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10.1002/dvdy.20982

http://scihub22266oqcxt.onion/10.1002/dvdy.20982
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17072878!ä!17072878

suck abstract from ncbi


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pmid17072878      Dev+Dyn 2006 ; 235 (12): 3413-22
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  • VE-cadherin-CreERT2 transgenic mouse: a model for inducible recombination in the endothelium #MMPMID17072878
  • Monvoisin A; Alva JA; Hofmann JJ; Zovein AC; Lane TF; Iruela-Arispe ML
  • Dev Dyn 2006[Dec]; 235 (12): 3413-22 PMID17072878show ga
  • To introduce temporal control in genetic experiments targeting the endothelium, we established a mouse line expressing tamoxifen-inducible Cre-recombinase (Cre-ERT2) under the regulation of the vascular endothelial cadherin promoter (VECad). Specificity and efficiency of Cre activity was documented by crossing VECad-Cre-ERT2 with the ROSA26R reporter mouse, in which a floxed-stop cassette has been placed upstream of the beta-galactosidase gene. We found that tamoxifen specifically induced widespread recombination in the endothelium of embryonic, neonatal, and adult tissues. Recombination was also documented in tumor-associated vascular beds and in postnatal angiogenesis assays. Furthermore, injection of tamoxifen in adult animals resulted in negligible excision (lower than 0.4%) in the hematopoietic lineage. The VECad-Cre-ERT2 mouse is likely to be a valuable tool to study the function of genes involved in vascular development, homeostasis, and in complex processes involving neoangiogenesis, such as tumor growth.
  • |Animals[MESH]
  • |Animals, Newborn[MESH]
  • |Antigens, CD/*genetics[MESH]
  • |Cadherins/*genetics[MESH]
  • |Endothelium, Vascular/embryology/growth & development/*metabolism[MESH]
  • |Female[MESH]
  • |Genes, Reporter[MESH]
  • |Integrases/*genetics[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Mice, Transgenic[MESH]
  • |Models, Genetic[MESH]
  • |Pregnancy[MESH]
  • |Recombination, Genetic/drug effects[MESH]


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