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2. Regulation of endocytic trafficking and acidification are independent of the cystic fibrosis transmembrane regulator. Dunn KW; Park J; Semrad CE; Gelman DL; Shevell T; McGraw TE J Biol Chem; 1994 Feb; 269(7):5336-45. PubMed ID: 7508934 [TBL] [Abstract][Full Text] [Related]
3. Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis. Clarke LL; Grubb BR; Gabriel SE; Smithies O; Koller BH; Boucher RC Science; 1992 Aug; 257(5073):1125-8. PubMed ID: 1380724 [TBL] [Abstract][Full Text] [Related]
4. cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator. Rommens JM; Dho S; Bear CE; Kartner N; Kennedy D; Riordan JR; Tsui LC; Foskett JK Proc Natl Acad Sci U S A; 1991 Sep; 88(17):7500-4. PubMed ID: 1715567 [TBL] [Abstract][Full Text] [Related]
5. Long-term cAMP activation of Na(+)-K(+)-2Cl- cotransporter activity in HT-29 human adenocarcinoma cells. Slotki IN; Breuer WV; Greger R; Cabantchik ZI Am J Physiol; 1993 Apr; 264(4 Pt 1):C857-65. PubMed ID: 7682775 [TBL] [Abstract][Full Text] [Related]
6. Increasing expression of the normal human CFTR cDNA in cystic fibrosis epithelial cells results in a progressive increase in the level of CFTR protein expression, but a limit on the level of cAMP-stimulated chloride secretion. Rosenfeld MA; Rosenfeld SJ; Danel C; Banks TC; Crystal RG Hum Gene Ther; 1994 Sep; 5(9):1121-9. PubMed ID: 7530494 [TBL] [Abstract][Full Text] [Related]
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]
9. Plasma membrane recycling in CFTR-expressing CHO cells. Dho S; Grinstein S; Foskett JK Biochim Biophys Acta; 1993 Nov; 1225(1):78-82. PubMed ID: 7694659 [TBL] [Abstract][Full Text] [Related]
10. Regulated trafficking of the CFTR chloride channel. Kleizen B; Braakman I; de Jonge HR Eur J Cell Biol; 2000 Aug; 79(8):544-56. PubMed ID: 11001491 [TBL] [Abstract][Full Text] [Related]
11. Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator. Schwiebert EM; Morales MM; Devidas S; Egan ME; Guggino WB Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2674-9. PubMed ID: 9482946 [TBL] [Abstract][Full Text] [Related]
12. Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents. Fulmer SB; Schwiebert EM; Morales MM; Guggino WB; Cutting GR Proc Natl Acad Sci U S A; 1995 Jul; 92(15):6832-6. PubMed ID: 7542778 [TBL] [Abstract][Full Text] [Related]
13. Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line. Kopelman H; Gauthier C; Bornstein M J Clin Invest; 1993 Mar; 91(3):1253-7. PubMed ID: 7680666 [TBL] [Abstract][Full Text] [Related]
14. Activation of the cystic fibrosis transmembrane regulator by cyclic AMP is not correlated with inhibition of endocytosis. Santos GF; Reenstra WW Biochim Biophys Acta; 1994 Oct; 1195(1):96-102. PubMed ID: 7522569 [TBL] [Abstract][Full Text] [Related]
15. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients. Dray-Charier N; Paul A; Scoazec JY; Veissière D; Mergey M; Capeau J; Soubrane O; Housset C Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100 [TBL] [Abstract][Full Text] [Related]