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Items: 1 to 20 of 277

1.

Huntington's disease--like 2 is associated with CUG repeat-containing RNA foci.

Rudnicki DD, Holmes SE, Lin MW, Thornton CA, Ross CA, Margolis RL.

Ann Neurol. 2007 Mar;61(3):272-82.

PMID:
17387722
2.

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, Henderson D, Schalling M, Swanson MS, Thornton CA.

Hum Mol Genet. 2001 Sep 15;10(19):2165-70.

3.

Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila.

Houseley JM, Wang Z, Brock GJ, Soloway J, Artero R, Perez-Alonso M, O'Dell KM, Monckton DG.

Hum Mol Genet. 2005 Mar 15;14(6):873-83.

4.

Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.

Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA.

J Cell Sci. 2005 Jul 1;118(Pt 13):2923-33.

5.

MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.

de Haro M, Al-Ramahi I, De Gouyon B, Ukani L, Rosa A, Faustino NA, Ashizawa T, Cooper TA, Botas J.

Hum Mol Genet. 2006 Jul 1;15(13):2138-45.

6.
7.

Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts.

Machuca-Tzili L, Thorpe H, Robinson TE, Sewry C, Brook JD.

Hum Genet. 2006 Nov;120(4):487-99.

PMID:
16927100
8.

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.

Mankodi A, Logigian E, Callahan L, McClain C, White R, Henderson D, Krym M, Thornton CA.

Science. 2000 Sep 8;289(5485):1769-73.

9.

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts.

Fardaei M, Larkin K, Brook JD, Hamshere MG.

Nucleic Acids Res. 2001 Jul 1;29(13):2766-71.

10.

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. Review.

11.

Muscleblind isoforms are functionally distinct and regulate alpha-actinin splicing.

Vicente M, Monferrer L, Poulos MG, Houseley J, Monckton DG, O'dell KM, Swanson MS, Artero RD.

Differentiation. 2007 Jun;75(5):427-40.

PMID:
17309604
12.

Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2.

Cardani R, Mancinelli E, Rotondo G, Sansone V, Meola G.

Eur J Histochem. 2006 Jul-Sep;50(3):177-82.

PMID:
16920640
13.

Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).

Santoro M, Modoni A, Masciullo M, Gidaro T, Broccolini A, Ricci E, Tonali PA, Silvestri G.

Exp Mol Pathol. 2010 Oct;89(2):158-68. doi: 10.1016/j.yexmp.2010.05.007.

PMID:
20685272
14.

CAG repeats mimic CUG repeats in the misregulation of alternative splicing.

Mykowska A, Sobczak K, Wojciechowska M, Kozlowski P, Krzyzosiak WJ.

Nucleic Acids Res. 2011 Nov 1;39(20):8938-51. doi: 10.1093/nar/gkr608.

15.

Hammerhead ribozyme-mediated destruction of nuclear foci in myotonic dystrophy myoblasts.

Langlois MA, Lee NS, Rossi JJ, Puymirat J.

Mol Ther. 2003 May;7(5 Pt 1):670-80.

PMID:
12718910
16.
17.

Nuclear RNA foci in the heart in myotonic dystrophy.

Mankodi A, Lin X, Blaxall BC, Swanson MS, Thornton CA.

Circ Res. 2005 Nov 25;97(11):1152-5.

18.

Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.

Fardaei M, Rogers MT, Thorpe HM, Larkin K, Hamshere MG, Harper PS, Brook JD.

Hum Mol Genet. 2002 Apr 1;11(7):805-14.

19.

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

Seznec H, Agbulut O, Sergeant N, Savouret C, Ghestem A, Tabti N, Willer JC, Ourth L, Duros C, Brisson E, Fouquet C, Butler-Browne G, Delacourte A, Junien C, Gourdon G.

Hum Mol Genet. 2001 Nov 1;10(23):2717-26.

20.

Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.

Ranum LP, Day JW.

Curr Neurol Neurosci Rep. 2002 Sep;2(5):465-70. Review.

PMID:
12169228
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