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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A mouse model of TSC1 reveals sex-dependent lethality from liver hemangiomas, and up-regulation of p70S6 kinase activity in Tsc1 null cells

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Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 525-534

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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Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model

By Gehrking Kristin M.   Andresen J. Michael   Duvick Lisa   Lough John   Zoghbi Huda Y.   Orr Harry T.  

Human Molecular Genetics, Vol. 20, Iss. 11, 2011-06 ,pp. : 2204-2212

Oxford University Press

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Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome?

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. : 802-804

John Wiley & Sons Inc

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