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14. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation. Dalemans W; Barbry P; Champigny G; Jallat S; Dott K; Dreyer D; Crystal RG; Pavirani A; Lecocq JP; Lazdunski M Nature; 1991 Dec 19-26; 354(6354):526-8. PubMed ID: 1722027 [TBL] [Abstract][Full Text] [Related]
15. 50 years ago in the Journal of Pediatrics: A note on studies of salt excretion in sweat: relationships between rate, conductivity, and electrolyte composition of sweat from patients with cystic fibrosis and from control subjects. Gibson, LE, di Sant’Agnese, PA. J Pediatr 1963;62:855-67. Gonska T J Pediatr; 2013 Jun; 162(6):1187. PubMed ID: 23708418 [No Abstract] [Full Text] [Related]
16. No way out. Nat Genet; 1992 Aug; 1(5):311-2. PubMed ID: 1284547 [No Abstract] [Full Text] [Related]
17. Pseudomonas-epithelial cell interactions dissected with DNA microarrays. Lory S; Ichikawa JK Chest; 2002 Mar; 121(3 Suppl):36S-39S. PubMed ID: 11893678 [No Abstract] [Full Text] [Related]
18. Failure of local defense mechanisms in cystic fibrosis. Proesmans M; De Boeck K Acta Otorhinolaryngol Belg; 2000; 54(3):367-72. PubMed ID: 11082773 [TBL] [Abstract][Full Text] [Related]
19. Cystic fibrosis transmembrane conductance regulator protein: what is its role in cystic fibrosis? Richardson PS; Alton EW Eur Respir J; 1993 Feb; 6(2):160-2. PubMed ID: 7680321 [No Abstract] [Full Text] [Related]
20. How mutant CFTR may contribute to Pseudomonas aeruginosa infection in cystic fibrosis. Pier GB; Grout M; Zaidi TS; Goldberg JB Am J Respir Crit Care Med; 1996 Oct; 154(4 Pt 2):S175-82. PubMed ID: 8876538 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]