A hypomorphic allele of Tsc2 highlights the role of TSC1/TSC2 in signaling to AKT and models mild human TSC2 alleles

By Pollizzi Kristen   Malinowska-Kolodziej Izabela   Doughty Cheryl   Betz Charles   Ma Jian   Goto June   Kwiatkowski David J.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2378-2387

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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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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Loss of Tsc1 , but not Pten , in renal tubular cells causes polycystic kidney disease by activating mTORC1

By Zhou Jing   Brugarolas James   Parada Luis F.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4428-4441

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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