...TSC2. The samples consisted of 103 unique sequence heterozygotes and 126 wild-type homozygous controls.,At the temperatu...
...TSC2 activity affecting neuronal migration.
...TSC2 gene product, in brain resections from children with and without tuberous sclerosis, to characterize the phenotype ...
...TSC2. We developed a murine model of Tsc2 disease using a gene targeting approach. Tsc2-null embryos die at embryonic da...
...TSC2 gene, was expressed. In 19 angiomyolipomas from a TSC2-linked patient, in whose angiomyolipomas loss of tuberin exp...
...TSC2 gene in the tumour. The primary mutation Q478X in this patient was identified in exon 13 of the TSC2 gene on chromo...
...TSC2, in peripheral blood leukocytes from the patient were analyzed by polymerase chain reaction-single strand conformat...
Two genes, mutations in which result in the phenotype of tuberous sclerosis (TSC), have recently been cloned. TSC2 on ch...
...TSC2 gene on chromosome 16 encodes a 1784-amino acid putative tumour suppressor protein, tuberin, that functions as a GT...
...TSC2 (16p13), and NF2 (22q12), but no known tumor suppressor gene localizes to 3q27. The mean fractional allelic loss am...
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