BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

338 related articles for article (PubMed ID: 11448935)

  • 1. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.
    Nakamura K; Jeong SY; Uchihara T; Anno M; Nagashima K; Nagashima T; Ikeda S; Tsuji S; Kanazawa I
    Hum Mol Genet; 2001 Jul; 10(14):1441-8. PubMed ID: 11448935
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [SCA17, a novel polyglutamine disease caused by the expansion of polyglutamine tracts in TATA-binding protein].
    Nakamura K
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1123-5. PubMed ID: 12235815
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.
    Fujigasaki H; Martin JJ; De Deyn PP; Camuzat A; Deffond D; Stevanin G; Dermaut B; Van Broeckhoven C; Dürr A; Brice A
    Brain; 2001 Oct; 124(Pt 10):1939-47. PubMed ID: 11571212
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
    Rolfs A; Koeppen AH; Bauer I; Bauer P; Buhlmann S; Topka H; Schöls L; Riess O
    Ann Neurol; 2003 Sep; 54(3):367-75. PubMed ID: 12953269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder.
    Rubinsztein DC; Leggo J; Crow TJ; DeLisi LE; Walsh C; Jain S; Paykel ES
    Am J Med Genet; 1996 Sep; 67(5):495-8. PubMed ID: 8886170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias--triple-labeling immunofluorescence study.
    Uchihara T; Fujigasaki H; Koyano S; Nakamura A; Yagishita S; Iwabuchi K
    Acta Neuropathol; 2001 Aug; 102(2):149-52. PubMed ID: 11563629
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
    Koide R; Kobayashi S; Shimohata T; Ikeuchi T; Maruyama M; Saito M; Yamada M; Takahashi H; Tsuji S
    Hum Mol Genet; 1999 Oct; 8(11):2047-53. PubMed ID: 10484774
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar Ataxia Type 17 (SCA17).
    Toyoshima Y; Takahashi H
    Adv Exp Med Biol; 2018; 1049():219-231. PubMed ID: 29427105
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synergistic Toxicity of Polyglutamine-Expanded TATA-Binding Protein in Glia and Neuronal Cells: Therapeutic Implications for Spinocerebellar Ataxia 17.
    Yang Y; Yang S; Guo J; Cui Y; Tang B; Li XJ; Li S
    J Neurosci; 2017 Sep; 37(38):9101-9115. PubMed ID: 28821675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6.
    Zühlke CH; Spranger M; Spranger S; Voigt R; Lanz M; Gehlken U; Hinrichs F; Schwinger E
    Eur J Hum Genet; 2003 Aug; 11(8):629-32. PubMed ID: 12891385
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease.
    Takahashi J; Tanaka J; Arai K; Funata N; Hattori T; Fukuda T; Fujigasaki H; Uchihara T
    J Neuropathol Exp Neurol; 2001 Apr; 60(4):369-76. PubMed ID: 11305872
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia.
    Zühlke C; Hellenbroich Y; Dalski A; Kononowa N; Hagenah J; Vieregge P; Riess O; Klein C; Schwinger E
    Eur J Hum Genet; 2001 Mar; 9(3):160-4. PubMed ID: 11313753
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes.
    Zühlke C; Dalski A; Schwinger E; Finckh U
    BMC Med Genet; 2005 Jul; 6():27. PubMed ID: 15989694
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation.
    Bech S; Petersen T; Nørremølle A; Gjedde A; Ehlers L; Eiberg H; Hjermind LE; Hasholt L; Lundorf E; Nielsen JE
    Parkinsonism Relat Disord; 2010 Jan; 16(1):12-5. PubMed ID: 19595623
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases.
    Wu YR; Fung HC; Lee-Chen GJ; Gwinn-Hardy K; Ro LS; Chen ST; Hsieh-Li HM; Lin HY; Lin CY; Li SN; Chen CM
    J Neural Transm (Vienna); 2005 Apr; 112(4):539-46. PubMed ID: 15365789
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinocerebellar ataxia type 17 associated with an expansion of 42 glutamine residues in TATA-box binding protein gene.
    Nolte D; Sobanski E; Wissen A; Regula JU; Lichy C; Müller U
    J Neurol Neurosurg Psychiatry; 2010 Dec; 81(12):1396-9. PubMed ID: 20587494
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.
    Trottier Y; Lutz Y; Stevanin G; Imbert G; Devys D; Cancel G; Saudou F; Weber C; David G; Tora L
    Nature; 1995 Nov; 378(6555):403-6. PubMed ID: 7477379
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular investigation of TBP allele length: a SCA17 cellular model and population study.
    Reid SJ; Rees MI; van Roon-Mom WM; Jones AL; MacDonald ME; Sutherland G; During MJ; Faull RL; Owen MJ; Dragunow M; Snell RG
    Neurobiol Dis; 2003 Jun; 13(1):37-45. PubMed ID: 12758065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.