An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria

By Davies Brandon S.J.   Barnes Richard H.   Tu Yiping   Ren Shuxun   Andres Douglas A.   Spielmann H. Peter   Lammerding Jan   Wang Yibin   Young Stephen G.   Fong Loren G.  

Human Molecular Genetics, Vol. 19, Iss. 13, 2010-07 ,pp. : 2682-2694

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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Nucleocytoplasmic transport signals affect the age at onset of abnormalities in knock-in mice expressing polyglutamine within an ectopic protein context

By Jackson W.S.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1621-1629

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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Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice

By Persichetti F.   Gines S.   Seong I.S.   Fossale E.   Ivanova E.   Gusella J.F.   Wheeler V.C.   Trettel F.   MacDonald M.E.  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 497-508

Oxford University Press

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