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Results: 1 to 20 of 107

Similar articles for PubMed (Select 23473314)

1.

The unstable repeats--three evolving faces of neurological disease.

Nelson DL, Orr HT, Warren ST.

Neuron. 2013 Mar 6;77(5):825-43. doi: 10.1016/j.neuron.2013.02.022. Review.

2.

Microsatellite repeat instability and neurological disease.

Brouwer JR, Willemsen R, Oostra BA.

Bioessays. 2009 Jan;31(1):71-83. doi: 10.1002/bies.080122. Review.

3.

CAG repeat RNA as an auxiliary toxic agent in polyglutamine disorders.

Wojciechowska M, Krzyzosiak WJ.

RNA Biol. 2011 Jul-Aug;8(4):565-71. doi: 10.4161/rna.8.4.15397. Epub 2011 Jul 1. Review.

4.

Trinucleotide repeats: mechanisms and pathophysiology.

Cummings CJ, Zoghbi HY.

Annu Rev Genomics Hum Genet. 2000;1:281-328. Review.

PMID:
11701632
5.

Trinucleotide repeat expansions in neurological disease.

Warren ST, Nelson DL.

Curr Opin Neurobiol. 1993 Oct;3(5):752-9. Review.

PMID:
8260825
6.

RNA-protein interactions in unstable microsatellite diseases.

Mohan A, Goodwin M, Swanson MS.

Brain Res. 2014 Oct 10;1584:3-14. doi: 10.1016/j.brainres.2014.03.039. Epub 2014 Apr 4. Review.

PMID:
24709120
7.

RNA-binding proteins in microsatellite expansion disorders: mediators of RNA toxicity.

Echeverria GV, Cooper TA.

Brain Res. 2012 Jun 26;1462:100-11. doi: 10.1016/j.brainres.2012.02.030. Epub 2012 Feb 22. Review.

8.

Trinucleotide repeat expansion in neurological disease.

La Spada AR, Paulson HL, Fischbeck KH.

Ann Neurol. 1994 Dec;36(6):814-22. Review.

PMID:
7998766
9.

Dominantly inherited, non-coding microsatellite expansion disorders.

Ranum LP, Day JW.

Curr Opin Genet Dev. 2002 Jun;12(3):266-71. Review.

PMID:
12076668
10.

RNA-mediated neuromuscular disorders.

Ranum LP, Cooper TA.

Annu Rev Neurosci. 2006;29:259-77. Review.

PMID:
16776586
11.

Heritable trinucleotide repeats and neurological disorders.

Shastry BS.

Experientia. 1994 Nov 30;50(11-12):1099-105. Review.

PMID:
7988670
12.

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.

Koshy BT, Zoghbi HY.

Brain Pathol. 1997 Jul;7(3):927-42. Review.

PMID:
9217976
13.

Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues.

Timchenko LT, Caskey CT.

FASEB J. 1996 Dec;10(14):1589-97. Review.

14.

Diseases of unstable repeat expansion: mechanisms and common principles.

Gatchel JR, Zoghbi HY.

Nat Rev Genet. 2005 Oct;6(10):743-55. Review.

PMID:
16205714
15.

Fragile X and other trinucleotide repeat diseases.

Wenstrom KD.

Obstet Gynecol Clin North Am. 2002 Jun;29(2):367-88, vii. Review.

PMID:
12108834
16.

Trinucleotide repeats in neurogenetic disorders.

Paulson HL, Fischbeck KH.

Annu Rev Neurosci. 1996;19:79-107. Review.

PMID:
8833437
17.

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.

Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL.

Am J Hum Genet. 2000 Mar;66(3):819-29.

18.

RNA-dominant diseases.

Osborne RJ, Thornton CA.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R162-9. Review.

19.

Coincident trinucleotide repeat expansions in a patient with myotonic dystrophy type 1 and spinocerebellar ataxia.

Kolb SJ, Kissel JT.

J Clin Neuromuscul Dis. 2008 Sep;10(1):22-3. doi: 10.1097/CND.0b013e318182105f.

PMID:
18772697
20.

[Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].

Matsuura T.

Rinsho Shinkeigaku. 2008 Nov;48(11):823-5. Review. Japanese.

PMID:
19198092
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