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5. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells. Rich DP; Anderson MP; Gregory RJ; Cheng SH; Paul S; Jefferson DM; McCann JD; Klinger KW; Smith AE; Welsh MJ Nature; 1990 Sep; 347(6291):358-63. PubMed ID: 1699126 [TBL] [Abstract][Full Text] [Related]
6. The gene defect in cystic fibrosis and clinical applications of the knowledge. Super M J R Soc Med; 1992; 85 Suppl 19(Suppl 19):6-8. PubMed ID: 1375961 [No Abstract] [Full Text] [Related]
7. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Welsh MJ; Smith AE Cell; 1993 Jul; 73(7):1251-4. PubMed ID: 7686820 [No Abstract] [Full Text] [Related]
8. Towards the biochemical defect in cystic fibrosis. Lancet; 1989 Dec; 2(8677):1433. PubMed ID: 2480500 [No Abstract] [Full Text] [Related]
9. Novel function discovered for the cystic fibrosis gene. Barinaga M Science; 1992 Apr; 256(5056):444-5. PubMed ID: 1373905 [No Abstract] [Full Text] [Related]
10. Pulmonary disease severity in men with deltaF508 cystic fibrosis and residual chloride secretion. Thomas SR; Jaffe A; Geddes DM; Hodson ME; Alton EW Lancet; 1999 Mar; 353(9157):984-5. PubMed ID: 10459916 [No Abstract] [Full Text] [Related]