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All Rights Reserved. http://resource.belframework.org/belframework/20131211/knowledge/small_corpus.bel http://purl.org/dc/elements/1.1/title BEL Framework Small Corpus Document http://resource.belframework.org/belframework/20131211/knowledge/small_corpus.bel http://purl.org/dc/terms/license Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported License http://resource.belframework.org/belframework/20131211/knowledge/small_corpus.bel http://purl.org/pav/authoredBy http://www.tkuhn.ch/bel2nanopub/RARZYVM5vY2W5NXWUWbEjIRXJIjpMh7j1f3gemibK7TGY#_6 http://resource.belframework.org/belframework/20131211/knowledge/small_corpus.bel http://purl.org/pav/version 20131211 http://www.tkuhn.ch/bel2nanopub/RARZYVM5vY2W5NXWUWbEjIRXJIjpMh7j1f3gemibK7TGY#_5 http://www.w3.org/ns/prov#value In SP-C/Dkk1 embryos, however, BMP4 expression is significantly reduced (Fig. 5J). As discussed above, at E12.5, the efficiency of β-catenin excision in many SP-C/rtTA:tetO-cre X β-cateninflox embryos is less than 100% in some embryos resulting in a mosaic pattern of β-catenin expression in the lung airway epithelium. However, this result proves advantageous since we can determine in a precise cell specific manner whether loss of β-catenin leads to a loss of BMP4. As expected, BMP4 and β-catenin are expressed at high levels in distal airway epithelium in wild-type lungs at E12.5 (Figs. 5K– M). Lungs exhibiting mosaic expression of β-catenin also express BMP4 in a mosaic pattern that closely correlates with presence of β-catenin (Figs. 5N–P). 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