Dynamics of protein and fluid secretion from the major salivary glands of rat: relevance of research findings to clinically observed defective secretion in cystic fibrosis D. Shori B. Asking Article Pages: S11 - S16
CFTR may play a role in regulated secretion by lymphocytes: a new hypothesis for the pathophysiology of cystic fibrosis James K. Bubien Article Pages: S36 - S39
Electrodiffusional ATP movement through CFTR and other ABC transporters H. Cantiello Article Pages: S22 - S27
Altered sialyl- and fucosyl-linkage on mucins in cystic fibrosis patients promotes formation of the sialyl-Lewis X determinant on salivary MUC-5B and MUC-7 D. Shori T. Genter I. Tsanakas Article Pages: S55 - S61
Role of snare proteins in CFTR and ENaC trafficking Kathryn W. PetersJuanjuan Qi R. Frizzell Article Pages: S65 - S69
Nucleoside diphosphate kinase – a component of the [Na+]- and [Cl–]-sensitive phosphorylation cascade in human and murine airway epithelium K. Treharne C. Riemen A. Mehta Article Pages: S97 - S102
Ca2+-activated Cl– channels: a newly emerging anion transport family Catherine M. FullerHong-Long JiDale J. Benos Article Pages: S107 - S110
Localisation of wild-type and ΔF508-CFTR in nasal epithelial cells R. Dormer C. McNeilly M. McPherson Article Pages: S117 - S120
EBIO, an agent causing maintained epithelial chloride secretion by co-ordinate actions at both apical and basolateral membranes L. MacVinish J. Keogh A. Cuthbert Article Pages: S127 - S131
Altered NaCl concentration of airway surface liquid in cystic fibrosis J. Widdicombe Article Pages: S8 - S10
Ultrastructural changes in exocrine tissues of a ΔF-508 CFTR mouse model G. Thomopoulos D. Shori W. Colledge Article Pages: S28 - S35
Effect of acute saline volume expansion in the anaesthetised ΔF508 cystic fibrosis mouse Jonathan D. KibbleAndrew NealChristopher J. Taylor Article Pages: S17 - S21
Relationship between IκBα deficiency, NFκB activity and interleukin-8 production in CF human airway epithelial cells Olivier TabarySandie EscotteJacky Jacquot Article Pages: S40 - S44
Sulphation of the salivary mucin MG1 (MUC-5B) is not correlated to the degree of its sialylation and is unaffected by cystic fibrosis D. Shori H. Kariyawasam A. Kalogeridis Article Pages: S50 - S54
Regulation of gap junctional communication in CFTR-expressing pancreatic epithelial cells Marc ChansonSusanne Suter Article Pages: S81 - S84
Endocytic adaptor complexes bind the C-terminal domain of CFTR K. Weixel N. Bradbury Article Pages: S70 - S74
Regulation of the CFTR channel by phosphorylation David DahanAlexandra EvagelidisTang Zhu Article Pages: S92 - S96
Non-CFTR chloride channels likely contribute to secretion in the murine small intestine Katalin GyömöreyElizabeth GaramiChristine E. Bear Article Pages: S103 - S106
Gadolinium as an opener of the outwardly rectifying Cl– channel (ORCC). Is there relevance for cystic fibrosis therapy? Friedrich ThinnesGötz WalterNorbert Hilschmann Article Pages: S111 - S116
Inhibition of amiloride-sensitive Na+ absorption by activation of CFTR in mouse endometrial epithelium L. Chan X. Wang H. Chan Article Pages: S132 - S136
The CFTR-mediated protein secretion defect: pharmacological correction M. McPherson M. Pereira R. Dormer Article Pages: S121 - S126
