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Results: 1 to 20 of 93

Similar articles for PubMed (Select 21173221)

1.

Non-ATG-initiated translation directed by microsatellite expansions.

Zu T, Gibbens B, Doty NS, Gomes-Pereira M, Huguet A, Stone MD, Margolis J, Peterson M, Markowski TW, Ingram MA, Nan Z, Forster C, Low WC, Schoser B, Somia NV, Clark HB, Schmechel S, Bitterman PB, Gourdon G, Swanson MS, Moseley M, Ranum LP.

Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):260-5. doi: 10.1073/pnas.1013343108. Epub 2010 Dec 20.

2.

Repeat associated non-ATG translation initiation: one DNA, two transcripts, seven reading frames, potentially nine toxic entities!

Pearson CE.

PLoS Genet. 2011 Mar;7(3):e1002018. doi: 10.1371/journal.pgen.1002018. Epub 2011 Mar 10. Review.

3.

Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.

Ikeda Y, Daughters RS, Ranum LP.

Cerebellum. 2008;7(2):150-8. doi: 10.1007/s12311-008-0010-7.

PMID:
18418692
4.

Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders.

Cleary JD, Ranum LP.

Curr Opin Genet Dev. 2014 Jun;26:6-15. doi: 10.1016/j.gde.2014.03.002. Epub 2014 May 22. Review.

5.

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.

6.

Repeat-associated non-ATG (RAN) translation in neurological disease.

Cleary JD, Ranum LP.

Hum Mol Genet. 2013 Oct 15;22(R1):R45-51. doi: 10.1093/hmg/ddt371. Epub 2013 Aug 4. Review.

7.

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP.

Nat Genet. 2006 Jul;38(7):758-69. Epub 2006 Jun 25.

PMID:
16804541
8.

RNA-mediated neuromuscular disorders.

Ranum LP, Cooper TA.

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

PMID:
16776586
9.

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
10.

Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis.

Galvão R, Mendes-Soares L, Câmara J, Jaco I, Carmo-Fonseca M.

Brain Res Bull. 2001 Oct-Nov 1;56(3-4):191-201. Review.

PMID:
11719250
11.

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.

Arch Neurol. 2004 May;61(5):727-33.

PMID:
15148151
12.

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.

13.

Dominantly inherited, non-coding microsatellite expansion disorders.

Ranum LP, Day JW.

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

PMID:
12076668
14.

RNA gain-of-function in spinocerebellar ataxia type 8.

Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner TJ, Swanson MS, Ranum LP.

PLoS Genet. 2009 Aug;5(8):e1000600. doi: 10.1371/journal.pgen.1000600. Epub 2009 Aug 14.

15.

Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells.

Huichalaf C, Sakai K, Jin B, Jones K, Wang GL, Schoser B, Schneider-Gold C, Sarkar P, Pereira-Smith OM, Timchenko N, Timchenko L.

FASEB J. 2010 Oct;24(10):3706-19. doi: 10.1096/fj.09-151159. Epub 2010 May 17.

16.
17.

Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S.

Psychiatr Genet. 2001 Dec;11(4):201-5.

PMID:
11807410
18.

Molecular genetics of spinocerebellar ataxia type 8 (SCA8).

Mosemiller AK, Dalton JC, Day JW, Ranum LP.

Cytogenet Genome Res. 2003;100(1-4):175-83. Review.

PMID:
14526178
19.

[Molecular genetic approach to spinocerebellar ataxias].

Ishikawa K, Ishiguro T, Takahashi M, Sato N, Amino T, Niimi Y, Mizusawa H.

Rinsho Shinkeigaku. 2009 Nov;49(11):907-9. Review. Japanese.

PMID:
20030245
20.

[Molecular basis of spinocerebellar ataxias subtype caused by nucleotide repeat expansion in noncoding region].

Wang JL, Tang BS.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Jun;25(3):293-6. Review. Chinese.

PMID:
18543219
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