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Demonstration of serum protein differences in cystic fibrosis by isoelectric focusing in thin-layer polyacrylamide gels.
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J Clin Invest. 1981 May;67(5):1574-9
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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.
Pflugers Arch. 1981 Aug;391(2):85-100
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Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.
N Engl J Med. 1981 Dec 17;305(25):1489-95
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Chloride impermeability in cystic fibrosis.
Nature. 1983 Feb 3;301(5899):421-2
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Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis.
N Engl J Med. 1983 May 19;308(20):1185-9
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Relative ion permeability of normal and cystic fibrosis nasal epithelium.
J Clin Invest. 1983 May;71(5):1410-7
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Abnormal ion permeation through cystic fibrosis respiratory epithelium.
Science. 1983 Sep 9;221(4615):1067-70
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The carbohydrate content of IgG from patients with cystic fibrosis.
Pediatr Res. 1983 Dec;17(12):931-5
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Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitro.
J Clin Invest. 1984 Jun;73(6):1763-71
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Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis.
N Engl J Med. 1985 Feb 7;312(6):329-34
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Persistence of abnormal chloride ion permeability in cystic fibrosis nasal epithelial cells in heterologous culture.
Lancet. 1985 Apr 27;1(8435):954-6
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Tissue localization and chromosomal assignment of a serum protein that tracks the cystic fibrosis gene.
Nature. 1985 Jun 6-12;315(6019):513-5
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Altered fucosylation of membrane glycoproteins from cystic fibrosis fibroblasts.
Pediatr Res. 1985 Apr;19(4):368-74
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Cystic fibrosis decreases the apical membrane chloride permeability of monolayers cultured from cells of tracheal epithelium.
Proc Natl Acad Sci U S A. 1985 Sep;82(18):6167-71
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Adrenergic secretory responses of submandibular tissues from control subjects and cystic fibrosis patients.
Clin Chim Acta. 1985 Jun 14;148(3):229-37
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Testing for cystic fibrosis.
Nature. 1985 Nov 28-Dec 4;318(6044):309
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Culture of human nasal epithelial cells on collagen matrix supports. A comparison of bioelectric properties of normal and cystic fibrosis epithelia.
Am Rev Respir Dis. 1985 Dec;132(6):1281-7
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An apical-membrane chloride channel in human tracheal epithelium.
Science. 1986 Jun 27;232(4758):1648-50
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Altered regulation of airway epithelial cell chloride channels in cystic fibrosis.
Science. 1986 Aug 1;233(4763):558-60
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Chloride and potassium channels in cystic fibrosis airway epithelia.
Nature. 1986 Jul 31-Aug 6;322(6078):467-70
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Missing Cl conductance in cystic fibrosis.
Am J Physiol. 1986 Oct;251(4 Pt 1):C649-52
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Cystic fibrosis and beta-adrenergic response of airway epithelial cell cultures.
Am J Physiol. 1986 Oct;251(4 Pt 2):R818-22
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Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.
J Clin Invest. 1986 Nov;78(5):1245-52
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Circulating and tissue angiotensin systems.
J Clin Invest. 1987 Jan;79(1):1-6
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Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.
J Clin Invest. 1987 Jan;79(1):80-5
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A clue to the basic defect in cystic fibrosis from cloning the CF antigen gene.
Nature. 1987 Apr 9-15;326(6113):614-7
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Cystic fibrosis. Classical and reverse genetics.
Nature. 1987 Apr 30-May 6;326(6116):824
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Permeability properties of cell membranes and tight junctions of normal and cystic fibrosis sweat ducts.
Pflugers Arch. 1987 May;408(5):505-10
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Development of a quantitative immunoassay for the cystic fibrosis gene.
Lancet. 1980 Feb 16;1(8164):330-1
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