CITATIONS
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JOP. J Pancreas (Online) 2001; 2(4 Suppl.):294-300.
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Charalabous P, Risk JM, Jenkins R, Birss AJ, Hart CA, Smalley JW. Characterization of a bifunctional catalase-peroxidase of Burkholderia cenocepacia. FEMS Immunol Med Microbiol 2007; 50(1):37-44. [More details] |
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Shin JH, Son EJ, Lee HS, Kim SJ, Kim K, Choi JY, et al. Molecular and functional expression of anion exchangers in cultured normal human nasal epithelial cells. Acta Physiol (Oxf) 2007; 191(2):99-110. [More details] |
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Sidani SM, Kirchhoff P, Socrates T, Stelter L, Ferreira E, Caputo C, Roberts KE, et al. DeltaF508 mutation results in impaired gastric acid secretion. J Biol Chem 2007; 282(9):6068-74. [More details] |
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Song Y, Salinas D, Nielson DW, Verkman AS. Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis. Am J Physiol Cell Physiol 2006; 290(3):C741-9. [More details] |
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Carraro S, Doherty J, Zaman K, Gainov I, Turner R, Vaughan J, et al. S-nitrosothiols regulate cell-surface pH buffering by airway epithelial cells during the human immune response to rhinovirus. Am J Physiol Lung Cell Mol Physiol 2006; 290(5):L827-32. [More details] |
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Edelman A, Fritsch J. Various aspects of regulating transepithelial ion transport in cystic fibrosis: Mechanisms of absorption and secretion, CFTR protein, other ion channels. Meine Therapeutique Pediatrie 2005; 8(3):135-49. [More details] |
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Wang Y, Lam CS, Wu F, Wang W, Duan Y, Huang P. Regulation of CFTR channels by HCO(3)--sensitive soluble adenylyl cyclase in human airway epithelial cells. Am J Physiol Cell Physiol 2005; 289(5):C1145-51. [More details] |
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Smart T, Peters J, Ashcroft F, et al. The nature reviews drug discovery ion channel questionnaire participants. Nat Rev Drug Discov 2004; 3(3):239-78. [More details] |
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Perez-Vilar J, Boucher RC. Reevaluating gel-forming mucins' roles in cystic fibrosis lung disease. Free Radic Biol Med 2004; 37(10):1564-77. [More details] |
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Ashcroft F, Benos D, Bezanilla F, Chien K, Choe S, Clapham D, et al. Twenty questions: Highlighting the pitfalls and possibilities of drug research. The state of ion channel research in 2004. Nat Rev Drug Discov 2004; 3(3):239-78. [More details] |
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Van Heeckeren AM, Scaria A, Schluchter MD, Ferkol TW, Wadsworth S, Davis PB. Delivery of CFTR by adenoviral vector to cystic fibrosis mouse lung in a model of chronic Pseudomonas aeruginosa lung infection. Am J Physiol Lung Cell Mol Physiol 2004; 286(4):L717-26. [More details] |
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Tomich M, Mohr CD. Transcriptional and posttranscriptional control of cable pilus gene expression in Burkholderia cenocepacia. J Bacteriol 2004; 186(4):1009-20. [More details] |
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Luckie DB, Wilterding JH, Krha M, Krouse ME. CFTR and MDR: ABC Transporters with Homologous Structure but Divergent Function. Curr Genomics 2003; 4(3):225-35. [More details] |
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Weiss DJ, Pilewski JM. The status of gene therapy for cystic fibrosis. Sem Resp Crit Care 2003; 24(6):749-70. [More details] |
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Lidell ME, Johansson ME, Hansson GC. An autocatalytic cleavage in the C terminus of the human MUC2 mucin occurs at the low pH of the late secretory pathway. J Biol Chem 2003; 278(16):13944-51. [More details] |
2 |
Verkman AS, Song Y, Thiagarajah JR. Role of airway surface liquid and submucosal glands in cystic fibrosis lung disease. Am J Physiol-Cell Ph 2003; 284(1):C2-C15. [More details] |
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Joo NS, Saenz Y, Krouse ME, Wine JJ. Mucus secretion from single submucosal glands of pig. Stimulation by carbachol and vasoactive intestinal peptide. J Biol Chem 2002; 277(31):28167-75. [More details] |