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2. Altered signal transduction pathways and induction of autophagy in human myotonic dystrophy type 1 myoblasts. Beffy P; Del Carratore R; Masini M; Furling D; Puymirat J; Masiello P; Simili M Int J Biochem Cell Biol; 2010 Dec; 42(12):1973-83. PubMed ID: 20797447 [TBL] [Abstract][Full Text] [Related]
3. Absence of a differentiation defect in muscle satellite cells from DM2 patients. Pelletier R; Hamel F; Beaulieu D; Patry L; Haineault C; Tarnopolsky M; Schoser B; Puymirat J Neurobiol Dis; 2009 Oct; 36(1):181-90. PubMed ID: 19632331 [TBL] [Abstract][Full Text] [Related]
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6. Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1. Thornell LE; Lindstöm M; Renault V; Klein A; Mouly V; Ansved T; Butler-Browne G; Furling D Neuropathol Appl Neurobiol; 2009 Dec; 35(6):603-13. PubMed ID: 19207265 [TBL] [Abstract][Full Text] [Related]
10. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1. Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511 [TBL] [Abstract][Full Text] [Related]
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12. Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1. Nakamori M; Kimura T; Kubota T; Matsumura T; Sumi H; Fujimura H; Takahashi MP; Sakoda S Neurology; 2008 Feb; 70(9):677-85. PubMed ID: 18299519 [TBL] [Abstract][Full Text] [Related]
13. Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cells. Bigot A; Klein AF; Gasnier E; Jacquemin V; Ravassard P; Butler-Browne G; Mouly V; Furling D Am J Pathol; 2009 Apr; 174(4):1435-42. PubMed ID: 19246640 [TBL] [Abstract][Full Text] [Related]
15. 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; 15(13):2138-45. PubMed ID: 16723374 [TBL] [Abstract][Full Text] [Related]
16. Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy. van den Broek WJ; Wansink DG; Wieringa B BMC Mol Biol; 2007 Jul; 8():61. PubMed ID: 17645799 [TBL] [Abstract][Full Text] [Related]
17. RNA pathogenesis of the myotonic dystrophies. Day JW; Ranum LP Neuromuscul Disord; 2005 Jan; 15(1):5-16. PubMed ID: 15639115 [TBL] [Abstract][Full Text] [Related]
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20. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes. Thornton CA; Johnson K; Moxley RT Ann Neurol; 1994 Jan; 35(1):104-7. PubMed ID: 8285579 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]