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Mouse Strains for the Ubiquitous or Conditional Overexpression of the Flii Gene

dc.contributor.authorThomsen, Nicole
dc.contributor.authorChappell, Anna
dc.contributor.authorAli, Radiya
dc.contributor.authorJones, Tamsin
dc.contributor.authorAdams, Damian H
dc.contributor.authorMatthaei, Klaus
dc.contributor.authorCampbell, Hugh
dc.contributor.authorCowin, Allison J
dc.contributor.authorArkell, Ruth
dc.date.accessioned2015-12-10T23:07:56Z
dc.date.issued2011
dc.date.updated2016-02-24T12:08:26Z
dc.description.abstractThe gelsolin related actin binding protein, Flii, is able to regulate wound healing; mice with decreased Flii expression show improved wound healing whereas mice with elevated Flii expression exhibit impaired wound healing. In both mice and humans Flii expression increases with age and amelioration of FLII activity represents a possible therapeutic strategy for improved wound healing in humans. Despite analysis of Flii function in a variety of organisms we know little of the molecular mechanisms underlying Flii action. Two new murine alleles of Flii have been produced to drive constitutive or tissue-specific expression of Flii. Each strain is able to rescue the embryonic lethality associated with a Flii null allele and to impair wound healing. These strains provide valuable resources for ongoing investigation of Flii function in a variety of biological processes. genesis 49:681-688, 2011.
dc.identifier.issn1526-954X
dc.identifier.urihttp://hdl.handle.net/1885/63083
dc.publisherWiley-Liss Inc
dc.sourceGenesis
dc.subjectKeywords: allele; animal cell; animal experiment; animal model; animal tissue; article; controlled study; female; Flii gene; gene; gene function; gene overexpression; lethality; mouse; mouse strain; nonhuman; null allele; priority journal; wound healing; Animals; B ROSA26; Wound healing
dc.titleMouse Strains for the Ubiquitous or Conditional Overexpression of the Flii Gene
dc.typeJournal article
local.bibliographicCitation.lastpage688
local.bibliographicCitation.startpage681
local.contributor.affiliationThomsen, Nicole, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationChappell, Anna, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationAli, Radiya, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationJones, Tamsin, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationAdams, Damian H, Women's and Children's Health Research Institute
local.contributor.affiliationMatthaei, Klaus, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationCampbell, Hugh, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationCowin, Allison J, Women's and Children's Health Research Institute
local.contributor.affiliationArkell, Ruth, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidThomsen, Nicole, u4515540
local.contributor.authoruidChappell, Anna, u3630997
local.contributor.authoruidAli, Radiya, u4391797
local.contributor.authoruidJones, Tamsin, u4500219
local.contributor.authoruidMatthaei, Klaus, u8200697
local.contributor.authoruidCampbell, Hugh, u7900069
local.contributor.authoruidArkell, Ruth, u4350791
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor060103 - Cell Development, Proliferation and Death
local.identifier.absfor060403 - Developmental Genetics (incl. Sex Determination)
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciences
local.identifier.ariespublicationu9511635xPUB767
local.identifier.citationvolume49
local.identifier.doi10.1002/dvg.20735
local.identifier.scopusID2-s2.0-80051565068
local.identifier.thomsonID000294177600005
local.type.statusPublished Version

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