Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in Hdh Q92 and Hdh Q111 knock-in mice

By Wheeler Vanessa C.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 503-513

Oxford University Press

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

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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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Genotypes and Phenotypes of 162 Families with a Glomulin Mutation

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A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

By Braunstein Kerstin E.   Eschbach Judith   Rna-Vrs Krisztina   Soylu Rana   Mikrouli Elli   Larmet Yves   Ren Frdrique   De Aguilar Jose-Luis Gonzalez   Loeffler Jean-Philippe   Mller Hans-Peter   Bucher Selina   Kaulisch Thomas   Niessen Heiko G.   Tillmanns Julia   Fischer Kristina   Schwalenstcker Birgit   Kassubek Jan   Pichler Bernd   Stiller Detlef   Petersen sa   Ludolph Albert C.   Dupuis Luc  

Human Molecular Genetics, Vol. 19, Iss. 22, 2010-11 ,pp. : 4385-4398

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