| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties. | Nature | 1993 | 3.43 |
| 2 | Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents. | J Gen Physiol | 1992 | 2.53 |
| 3 | Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium. | Am J Physiol | 1994 | 1.23 |
| 4 | The amino-terminal portion of CFTR forms a regulated Cl- channel. | Cell | 1994 | 1.21 |