The Eker rat is an animal model of tuberous sclerosis caused by a mutation in the Tsc2 gene encoding a tumor suppressor ...
...TSC2. Western blot analyses confirmed the deregulation of 14-3-3 proteins upon ectopic overexpression of TSC1 and TSC2. ...
...TSC2, and the small guanosine triphosphatase, Rheb. In cells, mTOR is found in a complex with two other proteins, raptor...
Tuberous Sclerosis Complex (TSC) is a genetic disorder that occurs through the loss of heterozygosity of either TSC1 or ...
...TSC2 tumour-suppressor genes. Hamartin and tuberin form a complex and antagonise phosphoinositide 3-kinase/protein kinas...
The tuberous sclerosis complex genes TSC1 and TSC2 were first identified by positional cloning strategies in the heritab...
...TSC2 contributes to the development of a wide range of hamartomatous lesions. These patients do not, however, show an in...
...TSC2 indicated the presence of the novel missense change 3106T-->C, 1036S-->P in all family members with seizures. The f...
...TSC2, but not a disease-associated TSC2 mutant, downregulates HIF. Rapamycin normalizes HIF levels in TSC2(-/-) cells, i...
Tuberous sclerosis complex (TSC), an autosomal dominant disease caused by mutations in either TSC1 or TSC2, is character...
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