Extracellular ATP and UTP induce chloride secretion in nasal epithelia of cystic fibrosis patients and normal subjects in vivo.

نویسندگان

  • M R Knowles
  • L L Clarke
  • R C Boucher
چکیده

1 Scanlin TF. Cystic fibrosis. In: Fishman AP, ed. Pulmonary diseases and disorders. 2nd ed. New York: McGraw-Hill, 1988:1273-94 2 Rommens JM, lanuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 1989; 245:1059-65 3 Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cos TK, Chakvarti A, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989; 245:1073-80 4 Riordan JR, Rommens JM, Kerem BS, Mon N, Rozmachel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of the complementary DNA. Science 1989; 245:1066-72 5 Harsch AD, Xu J, Glick MC, Bevins CL, Zeithn PL, Scanlin iT. Antibodies to peptides from the cystic fibrosis transmembrane conductance regulator (CF’TR) identify a high molecular weight protein in surface membranes of CF airway epithelial cells. Am Rev Respir Dis 1991; 143:298 6 Zeitlin PL, Lu L, Rhim J, Cutting G, Stetten G, Kiefer KA, et al. A cystic fibrosis bronchial epithelial cell line: immortalization by adeno 12-SV4O infection. Am J Respir Cell Mol Biol 1991; 4:313-19 7 Xu J, Harsch AD, Glick MC, Zasloff MA, Bevins CL, Zeitlin PL, et al. Cystic fibrosis transmembrane conductance regulator (CVFR) localization in surface membranes of airway epithelial cells. FASEB J 1991; 5:463.

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عنوان ژورنال:
  • Chest

دوره 101 3 Suppl  شماره 

صفحات  -

تاریخ انتشار 1992