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dc.contributor.authorGeorgiades, Pantelisen
dc.contributor.authorOgilvy, S.en
dc.contributor.authorDuval, H.en
dc.contributor.authorLicence, D. R.en
dc.contributor.authorCharnock-Jones, D. S.en
dc.contributor.authorSmith, S. K.en
dc.contributor.authorPrint, C. G.en
dc.creatorGeorgiades, Pantelisen
dc.creatorOgilvy, S.en
dc.creatorDuval, H.en
dc.creatorLicence, D. R.en
dc.creatorCharnock-Jones, D. S.en
dc.creatorSmith, S. K.en
dc.creatorPrint, C. G.en
dc.date.accessioned2019-11-04T12:50:37Z
dc.date.available2019-11-04T12:50:37Z
dc.date.issued2002
dc.identifier.issn1526-954X
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53092
dc.description.abstractCre transgenic mice can be used to delete gene sequences flanked by loxP sites in specific somatic tissues. We have generated vavCre transgenic mice, which can be used to inactivate genes specifically in adult hematopoietic and endothelial cells. In these animals, a Cre transgene is expressed under control of murine vav gene regulatory elements. To assess their usefulness, vavCre transgenic mice were bred with R26R mice, which express a lacZ reporter gene only in cells where Cre-mediated recombination has occurred. VavCre/R26R double-heterozygous offspring were analyzed by β-galactosidase histochemistry and flow cytometry. VavCre-mediated recombination occurred in most hematopoietic cells of all hematopoietic organs, including the hematopoietic progenitor-rich bone marrow. Recombination also occurred In most endothelial and germ cells, but only rarely in other cell types. The recombination in both hematopoietic and endothelial lineages may partly reflect their putative shared ontogeny and provides a unique tool for simultaneous pan-hematopoietic and endothelial mutagenesis. © 2002 Wiley-Liss, Inc.en
dc.sourceGenesisen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-6444245017&doi=10.1002%2fgene.10161&partnerID=40&md5=79fac1ccab75622f34449b3ed088f591
dc.subjectarticleen
dc.subjectpriority journalen
dc.subjectgenotypeen
dc.subjectgene expression regulationen
dc.subjectnonhumanen
dc.subjectimmunocytochemistryen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal cellen
dc.subjectmouseen
dc.subjectpolymerase chain reactionen
dc.subjectViral Proteinsen
dc.subjectHematopoietic Stem Cellsen
dc.subjectnucleotide sequenceen
dc.subjectAnimaliaen
dc.subjectMurinaeen
dc.subjectgenetic recombinationen
dc.subjectbeta galactosidaseen
dc.subjectOncogene Proteinsen
dc.subjectmutagenesisen
dc.subjectRecombination, Geneticen
dc.subjectMus musculusen
dc.subjecthistochemistryen
dc.subjectcomplementary DNAen
dc.subjectcre recombinaseen
dc.subjectIntegrasesen
dc.subjectCell Lineageen
dc.subjectCreen
dc.subjectEndothelialen
dc.subjectEndotheliumen
dc.subjectendothelium cellen
dc.subjectFlow Cytometryen
dc.subjectfluorescence activated cell sortingen
dc.subjectGenes, Reporteren
dc.subjectHematopoieticen
dc.subjecthematopoietic cellen
dc.subjectLeukocytesen
dc.subjectMice, Transgenicen
dc.subjectProto-Oncogene Proteins c-vaven
dc.subjectreporter geneen
dc.subjectTransgenesen
dc.subjecttransgenic mouseen
dc.subjectvaven
dc.titlevavCre transgenic mice: A tool for mutagenesis in hematopoietic and endothelial lineagesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/gene.10161
dc.description.volume34
dc.description.startingpage251
dc.description.endingpage256
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :74</p>en
dc.source.abbreviationGenesisen
dc.contributor.orcidGeorgiades, Pantelis [0000-0002-5538-3163]
dc.gnosis.orcid0000-0002-5538-3163


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