Literatura académica sobre el tema "Mutation"
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Artículos de revistas sobre el tema "Mutation"
GARCÍA-DORADO, A., C. LÓPEZ-FANJUL y A. CABALLERO. "Properties of spontaneous mutations affecting quantitative traits". Genetical Research 74, n.º 3 (diciembre de 1999): 341–50. http://dx.doi.org/10.1017/s0016672399004206.
Texto completoEllis, Nathan A. "Mutation-causing mutations". Nature 381, n.º 6578 (mayo de 1996): 110–11. http://dx.doi.org/10.1038/381110a0.
Texto completoMatsutani, Taro, Yuki Ueno, Tsukasa Fukunaga y Michiaki Hamada. "Discovering novel mutation signatures by latent Dirichlet allocation with variational Bayes inference". Bioinformatics 35, n.º 22 (16 de abril de 2019): 4543–52. http://dx.doi.org/10.1093/bioinformatics/btz266.
Texto completoLee, Joon-Hyop, Jiyoung Ahn, Won Seo Park, Eun Kyung Choe, Eunyoung Kim, Rumi Shin, Seung Chul Heo et al. "Colorectal Cancer Prognosis is Not Associated with BRAF and KRAS Mutations-A STROBE Compliant Study". Journal of Clinical Medicine 8, n.º 1 (17 de enero de 2019): 111. http://dx.doi.org/10.3390/jcm8010111.
Texto completoBustamante, A. V., A. M. Sanso, D. O. Segura, A. E. Parma y P. M. A. Lucchesi. "Dynamic of Mutational Events in Variable Number Tandem Repeats ofEscherichia coliO157:H7". BioMed Research International 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/390354.
Texto completoPawlik, Timothy M., Darrell R. Borger, Yuhree Kim, David Cosgrove, Sorin Alexandrescu, Ryan Thomas Groeschl, Vikram Deshpande et al. "Genomic profiling of intrahepatic cholangiocarcinoma: Refining prognostic determinants and identifying therapeutic targets." Journal of Clinical Oncology 32, n.º 3_suppl (20 de enero de 2014): 210. http://dx.doi.org/10.1200/jco.2014.32.3_suppl.210.
Texto completoRobinson, Philip S., Tim H. H. Coorens, Claire Palles, Emily Mitchell, Federico Abascal, Sigurgeir Olafsson, Bernard C. H. Lee et al. "Increased somatic mutation burdens in normal human cells due to defective DNA polymerases". Nature Genetics 53, n.º 10 (30 de septiembre de 2021): 1434–42. http://dx.doi.org/10.1038/s41588-021-00930-y.
Texto completoTrindade, Sandra, Lilia Perfeito y Isabel Gordo. "Rate and effects of spontaneous mutations that affect fitness in mutator Escherichia coli". Philosophical Transactions of the Royal Society B: Biological Sciences 365, n.º 1544 (27 de abril de 2010): 1177–86. http://dx.doi.org/10.1098/rstb.2009.0287.
Texto completoWatters, M. K. y D. R. Stadler. "Spontaneous mutation during the sexual cycle of Neurospora crassa." Genetics 139, n.º 1 (1 de enero de 1995): 137–45. http://dx.doi.org/10.1093/genetics/139.1.137.
Texto completoLee, Seung-Shin, Jae-Sook Ahn, Taehyung Kim, Hyeoung Joon Kim, Yeo-Kyeoung Kim, Seo-Yeon Ahn, Sung-Hoon Jung et al. "RUNX1 Mutation in Cytogenetically Normal Acute Myeloid Leukemia : Clinical Implications, Co-Mutation Analysis". Blood 128, n.º 22 (2 de diciembre de 2016): 5253. http://dx.doi.org/10.1182/blood.v128.22.5253.5253.
Texto completoTesis sobre el tema "Mutation"
Komp, Lindgren Patricia. "Mutations and Mutation Rate in the Development of Fluoroquinolone Resistance". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8275.
Texto completoIbrahim, Daniel Murad. "ChIP-seq reveals mutation-specific pathomechanisms of HOXD13 missense mutations". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2015. http://dx.doi.org/10.18452/17102.
Texto completoMutations in transcription factors (TF) do not only affect the function of the TF, but also the expression of its target genes and are frequently underlying congenital malformations. More than 20 distinct pathogenic mutations in HOXD13, a TF controlling limb development, have been associated with a broad range of limb malformations. However, a molecular basis underlying the variability of HOXD13-associated phenotypes remains elusive. To date, the experimental methods used to functionally characters TF mutations have allowed only limited insights into the underlying molecular pathomechanisms. The recently developed ChIP-seq technology has proven to be a powerful method to profile the binding characteristics of TFs; however a number of technical hurdles hinder its application for functional characterization of mutant TFs. This work describes the establishment of a ChIP-seq approach to investigate a wide spectrum of TFs and TF mutations. The approach was applied to characterize two previously unknown missense mutations in HOXD13, p.Q317K and p.R298Q, which both alter the DNA-binding domain of HOXD13 but cause very different disease phenotypes. The results show that the HOXD13Q317K mutant has an altered sequence specificity that resembles the recognition sequence of another TF, PITX1. Further, the genome-wide binding pattern of HOXD13Q317K shifts towards a more PITX1-like binding pattern. Even further analysis and viral overexpression in chicken limb buds confirm that the mutation partially converts HOXD13Q317K into a TF with PITX1-like properties. The HOXD13R298Q has a largely unchanged sequence specificity, but an altered composition of genomic binding sites. This, in combination with the human phenotype, indicates that the mutant might act in a dominant-negative manner. Collectively, this work shows through generation of direct experimental evidence, that clearly distinct molecular mechanisms underlie the pathogenicity of HOXD13Q317K and HOXD13R298Q mutations.
Hagman, Hans. "Mutation Testing : A comparison of mutation selection methods". Thesis, Högskolan i Skövde, Institutionen för kommunikation och information, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-6569.
Texto completoKrasovec, Marc. "Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote". Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066371/document.
Texto completoMutations are the main source of diversity on which selection acts to allow species to adapt. Studies of the effect of mutations on survival and estimation of spontaneous mutation rates are essential to better understand evolution. Using mutation accumulation experimental approach, we investigated the issues of mutation effects and mutation rate in five models of green algae (Ostreococcus tauri, O. mediterraneus, Bathycoccus Prasinos, Micromonas pusilla, and Picochlorum RCC4223). It highlighted a decline in fitness over time because of deleterious mutations, and a significant genotype-environment interaction on the fitness effect of mutations. The mutation rate varies at inter-specific and intra-genomic scales, with two main results: a raise of the mutation rate in non-coding regions in accordance with trancriptional-coupled repair, and an increase of the mutation rate with an increase of the genome size in eukaryotes and the GC content deviation from the equilibrium. Also, a new Picochlorum genome is provided to investigate the role of horizontal gene transfer in the Chlorophyta group
Krasovec, Marc. "Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote". Electronic Thesis or Diss., Paris 6, 2016. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2016PA066371.pdf.
Texto completoMutations are the main source of diversity on which selection acts to allow species to adapt. Studies of the effect of mutations on survival and estimation of spontaneous mutation rates are essential to better understand evolution. Using mutation accumulation experimental approach, we investigated the issues of mutation effects and mutation rate in five models of green algae (Ostreococcus tauri, O. mediterraneus, Bathycoccus Prasinos, Micromonas pusilla, and Picochlorum RCC4223). It highlighted a decline in fitness over time because of deleterious mutations, and a significant genotype-environment interaction on the fitness effect of mutations. The mutation rate varies at inter-specific and intra-genomic scales, with two main results: a raise of the mutation rate in non-coding regions in accordance with trancriptional-coupled repair, and an increase of the mutation rate with an increase of the genome size in eukaryotes and the GC content deviation from the equilibrium. Also, a new Picochlorum genome is provided to investigate the role of horizontal gene transfer in the Chlorophyta group
Lee, Angela Waishan. "Hair-loss mutation (dep) caused by a mutation in palmitoyl transferase Zdhhc21". Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/29217.
Texto completoDrechsel, Dieter. "Evolution and Mutation Physics". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-69962.
Texto completoDuncan, Ishbel M. M. "Strong mutation testing strategies". Thesis, Durham University, 1993. http://etheses.dur.ac.uk/5771/.
Texto completoWilliamson, David. "Haemoglobin mutation and instability". Thesis, Open University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315297.
Texto completoJia, Y. "Higher order mutation testing". Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1401264/.
Texto completoLibros sobre el tema "Mutation"
Robin, Cook. Mutation. New York: Putnam's, 1989.
Buscar texto completoApplegate, Katherine. Mutation. London: Scholastic, 2002.
Buscar texto completoRobin, Cook. Mutation. London: Guild Publishing, 1989.
Buscar texto completoRobin, Cook. Mutation. London: Pan Books, 1989.
Buscar texto completoRobin, Cook. Mutation. New York: Berkley Books, 1990.
Buscar texto completoRobin, Cook. Mutation. New York: Putnam, 1989.
Buscar texto completo1962-, Cordy Michael, ed. Mutation: Roman. München: Diana-Verl., 2000.
Buscar texto completoLogie, Colin. Point mutation. Rijeka: InTech, 2012.
Buscar texto completoApplegate, Katherine. The mutation. Milwaukee, WI: Gareth Stevens Pub., 2000.
Buscar texto completoApplegate, Katherine. The mutation. London: Hippo, 2001.
Buscar texto completoCapítulos de libros sobre el tema "Mutation"
Konzak, C. F. "Mutations and Mutation Breeding". En Agronomy Monographs, 428–43. Madison, WI, USA: American Society of Agronomy, Crop Science Society of America, Soil Science Society of America, 2015. http://dx.doi.org/10.2134/agronmonogr13.2ed.c24.
Texto completoLee, L. Slade, Bradley J. Till, Helen Hill, Owen A. Huynh y Joanna Jankowicz-Cieslak. "Mutation and Mutation Screening". En Methods in Molecular Biology, 77–95. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-715-0_8.
Texto completoSmith, C. A. y E. J. Wood. "Mutation". En Molecular Biology and Biotechnology, 156–84. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3866-0_8.
Texto completoVogel, Friedrich y Arno G. Motulsky. "Mutation". En Human Genetics, 334–432. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8_6.
Texto completoBrennan, Michael. "Mutation". En Encyclopedia of Personality and Individual Differences, 3057–58. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-24612-3_1551.
Texto completoDoolittle, Donald P. "Mutation". En Advanced Series in Agricultural Sciences, 74–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71734-5_15.
Texto completoShekhar, Shashi y Hui Xiong. "Mutation". En Encyclopedia of GIS, 765. Boston, MA: Springer US, 2008. http://dx.doi.org/10.1007/978-0-387-35973-1_857.
Texto completoSmith-Keary, Peter. "Mutation". En Molecular Genetics, 182–203. London: Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-11732-1_11.
Texto completoLázaro, Ester. "Mutation". En Encyclopedia of Astrobiology, 1102–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1037.
Texto completoForsdyke, Donald R. "Mutation". En Evolutionary Bioinformatics, 131–51. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-7771-7_7.
Texto completoActas de conferencias sobre el tema "Mutation"
Souza, Beatriz y Rohit Gheyi. "A Lightweight Technique to Identify Equivalent Mutants". En XI Congresso Brasileiro de Software: Teoria e Prática. Sociedade Brasileira de Computação - SBC, 2020. http://dx.doi.org/10.5753/cbsoft_estendido.2020.14630.
Texto completoCambraia, Amanda, Mario Campos Junior, Fernanda Gubert, Juliana Ferreira Vasques, Marli Pernes da Silva Loureiro, Claudio Heitor Gress, José Mauro Bráz de Lima, Rosalia Mendez Otero y Verônica Marques Zembrzuski. "A novel mutation in the RRM2 domain of TDP-43 in a Brazilian sporadic ALS patient." En XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.486.
Texto completoOffutt, Jeff, Paul Ammann y Lisa (Ling) Liu. "Mutation Testing implements Grammar-Based Testing". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.11.
Texto completoSen, Sagar y Benoit Baudry. "Mutation-based Model Synthesis in Model Driven Engineering". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.12.
Texto completoGallardo, Guillermo, John May y Julio C. Gallardo. "Assessment of Data Diversity Methods for Software Fault Tolerance Based on Mutation Analysis". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.1.
Texto completoBradbury, Jeremy S., James R. Cordy y Juergen Dingel. "Mutation Operators for Concurrent Java (J2SE 5.0)". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.10.
Texto completoTuya, Javier, Ma Jose Suarez-Cabal y Claudio de la Riva. "SQLMutation: A tool to generate mutants of SQL database queries". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.13.
Texto completoCrouzet, Yves, Helene Waeselynck, Benjamin Lussier y David Powell. "The SESAME Experience: from Assembly Languages to Declarative Models". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.14.
Texto completoBelli, Fevzi, Christof J. Budnik y W. Eric Wong. "Basic Operations for Generating Behavioral Mutants". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.2.
Texto completoAnbalagan, Prasanth y Tao Xie. "Efficient Mutant Generation for Mutation Testing of Pointcuts in Aspect-Oriented Programs". En Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.3.
Texto completoInformes sobre el tema "Mutation"
Silverstein, Eva. Dimensional Mutation and Spacelike Singularities. Office of Scientific and Technical Information (OSTI), octubre de 2005. http://dx.doi.org/10.2172/878029.
Texto completoNeel, J. V. Studies of human mutation rates. Office of Scientific and Technical Information (OSTI), julio de 1991. http://dx.doi.org/10.2172/5025881.
Texto completoNeel, J. V. Studies of human mutation rates. Office of Scientific and Technical Information (OSTI), enero de 1990. http://dx.doi.org/10.2172/6368357.
Texto completoNeel, J. V. The study of human mutation rates. Office of Scientific and Technical Information (OSTI), enero de 1992. http://dx.doi.org/10.2172/7175958.
Texto completoHarris, Reuben S. Enzyme-Catalyzed Mutation in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2014. http://dx.doi.org/10.21236/ada613711.
Texto completoAndrews, Paul W., Raymond R. Tice y Diane Satterfield. Salmonella Typhimurium Microsome Reverse Mutation Assay. Fort Belvoir, VA: Defense Technical Information Center, marzo de 1996. http://dx.doi.org/10.21236/ada589278.
Texto completoPonder, Rebecca y Susan Rosenberg. Mechanism of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, julio de 2001. http://dx.doi.org/10.21236/ada396622.
Texto completoPetrosino, Joseph F. Mechanisms of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, mayo de 2002. http://dx.doi.org/10.21236/ada406067.
Texto completoPonder, Rebecca G. y Susan Rosenberg. Mechanism of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, julio de 2002. http://dx.doi.org/10.21236/ada408728.
Texto completoPetrosino, Joseph F. y Susan Rosenberg. Mechanisms of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, mayo de 2003. http://dx.doi.org/10.21236/ada416708.
Texto completo