232 related articles for article (PubMed ID: 20457914)
1. A molecular mechanism underlying the neural-specific defect in torsinA mutant mice.
Kim CE; Perez A; Perkins G; Ellisman MH; Dauer WT
Proc Natl Acad Sci U S A; 2010 May; 107(21):9861-6. PubMed ID: 20457914
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Cell-intrinsic effects of TorsinA(ΔE) disrupt dopamine release in a mouse model of TOR1A dystonia.
Downs AM; Fan X; Kadakia RF; Donsante Y; Jinnah HA; Hess EJ
Neurobiol Dis; 2021 Jul; 155():105369. PubMed ID: 33894367
[TBL] [Abstract][Full Text] [Related]
4. Silencing primary dystonia: lentiviral-mediated RNA interference therapy for DYT1 dystonia.
Gonzalez-Alegre P; Bode N; Davidson BL; Paulson HL
J Neurosci; 2005 Nov; 25(45):10502-9. PubMed ID: 16280588
[TBL] [Abstract][Full Text] [Related]
5. The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component.
Jungwirth MT; Kumar D; Jeong DY; Goodchild RE
BMC Cell Biol; 2011 May; 12():24. PubMed ID: 21627841
[TBL] [Abstract][Full Text] [Related]
6. TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models.
Li J; Liang CC; Pappas SS; Dauer WT
Elife; 2020 Mar; 9():. PubMed ID: 32202496
[TBL] [Abstract][Full Text] [Related]
7. Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs.
Tanabe LM; Liang CC; Dauer WT
Cell Rep; 2016 Sep; 16(12):3322-3333. PubMed ID: 27653693
[TBL] [Abstract][Full Text] [Related]
8. A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation.
Weisheit CE; Dauer WT
Hum Mol Genet; 2015 Nov; 24(22):6459-72. PubMed ID: 26370418
[TBL] [Abstract][Full Text] [Related]
9. TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration.
Liang CC; Tanabe LM; Jou S; Chi F; Dauer WT
J Clin Invest; 2014 Jul; 124(7):3080-92. PubMed ID: 24937429
[TBL] [Abstract][Full Text] [Related]
10. Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons.
Koh JY; Iwabuchi S; Harata NC
Neuroscience; 2013 Dec; 253():316-29. PubMed ID: 24025868
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Structure of the Golgi apparatus is not influenced by a GAG deletion mutation in the dystonia-associated gene Tor1a.
Mitchell SB; Iwabuchi S; Kawano H; Yuen TMT; Koh JY; Ho KWD; Harata NC
PLoS One; 2018; 13(11):e0206123. PubMed ID: 30403723
[TBL] [Abstract][Full Text] [Related]
13. Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?
Cascalho A; Jacquemyn J; Goodchild RE
Mov Disord; 2017 Mar; 32(3):371-381. PubMed ID: 27911022
[TBL] [Abstract][Full Text] [Related]
14. Genetic background modulates the phenotype of a mouse model of DYT1 dystonia.
Tanabe LM; Martin C; Dauer WT
PLoS One; 2012; 7(2):e32245. PubMed ID: 22393392
[TBL] [Abstract][Full Text] [Related]
15. Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice.
Uluğ AM; Vo A; Argyelan M; Tanabe L; Schiffer WK; Dewey S; Dauer WT; Eidelberg D
Proc Natl Acad Sci U S A; 2011 Apr; 108(16):6638-43. PubMed ID: 21464304
[TBL] [Abstract][Full Text] [Related]
16. The zebrafish homologue of the human DYT1 dystonia gene is widely expressed in CNS neurons but non-essential for early motor system development.
Sager JJ; Torres GE; Burton EA
PLoS One; 2012; 7(9):e45175. PubMed ID: 23028827
[TBL] [Abstract][Full Text] [Related]
17. Synaptic vesicle recycling is enhanced by torsinA that harbors the DYT1 dystonia mutation.
Kakazu Y; Koh JY; Ho KW; Gonzalez-Alegre P; Harata NC
Synapse; 2012 May; 66(5):453-64. PubMed ID: 22213465
[TBL] [Abstract][Full Text] [Related]
18. Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations.
Vulinovic F; Lohmann K; Rakovic A; Capetian P; Alvarez-Fischer D; Schmidt A; Weißbach A; Erogullari A; Kaiser FJ; Wiegers K; Ferbert A; Rolfs A; Klein C; Seibler P
Hum Mutat; 2014 Sep; 35(9):1114-22. PubMed ID: 24931141
[TBL] [Abstract][Full Text] [Related]
19. A unique redox-sensing sensor II motif in TorsinA plays a critical role in nucleotide and partner binding.
Zhu L; Millen L; Mendoza JL; Thomas PJ
J Biol Chem; 2010 Nov; 285(48):37271-80. PubMed ID: 20861018
[TBL] [Abstract][Full Text] [Related]
20. Developmental patterns of torsinA and torsinB expression.
Vasudevan A; Breakefield XO; Bhide PG
Brain Res; 2006 Feb; 1073-1074():139-45. PubMed ID: 16458269
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
