Overexpression of yeast hsp104 reduces polyglutamine aggregation and prolongs survival of a transgenic mouse model of Huntington's disease

By Vacher Coralie   Garcia-Oroz Lourdes   Rubinsztein David C.  

Human Molecular Genetics, Vol. 14, Iss. 22, 2005-11 ,pp. : 3425-3433

Oxford University Press

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Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

By Khelfaoui Malik   Pavlowsky Alice   Powell Andrew D.   Valnegri Pamela   Cheong Kenneth W.   Blandin Yann   Passafaro Maria   Jefferys John G.R.   Chelly Jamel   Billuart Pierre  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2575-2583

Oxford University Press

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Embryonic motor axon development in the severe SMA mouse

By McGovern Vicki L.   Gavrilina Tatiana O.   Beattie Christine E.   Burghes Arthur H.M.  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2900-2909

Oxford University Press

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Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of Tuberous Sclerosis Complex

By Zeng Ling-Hui   Rensing Nicholas R.   Zhang Bo   Gutmann David H.   Gambello Michael J.   Wong Michael  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 445-454

Oxford University Press

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Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy

By Callizot N.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 499-505

Oxford University Press

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