Relevant bibliographies by topics / CLFV

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Academic literature on the topic 'CLFV'

Author: Grafiati
Published: 14 March 2023

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Journal articles on the topic "CLFV"

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Cei, F., and D. Nicolò. "Lepton Flavour Violation Experiments." Advances in High Energy Physics 2014 (2014): 1–31. http://dx.doi.org/10.1155/2014/282915.

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Lepton Flavour Violation in the charged lepton sector (CLFV) is forbidden in the Minimal Standard model and strongly suppressed in extensions of the model to include finite neutrino mixing. On the other hand, a wide class of Supersymmetric theories, even coupled with Grand Unification models (SUSY-GUT models), predict CLFV processes at a rate within the reach of new experimental searches operated with high resolution detectors at high intensity accelerators. As the Standard model background is negligible, the observation of one or more CLFV events would provide incontrovertible evidence for physics beyond Standard model, while a null effect would severely constrain the set of theory parameters. Therefore, a big experimental effort is currently (and will be for incoming years) accomplished to achieve unprecedented sensitivity on several CLFV processes. In this paper we review past and recent results in this research field, with focus on CLFV channels involving muons and tau's. We present currently operating experiments as well as future projects, with emphasis laid on how sensitivity enhancements are accompanied by improvements on detection techniques. Limitations due to systematic effects are also discussed in detail together with the solutions being adopted to overcome them.
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Pikies, M. "cLFV Searches at LHCb." Acta Physica Polonica B 49, no. 6 (2018): 1309. http://dx.doi.org/10.5506/aphyspolb.49.1309.

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Mihara, S. "Prospects for CLFV experiments." Journal of Physics: Conference Series 408 (February 7, 2013): 012017. http://dx.doi.org/10.1088/1742-6596/408/1/012017.

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Hitlin, David G. "CLFV Decays at BaBar." Nuclear Physics B - Proceedings Supplements 248-250 (March 2014): 64–66. http://dx.doi.org/10.1016/j.nuclphysbps.2014.02.012.

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Paradisi, Paride. "Interrelationship among , EDMs and cLFV." Nuclear Physics B - Proceedings Supplements 248-250 (March 2014): 8–12. http://dx.doi.org/10.1016/j.nuclphysbps.2014.02.003.

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Kriewald, J., A. Abada, and A. M. Teixeira. "The role of leptonic CPV phases in cLFV observables." Journal of Physics: Conference Series 2156, no. 1 (December 1, 2021): 012154. http://dx.doi.org/10.1088/1742-6596/2156/1/012154.

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Abstract In models where the Standard Model is extended by Majorana fermions, interference effects due to the presence of CP violating phases have been shown to play a crucial role in lepton number violating processes. However, important effects can also arise in lepton number conserving, but charged lepton flavour violating (cLFV) transitions and decays. Here we show that the presence of CP violating (Dirac and Majorana) phases can have a striking impact for the predicted rates of cLFV observables. We explore the interference effects in several cLFV observables, carrying for the first time a thorough analysis of the different observables and the implications for future observation. We discuss how the presence of leptonic CP violating phases might lead to a loss of correlation between observables (typically present in simple SM extensions via heavy sterile fermions), or even to the suppression of certain channels; these effects can be interpreted as suggestive of non-vanishing phases.
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Natori, Hiroaki. "COMET, an Experiment to Search for mu-e Conversion in a Nuclear Field." International Journal of Modern Physics: Conference Series 46 (January 2018): 1860065. http://dx.doi.org/10.1142/s2010194518600650.

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Charged lepton flavor violating (CLFV) process is predicted to be out of experimental reach by the Standard Model of elementary particle physics (SM). However, many models of the new physics beyond the SM predicts that it is just below the current experimental limit. COMET searches for one of the CLFV process, mu-e conversion in a nuclear field, improving the sensitivity by a factor of approximately [Formula: see text] for Phase-I and [Formula: see text] for Phase-II experiment from a past experiment.
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Hambye, Thomas. "CLFV and the origin of neutrino masses." Nuclear Physics B - Proceedings Supplements 248-250 (March 2014): 13–19. http://dx.doi.org/10.1016/j.nuclphysbps.2014.02.004.

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Shoukavy, Dzmitry. "COMET status and plans." EPJ Web of Conferences 212 (2019): 01006. http://dx.doi.org/10.1051/epjconf/201921201006.

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Lepton Flavour Violation in the charged lepton sector (CLFV) is forbidden in the Standard Model. Therefore, the observation of CLFV process would be clear evidence of physics beyond the Standard Model. The COMET (COherent Muon to Electron Transitions) experiment will measure one of these processes: µN → eN at the Japan Proton Accelerator Research Complex in Tokai, Japan. The COMET experiment will be carried out using a two-staged approach. Phase-I of the experiment is aiming at a signal sensitivity of 3.1 × 10−15. Phase-II will use much more intense beam and a more complex transport system to achieve a single-event sensitivity of 3 × 10−17. The article gives an overview of construction and status of the COMET experiment.
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Jasien, Paul G. "Stabilities of hypervalent chlorine fluorides (ClF3, ClF5 and ClF7)." Chemical Physics Letters 188, no. 1-2 (January 1992): 135–39. http://dx.doi.org/10.1016/0009-2614(92)85102-g.

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Dissertations / Theses on the topic "CLFV"

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MORESCALCHI, LUCA. "Study of the calorimetric detection of the muon to electron conversion in the Mu2e experiment." Doctoral thesis, Università di Siena, 2017. http://hdl.handle.net/11365/1030437.

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The Mu2e experiment will search for Charged Lepton Flavor Violation (CLFV), looking at the coherent conversion of a muon into an electron in the field of an aluminum nucleus. The knowledge of such a CLFV reaction allows to indirectly probe new physics at energy scales up to thousands of TeV, inaccessible with direct searches at either present or planned high energy colliders. For this reason, Mu2e will measure the muon-to-electron conversion rate R_{\mu e} with an unprecedented accuracy, so to improve of a factor 10^4 the best current measurement and, in case of no observation, to constrain its value below 6 x 10^-17 at 90% of CL. To reach this ambitious sensitivity, about 10^18 muonic atom decays have to be observed: Mu2e is expected to use an intense pulsed muon beam, and rely on a detector system composed of a straw tube tracker and an electromagnetic calorimeter. The calorimeter is composed of 1348 un-doped CsI crystals, each coupled to two large area Silicon Photomultipliers (SiPMs). It plays a central role in the Mu2e measurement, providing particle identification capabilities that are necessary to reject the cosmic muons and antiprotons induced background. Moreover, the calorimeter has to help the tracker providing a seed for the pattern recognition and to provide a fast independ trigger. Having these experimental requests as pivotal reference, a set of Quality Assurance (QA) criteria for the calorimeter active components have been defined. Following the corresponding QA procedures, a first batch of crystals and photosensors has been characterized and used to assemble a medium scale prototype of the calorimeter (Module-0). The Module-0 has been studied by means of a 100 MeV electron beam, confirming that expected calorimeter performances well satisfy the Mu2e requirements.
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Rebenstorf, Kathrin. "Untersuchungen zur Epidemiologie des Cherry leaf roll virus (CLRV)." Doctoral thesis, Humboldt-Universität zu Berlin, Landwirtschaftlich-Gärtnerische Fakultät, 2005. http://dx.doi.org/10.18452/15335.

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Das Cherry leaf roll virus (CLRV) ist ein weltweit verbreitetes Pflanzenvirus, das eine Vielzahl an Laubgehölzen und Stauden infiziert. In der vorliegenden Arbeit wurden phylogenetische und serologische Analysen der Populationsstruktur des CLRV durchgeführt und ihre Korrelation mit epidemiologischen Faktoren, wie der geographischen Verbreitung und der Wirtspflanzenart, untersucht. Der Nachweis von CLRV erfolgte mittels Immunocapture - Reverse Transkription -Polymerase Kettenreaktion (IC-RT-PCR). Dabei konnte CLRV in 20 verschiedenen Gehölzarten an 33 Standorten in Deutschland nachgewiesen werden. Außerdem wurden Isolate aus 6 anderen Ländern, die von Kollegen zur Verfügung gestellt worden waren, in die Untersuchungen einbezogen. Der Vergleich der Symptomausprägungen auf verschiedenen Testpflanzen zeigte keine auffälligen biologischen Unterschiede bei den gewonnenen CLRV-Isolaten. Untersuchungen zur RNA-Populationsstruktur basierend auf einem 380 bp langen Teilbereichs der 3’-nicht-translatierten Region (3’UTR) der genomischen RNA1 und RNA2 zeigte eine homogene Basenzusammensetzung innerhalb der Virusisolate. Hingegen traten zwischen den 73 untersuchten CLRV-Isolaten Sequenzunterschiede bis zu 15,5 % auf. Die phylogenetische Analyse der 3’UTR deckte eine Gruppierung der Virusisolate nach den natürlichen Wirtspflanzenarten auf, die durch statistischen Analysen mittels GST-Koeffizient bzw. Mantel-Test verifiziert werden konnten. Der Vergleich der phylogenetischen mit der serologischen Gruppierung, die unter der Verwendung monoklonaler Antikörper analysiert wurde, zeigte für 24 CLRV-Isolate eine hohe Korrelation in Bezug auf die Gruppenzuordnung. Auch beim phylogenetischen Vergleich der Hüllprotein-Sequenzen für 9 CLRV-Isolate ergaben sich die gleichen Gruppen. Innerhalb der 380 bp langen 3’UTR wurde mittels Computer-Modellierung der Sekundärstruktur unter Verwendung von 67 CLRV-Sequenzen zwei konservierte Stemloops identifiziert, die die Ergebnisse anderer Autoren bestätigen und die funktionelle Bedeutung der 3’UTR belegt.
Cherry leaf roll virus (CLRV) is worldwide distributed and is infecting a variety of deciduous trees and shrubs. In this study phylogenetic and serological analyses of the population diversity of CLRV and the correlation with the epidemiological factors geographical distribution and host plant species, have been investigated. During a survey in Germany plants were tested by IC-RT-PCR and virus isolates recovered from a range of woody plants from different geographical regions. CLRV was detected in 20 different plant species from 33 locations in Germany. Also isolates from 6 other countries received from colleagues were included in the study. Comparison of symptom expression on different indicator plants did not show obvious biological differences between the recovered CLRV isolates. Investigations of the RNA population structure based on a 380 bp long fragment of the 3''-non-translated region (3''UTR) of genomic RNA1 and RNA2 revealed a homogeneous base composition for single isolates. However, between 73 CLRV isolates 3’UTR sequences showed up to 15.5 % divergence. Phylogenetic analysis of the 3''UTR uncovered a grouping of the virus isolates according to the natural host plant species, which was verified by statistic analyses using GST coefficient and Mantel test. The comparison of the phylogenetic grouping with the serological grouping of 24 selected CLRV isolates, which was analyzed using a set of seven monoclonal antibodies, showed a high correlation regarding the group arrangement. The phylogenetic comparison of the coat protein sequences for 9 CLRV isolates also revealed the same group arrangement. Secondary structure analysis by computer modelling of the consensus sequence of the 380 bp long 3''UTR using 67 CLRV sequences identified two conserved stem loop regions supporting the results of other authors and indicating the functional significance of the 3''UTR.
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Fuchs, Franz Xaver. "Clock-feedthrough compensation in MOS sample-and-hold circuits." Thesis, University of Plymouth, 2001. http://hdl.handle.net/10026.1/2354.

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All MOS sample-and-hold circuits suffer to a greater or lesser extent from clock-feedthrough (CLFT), also called charge-injection. During the transition from sample to hold mode, charge is transferred from an MOS transistor switch onto the hold capacitor, thus the name charge-injection. This error can lead to considerable voltage change across the capacitor, and predicting the extent of the induced error potentials is important to circuit designers. Previous studies have shown a considerable dependency of CLFT on signal voltage, circuit impedances, clock amplitude and clock fall-time. The focus of this work was on the signal dependency of the CLFT error and on the CLFT induced signal distortion in open-loop sample-and-hold circuits. CLFT was found to have a strongly non-linear, signal dependent, component, which may cause considerable distortion of the sampled signal. The parameters influencing this distortion were established. It was discovered that distortion could be reduced by more than 20dB through careful adjustment of the clock fall-rate. Several circuit solutions that can help reduce the level of distortion arising from CLFT are presented. These circuits can also reduce the absolute level of CLFT. Simulations showed their effectiveness, which was also proven in silicon. The CLFT reduction methods used in these circuits are easily transferable to other switched-capacitor circuits and are suitable for applications where space is at a premium (as, for example, in analogue neural networks). A new saturation mode contribution to CLFT was found. It is shown to give rise to increased CLFT under high injection conditions.
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Ribeiro, Hugo Miguel Antunes. "Ensaios sobre microenxertia em nogueira (Juglans regia L.)." Master's thesis, Universidade de Évora, 2021. http://hdl.handle.net/10174/29912.

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As técnicas de cultura in vitro têm contribuído para a optimização de protocolos de propagação do género Juglans. Neste trabalho foi testada a técnica de microenxertia de J. regia em híbrido ‘Paradox’. Foi efectuado o enraizamento ex vitro em simultâneo com a enxertia. Foi avaliada a influência da presença de folhas no enxerto e no porta-enxerto na taxa de sucesso da técnica, assim como o despiste de Cherry leaf roll virus. Verificou-se que a presença de folhas foi um requisito obrigatório para o sucesso da enxertia e do enraizamento. A enxertia apresentou uma taxa média de sucesso de 84,6 % e a taxa de aclimatização aos 60 dias foi 86,4 %. Detectaram-se amostras suspeitas de serem positivas para a presença de Cherry leaf roll virus. A técnica de microenxertia apresentada mostrou-se viável tecnicamente e eventualmente com condições de competir com as técnicas tradicionais de enxertia em viveiro; ABSTRACT: Trials about walnut (Juglans regia L.) micrografting. In vitro culture techniques have contributed to the optimization of propagation protocols of the genus Juglans. Here the micrografting technique was tested with J. regia grafted in a 'Paradox' hybrid. Rooting ex vitro was performed simultaneously with grafting. The influence of the presence of leaves on the graft and rootstock on the success rate of the technique was evaluated, as well as the screening of Cherry leaf roll virus. It was found that the presence of leaves, in the graft or in the rootstock, or in both, was a mandatory requirement for the grafting success. The grafting success presented a final global average of 84.6% and the acclimatization rate at 60 days was 86.4%. Samples putatively positive for the presence of Cherry leaf roll virus were detected. The micrografting technique here presented seems to be technically feasible and maybe able to compete with the traditional techniques of nursery grafting.
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Wilson, K. Craig. "Using marginal analysis to load Combat Logistics Force (CLF) ships." Thesis, Monterey, Calif. : Springfield, Va. : Naval Postgraduate School ; Available from National Technical Information Service, 1994. http://handle.dtic.mil/100.2/ADA293136.

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Thesis (M.S. in Management) Naval Postgraduate School, December 1994.
Thesis advisor(s): Paul J. Fields, Katsuaki L. Terasawa. "December 1994." Includes bibliographical references. Also available online.
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Mock, Philip J. "Measuring Combat Logistics Force (CLF) Adequacy in Supporting Naval Operations." Thesis, Monterey, California. Naval Postgraduate School, 2012. http://hdl.handle.net/10945/6837.

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Approved for public release, distribution unlimited
We uses the existing outputs of the Combat Logistics Force (CLF) Planner tool to (1) assess the minimum level of support required for a specified force in a multi-stage naval combat scenario and (2) compare CLF adequacy, surplus mission capability, and logistics shortfalls that a minimum level of support provides to combat forces of varying compositions. We examine the potential impact of the transition from a traditional nuclear-powered aircraft carrier strike group to a more distributed conventionally-powered one. We find that the logistical demands of a small conventionally powered carrier strike group with comparable striking power require significant increases in CLF end strength, and therefore that logistical supportability must be an integral part of future fleet planning.
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Jablecka, Marta. "Modelling CLV in the Insurance Industry Using Deep Learning Methods." Thesis, KTH, Matematisk statistik, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-273607.

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This paper presents a master’s thesis project in which deep learning methods are used to both calculate and subsequently attempt to maximize Customer Lifetime Value (CLV) for an insurance provider’s customers. Specifically, the report investigates whether panel data comprised of customers monthly insurance policy subscription history can be used with Recurrent Neural Networks (RNN) to achieve better predictive performance than the naïve forecasting model. In order to do this, the use of Long Short Term Memory (LSTM) for anomaly detection in a supervised manner is explored to determine which customers are more likely to change their subscription policies. Whether Deep Reinforcement Learning (DRL) can be used in this setting in order to maximize CLV is also investigated. The study found that the best RNN models outperformed the naïve model in terms of precision on the data set containing customers which are more likely to change their subscription policies. The models suffer, however, from several notable limitations so further research is advised. Selecting those customers was shown to be successful in terms of precision but not sensitivity which suggest that there is a room for improvement. The DRL models did not show a substantial improvement in terms of CLV maximization.
I detta examensarbete presenteras metoder där djupinlärning används för att både beräkna och maximera kundens lönsamhet över tid, Customer Lifetime Value (CLV), för en försäkringsleverantörs kunder. Specifikt undersöker rapporten historisk paneldata som består av kunders månatliga försäkringsinnehav där Recurrent Neural Networks (RNN) används för att uppnå bättre prediktiv prestanda än en naiv prognosmodell. Detta undersöks tillsammans med det neurala nätverket Long Short Term Memory (LSTM), där vi försöker finna anomalier på ett övervakat sätt. Där anomalier syftar på kunder som är mer benägna att ändra sin försäkringspolicy, då den största delen av populationen har samma innehav på månadsbasis. Även en gren av djupinlärning, Deep Reinforcement Learning (DRL), används för att undersöka möjligheten att maximera CLV för denna typ av data. Studien fann att de bästa RNN-modellerna överträffade den naiva modellen i termer av precision i data där kunder är mer benägna att ändra sin försäkringspolicy. Modellerna lider dock av flera anmärkningsvärda begränsningar, så ytterligare forskning rekommenderas. Att välja kunder med hjälp av LSTM visade sig vara framgångsrikt när det gäller precision men inte känslighet vilket tyder på att det finns utrymme för förbättring. DRL-modellerna visade inte någon väsentlig förbättring vad gäller CLV-maximering.
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Agüero, González Jesús. "Desarrollo de vectores virales basados en el virus del manchado foliar de los cítricos (CLBV)." Doctoral thesis, Universitat Politècnica de València, 2013. http://hdl.handle.net/10251/34342.

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Los cítricos son el cultivo frutal económicamente más importante tanto en España como en el resto de los países productores. La clave para mantener la competitividad de este sector consiste en obtener material vegetal de alta calidad, para lo cual son indispensables los programas de mejora. La mejora de cítricos por métodos clásicos es muy complicada, por lo que hay que recurrir a las nuevas tecnologías para intentar acelerar y optimizar el procedimiento. La reciente secuenciación del genoma de dos especies de cítricos ha permitido identificar una larga lista de genes candidatos a participar en determinados procesos biológicos. Sin embargo, son necesarios nuevos análisis para asociar cada gen a un fenotipo específico o función biológica. El empleo de vectores virales para determinar la función de genes mediante silenciamiento génico inducido por virus (VIGS) ha demostrado ser una herramienta muy útil para los estudios de genética reversa realizados en plantas. Este sistema presenta ventajas respecto a los métodos tradicionales para estudiar la función de genes como son la mutagénesis o la transformación genética, ya que permite ensayar la función de numerosos genes en un corto periodo de tiempo. Esto es especialmente crítico en el caso de los cítricos, que poseen largos periodos juveniles de entre 6 y 8 años y donde la transformación de plantas adultas es muy difícil. Además, permite estudiar la función de genes que son esenciales para el crecimiento o el desarrollo de la planta y cuyo análisis es inviable con los métodos tradicionales. Al comienzo de la tesis se había desarrollado un vector viral para cítricos basado en el virus de la tristeza de los cítricos (CTV) con el que se pueden expresar proteínas pero que no se ha ensayado para estudiar la función de genes mediante VIGS. En el laboratorio disponíamos de un clon infeccioso de cDNA del genoma completo del virus del manchado foliar de los cítricos (CLBV), un virus que infecta a todas las especies y variedades de cítricos ensayadas y es asintomático en la mayoría de ellas. Este clon infeccioso se ha modificado para obtener vectores virales basados en el genoma de CLBV que pueden servir tanto para expresar proteínas como para silenciar mediante VIGS genes de cítricos para la mejora genética de este cultivo. Para ello, se ha introducido un punto de corte único PmlI en dos zonas del genoma de CLBV: en el extremo 3¿ no traducible (vector clbv3¿) o en la zona intergénica localizada entre los genes de las proteínas de movimiento y cápsida (CP) (vector clbvIN). Para la expresión de secuencias foráneas mediante la formación de un nuevo RNA subgenómico (sgRNA) se delimitó la secuencia mínima promotora del sgRNA CP mediante clonación de fragmentos de distinta longitud en torno al origen de transcripción de dicho sgRNA en el vector clbv3'. El fragmento de 92 bases localizado entre los nt -42 y +50 respecto al inicio de transcripción del sgRNA CP contenía todos los elementos necesarios para la promoción de un nuevo sgRNA in vivo. Esta secuencia mínima promotora se clonó en los 2 vectores virales previamente desarrollados para generar los vectores clbv3¿pr y clbvINpr, respectivamente. Ambos vectores fueron capaces de producir un nuevo sgRNA y de expresar proteínas recombinantes. Para determinar la estabilidad de los vectores obtenidos se clonaron en ellos fragmentos de secuencias lineales de distinto tamaño, o en tándem invertido para la formación de una estructura en horquilla, y se inocularon en plantas de N. benthamiana y cítricos. Todas las construcciones derivadas del vector clbv3' se mostraron estables a lo largo de las diferentes brotaciones analizadas durante al menos 3 años, comprobándose la replicación viral e integridad del inserto. Sin embargo, no se detectó multiplicación viral con ninguna de las construcciones derivadas del vector clbvIN. La estabilidad de las construcciones derivadas de los vectores con el promotor duplicado dependía del tamaño del inserto. Con todas ellas se detectó replicación viral pero se observaron eventos de recombinación cuando se clonaban fragmentos superiores a 720 nt en el vector clbvINpr o 408 nt en el vector clbv3'pr. Un factor importante para determinar la eficiencia y funcionalidad de los vectores desarrollados es conocer cómo se mueve y se distribuye el virus en los distintos tejidos de la planta. Para ello se inocularon plantas de N. benthamiana y cítricos con la construcción clbv3¿pr-GFP, que expresa GFP en los tejidos donde se localiza el virus. En N. benthamiana, la observación de GFP permitió detectar la presencia de CLBV en la mayoría de tejidos, acumulándose preferentemente en óvulos y regiones meristemáticas. En cítricos no se pudo visualizar GFP pero el virus se detectó en regiones meristemáticas mediante RT-PCR a tiempo real e hibridación molecular. La acumulación de CLBV en tejidos meristemáticos explicaría la dificultad de eliminar este virus mediante microinjerto. Para evaluar la capacidad de los vectores clbv3'pr y clbvINpr para expresar proteínas se clonó en ellos la secuencia completa del gen gfp y se cuantificó la cantidad de proteína GFP sintetizada en las plantas infectadas. En N. benthamiana la cantidad de GFP estimada para el vector clbv3'pr fue de 16 µg de proteína por gramo de peso fresco, cantidad que resultó entre 5 y 6 veces superior a la estimada para el vector clbvINpr. Sin embargo, en cítricos, debido a la inestabilidad del vector clbv3'pr, sólo se pudo cuantificar la proteína expresada por la construcción del vector clbvINpr, estimándose en 0.6 µg de GFP por gramo de peso fresco. La efectividad de los vectores clbv3', clbv3'pr y clbvINpr para silenciar genes mediante VIGS se ensayó clonando fragmentos de genes tanto endógenos de plantas (pds, actina, sulfur) como el gen gfp introducido experimentalmente en plantas transgénicas. En cítricos todas las construcciones de los tres vectores indujeron fenotipo de silenciamiento del gen ensayado, aunque el vector clbv3' fue el más efectivo para el estudio de VIGS en este huésped. Sin embargo, en N. benthamiana sólo se desencadenó el silenciamiento en las plantas inoculadas con la construcción clbv3¿pr-hp58PDS, que expresa una horquilla de doble cadena de un fragmento de 58 nt del gen pds. En todas las plantas silenciadas se detectó una disminución del correspondiente mRNA del gen ensayado y una acumulación de siRNAs derivados tanto del mRNA del gen insertado como del RNA genómico del virus. Por otro lado, el fenotipo de silenciamiento de los genes ensayados se observó en sucesivas brotaciones, lo que confirma la gran estabilidad de los vectores basados en el genoma de CLBV. Los vectores virales desarrollados en esta tesis constituyen una herramienta eficiente para el estudio de la función de genes mediante genética reversa utilizando la técnica VIGS. También pueden ser útiles para estudio de genética directa mediante expresión de proteínas o para la protección del cultivo frente a enfermedades producidas por virus, bacterias y hongos o frente a plagas de invertebrados.
Agüero González, J. (2013). Desarrollo de vectores virales basados en el virus del manchado foliar de los cítricos (CLBV) [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/34342
TESIS
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Bargheer, Matias. "Ultrafast photodynamics in condensed phase ClF, Cl2 and I2 in solid rare gases /." [S.l. : s.n.], 2002. http://www.diss.fu-berlin.de/2002/206/index.html.

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Kerouedan, Sylvie. "Conception et réalisation de circuits VLSI-CLF pour le traitement de l'information optique." Brest, 1998. http://www.theses.fr/1998BRES2012.

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Le contexte de cette these est l'etude de circuits integres optoelectroniques sur substrat silicium interfacant entrees optiques (photodiodes) et sorties optiques (cristal liquide ferroelectrique). Pour valider les relations entre les composants optiques et les fonctions electroniques integrees, deux circuits ont ete realises. La premiere realisation, un aiguilleur optique a adressage integre met en evidence la relation circuit integre et clf, en particulier elle montre les difficultes technologiques du depot de clf sur ci. Cette application de routage electronique entre fibres optiques monomodes permet d'envisager l'integration sur un meme support, le silicium, de la fonction d'adressage et des miroirs optiques. Ces miroirs assurent la creation de chemins optiquement transparents et reconfigurables entre 2 fibres quelconques. La deuxieme realisation, une retine de detection de contours permet d'illustrer les problemes d'interconnexions dans les systemes a base de pixels fortement interconnectes. Elle montre egalement que le choix de l'algorithme s'avere tres important : sa complexite entrainera un rapport surface photosensible par pixel/surface totale du pixel plus ou moins convenable dans des applications de traitements d'images. A la suite de ces realisations, nous cherchons a donner quelques pistes de reflexion pour repondre a quelques questions sur les traitements optoelectroniques complexes : comment peut-on les implanter sur silicium ? quand est-il preferable d'effectuer des operations optiques plutot que des operations electroniques ? quels sont les avantages des systemes d'interconnexions optiques ?
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Books on the topic "CLFV"

1

Fenigstein, Victor. Shakespeare's sonnets I-CLIV. [Luxemburg]: Fonds culturel national du Grand-duché de Luxembourg, 1988.

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author, Fanai Vanlalruata, Joy Sara author, Nandy Srejita author, and Export-Import Bank of India, eds. Enhancing India's engagement in healthcare sector of CLMV countries. Mumbai: Export-Import Bank of India, 2018.

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Sotharith, Chap. Development strategy for CLMV in the age of economic integration. [Vientiane]: [s.n.], 2008.

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Akira, Suehiro. Chūgoku no taigai bōchō to Dai Mekon-ken (GMS) CLMV. Tōkyō: Tōkyō Daigaku Shakai Kagaku Kenkyūjo Gendai Chūgoku Kenkyū Kyoten, 2011.

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Amakawa, Naoko. Kōhatsu ASEAN shokoku no kōgyōka: CLMV shokoku no keiken to tenbō. Chiba-ken Chiba-shi: Ajia Keizai Kenkyūjo, 2006.

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Sangyōshō, Japan Keizai. Study for special economic zone development in CLMV countries: Final report. Tokyo: Ministry of Economy, Trade and Industry, 2007.

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author, Fanai Vanlalruata, Bangera Snehal author, and Export-Import Bank of India, eds. Act East, enhancing India's engagements with Cambodia, Lao PDR, Myanmar, Vietnam (CLMV). Mumbai: Export-Import Bank of India, 2016.

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Corporation, SMR Research, ed. Dangerous customers: A study of current CLTV ratios of U.S. mortgage debtors. Hackettstown, NJ: SMR Research Corp., 2007.

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Srithilat, Khaisy. Financial development, trade openness and economic growth in CLV countries. Khon Kaen, Thailand: Mekong Institute, 2013.

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India's trade and investment relations with Cambodia, Lao PDR, Myanmar, Vietnam (CLMV): Enhancing economic cooperation. Mumbai: Export-Import Bank of India, 2013.

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Book chapters on the topic "CLFV"

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Kettle, Peter-Raymond. "The “Golden” cLFV channels μ → eγ and μ → eee — the high-intensity frontier." In SSP 2012, 47–54. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6485-9_7.

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Strader, Ted N., Christopher Kokoski, David Collins, Steven Shamblen, and Patrick Mckiernan. "CLFC Fatherhood Program." In Encyclopedia of Couple and Family Therapy, 454–59. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-49425-8_990.

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van Weert, Henk. "50 Eksteroog/clav." In Kleine kwalen en alledaagse klachten bij ouderen, 287–92. Houten: Bohn Stafleu van Loghum, 2016. http://dx.doi.org/10.1007/978-90-368-1082-1_50.

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Strader, Ted N., Christopher Kokoski, David Collins, Steven Shamblen, and Patrick Mckiernan. "CLFC Fatherhood Program." In Encyclopedia of Couple and Family Therapy, 1–6. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-15877-8_990-1.

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Vogt, J. "755 ClFO Chlorosyl fluoride." In Asymmetric Top Molecules. Part 3, 296–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_177.

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Vogt, J. "759 ClF3 Chlorine trifluoride." In Asymmetric Top Molecules. Part 3, 306–7. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_181.

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Strader, Ted N., Christopher Kokoski, David Collins, Steven Shamblen, and Patrick Mckiernan. "CLFC Marriage Enhancement Program." In Encyclopedia of Couple and Family Therapy, 459–63. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-49425-8_989.

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Holze, Rudolf. "Ionic conductivities of ClF3." In Electrochemistry, 327. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_310.

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Strader, Ted N., Christopher Kokoski, David Collins, Steven Shamblen, and Patrick Mckiernan. "CLFC Marriage Enhancement Program." In Encyclopedia of Couple and Family Therapy, 1–5. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-15877-8_989-1.

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Vogt, J. "757 ClFS Sulfur chloride fluoride." In Asymmetric Top Molecules. Part 3, 303–4. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_179.

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Conference papers on the topic "CLFV"

1

Baldini, A. M. "Charged Lepton Flavor Violations (CLFV)." In The 28th International Symposium on Lepton Photon Interactions at High Energies. WORLD SCIENTIFIC, 2020. http://dx.doi.org/10.1142/9789811207402_0010.

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Mihara, Satoshi. "cLFV/g-2/EDM Experiments." In The 39th International Conference on High Energy Physics. Trieste, Italy: Sissa Medialab, 2019. http://dx.doi.org/10.22323/1.340.0714.

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Dittmeier, Sebastian. "Searching for cLFV with the Mu3e experiment." In 41st International Conference on High Energy physics. Trieste, Italy: Sissa Medialab, 2022. http://dx.doi.org/10.22323/1.414.0692.

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De Gerone, Matteo. "A REVIEW OF cLFV EXPERIMENTS: THE MUON CHANNEL." In Nineteenth Lomonosov Conference on Elementary Particle Physics. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811233913_0050.

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Ieki, Kei. "SEARCH OF cLFV PROCESSES WITH MUONS AND OTHERS." In Eighteenth Lomonosov Conference on Elementary Particle Physics. WORLD SCIENTIFIC, 2019. http://dx.doi.org/10.1142/9789811202339_0076.

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Mihara, Satoshi. "cLFV searches using DC muon beam at PSI." In Flavor Physics & CP Violation 2015. Trieste, Italy: Sissa Medialab, 2016. http://dx.doi.org/10.22323/1.248.0033.

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Kriewald, Jonathan, Asmaa Abada, and Ana M. Teixeira. "The role of leptonic CPV phases in cLFV observables." In The 22nd International Workshop on Neutrinos from Accelerators. Trieste, Italy: Sissa Medialab, 2022. http://dx.doi.org/10.22323/1.402.0203.

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Mihara, Satoshi. "New cLFV search experiments using the mu-e conversion process." In The Xth Nicola Cabibbo International Conference on Heavy Quarks and Leptons. Trieste, Italy: Sissa Medialab, 2011. http://dx.doi.org/10.22323/1.128.0053.

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Yamanaka, Masato, Michihisa Takeuchi, and Yuichi Uesaka. "Higgs mediated CLFV processes $\mu N (eN) \rightarrow \tau X$ via gluon operators." In The 19th International Workshop on Neutrinos from Accelerators NUFACT2017. Trieste, Italy: Sissa Medialab, 2017. http://dx.doi.org/10.22323/1.295.0110.

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Uesaka, Yuichi, YOSHITAKA KUNO, Joe Sato, Toru Sato, and Masato YAMANAKA. "Improved analysis of the CLFV decay of muonic atoms $\mu e\rightarrow e e$." In Flavor Physics & CP Violation 2015. Trieste, Italy: Sissa Medialab, 2016. http://dx.doi.org/10.22323/1.248.0055.

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Reports on the topic "CLFV"

1

Jordan, Jason P. Organizing CLF Replenishment Events into CLF Voyages - The CLF Voyages Template. Fort Belvoir, VA: Defense Technical Information Center, July 2009. http://dx.doi.org/10.21236/ada510230.

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Jones, Russell I. Command Relationships for Amphibious Operations: CATF/CLF Undergo a Transformation. Fort Belvoir, VA: Defense Technical Information Center, May 2001. http://dx.doi.org/10.21236/ada390348.

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Salgueiro, G., V. Gurbani, and A. B. Roach. Format for the Session Initiation Protocol (SIP) Common Log Format (CLF). RFC Editor, February 2013. http://dx.doi.org/10.17487/rfc6873.

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Elwing, David W. CATF and CLF - Will These Traditional Roles Carry Us Into the 21st Century? Fort Belvoir, VA: Defense Technical Information Center, February 1998. http://dx.doi.org/10.21236/ada348820.

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Trowbridge, L. D. Reinterpretation of rate data for the reaction of ClF and F{sub 2}. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/10117670.

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Anjali, T., H. Abdelnur, and O. Festor. The Common Log Format (CLF) for the Session Initiation Protocol (SIP): Framework and Information Model. Edited by V. Gurbani and E. Burger. RFC Editor, February 2013. http://dx.doi.org/10.17487/rfc6872.

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Salgueiro, G., V. Pascual, A. Roman, and S. Garcia. Indicating WebSocket Protocol as a Transport in the Session Initiation Protocol (SIP) Common Log Format (CLF). RFC Editor, September 2014. http://dx.doi.org/10.17487/rfc7355.

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Ohad, Nir, and Robert Fischer. Regulation of Fertilization-Independent Endosperm Development by Polycomb Proteins. United States Department of Agriculture, January 2004. http://dx.doi.org/10.32747/2004.7695869.bard.

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Arabidopsis mutants that we have isolated, encode for fertilization-independent endosperm (fie), fertilization-independent seed2 (fis2) and medea (mea) genes, act in the female gametophyte and allow endosperm to develop without fertilization when mutated. We cloned the FIE and MEA genes and showed that they encode WD and SET domain polycomb (Pc G) proteins, respectively. Homologous proteins of FIE and MEA in other organisms are known to regulate gene transcription by modulating chromatin structure. Based on our results, we proposed a model whereby both FIE and MEA interact to suppress transcription of regulatory genes. These genes are transcribed only at proper developmental stages, as in the central cell of the female gametophyte after fertilization, thus activating endosperm development. To test our model, the following questions were addressed: What is the Composition and Function of the Polycomb Complex? Molecular, biochemical, genetic and genomic approaches were offered to identify members of the complex, analyze their interactions, and understand their function. What is the Temporal and Spatial Pattern of Polycomb Proteins Accumulation? The use of transgenic plants expressing tagged FIE and MEA polypeptides as well as specific antibodies were proposed to localize the endogenous polycomb complex. How is Polycomb Protein Activity Controlled? To understand the molecular mechanism controlling the accumulation of FIE protein, transgenic plants as well as molecular approaches were proposed to determine whether FIE is regulated at the translational or posttranslational levels. The objectives of our research program have been accomplished and the results obtained exceeded our expectation. Our results reveal that fie and mea mutations cause parent-of-origin effects on seed development by distinct mechanisms (Publication 1). Moreover our data show that FIE has additional functions besides controlling the development of the female gametophyte. Using transgenic lines in which FIE was not expressed or the protein level was reduced during different developmental stages enabled us for the first time to explore FIE function during sporophyte development (Publication 2 and 3). Our results are consistent with the hypothesis that FIE, a single copy gene in the Arabidopsis genome, represses multiple developmental pathways (i.e., endosperm, embryogenesis, shot formation and flowering). Furthermore, we identified FIE target genes, including key transcription factors known to promote flowering (AG and LFY) as well as shoot and leaf formation (KNAT1) (Publication 2 and 3), thus demonstrating that in plants, as in mammals and insects, PcG proteins control expression of homeobox genes. Using the Yeast two hybrid system and pull-down assays we demonstrated that FIE protein interact with MEA via the N-terminal region (Publication 1). Moreover, CURLY LEAF protein, an additional member of the SET domain family interacts with FIE as well. The overlapping expression patterns of FIE, with ether MEA or CLF and their common mutant phenotypes, demonstrate the versatility of FIE function. FIE association with different SET domain polycomb proteins, results in differential regulation of gene expression throughout the plant life cycle (Publication 3). In vitro interaction assays we have recently performed demonstrated that FIE interacts with the cell cycle regulatory component Retinobalsoma protein (pRb) (Publication 4). These results illuminate the potential mechanism by which FIE may restrain embryo sac central cell division, at least partly, through interaction with, and suppression of pRb-regulated genes. The results of this program generated new information about the initiation of reproductive development and expanded our understanding of how PcG proteins regulate developmental programs along the plant life cycle. The tools and information obtained in this program will lead to novel strategies which will allow to mange crop plants and to increase crop production.
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