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Pathophysiologic consequences following inhibition of a CFTR-dependent developmental cascade in the lung
BACKGROUND: Examination of late gestation developmental genes in vivo may be limited by early embryonic lethality and compensatory mechanisms. This problem is particularly apparent in evaluating the developmental role of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in the cyst...
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| Publicat a: | BMC Dev Biol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2005
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC549215/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15694001/ https://ncbi.nlm.nih.govhttps://doi.org/10.1186/1471-213X-5-2 |
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