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Items: 1 to 20 of 142

1.

Genetic background modulates the phenotype of a mouse model of DYT1 dystonia.

Tanabe LM, Martin C, Dauer WT.

PLoS One. 2012;7(2):e32245. doi: 10.1371/journal.pone.0032245. Epub 2012 Feb 29.

2.

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 19;108(16):6638-43. doi: 10.1073/pnas.1016445108. Epub 2011 Apr 4.

3.

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. doi: 10.1172/JCI72830. Epub 2014 Jun 17.

4.

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 1;430(1-2):105-15. doi: 10.1016/j.gene.2008.10.023. Epub 2008 Nov 6.

PMID:
19028553
5.

Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia.

Song CH, Bernhard D, Hess EJ, Jinnah HA.

Neurobiol Dis. 2014 Feb;62:372-80. doi: 10.1016/j.nbd.2013.10.003. Epub 2013 Oct 11.

6.

Regional specificity of synaptic plasticity deficits in a knock-in mouse model of DYT1 dystonia.

Martella G, Maltese M, Nisticò R, Schirinzi T, Madeo G, Sciamanna G, Ponterio G, Tassone A, Mandolesi G, Vanni V, Pignatelli M, Bonsi P, Pisani A.

Neurobiol Dis. 2014 May;65:124-32. doi: 10.1016/j.nbd.2014.01.016. Epub 2014 Feb 3.

PMID:
24503369
7.

Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.

Song CH, Fan X, Exeter CJ, Hess EJ, Jinnah HA.

Neurobiol Dis. 2012 Oct;48(1):66-78. doi: 10.1016/j.nbd.2012.05.009. Epub 2012 May 31.

8.

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. doi: 10.1002/humu.22604. Epub 2014 Jul 17.

PMID:
24931141
9.

Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout mice.

Yokoi F, Dang MT, Li J, Standaert DG, Li Y.

PLoS One. 2011;6(9):e24539. doi: 10.1371/journal.pone.0024539. Epub 2011 Sep 12.

10.

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. Epub 2005 Oct 20.

PMID:
16242683
11.

DYT1 knock-in mice are not sensitized against mitochondrial complex-II inhibition.

Bode N, Massey C, Gonzalez-Alegre P.

PLoS One. 2012;7(8):e42644. doi: 10.1371/journal.pone.0042644. Epub 2012 Aug 3.

12.

Pre-synaptic release deficits in a DYT1 dystonia mouse model.

Yokoi F, Cheetham CC, Campbell SL, Sweatt JD, Li Y.

PLoS One. 2013 Aug 13;8(8):e72491. doi: 10.1371/journal.pone.0072491. eCollection 2013.

13.

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 25;107(21):9861-6. doi: 10.1073/pnas.0912877107. Epub 2010 May 10.

14.

Miniature release events of glutamate from hippocampal neurons are influenced by the dystonia-associated protein torsinA.

Kakazu Y, Koh JY, Iwabuchi S, Gonzalez-Alegre P, Harata NC.

Synapse. 2012 Sep;66(9):807-22. doi: 10.1002/syn.21571. Epub 2012 Jun 20.

PMID:
22588999
15.

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. doi: 10.1371/journal.pone.0045175. Epub 2012 Sep 28.

16.

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 31;12:24. doi: 10.1186/1471-2121-12-24.

17.

The ubiquitin ligase F-box/G-domain protein 1 promotes the degradation of the disease-linked protein torsinA through the ubiquitin-proteasome pathway and macroautophagy.

Gordon KL, Glenn KA, Bode N, Wen HM, Paulson HL, Gonzalez-Alegre P.

Neuroscience. 2012 Nov 8;224:160-71. doi: 10.1016/j.neuroscience.2012.08.023. Epub 2012 Aug 20.

18.

Silencing primary dystonia: lentiviral-mediated RNA interference therapy for DYT1 dystonia.

Gonzalez-Alegre P, Bode N, Davidson BL, Paulson HL.

J Neurosci. 2005 Nov 9;25(45):10502-9.

19.

Impairment of bidirectional synaptic plasticity in the striatum of a mouse model of DYT1 dystonia: role of endogenous acetylcholine.

Martella G, Tassone A, Sciamanna G, Platania P, Cuomo D, Viscomi MT, Bonsi P, Cacci E, Biagioni S, Usiello A, Bernardi G, Sharma N, Standaert DG, Pisani A.

Brain. 2009 Sep;132(Pt 9):2336-49. doi: 10.1093/brain/awp194. Epub 2009 Jul 29.

20.

Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice.

Yokoi F, Chen HX, Dang MT, Cheetham CC, Campbell SL, Roper SN, Sweatt JD, Li Y.

PLoS One. 2015 Mar 23;10(3):e0120916. doi: 10.1371/journal.pone.0120916. eCollection 2015. Erratum in: PLoS One. 2015;10(4):e0126539.

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