These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 26663046)

  • 1. [Genetic and clinical analysis in a Parkinson's disease family caused by expansion of SCA2].
    Zhang Y; Lu X; Cen Z; Cao J; Ouyang Z; Wang B; Luo W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):776-9. PubMed ID: 26663046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
    Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
    Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism.
    Kim JM; Hong S; Kim GP; Choi YJ; Kim YK; Park SS; Kim SE; Jeon BS
    Arch Neurol; 2007 Oct; 64(10):1510-8. PubMed ID: 17923635
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
    Wang JL; Xiao B; Cui XX; Guo JF; Lei LF; Song XW; Shen L; Jiang H; Yan XX; Pan Q; Long ZG; Xia K; Tang BS
    Mov Disord; 2009 Oct; 24(13):2007-11. PubMed ID: 19672991
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence.
    McGurk L; Rifai OM; Shcherbakova O; Perlegos AE; Byrns CN; Carranza FR; Zhou HW; Kim HJ; Zhu Y; Bonini NM
    Hum Mol Genet; 2021 Sep; 30(19):1797-1810. PubMed ID: 34077532
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications.
    Chen CM; Lee LC; Soong BW; Fung HC; Hsu WC; Lin PY; Huang HJ; Chen FL; Lin CY; Lee-Chen GJ; Wu YR
    Clin Chim Acta; 2010 Mar; 411(5-6):375-80. PubMed ID: 20004653
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat.
    Scoles DR; Ho MH; Dansithong W; Pflieger LT; Petersen LW; Thai KK; Pulst SM
    PLoS One; 2015; 10(6):e0128769. PubMed ID: 26086378
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis.
    Li PP; Sun X; Xia G; Arbez N; Paul S; Zhu S; Peng HB; Ross CA; Koeppen AH; Margolis RL; Pulst SM; Ashizawa T; Rudnicki DD
    Ann Neurol; 2016 Oct; 80(4):600-15. PubMed ID: 27531668
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SCA2 family presenting as typical Parkinson's disease: 34 year follow up.
    Kim YE; Jeon B; Farrer MJ; Scott E; Guella I; Park SS; Kim JM; Park HY; Kim A; Son YD; Cho ZH
    Parkinsonism Relat Disord; 2017 Jul; 40():69-72. PubMed ID: 28462804
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    Hum Genet; 2012 Apr; 131(4):625-38. PubMed ID: 22037902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2.
    Almaguer-Mederos LE; Mesa JML; González-Zaldívar Y; Almaguer-Gotay D; Cuello-Almarales D; Aguilera-Rodríguez R; Falcón NS; Gispert S; Auburger G; Velázquez-Pérez L
    Clin Genet; 2018 Oct; 94(3-4):346-350. PubMed ID: 29756284
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Simultaneous ALS and SCA2 associated with an intermediate-length
    Ghahremani Nezhad H; Franklin JP; Alix JJP; Moll T; Pattrick M; Cooper-Knock J; Shanmugarajah P; Beauchamp NJ; Hadjivissiliou M; Paling D; Mcdermott C; Shaw PJ; Jenkins TM
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Nov; 22(7-8):579-582. PubMed ID: 33284045
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia.
    Rubino E; Mancini C; Boschi S; Ferrero P; Ferrone M; Bianca S; Zucca M; Orsi L; Pinessi L; Govone F; Vacca A; Gai A; Giordana MT; Brusco A; Rainero I
    Neurobiol Aging; 2019 Jan; 73():231.e7-231.e9. PubMed ID: 30342763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
    Charles P; Camuzat A; Benammar N; Sellal F; Destée A; Bonnet AM; Lesage S; Le Ber I; Stevanin G; Dürr A; Brice A;
    Neurology; 2007 Nov; 69(21):1970-5. PubMed ID: 17568014
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ATXN2 trinucleotide repeat length correlates with risk of ALS.
    Sproviero W; Shatunov A; Stahl D; Shoai M; van Rheenen W; Jones AR; Al-Sarraj S; Andersen PM; Bonini NM; Conforti FL; Van Damme P; Daoud H; Del Mar Amador M; Fogh I; Forzan M; Gaastra B; Gellera C; Gitler AD; Hardy J; Fratta P; La Bella V; Le Ber I; Van Langenhove T; Lattante S; Lee YC; Malaspina A; Meininger V; Millecamps S; Orrell R; Rademakers R; Robberecht W; Rouleau G; Ross OA; Salachas F; Sidle K; Smith BN; Soong BW; Sorarù G; Stevanin G; Kabashi E; Troakes C; van Broeckhoven C; Veldink JH; van den Berg LH; Shaw CE; Powell JF; Al-Chalabi A
    Neurobiol Aging; 2017 Mar; 51():178.e1-178.e9. PubMed ID: 28017481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
    Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients.
    Modoni A; Contarino MF; Bentivoglio AR; Tabolacci E; Santoro M; Calcagni ML; Tonali PA; Neri G; Silvestri G
    Mov Disord; 2007 Feb; 22(3):324-7. PubMed ID: 17149720
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats.
    Yu Z; Zhu Y; Chen-Plotkin AS; Clay-Falcone D; McCluskey L; Elman L; Kalb RG; Trojanowski JQ; Lee VM; Van Deerlin VM; Gitler AD; Bonini NM
    PLoS One; 2011 Mar; 6(3):e17951. PubMed ID: 21479228
    [TBL] [Abstract][Full Text] [Related]  

  • 19. C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism.
    Zhang M; Xi Z; Misquitta K; Sato C; Moreno D; Liang Y; Slow E; Rogaeva E; Tartaglia MC
    Mov Disord; 2017 Jan; 32(1):158-162. PubMed ID: 28124431
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
    Schraen-Maschke S; Brique S; Chartier-Harlin MC; Brique E; Destée A; Sablonnière B
    Am J Med Genet; 1999 Dec; 88(6):738-41. PubMed ID: 10581499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.