Annals of Human Genetics · 1995 · 79 citations · 41 references
MedicineGeneticsMolecular GeneticsGene ExpressionMedical GeneticsOncogenesOncogene MutationsOncogenic Signaling PathwaysTuberous Sclerosis ComplexCritical RegionDirect Rna SequencingTsc1 GeneTsc1 Mutations
A novel widely expressed homologue of the VAV oncogene, VAV2 (53% identical residues), has been identified within the critical region for the tuberous sclerosis gene, TSC1, on human chromosome 9q34. By Southern blot analysis, analysis of allele-specific transcription, and direct sequencing of the VAV2 mRNA/cDNA from patient lymphoblastoid cell lines, we demonstrate that both alleles of this gene are expressed in TSC patients and there are no significant mutations. VAV consists of a novel array of signalling domains and is thought to play an important role in signal transduction in haematopoietic tissues where it is exclusively expressed. VAV2 is likely to serve a similar role more generally in mammalian cells, but is not the TSC1 gene.
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Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene
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Strategies for multilocus linkage analysis in humans.
G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text
Life Sciences, Genetics, Genomics +16
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
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