Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities

By Hofmann-Radvanyi H.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1285-1291

Oxford University Press

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Somatic expansion behaviour of the (CTG) n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch–repair proteins

By te Riele H.   van den Broek W.J.A.A.   Nelen M.R.   Wansink D.G.   Coerwinkel M.M.   Groenen P.J.T.A.   Wieringa B.  

Human Molecular Genetics, Vol. 11, Iss. 2, 2002-01 ,pp. : 191-198

Oxford University Press

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Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients

By Martorell L.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 307-312

Oxford University Press

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Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability

By Seznec Hervé   Lia-Baldini Anne-Sophie  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1185-1194

Oxford University Press

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Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues

By Lpez Castel Arturo   Nakamori Masayuki   Tom Stephanie   Chitayat David   Gourdon Genevive   Thornton Charles A.   Pearson Christopher E.  

Human Molecular Genetics, Vol. 20, Iss. 1, 2011-01 ,pp. : 1-15

Oxford University Press

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