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Items: 1 to 20 of 30

1.

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. Epub 2005 Dec 19.

PMID:
16361107
2.

TorsinA and DYT1 dystonia: a synaptopathy?

Warner TT, Granata A, Schiavo G.

Biochem Soc Trans. 2010 Apr;38(2):452-6. doi: 10.1042/BST0380452. Review.

PMID:
20298201
3.

TorsinA and dystonia: from nuclear envelope to synapse.

Granata A, Schiavo G, Warner TT.

J Neurochem. 2009 Jun;109(6):1596-609. doi: 10.1111/j.1471-4159.2009.06095.x. Epub 2009 Apr 8. Review.

4.

TorsinA: movement at many levels.

Breakefield XO, Kamm C, Hanson PI.

Neuron. 2001 Jul 19;31(1):9-12. Review.

5.

Genetics and treatment of dystonia.

Schwarz CS, Bressman SB.

Neurol Clin. 2009 Aug;27(3):697-718, vi. doi: 10.1016/j.ncl.2009.04.010. Review.

PMID:
19555827
6.

Dystonia and the nuclear envelope.

Cookson MR, Clarimon J.

Neuron. 2005 Dec 22;48(6):875-7. Review.

7.

TorsinA, microtubules and cell polarity.

Ferrari Toninelli G, Spano P, Memo M.

Funct Neurol. 2003 Jan-Mar;18(1):7-10. Review.

PMID:
12760408
8.

Developments in the molecular biology of DYT1 dystonia.

Walker RH, Shashidharan P.

Mov Disord. 2003 Oct;18(10):1102-7. Review.

PMID:
14534912
9.

Early onset torsion dystonia (Oppenheim's dystonia).

Kamm C.

Orphanet J Rare Dis. 2006 Nov 27;1:48. Review.

10.

Genetics of dystonia: an overview.

Bressman SB.

Parkinsonism Relat Disord. 2007;13 Suppl 3:S347-55. doi: 10.1016/S1353-8020(08)70029-4. Review.

PMID:
18267263
11.

The role of torsinA in dystonia.

Granata A, Warner TT.

Eur J Neurol. 2010 Jul;17 Suppl 1:81-7. doi: 10.1111/j.1468-1331.2010.03057.x. Review.

PMID:
20590813
12.

TorsinA and early-onset torsion dystonia.

Bragg DC, Slater DJ, Breakefield XO.

Adv Neurol. 2004;94:87-93. Review. No abstract available.

PMID:
14509659
13.

Molecular chaperones and the cytoskeleton.

Liang P, MacRae TH.

J Cell Sci. 1997 Jul;110 ( Pt 13):1431-40. Review.

14.

Torsins: not your typical AAA+ ATPases.

Rose AE, Brown RS, Schlieker C.

Crit Rev Biochem Mol Biol. 2015;50(6):532-49. doi: 10.3109/10409238.2015.1091804. Epub 2015 Oct 13. Review.

15.

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. doi: 10.1002/mds.26880. Epub 2016 Dec 2. Review.

PMID:
27911022
16.

Genetic mutations strengthen functional association of LAP1 with DYT1 dystonia and muscular dystrophy.

Rebelo S, da Cruz E Silva EF, da Cruz E Silva OA.

Mutat Res Rev Mutat Res. 2015 Oct-Dec;766:42-7. doi: 10.1016/j.mrrev.2015.07.004. Epub 2015 Aug 5. Review.

PMID:
26596547
17.

TorsinA and torsion dystonia: Unraveling the architecture of the nuclear envelope.

Gerace L.

Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):8839-40. Epub 2004 Jun 8. Review. No abstract available.

18.

Cytoskeletal competence requires protein chaperones.

Quinlan R.

Prog Mol Subcell Biol. 2002;28:219-33. Review. No abstract available.

PMID:
11908062
19.

Quality control of cytoskeletal proteins and human disease.

Lundin VF, Leroux MR, Stirling PC.

Trends Biochem Sci. 2010 May;35(5):288-97. doi: 10.1016/j.tibs.2009.12.007. Epub 2010 Jan 28. Review.

PMID:
20116259
20.

Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature.

Edwards M, Wood N, Bhatia K.

Mov Disord. 2003 Jun;18(6):706-11. Review.

PMID:
12784278

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