Dissertationen zum Thema „Les Virus“
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Kamitani, Mari. „Analysis on virus-virus and virus-host interactions in Brassicaceae in natural environments“. 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225436.
Der volle Inhalt der QuelleGubser, Caroline. „Camelpox virus : the closest known virus to variola virus, the cause of smallpox“. Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393229.
Der volle Inhalt der QuelleNettleton, Peter Francis. „Studies on the relationship between bovine virus diarrhoea virus and border disease virus“. Thesis, University of Edinburgh, 1985. http://hdl.handle.net/1842/30569.
Der volle Inhalt der QuelleBentley, Emma. „The study of highly pathogenic emerging zoonotic virus envelope proteins through pseudotyped virus generation“. Thesis, University of Westminster, 2017. https://westminsterresearch.westminster.ac.uk/item/q4yzx/the-study-of-highly-pathogenic-emerging-zoonotic-virus-envelope-proteins-through-pseudotyped-virus-generation.
Der volle Inhalt der QuelleAravapalli, Sridhar. „Dengue virus and West Nile virus protease inhibitors“. Diss., Wichita State University, 2013. http://hdl.handle.net/10057/6719.
Der volle Inhalt der QuelleThesis (Ph.D.)--Wichita State University, Fairmount College of Liberal Arts and Sciences, Dept. of Chemistry
Koelzer, Anja Kathrin. „TT Virus“. Diss., lmu, 2002. http://nbn-resolving.de/urn:nbn:de:bvb:19-7124.
Der volle Inhalt der QuelleHolt, Jim. „Zika Virus“. Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etsu-works/6468.
Der volle Inhalt der QuelleChan, Kenneth See Kit. „Nef from pathogenic simian immunodeficiency virus attenuates vaccinia virus /“. For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2004. http://uclibs.org/PID/11984.
Der volle Inhalt der QuelleSchupp, Dorothee Carolin. „Elucidating virus uptake and fusion by single virus tracing“. Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-148690.
Der volle Inhalt der QuelleMcHugh, Paul H. „Studies on the antigenicity of bovine virus diarrhoea virus“. Thesis, Queen's University Belfast, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317512.
Der volle Inhalt der QuelleWard, Rebecca. „Bluetongue virus non-structural protein 1 : virus-host interactions“. Thesis, London School of Hygiene and Tropical Medicine (University of London), 2006. http://researchonline.lshtm.ac.uk/4646527/.
Der volle Inhalt der QuelleBajric, Amina. „Validering av Varicella Zoster virus och Herpes Simplex virus“. Thesis, Malmö universitet, Fakulteten för hälsa och samhälle (HS), 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-24474.
Der volle Inhalt der QuelleThe approach of this validation study is to evaluate the adequacy for transferring the manual analysis method of ongoing infection of Varicella Zoster Virus (aVZV IgM) and Herpes Simplex Virus (aHSV IgM) with SIEMENS Enzygnost® to one of the automated instruments EUROIMMUN Analyzer I (ELISA) or DiaSorin LIAISON® XL. The study was carried out at Clinical Microbiology in Lund. Consecutive serum samples for VZV IgM (n=108) and HSV IgM (n=116) from the daily local flow of tests were analyzed, along with 10 positive for primary infection of VZV and HSV, confirmed by PCR or seroconversion, and 10 with reactivated infection of VZV and HSV. Beyond those, 10 serum samples confirmed positive for Cytomegalovirus (CMV) respectively 10 for Epstein-Barr Virus (EBV) to test the cross-reaction between the three methods. The results from the validation of VZV in Analyzer I and LIAISON® XL gave an agreement of 93% and 94% respectively in the consecutive tests, 71% and 86% respectively in the primary infected tests and 75% and 58% respectively in the reactivated tests, and also a cross-reactivity (both positive and in between-values) at a total of 33% respectively 20% of the tests. The results from the validation of HSV in Analyzer I and LIAISON® XL gave an agreement of 84% and 87% respectively in the consecutive tests, 82% and 18% respectively in the primary infected tests and 40% and 10% respectively in the reactivated tests, and also a cross-reactivity (both positive and in between-values) at a total of 67% respectively 47% of the tests. According recommendations after the performance of this study, the analysis of HSV IgM should be excluded from both of the automated methods while VZV IgM should be controlled further in Analyzer I, with hopes that this new method could be more sensitive.
Danet, Nicolas. „Molecular characterisation of the recombinant Vesicular Stomatitis Virus- ZEBOV-GP virus, prototype vaccine against Ebola virus“. Thesis, Lyon, 2019. http://www.theses.fr/2019LYSE1009/document.
Der volle Inhalt der QuelleThe filovirus Ebolavirus (EBOV) is the causative agent of severe viral hemorrhagic fevers in humans that can be lethal in 90% of cases. The current outbreak in the Democratic Republic of Congo and the extraordinary scale of the 2014-2016 outbreak in West Africa, that caused the death of more than 11 000 disease victims, lead the international public health agencies to test several therapeutic approach to limit viral spreading and mortality. Amongst those, the recombinant replication-competent rVSV-ZEBOV virus, that expressed EBOV GP glycoprotein, appears to offer the best protection in animal models and outbreak settings. While its effectiveness and safety have been widely investigated before human trials and despite numerous studies that showed the importance the nature of the glycoproteins which are produced during the infection from the EBOV GP gene that has been inserted in VSV genome are unknown. In this respect, the molecular characterisations of the viral glycoproteins synthesised during rVSV-GP presented in this thesis, offer new insights with which to understand the success of the rVSV-GP vaccine but also the potential viral origins of the severe adverse side effects observed during vaccination and could help in developing a safer vaccine, which currently cannot be used in an immunocompromised population
HUGUENOT, CLAIRE. „Etude immunochimique de deux virus de plantes : le tomato spotted wilt virus et le peanut clump virus“. Université Louis Pasteur (Strasbourg) (1971-2008), 1989. http://www.theses.fr/1989STR13198.
Der volle Inhalt der QuelleRollison, Dana Elise Maher. „The association between the polyomaviruses JC virus, BK virus, and simian virus 40, and human brain tumors“. Available to US Hopkins community, 2002. http://wwwlib.umi.com/dissertations/dlnow/3080754.
Der volle Inhalt der QuelleDhillon, Simrat. „Investigating virus entry using cell-culture adapted hepatitis C virus“. Thesis, University of Glasgow, 2012. http://theses.gla.ac.uk/3616/.
Der volle Inhalt der QuelleKallies, René [Verfasser]. „Ljungan virus – prevalence in rodents and virus pathogenesis / René Kallies“. Berlin : Freie Universität Berlin, 2012. http://d-nb.info/1030291136/34.
Der volle Inhalt der QuelleThuenemann, Eva. „Virus-like particle production using cowpea mosaic virus-based vectors“. Thesis, University of East Anglia, 2010. https://ueaeprints.uea.ac.uk/20539/.
Der volle Inhalt der QuelleBouraï, Mehdi. „Caractérisation d'un interactome virus-hôte : l'exemple du virus du Chikungunya“. Paris 7, 2011. http://www.theses.fr/2011PA077183.
Der volle Inhalt der QuelleThe lifting of many technological barriers in recent years has allowed the development of « functional genomics », an innovative systemic approach to molecular and cell biology. Viruses, being intracellular parasites, interact with several components of the cell to replicate. Thus, defining and improving our knowledge of the interactions between viral and cellular proteins ensures a better understanding of the viral replication cycle and pathogenesis and opens the pathway to new therapeutic approaches. In my thesis, I defined the interaction map, or interactome, of the chikungunya virus (CHIKV), a virus whose interactions with the cell at the molecular level have been poorly understood. For this, I performed high throughput two-hybrid approaches in yeast (HT-Y2H) and validations in mammalian cells (including protein complementation assay technique or PCA). We screened all the CHIKV mature proteins across three different human cDNA libraries and a normalized 12,000 human full-length open reading frames (ORF) library. We identified 22 interactions, the majority of which involve non-structural protein 2 (nsP2) of CHIKV. Among the identified cellular interactors, we showed the important role of hnRNP-K (heterogeneous nuclear ribonucleoprotein K) and ubiquilin 4 in virus replication in vitro. Furthermore, we demonstrated the involvement of the TTC7B protein (tétratricopeptide 7B) in the transcriptional inhibition activity induced by the nsP2 protein of CHIKV. Such techniques conducted in the laboratory also allowed me to participate in thé charaterization of three virus-host interactions identified by a fellow PhD student and contribute to researching the replication of measles virus (MV) and type 3 human parainfluenza virus (hPIV3). In particular, I was able to accurately map the peptide domains involved in these interactions, using a technique adapted from Y2H. This work has allowed me to not only understand the current techniques for defining virus-host interactomes and consequently produce a map of virus-host interactions for CHIKV, but also to shed some light on the viral mechanisms involved in the replication cycle and the pathogenesis of this virus
Upadhyay, Mohita. „Dinucleotide frequencies in DNA virus genomes: implications on virus evolution“. Thesis, IIT Delhi, 2016. http://localhost:8080/xmlui/handle/12345678/6989.
Der volle Inhalt der QuelleCullen, Ben Sandford 1964-1995. „The cultural virus“. Phd thesis, School of Archaeology, Classics and Ancient History, 1993. http://hdl.handle.net/2123/9055.
Der volle Inhalt der QuelleNelson, M. R., A. Nadeem, W. Ahmed und T. V. Orum. „Cotton Virus Diseases“. College of Agriculture, University of Arizona (Tucson, AZ), 1998. http://hdl.handle.net/10150/210398.
Der volle Inhalt der QuelleHöfer, Chris Tina. „Influenza virus assembly“. Doctoral thesis, Humboldt-Universität zu Berlin, Lebenswissenschaftliche Fakultät, 2015. http://dx.doi.org/10.18452/17251.
Der volle Inhalt der QuelleInfluenza A viruses have a segmented single-stranded RNA genome, which is packed in form of viral ribonucleoprotein (vRNP) complexes. While the viral genome is replicated and transcribed in the host cell nucleus, assembly and budding of mature virus particles take place at the apical plasma membrane. Efficient virus formation requires delivery of all viral components to this site. While intrinsic apical targeting signals of the viral transmembrane proteins have been identified, it still remains poorly understood how the viral genome is transported and targeted into progeny virus particles. In this study, potential targeting mechanisms were investigated like the ability of vRNPs to associate with lipid membranes and the intrinsic ability of the viral nucleoprotein (NP) – which is the major protein component of vRNPs – for subcellular targeting. It could be shown that vRNPs are not able to associate with model membranes in vitro, which was demonstrated by flotation of purified vRNPs with liposomes of different lipid compositions. Results indicated, however, that the matrix protein M1 can mediate binding of vRNPs to negatively charged lipid bilayers. Intrinsic subcellular targeting of NP was further investigated by expression of fluorescent NP fusion protein and fluorescence photoactivation, revealing that NP by itself does not target cytoplasmic structures. It was found to interact extensively with the nuclear compartment instead and to target specific nuclear domains with high affinity, in particular nucleoli and small interchromatin domains that frequently localized in close proximity to Cajal bodies and PML bodies. An experimental approach was finally established that allowed monitoring the transport of vRNP-like complexes in living infected cells by fluorescence detection. It was possible to perform single particle tracking and to describe different stages of vRNP transport between the nucleus and the plasma membrane. A model of three-stage transport is suggested.
Smith, H. G. „Comparative epidemiology and host : Virus interactions of beet yellow virus and beet mild yellowing virus in sugar beet“. Thesis, University of East Anglia, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.374298.
Der volle Inhalt der QuelleCosta, Ana Catarina de Almeida. „Serological surveillance of West Nile virus and molecular diagnostic of West Nile virus, Usutu virus, avian influenza and Newcastle disease virus in wild birds of Portugal“. Master's thesis, Universidade de Lisboa, Faculdade de Medicina Veterinária, 2021. http://hdl.handle.net/10400.5/21604.
Der volle Inhalt der QuelleABSTRACT - The worldwide changes in the environment and climate of natural ecosystems detected in the last few decades have been responsible for the emergence of new infectious diseases in both animals and humans. This work focused on surveillance of four zoonotic pathogens, namely West Nile virus (WNV), Usutu virus (USUV), avian orthoavulavirus-1 (AOaV-1), also known as Newcastle disease virus (NDV), and influenza A virus (IAV) in wild birds of continental Portugal. Blood and tissues samples from both live and dead birds (were collected in three wildlife rehabilitation centres of Portugal between 2018 and 2019: Wildlife Rehabilitation and Research Centre of Ria Formosa, Wildlife Rehabilitation Centre of Lisbon and University of Trás-os-Montes and Alto Douro Veterinary Teaching Hospital – Wildlife Rehabilitation Centre. Samples from a total of 192 animal were collected (82 in vivo and 110 post-mortem). A total of one hundred and eighty-two samples were tested for WNV, USUV, IAV and for AOaV-1 by real time RT-PCR (RT-qPCR) or RT-PCR. AOaV-1 positive samples from two Eurasian collared doves (Streptopelia decaocto) (1.10% sample positivity) collected in the south of Portugal were sequenced, and their phylogenetic relationships analysed. Phylogenetic analysis confirmed that these sequences clustered with other AOaV-1 sequences from genotype XXI, subgenotype XXI.2. Tissue samples were all negative for WNV, USUV and IAV. Plasma samples were also tested for WNV antibodies by seroneutralization test. WNV neutralizing antibodies were detected in ten (13.70%) out of 73 samples namely: four Buteo buteo, two Hieraaetus pennatus, an Accipiter nisus, a Aegypius monachus, a Circaetus gallicus, and a Ciconia ciconia. This study has established a baseline for future epidemiological studies of WNV and AOaV-1 in wild birds of continental Portugal. Further monitoring and epidemiological studies of both diseases in Portugal is advised, considering the threat that both diseases can pose to humans, animals and to the ecosystems themselves.
RESUMO - MONITORIZAÇÃO SEROLÓGICA DO VÍRUS DO NILO OCIDENTAL E DIAGNÓSTICO MOLECULAR DO VÍRUS DO NILO OCIDENTAL, VÍRUS USUTU, INFLUENZA AVIÁRIA E VÍRUS DA DOENÇA DE NEWCASTLE EM AVES SELVAGENS DE PORTUGAL - As profundas alterações ambientais e climáticas dos ecossistemas naturais que o mundo tem sofrido nas últimas décadas têm sido responsáveis pelo aparecimento de novas doenças infeciosas em animais e humanos. Este trabalho focou-se na monitorização de quatro agentes zoonóticos em aves selvagens de Portugal continental, nomeadamente vírus do Nilo Ocidental (WNV), vírus Usutu (USUV), orthoavulavirus-1 aviário, também conhecido como vírus da doença de Newcastle (NDV) e vírus influenza A (IAV). Amostras de sangue e tecidos de animais vivos e mortos foram recolhidas entre 2018 e 2019 em três centros de recuperação de fauna selvagem em Portugal: Centro de Recuperação e Investigação de Animais Selvagens da Ria Formosa, Centro de Recuperação de Animais Silvestres de Lisboa e Centro de Recuperação de Animais Selvagens do Hospital Veterinário da UTAD. Foram recolhidas amostras de um total de 192 animais (82 in vivo e 110 post-mortem). Um total de cento e oitenta e duas amostras foram testadas para a presença de WNV, USUV, IAV e AOaV-1 por RT-PCR em tempo real (RT-qPCR) e RT-PCR convencional. Duas amostras positivas de duas rolas turcas (Streptopelia decaocto) (1.10% positividade) recolhidas no sul de Portugal foram sequenciadas e as suas relações filogenéticas foram analisadas. A análise filogenética confirmou que estas sequências agrupam com estirpes de AOaV-1 do genótipo XXI, subgenótipo XXI.2. Amostras de tecidos foram todas negativas para a presença de WNV, USUV e IAV. Amostras de plasma foram testadas para a presença de anticorpos neutralizantes de WNV pelo teste da seroneutralização. Das 73 amostras, dez (13.70%) apresentavam anticorpos neutralizantes para WNV: quatro Buteo buteo, duas Hieraaetus pennatus, um Accipiter nisus, um Aegypius monachus, uma Circaetus gallicus e uma Ciconia ciconia. Este estudo estabeleceu uma base para futuros estudos epidemiológicos sobre WNV e AOaV-1 em aves selvagens em Portugal continental. Aconselha-se a realização futura de outros estudos epidemiológicos e monitorizações, considerando a ameaça que ambas as doenças apresentam para humanos, animais e para os próprios ecossistemas.
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Gao, Zhanhai School of Mathematics UNSW. „Modelling Human Immunodeficiency Virus and Hepatitis C Virus Epidemics in Australia“. Awarded by:University of New South Wales. School of Mathematics, 2001. http://handle.unsw.edu.au/1959.4/18187.
Der volle Inhalt der QuelleHalasz, Robert. „Epidemiology and clinical importance of GB virus C/hepatitis G virus /“. Stockholm, 2000. http://diss.kib.ki.se/2000/91-628-3997-7/.
Der volle Inhalt der QuelleLaw, Mansun. „Vaccinia virus spread : the roles of virus proteins, antibody and complement“. Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365358.
Der volle Inhalt der QuelleSpagnuolo-Weaver, Martha. „Studies on the pathogenesis of bovine virus diarrhoea virus in calves“. Thesis, Queen's University Belfast, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388078.
Der volle Inhalt der QuelleSorensen, George Edwin Peter. „Host-virus interactions in porcine reproductive and respiratory syndrome virus infection“. Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/10040.
Der volle Inhalt der QuelleColledge, W. H. „Cellular transformation by simian virus 40 and Abelson murine leukaemia virus“. Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/38266.
Der volle Inhalt der QuelleBęczkowski, Paweł. „Virus evolution in the progression of natural feline immunodeficiency virus infection“. Thesis, University of Glasgow, 2013. http://theses.gla.ac.uk/4186/.
Der volle Inhalt der QuelleBadge, Joanne Louise. „The molecular characterisation of Narcissus latent virus and Maclura mosaic virus“. Thesis, University of Leicester, 1997. http://hdl.handle.net/2381/35608.
Der volle Inhalt der QuelleGaston, Fabrice. „Développement d’inhibiteurs d’entrée du virus VIH [Virus de l’Immunodéficience Humaine]-1“. Aix-Marseille 1, 2008. http://theses.univ-amu.fr.lama.univ-amu.fr/2008AIX11021.pdf.
Der volle Inhalt der QuellePore, Adam. „Studies on Host-Virus interaction for Viral Hemorrhagic Septicemia Virus (VHSv)“. University of Toledo / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1336766667.
Der volle Inhalt der QuelleChewachong, Godwill Mih. „Engineering Plant Virus " Vaccines" Using Pepino mosaic virus as a Model“. The Ohio State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=osu1384203201.
Der volle Inhalt der QuelleCuceanu, Narcisa Manuela. „Structural and genetic analysis of hepatitis G virus/GB virus-C“. Thesis, University of Edinburgh, 1999. http://hdl.handle.net/1842/22126.
Der volle Inhalt der QuelleMagoffin, Danielle E. „Molecular analysis of J-virus and Beilong virus using reverse genetics“. Thesis, Curtin University, 2006. http://hdl.handle.net/20.500.11937/560.
Der volle Inhalt der QuelleMagoffin, Danielle E. „Molecular analysis of J-virus and Beilong virus using reverse genetics“. Curtin University of Technology. Division of Health Sciences, 2006. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=17641.
Der volle Inhalt der QuelleTo gain an understanding of the biology of JPV and BeiPV, viral surface proteins from JPV were expressed and evaluated. Chimeric JPV virions containing recombinant surface proteins were generated and electron microscopy was used to determine the localisation of the proteins encoded by those JPV genes which are uncommon in other paramyxoviruses. Analysis of the attachment protein gene of JPV indicated that the virus was able to assemble an exceptionally large protein (156 kDa) into the virion structure, providing evidence in support of the hypothesis that JPV and BeiPV may represent an ancient lineage of viruses within the family Paramyxoviridae. In order to determine tissue tropism of JPV during experimental infection and to aid future work with a full-length JPV infectious clone, a real-time PCR assay for JPV was developed and assessed on tissues collected from mice infected with JPV. A multiplex microsphere assay for JPV and BeiPV was developed and used to analyse the seroprevalence of these viruses in Australian and Malaysian rodents. Although there is currently no evidence for disease caused by JPV or BeiPV, this does not preclude the emergence of a zoonotic rodent paramyxovirus related to these viruses. If this were to occur, the tools for virus detection and serological monitoring are now established.
Jalouli, Jamshid. „Human Papilloma Virus, Epstein-Barr Virus, and Herpes Simplex Virus Type-1 in Oral Squamous Cell Carcinomas from Three Populations“. Doctoral thesis, Uppsala universitet, Käkkirurgi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-128912.
Der volle Inhalt der QuelleRuiss, Romana. „Induktion Epstein-Barr Virus-spezifischer Immunantworten durch Exosomen und Virus-like Particles“. Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-119153.
Der volle Inhalt der QuelleWanas, Essam A. „Cloning and expression of the glycoproteins of pichinde virus by vaccinia virus“. Thesis, University of Ottawa (Canada), 1993. http://hdl.handle.net/10393/6489.
Der volle Inhalt der QuelleJohal, Harpreet Biotechnology & Biomolecular Sciences Faculty of Science UNSW. „The mouse mammary tumour virus - like virus in hormonally influenced human tissues“. Awarded by:University of New South Wales. Biotechnology & Biomolecular Sciences, 2009. http://handle.unsw.edu.au/1959.4/44734.
Der volle Inhalt der QuelleSchupp, Dorothee Carolin [Verfasser]. „Elucidating virus uptake and fusion by single virus tracing / Dorothee Carolin Schupp“. München : Verlag Dr. Hut, 2012. http://d-nb.info/1028783922/34.
Der volle Inhalt der QuelleSamman, Ayman. „The role of virus neutralisation in immunity to feline immunodeficiency virus infection“. Thesis, University of Glasgow, 2010. http://theses.gla.ac.uk/1554/.
Der volle Inhalt der QuelleWatson, J. P. „Hepatitis C virus : studies of the molecular basis of virus/host interaction“. Thesis, University of Newcastle Upon Tyne, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319188.
Der volle Inhalt der QuelleMartin, Caroline. „Hepatitis C virus - cell interactions : comparisons of virus and host lipoprotein binding“. Thesis, University of Newcastle Upon Tyne, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424130.
Der volle Inhalt der QuelleGreen, P. C. „Serological and immunocytochemical studies on influenza virus and influenza virus infected cells“. Thesis, University of Manchester, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356114.
Der volle Inhalt der QuelleWilliams, Cigdem Hayat. „Mutagenesis and virus blocking studies on virus-receptor interactions of Coxsackievirus A9“. Thesis, University of Essex, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390959.
Der volle Inhalt der QuelleSoards, Avril Jacqueline. „The Cucumber mosaic virus 2b protein : influences on the plant-virus interaction“. Thesis, University of Cambridge, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.619971.
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