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In this report, we identified a model caused by a mutation in kinesin motor family gene\n                    <jats:italic>kinesin family member 7<\/jats:italic>\n                    . We determined that this gene is required to regulate cell proliferation, patterning, and differentiation in the embryonic diaphragm. We ascertained several functions of retinoid signaling in diaphragm development and gained insight into how perturbations in this signaling network promote the pathogenesis of congenital diaphragmatic hernia.\n                  <\/jats:p>","DOI":"10.1073\/pnas.1222797110","type":"journal-article","created":{"date-parts":[[2013,5,7]],"date-time":"2013-05-07T00:00:47Z","timestamp":1367884847000},"update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":34,"title":["<i>Kif7<\/i>\n                    is required for the patterning and differentiation of the diaphragm in a model of syndromic congenital diaphragmatic hernia"],"prefix":"10.1073","volume":"110","author":[{"given":"Garry L.","family":"Coles","sequence":"first","affiliation":[{"name":"Department of Biomedical Genetics and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kate G.","family":"Ackerman","sequence":"additional","affiliation":[{"name":"Department of 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