Transgenic Res. 1999;8(6):451-8. Unique Identifier : AIDSLINE GENBANK/AF064783
Neilan EG; Barsh GS; Department of Pediatrics, Stanford University, Palo Alto, CA; 94305, USA.
Abstract: Insertional mutagenesis based on gene trap vectors that capture endogenous splice sites is a promising tool for functional genomics. Several groups have proposed large-scale gene trap screens, but questions remain as to the type of vectors and their design. We report a set of plasmid-encoded gene trap vectors and the disruption of two novel genes. Our results include a comparison of the relative gene trapping efficiencies of two different splice acceptor sequences in ES cells and an analysis of the structure of several gene trap insertions.
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