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Artykuły w czasopismach na temat "Mutation"
GARCÍA-DORADO, A., C. LÓPEZ-FANJUL i A. CABALLERO. "Properties of spontaneous mutations affecting quantitative traits". Genetical Research 74, nr 3 (grudzień 1999): 341–50. http://dx.doi.org/10.1017/s0016672399004206.
Pełny tekst źródłaEllis, Nathan A. "Mutation-causing mutations". Nature 381, nr 6578 (maj 1996): 110–11. http://dx.doi.org/10.1038/381110a0.
Pełny tekst źródłaMatsutani, Taro, Yuki Ueno, Tsukasa Fukunaga i Michiaki Hamada. "Discovering novel mutation signatures by latent Dirichlet allocation with variational Bayes inference". Bioinformatics 35, nr 22 (16.04.2019): 4543–52. http://dx.doi.org/10.1093/bioinformatics/btz266.
Pełny tekst źródłaLee, Joon-Hyop, Jiyoung Ahn, Won Seo Park, Eun Kyung Choe, Eunyoung Kim, Rumi Shin, Seung Chul Heo i in. "Colorectal Cancer Prognosis is Not Associated with BRAF and KRAS Mutations-A STROBE Compliant Study". Journal of Clinical Medicine 8, nr 1 (17.01.2019): 111. http://dx.doi.org/10.3390/jcm8010111.
Pełny tekst źródłaBustamante, A. V., A. M. Sanso, D. O. Segura, A. E. Parma i 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.
Pełny tekst źródłaPawlik, Timothy M., Darrell R. Borger, Yuhree Kim, David Cosgrove, Sorin Alexandrescu, Ryan Thomas Groeschl, Vikram Deshpande i in. "Genomic profiling of intrahepatic cholangiocarcinoma: Refining prognostic determinants and identifying therapeutic targets." Journal of Clinical Oncology 32, nr 3_suppl (20.01.2014): 210. http://dx.doi.org/10.1200/jco.2014.32.3_suppl.210.
Pełny tekst źródłaRobinson, Philip S., Tim H. H. Coorens, Claire Palles, Emily Mitchell, Federico Abascal, Sigurgeir Olafsson, Bernard C. H. Lee i in. "Increased somatic mutation burdens in normal human cells due to defective DNA polymerases". Nature Genetics 53, nr 10 (30.09.2021): 1434–42. http://dx.doi.org/10.1038/s41588-021-00930-y.
Pełny tekst źródłaTrindade, Sandra, Lilia Perfeito i 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, nr 1544 (27.04.2010): 1177–86. http://dx.doi.org/10.1098/rstb.2009.0287.
Pełny tekst źródłaWatters, M. K., i D. R. Stadler. "Spontaneous mutation during the sexual cycle of Neurospora crassa." Genetics 139, nr 1 (1.01.1995): 137–45. http://dx.doi.org/10.1093/genetics/139.1.137.
Pełny tekst źródłaLee, Seung-Shin, Jae-Sook Ahn, Taehyung Kim, Hyeoung Joon Kim, Yeo-Kyeoung Kim, Seo-Yeon Ahn, Sung-Hoon Jung i in. "RUNX1 Mutation in Cytogenetically Normal Acute Myeloid Leukemia : Clinical Implications, Co-Mutation Analysis". Blood 128, nr 22 (2.12.2016): 5253. http://dx.doi.org/10.1182/blood.v128.22.5253.5253.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaIbrahim, 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.
Pełny tekst źródłaMutations 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.
Pełny tekst źródłaKrasovec, 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.
Pełny tekst źródłaMutations 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.
Pełny tekst źródłaMutations 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.
Pełny tekst źródłaDrechsel, Dieter. "Evolution and Mutation Physics". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-69962.
Pełny tekst źródłaDuncan, Ishbel M. M. "Strong mutation testing strategies". Thesis, Durham University, 1993. http://etheses.dur.ac.uk/5771/.
Pełny tekst źródłaWilliamson, David. "Haemoglobin mutation and instability". Thesis, Open University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315297.
Pełny tekst źródłaJia, Y. "Higher order mutation testing". Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1401264/.
Pełny tekst źródłaKsiążki na temat "Mutation"
Robin, Cook. Mutation. New York: Putnam's, 1989.
Znajdź pełny tekst źródłaApplegate, Katherine. Mutation. London: Scholastic, 2002.
Znajdź pełny tekst źródłaRobin, Cook. Mutation. London: Guild Publishing, 1989.
Znajdź pełny tekst źródłaRobin, Cook. Mutation. London: Pan Books, 1989.
Znajdź pełny tekst źródłaRobin, Cook. Mutation. New York: Berkley Books, 1990.
Znajdź pełny tekst źródłaRobin, Cook. Mutation. New York: Putnam, 1989.
Znajdź pełny tekst źródła1962-, Cordy Michael, red. Mutation: Roman. München: Diana-Verl., 2000.
Znajdź pełny tekst źródłaLogie, Colin. Point mutation. Rijeka: InTech, 2012.
Znajdź pełny tekst źródłaApplegate, Katherine. The mutation. Milwaukee, WI: Gareth Stevens Pub., 2000.
Znajdź pełny tekst źródłaApplegate, Katherine. The mutation. London: Hippo, 2001.
Znajdź pełny tekst źródłaCzęści książek na temat "Mutation"
Konzak, C. F. "Mutations and Mutation Breeding". W 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.
Pełny tekst źródłaLee, L. Slade, Bradley J. Till, Helen Hill, Owen A. Huynh i Joanna Jankowicz-Cieslak. "Mutation and Mutation Screening". W Methods in Molecular Biology, 77–95. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-715-0_8.
Pełny tekst źródłaSmith, C. A., i E. J. Wood. "Mutation". W Molecular Biology and Biotechnology, 156–84. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3866-0_8.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. "Mutation". W Human Genetics, 334–432. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8_6.
Pełny tekst źródłaBrennan, Michael. "Mutation". W 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.
Pełny tekst źródłaDoolittle, Donald P. "Mutation". W 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.
Pełny tekst źródłaShekhar, Shashi, i Hui Xiong. "Mutation". W Encyclopedia of GIS, 765. Boston, MA: Springer US, 2008. http://dx.doi.org/10.1007/978-0-387-35973-1_857.
Pełny tekst źródłaSmith-Keary, Peter. "Mutation". W Molecular Genetics, 182–203. London: Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-11732-1_11.
Pełny tekst źródłaLázaro, Ester. "Mutation". W Encyclopedia of Astrobiology, 1102–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1037.
Pełny tekst źródłaForsdyke, Donald R. "Mutation". W Evolutionary Bioinformatics, 131–51. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-7771-7_7.
Pełny tekst źródłaStreszczenia konferencji na temat "Mutation"
Souza, Beatriz, i Rohit Gheyi. "A Lightweight Technique to Identify Equivalent Mutants". W XI Congresso Brasileiro de Software: Teoria e Prática. Sociedade Brasileira de Computação - SBC, 2020. http://dx.doi.org/10.5753/cbsoft_estendido.2020.14630.
Pełny tekst źródłaCambraia, 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 i Verônica Marques Zembrzuski. "A novel mutation in the RRM2 domain of TDP-43 in a Brazilian sporadic ALS patient." W XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.486.
Pełny tekst źródłaOffutt, Jeff, Paul Ammann i Lisa (Ling) Liu. "Mutation Testing implements Grammar-Based Testing". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.11.
Pełny tekst źródłaSen, Sagar, i Benoit Baudry. "Mutation-based Model Synthesis in Model Driven Engineering". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.12.
Pełny tekst źródłaGallardo, Guillermo, John May i Julio C. Gallardo. "Assessment of Data Diversity Methods for Software Fault Tolerance Based on Mutation Analysis". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.1.
Pełny tekst źródłaBradbury, Jeremy S., James R. Cordy i Juergen Dingel. "Mutation Operators for Concurrent Java (J2SE 5.0)". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.10.
Pełny tekst źródłaTuya, Javier, Ma Jose Suarez-Cabal i Claudio de la Riva. "SQLMutation: A tool to generate mutants of SQL database queries". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.13.
Pełny tekst źródłaCrouzet, Yves, Helene Waeselynck, Benjamin Lussier i David Powell. "The SESAME Experience: from Assembly Languages to Declarative Models". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.14.
Pełny tekst źródłaBelli, Fevzi, Christof J. Budnik i W. Eric Wong. "Basic Operations for Generating Behavioral Mutants". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.2.
Pełny tekst źródłaAnbalagan, Prasanth, i Tao Xie. "Efficient Mutant Generation for Mutation Testing of Pointcuts in Aspect-Oriented Programs". W Second Workshop on Mutation Analysis (Mutation 2006 - ISSRE Workshops 2006). IEEE, 2006. http://dx.doi.org/10.1109/mutation.2006.3.
Pełny tekst źródłaRaporty organizacyjne na temat "Mutation"
Silverstein, Eva. Dimensional Mutation and Spacelike Singularities. Office of Scientific and Technical Information (OSTI), październik 2005. http://dx.doi.org/10.2172/878029.
Pełny tekst źródłaNeel, J. V. Studies of human mutation rates. Office of Scientific and Technical Information (OSTI), lipiec 1991. http://dx.doi.org/10.2172/5025881.
Pełny tekst źródłaNeel, J. V. Studies of human mutation rates. Office of Scientific and Technical Information (OSTI), styczeń 1990. http://dx.doi.org/10.2172/6368357.
Pełny tekst źródłaNeel, J. V. The study of human mutation rates. Office of Scientific and Technical Information (OSTI), styczeń 1992. http://dx.doi.org/10.2172/7175958.
Pełny tekst źródłaHarris, Reuben S. Enzyme-Catalyzed Mutation in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2014. http://dx.doi.org/10.21236/ada613711.
Pełny tekst źródłaAndrews, Paul W., Raymond R. Tice i Diane Satterfield. Salmonella Typhimurium Microsome Reverse Mutation Assay. Fort Belvoir, VA: Defense Technical Information Center, marzec 1996. http://dx.doi.org/10.21236/ada589278.
Pełny tekst źródłaPonder, Rebecca, i Susan Rosenberg. Mechanism of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada396622.
Pełny tekst źródłaPetrosino, Joseph F. Mechanisms of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, maj 2002. http://dx.doi.org/10.21236/ada406067.
Pełny tekst źródłaPonder, Rebecca G., i Susan Rosenberg. Mechanism of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2002. http://dx.doi.org/10.21236/ada408728.
Pełny tekst źródłaPetrosino, Joseph F., i Susan Rosenberg. Mechanisms of Mutation in Non-Dividing Cells. Fort Belvoir, VA: Defense Technical Information Center, maj 2003. http://dx.doi.org/10.21236/ada416708.
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