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Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung
The CFTR gene encodes a transmembrane conductance regulator, which is dysfunctional in patients with cystic fibrosis (CF). The mechanism by which defective CFTR (CF transmembrane conductance regulator) leads to undersialylation of plasma membrane glycoconjugates, which in turn promote lung pathology...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The National Academy of Sciences
2001
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC61151/ https://ncbi.nlm.nih.gov/pubmed/11717455 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.241182598 |
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