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

Access to resources Recommend Favorite

The UTX gene escapes X inactivation in mice and humans

By Willard H.F.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 737-742

Oxford University Press

Access to resources Recommend Favorite

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

By Chavali Venkata R.M.   Khan Naheed W.   Cukras Catherine A.   Bartsch Dirk-Uwe   Jablonski Monica M.   Ayyagari Radha  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 2000-2014

Oxford University Press

Access to resources Recommend Favorite

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage

By Ferrer Isidre   Kapfhammer Josef P.   Hindelang Colette   Kemp Stephan   Troffer-Charlier Nathalie   Broccoli Vania   Callyzot Noëlle   Mooyer Petra   Selhorst Jacqueline   Vreken Peter   Wanders Ronald J.A.   Mandel Jean Louis   Pujol Aurora  

Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3565-3577

Oxford University Press

Access to resources Recommend Favorite

PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotype

By Okazawa H.  

Human Molecular Genetics, Vol. 12, Iss. 7, 2003-04 ,pp. : 711-725

Oxford University Press

Access to resources Recommend Favorite