...TSC2. Among sporadic TSC cases, mutations in TSC2 are more frequent and often accompanied by more severe neurologic defi...
...TSC2 gene, was expressed. In 19 angiomyolipomas from a TSC2-linked patient, in whose angiomyolipomas loss of tuberin exp...
...TSC2, or VHL gene regions, and no alterations in the VHL gene were detected using single-strand conformation polymorphis...
...TSC2, a gene mutated in half of TSC patients. Clones of gigas mutant cells induced in imaginal discs differentiate norma...
...Tsc2 is the rate-limiting step for renal carcinogenesis in the Eker rat model. Although inactivation of Tsc2 results in ...
...TSC2, in peripheral blood leukocytes from the patient were analyzed by polymerase chain reaction-single strand conformat...
...TSC2. In five families, somatic mosaicism was present in a mildly affected parent of an index patient. In one family wit...
...TSC2 activity affecting neuronal migration.
...TSC2. The samples consisted of 103 unique sequence heterozygotes and 126 wild-type homozygous controls.,At the temperatu...
Alterations in the rat tuberous sclerosis gene (Tsc2) are responsible for the hereditary renal carcinomas (RCs) of Eker ...
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