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

Access to resources Recommend Favorite

Thoracic aortic disease in tuberous sclerosis complex: molecular pathogenesis and potential therapies in Tsc2 / mice

By Cao Jiumei   Gong Limin   Guo Dong-chuan   Mietzsch Ulrike   Kuang Shao-Qing   Kwartler Callie S.   Safi Hazim   Estrera Anthony   Gambello Michael J.   Milewicz Dianna M.  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1908-1920

Oxford University Press

Access to resources Recommend Favorite

Primary intestinal lymphangiectasia treated with rapamycin in a child with tuberous sclerosis complex (TSC)

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2209-2212

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite