The TSC1 gene product, hamartin, negatively regulates cell proliferation

By Miloloza Angelina   Rosner Margit   Nellist Mark   Halley Dicky   Bernaschek Gerhard   Hengstschläger Markus  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1721-1727

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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Hypoxia-inducible factor 1a is a Tsc1 -regulated survival factor in newborn neurons in tuberous sclerosis complex

By Feliciano David M.   Zhang Shiliang   Quon Jennifer L.   Bordey Angélique  

Human Molecular Genetics, Vol. 22, Iss. 9, 2013-05 ,pp. : 1725-1734

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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The GAP-Related Domain of Tuberin, the Product of the TSC2 Gene, is a Target for Missense Mutations in Tuberous Sclerosis

By Maheshwar Magitha M.   Cheadle Jeremy P.   Jones Alistair C.   Myring Jenny   Fryer Alan E.   Harris Peter C.   Sampson Julian R.  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1991-1996

Oxford University Press

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