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dc.contributor.authorGierut, J. J.
dc.contributor.authorHaigis, K. M.
dc.contributor.authorJacks, Tyler E.
dc.date.accessioned2018-06-25T18:25:06Z
dc.date.available2018-06-25T18:25:06Z
dc.date.issued2014-04
dc.identifier.issn1559-6095
dc.identifier.urihttp://hdl.handle.net/1721.1/116576
dc.description.abstractThe laboratory mouse is an ideal model organism for studying disease because it is physiologically similar to human and also because its genome is readily manipulated. Genetic engineering allows researchers to introduce specific loss-of-function or gain-of-function mutations into genes and then to study the resulting phenotypes in an in vivo context. One drawback of using traditional transgenic and knockout mice to study human diseases is that many mutations passed through the germline can profoundly affect development, thus impeding the study of disease phenotypes in adults. New technology has made it possible to generate conditional mutations that can be introduced in a spatially and/ or temporally restricted manner. Mouse strains carrying conditional mutations represent valuable experimental models for the study of human diseases and they can be used to develop strategies for prevention and treatment of these diseases. In this article, we will describe the most widely used DNA recombinase systems used to achieve conditional gene mutation in mouse models and discuss how these systems can be employed in vivo.en_US
dc.publisherCold Spring Harbor Laboratory Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1101/PDB.TOP069807en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleStrategies to Achieve Conditional Gene Mutation in Miceen_US
dc.typeArticleen_US
dc.identifier.citationGierut, J. J. et al. “Strategies to Achieve Conditional Gene Mutation in Mice.” Cold Spring Harbor Protocols 2014, 4 (April 2014): 339-349 © 2014 Cold Spring Harbor Laboratory Pressen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorJacks, Tyler E.
dc.relation.journalCold Spring Harbor Protocolsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-06-25T17:02:34Z
dspace.orderedauthorsGierut, J. J.; Jacks, T. E.; Haigis, K. M.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5785-8911
dspace.mitauthor.errortrue
mit.licenseOPEN_ACCESS_POLICYen_US


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