| Title |
Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease
|
|---|---|
| Published by |
John Wiley & Sons, Ltd, November 2013
|
| DOI | 10.1002/14651858.cd005599.pub4 |
| Pubmed ID | |
| Authors |
Lee, Tim WR, Southern, Kevin W |
| Abstract |
Cystic fibrosis is caused by a defective gene encoding a protein called the cystic fibrosis transmembrane conductance regulator (CFTR), and is characterised by chronic lung infection resulting in inflammation and progressive lung damage that results in a reduced life expectancy. |
X Demographics
The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 1 | 100% |
Demographic breakdown
| Type | Count | As % |
|---|---|---|
| Members of the public | 1 | 100% |
Mendeley readers
The data shown below were compiled from readership statistics for 39 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 39 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Bachelor | 12 | 31% |
| Researcher | 6 | 15% |
| Student > Ph. D. Student | 6 | 15% |
| Student > Master | 3 | 8% |
| Professor > Associate Professor | 2 | 5% |
| Other | 1 | 3% |
| Unknown | 9 | 23% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 7 | 18% |
| Agricultural and Biological Sciences | 6 | 15% |
| Biochemistry, Genetics and Molecular Biology | 4 | 10% |
| Psychology | 4 | 10% |
| Nursing and Health Professions | 2 | 5% |
| Other | 5 | 13% |
| Unknown | 11 | 28% |