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Journal Abstract Search

333 related items for PubMed ID: 11017075

  • 1. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
    Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T.
    Nat Genet; 2000 Oct; 26(2):191-4. PubMed ID: 11017075
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  • 2. [Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].
    Ashizawa T, Matsuura T.
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1120-2. PubMed ID: 12235814
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  • 7. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
    Matsuura T, Fang P, Pearson CE, Jayakar P, Ashizawa T, Roa BB, Nelson DL.
    Am J Hum Genet; 2006 Jan; 78(1):125-9. PubMed ID: 16385455
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  • 8. Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
    McFarland KN, Liu J, Landrian I, Gao R, Sarkar PS, Raskin S, Moscovich M, Gatto EM, Teive HA, Ochoa A, Rasmussen A, Ashizawa T.
    Eur J Hum Genet; 2013 Nov; 21(11):1272-6. PubMed ID: 23443018
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  • 9. Recent progress in spinocerebellar ataxia type-10 (SCA10).
    Lin X, Ashizawa T.
    Cerebellum; 2005 Nov; 4(1):37-42. PubMed ID: 15895557
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  • 10. Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
    McFarland KN, Liu J, Landrian I, Zeng D, Raskin S, Moscovich M, Gatto EM, Ochoa A, Teive HA, Rasmussen A, Ashizawa T.
    Neurogenetics; 2014 Mar; 15(1):59-64. PubMed ID: 24318420
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  • 11. Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population.
    Goel D, Suroliya V, Shamim U, Mathur A, Faruq M.
    eNeurologicalSci; 2019 Dec; 17():100211. PubMed ID: 31737797
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  • 14. SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.
    McFarland KN, Liu J, Landrian I, Godiska R, Shanker S, Yu F, Farmerie WG, Ashizawa T.
    PLoS One; 2015 Dec; 10(8):e0135906. PubMed ID: 26295943
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  • 15. Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
    Bampi GB, Bisso-Machado R, Hünemeier T, Gheno TC, Furtado GV, Veliz-Otani D, Cornejo-Olivas M, Mazzeti P, Bortolini MC, Jardim LB, Saraiva-Pereira ML, Rede Neurogenetica.
    Neuromolecular Med; 2017 Dec; 19(4):501-509. PubMed ID: 28905220
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  • 16. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
    Teive HA, Roa BB, Raskin S, Fang P, Arruda WO, Neto YC, Gao R, Werneck LC, Ashizawa T.
    Neurology; 2004 Oct 26; 63(8):1509-12. PubMed ID: 15505178
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  • 17. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May 26; 61(5):727-33. PubMed ID: 15148151
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  • 18. Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.
    Grewal RP, Achari M, Matsuura T, Durazo A, Tayag E, Zu L, Pulst SM, Ashizawa T.
    Arch Neurol; 2002 Aug 26; 59(8):1285-90. PubMed ID: 12164725
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  • 19. A FEMALE CASE OF SPINOCEREBELLAR ATAXIA TYPE 10 WITH SUICIDAL BEHAVIOR AND ENDOCRINPATHIES ASSOCIATED WITH A MASSIVE EXPANSION (ATTCT) OF THE GENE ATXN10.
    Ramirez-Garcia SA, Sánchez-Corona J, Volpini-Bertran V, Moran-Moguel MC, Gutiérrez-Rubio SA, Castañeda-Cisneros G, Jiménez-Gil J, Garcia-Cruz D.
    Actas Esp Psiquiatr; 2022 Jan 26; 50(1):58-62. PubMed ID: 35103298
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  • 20. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
    Raskin S, Ashizawa T, Teive HA, Arruda WO, Fang P, Gao R, White MC, Werneck LC, Roa B.
    Arch Neurol; 2007 Apr 26; 64(4):591-4. PubMed ID: 17420323
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