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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Identification of the coding sequences responsible for Tsc2 -mediated tumor suppression using a transgenic rat system

By Momose S.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 2997-3006

Oxford University Press

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Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms

By Lux Andreas   Gallione Carol J.   Marchuk Douglas A.  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 745-755

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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Comparative analysis of the phosphomannomutase genes PMM1 , PMM2 and PMM2 : the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene

By Schollen E.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 157-164

Oxford University Press

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