL ("PHoÂto-InÂjecÂtor at LAL") is a new elecÂtron beam acÂcelÂerÂaÂtor at LAL. This acÂcelÂerÂaÂtor is dedÂiÂcatÂed to test and charÂacÂterÂize elecÂtron RF-guns and to deÂlivÂer elecÂtron beam to users. This maÂchine has been deÂsigned to proÂduce and charÂacÂterise low enÂerÂgy (E<10 MeV), small emitÂtance (e<10 p.âmm.âmrad), high brilÂliance elecÂtrons bunch at low repÂeÂtiÂtion freÂquenÂcy (n<10Hz). The first beam has been obÂtained on the 4th of NovemÂber 2009. The curÂrent RF-gun testÂed on PHIL is the AlÂphaX gun, a 2.5 cell S-band cavÂiÂty deÂsigned by LAL for the plasÂma acÂcelÂerÂaÂtor studÂies perÂformed at the StrathÂclyde uniÂverÂsiÂty. This paper will preÂsent the first AlÂphaX RF-gun charÂacÂterÂiÂzaÂtions perÂformed at LAL on PHIL acÂcelÂerÂaÂtor, and will show comÂparÂisons beÂtween meaÂsureÂments and PARMELA simÂuÂlaÂtions
Netrin-3 Signals Through Serine Phosphorylation in Tetrahymena thermophila
The netrin family of proteins are structurally related to laminin and, while first discovered in the nematode Caenorhabditis elegans, are now known to be present in species throughout the animal kingdom, including humans. These proteins also have a wide variety of roles that include inhibition of apoptosis, chemorepulsion, and axonal guidance. Due to the results of previous studies involving netrin-1 in vertebrate systems, the current prevailing assumption is that netrins, when acting as chemorepellents, signal using tyrosine kinases. However, data that we gathered through phosphoserine-targeting ELISA assays and immunofluorescence microscopy demonstrates that the netrin-3 peptides signal Tetrahymena thermophila through serine phosphorylation instead, causing the ciliate protists to avoid netrin-3 peptides in response. Treatment with netrin-3 peptides also seems to cause mitotic inhibition in Tetrahymena, which can be reversed by addition of a serine kinase inhibitor. This new information suggests that netrin-3 may have physiological roles that have previously been unexplored
Erratum to: Providing Patients with Implantable Cardiac Device Data through a Personal Health Record: A Qualitative Study
Erratum to: Providing Patients with Implantable Cardiac Device Data through a Personal Health Record: A Qualitative Study. [Appl Clin Inform. 2017
InterGEO: a digital platform for university education on geomorphological heritage
The project InterGEO was carried out with the objective to disseminate knowledge on geomorphological heritage by developing a digital learning platform. It aims at improving students' autonomy by the reduction of face-to-face teaching and increasing autonomous learning as well as promoting international interactions between students interested in geomorphological heritage. A completely free-access virtual course on geomorphosites was developed with the Learning Management System Moodle. The course is divided into 24 thematic chapters, each of them containing a short description, a list of references and selected publications, as well as other educational material (videos, virtual fieldtrips, etc.). In particular, several videos allow presenting in a dynamic way concepts and examples. The paper presents the tool and its use in academic programmes in six European universities, where it was tested, in various contexts (Bachelors' and Masters' programmes; students in geography or geology; general courses in geomorphology and specific courses on geoheritage and geoconservation), before discussing the advantages and challenges the tool is facing. The InterGEO platform is an easy-to-use and friendly educational tool, which allows developing blended learning activities; it is flexible and adaptable in various learning contexts.The coordination tasks (appointment of an assistant) and two workshops in Lausanne were financed by the University of Lausanne (Teaching Innovation Fund and Investment Fund of the Faculty of Geosciences and Environment, FGSE). The videos were designed and created with support of the universities of Lausanne (TIF) and Savoie Mont Blanc (IDEFI Promising and ReflexPro; LabEx ITEM)
Commissioning of the ALTO 50 MeV electron linac
online : http://accelconf.web.cern.ch/AccelConf/e06/PAPERS/MOPLS113.pdfThe ALTO 50 MeV electron linac is dedicated to the production of neutron-rich radioactive nuclei using the photo-fission process and the optimisation of the targetion source system for SPIRAL 2 and EURISOL projects. The accelerator consists of a 3 MeV injector (old test station of LAL, Laboratoire de l'Accélérateur Linéaire d'Orsay), LIL (Linac Injector of LEP) accelerating structure, RF power plant, beam line, control system and diagnostics. Specified and measured beam parameters will be compared to show the performances of the photofission process and eventually other applications
The Peptidyl Prolyl Isomerase Rrd1 Regulates the Elongation of RNA Polymerase II during Transcriptional Stresses
Rapamycin is an anticancer agent and immunosuppressant that acts by inhibiting the TOR signaling pathway. In yeast, rapamycin mediates a profound transcriptional response for which the RRD1 gene is required. To further investigate this connection, we performed genome-wide location analysis of RNA polymerase II (RNAPII) and Rrd1 in response to rapamycin and found that Rrd1 colocalizes with RNAPII on actively transcribed genes and that both are recruited to rapamycin responsive genes. Strikingly, when Rrd1 is lacking, RNAPII remains inappropriately associated to ribosomal genes and fails to be recruited to rapamycin responsive genes. This occurs independently of TATA box binding protein recruitment but involves the modulation of the phosphorylation status of RNAPII CTD by Rrd1. Further, we demonstrate that Rrd1 is also involved in various other transcriptional stress responses besides rapamycin. We propose that Rrd1 is a novel transcription elongation factor that fine-tunes the transcriptional stress response of RNAPII
Identifying invasive species threats, pathways, and impacts to improve biosecurity
Managing invasive species with prevention and early-detection strategies can avert severe ecological and economic impacts. Horizon scanning, an evidence-based process combining risk screening and consensus building to identify threats, has become a valuable tool for prioritizing invasive species management and prevention. We assembled a working group of experts from academic, government, and nonprofit agencies and organizations, and conducted a multi-taxa horizon scan for Florida, USA, the first of its kind in North America. Our primary objectives were to identify high-risk species and their introduction pathways, to detail the magnitude and mechanism of potential impacts, and, more broadly, to demonstrate the utility of horizon scanning. As a means to facilitate future horizon scans, we document the process used to generate the list of taxa for screening. We evaluated 460 taxa for their potential to arrive, establish, and cause negative ecological and socioeconomic impacts, and identified 40 potential invaders, including alewife, zebra mussel, crab-eating macaque, and red swamp crayfish. Vertebrates and aquatic invertebrates posed the greatest invasion threat, over half of the high-risk taxa were omnivores, and there was high confidence in the scoring of high-risk taxa. Common arrival pathways were ballast water, biofouling of vessels, and escape from the pet/aquarium/horticulture trade. Competition, predation, and damage to agriculture/forestry/aquaculture were common impact mechanisms. We recommend full risk analysis for the high-risk taxa; increased surveillance at Florida's ports, state borders, and high-risk pathways; and periodic review and revision of the list. Few horizon scans detail the comprehensive methodology (including list-building), certainty estimates for all scoring categories and the final score, detailed pathways, and the magnitude and mechanism of impact. Providing this information can further inform prevention efforts and can be efficiently replicated in other regions. Moreover, harmonizing methodology can facilitate data sharing and enhance interpretation of results for stakeholders and the general public.</p
Does rapid HIV disease progression prior to combination antiretroviral therapy hinder optimal CD4 + T-cell recovery once HIV-1 suppression is achieved?
Objective: This article compares trends in CD4+ T-cell recovery and proportions achieving optimal restoration (>=500 cells/”l) after viral suppression following combination antiretroviral therapy (cART) initiation between rapid and nonrapid progressors. Methods: We included HIV-1 seroconverters achieving viral suppression within 6 months of cART. Rapid progressors were individuals experiencing at least one CD4+ less than 200 cells/”l within 12 months of seroconverters before cART. We used piecewise linear mixed models and logistic regression for optimal restoration. Results: Of 4024 individuals, 294 (7.3%) were classified as rapid progressors. At the same CD4+ T-cell count at cART start (baseline), rapid progressors experienced faster CD4+ T-cell increases than nonrapid progressors in first month [difference (95% confidence interval) in mean increase/month (square root scale): 1.82 (1.61; 2.04)], which reversed to slightly slower increases in months 1â18 [-0.05 (-0.06; -0.03)] and no significant differences in 18â60 months [-0.003 (-0.01; 0.01)]. Percentage achieving optimal restoration was significantly lower for rapid progressors than nonrapid progressors at months 12 (29.2 vs. 62.5%) and 36 (47.1 vs. 72.4%) but not at month 60 (70.4 vs. 71.8%). These differences disappeared after adjusting for baseline CD4+ T-cell count: odds ratio (95% confidence interval) 0.86 (0.61; 1.20), 0.90 (0.38; 2.17) and 1.56 (0.55; 4.46) at months 12, 36 and 60, respectively. Conclusion: Among people on suppressive antiretroviral therapy, rapid progressors experience faster initial increases of CD4+ T-cell counts than nonrapid progressors, but are less likely to achieve optimal restoration during the first 36 months after cART, mainly because of lower CD4+ T-cell counts at cART initiation
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