| 1 | 1279436 | Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding. | Nature | 1992 Nov 5 |
5 |
| 2 | 1281032 | Milestones in cystic fibrosis. | Br Med Bull | 1992 Oct |
3 |
| 3 | 1281035 | Abnormalities in intracellular regulation in cystic fibrosis. | Br Med Bull | 1992 Oct |
2 |
| 4 | 1281220 | Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents. | J Gen Physiol | 1992 Oct |
15 |
| 5 | 1282296 | Antisense oligonucleotides to CFTR confer a cystic fibrosis phenotype on B lymphocytes. | Am J Physiol | 1992 Dec |
3 |
| 6 | 1282304 | CFTR channels in immortalized human airway cells. | Am J Physiol | 1992 Dec |
6 |
| 7 | 1284810 | [Molecular biological analysis of cystic fibrosis--a model example for the strategy of "reverse genetics"]. | Padiatr Grenzgeb | 1992 |
2 |
| 8 | 1302038 | Deficient nifedipine oxidation: a rare inherited trait associated with cystic fibrosis kindreds. | Pharmacogenetics | 1992 Feb |
1 |
| 9 | 1347041 | P-glycoprotein. ATP hydrolysis by the N-terminal nucleotide-binding domain. | J Biol Chem | 1992 Mar 5 |
2 |
| 10 | 1365829 | The molecular biology of chloride channels. | Curr Opin Nephrol Hypertens | 1992 Oct |
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| 11 | 1370488 | Biochemical characterization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis epithelial cells. | J Biol Chem | 1992 Jan 25 |
2 |
| 12 | 1370653 | In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium. | Cell | 1992 Jan 10 |
2 |
| 13 | 1370810 | Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. | Hum Genet | 1992 Jan |
2 |
| 14 | 1371114 | Human lymphocytes transcribe the cystic fibrosis transmembrane conductance regulator gene and exhibit CF-defective cAMP-regulated chloride current. | J Biol Chem | 1992 Feb 15 |
6 |
| 15 | 1371239 | Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR). | Cell | 1992 Feb 21 |
1 |
| 16 | 1371598 | Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein. | Nature | 1992 Feb 27 |
1 |
| 17 | 1371641 | Antibodies against the cystic fibrosis transmembrane regulator. | Am J Physiol | 1992 Feb |
3 |
| 18 | 1371876 | Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein. | Proc Natl Acad Sci U S A | 1992 Mar 1 |
2 |
| 19 | 1372005 | Cellular differentiation is required for cAMP but not Ca(2+)-dependent Cl- secretion in colonic epithelial cells expressing high levels of cystic fibrosis transmembrane conductance regulator. | J Biol Chem | 1992 Mar 15 |
1 |
| 20 | 1372253 | Transfection of wild-type CFTR into cystic fibrosis lymphocytes restores chloride conductance at G1 of the cell cycle. | EMBO J | 1992 Mar |
2 |
| 21 | 1372390 | Down-regulation of cystic fibrosis transmembrane conductance regulator gene expression by agents that modulate intracellular divalent cations. | Mol Cell Biol | 1992 Apr |
8 |
| 22 | 1372891 | The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide. | J Biol Chem | 1992 Mar 25 |
5 |
| 23 | 1373728 | Antibody against a cystic fibrosis transmembrane conductance regulator-derived synthetic peptide inhibits anion currents in human colonic cell line T84. | J Biol Chem | 1992 Apr 25 |
5 |
| 24 | 1373908 | Regulation of plasma membrane recycling by CFTR. | Science | 1992 Apr 24 |
4 |
| 25 | 1375156 | Quantitative expression patterns of multidrug-resistance P-glycoprotein (MDR1) and differentially spliced cystic-fibrosis transmembrane-conductance regulator mRNA transcripts in human epithelia. | Eur J Biochem | 1992 May 15 |
2 |
| 26 | 1375221 | Induction of expression of the cystic fibrosis transmembrane conductance regulator. | J Biol Chem | 1992 May 25 |
3 |
| 27 | 1375432 | cAMP-activated Cl channels in CFTR-transfected cystic fibrosis pancreatic epithelial cells. | Am J Physiol | 1992 May |
5 |
| 28 | 1376017 | Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians. | Am J Hum Genet | 1992 Jun |
1 |
| 29 | 1376923 | A1 adenosine-receptor antagonists activate chloride efflux from cystic fibrosis cells. | Proc Natl Acad Sci U S A | 1992 Jun 15 |
1 |
| 30 | 1377674 | Phosphorylation of the cystic fibrosis transmembrane conductance regulator. | J Biol Chem | 1992 Jun 25 |
3 |
| 31 | 1378393 | Regulation of CFTR expression and function during differentiation of intestinal epithelial cells. | EMBO J | 1992 Jul |
1 |
| 32 | 1378996 | Altered sulfate transport via anion exchange in CFPAC is corrected by retrovirus-mediated CFTR gene transfer. | Am J Physiol | 1992 Jul |
3 |
| 33 | 1379413 | Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus. | Am J Hum Genet | 1992 Aug |
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| 34 | 1379589 | Expression of the cystic fibrosis transmembrane conductance regulator gene can be regulated by protein kinase C. | J Biol Chem | 1992 Aug 15 |
11 |
| 35 | 1379613 | Localization of cystic fibrosis transmembrane conductance regulator mRNA in human fetal lung tissue by in situ hybridization. | J Clin Invest | 1992 Aug |
6 |
| 36 | 1379720 | Antisense oligodeoxynucleotides to the cystic fibrosis transmembrane conductance regulator inhibit cAMP-activated but not calcium-activated chloride currents. | Proc Natl Acad Sci U S A | 1992 Aug 1 |
10 |
| 37 | 1380673 | Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive. | Nature | 1992 Aug 27 |
4 |
| 38 | 1380724 | Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis. | Science | 1992 Aug 21 |
2 |
| 39 | 1381146 | CFTR! | Am J Physiol | 1992 Aug |
2 |
| 40 | 1381442 | Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease. | J Med Genet | 1992 Aug |
1 |
| 41 | 1381723 | Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis. | J Clin Invest | 1992 Sep |
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| 42 | 1382316 | Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains. | Science | 1992 Sep 18 |
8 |
| 43 | 1384582 | Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium. | Am J Respir Cell Mol Biol | 1992 Nov |
7 |
| 44 | 1385255 | The origin of and subcellular mechanisms causing pancreatic bicarbonate secretion. | Gastroenterology | 1992 Nov |
3 |
| 45 | 1551244 | Cystic fibrosis in adolescents and adults. The coming of age of cystic fibrosis. | Dig Dis | 1992 |
2 |
| 46 | 1691449 | A frame-shift mutation in the cystic fibrosis gene. | Nature | 1990 Apr 12 |
1 |
| 47 | 1695717 | A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. | Nature | 1990 Jul 26 |
1 |
| 48 | 1698126 | Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer. | Cell | 1990 Sep 21 |
4 |
| 49 | 1705179 | Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance. | Cell | 1991 Feb 22 |
2 |
| 50 | 1706279 | Immunological localization of cystic fibrosis candidate gene products. | Exp Cell Res | 1991 Apr |
2 |