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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Therapeutic value of prenatal rapamycin treatment in a mouse brain model of tuberous sclerosis complex

By Anderl Stefanie   Freeland Megan   Kwiatkowski David J.   Goto June  

Human Molecular Genetics, Vol. 20, Iss. 23, 2011-12 ,pp. : 4597-4604

Oxford University Press

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Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

By Lin Xiaoyan   Miller Jill W.   Mankodi Ami   Kanadia Rahul N.   Yuan Yuan   Moxley Richard T.   Swanson Maurice S.   Thornton Charles A.  

Human Molecular Genetics, Vol. 15, Iss. 13, 2006-07 ,pp. : 2087-2097

Oxford University Press

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The galactocerebrosidase enzyme contributes to maintain a functional neurogenic niche during early post-natal CNS development

By Santambrogio Sara   Ricca Alessandra   Maderna Claudio   Ieraci Alessandro   Aureli Massimo   Sonnino Sandro   Kulik Willem   Aimar Patrizia   Bonfanti Luca   Martino Sabata   Gritti Angela  

Human Molecular Genetics, Vol. 21, Iss. 21, 2012-11 ,pp. : 4732-4750

Oxford University Press

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The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome

By Dauphinot L.  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 373-384

Oxford University Press

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