| pubmed-article:18601749 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18601749 | lifeskim:mentions | umls-concept:C0105770 | lld:lifeskim |
| pubmed-article:18601749 | lifeskim:mentions | umls-concept:C1160389 | lld:lifeskim |
| pubmed-article:18601749 | lifeskim:mentions | umls-concept:C0037083 | lld:lifeskim |
| pubmed-article:18601749 | lifeskim:mentions | umls-concept:C1413365 | lld:lifeskim |
| pubmed-article:18601749 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
| pubmed-article:18601749 | pubmed:dateCreated | 2008-7-15 | lld:pubmed |
| pubmed-article:18601749 | pubmed:abstractText | Cystic fibrosis transmembrane conductance regulator (CFTR) was shown previously to modify stretch induced differentiation in the lung. The mechanism for CFTR modulation of lung development was examined by in utero gene transfer of either a sense or antisense construct to alter CFTR expression levels. The BAT-gal transgenic reporter mouse line, expressing beta-galactosidase under a canonical Wnt/beta-catenin-responsive promoter, was used to assess the relative roles of CFTR, Wnt, and parathyroid hormone-related peptide (PTHrP) in lung organogenesis. Adenoviruses containing full-length CFTR, a short anti-sense CFTR gene fragment, or a reporter gene as control were used in an intra-amniotic gene therapy procedure to transiently modify CFTR expression in the fetal lung. | lld:pubmed |
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| pubmed-article:18601749 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18601749 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18601749 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18601749 | pubmed:issn | 1471-213X | lld:pubmed |
| pubmed-article:18601749 | pubmed:author | pubmed-author:TakemaruKen-I... | lld:pubmed |
| pubmed-article:18601749 | pubmed:author | pubmed-author:KilleenErinE | lld:pubmed |
| pubmed-article:18601749 | pubmed:author | pubmed-author:LarsonJanet... | lld:pubmed |
| pubmed-article:18601749 | pubmed:author | pubmed-author:CohenJ... | lld:pubmed |
| pubmed-article:18601749 | pubmed:author | pubmed-author:LoveDamonD | lld:pubmed |
| pubmed-article:18601749 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18601749 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:18601749 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18601749 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18601749 | pubmed:pagination | 70 | lld:pubmed |
| pubmed-article:18601749 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:18601749 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18601749 | pubmed:articleTitle | CFTR and Wnt/beta-catenin signaling in lung development. | lld:pubmed |
| pubmed-article:18601749 | pubmed:affiliation | The Brady Laboratory, Section of Neonatology, Department of Pediatrics, Stony Brook University, School of Medicine, Stony Brook, New York, USA. jcraig.cohen@stonybrook.edu | lld:pubmed |
| pubmed-article:18601749 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18601749 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18601749 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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