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Artigos de revistas sobre o assunto "Les Mutations"
Tarlock, Katherine, Todd M. Cooper, Todd A. Alonzo, Robert Gerbing, Jessica Pollard, Richard Aplenc, E. Anders Kolb, Alan S. Gamis e Soheil Meshinchi. "Mutational Concordance from Diagnosis and Relapse in Pediatric Acute Myeloid Leukemia: A Report from the Children's Oncology Group". Blood 128, n.º 22 (2 de dezembro de 2016): 2846. http://dx.doi.org/10.1182/blood.v128.22.2846.2846.
Texto completo da fonteGARCÍA-DORADO, A., C. LÓPEZ-FANJUL e A. CABALLERO. "Properties of spontaneous mutations affecting quantitative traits". Genetical Research 74, n.º 3 (dezembro de 1999): 341–50. http://dx.doi.org/10.1017/s0016672399004206.
Texto completo da fonteWatters, M. K., e D. R. Stadler. "Spontaneous mutation during the sexual cycle of Neurospora crassa." Genetics 139, n.º 1 (1 de janeiro de 1995): 137–45. http://dx.doi.org/10.1093/genetics/139.1.137.
Texto completo da fonteEllis, Nathan A. "Mutation-causing mutations". Nature 381, n.º 6578 (maio de 1996): 110–11. http://dx.doi.org/10.1038/381110a0.
Texto completo da fontePawlik, 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 janeiro de 2014): 210. http://dx.doi.org/10.1200/jco.2014.32.3_suppl.210.
Texto completo da fonteKang, S., S. S. Seo, H. J. Chang, C. W. Yoo, S. Y. Park e S. M. Dong. "Mutual exclusiveness between PIK3CA and KRAS mutations in endometrial carcinoma". International Journal of Gynecologic Cancer 18, n.º 6 (2008): 1339–43. http://dx.doi.org/10.1111/j.1525-1438.2007.01172.x.
Texto completo da fonteChao, Mwe, Kathrin Thomay, Gudrun Goehring, Marcin Wlodarski, Victor Pastor, Brigitte Schlegelberger, Detlev Schindler, Christian Kratz e Charlotte Niemeyer. "Mutational Spectrum of Fanconi Anemia Associated Myeloid Neoplasms". Klinische Pädiatrie 229, n.º 06 (novembro de 2017): 329–34. http://dx.doi.org/10.1055/s-0043-117046.
Texto completo da fonteHughes, Timothy, Giuseppe Saglio, Giovanni Martinelli, Dong-Wook Kim, S. Soverini, Martin Mueller, A. Haque et al. "Responses and Disease Progression in CML-CP Patients Treated with Nilotinib after Imatinib Failure Appear To Be Affected by the BCR-ABL Mutation Status and Types." Blood 110, n.º 11 (16 de novembro de 2007): 320. http://dx.doi.org/10.1182/blood.v110.11.320.320.
Texto completo da fontePálinkás, Hajnalka Laura, Lőrinc Pongor, Máté Balajti, Ádám Nagy, Kinga Nagy, Angéla Békési, Giampaolo Bianchini, Beáta G. Vértessy e Balázs Győrffy. "Primary Founder Mutations in the PRKDC Gene Increase Tumor Mutation Load in Colorectal Cancer". International Journal of Molecular Sciences 23, n.º 2 (6 de janeiro de 2022): 633. http://dx.doi.org/10.3390/ijms23020633.
Texto completo da fonteAhn, TaeJin, e Taesung Park. "Pathway-Driven Discovery of Rare Mutational Impact on Cancer". BioMed Research International 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/171892.
Texto completo da fonteTeses / dissertações sobre o assunto "Les Mutations"
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 completo da fonteIbrahim, 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 completo da fonteMutations 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.
Krasovec, 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 completo da fonteMutations 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 completo da fonteMutations 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
Maxwell, Megan Amanda, e n/a. "PEX1 Mutations in Australasian Patients with Disorders of Peroxisome Biogenesis". Griffith University. School of Biomolecular and Biomedical Science, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20040219.100649.
Texto completo da fonteMaxwell, Megan Amanda. "PEX1 Mutations in Australasian Patients with Disorders of Peroxisome Biogenesis". Thesis, Griffith University, 2004. http://hdl.handle.net/10072/366184.
Texto completo da fonteThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Biomedical Sciences
Full Text
COCCIADIFERRO, DARIO. "Mutational analysis of Kabuki Syndrome patients and functional dissection of KMT2D mutations". Doctoral thesis, Università di Foggia, 2018. http://hdl.handle.net/11369/369451.
Texto completo da fonteDavis, Brad. "Compensatory and deleterious mutations". Thesis, University of British Columbia, 2009. http://hdl.handle.net/2429/7722.
Texto completo da fonteBendall, Kate E. "Inheritance of mitochondrial mutations". Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320141.
Texto completo da fonteSalamat, Majid. "Coalescent, recombinaisons et mutations". Thesis, Aix-Marseille 1, 2011. http://www.theses.fr/2011AIX10059.
Texto completo da fonteThis thesis is concentrated on some sub jects on population genetics. In the first part we give formulae including the expectation and variance of the height and the length of the ancestral recombination graph (ARG) and the expectation and variance of the number of recombination events and we show that the expectation of the length of the ARG is a linear combination of the expectation of the length of Kingman's coalescent and the expectation of the height of the ARG. Also we show give a relation between the expectation of the ARG and the expectation of the number of recombination events. At the end of this part we show that the ARG comes down from infinity in the sense that we can dfine it with X_0 = ∞, while X_t <∞ ; for all t and we find the speed that the ARG comes down from infinity. In the second part wfind a generalization of the the Ewens sampling formula (GESF) in the presence of recombination for sample of sizes n = 2 and n = 3. In the third part of the thesis we study the ARG along the genome and we we find the distribution of the number of mutations when we have one recombination event in the genealogy of the sample
Livros sobre o assunto "Les Mutations"
Thomas, Hugh. Mutations. Toronto: BookThug, 2004.
Encontre o texto completo da fonteCentre d'études et de recherche sur les civilisations et les littératures européennes (Boulogne-sur-Mer, France) e Université du Littoral Côte d'Opale. Équipe de recherche "HLLI.", eds. Mutations de société, mutations de cinéma. Aachen: Shaker Verlag, 2015.
Encontre o texto completo da fonteAubin, Denis. Mutations/fluctuations. [Outremont, Québec]: NBJ, 1985.
Encontre o texto completo da fonteWedge, Martin. Per-mutations. Belfast: Ormeau Baths Gallery, 1997.
Encontre o texto completo da fonteFrancesco, Casetti, Odin Roger e Centre d'études transdisciplinaires, eds. Télévisions mutations. Paris: Éditions du Seuil [for] Centre d'Études Transdisciplinaires, 1990.
Encontre o texto completo da fonteCarlos, Pacheco, Townsend Timothy, Hosek Dan, Harris Bob e Atomic Media, eds. X-Men: Mutations. New York: Marvel Comics, 1996.
Encontre o texto completo da fonteJay, Prosser, ed. Sublime mutations: Photographs. Tübingen: Konkursbuch Verlag, 2000.
Encontre o texto completo da fonteinternational, Institut CEDIMES Colloque, ed. Mutations contemporaines & développement. Paris: CEDIMES, 2003.
Encontre o texto completo da fonteCastella, Vincenzo, Davis Lynn 1944- e Roberto Pugliese. Recursions and mutations. Cinisello Balsamo, Milano: Silvana editoriale, 2019.
Encontre o texto completo da fonteCouturier, Stéphane. Stéphane Couturier: Mutations. [Paris]: Bibliothèque nationale de France, 2004.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Les Mutations"
Konzak, C. F. "Mutations and Mutation Breeding". In 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 completo da fonteSebald, Madeleine. "Mutations". In Brock/Springer Series in Contemporary Bioscience, 64–97. New York, NY: Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4615-7087-5_5.
Texto completo da fonteSharma, Dhirendra Kumar. "Mutations". In Encyclopedia of Animal Cognition and Behavior, 4519–24. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-319-55065-7_567.
Texto completo da fonteSharma, Dhirendra Kumar. "Mutations". In Encyclopedia of Animal Cognition and Behavior, 1–6. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-47829-6_567-1.
Texto completo da fonteBiswas, Nabendu. "Mutations". In Practical GraphQL, 49–75. Berkeley, CA: Apress, 2023. http://dx.doi.org/10.1007/978-1-4842-9621-9_3.
Texto completo da fontevan Eyk, Clare L., e Robert I. Richards. "Dynamic Mutations". In Advances in Experimental Medicine and Biology, 55–77. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5434-2_5.
Texto completo da fonteMichaelides, K., R. Schwaab, M. R. A. Lalloz, W. Schmidt, e E. G. D. Tuddenham. "Mutational analysis: new mutations". In PCR2, 255–88. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0013.
Texto completo da fonteNewton, Clive R. "Mutational analysis: known mutations". In PCR2, 219–54. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780199634255.003.0012.
Texto completo da fonteLevine, Michael A., e Steven A. Lietman. "Molecular and Clinical Characteristics of the McCune–Albright Syndrome". In Oxford Textbook of Endocrinology and Diabetes 3e, editado por John A. H. Wass, Wiebke Arlt e Robert K. Semple, 1075–88. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198870197.003.0121.
Texto completo da fonteJennings, Barbara, Nandu Thalange e Gavin Willis. "Mutations and Genetic Variation". In Genetics in Medicine. Oxford University Press, 2020. http://dx.doi.org/10.1093/hesc/9780198841555.003.0002.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Les Mutations"
SEPE, MARICHELA. "MEASURING UNCERTAINTY: FACING PLACE MUTATIONS SUSTAINABLY". In SDP 2024, 155–64. Southampton UK: WIT Press, 2024. http://dx.doi.org/10.2495/sdp240131.
Texto completo da fonteSouza, Beatriz, e Rohit Gheyi. "A Lightweight Technique to Identify Equivalent Mutants". In 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 completo da fonteCambraia, 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 e Verônica Marques Zembrzuski. "A novel mutation in the RRM2 domain of TDP-43 in a Brazilian sporadic ALS patient." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.486.
Texto completo da fonteIliushchenko, D. V., B. E. Efimenko, K. V. Gunbin e K. Y. Popadin. "DEEP MUTATIONAL SPECTRUM OF MITOCHONDRIAL GENOME IN VERTEBRATES AS A NEW TYPE OF SPECIES — SPECIFIC MOLECULAR PHENOTYPE". In OpenBio-2023. ИПЦ НГУ, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-4.
Texto completo da fonteMukhopadhyay, Asima, Nicola Curtin e Richard Edmondson. "Evaluation of different methods to assess homologous recombination status and sensitivity to PARP inhibitors in ovarian cancer". In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685289.
Texto completo da fonteBittencourt, Yuri Cardoso Rodrigues Beckedorff, Lucas Soares Almada, Tatiana Strava Corrêa, Daniele Xavier Assad, Marina Sahade Gonçalves, Andrea Kazumi Shimada, Artur Katz e Romualdo Barroso-Sousa. "SOMATIC MUTATIONAL LANDSCAPE CHARACTERIZATION OF METASTATIC BREAST CANCER IN BRAZIL". In Brazilian Breast Cancer Symposium 2022. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s2025.
Texto completo da fonteBirch, David G., Gabriel H. Travis, Kirsten G. Locke e Donald C. Hood. "Rod Ergs in Mice and Humans with Putative Null Mutations in the RDS Gene". In Vision Science and its Applications. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/vsia.1997.ma.4.
Texto completo da fonteAntonarakis, E. "The Molecular Genetics of Hemophilia A Stylianos". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643980.
Texto completo da fonteHiguchi, M., L. Kochhan, R. Schwaab, H. H. Brackmann, H. Egli e K. Olek. "DETECTION OF MUTATIONS IN HEMOPHILIA A". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644012.
Texto completo da fonteYoussoufiän, H., A. Patel, D. Phillips, H. H. Kazazian e S. E. Antonarakis. "RECURRENT MUTATIONS AND AN UNUSUAL DELETION IN HEMOPHILIA A". In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644014.
Texto completo da fonteRelatórios de organizações sobre o assunto "Les Mutations"
Yang, Mengge, e Lin Liao. Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, dezembro de 2022. http://dx.doi.org/10.37766/inplasy2022.12.0031.
Texto completo da fonteHenry, Stephen Michael, Mark A. Smith e John P. Eddy. Holistic Portfolio Optimization using Directed Mutations. Office of Scientific and Technical Information (OSTI), fevereiro de 2016. http://dx.doi.org/10.2172/1618206.
Texto completo da fonteYeung, Anthony T. Detection of Mutations Using a Novel Endonuclease. Fort Belvoir, VA: Defense Technical Information Center, junho de 1998. http://dx.doi.org/10.21236/adb238444.
Texto completo da fonteDr. Elizabeth Iorns, Dr Elizabeth Iorns. Can we prevent the transmission of BRCA mutations? Experiment, fevereiro de 2013. http://dx.doi.org/10.18258/0090.
Texto completo da fonteLapedes, A. S., B. G. Giraud, L. C. Liu e G. D. Stormo. Correlated mutations in protein sequences: Phylogenetic and structural effects. Office of Scientific and Technical Information (OSTI), dezembro de 1998. http://dx.doi.org/10.2172/296863.
Texto completo da fonteBeernink, P., D. Barsky e B. Pesavento. Mutations that Cause Human Disease: A Computational/Experimental Approach. Office of Scientific and Technical Information (OSTI), janeiro de 2006. http://dx.doi.org/10.2172/898012.
Texto completo da fonteGrapes, Laura, Stephen Rudd, Rohan L. Fernando, Karine Megy, Dominique Rocha e Max F. Rothschild. Searching for mutations in pigs using the human genome. Ames (Iowa): Iowa State University, janeiro de 2005. http://dx.doi.org/10.31274/ans_air-180814-1070.
Texto completo da fonteBarkan, A. Transposon-induced nuclear mutations that alter chloroplast gene expression. Office of Scientific and Technical Information (OSTI), janeiro de 1992. http://dx.doi.org/10.2172/6686800.
Texto completo da fonteNelson, Peter S. Global Characterization of Protein-Altering Mutations in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2012. http://dx.doi.org/10.21236/ada568599.
Texto completo da fonteSieburth, Derek. Genetic and Molecular Analysis of Suppressors of Ras Mutations. Fort Belvoir, VA: Defense Technical Information Center, outubro de 1997. http://dx.doi.org/10.21236/ada340946.
Texto completo da fonte