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Ratcliff, Frank Giles. "Novel aspects of plant-virus interactions". Thesis, University of East Anglia, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302040.
Pełny tekst źródłaChewachong, 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.
Pełny tekst źródłaTungadi, Trisna Dewi. "Cucumber mosaic virus modifies plant-aphid interactions". Thesis, University of Cambridge, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708288.
Pełny tekst źródłavan, Zyl Albertha R. "Development of plant-produced Bluetongue virus vaccines". Doctoral thesis, University of Cape Town, 2014. http://hdl.handle.net/11427/28248.
Pełny tekst źródłaMurray, Abner A. "Plant Virus Nanoparticle In Situ Cancer Immunotherapies". Case Western Reserve University School of Graduate Studies / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=case1532370850718292.
Pełny tekst źródłaAitken, Angus Iain. "Membrane interactions of plant virus movement proteins". Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/15617.
Pełny tekst źródłaSoards, 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.
Pełny tekst źródłaGaafar, Yahya Zakaria Abdou [Verfasser]. "Plant virus identification and virus-vector-host interactions / Yahya Zakaria Abdou Gaafar". Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://d-nb.info/1220909262/34.
Pełny tekst źródłaChun, Elizabeth M. "Developing a Recombinant Plant Virus Nanoparticle Vaccine for Rift Valley Fever Virus". Scholarship @ Claremont, 2019. https://scholarship.claremont.edu/scripps_theses/1345.
Pełny tekst źródłaChare, Elizabeth R. "Recombination in RNA viruses and plant virus evolution". Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433381.
Pełny tekst źródłaWestwood, Jack Henry. "Cucumber mosaic virus infection and plant-aphid interactions". Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608811.
Pełny tekst źródłaLi, Hua. "Molecular approaches to plant virus resistance in lupins". Thesis, Li, Hua (2000) Molecular approaches to plant virus resistance in lupins. PhD thesis, Murdoch University, 2000. https://researchrepository.murdoch.edu.au/id/eprint/52579/.
Pełny tekst źródłaShamandi, Nahid. "Functional analysis of plant RNaseIII enzymes". Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112157/document.
Pełny tekst źródłaSmall RNAs, including miRNA and siRNA, play essential regulatory roles in genome stability, development and stress responses in most eukaryotes. Plants encode four DICER-LIKE (DCL) RNaseIII enzymes. DCL1 produces miRNAs, while DCL2, DCL3 and DCL4 produce diverse size classes of siRNA. Plants also encode RNASE THREE-LIKE (RTL) enzymes that lack DCL-specific domains and whose function is largely unknown. Arabidopsis plants over-expressing RTL1 exhibit morphological defects and lack all types of small RNAs produced by DCL2, DCL3 and DCL4, indicating that RTL1 is a general suppressor of plant siRNA pathways. RTL1 activity requires a functional RNaseIII domain. RTL1 is naturally expressed only weakly in roots, but virus infection strongly induces its expression in leaves, suggesting that RTL1 induction is a general strategy used by viruses to counteract the siRNA-based plant antiviral defense. Accordingly, transgenic plants over-expressing RTL1 are more sensitive to TYMV infection than wild-type plants, likely because RTL1 prevents the production of antiviral siRNAs. However, TCV, TVCV and CMV, which encode stronger suppressors of RNA silencing (VSR) than TYMV, are insensitive to RTL1 over-expression. Indeed, TCV VSR inhibits RTL1 activity, suggesting that inducing RTL1 expression and dampening RTL1 activity is a dual strategy used by viruses to establish a successful infection. Plants over-expressing RTL2 and rtl2 mutants do not exhibit morphological defects and do not show major changes in the endogenous small RNA repertoire. However, RTL2 over-expression enhances the accumulation of exogenous siRNAs in transient assays, and this activity requires a functional RNaseIII domain. Therefore, it is possible that plant RTL2 processes certain substrates to facilitate the action of DCL enzymes
Chingandu, Nomatter, i Nomatter Chingandu. "Genomic Characterization of the Cacao Swollen Shoot Virus Complex and other Theobroma Cacao-Infecting Badnaviruses". Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/621859.
Pełny tekst źródłaHarker, C. L. "The detection of virus coded proteins in cauliflower mosaic virus infected plants and protoplasts". Thesis, Bucks New University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376417.
Pełny tekst źródłaCarr, Tyrell. "Genetic and molecular investigation of compatible plant-virus interactions". [Ames, Iowa : Iowa State University], 2007.
Znajdź pełny tekst źródłaBrown, J. K., D. Goldstein i M. R. Nelson. "Plant Virus Diseases that Threaten Cucurbit Production in Arizona". College of Agriculture, University of Arizona (Tucson, AZ), 1986. http://hdl.handle.net/10150/214137.
Pełny tekst źródłaJeffries, Alex Craig. "The study at the molecular level of the New Zealand isolate of Lucerne transient streak sobemovirus and its satellite RNA". Title page, contents and summary only, 1993. http://web4.library.adelaide.edu.au/theses/09PH/09phj47.pdf.
Pełny tekst źródłaCole, Anthony Blaine Thomas. "Investigations into the hypersensitive response of Nicotiana species to virus infections /". free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3012960.
Pełny tekst źródłaAsare-Bediako, Elvis. "Brassicaceae : Turnip yellows virus interactions". Thesis, University of Warwick, 2011. http://wrap.warwick.ac.uk/44041/.
Pełny tekst źródłaMoshref, Mahmood. "Investigation of plant extracts for antimicrobial activity". Thesis, University of Sheffield, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388711.
Pełny tekst źródłaVaitkunas, Katrina Emilee. "The genetics of TCV resistance". Link to electronic thesis, 2003. http://www.wpi.edu/Pubs/ETD/Available/etd-0428103-102720.
Pełny tekst źródłaAl-Kaff, Nadia Saleh Ahmed. "Biological and molecular diversity of cauliflower mosaic virus". Thesis, University of East Anglia, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240834.
Pełny tekst źródłaChapman, Sean Nicholas. "A molecular analysis of potato virus X". Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386398.
Pełny tekst źródłaBalcı, Evrim Doğanlar Sami. "Genetic characterization of cucumber mosaic virus(CMV)resistance in tomato and pepper". [s.l.]: [s.n.], 2005. http://library.iyte.edu.tr/tezler/master/biyoloji/T000388.pdf.
Pełny tekst źródłaWasswa, Peter. "Sweet potato viruses in Uganda : identification of a new virus, a mild strain of an old virus and reversion". Thesis, University of Greenwich, 2012. http://gala.gre.ac.uk/9091/.
Pełny tekst źródłaLin, Junyan. "NONHOST RESISTANCE TO BEAN POD MOTTLE VIRUS IN NICOTIANA BENTHAMIANA". The Ohio State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=osu1372723537.
Pełny tekst źródłaFreitas, Debora Maria Sansini. "Novas observações sobre a proteção com estirpes fracas do Papaya ringspot virus - type W e do Zucchini yellow mosaic virus em plantas de abobrinha-de-moita". Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-17082007-095734/.
Pełny tekst źródłaPapaya ringspot virus - type W (PRSV-W) and Zucchini yellow mosaic virus (ZYMV) are two potyviruses associated with severe yield losses on cucurbit crops in the State of São Paulo and other parts of the Brazilian territory. Preimmunization with mild strains has proved to be a good alternative for the control of both viruses in susceptible cultivars. The main purpose of this work was to evaluate the competition for infectable sites as a possible mechanism of cross protection between the mild strain PRSV-W-1 and the severe strain PRSV-W-C in zucchini squash (Cucurbita pepo cv. Caserta). Protective inoculation with the mild strain was done at the cotyledon and the challenge inoculation with the severe strain was applied on the first true expanded leaf, and viceversa. Different plants were challenged at three, six and nine days, respectively. No challenge protected plants and healthy plants infected with the severe strain were used as controls. Evaluations were based on the expression of the symptoms at 30 days after challenge inoculation. Attempts to recover the challenge strain from challenge inoculated and new developed leaves were also done at eight days after challenge inoculation. RT-PCR with specific pairs of primers was also used to detect both stains in some of these samples. Regardless the leaf on which the protective strain was applied (cotyledon or first true expanded leaf) there appear to be some infectable sites available for superinfection with the severe strain. When the challenge inoculation was done at three days after preimmunization, the severe strain was able to superinfect some plants, move systemically and overcome the mild strain, since these plants expressed severe symptoms. All plants become protected against the expression of the symptoms induced by the severe strain when the challenge inoculation was done at six and nine days after preimmunization. However, the severe strain was still detected in the inoculated and upper leaves of few test-plants, eight days after challenge inoculation. In addition to this, it was also determined the period of time necessary to protect zucchini squash plants with a mild strain of ZYMV, named ZYMV-M, alone and in mixture with mild strain PRSV-W-1. The results indicated that single and double preimmunized plants were protected against infection and/or expression of the homologous severe strain seven days after protective inoculation.
George, Gavin M. (Gavin Mager). "Virus induced gene silencing for the study of starch metabolism". Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/4024.
Pełny tekst źródłaENGLISH ABSTRACT: Virus Induced Gene Silencing (VIGS) was optimized to allow for the study of starch metabolism. The plastidial inorganic pyrophosphatase gene, for which a mutant has never been identified, was studied using VIGS and it was found to have a broad role in this subcellular compartment. The accumulation of inorganic pyrophosphate limited the production of starch, carotenoids, chlorophyll, and increased the plants susceptibility to drought stress. These effects highlight the importance of this enzyme in maintaining a low intraplastidial concentration of PPi providing an environment which facilitates these anabolic processes. Several genes involved in starch synthesis and degradation were also targeted with the aim of establishing a system of multiple gene silencing for the study of metabolic pathways. One, two and three genes were successfully silenced using this system which was validated based on previously published data. Interestingly, simultaneous silencing of the two isoforms of disproportionating enzyme led to a novel phenotype as a large reduction in starch instead of the expected increase was observed.
No Afrikaans abstract available
Bustamante-Gallardo, Pedro. "Molecular studies on Rice hoja blanca virus (RHBV)". Thesis, University of East Anglia, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338096.
Pełny tekst źródłaEscaler, Margarita. "Changes in host gene expression associated with plant virus replication". Thesis, University of East Anglia, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302215.
Pełny tekst źródłaSeymour, Maile Elizabeth Kahawaluiaakalani. "Process considerations in the extraction and recovery of plant virus". Thesis, University College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398938.
Pełny tekst źródłaZhang, Xu-Sheng. "Mathematical models of plant disease epidemics that involve virus interactions". Thesis, University of Greenwich, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327341.
Pełny tekst źródłaTakeda, Atsushi. "Analysis of Plant Virus Movement Proteins and RNA Silencing Suppressors". Kyoto University, 2004. http://hdl.handle.net/2433/147760.
Pełny tekst źródła0048
新制・課程博士
博士(農学)
甲第10911号
農博第1417号
新制||農||891(附属図書館)
学位論文||H16||N3922(農学部図書室)
UT51-2004-G758
京都大学大学院農学研究科応用生物科学専攻
(主査)教授 奥野 哲郎, 教授 遠藤 隆, 教授 西岡 孝明
学位規則第4条第1項該当
Maree, H. J. (Hans Jacob). "The expression of Dianthin 30, a ribosome inactivating protein". Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53633.
Pełny tekst źródłaENGLISH ABSTRACT: Ribosome inactivating proteins (RIPs) are currently classified as rRNA N-glycosidases, but also have polynucleotide: adenosine glycosidase activity. RIPs are believed to have anti-viral and anti-fungal properties, but the exact mechanism of these proteins still need to be elucidated.The mechanism of resistance however, appears to be independent of the pathogen. For resistance the RIP terminates virus infected plant cells and stops the reproduction and spread of the virus. Transgenic plants containing RIPs should thus be resistant to a wide range of viruses. The ultimate goal of the larger project of which this forms part is the development of virus resistant plants. To monitor the expression of a RIP in a transgenic plant a detection method had to be developed. Antibody detection of the RIP was decided upon as the most cost effective method. The RIP, Dianthin 30 from Dianthus caryophyllus (carnation), was used and expressed in bacterial and insect expression systems. The bacterial expression experiments were done using the pET expression system in BL21(DE3)pLysS cells. The expression in this system yielded recombinant protein at a very low concentration. Expression experiments were also performed in insect tissue culture with the baculovirus vector BAC-TO-BAC™.With this system the expression was also too low to be used for the production of antibodies. A Dianthin 30 specific peptide was then designed and then produced by Bio-Synthesis. This peptide was then used to raise antibodies to detect Dianthin 30. These antibodies were tested on Dianthus caryophyllus proteins. To establish if this detection method was effective to monitor the expression in plants, tobacco plants were transformed with Agrobacterium tumefaciens containing Dianthin 30 in the pART27 plant expression vector. The putative transformed plants were analysed with peR and Southern blots.
AFRIKAANSE OPSOMMING: Tans word Ribosomale-inaktiverende proteïene (RIPs) geklassifiseer as rRNA N-glikosidase wat ook polinukleotied: adenosien glikosidase aktiwiteit bevat. Daar word geglo dat RIPs anti-virale en anti-fungus eienskappe bevat, maar die meganisme van beskerming word nog nie ten volle verstaan nie. Dit is wel bewys dat die meganisme van weerstand onafhanklik is van die patogeen. Virus geinfekteerde plantselle word deur die RIP gedood om die voortplanting en verspreiding te bekamp en sodoende word weerstand bewerkstellig. Transgeniese plante wat dan 'n RIP bevat sal dus weerstandbiedend wees teen 'n wye spektrum virusse. Die hoofdoel van die breër projek, waarvan die projek deel uitmaak: is die ontwikkeling van virusbestande plante. Om die uitdrukking van die RIP in die transgeniese plante te kontroleer, moes 'n deteksie metode ontwikkel word. Die mees koste effektiewe deteksie metode is met teenliggame. Die RIP, Dianthin 30 from Dianthus caryophyllus (angelier) was gebruik vir uitdrukking in bakteriele- en insekweefselkultuur. Die bakteriele uitdrukkingseksperimente was gedoen met die pET uitdrukkings sisteem III BL21(DE3)pLysS selle. Die uitdrukking in die sisteem het slegs rekombinante proteïene gelewer in uiters lae konsentrasies. Uitdrukkingseksperimente was ook gedoen in insekweefselkultuur met die baculovirus vektor BAC-To- BACTM. Met die sisteem was die uitdrukking ook veels te laag om bruikbaar te wees vir die produksie van teenliggame. Daar is toe 'n peptied ontwerp wat Dianthin 30 kan verteenwoordig vir die produksie van teenliggame. Die teenliggame is getoets teen Dianthus caryophyllus proteïene. Om vas te stel of die deteksiemetode wel die uitdrukking van Dianthin 30 sal kan monitor, is tabak ook getransformeer met Dianthin 30. Die transformasies is gedoen met die hulp van Agrobacterium tumefaciens en die pART27 plant uitdrukkings vektor. Die plante is getoets met die polimerase ketting reaksie en Southern klad tegnieke.
Shih, Sharon Min-Hsuan Biotechnology & Biomolecular Sciences Faculty of Science UNSW. "Transient viral infection of plant tissue culture and plants for production of virus and foreign protein". Awarded by:University of New South Wales, 2007. http://handle.unsw.edu.au/1959.4/34967.
Pełny tekst źródłaGiampan, José Segundo. "Infectividade e proteção de três estirpes fracas do Papaya ringspot virus em plantas de melancia". Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-25022003-134805/.
Pełny tekst źródłaThe purpose of this work was to evaluate the infectivity of three mild strains of Papaya ringspot virus - type W (PRSV-W) on watermelon (Citrullus lanatus). The effect of the origin of the mild strain, the concentration of the inoculum, the species of the source of the inoculum and the age of the test-plant on the infectivity of mechanically inoculated watermelon were also evaluated. The protective effect of these mild strains on preimmunized watermelon plants was evaluated under greenhouse and field conditions. Mild strains were selected from blisters formed on mosaic leaves of naturally infected watermelon plants. The infectivity of the selected mild strain was compared with that of mild strains PRSV-W-1 and PRSV-W-2, which were previously obtained from blisters formed on mosaic leaves of zucchini squash (Cucurbita pepo cv. Caserta). A severe strain isolated from zucchini squash (PRSV-W-C) was used as control. The effect of the concentration and the species source of inoculum of the mild strains on the infectivity of watermelon plants was studied with inoculum extracted from 4, 8, 12 and 16 leaf discs of zucchini squash and watermelon plants, separately infected with the mild and severe strains, diluted in 2 mL of phosphate buffer. Four stages of development of watermelon plants, starting at the cotyledonal stage, were tested for the infectivity with the mild strains. Inocula were prepared with extracts of 12 leaf discs diluted in 2 mL of phosphate buffer. The protective effect of the mild strain selected from blisters on mosaic leaves of watermelon plants was evaluated on preimmunized plants challenge inoculated with severe strain PRSV-W-C, under greenhouse and field conditions. Watermelon plants preimmunized with mild strains PRSV-W-1 and PRSV-W-2 and unprotected plants were also included in the field trial. Protection was evaluated based on plant simptons, yield and sugar content in the fruits. One mild strain, named PRSV-W-3, was obtained from blisters on mosaic leaves of watermelon plants. The rate of infection of watermelon plants with mild strain PRSV-W-3 was similar to that with mild strains PRSV-W-1 and PRSV-W-2 in all infectivity tests, independently of the concentration of the inoculum, species source of the inoculum and stage of development of the inoculated test-plant, reaching 100% in some cases. Rate of infectivity with severe strain PRSV-W-C was always 100%. Apparently, the infectivity of the mild strains on watermelon was more directly related with the intensity of the abrasion produced by mechanical inoculation than with the above studied variables. The selected mild strain PRSV-W-3 protected watermelon plants against superinfection with the severe strain in the greenhouse tests. Protection was also effective under field conditions. Yield of plants preimmunized with all three mild strains and unprotected plants were statistically similar. The sugar content and the quality of the pulp of the fruits were similar for all treatments.
Pinto, Yvonne Maria. "Characterization of a Nigerian isolate of rice yellow mottle virus". Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243556.
Pełny tekst źródłaPerbal, Marie-Christine. "A functional analysis of the cauliflower mosaic virus movement protein". Thesis, University of East Anglia, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359335.
Pełny tekst źródłaWeng, Ziming. "Replication and recombination of the Red clover necrotic mosaic virus". Diss., The University of Arizona, 2002. http://hdl.handle.net/10150/280079.
Pełny tekst źródłaBrigneti, Gianinna. "Molecular and genetical analysis of the Ry-mediated resistance to potato virus Y in potato". Thesis, University of East Anglia, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389221.
Pełny tekst źródłaHamdollah-Zadeh, Akram. "Transgenic resistance to pollen transmission of tobacco ringspot virus". Thesis, University of Bristol, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364912.
Pełny tekst źródłaLutz, Lindy Michelle. "Cauliflower mosaic virus P6 protein interactions: a complex story". University of Toledo / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1393863253.
Pełny tekst źródłaSisco, Daniel. "Adeno-associated virus rep78 expression in Arabidopsis thaliana". Thesis, Virginia Tech, 2002. http://hdl.handle.net/10919/9706.
Pełny tekst źródłaMaster of Science
Zhan, Ye. "Molecular analysis of turnip crinkle virus coat protein mutations". Link to electronic thesis, 2002. http://www.wpi.edu/Pubs/ETD/Available/etd-0430102-142639.
Pełny tekst źródłaPitzalis, Nicolas. "Plant-virus interactions : role of virus- and host-derived small non-coding RNAs during infection and disease". Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAJ103.
Pełny tekst źródłaIn this thesis, I investigated the role of host- and virus-derived sRNAs during infection of Rapeseed (Brassica napus, Canola) by the UK1 strain of Turnip mosaic virus (TuMV-UK1). By using a TuMV derivative tagged with a gene encoding green fluorescent protein (TuMV-GFP), two rapeseed cultivars (‘Drakkar’ and ‘Tanto’) that differ in susceptibility to this virus were identified. Transcriptional profiling of local infection foci in Drakkar and Tanto leaves by next generation sequencing (NGS) revealed numerous differentially expressed genes. The same RNA samples from mock- and virus- treated Drakkar and Tanto leaves were also used for the global NGS profiling of sRNAs (sRNAseq) and their potential RNA targets (PAREseq). The bioinformatic analysis and their in vivo validation led to the identification of transcript cleavage events involving known and yet unknown miRNAs. Importantly, the results indicate that TuMV hijacks the host RNA silencing pathway with siRNAs derived from its own genome (vsiRNAs) to target host genes. The virus also triggers the widespread targeting of host messenger RNAs (mRNAs) through activation of phased, secondary siRNA production from PHAS loci. In turn, both vsiRNAs and host-derived siRNAs (hsRNAs) target and cleave the viral RNA by the RISC-mediated pathway. These observations illuminate the role of host and virus-derived sRNAs in the coordination of virus infection. Another chapter of this thesis is dedicated to the analysis of virus-induced diseases by using Arabidopsis plants infected with the Oilseed rape mosaic tobamovirus (ORMV) as a model. Initially, the infected plants develop leaves with strong disease symptoms. However, at a later stage, disease-free, “recovered” leaves start to appear. Analysis of symptoms recovery led to the identification of a mechanism in which the VSR and virus derived-siRNAs play a central role. I used Arabidopsis mutants impaired in transcriptional and post-transcriptional silencing pathways (TGS and PTGS respectively) and a plant line carrying a promoter-driven GFP transgene silenced by PTGS (Arabidopsis line 8z2). Using various techniques able to monitor virus infection, small and long viral RNA molecules, VSR activity, as well as phloem-mediated transport with in these lines, this study led to the identification of genes required for disease symptoms and disease symptom recovery. Moreover, the observations allowed to propose a model in which symptoms recovery occurs upon robust delivery of antiviral secondary vsiRNAs from source to sink tissues, and establishment of a vsiRNA dosage able to block the VSR activity involved in the formation of disease symptoms
Cruz, Luisa Fernanda. "Resistance to Wheat streak mosaic virus and Triticum mosaic virus in wheat mediated by RNAi". Thesis, Manhattan, Kan. : Kansas State University, 2009. http://hdl.handle.net/2097/1653.
Pełny tekst źródłaKirály, Lóránt. "Interactions between cauliflower mosaic virus isolates and nicotiana species that determine systemic necrosis /". free to MU campus, to others for purchase, 1997. http://wwwlib.umi.com/cr/mo/fullcit?p9841160.
Pełny tekst źródłaCleveland, S. Matthew. "HIV-1-specific antibody responses to a plant virus-HIV chimera". Thesis, University of Warwick, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340090.
Pełny tekst źródłaNagano, Hideaki. "Studies on Plant-Virus Cell-to-Cell Movement Using Chimeric Viruses". Kyoto University, 2000. http://hdl.handle.net/2433/78105.
Pełny tekst źródła0048
新制・課程博士
博士(農学)
甲第8438号
農博第1122号
新制||農||801(附属図書館)
学位論文||H12||N3395(農学部図書室)
UT51-2000-F342
京都大学大学院農学研究科農林生物学専攻
(主査)教授 古澤 巌, 教授 泉井 桂, 教授 津田 盛也
学位規則第4条第1項該当