Cystic fibrosis: lessons from the sweat gland.
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[1] D. Andersen. CYSTIC FIBROSIS OF THE PANCREAS AND ITS RELATION TO CELIAC DISEASE: A CLINICAL AND PATHOLOGIC STUDY , 1938 .
[2] D. Andersen. CELIAC SYNDROME: III. DIETARY THERAPY FOR CONGENITAL PANCREATIC DEFICIENCY , 1945 .
[3] P. di Sant'Agnese,et al. Celiac syndrome; chemotherapy in infections of the respiratory tract associated with cystic fibrosis of the pancreas; observations with penicillin and drugs of the sulfonamide group, with special reference to penicillin aerosol. , 1946, American journal of diseases of children.
[4] R. G. Hodges,et al. Celiac syndrome; genetics of cystic fibrosis of the pancreas, with a consideration of etiology. , 1946, American journal of diseases of children.
[5] W. Zuelzer,et al. The pathogenesis of fibrocystic disease of the pancreas; a study of 36 cases with special reference to the pulmonary lesions. , 1949, Pediatrics.
[6] D. Andersen,et al. Heat prostration in fibrocystic disease of the pancreas and other conditions. , 1951, Pediatrics.
[7] J. Weiner,et al. A comparison of arm‐bag sweat and body sweat , 1952, Journal of Physiology.
[8] P. diSant’Agnese,et al. ELECTROLYTE ABNORMALITIES OF THE SWEAT IN FIBROCYSTIC DISEASE OF THE PANCREAS° , 1953, The American journal of the medical sciences.
[9] Darling Rc,et al. Electrolyte abnormalities of the sweat in fibrocystic disease of the pancreas. , 1953 .
[10] P. di Sant'Agnese,et al. Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas; clinical significance and relationship to the disease. , 1953, Pediatrics.
[11] N. Thorn,et al. Excretion of sodium, potassium, chloride and carbon dioxide in human parotid saliva. , 1954, The American journal of physiology.
[12] P. A. Sant'agnese,et al. Fibrocystic disease of the pancreas with normal or partial pancreatic function; current views on pathogenesis and diagnosis. , 1955, Pediatrics.
[13] P. di Sant'Agnese. Fibrocystic disease of the pancreas with normal or partial pancreatic function; current views on pathogenesis and diagnosis. , 1955, Pediatrics.
[14] J. Rendle–Short. Fibrocystic Disease of the Pancreas Presenting with Acute Salt Depletion , 1956, Archives of disease in childhood.
[15] I L SCHWARTZ,et al. Excretion of sodium and potassium in human sweat. , 1956, The Journal of clinical investigation.
[16] P. A. Sant'agnese,et al. Cystic fibrosis of the pancreas , 1956 .
[17] [Celiac syndrome]. , 1956, Pediatria polska.
[18] G. Barbero,et al. A simplified technique for the sweat test in the diagnosis of fibrocystic disease of the pancreas. , 1956, Pediatrics.
[19] A. Mauer,et al. A simple method for collection and analysis of sweat for chloride. , 1956, A.M.A. journal of diseases of children.
[20] C. Vink. The sweat test in cystic fibrosis of the pancreas. , 1957, A.M.A. journal of diseases of children.
[21] H. Shwachman,et al. Measurement of the electrical conductivity of sweat; its application to the study of cystic fibrosis of the pancreas. , 1957, Clinical chemistry.
[22] Sweat Test for the Diagnosis of Fibrocystic Disease of the Pancreas , 1958, Archives of disease in childhood.
[23] Cystic fibrosis of the pancreas. , 1958 .
[24] D. Hsia,et al. Studies on the genetic mechanism of cystic fibrosis of the pancreas. , 1959, A.M.A. journal of diseases of children.
[25] Fundamental defect in fibrocystic disease of the pancreas. , 1959, Lancet.
[26] R E COOKE,et al. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. , 1959, Pediatrics.
[27] E. M. Peterson. Consideration of cystic fibrosis in adults, with a study of sweat electrolyte values. , 1959, Journal of the American Medical Association.
[28] The hazard of induction of sweating in cystic fibrosis of the pancreas. , 1960, Pediatrics.
[29] B. Munger,et al. An electron microscopic study of eccrine sweat glands in patients with cystic fibrosis of the pancreas. , 1961, The Journal of pediatrics.
[30] P. A. Sant'agnese,et al. THE ECCRINE SWEAT DEFECT IN CYSTIC FIBROSIS OF THE PANCREAS (MUCOVISCIDOSIS) , 1962 .
[31] W. Gaisford. The Nails , 1965 .
[32] L. Gibson,et al. Studies of salt excretion in sweat. Relationships between rate, conductivity, and electrolyte composition of sweat from patients with cystic fibrosis and from control subjects. , 1963, The Journal of pediatrics.
[33] J. Pallavicini,et al. ISOLATION AND CHARACTERIZATION OF CARBOHYDRATE‐PROTEIN COMPLEXES FROM HUMAN SWEAT , 1963 .
[34] J. Slegers. THE MECHANISM OF ECCRINE SWEAT-GLAND FUNCTION IN NORMAL SUBJECTS AND IN PATIENTS WITH MUCOVISCOIDOSIS. , 1963, Dermatologica.
[35] G. Cage,et al. SODIUM SECRETION AND REABSORPTION IN THE HUMAN ECCRINE SWEAT GLAND. , 1965, The Journal of clinical investigation.
[37] Density and secretory activity of accrine sweat glands in patients with cystic fibrosis and in health controls. , 1966, Pediatrics.
[38] G. Cage,et al. Sweat gland function in cystic fibrosis. , 1966, The Journal of clinical investigation.
[39] J. Orloff,et al. Preparation and study of fragments of single rabbit nephrons. , 1966, The American journal of physiology.
[40] The influx and outflux of sodium in the sweat-gland. , 1966, Dermatologica.
[41] H. Heick,et al. Abnormal Serum Factor in Patients with Cystic Fibrosis of the Pancreas , 1967, Pediatric Research.
[42] H. Shwachman,et al. Pilocarpine iontophoresis sweat testing results of seven years' experience. , 1967, Bibliotheca paediatrica.
[43] Slegers Jf,et al. A mathematical approach to the two-step reabsorption hypothesis. , 1967 .
[44] J. Slegers. A mathematical approach to the two-step reabsorption hypothesis. , 1967, Bibliotheca paediatrica.
[45] J. Mangos,et al. Sodium Transport: Inhibitory Factor in Sweat of Patients with Cystic Fibrosis , 1967, Science.
[46] Clinical findings and research in cystic fibrosis. , 1967 .
[47] C. Lobeck,et al. The ionic composition of pilocarpine induced sweat in relation to gland output during aging and in cystic fibrosis. , 1967, Bibliotheca paediatrica.
[48] J. Mangos,et al. Studies on the Mechanism of Inhibition of Sodium Transport in Cystic Fibrosis of the Pancreas , 1968, Pediatric Research.
[49] H. Emrich,et al. Sweat Composition in Relation to Rate of Sweating in Patients with Cystic Fibrosis of the Pancreas , 1968, Pediatric Research.
[50] V. Schwarz,et al. Biochemical Studies of Sweat Secretion in Cystic Fibrosis , 1968, Proceedings of the Royal Society of Medicine.
[51] I. Schulz. Micropuncture studies of the sweat formation in cystic fibrosis patients. , 1969, The Journal of clinical investigation.
[52] M. McCombs,et al. Oyster Ciliary Inhibition by Cystic Fibrosis Factor , 1969, Science.
[53] P. Minihan,et al. Hyperpermeable mucus in cystic fibrosis. , 1970, Lancet.
[54] E. Oppenheimer,et al. Cervical mucus in cystic fibrosis: a possible cause of infertility. , 1970, American journal of obstetrics and gynecology.
[55] H. Shwachman,et al. Water and electrolytes in cervical mucus from patients with cystic fibrosis. , 1973, Fertility and sterility.
[56] G. Harrison,et al. Cystic fibrosis: reversal of ciliary inhibition in serum and saliva by heparin. , 1973, Texas reports on biology and medicine.
[57] D. Kaiser,et al. Diminished Excretion of Bicarbonate from the Single Sweat Gland of Patients with Cystic Fibrosis of the Pancreas * , 1974, European journal of clinical investigation.
[58] H. Shwachman,et al. Gastrointestinal manifestations of cystic fibrosis. , 1975, Pediatric clinics of North America.
[59] Beta-adrenergic receptors, cyclic AMP, and ion transport in the avian erythrocyte. , 1975, Advances in cyclic nucleotide research.
[60] J. Sturgess,et al. Cystic fibrosis: effects of serum factors on mucus secretion. , 1976, Laboratory investigation; a journal of technical methods and pathology.
[61] G. B. Wilson,et al. Detection of cystic fibrosis protein by electrofocusing. , 1976, Pediatric research.
[62] T. Nelson,et al. Cystic Fibrosis: Enzymatic Detection of a Ciliostatic Factor , 1976, Pediatric Research.
[63] Kunie Nakamura,et al. EFFECT OF SERA FROM CYSTIC FIBROSIS HOMOZYGOTES AND HETEROZYGOTES ON GLUCOSE METABOLISM IN VERO CELLS , 1978, The Lancet.
[64] C. Denning,et al. Biological activities of cystic fibrosis serum. III. CF serum induced uptake of 45Ca++ by rabbit tracheal explants. , 1979, Biochemical and biophysical research communications.
[65] G. Gibbs,et al. Cystic Fibrosis Serum Effect on the Short Circuit Current of Rat Jejunum , 1979, Pediatric Research.
[66] P. Allen,et al. Cystic Fibrosis Serum Effects on Rabbit Tracheal Epithelium: an Ultrastructural Analysis , 1980, Pediatric Research.
[67] J. Lieberman,et al. Presence of a serum hemagglutinin (lectinlike factor) in cystic fibrosis homozygotes and heterozygotes. , 1981, The Journal of laboratory and clinical medicine.
[68] G. B. Wilson,et al. Cystic fibrosis ciliary dyskinesia substances and pulmonary disease. Effects of ciliary dyskinesia substances on neutrophil movement in vitro. , 1981, The Journal of clinical investigation.
[69] M. Knowles,et al. Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis. , 1981, The New England journal of medicine.
[70] P. Quinton. Suggestion of an Abnormal Anion Exchange Mechanism in Sweat Glands of Cystic Fibrosis Patients , 1982, Pediatric Research.
[71] M. Knowles,et al. Abnormal ion permeation through cystic fibrosis respiratory epithelium. , 1983, Science.
[72] F Beck. Fluid and Electrolyte Abnormalities in Exocrine Glands in Cystic Fibrosis , 1983 .
[73] P. Quinton,et al. Chloride impermeability in cystic fibrosis , 1983, Nature.
[74] P. Quinton,et al. Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis. , 1983, The New England journal of medicine.
[75] Abnormal anion exchange mechanism operates in the sweat glands of cystic fibrosis patients. , 1984, Pediatric research.
[76] P. Quinton,et al. Apparent Absence of Cystic Fibrosis Sweat Factor on Ion-selective and Transport Properties of the Perfused Human Sweat Duct , 1984, Pediatric Research.
[77] K. Sato,et al. Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitro. , 1984, The Journal of clinical investigation.
[78] P. Quinton,et al. Influence of abnormal Cl- impermeability on sweating in cystic fibrosis. , 1984, The American journal of physiology.
[79] M. Blitzer,et al. A Purified Serum Glycopeptide from Controls and Cystic Fibrosis Patients. III. The Association of the Ciliary Dyskinetic Activity with the Oligosaccharide Component , 1984, Pediatric Research.
[80] M. Knowles,et al. Increased nasal potential difference and amiloride sensitivity in neonates with cystic fibrosis , 1986 .
[81] R. Shoemaker,et al. Altered regulation of airway epithelial cell chloride channels in cystic fibrosis. , 1986, Science.
[82] P. Quinton. Missing Cl conductance in cystic fibrosis. , 1986, The American journal of physiology.
[83] M. Welsh,et al. Chloride and potassium channels in cystic fibrosis airway epithelia , 1986, Nature.
[84] L. Cantley,et al. Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation. , 1986, The Journal of clinical investigation.
[85] P. Quinton,et al. Lactate and Bicarbonate Uptake in the Sweat Duct of Cystic Fibrosis and Normal Subjects , 1987, Pediatric Research.
[86] J. Wine,et al. Hyposecretion of β-Adrenergically Induced Sweating in Cystic Fibrosis Heterozygotes , 1987, Pediatric Research.
[87] R. Barthelson,et al. Cyclic adenosine monophosphate-dependent kinase in cystic fibrosis tracheal epithelium. , 1987, The Journal of clinical investigation.
[88] I. Forgacs. GASTROENTEROLOGY , 1988, The Lancet.
[89] G. Rechkemmer,et al. Apical membrane chloride channels in a colonic cell line activated by secretory agonists. , 1988, The American journal of physiology.
[90] K. Sato,et al. Variable reduction in beta-adrenergic sweat secretion in cystic fibrosis heterozygotes. , 1988, The Journal of laboratory and clinical medicine.
[91] A. Beaudet. Cellular and molecular basis of cystic fibrosis. , 1988 .
[92] P. Quinton,et al. Localization of Cl- conductance in normal and Cl- impermeability in cystic fibrosis sweat duct epithelium. , 1989, The American journal of physiology.
[93] P. Quinton,et al. Cl‐ Conductance and Acid Secretion in the Human Sweat Duct , 1989, Annals of the New York Academy of Sciences.
[94] Altered electrical potential profile of human reabsorptive sweat duct cells in cystic fibrosis. , 1989, The American journal of physiology.
[95] L. Tsui,et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. , 1989, Science.
[96] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.
[97] L. Tsui,et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. , 1989, Science.
[98] Cystic fibrosis. Righting the wrong protein. , 1990, Nature.
[99] Na+, K+, H+, Cl-, and Ca2+ concentrations in cystic fibrosis eccrine sweat in vivo and in vitro. , 1990, The Journal of laboratory and clinical medicine.
[100] P. Quinton. Cystic fibrosis: a disease in electrolyte transport , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[101] J. Marshall,et al. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis , 1990, Cell.
[102] J. Cohn,et al. CFTR: development of high- affinity antibodies and localization in sweat gland. , 1991, Biochemical and biophysical research communications.
[103] B. Brown,et al. Measurement of intracellular mediators in enterocytes isolated from jejunal biopsy specimens of control and cystic fibrosis patients. , 1991, Gut.
[104] David J Brayden,et al. Cystic fibrosis, the CFTR, and rectifying Cl- channels. , 1991, Advances in experimental medicine and biology.
[105] R. Busch. On the history of cystic fibrosis , 1991, Nordisk medicinhistorisk arsbok.
[106] Matthew P. Anderson,et al. Nucleoside triphosphates are required to open the CFTR chloride channel , 1991, Cell.
[107] Regulation of airway mucosal ion transport. , 1991, International archives of allergy and applied immunology.
[108] P. Quinton,et al. Regulation of absorption in the human sweat duct. , 1991, Advances in experimental medicine and biology.
[109] J. Wine,et al. The basic defect in cystic fibrosis. , 1991, Trends in biochemical sciences.
[110] P. Quinton,et al. Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding , 1992, Nature.
[111] P. Quinton,et al. T84 cells: anion selectivity demonstrates expression of Cl- conductance affected in cystic fibrosis. , 1992, The American journal of physiology.
[112] A. Gilman,et al. Adenylyl cyclases , 1992, Cell.
[113] A. Pavirani,et al. Immunocytochemical analysis reveals differences between the subcellular localization of normal and delta Phe508 recombinant cystic fibrosis transmembrane conductance regulator. , 1992, Experimental cell research.
[114] James M. Wilson,et al. Submucosal glands are the predominant site of CFTR expression in the human bronchus , 1992, Nature Genetics.
[115] A. Pavirani,et al. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium. , 1992, American journal of respiratory cell and molecular biology.
[116] J. Riordan,et al. Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland , 1992, Nature Genetics.
[117] John P. Johnson. The identification of the CF (Cystic fibrosis) gene: Recent progress and new research strategies , 1992 .
[118] M. Gray,et al. cAMP-regulated whole cell chloride currents in pancreatic duct cells. , 1993, The American journal of physiology.
[119] H. A. Berger,et al. Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by specific protein kinases and protein phosphatases. , 1993, The Journal of biological chemistry.
[120] P. Quinton. Human Genetics: What is good about cystic fibrosis? , 1994, Current Biology.
[121] H. Cantiello,et al. The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel. , 1994, The Journal of biological chemistry.
[122] J. Yankaskas,et al. Mechanism of sodium hyperabsorption in cultured cystic fibrosis nasal epithelium: a patch-clamp study. , 1994, The American journal of physiology.
[123] R. Boucher. Human airway ion transport. Part one. , 1994, American journal of respiratory and critical care medicine.
[124] W. Guggino,et al. Rectal epithelial expression of protein kinase A phosphorylation of cystic fibrosis transmembrane conductance regulator. , 1994, Gastroenterology.
[125] P. Pedersen,et al. The First Nucleotide Binding Fold of the Cystic Fibrosis Transmembrane Conductance Regulator Can Function as an Active ATPase (*) , 1995, The Journal of Biological Chemistry.
[126] W. Colledge,et al. The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study. , 1995, The Journal of physiology.
[127] J C Olsen,et al. CFTR as a cAMP-dependent regulator of sodium channels , 1995, Science.
[128] A. Nairn,et al. Isotype-specific Activation of Cystic Fibrosis Transmembrane Conductance Regulator-Chloride Channels by cGMP-dependent Protein Kinase II (*) , 1995, The Journal of Biological Chemistry.
[129] M. Donowitz,et al. Genistein and tyrphostin 47 stimulate CFTR-mediated Cl- secretion in T84 cell monolayers. , 1995, The American journal of physiology.
[130] K. Gunderson,et al. Conformational states of CFTR associated with channel gating: The role of ATP binding and hydrolysis , 1995, Cell.
[131] David H. Dreyfus,et al. CYSTIC FIBROSIS HETEROZYGOTE RESISTANCE TO CHOLERA TOXIN IN THE CYSTIC FIBROSIS MOUSE MODEL , 1995, Pediatrics.
[132] M. Corey,et al. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations. , 1995, The Journal of pediatrics.
[133] J. Widdicombe,et al. cAMP-independent activation of CFTR Cl channels by the tyrosine kinase inhibitor genistein. , 1995, The American journal of physiology.
[134] J. Rommens,et al. ATPase Activity of the Cystic Fibrosis Transmembrane Conductance Regulator* , 1996, The Journal of Biological Chemistry.
[135] T. Machen,et al. Alternate stimulation of apical CFTR by genistein in epithelia. , 1996, The American journal of physiology.
[136] R. Frizzell,et al. Lack of Conventional ATPase Properties in CFTR Chloride Channel Gating , 1996, The Journal of Membrane Biology.
[137] K. Gunderson,et al. Failure of the Cystic Fibrosis Transmembrane Conductance Regulator to Conduct ATP , 1996, Science.
[138] P. Quinton,et al. Hydrolytic and nonhydrolytic interactions in the ATP regulation of CFTR Cl- conductance. , 1996, The American journal of physiology.
[139] P. Quinton,et al. Deactivation of CFTR-Cl conductance by endogenous phosphatases in the native sweat duct. , 1996, The American journal of physiology.
[140] P. Farrell,et al. Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis. , 1996, Pediatrics.
[141] H. Rossmann,et al. A functional CFTR protein is required for mouse intestinal cAMP‐, cGMP‐ and Ca2+‐dependent HCO3− secretion , 1997, The Journal of physiology.
[142] C. Bear,et al. Coupling of ATP Hydrolysis with Channel Gating by Purified, Reconstituted CFTR , 1997, Journal of bioenergetics and biomembranes.
[143] L. Tsui,et al. Permeability of Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels to Polyatomic Anions , 1997, The Journal of general physiology.
[144] H. Cantiello. Nucleotide Transport Through the Cystic Fibrosis Transmembrane Conductance Regulator , 1997, Bioscience reports.
[145] R. Boucher,et al. Enhanced colonic Na+ absorption in cystic fibrosis mice versus normal mice. , 1997, The American journal of physiology.
[146] R. Schreiber,et al. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways. , 1998, The Journal of clinical investigation.
[147] A. Hamosh,et al. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. , 1998, The Journal of pediatrics.
[148] A. Nairn,et al. ATP hydrolysis cycles and the gating of CFTR Cl- channels. , 1998, Acta physiologica Scandinavica. Supplementum.
[149] P. Quinton. Physiological basis of cystic fibrosis: a historical perspective. , 1999, Physiological reviews.
[150] P. Quinton,et al. Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function , 1999, Nature.
[151] Ashvani K. Singh,et al. Bicarbonate and Chloride Secretion in Calu-3 Human Airway Epithelial Cells , 1999, The Journal of general physiology.
[152] C. Högenauer,et al. Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion. , 2000, American journal of human genetics.
[153] Min Goo Lee,et al. Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis , 2001, Nature.
[154] P. Quinton,et al. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances. , 2001, JOP : Journal of the pancreas.
[155] H. Cantiello. Electrodiffusional ATP movement through CFTR and other ABC transporters , 2001, Pflügers Archiv.
[156] P. Quinton,et al. Apical Heterotrimeric G-proteins Activate CFTR in the Native Sweat Duct , 2001, The Journal of Membrane Biology.
[157] C. Wiuf. Do delta F508 heterozygotes have a selective advantage? , 2001, Genetical research.
[158] A. Evagelidis,et al. Regulation of the CFTR channel by phosphorylation , 2001, Pflügers Archiv.
[159] P. Quinton,et al. Functional interaction of CFTR and ENaC in sweat glands , 2002, Pflügers Archiv.
[160] R. Tarran,et al. Thin-film measurements of airway surface liquid volume/composition and mucus transport rates in vitro. , 2002, Methods in molecular medicine.
[161] S. Donaldson,et al. Update on pathogenesis of cystic fibrosis lung disease , 2003, Current opinion in pulmonary medicine.
[162] On the Mechanism of MgATP-dependent Gating of CFTR Cl− Channels , 2003, The Journal of general physiology.
[163] J. Filkowski,et al. Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells , 2003, Nature.
[164] J. Fordtran,et al. Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect. , 2003, The Journal of clinical investigation.
[165] J. Slegers. Patho-physiological studies of the sweat gland , 2004, Pflüger's Archiv für die gesamte Physiologie des Menschen und der Tiere.
[166] Permeability properties of cell membranes and tight junctions of normal and cystic fibrosis sweat ducts , 1987, Pflügers Archiv.
[167] R. Greger,et al. Characterization of human sweat duct chloride conductance by chloride channel blockers , 1987, Pflügers Archiv.
[168] P. Quinton,et al. cAMP activation of CF-affected Cl− conductance in both cell membranes of an absorptive epithelium , 1992, The Journal of Membrane Biology.
[169] P. Quinton,et al. Rapid regulation of electrolyte absorption in sweat duct , 1994, The Journal of Membrane Biology.
[170] Richard C Boucher,et al. Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice , 2004, Nature Medicine.
[171] Effects of some ion transport inhibitors on secretion and reabsorption in intact and perfused single human sweat glands , 1981, Pflügers Archiv.
[172] M. Stutts,et al. Local regulation of cystic fibrosis transmembrane regulator and epithelial sodium channel in airway epithelium. , 2004, Proceedings of the American Thoracic Society.
[173] Intracellular potentials of microperfused human sweat duct cells , 1987, Pflügers Archiv - European Journal of Physiology.
[174] S. Muallem,et al. Gating of CFTR by the STAS domain of SLC26 transporters , 2004, Nature Cell Biology.
[175] P. Quinton,et al. Localization of Na/K-ATPase sites in the secretory and reabsorptive epithelia of perfused eccrine sweat glands: A question to the role of the enzyme in secretion , 1976, The Journal of Membrane Biology.
[176] Paola Vergani,et al. CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains , 2005, Nature.
[177] H. M. Emrich,et al. pH of sweat of patients with cystic fibrosis , 1976, Klinische Wochenschrift.
[178] P. Quinton,et al. Normal CFTR Activity and Reversed Skin Potentials in Pseudohypoaldosteronism , 2005, The Journal of Membrane Biology.
[179] J. Massie,et al. The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era. , 2005, The Clinical biochemist. Reviews.
[180] P. Quinton,et al. Predominant constitutive CFTR conductance in small airways , 2005, Respiratory research.
[181] J. Best,et al. Salivary secretion assay for drug efficacy for cystic fibrosis in mice , 2005, Experimental physiology.
[182] P. Quinton,et al. ENaC Activity Requires CFTR Channel Function Independently of Phosphorylation in Sweat Duct , 2005, The Journal of Membrane Biology.
[183] P. Quinton,et al. Intracellular potassium activity and the role of potassium in transepithelial salt transport in the human reabsorptive sweat duct , 1991, The Journal of Membrane Biology.
[184] M. Corey,et al. Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. , 2006, American journal of respiratory and critical care medicine.
[185] M. Knowles,et al. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. , 2006, The New England journal of medicine.
[186] A. Mehta,et al. CFTR, chloride concentration and cell volume: could mammalian protein histidine phosphorylation play a latent role? , 2006, Experimental physiology.
[187] P. Quinton,et al. Cytosolic potassium controls CFTR deactivation in human sweat duct. , 2006, American journal of physiology. Cell physiology.
[188] P. Davis,et al. Cystic fibrosis since 1938. , 2006, American journal of respiratory and critical care medicine.