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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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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Cln3 Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth

By Lerner T.J.  

Human Molecular Genetics, Vol. 11, Iss. 22, 2002-10 ,pp. : 2709-2721

Oxford University Press

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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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Neurological abnormalities in a knock-in mouse model of Huntington’s disease

By Detloff P.J.  

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