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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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

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Absence of progeria-like disease phenotypes in knock-in mice expressing a non-farnesylated version of progerin

By Yang Shao H.   Chang Sandy Y.   Ren Shuxun   Wang Yibin   Andres Douglas A.   Spielmann H. Peter   Fong Loren G.   Young Stephen G.  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 436-444

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Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse

By Joyner A.L.  

Human Molecular Genetics, Vol. 8, Iss. 1, 1999-01 ,pp. : 115-122

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A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice

By Iannicola C.  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 763-774

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