Literatura académica sobre el tema "Virus induced gene silencing"

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Artículos de revistas sobre el tema "Virus induced gene silencing"

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Brigneti, Gianinna, Ana M. Martín-Hernández, Hailing Jin, Judy Chen, David C. Baulcombe, Barbara Baker y Jonathan D. G. Jones. "Virus-induced gene silencing inSolanumspecies". Plant Journal 39, n.º 2 (julio de 2004): 264–72. http://dx.doi.org/10.1111/j.1365-313x.2004.02122.x.

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Unver, Turgay y Hikmet Budak. "Virus-Induced Gene Silencing, a Post Transcriptional Gene Silencing Method". International Journal of Plant Genomics 2009 (15 de junio de 2009): 1–8. http://dx.doi.org/10.1155/2009/198680.

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Virus-induced gene silencing (VIGS) is one of the reverse genetics tools for analysis of gene function that uses viral vectors carrying a target gene fragment to produce dsRNA which trigger RNA-mediated gene silencing. There are a number of viruses which have been modified to silence the gene of interest effectively with a sequence-specific manner. Therefore, different types of methodologies have been advanced and modified for VIGS approach. Virus-derived inoculations are performed on host plants using different methods such as agro-infiltration and in vitro transcriptions. VIGS has many advantages compared to other loss-of-gene function approaches. The approach provides the generation of rapid phenotype and no need for plant transformation. The cost of VIGS experiment is relatively low, and large-scale analysis of screening studies can be achieved by the VIGS. However, there are still limitations of VIGS to be overcome. Nowadays, many virus-derived vectors are optimized to silence more than one host plant such as TRV-derived viral vectors which are used for Arabidopsis and Nicothiana benthamiana. By development of viral silencing systems monocot plants can also be targeted as silencing host in addition to dicotyledonous plants. For instance, Barley stripe mosaic virus (BSMV)-mediated VIGS allows silencing of barley and wheat genes. Here we summarize current protocols and recent modified viral systems to lead silencing of genes in different host species.
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Lu, R. "Virus-induced gene silencing in plants". Methods 30, n.º 4 (agosto de 2003): 296–303. http://dx.doi.org/10.1016/s1046-2023(03)00037-9.

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Liu, Yule, Michael Schiff y S. P. Dinesh-Kumar. "Virus-induced gene silencing in tomato". Plant Journal 31, n.º 6 (septiembre de 2002): 777–86. http://dx.doi.org/10.1046/j.1365-313x.2002.01394.x.

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Gammelgård, Elin, Maradumane Mohan y Jari P. T. Valkonen. "Potyvirus-induced gene silencing: the dynamic process of systemic silencing and silencing suppression". Journal of General Virology 88, n.º 8 (1 de agosto de 2007): 2337–46. http://dx.doi.org/10.1099/vir.0.82928-0.

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Potato virus A (PVA; genus Potyvirus) was used for virus-induced gene silencing in a model system that included transgenic Nicotiana benthamiana (line 16c) expressing the gfp transgene for green fluorescent protein (GFP) and chimeric PVA (PVA–GFP) carrying gfp in the P1-encoding region. Infection of the 16c plants with PVA–GFP in five experiments resulted in a reproducible pattern of systemic gfp transgene silencing, despite the presence of the strong silencing-suppressor protein, HC-Pro, produced by the virus. PVA–GFP was also targeted by silencing, and virus-specific short interfering RNA accumulated from the length of the viral genome. Viral deletion mutants lacking the gfp insert appeared in systemically infected leaves and reversed silencing of the gfp transgene in limited areas. However, systemic gfp silencing continued in newly emerging leaves in the absence of the gfp-carrying virus, which implicated a systemic silencing signal that moved from lower leaves without interference by HC-Pro. Use of GFP as a visual marker revealed a novel, mosaic-like recovery phenotype in the top leaves. The leaf areas appearing red or purple under UV light (no GFP expression) contained little PVA and gfp mRNA, and corresponded to the dark-green islands observed under visible light. The surrounding green fluorescent tissues contained actively replicating viral deletion mutants that suppressed GFP silencing. Taken together, systemic progression of gene silencing and antiviral defence (RNA silencing) and circumvention of the silencing by the virus could be visualized and analysed in a novel manner.
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Corbin, Cyrielle, Florent Lafontaine, Liuda Johana Sepúlveda, Ines Carqueijeiro, Martine Courtois, Arnaud Lanoue, Thomas Dugé de Bernonville et al. "Virus-induced gene silencing in Rauwolfia species". Protoplasma 254, n.º 4 (24 de enero de 2017): 1813–18. http://dx.doi.org/10.1007/s00709-017-1079-y.

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Burch-Smith, Tessa M., Michael Schiff, Yule Liu y S. P. Dinesh-Kumar. "Efficient Virus-Induced Gene Silencing in Arabidopsis". Plant Physiology 142, n.º 1 (30 de junio de 2006): 21–27. http://dx.doi.org/10.1104/pp.106.084624.

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Shao, Y., H. L. Zhu, H. Q. Tian, X. G. Wang, X. J. Lin, B. Z. Zhu, Y. H. Xie y Y. B. Luo. "Virus-induced gene silencing in plant species". Russian Journal of Plant Physiology 55, n.º 2 (marzo de 2008): 168–74. http://dx.doi.org/10.1134/s1021443708020027.

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Fu, Da-Qi, Ben-Zhong Zhu, Hong-Liang Zhu, Wei-Bo Jiang y Yun-Bo Luo. "Virus-induced gene silencing in tomato fruit". Plant Journal 43, n.º 2 (10 de junio de 2005): 299–308. http://dx.doi.org/10.1111/j.1365-313x.2005.02441.x.

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Martin, Ruth C., Kira Glover-Cutter, Robert R. Martin y James E. Dombrowski. "Virus induced gene silencing in Lolium temulentum". Plant Cell, Tissue and Organ Culture (PCTOC) 113, n.º 2 (29 de noviembre de 2012): 163–71. http://dx.doi.org/10.1007/s11240-012-0257-z.

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Tesis sobre el tema "Virus induced gene silencing"

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Payne, Richard. "Gene discovery in Catharanthus roseus using virus induced gene silencing". Thesis, University of East Anglia, 2015. https://ueaeprints.uea.ac.uk/59379/.

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This thesis presents the use of Virus Induced Gene Silencing (VIGS) for the discovery of enzymes and transporters involved in monoterpene indole alkaloid (MIA) metabolism in the medicinal plant Catharanthus roseus. C. roseus is the source of a number of MIAs that are used as chemotherapeutic agents in the treatment of a variety of cancers, however the complete biosynthetic pathway for these metabolites remains to be elucidated. Additionally, this metabolic pathway is subcellulary compartmented with the key branch point enzyme, strictosidine synthase, localised to the plant vacuole. There is therefore a need for the import of the substrates for strictosidine biosynthesis; secologanin and tryptamine, across the vacuolar membrane, and export of the product, strictosidine, for synthesis of the downstream alkaloids. This thesis presents the identification of two proteins that act as trans-tonoplastic transporters in MIA metabolism. The multidrug and toxic compound extrusion (MATE) protein, CrMATE1952, was localised to the vacuolar membrane and silencing its expression in planta resulted in the accumulation of a secologanin derivative. This implicates CrMATE1952 in the transport of secologanin into the vacuole and highlights the importance of the spatial organisation of the pathway in preventing secologanin derivatisation. Secondly silencing the expression of a tonoplast localised nitrate/peptide (NPF) transporter, CrNPF2.9, resulted in the 20-fold accumulation of strictosidine, suggesting this transporter is the exporter of strictosidine from the vacuole. Furthermore, VIGS also allowed the identification of a reticuline oxidase like protein, CrRO, which resulted in the accumulation of two new MIAs in leaf tissue upon silencing. This thesis highlights a reverse genetics strategy for gene identification in metabolic pathways and is the first time the MATE and NPF transporters, and the reticuline oxidase like enzymes, have been shown to be involved in MIA metabolism in C. roseus.
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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.

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Thesis (PhD (Plant Biotechnology))--University of Stellenbosch, 2010.
ENGLISH 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.
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Starkus, Laura. "Virus-induced gene silencing of putative Diuraphis noxia (Kurdjumov) resistance genes in wheat". Thesis, Manhattan, Kan. : Kansas State University, 2010. http://hdl.handle.net/2097/4193.

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Jaggard, Daniel Andrew William. "The structure and function of RPW8.1 and RPW8.2, powdery mildew disease resistance proteins from Arabidopsis thaliana (L.) Heyhn". Thesis, University of East Anglia, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251898.

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Kawai, Takashi. "Virus-induced gene silencing in Prunus fruit and nut tree species by Apple latent spherical virus vector". Kyoto University, 2017. http://hdl.handle.net/2433/217995.

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Kyoto University (京都大学)
0048
新制・論文博士
博士(農学)
乙第13073号
論農博第2843号
新制||農||1046(附属図書館)
学位論文||H29||N5029(農学部図書室)
33224
京都大学大学院農学研究科農学専攻
(主査)教授 北島 宣, 教授 土井 元章, 教授 田尾 龍太郎
学位規則第4条第2項該当
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Peart, Jack Robert. "The use of virus-induced gene silencing to identify genes required for N-mediated resistance against tobacco mosaic virus". Thesis, University of East Anglia, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247101.

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Demircan, Turan. "Application Of Virus Induced Gene Silencing Of Brachypodium Distachyon, A Model Organism For Crops". Master's thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/12610649/index.pdf.

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Grass family is most important family in plant kingdom due to intensive usage of crops in agriculture. To date, molecular biology researches on grass family have had limitations because of inappropriate characteristics of barley and wheat to conduct experiments on them. Brachypodium distachyon that belongs to grass family has recently emerged as a model organism for crops. It shares common characteristics for a model plant due to its small genome, small physical plant size, a short lifecycle, and less demanding growth requirements
as other model organisms
Arabidopsis thaliana, Oryza sativa, and Zea mays (Draper et al. 2001). Especially after appreciating, the genetic distance of O. sativa to grasses (Garvin et al. 2008), it become a key organism to understand complicated genomic organization of agriculturally valuable grasses. Virus-induced gene silencing (VIGS) is one of the revolutionary methods allowing a rapid and effective loss of a gene function through RNA interference (Holzberg et al. 2002
Liu et al. 2008). Barley stripe mosaic virus (BSMV) is still the most effective vector used in monocot gene silencing. It has a tripartite RNA genome having a wide range of infection ability for monocots including barley, oat, wheat, and maize as host (Holzberg et al. 2002
Scofield 2005). In this thesis, Phytoene desaturase (PDS) gene of Brachypodium distachyon was silenced via BSMV mediated VIGS. Additionally, with Green fluorescence protein (GFP) bearing BSMV transcripts, GFP expression was observed under fluorescent microscope. To our knowledge, this is the first report demonstrating a VIGS via BSMV in Brachypodium distachyon. The success of virus induced gene silencing method in Brachypodium distachyon, will be a new convenient tool for evaluating functions of crop genes in this model organism.
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Lu, Rui. "High throughput virus induced gene silencing for the analysis of disease resistance in plants". Thesis, University of East Anglia, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398556.

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Lee, Jack Alexander. "The use of virus induced gene silencing to investigate Septoria leaf blotch in wheat". Thesis, Durham University, 2016. http://etheses.dur.ac.uk/11465/.

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Septoria leaf blotch, caused by the fungal pathogen Zymoseptoria tritici, is one of the most damaging diseases of wheat (Triticum aestivum), a crop plant of significant worldwide importance. Using the system of Virus-Induced Gene Silencing, to create transient knockdowns of target genes, a novel wheat gene, TaR1, was identified as playing a key role in the host response to this pathogen. Silencing this gene leads to the earlier onset of disease symptoms, but reduced reproduction of the causal pathogen. Sequence analysis, confocal microscopy and protein-protein interaction assays were used to determine that the protein TaR1 localises the nucleus, where its function involves the binding of histones. Precisely, TaR1 is able to bind the Histone 3 subunit, specifically methylated on Lysine 4. Through this action, the host defence response is delayed, and successful pathogen colonisation is promoted. It is hypothesised that this is an example of the pathogen ‘hi-jacking’ TaR1 from its original function, in order to complete its lifecycle.
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Bozhanaj, Kreshnik. "The Effect Of Virus Induced Gene Silencing Of Fas Associated Factor1 In Blumeria Graminis Infected Barley". Master's thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/12611139/index.pdf.

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Cereal loss due to fungal pathogens is an ongoing setback in agriculture. Elucidating plant&rsquo
s resistance and susceptibility mechanisms against these cereal killers, promises progress in agriculture. In the way of understanding barley resistance against fungus Blumeria Graminis we silenced FAS-Associated Factor 1 (FAF1) gene in its mRNA level with Virus Induced Gene Silencing (VIGS) technique. Previous research in our lab had shown an augmentation in mRNA levels of FAF1 gene in fungus infected wheat, suggesting a role of this gene in the resistance mechanism. We hypothesized that the apoptotic role of FAF1 protein in metazoan is conserved in plants by including FAF1 as a factor in hypersensitive response. Barley lines Pallas01 and Pallas03 which are respectively resistant and susceptible against fungus Blumeria graminis hordei 103 (Bgh103) were used for fungal inoculations after FAF1 silencing, to test if the hypersensitive response against fungus Bgh103 was prevented. In this aspect the formation of death lesions on the Pallas01 leaf due to fungal resistance was not prevented demonstrating that FAF1 silencing with VIGS in the resistant Pallas01 line of barley is not sufficient to stop apoptosis. On the other hand the FAF1-silenced barley susceptible line Pallas03 became more sensitive to fungal stress based on conidia (body part of the fungus) counting after trypan blue staining of the infected leaves. In the C-terminus of FAF1 an ubiquitin like domain-X (UBX) is found, which is the cause of stress sensitivity based on the reported data obtained about this domain&rsquo
s loss of function in other proteins. These results suggest that FAF1 is a catalyst in the hypersensitive response and its loss of function makes barley more susceptible to fungal stress. On the other hand a short mRNA homology was found among FAF1 and many pathogen disease related proteins making this homology a possible target site for VIGS of FAF1 generated siRNAs, which might cause some other protein to be responsible for the barley susceptibility against the fungus.
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Libros sobre el tema "Virus induced gene silencing"

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Becker, Annette, ed. Virus-Induced Gene Silencing. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-278-0.

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Courdavault, Vincent y Sébastien Besseau, eds. Virus-Induced Gene Silencing in Plants. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0751-0.

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Hayes, Ian MacDonald. Virus-induced changes in host gene expression in infected cowpeas. Norwich: University of East Anglia, 1990.

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Plows, David John. Natural and induced variation in the fusion glycoprotein gene of human respiratory syncytial virus subgroup A. [s.l.]: typescript, 1994.

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Antiviral RNAi: Concepts, methods, and applications. New York: Humana Press/Springer Science, 2011.

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Munroe, Donald Gordon. Expression and mutation of the p53 gene in friend virus-induced murine erythroleukemia. 1991.

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Capítulos de libros sobre el tema "Virus induced gene silencing"

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Kachroo, Aardra y Said Ghabrial. "Virus-Induced Gene Silencing in Soybean". En Methods in Molecular Biology, 287–97. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-882-5_19.

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Palmer, Lira y Sarah E. O’Connor. "Virus-Induced Gene Silencing in Nepeta". En Methods in Molecular Biology, 111–21. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0751-0_9.

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Jia, Haifeng y Yuanyue Shen. "Virus-Induced Gene Silencing in Strawberry Fruit". En Methods in Molecular Biology, 211–18. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-278-0_16.

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Todd, Andrea T., Enwu Liu y Jonathan E. Page. "cDNA Libraries for Virus-Induced Gene Silencing". En Plant Epigenetics, 221–36. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-646-7_16.

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Jiang, Cai-Zhong, Jen-Chih Chen y Michael Reid. "Virus-Induced Gene Silencing in Ornamental Plants". En Methods in Molecular Biology, 81–96. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-123-9_6.

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Yan, Huijun, Zhao Zhang, Jean-Louis Magnard, Benoît Boachon, Sylvie Baudino y Kaixue Tang. "Virus-Induced Gene Silencing in Rose Flowers". En Methods in Molecular Biology, 223–32. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0751-0_16.

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Bachan, Shawn y Savithramma P. Dinesh-Kumar. "Tobacco Rattle Virus (TRV)-Based Virus-Induced Gene Silencing". En Methods in Molecular Biology, 83–92. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-882-5_6.

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Ricci, Angela, Silvia Sabbadini, Laura Miozzi, Bruno Mezzetti y Emanuela Noris. "Host-induced gene silencing and spray-induced gene silencing for crop protection against viruses." En RNAi for plant improvement and protection, 72–85. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0072.

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Abstract Since the beginning of agriculture, plant virus diseases have been a strong challenge for farming. Following its discovery at the very beginning of the 1990s, the RNA interference (RNAi) mechanism has been widely studied and exploited as an integrative tool to obtain resistance to viruses in several plant species, with high target-sequence specificity. In this chapter, we describe and review the major aspects of host-induced gene silencing (HIGS), as one of the possible plant defence methods, using genetic engineering techniques. In particular, we focus our attention on the use of RNAi-based gene constructs to introduce stable resistance in host plants against viral diseases, by triggering post-transcriptional gene silencing (PTGS). Recently, spray-induced gene silencing (SIGS), consisting of the topical application of small RNA molecules to plants, has been explored as an alternative tool to the stable integration of RNAi-based gene constructs in plants. SIGS has great and innovative potential for crop defence against different plant pathogens and pests and is expected to raise less public and political concern, as it does not alter the genetic structure of the plant.
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Ricci, Angela, Silvia Sabbadini, Laura Miozzi, Bruno Mezzetti y Emanuela Noris. "Host-induced gene silencing and spray-induced gene silencing for crop protection against viruses." En RNAi for plant improvement and protection, 72–85. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0008.

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Abstract Since the beginning of agriculture, plant virus diseases have been a strong challenge for farming. Following its discovery at the very beginning of the 1990s, the RNA interference (RNAi) mechanism has been widely studied and exploited as an integrative tool to obtain resistance to viruses in several plant species, with high target-sequence specificity. In this chapter, we describe and review the major aspects of host-induced gene silencing (HIGS), as one of the possible plant defence methods, using genetic engineering techniques. In particular, we focus our attention on the use of RNAi-based gene constructs to introduce stable resistance in host plants against viral diseases, by triggering post-transcriptional gene silencing (PTGS). Recently, spray-induced gene silencing (SIGS), consisting of the topical application of small RNA molecules to plants, has been explored as an alternative tool to the stable integration of RNAi-based gene constructs in plants. SIGS has great and innovative potential for crop defence against different plant pathogens and pests and is expected to raise less public and political concern, as it does not alter the genetic structure of the plant.
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Serwatowska, Joanna, Ole Søgaard Lund y Ida Elisabeth Johansen. "Transient Posttranscriptional Gene Silencing in Medicago truncatula: Virus-Induced Gene Silencing (VIGS)". En Methods in Molecular Biology, 115–22. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8633-0_8.

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Actas de conferencias sobre el tema "Virus induced gene silencing"

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Fenwick, Ann, Rebecca L. Larson, Patrick A. Reeves, Christopher M. Richards y Lee Panella. "Virus induced gene silencing of a gene repressing flowering in sugar beet". En American Society of Sugar Beet Technologist. ASSBT, 2007. http://dx.doi.org/10.5274/assbt.2007.30.

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Wintermantel, William M. y Laura L. Hladky. "Resistance to curly top viruses through virus induced gene silencing." En American Society of Sugarbeet Technologist. ASSBT, 2009. http://dx.doi.org/10.5274/assbt.2009.35.

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Wintermantel, William M., Amy G. Anchieta y Particia A. Nicely. "Development of novel sources of resistance to Beet curly top virus through virus-induced gene silencing". En American Society of Sugar Beet Technologist. ASSBT, 2007. http://dx.doi.org/10.5274/assbt.2007.35.

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Suprunova, T. P., N. V. Markin, A. N. Ignatov, A. G. Solovyov, N. O. Kalinina y M. E. Talyansky. "Use of dsRNA-based antiviral compounds to protect potato plants". En Растениеводство и луговодство. Тимирязевская сельскохозяйственная академия, 2020. http://dx.doi.org/10.26897/978-5-9675-1762-4-2020-132.

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One of the most important food crops in the world, the potato (Solanum tuberosum L.) is infected with many viruses, of which the y virus (Potato virus Y, PVY) is the most important economically, causing significant crop losses. Several alternative methods of dsRNA delivery have been tested, with the most promising being spray - induced gene silencing (SIGS). The results showed a high effect of preventive use of dsRNA. Treatment with the initial working concentration of dsRNA protected 100% and 65% of plants from virus propagation for 14 and 21 days, respectively, and 65% of plants were protected by the minimum tested concentration (10 ng/MCL) for 14 days. Therapeutic use of dsRNA 3 days after inoculation did not significantly affect the dynamics of virus accumulation in the plant. Thus, in the course of the experiment, a high biological antiviral effectiveness of dsRNA was demonstrated in the preventive treatment of potato plants against the background of artificial infection of plants with the PVY virus.
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Schulman, ES, SC Pugliese, S. Ansaloni, P. Mannam, H. Nishi, M. Bouchard y SA Saunders. "RNA Interference-Induced Gene Silencing of Histidine Decarboxylase Produces Human Mast Cells Deficient in Histamine." En American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a3708.

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Allen, Brittany N., Michal Masternak y Mark Muller. "Abstract A43: DNA repair by non-homologous end joining induced gene silencing via DNA hypermethylation". En Abstracts: AACR Special Conference: Chromatin and Epigenetics in Cancer; September 24-27, 2015; Atlanta, GA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.chromepi15-a43.

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Huang, Tao, Guohui Ding, Yixue Li, Lei Liu, Eugene Tan, Hongyue Dai, Qi Liu, Zhidong Tu y Lu Xie. "Dysfunctional gene/protein networks in hepatitis C virus-induced hepatocellular cirrhosis and carcinoma". En the First ACM International Conference. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/1854776.1854873.

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Schuurhof, Annemieke, Louis Bont, Jeroen Pennings, Hennie Hodemaekers, Piet Wester, Annemarie Buisman, Lia D. Rond et al. "Gene Expression Differences Between Vaccine-Induced And Natural Immunity After Respiratory Syncytial Virus Infection". En American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a1806.

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Yu, Lunyin y Charles A. Hales. "Silencing Of NHE1 Gene Decreases Hypoxia-induced Proliferation And Cell Cycle Progression Of Human Pulmonary Artery Smooth Muscle Cells". En American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3950.

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Hussin, Ainulkhir, Norefrina Shafinaz Md Nor y Nazlina Ibrahim. "Amino acid substitutions in the thymidine kinase gene of induced acyclovir-resistant herpes simplex virus type 1". En THE 2013 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2013 Postgraduate Colloquium. AIP Publishing LLC, 2013. http://dx.doi.org/10.1063/1.4858664.

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Informes sobre el tema "Virus induced gene silencing"

1

Turker, Mitchell. Environmentally Induced Gene Silencing in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, julio de 2008. http://dx.doi.org/10.21236/ada493645.

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Turker, Mitchell. Environmentally Induced Gene Silencing in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, julio de 2007. http://dx.doi.org/10.21236/ada473698.

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