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pubmed-article:15048813pubmed:abstractTextAlteration of the mouse genome through homologous recombination in embryonic stem (ES) cells is the most accurate and versatile way to dissect gene function in a vertebrate model. Most often, a selectable marker is used to create a knockout allele by replacing an essential part of the gene. However, knockout strategies are limited because the mutation is present constitutively. Conditional approaches based on the Cre-loxP site-specific recombination (SSR) system address this limitation; however, it requires that all parts of the targeted gene remain in ES cells. Here we report success with a "knockout-first" strategy that ablates gene function by insertion of RNA processing signals without deletion of any of the target gene. Incorporation of site-specific recombination target sites creates a multipurpose allele for both knockout and conditional applications.lld:pubmed
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pubmed-article:15048813pubmed:authorpubmed-author:ZhangYoumingYlld:pubmed
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pubmed-article:15048813pubmed:authorpubmed-author:GlaserStefanSlld:pubmed
pubmed-article:15048813pubmed:copyrightInfoCopyright 2004 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:15048813pubmed:articleTitleA reliable lacZ expression reporter cassette for multipurpose, knockout-first alleles.lld:pubmed
pubmed-article:15048813pubmed:affiliationBiotec, Technische Universität Dresden, c/o Max Planck Institute of Molecular cell Biology and Genetics, Dresden, Germany.lld:pubmed
pubmed-article:15048813pubmed:publicationTypeJournal Articlelld:pubmed
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