A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene : a site for rare mutationsMERCIER, B; LISSENS, W; SAVOV, A et al.Journal of medical genetics. 1994, Vol 31, Num 9, pp 731-734, issn 0022-2593Article

Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gatingGUNDERSON, K. L; KOPITO, R. R.The Journal of biological chemistry (Print). 1994, Vol 269, Num 30, pp 19349-19353, issn 0021-9258Article

Partial purification of the cystic fibrosis transmembrane conductance regulatorOSTEDGAARD, L. S; WELSH, M. J.The Journal of biological chemistry (Print). 1992, Vol 267, Num 36, pp 26142-26149, issn 0021-9258Article

Activation of the cystic fibrosis transmembrane conductance regulator by cGMP in the human colonic cancer cell line, caco-2XIAO-YING TIEN; BRASITUS, T. A; KAETZEL, M. A et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 1, pp 51-54, issn 0021-9258Article

Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl^- conductanceSTUTTS, M. J; GABRIEL, S. E; PRICE, E. M et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 12, pp 8667-8674, issn 0021-9258Article

The cystic fibrosis transmembrane conductance regulator : overexpression, purification, and characterization of wild type and ΔF508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding proteinYOUNG HEE KO; THOMAS, P. J; DELANNOY, M. R et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 32, pp 24330-24338, issn 0021-9258Article

CFTR : development of high- affinity antibodies and localization in sweat glandCOHN, J. A; MELHUS, O; PAGE, L. J et al.Biochemical and biophysical research communications (Print). 1991, Vol 181, Num 1, pp 36-43, issn 0006-291XArticle

Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sitesXIU-BAO CHANG; TABCHARANI, J. A; YUE-XIAN HOU et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 15, pp 11304-11311, issn 0021-9258Article

Protein kinase C mediates down-regulation of cystic fibrosis transmenbrane conductance regulator levels in epithelial cellsBREUER, W; GLICKSTEIN, H; KARTNER, N et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 19, pp 13935-13939, issn 0021-9258Article

Biochemical characterization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis epithalial cellsSARKADI, B; BAUZON, D; HUCKLE, W. R et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 3, pp 2087-2095, issn 0021-9258Article

Ultrastructural localization of variant forms of cystic fibrosis transmembrane conductance regulator in human bronchial epithelia of xenograftsYIPING YANG; ENGELHARDT, J. F; WILSON, J. M et al.American journal of respiratory cell and molecular biology. 1994, Vol 11, Num 1, pp 7-15, issn 1044-1549Article

Characterization of the cystic fibrosis transmembrane conductance regulator promoter region : chromatin context and tissue-specificityKOH, J; SFERRA, T. J; COLLINS, F. S et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 21, pp 15912-15921, issn 0021-9258Article

Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulatorTRAVIS, S. M; CARSON, M. R; RIES, D. R et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 21, pp 15336-15339, issn 0021-9258Article

The δF508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane : determination of functional half-lives on transfected cellsLUKACS, G. L; XIU-BAO CHANG; BEAR, C et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 29, pp 21592-21598, issn 0021-9258Article

Aberrant CFTR-dependent HCO₃^- transport in mutations associated with cystic fibrosisJOO YOUNG CHOL; MUALLEM, Danlella; KISELYOV, Kirill et al.Nature (London). 2001, Vol 410, Num 6824, pp 94-97, issn 0028-0836Article

Cystic fibrosis and the pancreas: Recent scientific advancesNOUSIA-ARVANITAKIS, S.Journal of clinical gastroenterology. 1999, Vol 29, Num 2, pp 138-142, issn 0192-0790Article

Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population : 43 mutations account for only 78% of CF chromosomesCHILLON, M; CASALS, T; GIMENEZ, J et al.Human genetics. 1994, Vol 93, Num 4, pp 447-451, issn 0340-6717Article

Effect of cAMP on intracellular and extracellular ATP content of Cl^--secreting epithelia and 3T3 fibroblastsTAKAHASHI, T; MATSUSHITA, K; WELSH, M. J et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 27, pp 17853-17857, issn 0021-9258Article

Functional consequences of heterologous expression of the cystic fibrosis transmembrane conductance regulator in fibroblastsSTUTTS, M. J; GABRIEL, S. E; OLSEN, J. C et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 27, pp 20653-20658, issn 0021-9258Article

Avances moleculares en la fibrosis quística = Molecular development in cystic fibrosisTRUJILLO, C. J.AMC. Acta médica colombiana. 1993, Vol 18, Num 1, pp 51-55, issn 0120-2448Conference Paper

Tumor necrosis factor modulation of expression of the cystic fibrosis transmembrane conductance regulator geneNAKAMURA, H; YOSHIMURA, K; BAJOCCHI, G et al.FEBS letters. 1992, Vol 314, Num 3, pp 366-370, issn 0014-5793Article

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulatorROMMENS, J. M; DHO, S; BEAR, C. E et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 17, pp 7500-7504, issn 0027-8424Article

X-ray microanalysis of cell elements in normal and cystic fibrosis jejunum : evidence for chloride secretion in villiO'LOUGHLIN, E. V; HUNT, D. M; BOSTROM, T. E et al.Gastroenterology (New York, NY. 1943). 1996, Vol 110, Num 2, pp 411-418, issn 0016-5085Article

A new missense mutation G126D in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneWAGNER, K; GREIL, I; SCHNEDITZ, P et al.Human heredity. 1994, Vol 44, Num 1, pp 56-57, issn 0001-5652Article

A two-domain model for the R domain of the cystic fibrosis transmembrane conductance regulator based on sequence similaritiesDULHANTY, A. M; RIORDAN, J. R.FEBS letters. 1994, Vol 343, Num 2, pp 109-114, issn 0014-5793Article