...Tsc2) gene. The Eker rat familial cancer syndrome serves as a unique animal model in which to study the molecular pathwa...
...TSC2). The TSC2 gene has been isolated. To date, only a small number of intragenic deletional and point mutations have b...
...TSC2 contiguous-gene syndrome, and the likely mutational mechanism in PKD1 is considered.
...TSC2 gene, which have severe infantile polycystic kidney disease, have also been characterised. The full length transcri...
...TSC2 gene may present phenotypically as mild skin signs and significant behavioural problems.
...TSC2 on chromosome 16p13.3. Loss of heterozygosity at 16p13.3-associated markers has been recently observed in hamartoma...
...TSC2). Germline deletions in the TSC2 gene have been shown in 5% of patients with tuberous sclerosis (TSC). These data s...
...TSC2. Intriguingly, the TSC2 product, tuberin, has an area of sequence homology with the GTPase activating protein rap1G...
...Tsc2) gene is localized, was found in the renal cell carcinomas which developed from hybrid F1 rats carrying the Eker mu...
Major genes which cause tuberous sclerosis (TSC) and autosomal dominant polycystic kidney disease (ADPKD), known as TSC2...
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