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 Instability of the Myotonic Dystrophy (CTG) n Repeat during Human Fetal Development

By Martorell Loreto  

Human Molecular Genetics, Vol. 6, Iss. 6, 1997-01 ,pp. : 877-880

Oxford University Press

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Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

By Agbulut O.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2717-2726

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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Pms2 is a genetic enhancer of trinucleotide CAG·CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion

By Gomes-Pereira Mário   Fortune M. Teresa   Ingram Laura   McAbney John P.   Monckton Darren G.  

Human Molecular Genetics, Vol. 13, Iss. 16, 2004-08 ,pp. : 1815-1825

Oxford University Press

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