Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

By Swami Meera   Hendricks Audrey E.   Gillis Tammy   Massood Tiffany   Mysore Jayalakshmi   Myers Richard H.   Wheeler Vanessa C.  

Human Molecular Genetics, Vol. 18, Iss. 16, 2009-08 ,pp. : 3039-3047

Oxford University Press

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Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice

By Borchelt D.R.  

Human Molecular Genetics, Vol. 11, Iss. 6, 2002-03 ,pp. : 633-640

Oxford University Press

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Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice

By Fossale E.   Wheeler V.C.   Vrbanac V.   Lebel L-A.   Teed A.   Mysore J.S.   Gusella J.F.   MacDonald M.E.   Persichetti F.  

Human Molecular Genetics, Vol. 11, Iss. 19, 2002-07 ,pp. : 2233-2241

Oxford University Press

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Absence of Disease Phenotype and Intergenerational Stability of the Cag Repeat in Transgenic Mice Expressing the Human Huntington Disease Transcript

By Goldberg Y. P.   Kalchman M. A.   Metzler M.   Nasir J.   Zeisler J.   Graham R.   Koide H. B.   O'Kusky J.   Sharp A. H.   Ross C. A.   Jirik F.   Hayden M. R.  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 177-185

Oxford University Press

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Gender of the embryo contributes to CAG instability in transgenic mice containing a Huntington’s disease gene

By Kovtun Irina V.  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2767-2775

Oxford University Press

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