Academic literature on the topic 'Viral traffic'
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Journal articles on the topic "Viral traffic"
Luethy, Lauren N., and Julie K. Pfeiffer. "Viral Infection Brings Mitochondrial Traffic to a Standstill." Cell Host & Microbe 11, no. 5 (May 2012): 420–21. http://dx.doi.org/10.1016/j.chom.2012.05.001.
Full textEnserink, M. "AVIAN INFLUENZA: Keeping Track of Viral Air Traffic." Science 310, no. 5747 (October 21, 2005): 428. http://dx.doi.org/10.1126/science.310.5747.428.
Full textMorse, Stephen S. "Emerging Viruses: Defining the Rules for Viral Traffic." Perspectives in Biology and Medicine 34, no. 3 (1991): 387–409. http://dx.doi.org/10.1353/pbm.1991.0038.
Full textRoman, Laura M., and Henrik Garoff. "Revelation through exploitation: the viral model for intracellular traffic." Trends in Biochemical Sciences 10, no. 11 (November 1985): 428–32. http://dx.doi.org/10.1016/0968-0004(85)90024-6.
Full textLidsky, Peter V., Stanleyson Hato, Maryana V. Bardina, Alexei G. Aminev, Ann C. Palmenberg, Eugene V. Sheval, Vladimir Y. Polyakov, Frank J. M. van Kuppeveld, and Vadim I. Agol. "Nucleocytoplasmic Traffic Disorder Induced by Cardioviruses." Journal of Virology 80, no. 6 (March 15, 2006): 2705–17. http://dx.doi.org/10.1128/jvi.80.6.2705-2717.2006.
Full textSuikkanen, Sanna, Tuula Aaltonen, Marjukka Nevalainen, Outi Välilehto, Laura Lindholm, Matti Vuento, and Maija Vihinen-Ranta. "Exploitation of Microtubule Cytoskeleton and Dynein during Parvoviral Traffic toward the Nucleus." Journal of Virology 77, no. 19 (October 1, 2003): 10270–79. http://dx.doi.org/10.1128/jvi.77.19.10270-10279.2003.
Full textHaupt, Sophie, Graham H. Cowan, Angelika Ziegler, Alison G. Roberts, Karl J. Oparka, and Lesley Torrance. "Two Plant–Viral Movement Proteins Traffic in the Endocytic Recycling Pathway." Plant Cell 17, no. 1 (December 17, 2004): 164–81. http://dx.doi.org/10.1105/tpc.104.027821.
Full textShimizu, Kenta, Kumiko Yoshimatsu, Takaaki Koma, Shumpei P. Yasuda, and Jiro Arikawa. "Role of nucleocapsid protein of hantaviruses in intracellular traffic of viral glycoproteins." Virus Research 178, no. 2 (December 2013): 349–56. http://dx.doi.org/10.1016/j.virusres.2013.09.022.
Full textIkonen, E., R. G. Parton, F. Lafont, and K. Simons. "Analysis of the role of p200-containing vesicles in post-Golgi traffic." Molecular Biology of the Cell 7, no. 6 (June 1996): 961–74. http://dx.doi.org/10.1091/mbc.7.6.961.
Full textJing, Peng, Farzin Haque, Dan Shu, Carlo Montemagno, and Peixuan Guo. "One-Way Traffic of a Viral Motor Channel for Double-Stranded DNA Translocation." Nano Letters 10, no. 9 (September 8, 2010): 3620–27. http://dx.doi.org/10.1021/nl101939e.
Full textDissertations / Theses on the topic "Viral traffic"
Rizkallah, Gergès. "Le role de l'interaction des cellules dendritiques avec le virus HTLV-1 dans la dissémination virale : capture ou infection productive ?" Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE1099/document.
Full textHTLV-1 (Human T cell leukemia/lymphoma virus type 1) is the etiological agent of Adult T cell Leukemia/Lymphoma (ATLL) and HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP). In chronically infected patients, the provirus is mainly detected in the CD4 T-cell population and, to a lesser extent in myeloid dendritic cells (DCs), plasmacytoid DCs (pDCs), macrophages and monocytes. Among the different DCs subsets found in vivo, myeloid DCs from the blood, tolerogenic or inflammatory DCs from mucosa may first encounter HTLV-1 during blood transmission, breast-feeding or sexual transmission, respectively. They would then be able to transmit HTLV-1 to CD4 + T cells. This hypothesis is supported by the recent work of our team that showed that monocyte derived dendritic cells (MDDCs) are more susceptible to HTLV-1 infection in comparison to autologous T cells. We therefore asked whether all these DCs subsets were equally susceptible to HTLV-1 and whether the nature of the DC subset would impact HTLV-1 spread to T-cells. Human monocytes obtained from healthy blood donors were differentiated into IL-4 DCs, TGF-ß DCs or IFN-a DCs. In vitro-derived immature IL-4 DCs, TGF-ß DCs and IFN-a DCs mimic myeloid, tolerogenic and inflammatory DCs, respectively. We also generated LPS-matured IL-4 DCs that exhibited a strong maturation profile with over-expression of maturation markers. We observed HTLV-1 protein expression and provirus accumulation in IL-4 DCs and TGF-ß DCs but not in IFN-a DCs and LPS-matured IL-4 DCs. Despite their increased ability to capture HTLV-1 virion compared to IL-4 DCs and TGF-ß DCs, IFN-a DCs and LPS-matured IL-4 DCs restricted HTLV-1 productive infection. This was not due to the antiviral activity of type–I interferon produced by IFN-a DC or LPS-matured IL-4 DCs. In contrast, we showed that these differences in susceptibility to HTLV-1 infection might be linked to the maturation phenotype of the DCs subsets and to a different trafficking of HTLV-1 in IL-4 DC vs. IFN-a DC. Finally, using IL-4DCs, LPS-matured IL-4 DCs and IFN-a DCs, we demonstrate that productive infection rather than trans-infection is required for HTLV-1 transmission from DCs to CD4 T-cells. Thus, our results demonstrate that the nature of the DCs encountered by HTLV-1 during primo-infection and the trafficking route of the virus through the vesicular pathway of these cells determine the efficiency of viral transmission to T-cells
Renault, Noémie. "Trafic intracellulaire de la protéine Gag du virus Foamy." Paris 7, 2009. http://www.theses.fr/2009PA077154.
Full textFoamy viruses (FVs) are complex exogenous animal retroviruses that differ in many aspects of their life cycle from the orthoretroviruses such as human immunodefîciency virus (HIV). In particular, in FVvs, Gag and Pol proteins are expressed independently of one another, and both proteins undergo single clivage events. None of the conventional Gag landmarks of exogenous retroviruses, such as the major homology region or Cys-His motifs, are found in this protein. Instead, FV Gag harbors conserved C-terminal basic motifs, referred to as Gly-Arg (GR) boxes. Although the first GR (GRI) box binds viral nucleic acids and is required for viral genome packaging, the second (GRII) harbors a nuclear localization sequence (NLS) at its C-terminus, targeting Gag to the nucleus early after infection. GRII also contains a chromatin binding sequence (CBS) in its N-terminus, tethering the FV incoming pre-integration complex onto host chromosomes. The present work focuses on the structural Gag proteins, in early and late stages of infection. Troviral Gag proteins are involved in early stages of infection such as trafficking of incoming viruses nd nuclear import. FV Gag protein uses the microtubule network to reach the nucleus. In cycling cells,FV articles are structured at the centrosome 4 h post-infection. Then, the viral protease helps capsid for ncoating. In quiescent cells, we have shown that viral particles remain structured at the centrosome during everal weeks and that uncoating does not occur : this step is a limiting factor for infection although viral articles are still infectious. Upon cells reactivation, viral capsids undergo proteolysis and disassembly, llowing infection to proceed. During the late stages of infection, Gag undergoes transient nuclear trafficking after it synthesis, before returning back to the cytoplasm for capsid assembly and virus egress. The functional role of this nuclear stage, as well as the molecular mechanisms responsible for Gag nuclear export, are not understood. Here, we identify a leptomycin-sensitive nuclear export sequence (NES) within the N-terminus of the primate foamy virus Gag protein that is absolutely required for the completion of late stages of virus replication. Point mutation of conserved residues within this motif leads to nuclear retention of Gag and dramatically affects viral replication. Moreover, complementation experiments demonstrate that nuclear export-defective Gag mutants negatively interfere with virus release by sequestering wild-type Gag in the nucleus
El, Meshri Salah Edin. "Etude du trafic intracellulaire de la protéine Gag du VIH et rôle de son domaine NCp7." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAJ025/document.
Full textThe Gag structural polyprotein of HIV-1 orchestrates viral particle assembly in producer cells, in a process that requires two platforms, the genomic RNA on the one hand and a membrane with a lipid bilayer, on the other. During its transportation from translating ribosomes to plasma membrane, Gag hijacks cellular proteins of the cytoskeleton and the ESCRT proteins like TSG101, Alix, etc., to egress viral particles. However, a number of questions remain to be answered before they are clearly apprehended. In this thesis, , we studied the role of the NC domain alone or as part of Gag (GagNC) in Gag-Gag and Gag-TSG101 interactions, which are essential for the assembly and budding of HIV-1 particles using quantitative fluorescent microscopy and biochemical approach. Results, showed that the absence of NC domain lead to (1) an accumulation of Gag as large aggregates that are dispersed in the cytoplasm, (2) a decrease of Gag-Gag condensation and (3) a delay for Gag-Gag complexes in reaching the PM, (4) improved interaction between Gag and TSG101, and (5) by its virtue in Gag trafficking docks TSG101 to the PM. This regulatory effect of NCp7 domain in either TSG101 or Gag or both protein- regulated pathways during virus budding can be exploited to develop inhibitors targeting HIV-1
Toledo, Marcelo Augusto Szymanski de 1987. "Trafego intracelular de vetores não-virais = desenvolvimento de proteínas de fusão para transporte de DNA plasmidial através da interação com proteínas motoras = Intracelullar traffic of non-viral vectors: development of recombinant fusion proteins to mediate plasmidial DNA transport by interaction with motor proteins." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316418.
Full textTese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-24T06:15:51Z (GMT). No. of bitstreams: 1 Toledo_MarceloAugustoSzymanskide_D.pdf: 15660446 bytes, checksum: 8e64c5b4455cf458c2eb0d9b8e030e70 (MD5) Previous issue date: 2013
Resumo: Apesar de seguros e simples de produzir, o uso de vetores não virais como o DNA plasmidial (DNAp) em estudos de terapia gênica e vacinação por DNA tem sido limitado pela baixa eficiência quando comparados aos vetores virais. Essa limitação provém principalmente da reduzida capacidade de superar as barreiras físicas, enzimáticas e difusionais encontradas durante o tráfego intracelular para o interior do núcleo das células alvo. Dentro deste contexto, o presente trabalho demonstra a utilização de cadeias leves modificadas de Dineína (Lc8 e Rp3) como vetores não-virais de entrega gênica. A escolha de cadeias leves de Dineína justifica-se pela possibilidade de utilizar o transporte retrógrado celular mediado por complexos motores de Dineína para facilitar o tráfego de material genético exógeno através do citoplasma em direção à periferia nuclear. Através da adição de pequenos domínios peptídicos, ricos em aminoácidos polares positivos (arginina e lisina), ao N-terminal de cadeias leves de Dineína foi possível conferir a estas proteínas a habilidade de interagir com material genético condensando-o em partículas. Ensaios de transfecção demonstraram que tais partículas apresentam elevada eficiência de entrega do material genético exógeno ao núcleo de células HeLa, eficiência esta superior àquela apresentada pelo peptídeo protamina, amplamente estudado como vetor não-viral de entrega gênica. A formação de complexos ternários utilizando-se DNA plasmidial, cadeias leves de Dineína modificadas e lipídios catiônicos apresentou eficiência de entrega superior àquelas apresentadas na ausência do lipídio. Adicionalmente, complexos de entrega formados apenas com DNA plasmidial e cadeias leves de Dineína modificadas apresentaram baixo efeito citotóxico em células HeLa, característica esta de grande relevância uma vez que a toxicidade dos vetores de entrega gênica atua como importante fator limitante em sua aplicação clínica. O mecanismo envolvido no processo de entrega gênica mediado por cadeias leves de Dineína modificadas também foi estudado, podendo ser observado que (1) a entrada dos complexos de entrega na célula é altamente dependente do processo de endocitose, (2) a eficiência de entrega observada depende da rede de microtúbulos e (3) parte significativa dos complexos de entrega é degradada na via de endossoma/lisossomo celular. Os vetores não-virais de entrega gênica descritos no presente estudo associam elevada eficiência de transfecção, baixa toxicidade celular e relativo baixo custo de produção, uma vez que as cadeias leves de Dineína recombinantes são produzidas em sistema heterólogo utilizando-se Escherichia coli. Ressalta-se ainda a possibilidade de adição de novos domínios peptídicos às cadeias leves de Dineína modificadas, agregando novas funções/capacidades que poderiam resultar em maior eficiência de entrega gênica através da otimização dos processos de internalização celular ou escape endossomal. A abordagem de se utilizar a via de transporte retrógrado celular para o desenvolvimento de vetores não-virais para entrega gênica é pouco explorada pela comunidade científica e o presente estudo apresenta-se entre os poucos da área, esperando assim contribuir para o desenvolvimento de vetores não-virais mais eficientes e seguros
Abstract: The use of non viral vectors such as plasmidial DNA (pDNA) in gene therapy and DNA vaccination protocols has been limited due to its low transfection efficiency when compared to viral vectors. This limitation occurs mainly due to the physical, enzymatic and diffusion barriers faced during the transport of the genetic material to the nucleus of target eukaryotic cells. Regarding this subject, the present work demonstrates the feasibility of using modified Dynein light chains (Lc8 and Rp3) as non viral vectors for gene delivery. The use of Dynein light chains relies on the possibility to exploit the Dynein based cellular retrograde transport in order to improve the exogenous genetic material transport across the citosol towards the nuclear periphery. By adding small peptide domains, based in positively charged aminoacids (arginine and lysine) to the N-terminal of Dynein light chains, the resulting recombinant proteins were able to interact and condense genetic material into delivery particles. Transfection assays demonstrated that these particles are highly efficient to delivery plasmidial DNA to nucleus of HeLa cells when compared to the transfection efficiency presented by protamine, a well characterized non viral vector peptide. Ternary complexes formed by modified Dynein light chains, pDNA and a cationic lipid showed even higher transfection efficiency. Additionally, the light chain based non viral delivery vectors presented low citotoxic effect to HeLa cells, a valuable feature as toxicity is regarded as one of the main concerns on delivery vectors development. The mechanism by which the modified Dynein light chain based vectors mediates gene delivery was also investigated and we could observe that (1) the internalization process deeply relies on endocytosis, (2) it depends on the microtubule network and (3) a significant fraction of the delivery complexes are trapped and degraded in the endocytic pathway. The non viral vectors developed in the present study combine high transfection efficiency, low toxicity and relative low production cost, as all modified proteins were produced in Escherichia coli prokaryotic host. Its noteworthy that additional peptide domains can be further associated to the delivery vectors described providing it with new abilities such as higher internalization or endosomal escape capacity. The approach to use the cellular retrograde transport in order to develop non viral vectors is poorly exploited by the scientific community and the present study stands among few in the field hopefully contributing to the development of more efficient and safer non viral vectors for gene delivery
Doutorado
Genetica de Microorganismos
Doutor em Genetica e Biologia Molecular
Bouard, David. "La glycoprotéine d'enveloppe rétrovirale : trafic intracellulaire et recrutement lors de l'assemblage viral." Lyon, École normale supérieure (sciences), 2008. http://www.theses.fr/2008ENSL0471.
Full textGrigorov, Boyan. "Studying the traffic and assembly of HIV-1 Gag." Lyon, École normale supérieure (sciences), 2007. http://www.theses.fr/2007ENSL0398.
Full textParis, Joris. "Trafic intranucléaire du rétrovirus Foamy." Paris 7, 2014. http://www.theses.fr/2014PA077053.
Full textThe structural Gag protein hijacks many cellular machineries to fulfill its distinct and fundamental roles in the replication of retroviruses. In the case of the prototype foamy virus (PFV), Gag contains a nuclear export signal (NES) which allows the gRNA-Gag complex to be exported to the cytoplasm prior to capsids assembly and virus egress. We identified a nucleolar localization sequence (NoLS) in the C-terminus of PFV Gag. This NoLS contains two regions, rich in arginine and glycine, which are necessary and sufficient for nucleolar targeting. The methylation of Arginine R540 by PRMT-1 regulates the functions NoLS vs CBS of Gag. To study the nucleolar step of PFV replication, we used different conditions that slow down intracellular trafficking (hypoxia and/or treatment with leptomycin B) and also a molecular trap system to retain Gag into the nucleolus. In both cases, Gag was detected in the nucleolus. We also developed an approach, based on a ribozyme fused to a snoRNA able to cleave specifically PFV gRNA in the nucleolus
Charrat, Coralie. "Formulation de nanoparticules d’ADN fonctionnalisées par des peptides ligands des chaînes LC8 de la dynéine pour améliorer le trafic intracellulaire dans le transfert de gènes non viral." Thesis, Nice, 2016. http://www.theses.fr/2016NICE4017/document.
Full textThe aim consists in engineering DNA carriers functionalized by peptide sequences, DLC8-AS, targeting the LC8 light chains of cytoplasmic dynein, to promote active transport towards the nucleus along the microtubules (MTs).Dépôt de thèseDonnées complémentairesPrevious works based on polystyrene fluospheres functionalized with DLC8-AS, showed a noteworthy transfection enhancement but as a cost of high levels of ligands. Such levels of functionalization are unsuitable for maintaining sufficient colloidal stability of DNA nanoparticles (NPs). In order to compensate for this, we developed in this thesis weakly functionalized DNA NPs (2-10 mol %) bearing dimers of DLC8-AS to benefit from a dimeric effect toward the dynein which increase the affinity. Among our designed systems, two revealed the benefit from taking advantage from the dimeric effect of DLC8-AS. The 1st one relies on a cationic and dimerizable cysteine based amphiphile, which was used with its dimerizable pegylated homologue containing DLC8-AS, to produce, through a thiol-disulfide oligomerisation process, a monodisperse population of small sized functionalized DNA NPs (~60 nm). Experiments carried out onto HeLa cells, showed that DNA NPs functionalized with DLC8-AS dimers exhibited enhanced transfection properties (~250 times) through a dynein/MTs dependant mechanism. The second consists in functionalizing the surface of PEI polyplexes with octaarginine amphiphiles carrying a mono- or bis-DLC8-AS. Remarkably, the transfection efficiency of polyplexes bearing the dimeric ligands was increased by a 50 times factor compared to the JetPEI golden standard. Here too, the mechanism strongly depends on MTs
Vertiz, Zavaleta Julio Cesar, and Avalos Victor Eduardo Ramon. "Propuesta de mejora de niveles de servicio en la intersección vial entre la carretera Panamericana Sur km 37.5 y el puente Arica en la ciudad de Lima." Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2020. http://hdl.handle.net/10757/648867.
Full textThe South Pan American Highway km. 37.5 and the Arica Bridge, is a Conventional Diamond-type road intersection without traffic lights, located in the district of Lurín and province of Lima. This intersection presents vehicular congestion causing loss of man-hours. Due to this, the current service levels were determined, through Synchro 8.0 software, through vehicle capacities taken in the field. The service levels obtained were very low and delays were high. As a consequence, different proposals were proposed and modeled with Synchro 8.0 software to solve vehicular congestion, such as; Implementation of traffic lights with different designs, implementation of mini ovals within the intersection and at the ends of the intersection, and a Divergent Diamond road interchange. The solution proposal begins with the comparison of results obtained from the alternatives for the current scenario and projected at 5 and 10 years. Consequently, two proposals were obtained that solve the current and projected vehicular congestion at 5 years. The first is the implementation of traffic light cruises with an exclusive lane for the free right turn and the second is the implementation of a new Divergent Diamond interchange, while the other proposals are not sustainable in the projection of future traffic. On the other hand, although it is true that both proposals improve and solve the problem posed, the second presents better levels of service and less delays in the 10-year projection.
Tesis
Huanca, Tarazona Samuel David, and Quispe Angel Abel Rojas. "Propuesta de mejora del diseño vial del óvalo La Curva de Chorrillos validado con el software Vissim 9.0." Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2019. http://hdl.handle.net/10757/626486.
Full textThis thesis is based on the analysis of vehicle flow, present in the La Curva oval, located in the district of Chorrillos, Department of Lima-Peru. The project evaluates service conditions, oval design and vehicular traffic. This evaluation is done through a microscopic model that is simulated in Vissim 9.0 software. The construction of the model consists of 4 phases. The first one deals with the previous analysis, which ranges from data collection to cabinet processing. On the one hand, the geometric measurements were taken on a day with less vehicular volume. On the other hand, vehicular and pedestrian traffic was performed on a typical day. The second phase consists of the initial modeling, which seeks to transfer the current geometric design to the Vissim to proceed with the microsimulation. Likewise, multiple runs were performed until the model was optimized, after preheating and calibrating it. The third phase analyzes the proposed design based on vehicle efficiency parameters, such as travel time (delays), tail length and service level. The proposal seeks to optimize the traffic signaling system, currently existing and inoperative, and a change of level in one of the avenues that has the greatest amount of traffic flow. In the last phase, the aim is to evaluate and compare the results, both of the current situation and of the proposed alternative. Finally, the parameters that present improvements in their service will be decisive to reduce the problem of vehicular congestion.
Tesis
Books on the topic "Viral traffic"
Castilla, Gustavo Ordoqui. Ley de tránsito y seguridad vial, 18,191. Montevideo, Uruguay: La Ley Uruguay, 2009.
Find full textSpain. Tráfico, circulación y seguridad vial. Madrid: Ministerio del Interior, Dirección General de Tráfico, 1990.
Find full textIsasi Ortiz de Barrón, Fernando, ed. Tráfico y seguridad vial. Cizur Menor (Navarra): Editorial Aranzadi, 2003.
Find full text1960-, Linamen Karen Scalf, ed. Vital connections. Colorado Springs, CO]: LearningRx, 2012.
Find full textSpain. Comisión Nacional de Seguridad de la Circulación Vial. Plan nacional de seguridad vial para el año 1991. Madrid: Dirección General de Tráfico, Ministerio del Interior, 1991.
Find full textJuan Manuel Herrero de Egaña Espinosa de los Monteros. Ley de seguridad vial: Infracciones y sanciones : procedimiento sancionador. Pamplona: Aranzadi Editorial, 1992.
Find full textLeón, Luis Carlos Rodríguez. Seguridad vial: Crónica de una reforma penal. Sevilla: Instituto Andaluz de Administración Pública, 2008.
Find full textLeón, Luis Carlos Rodríguez. Seguridad vial: Crónica de una reforma penal. Sevilla: Instituto Andaluz de Administración Pública, 2008.
Find full textBook chapters on the topic "Viral traffic"
Arias, C. F., D. Silva-Ayala, P. Isa, M. A. Díaz-Salinas, and S. López. "Rotavirus Attachment, Internalization, and Vesicular Traffic." In Viral Gastroenteritis, 103–19. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-12-802241-2.00006-7.
Full text"AIDS and Beyond: Defining the Rules for Viral Traffic." In AIDS, 23–48. University of California Press, 1992. http://dx.doi.org/10.1525/9780520912441-002.
Full textRoldan, Malu. "The Evolution of Web Marketing Practice." In Internet Marketing Research, 31–46. IGI Global, 2001. http://dx.doi.org/10.4018/978-1-878289-97-1.ch002.
Full textArmstrong, John. "The Role of Coastal Shipping in UK Transport: An Estimate of Comparative Traffic Movements in 1910." In The Vital Spark, 243–60. Liverpool University Press, 2009. http://dx.doi.org/10.5949/liverpool/9780986497308.003.0013.
Full textAkhter, Shamim, Rahatur Rahman, and Ashfaqul Islam. "Neural Network (NN) Based Route Weight Computation for Bi-Directional Traffic Management System." In Deep Learning and Neural Networks, 750–65. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-0414-7.ch042.
Full textJamal, Arshad, Hassan M. Al-Ahmadi, Farhan Muhammad Butt, Mudassir Iqbal, Meshal Almoshaogeh, and Sajid Ali. "Metaheuristics for Traffic Control and Optimization: Current Challenges and Prospects." In Search Algorithm - Essence of Optimization [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99395.
Full textNarayan, Valliammal, and Shanmugapriya D. "Big Data Analytics With Machine Learning and Deep Learning Methods for Detection of Anomalies in Network Traffic." In Handbook of Research on Machine and Deep Learning Applications for Cyber Security, 317–46. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-5225-9611-0.ch015.
Full textAlejos, Ana Vazquez, Paula Gómez Pérez, Manuel Garcia Sanchez, and Muhammad Dawood. "SimuMANET." In Technological Advancements and Applications in Mobile Ad-Hoc Networks, 408–43. IGI Global, 2012. http://dx.doi.org/10.4018/978-1-4666-0321-9.ch022.
Full textSingh, Surabhi. "Student's Perception Towards Digital Learning for Skill Enhancement Programs." In Driving Traffic and Customer Activity Through Affiliate Marketing, 129–40. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-2656-8.ch009.
Full textRakhee and M. B. Srinivas. "A Soft Computing Approach for Data Routing in Hospital Area Networks (HAN)." In Hospital Management and Emergency Medicine, 71–83. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-2451-0.ch004.
Full textConference papers on the topic "Viral traffic"
Willis, P. J. "Emerging (IP) network traffic measurements and QoS implications." In IEE Seminar Telecommunications Quality of Service (QoS): Vital Ingredient for Success. IEE, 2003. http://dx.doi.org/10.1049/ic:20030200.
Full textErdmann, Jakob, Robert Oertel, and Peter Wagner. "VITAL: A Simulation-Based Assessment of New Traffic Light Controls." In 2015 IEEE 18th International Conference on Intelligent Transportation Systems - (ITSC 2015). IEEE, 2015. http://dx.doi.org/10.1109/itsc.2015.12.
Full textSalaani, M. Kamel, Gary J. Heydinger, Paul A. Grygier, and W. Riley Garrott. "Transport Delay Compensation for the Image Generator Used in the National Advanced Driving Simulator." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-42975.
Full textBień, J., and M. Salamak. "Management of Bridge Structures – Challenges and Possibilities." In IABSE Symposium, Wroclaw 2020: Synergy of Culture and Civil Engineering – History and Challenges. Zurich, Switzerland: International Association for Bridge and Structural Engineering (IABSE), 2020. http://dx.doi.org/10.2749/wroclaw.2020.0002.
Full textPetelin, Stojan, Marko Perkovic, Peter Vidmar, and Katja Petelin. "Ship’s Engine Room Fire Modelling." In International Joint Power Generation Conference collocated with TurboExpo 2003. ASMEDC, 2003. http://dx.doi.org/10.1115/ijpgc2003-40176.
Full textMakhoul, Nisrine. "Performance-based assessment of Nahr Al-Fidar bridge." In IABSE Symposium, Guimarães 2019: Towards a Resilient Built Environment Risk and Asset Management. Zurich, Switzerland: International Association for Bridge and Structural Engineering (IABSE), 2019. http://dx.doi.org/10.2749/guimaraes.2019.1237.
Full textCollyer, Robert, Hasan Ahmed, Raj Navalurkar, and Dawn Harrison. "Urban Infrastructure: Design and Preservation - Brooklyn Bridge Rehabilitation Program." In IABSE Congress, New York, New York 2019: The Evolving Metropolis. Zurich, Switzerland: International Association for Bridge and Structural Engineering (IABSE), 2019. http://dx.doi.org/10.2749/newyork.2019.2753.
Full textPouryousef, Hamed, Paulo Teixeira, and Joseph Sussman. "Track Maintenance Scheduling and Its Interactions With Operations: Dedicated and Mixed High-Speed Rail (HSR) Scenarios." In 2010 Joint Rail Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/jrc2010-36125.
Full textWang, Zezhou, Xiang Liu, Yongxin Wang, Chaitanya Yavvari, Matthew Jablonski, Duminda Wijesekera, Brian Sykes, and Keith Holt. "Cyber Security Analysis for Advanced Train Control System (ATCS) in CTC Systems: Concepts and Methods." In 2019 Joint Rail Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/jrc2019-1236.
Full textTreacy, Mark, Danilo Della Ca', and Niculin Meng. "Recent advancements in the monitoring of bridges using “smart” components." In IABSE Congress, New York, New York 2019: The Evolving Metropolis. Zurich, Switzerland: International Association for Bridge and Structural Engineering (IABSE), 2019. http://dx.doi.org/10.2749/newyork.2019.0811.
Full textReports on the topic "Viral traffic"
Chiavassa, Nathalie, and Raphael Dewez. Technical Note on Road Safety in Haiti. Inter-American Development Bank, January 2021. http://dx.doi.org/10.18235/0003250.
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