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CFTR Expression Regulation by the Unfolded Protein Response
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel and key regulator of epithelial functions. Mutations in the CFTR gene lead to reduced or dysfunctional CFTR protein and cause cystic fibrosis (CF), a generalized exocrinopathy affecting multiple organs. In the airwa...
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| Publicado no: | Methods Enzymol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4415166/ https://ncbi.nlm.nih.gov/pubmed/21329791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/B978-0-12-385928-0.00001-8 |
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