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1 We generated mice lacking Fbxw8 by gene trapping.
2 are accessible by either targeted or random gene trapping.
3 findings suggest that the probability that a gene trapping AAV integration event occurs is influenced
4 ivation by stable inversion of the cassette, gene trapping and mRFP expression, and the expected muta
10 epidermal differentiation, we used enzymatic gene trapping combined with immunohistochemical, ultrast
11 reated by either targeted gene disruption or gene trapping display a wide range of phenotypes associa
16 rovirus-mediated mutagenesis method based on gene trapping in embryonic stem cells was used to identi
22 se using a combination of gene targeting and gene trapping in mouse embryonic stem (ES) cells and to
30 hly scalable approach integrating methods of gene-trapping, microarray-based expression analysis, and
34 ay alter normal gene transcription either by gene-trapping or by introducing PTCs through exonization
35 demonstrate that intronic insertions in the gene-trapping orientation severely disrupt the expressio
40 Our results demonstrate that the inducible gene trapping system described here can be used to enric
41 Complex trait analysis, gene-targeting and gene-trapping technologies, as well as insertional and c
42 high-throughput mutagenesis method based on gene trapping that allows the automated identification o
43 c analysis using homologous recombination or gene trapping to produce deletion or insertion mutants.
44 hat had been trapped by random (nontargeted) gene trapping with the same vector shows that virtually