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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1971 1
1976 1
1978 1
1982 1
1983 1
1987 1
1989 1
1990 3
1992 3
1993 3
1994 3
1995 3
1996 4
1997 3
1998 8
1999 3
2000 4
2001 1
2002 3
2003 1
2004 6
2005 1
2006 2
2007 2
2009 1
2010 2
2011 5
2012 3
2013 1
2014 1
2015 1
2016 1
2017 1
2020 1
2022 1
2024 0

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PubMed (cited) for id: 183090

74 results

Results by year

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Page 1
ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
Glass JD, Dewan R, Ding J, Gibbs JR, Dalgard C, Keagle PJ, Shankaracharya, García-Redondo A, Traynor BJ, Chia R, Landers JE. Glass JD, et al. Brain. 2022 Aug 27;145(8):2671-2676. doi: 10.1093/brain/awac167. Brain. 2022. PMID: 35521889 Free PMC article.
Features of speech and swallowing dysfunction in pre-ataxic spinocerebellar ataxia type 2.
Vogel AP, Magee M, Torres-Vega R, Medrano-Montero J, Cyngler MP, Kruse M, Rojas S, Cubillos SC, Canento T, Maldonado F, Vazquez-Mojena Y, Ilg W, Rodríguez-Labrada R, Velázquez-Pérez L, Synofzik M. Vogel AP, et al. Neurology. 2020 Jul 14;95(2):e194-e205. doi: 10.1212/WNL.0000000000009776. Epub 2020 Jun 11. Neurology. 2020. PMID: 32527970
Antisense oligonucleotide therapy for spinocerebellar ataxia type 2.
Scoles DR, Meera P, Schneider MD, Paul S, Dansithong W, Figueroa KP, Hung G, Rigo F, Bennett CF, Otis TS, Pulst SM. Scoles DR, et al. Nature. 2017 Apr 20;544(7650):362-366. doi: 10.1038/nature22044. Epub 2017 Apr 12. Nature. 2017. PMID: 28405024 Free PMC article.
ATXN2 polyQ intermediate repeats are a modifier of ALS survival.
Chiò A, Calvo A, Moglia C, Canosa A, Brunetti M, Barberis M, Restagno G, Conte A, Bisogni G, Marangi G, Moncada A, Lattante S, Zollino M, Sabatelli M, Bagarotti A, Corrado L, Mora G, Bersano E, Mazzini L, D'Alfonso S; PARALS. Chiò A, et al. Neurology. 2015 Jan 20;84(3):251-8. doi: 10.1212/WNL.0000000000001159. Epub 2014 Dec 19. Neurology. 2015. PMID: 25527265 Free article.
Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications.
Laffita-Mesa JM, Bauer PO, Kourí V, Peña Serrano L, Roskams J, Almaguer Gotay D, Montes Brown JC, Martínez Rodríguez PA, González-Zaldívar Y, Almaguer Mederos L, Cuello-Almarales D, Aguiar Santiago J. Laffita-Mesa JM, et al. Hum Genet. 2012 Apr;131(4):625-38. doi: 10.1007/s00439-011-1101-y. Epub 2011 Oct 30. Hum Genet. 2012. PMID: 22037902
Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.
Laffita-Mesa JM, Velázquez-Pérez LC, Santos Falcón N, Cruz-Mariño T, González Zaldívar Y, Vázquez Mojena Y, Almaguer-Gotay D, Almaguer Mederos LE, Rodríguez Labrada R. Laffita-Mesa JM, et al. Eur J Hum Genet. 2012 Jan;20(1):41-9. doi: 10.1038/ejhg.2011.154. Epub 2011 Sep 21. Eur J Hum Genet. 2012. PMID: 21934711 Free PMC article.
Ataxin-2 repeat-length variation and neurodegeneration.
Ross OA, Rutherford NJ, Baker M, Soto-Ortolaza AI, Carrasquillo MM, DeJesus-Hernandez M, Adamson J, Li M, Volkening K, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Woodruff BK, Knopman DS, White CL 3rd, Van Gerpen JA, Meschia JF, Mackenzie IR, Boylan K, Boeve BF, Miller BL, Strong MJ, Uitti RJ, Younkin SG, Graff-Radford NR, Petersen RC, Wszolek ZK, Dickson DW, Rademakers R. Ross OA, et al. Hum Mol Genet. 2011 Aug 15;20(16):3207-12. doi: 10.1093/hmg/ddr227. Epub 2011 May 24. Hum Mol Genet. 2011. PMID: 21610160 Free PMC article.
74 results