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

Access to resources Recommend Favorite

TSC2 missense mutations inhibit tuberin phosphorylation and prevent formation of the tuberin–hamartin complex

By Nellist M.   Verhaaf B.   Goedbloed M.A.   Reuser A.J.J.   van den Ouweland A.M.W.   Halley D.J.J.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2889-2898

Oxford University Press

Access to resources Recommend Favorite

The TSC1 gene product, hamartin, negatively regulates cell proliferation

By Miloloza Angelina   Rosner Margit   Nellist Mark   Halley Dicky   Bernaschek Gerhard   Hengstschläger Markus  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1721-1727

Oxford University Press

Access to resources Recommend Favorite

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

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