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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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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2005
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC549215/ https://ncbi.nlm.nih.gov/pubmed/15694001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-213X-5-2 |
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