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5. 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]
6. Toward defining the function of the cystic fibrosis gene product. Forstner GG J Pediatr Gastroenterol Nutr; 1991 Nov; 13(4):432-3. PubMed ID: 1723427 [No Abstract] [Full Text] [Related]
7. Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties. Sheppard DN; Rich DP; Ostedgaard LS; Gregory RJ; Smith AE; Welsh MJ Nature; 1993 Mar; 362(6416):160-4. PubMed ID: 7680769 [TBL] [Abstract][Full Text] [Related]
8. Cystic fibrosis. The mutant protein responds. Wine JJ Nature; 1991 Dec 19-26; 354(6354):503-4. PubMed ID: 1722026 [No 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]
10. Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells. Schoumacher RA; Shoemaker RL; Halm DR; Tallant EA; Wallace RW; Frizzell RA Nature; 1987 Dec 24-31; 330(6150):752-4. PubMed ID: 2447502 [TBL] [Abstract][Full Text] [Related]
11. No way out. Nat Genet; 1992 Aug; 1(5):311-2. PubMed ID: 1284547 [No Abstract] [Full Text] [Related]
12. Studies on human porin XXI: gadolinium opens Up cell membrane standing porin channels making way for the osmolytes chloride or taurine-A putative approach to activate the alternate chloride channel in cystic fibrosis. Thinnes FP; Hellmann KP; Hellmann T; Merker R; Schwarzer C; Walter G; Götz H; Hilschmann N Mol Genet Metab; 2000 Mar; 69(3):240-51. PubMed ID: 10767179 [TBL] [Abstract][Full Text] [Related]