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Dimeric cystic fibrosis transmembrane conductance regulator exists in the plasma membrane.
CFTR (cystic fibrosis transmembrane conductance regulator) mediates chloride conduction across the apical membrane of epithelia, and mutations in CFTR lead to defective epithelial fluid transport. Recently, there has been considerable interest in determining the quaternary structure of CFTR at the c...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1223644/ https://ncbi.nlm.nih.gov/pubmed/12820897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20030683 |
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