Artículos de revistas sobre el tema "Triplet repeat diseases"
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Pan, Feng, Pengning Xu, Christopher Roland, Celeste Sagui y Keith Weninger. "Structural and Dynamical Properties of Nucleic Acid Hairpins Implicated in Trinucleotide Repeat Expansion Diseases". Biomolecules 14, n.º 10 (10 de octubre de 2024): 1278. http://dx.doi.org/10.3390/biom14101278.
Texto completoMonckton, Darren G. y C. Thomas Caskey. "Unstable Triplet Repeat Diseases". Circulation 91, n.º 2 (15 de enero de 1995): 513–20. http://dx.doi.org/10.1161/01.cir.91.2.513.
Texto completoJasinska, Anna J., Piotr Kozlowski y Wlodzimierz J. Krzyzosiak. "Expression characteristics of triplet repeat-containing RNAs and triplet repeat-interacting proteins in human tissues." Acta Biochimica Polonica 55, n.º 1 (30 de enero de 2008): 1–8. http://dx.doi.org/10.18388/abp.2008_3090.
Texto completoBates, Gillian P. y Roman Gonitel. "Mouse Models of Triplet Repeat Diseases". Molecular Biotechnology 32, n.º 2 (2006): 147–58. http://dx.doi.org/10.1385/mb:32:2:147.
Texto completoDi Prospero, Nicholas A. y Kenneth H. Fischbeck. "Therapeutics development for triplet repeat expansion diseases". Nature Reviews Genetics 6, n.º 10 (octubre de 2005): 756–66. http://dx.doi.org/10.1038/nrg1690.
Texto completoLi, Rena y Rif S. El-Mallakh. "Triplet Repeat Gene Sequences in Neuropsychiatric Diseases". Harvard Review of Psychiatry 5, n.º 2 (enero de 1997): 66–74. http://dx.doi.org/10.3109/10673229709034729.
Texto completoGorbunova, Vera, Andrei Seluanov, Vincent Dion, Zoltan Sandor, James L. Meservy y John H. Wilson. "Selectable System for Monitoring the Instability of CTG/CAG Triplet Repeats in Mammalian Cells". Molecular and Cellular Biology 23, n.º 13 (1 de julio de 2003): 4485–93. http://dx.doi.org/10.1128/mcb.23.13.4485-4493.2003.
Texto completoSinnreich, Michael, Eric J. Sorenson y Christopher J. Klein. "Neurologic Course, Endocrine Dysfunction and Triplet Repeat Size in Spinal Bulbar Muscular Atrophy". Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 31, n.º 3 (agosto de 2004): 378–82. http://dx.doi.org/10.1017/s0317167100003486.
Texto completoOlejniczak, Marta, Martyna O. Urbanek y Wlodzimierz J. Krzyzosiak. "The Role of the Immune System in Triplet Repeat Expansion Diseases". Mediators of Inflammation 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/873860.
Texto completoServadio, Antonio, Angelo Poletti, Antonio Servadio y Franco Taroni. "Triplet repeat diseases: from basic to clinical aspects". Brain Research Bulletin 56, n.º 3-4 (noviembre de 2001): 159. http://dx.doi.org/10.1016/s0361-9230(01)00750-x.
Texto completoGalka-Marciniak, Paulina, Martyna O. Urbanek y Wlodzimierz J. Krzyzosiak. "Triplet repeats in transcripts: structural insights into RNA toxicity". Biological Chemistry 393, n.º 11 (1 de noviembre de 2012): 1299–315. http://dx.doi.org/10.1515/hsz-2012-0218.
Texto completoRandall, Teri. "Triplet Repeat Mutations: Amplification Within Pedigrees Generates Three Human Diseases". JAMA: The Journal of the American Medical Association 269, n.º 5 (3 de febrero de 1993): 558. http://dx.doi.org/10.1001/jama.1993.03500050016004.
Texto completoRandall, T. "Triplet repeat mutations: amplification within pedigrees generates three human diseases". JAMA: The Journal of the American Medical Association 269, n.º 5 (3 de febrero de 1993): 558. http://dx.doi.org/10.1001/jama.269.5.558.
Texto completoWilliams, Gregory M., Vasileios Paschalis, Janice Ortega, Frederick W. Muskett, James T. Hodgkinson, Guo-Min Li, John W. R. Schwabe y Robert S. Lahue. "HDAC3 deacetylates the DNA mismatch repair factor MutSβ to stimulate triplet repeat expansions". Proceedings of the National Academy of Sciences 117, n.º 38 (8 de septiembre de 2020): 23597–605. http://dx.doi.org/10.1073/pnas.2013223117.
Texto completoGonzalez-Alegre, Pedro. "Recent advances in molecular therapies for neurological disease: triplet repeat disorders". Human Molecular Genetics 28, R1 (22 de junio de 2019): R80—R87. http://dx.doi.org/10.1093/hmg/ddz138.
Texto completoNahalka, Jozef. "1-L Transcription in Prion Diseases". International Journal of Molecular Sciences 25, n.º 18 (15 de septiembre de 2024): 9961. http://dx.doi.org/10.3390/ijms25189961.
Texto completoTruant, Ray, Lynn A. Raymond, Jianrun Xia, Deborah Pinchev, Anjee Burtnik y Randy Singh Atwal. "Canadian Association of Neurosciences Review: Polyglutamine Expansion Neurodegenerative Diseases". Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 33, n.º 3 (agosto de 2006): 278–91. http://dx.doi.org/10.1017/s031716710000514x.
Texto completoVölker, Plum, Gindikin y Breslauer. "Dynamic DNA Energy Landscapes and Substrate Complexity in Triplet Repeat Expansion and DNA Repair". Biomolecules 9, n.º 11 (6 de noviembre de 2019): 709. http://dx.doi.org/10.3390/biom9110709.
Texto completoKelley, Karen, Shin-Ju E. Chang y Shi-Lung Lin. "Mechanism of Repeat-Associated MicroRNAs in Fragile X Syndrome". Neural Plasticity 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/104796.
Texto completoBhattacharyya, Saumitri, Michael L. Rolfsmeier, Michael J. Dixon, Kara Wagoner y Robert S. Lahue. "Identification of RTG2 as a Modifier Gene for CTG·CAG Repeat Instability in Saccharomyces cerevisiae". Genetics 162, n.º 2 (1 de octubre de 2002): 579–89. http://dx.doi.org/10.1093/genetics/162.2.579.
Texto completoVolker, J., N. Makube, G. E. Plum, H. H. Klump y K. J. Breslauer. "Conformational energetics of stable and metastable states formed by DNA triplet repeat oligonucleotides: Implications for triplet expansion diseases". Proceedings of the National Academy of Sciences 99, n.º 23 (4 de noviembre de 2002): 14700–14705. http://dx.doi.org/10.1073/pnas.222519799.
Texto completoHasan, Qurratulain, Ravindra Varma Alluri, Pragna Rao y Yog Raj Ahuja. "Role of Glutamine Deamidation in Neurodegenerative Diseases Associated With Triplet Repeat Expansions: A Hypothesis". Journal of Molecular Neuroscience 29, n.º 1 (2006): 29–34. http://dx.doi.org/10.1385/jmn:29:1:29.
Texto completoHoffman-Zacharska, Dorota y Anna Sulek. "The New Face of Dynamic Mutation—the CAA [CAG]n CAA CAG Motif as a Mutable Unit in the TBP Gene Causative for Spino-Cerebellar Ataxia Type 17". International Journal of Molecular Sciences 25, n.º 15 (26 de julio de 2024): 8190. http://dx.doi.org/10.3390/ijms25158190.
Texto completoShen, Tao, Yukari Nagai, M. Udayakumar, K. Narasimhan, R. K. Arvind Shriram, N. Mohanraj y V. Elamaran. "Automated Genomic Signal Processing for Diseased Gene Identification". Journal of Medical Imaging and Health Informatics 9, n.º 6 (1 de agosto de 2019): 1254–61. http://dx.doi.org/10.1166/jmihi.2019.2726.
Texto completoRaaijmakers, Renée H. L., Lise Ripken, C. Rosanne M. Ausems y Derick G. Wansink. "CRISPR/Cas Applications in Myotonic Dystrophy: Expanding Opportunities". International Journal of Molecular Sciences 20, n.º 15 (27 de julio de 2019): 3689. http://dx.doi.org/10.3390/ijms20153689.
Texto completoKIMMEL, MAREK. "WHY MATHEMATICS IS NEEDED TO UNDERSTAND COMPLEX GENETICS DISEASES". Journal of Biological Systems 10, n.º 04 (diciembre de 2002): 359–80. http://dx.doi.org/10.1142/s0218339002000688.
Texto completoWells, Robert D., Pawel Parniewski, Anna Pluciennik, Albino Bacolla, Robert Gellibolian y Adam Jaworski. "Small Slipped Register Genetic Instabilities inEscherichia coliin Triplet Repeat Sequences Associated with Hereditary Neurological Diseases". Journal of Biological Chemistry 273, n.º 31 (31 de julio de 1998): 19532–41. http://dx.doi.org/10.1074/jbc.273.31.19532.
Texto completoShimizu, M., R. Fujita, N. Tomita, H. Shindo y R. D. Wells. "Chromatin structure of yeast minichromosomes containing triplet repeat sequences associated with human hereditary neurological diseases". Nucleic Acids Symposium Series 1, n.º 1 (1 de noviembre de 2001): 71–72. http://dx.doi.org/10.1093/nass/1.1.71.
Texto completoMatsuo, Kazuya, Susumu Ikenoshita, Yasushi Yabuki, Kosuke Kawakubo, Sefan Asamitsu, Hiroshi Sugiyama y Norifumi Shioda. "Development of a mutant allele-specific transcriptional repressive agent in CAG/CTG triplet repeat diseases". Proceedings for Annual Meeting of The Japanese Pharmacological Society 96 (2022): YIA08–1. http://dx.doi.org/10.1254/jpssuppl.96.0_yia08-1.
Texto completoKawakubo, Kosuke, Susumu Ikenoshita, Kazuya Matsuo, Sefan Asamitsu, Yasushi Yabuki, Hiroshi Sugiyama y Norifumi Shioda. "Therapeutic targeting expanded DNA using cyclic pyrrole-imidazole polyamide in CAG/CTG triplet repeat neurological diseases." Proceedings for Annual Meeting of The Japanese Pharmacological Society 95 (2022): 1—SS—27. http://dx.doi.org/10.1254/jpssuppl.95.0_1-ss-27.
Texto completoHou, M. H. "Crystal structure of actinomycin D bound to the CTG triplet repeat sequences linked to neurological diseases". Nucleic Acids Research 30, n.º 22 (15 de noviembre de 2002): 4910–17. http://dx.doi.org/10.1093/nar/gkf619.
Texto completoVolker, J., H. H. Klump y K. J. Breslauer. "DNA energy landscapes via calorimetric detection of microstate ensembles of metastable macrostates and triplet repeat diseases". Proceedings of the National Academy of Sciences 105, n.º 47 (17 de noviembre de 2008): 18326–30. http://dx.doi.org/10.1073/pnas.0810376105.
Texto completoSERMON, K. "PGD in the lab for triplet repeat diseases ? myotonic dystrophy, Huntington's disease and Fragile-X syndrome". Molecular and Cellular Endocrinology 183 (octubre de 2001): S77—S85. http://dx.doi.org/10.1016/s0303-7207(01)00572-x.
Texto completoMaduro, Maria Rosa, Roberto Casella, Alex G. Smith y Dolores J. Lamb. "Increased incidence of triplet repeat diseases expanded alleles in azoospermic men: a new concern for ICSI?" Fertility and Sterility 78 (septiembre de 2002): S32. http://dx.doi.org/10.1016/s0015-0282(02)03465-9.
Texto completoWhite, Peter J., Rhona H. Borts y Mark C. Hirst. "Stability of the Human Fragile X (CGG)n Triplet Repeat Array inSaccharomyces cerevisiae Deficient in Aspects of DNA Metabolism". Molecular and Cellular Biology 19, n.º 8 (1 de agosto de 1999): 5675–84. http://dx.doi.org/10.1128/mcb.19.8.5675.
Texto completoHuntley, Melanie A., Sanaa Mahmood y G. Brian Golding. "Simple sequence in brain and nervous system specific proteins". Genome 48, n.º 2 (1 de abril de 2005): 291–301. http://dx.doi.org/10.1139/g04-124.
Texto completoLiu, Yuan, Haihua Zhang, Janaki Veeraraghavan, Robert A. Bambara y Catherine H. Freudenreich. "Saccharomyces cerevisiae Flap Endonuclease 1 Uses Flap Equilibration To Maintain Triplet Repeat Stability". Molecular and Cellular Biology 24, n.º 9 (1 de mayo de 2004): 4049–64. http://dx.doi.org/10.1128/mcb.24.9.4049-4064.2004.
Texto completoSaido, T. C. "Involvement of polyglutamine endolysis followed by pyroglutamate formation in the pathogenesis of triplet repeat/polyglutamine-expansion diseases". Medical Hypotheses 54, n.º 3 (marzo de 2000): 427–29. http://dx.doi.org/10.1054/mehy.1999.0866.
Texto completoThirugnanasambandam, Arunachalam, Selvam Karthik, Pradeep Kumar Mandal y Namasivayam Gautham. "The novel double-folded structure of d(GCATGCATGC): a possible model for triplet-repeat sequences". Acta Crystallographica Section D Biological Crystallography 71, n.º 10 (30 de septiembre de 2015): 2119–26. http://dx.doi.org/10.1107/s1399004715013930.
Texto completoFischer, K. M. "Etiology of (CAG)n triplet repeat neurodegenerative diseases such as Huntington's disease is connected to stimulation of glutamate receptors". Medical Hypotheses 48, n.º 5 (mayo de 1997): 393–98. http://dx.doi.org/10.1016/s0306-9877(97)90034-7.
Texto completoFreudenreich, C. H., J. B. Stavenhagen y V. A. Zakian. "Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome." Molecular and Cellular Biology 17, n.º 4 (abril de 1997): 2090–98. http://dx.doi.org/10.1128/mcb.17.4.2090.
Texto completoBichara, M., S. Schumacher y R. P. Fuchs. "Genetic instability within monotonous runs of CpG sequences in Escherichia coli." Genetics 140, n.º 3 (1 de julio de 1995): 897–907. http://dx.doi.org/10.1093/genetics/140.3.897.
Texto completoSzwarocka, Sylwia T., Paweł Stączek y Paweł Parniewski. "Chromosomal model for analysis of a long CTG/CAG tract stability in wild-type Escherichia coli and its nucleotide excision repair mutants". Canadian Journal of Microbiology 53, n.º 7 (julio de 2007): 860–68. http://dx.doi.org/10.1139/w07-047.
Texto completoLee, Suman y Min S. Park. "Human FEN-1 can process the 5'-flap DNA of CTG/CAG triplet repeat derived from human genetic diseases by length and sequence dependent manner". Experimental & Molecular Medicine 34, n.º 4 (septiembre de 2002): 313–17. http://dx.doi.org/10.1038/emm.2002.44.
Texto completoShimada, Makoto K. "Splicing Modulators Are Involved in Human Polyglutamine Diversification via Protein Complexes Shuttling between Nucleus and Cytoplasm". International Journal of Molecular Sciences 24, n.º 11 (1 de junio de 2023): 9622. http://dx.doi.org/10.3390/ijms24119622.
Texto completoMcDonough, Paul G. "Triple repeat diseases and unstable gonadal function". Fertility and Sterility 88, n.º 5 (noviembre de 2007): 1477–78. http://dx.doi.org/10.1016/j.fertnstert.2007.07.021.
Texto completoPastore, Lisa M., JoAnn V. Pinkerton y Christopher D. Williams. "Triple repeat diseases and unstable gonadal function". Fertility and Sterility 88, n.º 5 (noviembre de 2007): 1477. http://dx.doi.org/10.1016/j.fertnstert.2007.07.023.
Texto completoWittenberger, Michael D. y Lawrence M. Nelson. "Reply: Triple repeat diseases and unstable gonadal function". Fertility and Sterility 88, n.º 5 (noviembre de 2007): 1477. http://dx.doi.org/10.1016/j.fertnstert.2007.07.022.
Texto completoTSUJI, Shoji. "Molecular Genetics of Triplet Repeats: Unstable Expansion of Triplet Repeats as a New Mechanism for Neurodegenerative Diseases." Internal Medicine 36, n.º 1 (1997): 3–8. http://dx.doi.org/10.2169/internalmedicine.36.3.
Texto completoUsdin, K. "NGG-triplet repeats form similar intrastrand structures: implications for the triplet expansion diseases". Nucleic Acids Research 26, n.º 17 (1 de septiembre de 1998): 4078–85. http://dx.doi.org/10.1093/nar/26.17.4078.
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