BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 20865765)

  • 1. Direct interaction between causative genes of DYT1 and DYT6 primary dystonia.
    Gavarini S; Cayrol C; Fuchs T; Lyons N; Ehrlich ME; Girard JP; Ozelius LJ
    Ann Neurol; 2010 Oct; 68(4):549-53. PubMed ID: 20865765
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6).
    Kaiser FJ; Osmanoric A; Rakovic A; Erogullari A; Uflacker N; Braunholz D; Lohnau T; Orolicki S; Albrecht M; Gillessen-Kaesbach G; Klein C; Lohmann K
    Ann Neurol; 2010 Oct; 68(4):554-9. PubMed ID: 20976771
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.
    Cheng FB; Feng JC; Ma LY; Miao J; Ott T; Wan XH; Grundmann K
    Mov Disord; 2014 Jul; 29(8):1079-83. PubMed ID: 24862462
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic evaluation of DYT1 and DYT6 primary dystonia in China.
    Cheng FB; Wan XH; Feng JC; Wang L; Yang YM; Cui LY
    Eur J Neurol; 2011 Mar; 18(3):497-503. PubMed ID: 20825472
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression.
    Hollstein R; Reiz B; Kötter L; Richter A; Schaake S; Lohmann K; Kaiser FJ
    Hum Mol Genet; 2017 Aug; 26(15):2975-2983. PubMed ID: 28486698
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
    Saunders-Pullman R; Fuchs T; San Luciano M; Raymond D; Brashear A; Ortega R; Deik A; Ozelius LJ; Bressman SB
    Mov Disord; 2014 May; 29(6):812-8. PubMed ID: 24500857
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited isolated dystonia: clinical genetics and gene function.
    Dauer W
    Neurotherapeutics; 2014 Oct; 11(4):807-16. PubMed ID: 25155315
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia.
    Dobričić VS; Kresojević ND; Svetel MV; Janković MZ; Petrović IN; Tomić AD; Novaković IV; Kostić VS
    J Neurol; 2013 Apr; 260(4):1037-42. PubMed ID: 23180184
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion.
    De Carvalho Aguiar P; Fuchs T; Borges V; Lamar KM; Silva SM; Ferraz HB; Ozelius L
    Mov Disord; 2010 Dec; 25(16):2854-7. PubMed ID: 20925076
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dystonia type 6 gene product Thap1: identification of a 50 kDa DNA-binding species in neuronal nuclear fractions.
    Ortiz-Virumbrales M; Ruiz M; Hone E; Dolios G; Wang R; Morant A; Kottwitz J; Ozelius LJ; Gandy S; Ehrlich ME
    Acta Neuropathol Commun; 2014 Sep; 2():139. PubMed ID: 25231164
    [TBL] [Abstract][Full Text] [Related]  

  • 11. THAP1/DYT6 sequence variants in non-DYT1 early-onset primary dystonia in China and their effects on RNA expression.
    Cheng FB; Ozelius LJ; Wan XH; Feng JC; Ma LY; Yang YM; Wang L
    J Neurol; 2012 Feb; 259(2):342-7. PubMed ID: 21800139
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Review: genetics and neuropathology of primary pure dystonia.
    Paudel R; Hardy J; Revesz T; Holton JL; Houlden H
    Neuropathol Appl Neurobiol; 2012 Oct; 38(6):520-34. PubMed ID: 22897341
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population.
    Wang L; Duan C; Gao Y; Xu W; Ding J; Liu VT; Wu Y
    Clin Neurol Neurosurg; 2016 Mar; 142():26-30. PubMed ID: 26803725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New THAP1 mutation and role of putative modifier in TOR1A.
    Piovesana LG; Torres FR; Azevedo PC; Amaral TP; Lopes-Cendes I; D'Abreu A
    Acta Neurol Scand; 2017 Feb; 135(2):183-188. PubMed ID: 26940431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia.
    Zech M; Boesch S; Sycha T; Mueller J; Poewe W; Winkelmann J
    Mov Disord; 2015 Nov; 30(13):1853-4. PubMed ID: 26506956
    [No Abstract]   [Full Text] [Related]  

  • 16. Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families.
    Zittel S; Moll CK; Brüggemann N; Tadic V; Hamel W; Kasten M; Lohmann K; Lohnau T; Winkler S; Gerloff C; Schönweiler R; Hagenah J; Klein C; Münchau A; Schneider SA
    Mov Disord; 2010 Oct; 25(14):2405-12. PubMed ID: 20687193
    [TBL] [Abstract][Full Text] [Related]  

  • 17. THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression.
    Erogullari A; Hollstein R; Seibler P; Braunholz D; Koschmidder E; Depping R; Eckhold J; Lohnau T; Gillessen-Kaesbach G; Grünewald A; Rakovic A; Lohmann K; Kaiser FJ
    Biochim Biophys Acta; 2014 Nov; 1839(11):1196-204. PubMed ID: 25088175
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The THAP-zinc finger protein THAP1 associates with coactivator HCF-1 and O-GlcNAc transferase: a link between DYT6 and DYT3 dystonias.
    Mazars R; Gonzalez-de-Peredo A; Cayrol C; Lavigne AC; Vogel JL; Ortega N; Lacroix C; Gautier V; Huet G; Ray A; Monsarrat B; Kristie TM; Girard JP
    J Biol Chem; 2010 Apr; 285(18):13364-71. PubMed ID: 20200153
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Intrafamilial variability of the primary dystonia DYT6 phenotype caused by p.Cys5Trp mutation in THAP1 gene.
    Jurek M; Hoffman-Zacharska D; Koziorowski D; Mądry J; Friedman A; Bal J
    Neurol Neurochir Pol; 2014; 48(4):254-7. PubMed ID: 25168324
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.
    Palada V; Stiern S; Glöckle N; Gómez-Garre P; Carrillo F; Mir P; Szczaluba K; Tinazzi M; Ajena D; Romani M; Valente EM; Müller U; Bauer P; Riess O; Ott T; Grundmann K
    Mov Disord; 2012 Jun; 27(7):917. PubMed ID: 22508326
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.