Citations for
1DYT1, TOR1A
Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China.
Zhang SS, Fang DF, Hu XH, Burgunder JM, Chen XP, Zhang YW, Shang HF.
Eur J Neurol ur J Neurol. 2010 Jan 26. [Epub ahead of print]PMID: 20113340 2010
2DYT1, TOR1A
Chemical enhancement of torsinA function in cell and animal models of torsion dystonia.
Cao S, Hewett JW, Yokoi F, Lu J, Buckley AC, Burdette AJ, Chen P, Nery FC, Li Y, Breakefield XO, Caldwell GA, Caldwell KA.
Dis Model Mech is Model Mech. 2010 Mar 11. [Epub ahead of print]PMID: 20223934 2010
3DYT1, TOR1A
Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia.
Calakos N, Patel VD, Gottron M, Wang G, Tran-Viet KN, Brewington D, Beyer JL, Steffens DC, Krishnan RR, Züchner S.
J Med Genet 47(9):646-50. Epub 2009 Dec 2.PMID: 19955557 2010
4DYT1, KLHL14, TOR1A
Printor, a novel torsinA-interacting protein implicated in dystonia pathogenesis.
Giles LM, Li L, Chin LS.
J Biol Chem 284(32):21765-75. Epub 2009 Jun 17.PMID: 19535332 2009
5DYT1, TOR1A
The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
Brüggemann N, Kock N, Lohmann K, König IR, Rakovic A, Hagenah J, Schmidt A, Ziegler A, Jabusch HC, Siebner H, Altenmüller E, Münchau A, Klein C.
Neurology 72(16):1441-3. No abstract available. PMID: 19380705 2009
6DYT1, DYT11, DYT12, DYT13, DYT15, DYT3, DYT5, DYT6, DYT7, DYT7, DYT8, DYT9, EKD1, EKD2
The pathophysiological basis of dystonias.
Breakefield XO, Blood AJ, Li Y, Hallett M, Hanson PI, Standaert DG.
Nat Rev Neurosci 9(3):222-34. 2008
7TOR1A, DYT1, SNAPIN
The dystonia-associated protein torsinA modulates synaptic vesicle recycling.
Granata A, Watson R, Collinson LM, Schiavo G, Warner TT.
J Biol Chem 283(12):7568-79. Epub 2007 Dec 31. 2008
8DYT1, TOR1A
Dystonia-associated mutations cause premature degradation of torsinA protein and cell-type-specific mislocalization to the nuclear envelope.
Giles LM, Chen J, Li L, Chin LS.
Hum Mol Genet 17(17):2712-22. Epub 2008 Jun 14. 2008
9DYT1, TOR1A
Intragenic Cis and Trans Modification of Genetic Susceptibility in DYT1 Torsion Dystonia.
Risch NJ, Bressman SB, Senthil G, Ozelius LJ.
Am J Hum Genet 80(6):1188-93. Epub 2007 Apr 27. 2007
10TOR1A, DYT1
Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells.
Hewett JW, Tannous B, Niland BP, Nery FC, Zeng J, Li Y, Breakefield XO.
Proc Natl Acad Sci U S A 104(17):7271-6. Epub 2007 Apr 11. 2007
11TOR1A, DYT1
Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier.
Kock N, Naismith TV, Boston HE, Ozelius LJ, Corey DP, Breakefield XO, Hanson PI.
Hum Mol Genet 15(8):1355-64. Epub 2006 Mar 14. 2006
12DYT1, TOR1A
TorsinA and torsion dystonia: Unraveling the architecture of the nuclear envelope.
Gerace L.
Proc Natl Acad Sci U S A 101(24):8839-40. Epub 2004 Jun 08. No abstract available. 2004
13TOR1A, DYT1
Effect of torsinA on membrane proteins reveals a loss of function and a dominant-negative phenotype of the dystonia-associated DeltaE-torsinA mutant.
Torres GE, Sweeney AL, Beaulieu JM, Shashidharan P, Caron MG.
Proc Natl Acad Sci U S A 101(44):15650-5. Epub 2004 Oct 25. 2004
14DYT1, TOR1A
TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion
Rostasy K, Augood SJ, Hewett JW, Leung JC, Sasaki H, Ozelius LJ, Ramesh V, Standaert DG, Breakefield XO, Hedreen JC.
Neurobiol Dis 12(1):11-24. 2003
15DYT1, TOR1A
Characterization of human torsinA and its dystonia-associated mutant form.
Liu Z, Zolkiewska A, Zolkiewski M.
Biochem J 374(Pt 1):117-22. 2003
16DYT1, TOR1A
Inherited and de novo mutations in sporadic cases of DYT1-dystonia.
Hjermind LE, Werdelin LM, Sorensen SA.
Eur J Hum Genet 10(3):213-6. 2002
17DYT1, TOR1B, TOR1A
Cellular distribution of torsin A and torsin B in normal human brain.
Konakova M, Huynh DP, Yong W, Pulst SM.
Arch Neurol 58(6):921-7. 2001
18DYT1, TOR1A
DYT1 mutation in French families with idiopathic torsion dystonia.
Lebre AS, et al.
Brain 122 ( Pt 1):41-5. 1999
19DYT1, TOR1A, TOR1B, TOR2A
The TOR1A (DYT1) gene family and its role in early onset torsion dystonia.
Ozelius LJ, Page CE, Klein C, Hewett JW, Mineta M, Leung J, Shalish C,Bressman SB, de Leon D, Brin MF, Fahn S, Corey DP, Breakefield XO.
Genomics 62(3):377-84. 1999
20DYT1,DYT7
Genetics of primary dystonia.
Klein C, Breakefield XO, Ozelius LJ.
Semin Neurol 19(3):271-80. Review. 1999
21DYT1, GCH1, TOR1A
A novel mutation of the GTP-cyclohydrolase I gene in a patient with hereditary progressive dystonia/dopa-responsive dystonia.
Imaiso Y, Taniwaki T, Yamada T, Yoshimura T, Hirano M, Ueno S, Kaneda N, Kira J.
Neurology 50(2):517-9. 1998
22DYT1, DYT3, PNKD, TOR1A
The dystonias.
Jarman PR, et al.
J Med Genet 35 : 314-318. 1998
23DYT1, TOR1A
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.
Klein C, et al.
Hum Mol Genet 7 : 1133-1136. 1998
24DYT1, TOR1A
Secondary dystonia and the DYTI gene.
Bressman SB, de Leon D, Raymond D, Greene PE, Brin MF, Fahn S, Ozelius LJ, Breakefield XO, Kramer PL, Risch NJ.
Neurology 48(6):1571-7. 1997
25TOR1B, DYT1, TOR1A
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO.
Nat Genet 17(1):40-8. 1997
26DYT1, TOR1A
Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.
Holmgren G, et al.
J Neurol Neurosurg Psychiatry 59 : 178-181. 1995
27DYT1, TOR1A
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.
Wahlstršm J, et al.
Clin Genet 45 : 88-92. 1994
28DYT1, TOR1A
The DYTI gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews.
Kramer PL, et al.
Am J Hum Genet 55 : 468-475. 1994
29DYT1, TOR1A
Dystonia in Ashkenazi Jews : clinical characterization of a founder mutation.
Bressman SB, et al.
Ann Neurol 36 : 771-777. 1994
30DYT1, TOR1A
Linkage analysis with chromosome 9 markers in hereditary essential tremor.
Conway D, et al.
Mov Disord 8 : 374-376. 1993
31DYT1, TOR1A
The familial dysautonomia gene maps to chromosome 9q31-33 and shows strong allelic association with D9S58.
Blumenfeld A, et al.
Am J Hum Genet 53 : 979. 1993
32DYT1, TOR1A
Evidence for locus heterogeneity in autosomal dominant torsion dystonia.
Ahmad F, et al.
Genomics 15 : 9-12. 1993
33DYT1, TOR1A
Strong allelic association between the torsion dystonia gene (DYTI) and loci on chromosome 9q34 in Ashkenazi Jews.
Ozelius LJ, et al.
Am J Hum Genet 50 : 619-628. 1992
34DYT1, TOR1A
Idiopathic torsion dystonia in Ashkenazim : a distinct phenotype of a single mutation.
Bressman SB, et al.
Am J Hum Genet 51 : A209. 1992
35DYT1, TOR1A
Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.
Kwiatkowski DJ, et al.
Am J Hum Genet 49 : 366-371. 1991
36DYT1, TOR1A
Evidence for genetic heterogeneity in autosomal dominant torsion dystonia.
Ahmad F, et al.
(HGM11) Cytogenet Cell Genet 58 : 1934. 1991
37DYT1, TOR1A
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus : exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.
Kwiatkowski DJ, et al.
Am J Hum Genet 48 : 121-128. 1991
38DYT1, TOR1A
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.
Kramer PL, et al.
Ann Neurol 27 : 114-120. 1990
39DYT1, TOR1A
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.
Risch NJ, et al.
Am J Hum Genet 46 : 533-538. 1990
40DYT1, TOR1A
The genetics of idiopathic torsion dystonia.
Fletcher NA.
J Med Genet 27 : 409-412. 1990
41CTLN1, DYT1, GSN, TOR1A
Highly informative (GT)n polymorphisms from 9q32-34 permit creation of a high resolution map and delineation of a region likely to contain genes for torsion dystonia (DYT1), tuberous sclerosis (TSC1), and nail-patella syndrome (NPS1).
Kwiatkowski DJ, et al.
Am J Hum Genet 47 : A187. 1990
42DYT1, TOR1A
Human gene for torsion dystonia located on chromosome 9q32-q34.
Ozelius L, et al.
Neuron 2 : 1427-1434. 1989