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                <identifier>oai:data.mendeley.com/x3r8fcnkpc.2</identifier>
                <datestamp>2020-04-02T16:23:10Z</datestamp>
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    <dc:creator>Lab, Simons</dc:creator>
    <dc:title>A study of SMCs phenotype in TGFβR2iSMC-Apoe and TGFβR2iSMC-Ldlr mice Chen et al. Related to Fig 2</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Data Related to Fig 2. A mouse line carrying floxed Tgfbr2 and SMC lineage-tracing mT/mG alleles under control of a myosin heavy chain (Myh11) promoter on an Ldlr null background (Ldlr-/-;Myh11CreERT2;mT/mGf/f;Tgfbr2f/f) hereafter called TGFβR2iSMC-Ldlr. These mice were treated with Tamoxifen at 6 week of age and fed high cholesterol high fat diet for 4 months. Ascending aorta smooth muscle cells from these mice express macrophage, chondrocyte, adipocyte, and osteoblast lineage markers as shown by immunocytochemistry and qRT-PCT from laser micro dissection tissues compared to controls.</dc:description>
    <dc:subject>Aorta</dc:subject>
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    <dc:identifier>oai:data.mendeley.com/x3r8fcnkpc.2</dc:identifier>
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