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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Altered LKB1/AMPK/TSC1/TSC2/mTOR signaling causes disruption of Sertoli cell polarity and spermatogenesis

By Tanwar Pradeep S.   Kaneko-Tarui Tomoko   Zhang LiHua   Teixeira Jose M.  

Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4394-4405

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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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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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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