Literatura académica sobre el tema "Microsatellite disorders"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Microsatellite disorders".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Microsatellite disorders"
Richard, Guy-Franck. "The Startling Role of Mismatch Repair in Trinucleotide Repeat Expansions". Cells 10, n.º 5 (26 de abril de 2021): 1019. http://dx.doi.org/10.3390/cells10051019.
Texto completoAvvaru, Akshay Kumar, Deepak Sharma, Archana Verma, Rakesh K. Mishra y Divya Tej Sowpati. "MSDB: a comprehensive, annotated database of microsatellites". Nucleic Acids Research 48, n.º D1 (10 de octubre de 2019): D155—D159. http://dx.doi.org/10.1093/nar/gkz886.
Texto completoRanum, Laura P. W. y John W. Day. "Dominantly inherited, non-coding microsatellite expansion disorders". Current Opinion in Genetics & Development 12, n.º 3 (junio de 2002): 266–71. http://dx.doi.org/10.1016/s0959-437x(02)00297-6.
Texto completoVolpe, G., B. Gamberi, C. Pastore, A. Roetto, M. Pautasso, G. Parvis, C. Camaschella, U. Mazza, G. Saglio y G. Gaidano. "Analysis of microsatellite instability in chronic lymphoproliferative disorders". Annals of Hematology 72, n.º 2 (febrero de 1996): 67–71. http://dx.doi.org/10.1007/bf00641310.
Texto completoVolpe, G., B. Gamberi, C. Pastore, A. Roetto, M. Pautasso, G. Parvis, C. Camaschella, U. Mazza, G. Saglio y G. Gaidano. "Analysis of microsatellite instability in chronic lymphoproliferative disorders". Annals of Hematology 72, n.º 2 (1 de febrero de 1996): 67–71. http://dx.doi.org/10.1007/s002770050139.
Texto completoPoggi, Lucie, Lisa Emmenegger, Stéphane Descorps-Declère, Bruno Dumas y Guy-Franck Richard. "Differential efficacies of Cas nucleases on microsatellites involved in human disorders and associated off-target mutations". Nucleic Acids Research 49, n.º 14 (7 de julio de 2021): 8120–34. http://dx.doi.org/10.1093/nar/gkab569.
Texto completoShoab Mansuri, Mohmmad, Mala Singh y Munira Jariwala. "Investigating the Association of Poly (ADP-Ribose) Polymerase-1 (PARP-1) and Nuclear Factor-κB (NF-κB) Polymorphisms with Vitiligo Susceptibility". International Journal of Research and Review 9, n.º 10 (17 de octubre de 2022): 277–85. http://dx.doi.org/10.52403/ijrr.20221032.
Texto completoEcheverria, Gloria V. y Thomas A. Cooper. "RNA-binding proteins in microsatellite expansion disorders: Mediators of RNA toxicity". Brain Research 1462 (junio de 2012): 100–111. http://dx.doi.org/10.1016/j.brainres.2012.02.030.
Texto completoHayward, Bruce E., Peter J. Steinbach y Karen Usdin. "A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders". Nucleic Acids Research 48, n.º 14 (3 de julio de 2020): 7856–63. http://dx.doi.org/10.1093/nar/gkaa573.
Texto completoGrespi, Valentina, Cecilia Caprera, Claudia Ricciolini, Ilaria Bicchi, Gianmarco Muzi, Matteo Corsi, Stefano Ascani, Angelo Luigi Vescovi y Maurizio Gelati. "Human neural stem cells drug product: Microsatellite instability analysis". PLOS ONE 17, n.º 8 (30 de agosto de 2022): e0273679. http://dx.doi.org/10.1371/journal.pone.0273679.
Texto completoTesis sobre el tema "Microsatellite disorders"
Poggi, Lucie. "Gene editing approaches of microsatellite disorders : shortening expanded repeats". Electronic Thesis or Diss., Sorbonne université, 2020. http://www.theses.fr/2020SORUS412.
Texto completoMicrosatellite disorders are a specific class of human diseases that are due to the expansion of repeated sequences above pathological thresholds. These disorders have varying symptoms and pathogenic mechanisms, caused by the expanded repeat. No cure exists for any of these dramatic conditions. This thesis is investigating new gene editing approaches to remove pathological expansions in the human genome. In a first part, a yeast-based screen was constructed to identify potent CRISPR-associated nucleases that can cut these microsatellites. The second part focuses on myotonic dystrophy type 1 (DM1), which is due to and expanded CTG repeat tract located at the 3’UTR of the DMKP gene. A nuclease, TALENCTG was designed to induce a double strand break into the CTG repeats. It was previously shown to be active in yeast cells, inducing contractions of CTG repeats from a DM1 patient integrated into the yeast genome. The TALEN was tested in DM1 patient cells. The nuclease was found to trigger some contraction events in patient cells. In vivo experiments were carried out in a mouse model of myotonic dystrophy type 1 containing a human genomic fragment from a patient and 1000 CTG. Intramuscular injections of recombinant AAV encoding the TALENCTG revealed that the nuclease is toxic and/or immunogenic in muscle cells in the tested experimental conditions. Finally, the reporter assay integrated in yeast to screen nucleases was transposed in HEK293FS cell line. The integrated cassette contains a CTG expansion from a myotonic dystrophy type 1 patient flanked by two halves of GFP genes. This system would enable to find nucleases active in human cells
Vaksman, Zalman. "Somatic microsatellite variability as a measure of DNA stability in cancer and DNA repair disorders". Diss., Virginia Tech, 2015. http://hdl.handle.net/10919/51174.
Texto completoPh. D.
Vaysse-Zinkhöfer, Wilhelm. "Mécanismes de réparations d’une cassure double-brin et résection au sein d’un microsatellite humain". Electronic Thesis or Diss., Sorbonne université, 2021. http://www.theses.fr/2021SORUS477.
Texto completoMicrosatellites are tandem repeats of a motif between one and nine base pairs. These repeats are found ubiquitously in all organisms and are particularly abundant in eukaryotic organisms. All these repeats are capable of forming secondary structures in vitro and possibly in vivo. Some microsatellites are prone to expansion, leading to many neurodegenerative diseases in humans such as myotonic dystrophy type 1 (DM1), the most frequently transmitted neurodegenerative disease. The onset and severity of symptoms are positively correlated with the number of repeats located in the 3'UTR of the DMPK gene. In previous work in the laboratory, a TALE nuclease (TALEN) was developed to introduce a double-strand break into a microsatellite (GTC)n from a DM1 patient. Understanding the mechanisms leading to repeat contraction in yeast is necessary to understand the mechanisms in humans. Thus, experiments were conducted in cells with altered CBD repair systems showing that RAD51, POL32 and DNL4 were not required for CBD repair within microsatellites. Only RAD50 and RAD52 appear to be required, indicating that the cell repairs CBDs in repeated regions by single-strand annealing. The objective of this thesis was to study the role of several genes (MRE11, EXO1, SGS1, DNA2, SAE2, RIF1 and RIF2), involved in the resection and repair of a single CBD within a CTG repeat region, in yeast
Rohilla, Kushal. "Cell-Based Models and RNA Biology for a Genetic Form of Lou Gehrig's Disease". OpenSIUC, 2020. https://opensiuc.lib.siu.edu/dissertations/1784.
Texto completoCapítulos de libros sobre el tema "Microsatellite disorders"
Goodwin, Marianne y Maurice S. Swanson. "RNA-Binding Protein Misregulation in Microsatellite Expansion Disorders". En Systems Biology of RNA Binding Proteins, 353–88. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1221-6_10.
Texto completoDias, Christel y Cynthia Gates Goodyer. "Association of a Human Growth Hormone Receptor (HGHR) Gene Microsatellite Polymorphism with Idiopathic Short Stature (ISS)". En CLINICAL/TRANSLATIONAL - Growth Disorders, P1–726—P1–726. The Endocrine Society, 2011. http://dx.doi.org/10.1210/endo-meetings.2011.part2.p19.p1-726.
Texto completoBarcellos, Lisa F., Soren Germer y William Klitz. "DNA pooling methods for association mapping of complex disease loci". En Molecular Epidemiology, 113–44. Oxford University PressOxford, 2007. http://dx.doi.org/10.1093/oso/9780199638116.003.0005.
Texto completoActas de conferencias sobre el tema "Microsatellite disorders"
Charbonneaux, Juliette y Karine Berthelot Guiet. "Of Seals and Humans. Media and scientific discourses about a caregiving medical device." En 14th International Conference on Applied Human Factors and Ergonomics (AHFE 2023). AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1003485.
Texto completo