PubMed (cited) for id: 605377

Year	Number of Results
1966	1
1969	1
1974	1
1990	1
1992	2
1993	6
1994	1
1995	5
1996	1
2000	1
2001	4
2002	2
2003	3
2004	5
2005	3
2006	8
2007	2
2008	2
2010	1
2024	0

1

Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.

Braida C, Stefanatos RK, Adam B, Mahajan N, Smeets HJ, Niel F, Goizet C, Arveiler B, Koenig M, Lagier-Tourenne C, Mandel JL, Faber CG, de Die-Smulders CE, Spaans F, Monckton DG. Braida C, et al. Hum Mol Genet. 2010 Apr 15;19(8):1399-412. doi: 10.1093/hmg/ddq015. Epub 2010 Jan 15. Hum Mol Genet. 2010. PMID: 20080938

2

Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy.

Orengo JP, Chambon P, Metzger D, Mosier DR, Snipes GJ, Cooper TA. Orengo JP, et al. Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2646-51. doi: 10.1073/pnas.0708519105. Epub 2008 Feb 13. Proc Natl Acad Sci U S A. 2008. PMID: 18272483 Free PMC article.

3

RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression.

Yadava RS, Frenzel-McCardell CD, Yu Q, Srinivasan V, Tucker AL, Puymirat J, Thornton CA, Prall OW, Harvey RP, Mahadevan MS. Yadava RS, et al. Nat Genet. 2008 Jan;40(1):61-8. doi: 10.1038/ng.2007.28. Epub 2007 Dec 16. Nat Genet. 2008. PMID: 18084293 Free PMC article.

4

Patients with primary cataract as a genetic pool of DMPK protomutation.

Medica I, Teran N, Volk M, Pfeifer V, Ladavac E, Peterlin B. Medica I, et al. J Hum Genet. 2007;52(2):123-128. doi: 10.1007/s10038-006-0091-4. Epub 2006 Dec 5. J Hum Genet. 2007. PMID: 17146587

5

A reversal of misfortune for myotonic dystrophy?

Cooper TA. Cooper TA. N Engl J Med. 2006 Oct 26;355(17):1825-7. doi: 10.1056/NEJMcibr064708. N Engl J Med. 2006. PMID: 17065646 No abstract available.

6

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. Machuca-Tzili L, et al. Hum Genet. 2006 Nov;120(4):487-99. doi: 10.1007/s00439-006-0228-8. Epub 2006 Aug 23. Hum Genet. 2006. PMID: 16927100

7

Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy.

Mahadevan MS, Yadava RS, Yu Q, Balijepalli S, Frenzel-McCardell CD, Bourne TD, Phillips LH. Mahadevan MS, et al. Nat Genet. 2006 Sep;38(9):1066-70. doi: 10.1038/ng1857. Epub 2006 Jul 30. Nat Genet. 2006. PMID: 16878132 Free PMC article.

8

Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy.

Kanadia RN, Shin J, Yuan Y, Beattie SG, Wheeler TM, Thornton CA, Swanson MS. Kanadia RN, et al. Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11748-53. doi: 10.1073/pnas.0604970103. Epub 2006 Jul 24. Proc Natl Acad Sci U S A. 2006. PMID: 16864772 Free PMC article.

9

RNA-mediated neuromuscular disorders.

Ranum LP, Cooper TA. Ranum LP, et al. Annu Rev Neurosci. 2006;29:259-77. doi: 10.1146/annurev.neuro.29.051605.113014. Annu Rev Neurosci. 2006. PMID: 16776586 Review.

10

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.

Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA. Lin X, et al. Hum Mol Genet. 2006 Jul 1;15(13):2087-97. doi: 10.1093/hmg/ddl132. Epub 2006 May 22. Hum Mol Genet. 2006. PMID: 16717059

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