Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberin

By Li S.   Braverman R.   DeClue J.E.   Hodges A.K.   Maynard J.   Parry L.   Cheadle J.P.   Sampson J.R.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2899-2905

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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Hamartin, the tuberous sclerosis complex 1 gene product, interacts with polo-like kinase 1 in a phosphorylation-dependent manner

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Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 287-297

Oxford University Press

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Bladder tumour-derived somatic TSC1 missense mutations cause loss of function via distinct mechanisms

By Pymar Louis S.   Platt Fiona M.   Askham Jon M.   Morrison Ewan E.   Knowles Margaret A.  

Human Molecular Genetics, Vol. 17, Iss. 13, 2008-07 ,pp. : 2006-2017

Oxford University Press

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