| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7636719 | Journal of Proteomics | 2014 | 39 Pages |
Abstract
Schematic drawing showing interactions between the cystic fibrosis transmembrane conductance regulator (CFTR) and the porosome complex at the cell plasma membrane in human airway epithelia. The possible regulation by CFTR on the quality of mucus secreted via the porosome complex, such as highly viscous mucus resulting from CFTR defects is hypothesized.120
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Authors
Xia Hou, Kenneth T. Lewis, Qingtian Wu, Sunxi Wang, Xuequn Chen, Amanda Flack, Guangzhao Mao, Douglas J. Taatjes, Fei Sun, Bhanu P. Jena,