309 related articles for article (PubMed ID: 9241283)
21. Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle.
Inukai A; Doyu M; Kato T; Liang Y; Kuru S; Yamamoto M; Kobayashi Y; Sobue G
Muscle Nerve; 2000 Sep; 23(9):1421-6. PubMed ID: 10951446
[TBL] [Abstract][Full Text] [Related]
22. Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
Jansen G; Groenen PJ; Bächner D; Jap PH; Coerwinkel M; Oerlemans F; van den Broek W; Gohlsch B; Pette D; Plomp JJ; Molenaar PC; Nederhoff MG; van Echteld CJ; Dekker M; Berns A; Hameister H; Wieringa B
Nat Genet; 1996 Jul; 13(3):316-24. PubMed ID: 8673131
[TBL] [Abstract][Full Text] [Related]
23. Genetic mapping of a second myotonic dystrophy locus.
Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
[TBL] [Abstract][Full Text] [Related]
24. Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.
Gennarelli M; Pavoni M; Amicucci P; Angelini C; Menegazzo E; Zelano G; Novelli G; Dallapiccola B
Neuromuscul Disord; 1999 Jun; 9(4):215-9. PubMed ID: 10399747
[TBL] [Abstract][Full Text] [Related]
25. Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.
Rubinsztein DC; Leggo J; Amos W; Barton DE; Ferguson-Smith MA
Hum Mol Genet; 1994 Nov; 3(11):2031-5. PubMed ID: 7874122
[TBL] [Abstract][Full Text] [Related]
26. [CTG-repeat in myotonin protein kinase].
Sorimachi H; Sasagawa N; Maruyama K; Arahata K; Ishiura S; Suzuki K
Rinsho Shinkeigaku; 1994 Dec; 34(12):1230-2. PubMed ID: 7774120
[TBL] [Abstract][Full Text] [Related]
27. [Molecular pathways to myotonic dystrophy].
Ishiura S
Nihon Rinsho; 2005 Mar; 63(3):515-21. PubMed ID: 15773354
[TBL] [Abstract][Full Text] [Related]
28. Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions.
Hamshere MG; Harley H; Harper P; Brook JD; Brookfield JF
J Med Genet; 1999 Jan; 36(1):59-61. PubMed ID: 9950368
[TBL] [Abstract][Full Text] [Related]
29. Myotonic dystrophies.
Huang CC; Kuo HC
Chang Gung Med J; 2005 Aug; 28(8):517-26. PubMed ID: 16265841
[TBL] [Abstract][Full Text] [Related]
30. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus.
Filippova GN; Thienes CP; Penn BH; Cho DH; Hu YJ; Moore JM; Klesert TR; Lobanenkov VV; Tapscott SJ
Nat Genet; 2001 Aug; 28(4):335-43. PubMed ID: 11479593
[TBL] [Abstract][Full Text] [Related]
31. Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs.
Jansen G; Mahadevan M; Amemiya C; Wormskamp N; Segers B; Hendriks W; O'Hoy K; Baird S; Sabourin L; Lennon G
Nat Genet; 1992 Jul; 1(4):261-6. PubMed ID: 1302022
[TBL] [Abstract][Full Text] [Related]
32. Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy.
Reddy S; Smith DB; Rich MM; Leferovich JM; Reilly P; Davis BM; Tran K; Rayburn H; Bronson R; Cros D; Balice-Gordon RJ; Housman D
Nat Genet; 1996 Jul; 13(3):325-35. PubMed ID: 8673132
[TBL] [Abstract][Full Text] [Related]
33. Hypermutable myotonic dystrophy CTG repeats in transgenic mice.
Monckton DG; Coolbaugh MI; Ashizawa KT; Siciliano MJ; Caskey CT
Nat Genet; 1997 Feb; 15(2):193-6. PubMed ID: 9020848
[TBL] [Abstract][Full Text] [Related]
34. Real-time RT-PCR for CTG repeat-containing genes.
Eriksson M
Methods Mol Biol; 2004; 277():77-84. PubMed ID: 15201450
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. Identification of two nuclear proteins which bind to RNA CUG repeats: significance for myotonic dystrophy.
Bhagavati S; Ghatpande A; Leung B
Biochem Biophys Res Commun; 1996 Nov; 228(1):55-62. PubMed ID: 8912635
[TBL] [Abstract][Full Text] [Related]
37. Myotonic dystrophy gene analysis in affected Israeli families.
Achiron A; Magal N; Shem-Tov N; Noy S; Shohat M; Gadoth N
Isr J Med Sci; 1994 Aug; 30(8):622-5. PubMed ID: 8045745
[TBL] [Abstract][Full Text] [Related]
38. An expanded CTG trinucleotide repeat causes trans RNA interference: a new hypothesis for the pathogenesis of myotonic dystrophy.
Sasagawa N; Takahashi N; Suzuki K; Ishiura S
Biochem Biophys Res Commun; 1999 Oct; 264(1):76-80. PubMed ID: 10527844
[TBL] [Abstract][Full Text] [Related]
39. [Somatic mosaicism of p(CTG)n expansion in a case of myotonic dystrophy with parotid tumor].
Ogata K; Takahashi A; Oguchi N; Ishitoya J; Fuse S; Shimpo T
Rinsho Shinkeigaku; 1998 Aug; 38(8):736-8. PubMed ID: 9916519
[TBL] [Abstract][Full Text] [Related]
40. Myotonic dystrophy: molecular genetics and diagnosis.
Gharehbaghi-Schnell E; Finsterer J; Korschineck I; Mamoli B; Binder BR
Wien Klin Wochenschr; 1998 Jan; 110(1):7-14. PubMed ID: 9499472
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]