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2. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Liquori CL; Ricker K; Moseley ML; Jacobsen JF; Kress W; Naylor SL; Day JW; Ranum LP Science; 2001 Aug; 293(5531):864-7. PubMed ID: 11486088 [TBL] [Abstract][Full Text] [Related]
3. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion]. Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170 [TBL] [Abstract][Full Text] [Related]
4. A reversal of misfortune for myotonic dystrophy? Cooper TA N Engl J Med; 2006 Oct; 355(17):1825-7. PubMed ID: 17065646 [No Abstract] [Full Text] [Related]
5. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1]. de Die-Smulders CE; Faber CG; Smeets HJ Ned Tijdschr Geneeskd; 2005 Sep; 149(37):2043-6. PubMed ID: 16184945 [TBL] [Abstract][Full Text] [Related]
7. Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles. Holt I; Mittal S; Furling D; Butler-Browne GS; Brook JD; Morris GE Genes Cells; 2007 Sep; 12(9):1035-48. PubMed ID: 17825047 [TBL] [Abstract][Full Text] [Related]
8. Triplet-repeat transcripts: a role for DNA in disease. Singer RH Science; 1998 May; 280(5364):696-7. PubMed ID: 9599147 [No Abstract] [Full Text] [Related]
9. Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophy. Chen W; Wang Y; Abe Y; Cheney L; Udd B; Li YP J Mol Biol; 2007 Apr; 368(1):8-17. PubMed ID: 17335846 [TBL] [Abstract][Full Text] [Related]
10. Myotonic dystrophy: discussion of molecular basis. Timchenko LT; Tapscott SJ; Cooper TA; Monckton DG Adv Exp Med Biol; 2002; 516():27-45. PubMed ID: 12611434 [No Abstract] [Full Text] [Related]
11. 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; 118(Pt 13):2923-33. PubMed ID: 15961406 [TBL] [Abstract][Full Text] [Related]
12. Absconding with the threesome. Sachidanandan C Trends Cell Biol; 2001 Dec; 11(12):462. PubMed ID: 11719038 [No Abstract] [Full Text] [Related]
13. RNA leaching of transcription factors disrupts transcription in myotonic dystrophy. Ebralidze A; Wang Y; Petkova V; Ebralidse K; Junghans RP Science; 2004 Jan; 303(5656):383-7. PubMed ID: 14657503 [TBL] [Abstract][Full Text] [Related]
14. [Clinical and molecular genetical features of myotonic dystrophy]. Furuya H Fukuoka Igaku Zasshi; 2002 Aug; 93(8):153-60. PubMed ID: 12382414 [No Abstract] [Full Text] [Related]
15. Giant hairpins formed by CUG repeats in myotonic dystrophy messenger RNAs might sterically block RNA export through nuclear pores. Koch KS; Leffert HL J Theor Biol; 1998 Jun; 192(4):505-14. PubMed ID: 9680723 [TBL] [Abstract][Full Text] [Related]
16. [Myotonic dystrophy as an RNA-mediated disease]. Ishiura S Rinsho Shinkeigaku; 2005 Nov; 45(11):828-30. PubMed ID: 16447737 [No Abstract] [Full Text] [Related]
18. Muscleblind-like 2 (Mbnl2) -deficient mice as a model for myotonic dystrophy. Hao M; Akrami K; Wei K; De Diego C; Che N; Ku JH; Tidball J; Graves MC; Shieh PB; Chen F Dev Dyn; 2008 Feb; 237(2):403-10. PubMed ID: 18213585 [TBL] [Abstract][Full Text] [Related]
19. MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain. Goodwin M; Mohan A; Batra R; Lee KY; Charizanis K; Fernández Gómez FJ; Eddarkaoui S; Sergeant N; Buée L; Kimura T; Clark HB; Dalton J; Takamura K; Weyn-Vanhentenryck SM; Zhang C; Reid T; Ranum LP; Day JW; Swanson MS Cell Rep; 2015 Aug; 12(7):1159-68. PubMed ID: 26257173 [TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular aspects of the myotonic dystrophies: a review. Machuca-Tzili L; Brook D; Hilton-Jones D Muscle Nerve; 2005 Jul; 32(1):1-18. PubMed ID: 15770660 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]