Dominant phenotypes produced by the HD mutation in ST Hdh Q111 striatal cells

By Trettel Flavia   Rigamonti Dorotea  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2799-2809

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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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh Q111 striatum

By Wheeler V.C.  

Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 273-281

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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Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice

By Lloret Alejandro   Dragileva Ella   Teed Allison   Espinola Janice   Fossale Elisa   Gillis Tammy   Lopez Edith   Myers Richard H.   MacDonald Marcy E.   Wheeler Vanessa C.  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 2015-2024

Oxford University Press

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