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Summary
| Description |
The CFTR protein is a channel protein that controls the flow of H2O and Cl- ions into and out of cells inside the lungs. When the CFTR protein is working correctly, as shown in Panel 1, ions freely flow in and out of the cells. However, when the CFTR protein is malfunctioning as in Panel 2, these ions cannot flow out of the cell due to a blocked channel. This causes Cystic Fibrosis, characterized by the buildup of thick mucus in the lungs. |
| Date | |
| Source | Own work |
| Author | Lbudd14 |
Licensing
I, the copyright holder of this work, hereby publish it under the following license:
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 13:02, 24 May 2013 | | 512 × 384 (94 KB) | Lbudd14 | New version uses all available space. |
| 17:06, 22 May 2013 |  | 512 × 384 (94 KB) | Lbudd14 | User created page with UploadWizard |
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