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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Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2 / mice

By Cao Jiumei   Gong Limin   Guo Dong-chuan   Mietzsch Ulrike   Kuang Shao-Qing   Kwartler Callie S.   Safi Hazim   Estrera Anthony   Gambello Michael J.   Milewicz Dianna M.  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1908-1920

Oxford University Press

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Comparative Analysis and Genomic Structure of the Tuberous Sclerosis 2 (TSC2) Gene in Human and Pufferfish

By Maheshwar Magitha M.   Sandford Richard   Nellist Mark   Cheadle Jeremy P.   Sgotto Barbara   Vaudin Mark   Sampson Julian R.  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 131-137

Oxford University Press

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Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC Patients

By Wilson Peter J.   Ramesh Vijaya   Kristiansen Arthur   Bove Catherine   Jozwiak Serguisy   Kwiatkowski David J.   Short M. Priscilla   Haines Jonathan L.  

Human Molecular Genetics, Vol. 5, Iss. 2, 1996-01 ,pp. : 249-256

Oxford University Press

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Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

By Sampson J.  

Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1053-1057

Oxford University Press

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