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 *

136 related articles for article (PubMed ID: 11591855)

  • 1. SCA8 repeat expansions in ataxia: a controversial association.
    Sobrido MJ; Cholfin JA; Perlman S; Pulst SM; Geschwind DH
    Neurology; 2001 Oct; 57(7):1310-2. PubMed ID: 11591855
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
    Ikeda Y; Dalton JC; Moseley ML; Gardner KL; Bird TD; Ashizawa T; Seltzer WK; Pandolfo M; Milunsky A; Potter NT; Shoji M; Vincent JB; Day JW; Ranum LP
    Am J Hum Genet; 2004 Jul; 75(1):3-16. PubMed ID: 15152344
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 61(5):727-33. PubMed ID: 15148151
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy.
    Cellini E; Nacmias B; Forleo P; Piacentini S; Guarnieri BM; Serio A; Calabrò A; Renzi D; Sorbi S
    Arch Neurol; 2001 Nov; 58(11):1856-9. PubMed ID: 11708995
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
    Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
    Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
    Topisirovic I; Dragasevic N; Savic D; Ristic A; Keckarevic M; Keckarevic D; Culjkovic B; Petrovic I; Romac S; Kostic VS
    Clin Genet; 2002 Oct; 62(4):321-4. PubMed ID: 12372061
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
    Mosemiller AK; Dalton JC; Day JW; Ranum LP
    Cytogenet Genome Res; 2003; 100(1-4):175-83. PubMed ID: 14526178
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.
    Wu YR; Lin HY; Chen CM; Gwinn-Hardy K; Ro LS; Wang YC; Li SH; Hwang JC; Fang K; Hsieh-Li HM; Li ML; Tung LC; Su MT; Lu KT; Lee-Chen GJ
    Clin Genet; 2004 Mar; 65(3):209-14. PubMed ID: 14756671
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.
    Wu YR; Chen IC; Soong BW; Kao SH; Lee GC; Huang SY; Fung HC; Lee-Chen GJ; Chen CM
    Hum Genet; 2009 May; 125(4):437-44. PubMed ID: 19229559
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
    Ikeda Y; Daughters RS; Ranum LP
    Cerebellum; 2008; 7(2):150-8. PubMed ID: 18418692
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.
    Moseley ML; Schut LJ; Bird TD; Koob MD; Day JW; Ranum LP
    Hum Mol Genet; 2000 Sep; 9(14):2125-30. PubMed ID: 10958651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.
    Silveira I; Alonso I; Guimarães L; Mendonça P; Santos C; Maciel P; Fidalgo De Matos JM; Costa M; Barbot C; Tuna A; Barros J; Jardim L; Coutinho P; Sequeiros J
    Am J Hum Genet; 2000 Mar; 66(3):830-40. PubMed ID: 10712199
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
    Mutsuddi M; Rebay I
    RNA Biol; 2005 Apr; 2(2):49-52. PubMed ID: 17132942
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.
    Cagnoli C; Michielotto C; Matsuura T; Ashizawa T; Margolis RL; Holmes SE; Gellera C; Migone N; Brusco A
    J Mol Diagn; 2004 May; 6(2):96-100. PubMed ID: 15096564
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of a fully penetrant spinocerebellar ataxia type 8 Brazilian family.
    Cintra VP; Lourenço CM; Rocha MMV; Tomaselli PJ; Marques W
    Acta Neurol Scand; 2017 Nov; 136(5):541-545. PubMed ID: 28229454
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The spinocerebellar ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in Drosophila.
    Mutsuddi M; Marshall CM; Benzow KA; Koob MD; Rebay I
    Curr Biol; 2004 Feb; 14(4):302-8. PubMed ID: 14972680
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
    Moseley ML; Zu T; Ikeda Y; Gao W; Mosemiller AK; Daughters RS; Chen G; Weatherspoon MR; Clark HB; Ebner TJ; Day JW; Ranum LP
    Nat Genet; 2006 Jul; 38(7):758-69. PubMed ID: 16804541
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Long repeat tracts at SCA8 in major psychosis.
    Vincent JB; Yuan QP; Schalling M; Adolfsson R; Azevedo MH; Macedo A; Bauer A; DallaTorre C; Medeiros HM; Pato MT; Pato CN; Bowen T; Guy CA; Owen MJ; O'Donovan MC; Paterson AD; Petronis A; Kennedy JL
    Am J Med Genet; 2000 Dec; 96(6):873-6. PubMed ID: 11121201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SCA8 CAG/CTG expansions, a tale of two TOXICities: a unique or common case?
    Merienne K; Trottier Y
    PLoS Genet; 2009 Aug; 5(8):e1000593. PubMed ID: 19680445
    [No Abstract]   [Full Text] [Related]  

  • 20. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.
    Izumi Y; Maruyama H; Oda M; Morino H; Okada T; Ito H; Sasaki I; Tanaka H; Komure O; Udaka F; Nakamura S; Kawakami H
    Am J Hum Genet; 2003 Mar; 72(3):704-9. PubMed ID: 12545428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.