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 *

202 related articles for article (PubMed ID: 8279460)

  • 1. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.
    Stevanin G; Le Guern E; Ravisé N; Chneiweiss H; Dürr A; Cancel G; Vignal A; Boch AL; Ruberg M; Penet C
    Am J Hum Genet; 1994 Jan; 54(1):11-20. PubMed ID: 8279460
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.
    Stevanin G; Cancel G; Dürr A; Chneiweiss H; Dubourg O; Weissenbach J; Cann HM; Agid Y; Brice A
    Am J Hum Genet; 1995 Jan; 56(1):193-201. PubMed ID: 7825578
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q.
    Stevanin G; Sousa PS; Cancel G; Dürr A; Dubourg O; Nicholson GA; Weissenbach J; Jardim E; Agid Y; Cassa E
    Neurobiol Dis; 1994 Nov; 1(1-2):79-82. PubMed ID: 9216989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I.
    Verschuuren-Bemelmans CC; Brunt ER; Burton M; Mensink RG; van der Meulen MA; Smit NH; Stolte-Dijkstra I; Buys CH; Scheffer H
    Hum Genet; 1995 Dec; 96(6):691-4. PubMed ID: 8522329
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
    Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
    Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C
    Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.
    Twells R; Yenchitsomanus PT; Sirinavin C; Allotey R; Poungvarin N; Viriyavejakul A; Cemal C; Weber J; Farrall M; Rodprasert P
    Hum Mol Genet; 1994 Jan; 3(1):177-80. PubMed ID: 8162021
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.
    Twist EC; Casaubon LK; Ruttledge MH; Rao VS; Macleod PM; Radvany J; Zhao Z; Rosenberg RN; Farrer LA; Rouleau GA
    J Med Genet; 1995 Jan; 32(1):25-31. PubMed ID: 7897622
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.
    Holmberg M; Johansson J; Forsgren L; Heijbel J; Sandgren O; Holmgren G
    Hum Mol Genet; 1995 Aug; 4(8):1441-5. PubMed ID: 7581386
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlation.
    Kubis N; Dürr A; Gugenheim M; Chneiweiss H; Mazzetti P; Brice A; Bouche P
    Muscle Nerve; 1999 Jun; 22(6):712-7. PubMed ID: 10366224
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
    Stevanin G; Trottier Y; Cancel G; Dürr A; David G; Didierjean O; Bürk K; Imbert G; Saudou F; Abada-Bendib M; Gourfinkel-An I; Benomar A; Abbas N; Klockgether T; Grid D; Agid Y; Mandel JL; Brice A
    Hum Mol Genet; 1996 Dec; 5(12):1887-92. PubMed ID: 8968739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS; Schelhaas JH; Ippel EF; Beemer FA; Pearson PL; Sinke RJ
    Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
    Pujana MA; Volpini V; Gratacós M; Corral J; Banchs I; Sánchez A; Genís D; Cervera C; Estivill X
    J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY; Lu YC; Cheng NC; Soong BW
    Brain; 2003 Jun; 126(Pt 6):1293-9. PubMed ID: 12764052
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.
    Worth PF; Giunti P; Gardner-Thorpe C; Dixon PH; Davis MB; Wood NW
    Am J Hum Genet; 1999 Aug; 65(2):420-6. PubMed ID: 10417284
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
    Belal S; Cancel G; Stevanin G; Hentati F; Khati C; Ben Hamida C; Auburger G; Agid Y; Ben Hamida M; Brice A
    Neurology; 1994 Aug; 44(8):1423-6. PubMed ID: 8058142
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
    Vale J; Bugalho P; Silveira I; Sequeiros J; Guimarães J; Coutinho P
    Eur J Neurol; 2010 Jan; 17(1):124-8. PubMed ID: 19659750
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.
    Twist EC; Farrer LA; Macleod PM; Radvany J; Chamberlain S; Rosenberg RN; Rouleau GA
    Hum Genet; 1994 Mar; 93(3):335-8. PubMed ID: 8125487
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.
    Lezin A; Cancel G; Stevanin G; Smadja D; Vernant JC; Dürr A; Martial J; Buisson GG; Bellance R; Chneiweiss H; Agid Y; Brice A
    Hum Genet; 1996 May; 97(5):671-6. PubMed ID: 8655151
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
    Benomar A; Krols L; Stevanin G; Cancel G; LeGuern E; David G; Ouhabi H; Martin JJ; Dürr A; Zaim A
    Nat Genet; 1995 May; 10(1):84-8. PubMed ID: 7647798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.