A mouse model of cardiac rhabdomyoma generated by loss of Tsc1 in ventricular myocytes

By Meikle Lynsey  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 429-435

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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Molecular Genetic and Phenotypic Analysis Reveals Differences between TSC1 and TSC2 Associated Familial and Sporadic Tuberous Sclerosis

By Jones Alistair C.   Daniells Claire E.   Snell Russell G.   Tachataki Maria   Idziaszczyk Shelley A.   Krawczak Michael   Sampson Julian R.   Cheadle Jeremy P.  

Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2155-2161

Oxford University Press

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Zebrafish Tsc1 reveals functional interactions between the cilium and the TOR pathway

By DiBella Linda M.   Park Alice   Sun Zhaoxia  

Human Molecular Genetics, Vol. 18, Iss. 4, 2009-02 ,pp. : 595-606

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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