| First Author | Gabriel SE | Year | 1994 |
| Journal | Science | Volume | 266 |
| Issue | 5182 | Pages | 107-9 |
| PubMed ID | 7524148 | Mgi Jnum | J:20778 |
| Mgi Id | MGI:68848 | Doi | 10.1126/science.7524148 |
| Citation | Gabriel SE, et al. (1994) Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model [see comments]. Science 266(5182):107-9 |
| abstractText | The effect of the number of cystic fibrosis (CF) alleles on cholera toxin (CT)-induced intestinal secretion was examined in the CF mouse model. CF mice that expressed no CF transmembrane conductance regulator (CFTR) protein did not secrete fluid in response to CT. Heterozygotes expressed 50 percent of the normal amount of CFTR protein in the intestinal epithelium and secreted 50 percent of the normal fluid and chloride ion in intestinal epithelium and secreted 50 percent of the normal fluid and chloride ion and fluid secretion suggests that CF heterozygotes might possess a selective advantage of resistance to cholera. |
