TSC2 missense mutations inhibit tuberin phosphorylation and prevent formation of the tuberin–hamartin complex

By Nellist M.   Verhaaf B.   Goedbloed M.A.   Reuser A.J.J.   van den Ouweland A.M.W.   Halley D.J.J.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2889-2898

Oxford University Press

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

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

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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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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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Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberin

By Li S.   Braverman R.   DeClue J.E.   Hodges A.K.   Maynard J.   Parry L.   Cheadle J.P.   Sampson J.R.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2899-2905

Oxford University Press

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