220 related articles for article (PubMed ID: 14534912)
1. Developments in the molecular biology of DYT1 dystonia.
Walker RH; Shashidharan P
Mov Disord; 2003 Oct; 18(10):1102-7. PubMed ID: 14534912
[TBL] [Abstract][Full Text] [Related]
2. Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia.
Dang MT; Yokoi F; McNaught KS; Jengelley TA; Jackson T; Li J; Li Y
Exp Neurol; 2005 Dec; 196(2):452-63. PubMed ID: 16242683
[TBL] [Abstract][Full Text] [Related]
3. 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; 2006 Apr; 15(8):1355-64. PubMed ID: 16537570
[TBL] [Abstract][Full Text] [Related]
4. Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope.
Goodchild RE; Kim CE; Dauer WT
Neuron; 2005 Dec; 48(6):923-32. PubMed ID: 16364897
[TBL] [Abstract][Full Text] [Related]
5. TorsinA, microtubules and cell polarity.
Ferrari Toninelli G; Spano P; Memo M
Funct Neurol; 2003; 18(1):7-10. PubMed ID: 12760408
[TBL] [Abstract][Full Text] [Related]
6. TorsinA and dystonia: from nuclear envelope to synapse.
Granata A; Schiavo G; Warner TT
J Neurochem; 2009 Jun; 109(6):1596-609. PubMed ID: 19457118
[TBL] [Abstract][Full Text] [Related]
7. Genetics of dystonia: an overview.
Bressman SB
Parkinsonism Relat Disord; 2007; 13 Suppl 3():S347-55. PubMed ID: 18267263
[TBL] [Abstract][Full Text] [Related]
8. Characterization of the porcine TOR1A gene: The first step towards generation of a pig model for dystonia.
Henriksen C; Madsen LB; Bendixen C; Larsen K
Gene; 2009 Feb; 430(1-2):105-15. PubMed ID: 19028553
[TBL] [Abstract][Full Text] [Related]
9. Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA.
Jungwirth M; Dear ML; Brown P; Holbrook K; Goodchild R
Hum Mol Genet; 2010 Mar; 19(5):888-900. PubMed ID: 20015956
[TBL] [Abstract][Full Text] [Related]
10. Dystonia-causing mutant torsinA inhibits cell adhesion and neurite extension through interference with cytoskeletal dynamics.
Hewett JW; Zeng J; Niland BP; Bragg DC; Breakefield XO
Neurobiol Dis; 2006 Apr; 22(1):98-111. PubMed ID: 16361107
[TBL] [Abstract][Full Text] [Related]
11. Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
Grundmann K; Laubis-Herrmann U; Bauer I; Dressler D; Vollmer-Haase J; Bauer P; Stuhrmann M; Schulte T; Schöls L; Topka H; Riess O
Arch Neurol; 2003 Sep; 60(9):1266-70. PubMed ID: 12975293
[TBL] [Abstract][Full Text] [Related]
12. Toward therapy for DYT1 dystonia: allele-specific silencing of mutant TorsinA.
Gonzalez-Alegre P; Miller VM; Davidson BL; Paulson HL
Ann Neurol; 2003 Jun; 53(6):781-7. PubMed ID: 12783425
[TBL] [Abstract][Full Text] [Related]
13. Genetics and treatment of dystonia.
Schwarz CS; Bressman SB
Neurol Clin; 2009 Aug; 27(3):697-718, vi. PubMed ID: 19555827
[TBL] [Abstract][Full Text] [Related]
14. [Inherited dystonia update].
Nomura Y
Rinsho Shinkeigaku; 2004 Nov; 44(11):929-31. PubMed ID: 15651334
[TBL] [Abstract][Full Text] [Related]
15. Brainstem pathology in DYT1 primary torsion dystonia.
McNaught KS; Kapustin A; Jackson T; Jengelley TA; Jnobaptiste R; Shashidharan P; Perl DP; Pasik P; Olanow CW
Ann Neurol; 2004 Oct; 56(4):540-7. PubMed ID: 15455404
[TBL] [Abstract][Full Text] [Related]
16. Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis.
Beauvais G; Bode NM; Watson JL; Wen H; Glenn KA; Kawano H; Harata NC; Ehrlich ME; Gonzalez-Alegre P
J Neurosci; 2016 Oct; 36(40):10245-10256. PubMed ID: 27707963
[TBL] [Abstract][Full Text] [Related]
17. Expression of the early-onset torsion dystonia gene (DYT1) in human brain.
Augood SJ; Penney JB; Friberg IK; Breakefield XO; Young AB; Ozelius LJ; Standaert DG
Ann Neurol; 1998 May; 43(5):669-73. PubMed ID: 9585364
[TBL] [Abstract][Full Text] [Related]
18. Inherited and de novo mutations in sporadic cases of DYT1-dystonia.
Hjermind LE; Werdelin LM; Sørensen SA
Eur J Hum Genet; 2002 Mar; 10(3):213-6. PubMed ID: 11973627
[TBL] [Abstract][Full Text] [Related]
19. Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.
Goodchild RE; Dauer WT
Proc Natl Acad Sci U S A; 2004 Jan; 101(3):847-52. PubMed ID: 14711988
[TBL] [Abstract][Full Text] [Related]
20. Dominant torsinA mutations in cellular systems.
Baptista MJ; O'Farrell CA; Cookson MR
Adv Neurol; 2004; 94():73-8. PubMed ID: 14509657
[No Abstract] [Full Text] [Related]
[Next] [New Search]
