BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 18949263)

  • 1. Spinocerebellar ataxia type 6 in Brazil.
    Teive HA; Munhoz RP; Raskin S; Werneck LC
    Arq Neuropsiquiatr; 2008 Sep; 66(3B):691-4. PubMed ID: 18949263
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
    Ishikawa K; Tanaka H; Saito M; Ohkoshi N; Fujita T; Yoshizawa K; Ikeuchi T; Watanabe M; Hayashi A; Takiyama Y; Nishizawa M; Nakano I; Matsubayashi K; Miwa M; Shoji S; Kanazawa I; Tsuji S; Mizusawa H
    Am J Hum Genet; 1997 Aug; 61(2):336-46. PubMed ID: 9311738
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
    Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.
    Sinke RJ; Ippel EF; Diepstraten CM; Beemer FA; Wokke JH; van Hilten BJ; Knoers NV; van Amstel HK; Kremer HP
    Arch Neurol; 2001 Nov; 58(11):1839-44. PubMed ID: 11708993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spinocerebellar ataxia type 6.
    Solodkin A; Gomez CM
    Handb Clin Neurol; 2012; 103():461-73. PubMed ID: 21827907
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
    Sasaki H; Kojima H; Yabe I; Tashiro K; Hamada T; Sawa H; Hiraga H; Nagashima K
    Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics.
    Du X; Gomez CM
    Adv Exp Med Biol; 2018; 1049():147-173. PubMed ID: 29427102
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Jiang H; Tang BS; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
    Chin Med J (Engl); 2005 May; 118(10):837-43. PubMed ID: 15989765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese.
    Yabe I; Sasaki H; Yamashita I; Tashiro K; Takei A; Suzuki Y; Kida H; Takiyama Y; Nishizawa M; Hokezu Y; Nagamatsu K; Oda T; Ohnishi A; Inoue I; Hata A
    J Med Genet; 2001 May; 38(5):328-33. PubMed ID: 11403042
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Pontine atrophy in spinocerebellar ataxia type 6.
    Sugawara M; Toyoshima I; Wada C; Kato K; Ishikawa K; Hirota K; Ishiguro H; Kagaya H; Hirata Y; Imota T; Ogasawara M; Masamune O
    Eur Neurol; 2000; 43(1):17-22. PubMed ID: 10601803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia.
    Yabe I; Sasaki H; Matsuura T; Takada A; Wakisaka A; Suzuki Y; Fukazawa T; Hamada T; Oda T; Ohnishi A; Tashiro K
    J Neurol Sci; 1998; 156(1):89-95. PubMed ID: 9559993
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen JT; Riess O
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY; Howell MJ; Roller MJ; Xie TD; Gomez CM
    Ann Neurol; 2005 Mar; 57(3):349-54. PubMed ID: 15732118
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
    Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.
    Restituito S; Thompson RM; Eliet J; Raike RS; Riedl M; Charnet P; Gomez CM
    J Neurosci; 2000 Sep; 20(17):6394-403. PubMed ID: 10964945
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular genetic approach to spinocerebellar ataxias].
    Ishikawa K; Ishiguro T; Takahashi M; Sato N; Amino T; Niimi Y; Mizusawa H
    Rinsho Shinkeigaku; 2009 Nov; 49(11):907-9. PubMed ID: 20030245
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
    Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE
    J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia.
    Morino H; Matsuda Y; Muguruma K; Miyamoto R; Ohsawa R; Ohtake T; Otobe R; Watanabe M; Maruyama H; Hashimoto K; Kawakami H
    Mol Brain; 2015 Dec; 8():89. PubMed ID: 26715324
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.