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7. 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]
8. [The cystic fibrosis gene: mutation and the function of CFTR protein]. Goossens M Ann Pediatr (Paris); 1991 Nov; 38(9):591-4. PubMed ID: 1721508 [TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis: current concepts. Abrons HL W V Med J; 1993 Jun; 89(6):236-40. PubMed ID: 7686701 [TBL] [Abstract][Full Text] [Related]
18. [Molecular basis of cystic fibrosis]. Bal J Postepy Biochem; 1991; 37(3-4):153-8. PubMed ID: 1725923 [No Abstract] [Full Text] [Related]
19. Complex mutation 4114 ATA-->TT in exon 22 of the cystic fibrosis gene CFTR. Dörk T; Fislage R; Tümmler B Hum Mutat; 1993; 2(6):489-91. PubMed ID: 7509237 [No Abstract] [Full Text] [Related]
20. Cystic fibrosis: a disease caused by a single defect in salt-transporting epithelial cells. Williams JC J S C Med Assoc; 1992 Jul; 88(7):331-8. PubMed ID: 1380107 [No Abstract] [Full Text] [Related] [Next] [New Search]