-
2
-
-
0028324349
-
Crohn's disease cystic fibrosis
-
Lloyd-Still JD: Crohn's disease and cystic fibrosis. Dig Dis Sci 1994, 39: 880-885.
-
(1994)
Dig. Dis. Sci.
, vol.39
, pp. 880-885
-
-
Lloyd-Still, J.D.1
-
4
-
-
0032934916
-
Role of CFTR in airway disease
-
Pilewski JM and Frizzell RA: Role of CFTR in airway disease. Physiol Rev 1999, 79(1 Suppl): S215-S255.
-
(1999)
Physiol. Rev.
, vol.79
, Issue.1 SUPPL.
-
-
Pilewski, J.M.1
Frizzell, R.A.2
-
5
-
-
0036097028
-
Novel role for CFTR in fluid absorption from the distal airspaces of the lung
-
Fang X, Fukuda N, Barbry P, Sartori C, Verkman AS and Matthay MA: Novel role for CFTR in fluid absorption from the distal airspaces of the lung. J Gen Physiol 2002, 119: 199-207.
-
(2002)
J. Gen. Physiol.
, vol.119
, pp. 199-207
-
-
Fang, X.1
Fukuda, N.2
Barbry, P.3
Sartori, C.4
Verkman, A.S.5
Matthay, M.A.6
-
6
-
-
0035184114
-
CFTR may play a role in regulated secretion by lymphocytes: A new hypothesis for the pathophysiology of cystic fibrosis
-
Bubien JK: CFTR may play a role in regulated secretion by lymphocytes: a new hypothesis for the pathophysiology of cystic fibrosis. Pflugers Arch 2001, 443(Suppl 1): S36-S39.
-
(2001)
Pflugers Arch.
, vol.443
, Issue.SUPPL. 1
-
-
Bubien, J.K.1
-
7
-
-
0036712439
-
Regulation of Murine Airway Surface Liquid Volume by CFTR Ca(2+)-activated Cl(-) Conductances
-
Tarran R, Loewen ME, Paradiso AM, Olsen JC, Gray MA, Argent BE, Boucher RC and Gabriel SE: Regulation of Murine Airway Surface Liquid Volume by CFTR and Ca(2+)-activated Cl(-) Conductances. J Gen Physiol 2002, 120: 407-418.
-
(2002)
J. Gen. Physiol.
, vol.120
, pp. 407-418
-
-
Tarran, R.1
Loewen, M.E.2
Paradiso, A.M.3
Olsen, J.C.4
Gray, M.A.5
Argent, B.E.6
Boucher, R.C.7
Gabriel, S.E.8
-
8
-
-
0029821863
-
Regulation of epithelial ion channels by the cystic fibrosis transmembrane conductance regulator
-
Greger R, Mall M, Bleich M, Ecke D, Warth R, Riedemann N and Kunzelmann K: Regulation of epithelial ion channels by the cystic fibrosis transmembrane conductance regulator. J Mol Med 1996, 74: 527-534.
-
(1996)
J. Mol. Med.
, vol.74
, pp. 527-534
-
-
Greger, R.1
Mall, M.2
Bleich, M.3
Ecke, D.4
Warth, R.5
Riedemann, N.6
Kunzelmann, K.7
-
9
-
-
0029935712
-
Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice
-
Hummler E, Barker P, Gatzy J, Beermann F, Verdumo C, Schmidt A, Boucher R and Rossier BC: Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice. Nat Genet 1996, 12: 325-328.
-
(1996)
Nat. Genet.
, vol.12
, pp. 325-328
-
-
Hummler, E.1
Barker, P.2
Gatzy, J.3
Beermann, F.4
Verdumo, C.5
Schmidt, A.6
Boucher, R.7
Rossier, B.C.8
-
10
-
-
0034045308
-
Control of epithelial Na+ conductance by the cystic fibrosis transmembrane conductance regulator
-
Kunzelmann K, Schreiber R, Nitschke R and Mall M: Control of epithelial Na+ conductance by the cystic fibrosis transmembrane conductance regulator. Pflugers Arch 2000, 440: 193-201.
-
(2000)
Pflugers Arch.
, vol.440
, pp. 193-201
-
-
Kunzelmann, K.1
Schreiber, R.2
Nitschke, R.3
Mall, M.4
-
11
-
-
0034607827
-
Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes
-
Jiang Q, Li J, Dubroff R, Ahn YJ, Foskett JK, Engelhardt J and Kleyman TR: Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes. J Biol Chem 2000, 275: 13266-13274.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 13266-13274
-
-
Jiang, Q.1
Li, J.2
Dubroff, R.3
Ahn, Y.J.4
Foskett, J.K.5
Engelhardt, J.6
Kleyman, T.R.7
-
12
-
-
0031921269
-
Cl-transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR ENaC
-
Briel M, Greger R and Kunzelmann K: Cl-transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC. J Physiol 1998, 508(Pt 3): 825-836.
-
(1998)
J. Physiol.
, vol.508
, Issue.PART 3
, pp. 825-836
-
-
Briel, M.1
Greger, R.2
Kunzelmann, K.3
-
13
-
-
0030970422
-
Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics
-
Stutts MJ, Rossier BC and Boucher RC: Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics. J Biol Chem 1997, 272: 14037-14040.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 14037-14040
-
-
Stutts, M.J.1
Rossier, B.C.2
Boucher, R.C.3
-
14
-
-
0034890007
-
X-ray microanalysis of airway surface liquid collected in cystic fibrosis mice
-
Zahm JM, Baconnais S, Davidson DJ, Webb S, Dorin J, Bonnet N, Balossier G and Puchelle E: X-ray microanalysis of airway surface liquid collected in cystic fibrosis mice. Am J Physiol Lung Cell Mol Physiol 2001, 281: L309-L313.
-
(2001)
Am. J. Physiol. Lung Cell Mol. Physiol.
, vol.281
-
-
Zahm, J.M.1
Baconnais, S.2
Davidson, D.J.3
Webb, S.4
Dorin, J.5
Bonnet, N.6
Balossier, G.7
Puchelle, E.8
-
15
-
-
0034939593
-
Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] pH but elevated viscosity
-
Jayaraman S, Joo NS, Reitz B, Wine JJ and Verkman AS: Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] and pH but elevated viscosity. Proc Natl Acad Sci U S A 2001, 98: 8119-8123.
-
(2001)
Proc. Natl. Acad. Sci. U S A
, vol.98
, pp. 8119-8123
-
-
Jayaraman, S.1
Joo, N.S.2
Reitz, B.3
Wine, J.J.4
Verkman, A.S.5
-
16
-
-
0035132659
-
Noninvasive in vivo fluorescence measurement of airway-surface liquid depth salt concentration pH
-
Jayaraman S, Song Y, Vetrivel L, Shankar L and Verkman AS: Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH. J Clin Invest 2001, 107: 317-324.
-
(2001)
J. Clin. Invest.
, vol.107
, pp. 317-324
-
-
Jayaraman, S.1
Song, Y.2
Vetrivel, L.3
Shankar, L.4
Verkman, A.S.5
-
17
-
-
0034125685
-
Osmotic water permeabilities of cultured well-differentiated normal cystic fibrosis airway epithelia
-
Matsui H, Davis CW, Tarran R and Boucher RC: Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia. J Clin Invest 2000, 105: 1419-1427.
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 1419-1427
-
-
Matsui, H.1
Davis, C.W.2
Tarran, R.3
Boucher, R.C.4
-
18
-
-
0032433707
-
Evidence for periciliary liquid layer depletion not abnormal ion composition in the pathogenesis of cystic fibrosis airways disease
-
Matsui H, Grubb BR, Tarran R, Randell SH, Gatzy JT, Davis CW and Boucher RC: Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease. Cell 1998, 95: 1005-1015.
-
(1998)
Cell
, vol.95
, pp. 1005-1015
-
-
Matsui, H.1
Grubb, B.R.2
Tarran, R.3
Randell, S.H.4
Gatzy, J.T.5
Davis, C.W.6
Boucher, R.C.7
-
19
-
-
0015885904
-
Water electrolytes in cervical mucus from patients with cystic fibrosis
-
Kopito LE, Kosasky HJ and Shwachman H: Water and electrolytes in cervical mucus from patients with cystic fibrosis. Fertil Steril 1973, 24: 512-516.
-
(1973)
Fertil. Steril.
, vol.24
, pp. 512-516
-
-
Kopito, L.E.1
Kosasky, H.J.2
Shwachman, H.3
-
20
-
-
0031916813
-
Experimental models for studying mucociliary clearance
-
King M: Experimental models for studying mucociliary clearance. Eur Respir J 1998, 11: 222-228.
-
(1998)
Eur. Respir. J.
, vol.11
, pp. 222-228
-
-
King, M.1
-
21
-
-
0031961860
-
Nasal mucociliary clearance of chronic sinusitis in relation to rheological properties of nasal mucus
-
Atsuta S and Majima Y: Nasal mucociliary clearance of chronic sinusitis in relation to rheological properties of nasal mucus. Ann Otol Rhinol Laryngol 1998, 107: 47-51.
-
(1998)
Ann. Otol. Rhinol. Laryngol.
, vol.107
, pp. 47-51
-
-
Atsuta, S.1
Majima, Y.2
-
22
-
-
0020082418
-
Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis control infants
-
Sturgess J and Imrie J: Quantitative evaluation of the development of tracheal submucosal glands in infants with cystic fibrosis and control infants. Am J Pathol 1982, 106: 303-311.
-
(1982)
Am. J. Pathol.
, vol.106
, pp. 303-311
-
-
Sturgess, J.1
Imrie, J.2
-
23
-
-
0033844485
-
Inflammation infection in naive human cystic fibrosis airway grafts
-
Tirouvanziam R, de Bentzmann S, Hubeau C, Hinnrasky J, Jacquot J, Peault B and Puchelle E: Inflammation and infection in naive human cystic fibrosis airway grafts. Am J Respir Cell Mol Biol 2000, 23: 121-127.
-
(2000)
Am. J. Respir. Cell Mol. Biol.
, vol.23
, pp. 121-127
-
-
Tirouvanziam, R.1
de Bentzmann, S.2
Hubeau, C.3
Hinnrasky, J.4
Jacquot, J.5
Peault, B.6
Puchelle, E.7
-
24
-
-
0031659351
-
Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo in vitro
-
Tabary O, Zahm JM, Hinnrasky J, Couetil JP, Cornillet P, Guenounou M, Gaillard D, Puchelle E and Jacquot J: Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo and in vitro. Am J Pathol 1998, 153: 921-930.
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 921-930
-
-
Tabary, O.1
Zahm, J.M.2
Hinnrasky, J.3
Couetil, J.P.4
Cornillet, P.5
Guenounou, M.6
Gaillard, D.7
Puchelle, E.8
Jacquot, J.9
-
25
-
-
0032531160
-
Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine human airway epithelial cells
-
Kelley TJ and Drumm ML: Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells. J Clin Invest 1998, 102: 1200-1207.
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1200-1207
-
-
Kelley, T.J.1
Drumm, M.L.2
-
26
-
-
0033846368
-
In vivo alterations of IFN regulatory factor-1 PIAS1 protein levels in cystic fibrosis epithelium
-
Kelley TJ and Elmer HL: In vivo alterations of IFN regulatory factor-1 and PIAS1 protein levels in cystic fibrosis epithelium. J Clin Invest 2000, 106: 403-410.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 403-410
-
-
Kelley, T.J.1
Elmer, H.L.2
-
27
-
-
0030021470
-
Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections
-
Pier GB, Grout M, Zaidi TS, Olsen JC, Johnson LG, Yankaskas JR and Goldberg JB: Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections. Science 1996, 271: 64-67.
-
(1996)
Science
, vol.271
, pp. 64-67
-
-
Pier, G.B.1
Grout, M.2
Zaidi, T.S.3
Olsen, J.C.4
Johnson, L.G.5
Yankaskas, J.R.6
Goldberg, J.B.7
-
28
-
-
0027428606
-
Pseudomonas aeruginosa pili bind to asialoGM1 which is increased on the surface of cystic fibrosis epithelial cells
-
Saiman L and Prince A: Pseudomonas aeruginosa pili bind to asialoGM1, which is increased on the surface of cystic fibrosis epithelial cells. J Clin Invest 1993, 92: 1875-1880.
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 1875-1880
-
-
Saiman, L.1
Prince, A.2
-
29
-
-
0026753576
-
Comparison of adherence of Pseudomonas aeruginosa to respiratory epithelial cells from cystic fibrosis patients healthy subjects
-
Saiman L, Cacalano G, Gruenert D and Prince A: Comparison of adherence of Pseudomonas aeruginosa to respiratory epithelial cells from cystic fibrosis patients and healthy subjects. Infect Immun 1992, 60: 2808-2814.
-
(1992)
Infect. Immun.
, vol.60
, pp. 2808-2814
-
-
Saiman, L.1
Cacalano, G.2
Gruenert, D.3
Prince, A.4
-
30
-
-
0024835905
-
Immunohistopathologic localization of Pseudomonas aeruginosa in lungs from patients with cystic fibrosis. Implications for the pathogenesis of progressive lung deterioration
-
Baltimore RS, Christie CD and Smith GJ: Immunohistopathologic localization of Pseudomonas aeruginosa in lungs from patients with cystic fibrosis. Implications for the pathogenesis of progressive lung deterioration. Am Rev Respir Dis 1989, 140: 1650-1661.
-
(1989)
Am. Rev. Respir. Dis.
, vol.140
, pp. 1650-1661
-
-
Baltimore, R.S.1
Christie, C.D.2
Smith, G.J.3
-
31
-
-
0032113268
-
Localization of Staphylococcus aureus in infected airways of patients with cystic fibrosis in a cell culture model of S. aureus adherence
-
Ulrich M, Herbert S, Berger J, Bellon G, Louis D, Munker G and Doring G: Localization of Staphylococcus aureus in infected airways of patients with cystic fibrosis and in a cell culture model of S. aureus adherence. Am J Respir Cell Mol Biol 1998, 19: 83-91.
-
(1998)
Am. J. Respir. Cell Mol. Biol.
, vol.19
, pp. 83-91
-
-
Ulrich, M.1
Herbert, S.2
Berger, J.3
Bellon, G.4
Louis, D.5
Munker, G.6
Doring, G.7
-
32
-
-
0035020777
-
Immunolocalisation of Burkholderia cepacia in the lungs of cystic fibrosis patients
-
Sajjan U, Corey M, Humar A, Tullis E, Cutz E, Ackerley C and Forstner J: Immunolocalisation of Burkholderia cepacia in the lungs of cystic fibrosis patients. J Med Microbiol 2001, 50: 535-546.
-
(2001)
J. Med. Microbiol.
, vol.50
, pp. 535-546
-
-
Sajjan, U.1
Corey, M.2
Humar, A.3
Tullis, E.4
Cutz, E.5
Ackerley, C.6
Forstner, J.7
-
33
-
-
17844377960
-
Inflammation in cystic fibrosis airways: Relationship to increased bacterial adherence
-
Scheid P, Kempster L, Griesenbach U, Davies JC, Dewar A, Weber PP, Colledge WH, Evans MJ, Geddes DM and Alton EW: Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence. Eur Respir J 2001, 17: 27-35.
-
(2001)
Eur. Respir. J.
, vol.17
, pp. 27-35
-
-
Scheid, P.1
Kempster, L.2
Griesenbach, U.3
Davies, J.C.4
Dewar, A.5
Weber, P.P.6
Colledge, W.H.7
Evans, M.J.8
Geddes, D.M.9
Alton, E.W.10
-
34
-
-
0032081281
-
Activation of NF-kappaB by adherent Pseudomonas aeruginosa in normal cystic fibrosis respiratory epithelial cells
-
DiMango E, Ratner AJ, Bryan R, Tabibi S and Prince A: Activation of NF-kappaB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells. J Clin Invest 1998, 101: 2598-2605.
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 2598-2605
-
-
DiMango, E.1
Ratner, A.J.2
Bryan, R.3
Tabibi, S.4
Prince, A.5
-
35
-
-
0028881698
-
Diverse Pseudomonas aeruginosa gene products stimulate respiratory epithelial cells to produce interleukin-8
-
DiMango E, Zar HJ, Bryan R and Prince A: Diverse Pseudomonas aeruginosa gene products stimulate respiratory epithelial cells to produce interleukin-8. J Clin Invest 1995, 96: 2204-2210.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 2204-2210
-
-
DiMango, E.1
Zar, H.J.2
Bryan, R.3
Prince, A.4
-
36
-
-
0031887898
-
The Pseudomonas aeruginosa flagellar cap protein, FliD, is responsible for mucin adhesion
-
Arora SK, Ritchings BW, Almira EC, Lory S and Ramphal R: The Pseudomonas aeruginosa flagellar cap protein, FliD, is responsible for mucin adhesion. Infect Immun 1998, 66: 1000-1007.
-
(1998)
Infect. Immun.
, vol.66
, pp. 1000-1007
-
-
Arora, S.K.1
Ritchings, B.W.2
Almira, E.C.3
Lory, S.4
Ramphal, R.5
-
37
-
-
0029910879
-
Recognition of mucin by the adhesin-flagellar system of Pseudomonas aeruginosa
-
Ramphal R, Arora SK and Ritchings BW: Recognition of mucin by the adhesin-flagellar system of Pseudomonas aeruginosa. Am J Respir Crit Care Med 1996, 154(4 Pt 2): S170-S174.
-
(1996)
Am. J. Respir. Crit. Care Med.
, vol.154
, Issue.4 PART 2
-
-
Ramphal, R.1
Arora, S.K.2
Ritchings, B.W.3
-
38
-
-
0031975347
-
Role of flagella in pathogenesis of Pseudomonas aeruginosa pulmonary infection
-
Feldman M, Bryan R, Rajan S, Scheffler L, Brunnert S, Tang H and Prince A: Role of flagella in pathogenesis of Pseudomonas aeruginosa pulmonary infection. Infect Immun 1998, 66: 43-51.
-
(1998)
Infect. Immun.
, vol.66
, pp. 43-51
-
-
Feldman, M.1
Bryan, R.2
Rajan, S.3
Scheffler, L.4
Brunnert, S.5
Tang, H.6
Prince, A.7
-
39
-
-
0023371348
-
Qualitative. quantitative microbiological analysis of sputa of 102 patients with cystic fibrosis
-
Bauernfeind A, Bertele RM, Harms K, Horl G, Jungwirth R, Petermuller C, Przyklenk B and Weisslein-Pfister C: Qualitative and quantitative microbiological analysis of sputa of 102 patients with cystic fibrosis. Infection 1987, 15: 270-277.
-
(1987)
Infection
, vol.15
, pp. 270-277
-
-
Bauernfeind, A.1
Bertele, R.M.2
Harms, K.3
Horl, G.4
Jungwirth, R.5
Petermuller, C.6
Przyklenk, B.7
Weisslein-Pfister, C.8
-
40
-
-
0026058195
-
Microbiology of airway disease in patients with cystic fibrosis
-
Gilligan PH: Microbiology of airway disease in patients with cystic fibrosis. Clin Microbiol Rev 1991, 4: 35-51.
-
(1991)
Clin. Microbiol. Rev.
, vol.4
, pp. 35-51
-
-
Gilligan, P.H.1
-
41
-
-
0032718969
-
Diagnostic accuracy of oropharyngeal cultures in infants young children with cystic fibrosis
-
Rosenfeld M, Emerson J, Accurso F, Armstrong D, Castile R, Grimwood K, Hiatt P, McCoy K, McNamara S, Ramsey B and Wagener J: Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis. Pediatr Pulmonol 1999, 28(2): 321-328.
-
(1999)
Pediatr. Pulmonol.
, vol.28
, Issue.2
, pp. 321-328
-
-
Rosenfeld, M.1
Emerson, J.2
Accurso, F.3
Armstrong, D.4
Castile, R.5
Grimwood, K.6
Hiatt, P.7
McCoy, K.8
McNamara, S.9
Ramsey, B.10
Wagener, J.11
-
42
-
-
0022463734
-
Biology of Pseudomonas aeruginosa in relation to pulmonary infection in cystic fibrosis
-
Pitt TL: Biology of Pseudomonas aeruginosa in relation to pulmonary infection in cystic fibrosis. J R Soc Med 1986, 79(Suppl 12): 13-18.
-
(1986)
J. R. Soc. Med.
, vol.79
, Issue.SUPPL. 12
, pp. 13-18
-
-
Pitt, T.L.1
-
43
-
-
0035087832
-
Multidrug efflux pumps antimicrobial resistance in Pseudomonas aeruginosa related organisms
-
Poole K: Multidrug efflux pumps and antimicrobial resistance in Pseudomonas aeruginosa and related organisms. J Mol Microbiol Biotechnol 2001, 3: 255-264.
-
(2001)
J. Mol. Microbiol. Biotechnol.
, vol.3
, pp. 255-264
-
-
Poole, K.1
-
44
-
-
0034685940
-
High Frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection
-
Oliver A, Canton R, Campo P, Baquero F and Blazquez J: High Frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. Science 2000, 288: 1251-1254.
-
(2000)
Science
, vol.288
, pp. 1251-1254
-
-
Oliver, A.1
Canton, R.2
Campo, P.3
Baquero, F.4
Blazquez, J.5
-
45
-
-
0036167851
-
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
-
Worlitzsch D, Tarran R, Ulrich M, Schwab U, Cekici A, Meyer KC, Birrer P, Bellon G, Berger J, Weiss T, Botzenhart K, Yankaskas JR, Randell S, Boucher RC and Doring G: Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. J Clin Invest 2002, 109: 317-325.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 317-325
-
-
Worlitzsch, D.1
Tarran, R.2
Ulrich, M.3
Schwab, U.4
Cekici, A.5
Meyer, K.C.6
Birrer, P.7
Bellon, G.8
Berger, J.9
Weiss, T.10
Botzenhart, K.11
Yankaskas, J.R.12
Randell, S.13
Boucher, R.C.14
Doring, G.15
-
46
-
-
0022529164
-
Pseudomonas aeruginosa : Biology mechanisms of virulence epidemiology
-
Vasil ML: Pseudomonas aeruginosa : biology, mechanisms of virulence, epidemiology. J Pediatr 1986, 108(5 Pt 2): 800-805.
-
(1986)
J. Pediatr.
, vol.108
, Issue.5 PART 2
, pp. 800-805
-
-
Vasil, M.L.1
-
47
-
-
0021269515
-
Nonspecific immunoglobulin synthesis elevated IgG levels in rabbits immunized with mucoid exopolysaccharide from cystic fibrosis isolates of Pseudomonas aeruginosa
-
Pier GB and Elcock ME: Nonspecific immunoglobulin synthesis and elevated IgG levels in rabbits immunized with mucoid exopolysaccharide from cystic fibrosis isolates of Pseudomonas aeruginosa. J Immunol 1984, 133: 734-739.
-
(1984)
J. Immunol.
, vol.133
, pp. 734-739
-
-
Pier, G.B.1
Elcock, M.E.2
-
48
-
-
0027499133
-
Immune complexes from immunized mice infected cystic fibrosis patients mediate murine human T cell killing of hybridomas producing protective opsonic antibody to Pseudomonas aeruginosa
-
Pier GB, Takeda S, Grout M and Markham RB: Immune complexes from immunized mice and infected cystic fibrosis patients mediate murine and human T cell killing of hybridomas producing protective, opsonic antibody to Pseudomonas aeruginosa. J Clin Invest 1993, 91: 1079-1087.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 1079-1087
-
-
Pier, G.B.1
Takeda, S.2
Grout, M.3
Markham, R.B.4
-
49
-
-
0025850634
-
Interaction between Pseudomonas aeruginosa and host defenses in cystic fibrosis
-
Marshall BC and Carroll KC: Interaction between Pseudomonas aeruginosa and host defenses in cystic fibrosis. Semin Respir Infect 1991, 6: 11-18.
-
(1991)
Semin. Respir. Infect.
, vol.6
, pp. 11-18
-
-
Marshall, B.C.1
Carroll, K.C.2
-
50
-
-
0028340887
-
Role of alginate lyase in cell detachment of Pseudomonas aeruginosa
-
Boyd A and Chakrabarty AM: Role of alginate lyase in cell detachment of Pseudomonas aeruginosa. Appl Environ Microbiol 1994, 60: 2355-2359.
-
(1994)
Appl. Environ. Microbiol.
, vol.60
, pp. 2355-2359
-
-
Boyd, A.1
Chakrabarty, A.M.2
-
51
-
-
0026135443
-
Longitudinal studies of virulence factors of Pseudomonas aeruginosa in cystic fibrosis
-
Burke V, Robinson JO, Richardson CJ and Bundell CS: Longitudinal studies of virulence factors of Pseudomonas aeruginosa in cystic fibrosis. Pathology 1991, 23: 145-148.
-
(1991)
Pathology
, vol.23
, pp. 145-148
-
-
Burke, V.1
Robinson, J.O.2
Richardson, C.J.3
Bundell, C.S.4
-
52
-
-
0029016495
-
Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection
-
Demko CA, Byard PJ and Davis PB: Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection. J Clin Epidemiol 1995, 48: 1041-1049.
-
(1995)
J. Clin. Epidemiol.
, vol.48
, pp. 1041-1049
-
-
Demko, C.A.1
Byard, P.J.2
Davis, P.B.3
-
53
-
-
0033584935
-
Specific lipopolysaccharide found in cystic fibrosis airway Pseudomonas aeruginosa
-
Ernst RK, Yi EC, Guo L, Lim KB, Burns JL, Hackett M and Miller SI: Specific lipopolysaccharide found in cystic fibrosis airway Pseudomonas aeruginosa. Science 1999, 286: 1561-1565.
-
(1999)
Science
, vol.286
, pp. 1561-1565
-
-
Ernst, R.K.1
Yi, E.C.2
Guo, L.3
Lim, K.B.4
Burns, J.L.5
Hackett, M.6
Miller, S.I.7
-
54
-
-
0024797909
-
Functional importance of cystic fibrosis immunoglobulin G fragments generated by Pseudomonas aeruginosa elastase
-
Bainbridge T and Fick RB Jr: Functional importance of cystic fibrosis immunoglobulin G fragments generated by Pseudomonas aeruginosa elastase. J Lab Clin Med 1989, 114: 728-733.
-
(1989)
J. Lab. Clin. Med.
, vol.114
, pp. 728-733
-
-
Bainbridge, T.1
Fick Jr., R.B.2
-
55
-
-
0020857013
-
Pseudomonas aeruginosa elastase its role in pseudomonas infections
-
Wretlind B and Pavlovskis OR: Pseudomonas aeruginosa elastase and its role in pseudomonas infections. Rev Infect Dis 1983, 5(Suppl): S998-S1004.
-
(1983)
Rev. Infect. Dis.
, vol.5
, Issue.SUPPL.
-
-
Wretlind, B.1
Pavlovskis, O.R.2
-
56
-
-
0021718398
-
Proteinases of Pseudomonas aeruginosa evoke mucin release by tracheal epithelium
-
Klinger JD, Tandler B, Liedtke CM and Boat TF: Proteinases of Pseudomonas aeruginosa evoke mucin release by tracheal epithelium. J Clin Invest 1984, 74: 1669-1678.
-
(1984)
J. Clin. Invest.
, vol.74
, pp. 1669-1678
-
-
Klinger, J.D.1
Tandler, B.2
Liedtke, C.M.3
Boat, T.F.4
-
57
-
-
0026593573
-
Acute lung injury induced by Pseudomonas aeruginosa elastase in hamsters
-
Williams JC, Lucas BJ, Knee C, Renzetti M and Donahue J: Acute lung injury induced by Pseudomonas aeruginosa elastase in hamsters. Exp Lung Res 1992, 18: 155-171.
-
(1992)
Exp. Lung Res.
, vol.18
, pp. 155-171
-
-
Williams, J.C.1
Lucas, B.J.2
Knee, C.3
Renzetti, M.4
Donahue, J.5
-
58
-
-
0036182477
-
Pulmonary inflammation induced by Pseudomonas aeruginosa lipopolysaccharide phospholipase C exotoxin A: Role of interferon regulatory factor 1
-
Wieland CW, Siegmund B, Senaldi G, Vasil ML, Dinarello CA and Fantuzzi G: Pulmonary inflammation induced by Pseudomonas aeruginosa lipopolysaccharide, phospholipase C, and exotoxin A: role of interferon regulatory factor 1. Infect Immun 2002, 70: 1352-1358.
-
(2002)
Infect. Immun.
, vol.70
, pp. 1352-1358
-
-
Wieland, C.W.1
Siegmund, B.2
Senaldi, G.3
Vasil, M.L.4
Dinarello, C.A.5
Fantuzzi, G.6
-
59
-
-
0030726075
-
The exoenzyme S regulon of Pseudomonas aeruginosa
-
Frank DW: The exoenzyme S regulon of Pseudomonas aeruginosa. Mol Microbiol 1997, 26: 621-629.
-
(1997)
Mol. Microbiol.
, vol.26
, pp. 621-629
-
-
Frank, D.W.1
-
60
-
-
0031816676
-
Pseudomonas aeruginosa exoenzyme S is a mitogen but not a superantigen for human T lymphocytes
-
Bruno TF, Buser DE, Syme RM, Woods DE and Mody CH: Pseudomonas aeruginosa exoenzyme S is a mitogen but not a superantigen for human T lymphocytes. Infect Immun 1998, 66: 3072-3079.
-
(1998)
Infect. Immun.
, vol.66
, pp. 3072-3079
-
-
Bruno, T.F.1
Buser, D.E.2
Syme, R.M.3
Woods, D.E.4
Mody, C.H.5
-
61
-
-
0025883003
-
Pseudomonas aeruginosa exoenzyme S is an adhesion
-
Baker NR, Minor V, Deal C, Shahrabadi MS, Simpson DA and Woods DE: Pseudomonas aeruginosa exoenzyme S is an adhesion. Infect Immun 1991, 59: 2859-2863.
-
(1991)
Infect. Immun.
, vol.59
, pp. 2859-2863
-
-
Baker, N.R.1
Minor, V.2
Deal, C.3
Shahrabadi, M.S.4
Simpson, D.A.5
Woods, D.E.6
-
62
-
-
0033752839
-
Pseudomonas aeruginosa exoenzyme S a bifunctional type-III secreted cytotoxin
-
Barbieri JT: Pseudomonas aeruginosa exoenzyme S, a bifunctional type-III secreted cytotoxin. Int J Med Microbiol 2000, 290: 381-387.
-
(2000)
Int. J. Med. Microbiol.
, vol.290
, pp. 381-387
-
-
Barbieri, J.T.1
-
63
-
-
0029902823
-
Fibronectin its alpha 5 beta 1-integrin receptor are involved in the wound-repair process of airway epithelium
-
Herard AL, Pierrot D, Hinnrasky J, Kaplan H, Sheppard D, Puchelle E and Zahm JM: Fibronectin and its alpha 5 beta 1-integrin receptor are involved in the wound-repair process of airway epithelium. Am J Physiol 1996, 271: L726-733.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Herard, A.L.1
Pierrot, D.2
Hinnrasky, J.3
Kaplan, H.4
Sheppard, D.5
Puchelle, E.6
Zahm, J.M.7
-
64
-
-
0036137206
-
In vivo rho GTPase- activating protein activity of Pseudomonas aeruginosa cytotoxin ExoS
-
Krall R, Sun J, Pederson KJ and Barbieri JT: In vivo rho GTPase- activating protein activity of Pseudomonas aeruginosa cytotoxin ExoS. Infect Immun 2002, 70: 360-367.
-
(2002)
Infect. Immun.
, vol.70
, pp. 360-367
-
-
Krall, R.1
Sun, J.2
Pederson, K.J.3
Barbieri, J.T.4
-
65
-
-
0022639413
-
Role of pyocyanin in the acquisition of iron from transferrin
-
Cox CD: Role of pyocyanin in the acquisition of iron from transferrin. Infect Immun 1986, 52: 263-270.
-
(1986)
Infect. Immun.
, vol.52
, pp. 263-270
-
-
Cox, C.D.1
-
66
-
-
0023108150
-
Pyocyanin 1-hydroxyphenazine produced by Pseudomonas aeruginosa inhibit the beating of human respiratory cilia in vitro
-
Wilson R, Pitt T, Taylor G, Watson D, MacDermot J, Sykes D, Roberts D and Cole P: Pyocyanin and 1-hydroxyphenazine produced by Pseudomonas aeruginosa inhibit the beating of human respiratory cilia in vitro. J Clin Invest 1987, 79: 221-229.
-
(1987)
J. Clin. Invest.
, vol.79
, pp. 221-229
-
-
Wilson, R.1
Pitt, T.2
Taylor, G.3
Watson, D.4
MacDermot, J.5
Sykes, D.6
Roberts, D.7
Cole, P.8
-
67
-
-
0027564440
-
Elevated exoenzyme expression by P. aeruginosa is correlated with exacerbations of lung disease in cystic fibrosis
-
Grimwood K, Semple RA, Rabin HR, Sokol PA and Woods DE: Elevated exoenzyme expression by P. aeruginosa is correlated with exacerbations of lung disease in cystic fibrosis. Pediatr Pulmonol 1993, 15: 135-139.
-
(1993)
Pediatr. Pulmonol.
, vol.15
, pp. 135-139
-
-
Grimwood, K.1
Semple, R.A.2
Rabin, H.R.3
Sokol, P.A.4
Woods, D.E.5
-
68
-
-
0028934314
-
Production of elastase exotoxin A alkaline protease in sputa during pulmonary exacerbation of cystic fibrosis in patients chronically infected by Pseudomonas aeruginosa
-
Jaffar-Bandjee MC, Lazdunski A, Bally M, Carrere J, Chazalette JP and Galabert C: Production of elastase, exotoxin A and alkaline protease in sputa during pulmonary exacerbation of cystic fibrosis in patients chronically infected by Pseudomonas aeruginosa. J Clin Microbiol 1995, 33: 924-929.
-
(1995)
J. Clin. Microbiol.
, vol.33
, pp. 924-929
-
-
Jaffar-Bandjee, M.C.1
Lazdunski, A.2
Bally, M.3
Carrere, J.4
Chazalette, J.P.5
Galabert, C.6
-
69
-
-
0036228505
-
Biofilms: Survival mechanisms of clinically relevant microorganisms
-
Donlan RM and Costerton JW: Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev 2002, 15: 167-193.
-
(2002)
Clin. Microbiol. Rev.
, vol.15
, pp. 167-193
-
-
Donlan, R.M.1
Costerton, J.W.2
-
70
-
-
0034641962
-
Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms
-
Singh PK, Schaefer AL, Parsek MR, Moninger TO, Welsh MJ and Greenberg EP: Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms. Nature 2000, 407: 762-764.
-
(2000)
Nature
, vol.407
, pp. 762-764
-
-
Singh, P.K.1
Schaefer, A.L.2
Parsek, M.R.3
Moninger, T.O.4
Welsh, M.J.5
Greenberg, E.P.6
-
71
-
-
0037129218
-
Pseudomonas biofilm formation antibiotic resistance are linked to phenotypic variation
-
Drenkard E and Ausubel FM: Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation. Nature 2002, 416: 740-743.
-
(2002)
Nature
, vol.416
, pp. 740-743
-
-
Drenkard, E.1
Ausubel, F.M.2
-
72
-
-
0037190575
-
Long term azithromycin in children with cystic fibrosis: A randomised placebo-controlled crossover trial
-
Equi A, Balfour-Lynn I, Bush A and Rosenthal M: Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial. Lancet 2002, 360: 978.
-
(2002)
Lancet
, vol.360
, pp. 978
-
-
Equi, A.1
Balfour-Lynn, I.2
Bush, A.3
Rosenthal, M.4
-
73
-
-
0036185807
-
Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: A randomised trial
-
Wolter J, Seeney S, Bell S, Bowler S, Masel P and McCormack J: Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial. Thorax 2002, 57: 212-216.
-
(2002)
Thorax
, vol.57
, pp. 212-216
-
-
Wolter, J.1
Seeney, S.2
Bell, S.3
Bowler, S.4
Masel, P.5
McCormack, J.6
-
75
-
-
0031660253
-
Burkholderia cepacia. Management issues new insights
-
LiPuma JJ: Burkholderia cepacia. Management issues and new insights. Clin Chest Med 1998, 19: 473-486.
-
(1998)
Clin. Chest Med.
, vol.19
, pp. 473-486
-
-
LiPuma, J.J.1
-
76
-
-
0033015044
-
Lipopolysaccharide (LPS) from Burkholderia cepacia is more active than LPS from Pseudomonas aeruginosa Stenotrophomonas maltophilia in stimulating tumor necrosis factor alpha from human monocytes
-
Zughaier SM, Ryley HC and Jackson SK: Lipopolysaccharide (LPS) from Burkholderia cepacia is more active than LPS from Pseudomonas aeruginosa and Stenotrophomonas maltophilia in stimulating tumor necrosis factor alpha from human monocytes. Infect Immun 1999, 67: 1505-1507.
-
(1999)
Infect. Immun.
, vol.67
, pp. 1505-1507
-
-
Zughaier, S.M.1
Ryley, H.C.2
Jackson, S.K.3
-
77
-
-
0030756397
-
Priming of neutrophil respiratory burst activity by lipopolysaccharide from Burkholderia cepacia
-
Hughes JE, Stewart J, Barclay GR and Govan JR: Priming of neutrophil respiratory burst activity by lipopolysaccharide from Burkholderia cepacia. Infect Immun 1997, 65: 4281-4287.
-
(1997)
Infect. Immun.
, vol.65
, pp. 4281-4287
-
-
Hughes, J.E.1
Stewart, J.2
Barclay, G.R.3
Govan, J.R.4
-
78
-
-
0032872906
-
Cystic fibrosis: Inflammatory response to infection with Burkholderia cepacia and Pseudomonas aeruginosa
-
Hendry J, Elborn JS, Nixon L, Shale DJ and Webb AK: Cystic fibrosis: Inflammatory response to infection with Burkholderia cepacia and Pseudomonas aeruginosa. Eur Respir J 1999, 14: 435-438.
-
(1999)
Eur. Respir. J.
, vol.14
, pp. 435-438
-
-
Hendry, J.1
Elborn, J.S.2
Nixon, L.3
Shale, D.J.4
Webb, A.K.5
-
79
-
-
0031035884
-
Nasal bronchoalveolar lavage fluid cytokines in early cystic fibrosis
-
Noah TL, Black HR, Cheng PW, Wood RE and Leigh MW: Nasal and bronchoalveolar lavage fluid cytokines in early cystic fibrosis. J Infect Dis 1997, 175: 638-647.
-
(1997)
J. Infect. Dis.
, vol.175
, pp. 638-647
-
-
Noah, T.L.1
Black, H.R.2
Cheng, P.W.3
Wood, R.E.4
Leigh, M.W.5
-
81
-
-
0028914085
-
Early pulmonary inflammation in infants with cystic fibrosis
-
Khan TZ, Wagener JS, Bost T, Martinez J, Accurso FJ and Riches DWH: Early pulmonary inflammation in infants with cystic fibrosis. Am J Respir Crit Care Med 1995, 151: 1075-1082.
-
(1995)
Am. J. Respir. Crit. Care Med.
, vol.151
, pp. 1075-1082
-
-
Khan, T.Z.1
Wagener, J.S.2
Bost, T.3
Martinez, J.4
Accurso, F.J.5
Riches, D.W.H.6
-
82
-
-
0030768159
-
Lower airway inflammation in infants young children with cystic fibrosis
-
Armstrong DS, Grimwood K, Carlin JB, Carzino R, Gutierrez JP, Hull J, Olinsky A, Phelan EM, Robertson CF and Phelan PD: Lower airway inflammation in infants and young children with cystic fibrosis. Am J Respir Crit Care Med 1997, 156: 1197-1204.
-
(1997)
Am. J. Respir. Crit. Care Med.
, vol.156
, pp. 1197-1204
-
-
Armstrong, D.S.1
Grimwood, K.2
Carlin, J.B.3
Carzino, R.4
Gutierrez, J.P.5
Hull, J.6
Olinsky, A.7
Phelan, E.M.8
Robertson, C.F.9
Phelan, P.D.10
-
83
-
-
0028784322
-
Inflammatory cytokines in cystic fibrosis lungs
-
Bonfield TL, Panuska JR, Konstan MW, Hillard KA, Hillard JB, Ghnaim H and Berger M: Inflammatory cytokines in cystic fibrosis lungs. Am J Respir Crit Care Med 1995, 152: 2111-2118.
-
(1995)
Am. J. Respir. Crit. Care Med.
, vol.152
, pp. 2111-2118
-
-
Bonfield, T.L.1
Panuska, J.R.2
Konstan, M.W.3
Hillard, K.A.4
Hillard, J.B.5
Ghnaim, H.6
Berger, M.7
-
84
-
-
0027682586
-
Leukotriene B4 is markedly elevated in the epithelial lining fluid of patients with cystic fibrosis
-
Konstan MW, Walenga RW, Hilliard KA and Hilliard JB: Leukotriene B4 is markedly elevated in the epithelial lining fluid of patients with cystic fibrosis. Am Rev Respir Dis 1993, 148: 896-901.
-
(1993)
Am. Rev. Respir. Dis.
, vol.148
, pp. 896-901
-
-
Konstan, M.W.1
Walenga, R.W.2
Hilliard, K.A.3
Hilliard, J.B.4
-
85
-
-
0029372481
-
Normal bronchial epithelial cells constitutively produce the anti-inflammatory cytokine interleukin-10 which is downregulated in cystic fibrosis
-
Bonfield TL, Konstan MW, Burfeind P, Panuska JR, Hillard JB and Berger M: Normal bronchial epithelial cells constitutively produce the anti-inflammatory cytokine interleukin-10, which is downregulated in cystic fibrosis. Am J Respir Cell Mol Biol 1995, 13: 257-261.
-
(1995)
Am. J. Respir. Cell Mol. Biol.
, vol.13
, pp. 257-261
-
-
Bonfield, T.L.1
Konstan, M.W.2
Burfeind, P.3
Panuska, J.R.4
Hillard, J.B.5
Berger, M.6
-
86
-
-
0032817772
-
Altered respiratory epithelial cell cytokine production in cystic fibrosis
-
Bonfield TL, Konstan MW and Berger M: Altered respiratory epithelial cell cytokine production in cystic fibrosis. J Allergy Clin Immunol 1999, 104: 72-78.
-
(1999)
J. Allergy Clin. Immunol.
, vol.104
, pp. 72-78
-
-
Bonfield, T.L.1
Konstan, M.W.2
Berger, M.3
-
87
-
-
0026474443
-
Modulation of airway inflammation in cystic fibrosis: In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor
-
McElvaney NG, Nakamura H, Birrer P, Hebert CA, Wong WL, Alphonso M, Baker JB, Catalano MA and Crystal RG: Modulation of airway inflammation in cystic fibrosis: In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor. J Clin Invest 1992, 90: 1296-1301.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 1296-1301
-
-
McElvaney, N.G.1
Nakamura, H.2
Birrer, P.3
Hebert, C.A.4
Wong, W.L.5
Alphonso, M.6
Baker, J.B.7
Catalano, M.A.8
Crystal, R.G.9
-
88
-
-
0026681802
-
Neutrophil elastase in respiratory epithelial lining fluid of individuals with cystic fibrosis induces interleukin-8 gene expression in human bronchial epithelial cell line
-
Nakamura H, Yoshimura K, McElvaney NG and Crystal RG: Neutrophil elastase in respiratory epithelial lining fluid of individuals with cystic fibrosis induces interleukin-8 gene expression in human bronchial epithelial cell line. J Clin Invest 1992, 89: 1478-1484.
-
(1992)
J. Clin. Invest.
, vol.89
, pp. 1478-1484
-
-
Nakamura, H.1
Yoshimura, K.2
McElvaney, N.G.3
Crystal, R.G.4
-
89
-
-
0025228983
-
Neutrophil elastase cathepsin G stimulate secretion from cultured bovine airway gland serous cells
-
Sommerhoff CP, Nadel JA, Basbaum CB and Caughey GH: Neutrophil elastase and cathepsin G stimulate secretion from cultured bovine airway gland serous cells. J Clin Invest 1990, 85: 682-689.
-
(1990)
J. Clin. Invest.
, vol.85
, pp. 682-689
-
-
Sommerhoff, C.P.1
Nadel, J.A.2
Basbaum, C.B.3
Caughey, G.H.4
-
90
-
-
0026599949
-
Neutrophil elastase stimulates tracheal submucosa gland secretion that is inhibited by ICI 200355
-
Schuster A, Ueki I and Nadel JA: Neutrophil elastase stimulates tracheal submucosa gland secretion that is inhibited by ICI 200,355. Am J Physiol 1992, 262: L86-L91.
-
(1992)
Am. J. Physiol.
, vol.262
-
-
Schuster, A.1
Ueki, I.2
Nadel, J.A.3
-
91
-
-
0018645925
-
Effect of human leukocyte enzymes on tracheal mucosa and mucociliary activity
-
Tegner H, Ohlsson K, Toremalm NG and von Mecklenbeurg C: Effect of human leukocyte enzymes on tracheal mucosa and mucociliary activity. Rhinology 1979, 17:199-206.
-
(1979)
Rhinology
, vol.17
, pp. 199-206
-
-
Tegner, H.1
Ohlsson, K.2
Toremalm, N.G.3
von Mecklenbeurg, C.4
-
92
-
-
0023766047
-
Functional differences between the 40 kDa 50 to 70 kDa IgG Fc receptors on human neutrophils revealed by elastase treatment antireceptor antibodies
-
Tosi MF and Berger M: Functional differences between the 40 kDa and 50 to 70 kDa IgG Fc receptors on human neutrophils revealed by elastase treatment and antireceptor antibodies. J Immunol 1988, 141:2097-2103.
-
(1988)
J. Immunol.
, vol.141
, pp. 2097-2103
-
-
Tosi, M.F.1
Berger, M.2
-
93
-
-
0026737931
-
Surface expression of Fc gamma receptor III (CD 16) on chemoattractant-stimulated neutrophils is determined by both surface shedding translocation from intracellular storage compartments
-
Tosi MF and Zakem H: Surface expression of Fc gamma receptor III (CD 16) on chemoattractant-stimulated neutrophils is determined by both surface shedding and translocation from intracellular storage compartments. J Clin Invest 1992, 90:462-470.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 462-470
-
-
Tosi, M.F.1
Zakem, H.2
-
94
-
-
0025374923
-
Neutrophil elastase cleaves C3bi on opsonized pseudomonas as well as CR1 on neutrophils to create a functionally important opsonin receptor mismatch
-
Tosi MF, Zakem H and Berger M: Neutrophil elastase cleaves C3bi on opsonized pseudomonas as well as CR1 on neutrophils to create a functionally important opsonin receptor mismatch. J Clin Invest 1990, 86:300-308.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 300-308
-
-
Tosi, M.F.1
Zakem, H.2
Berger, M.3
-
95
-
-
0024459145
-
Complement receptor expression on neutrophils at an inflammatory site the pseudomonas-infected lung in cystic fibrosis
-
Berger M, Sorensen RU, Tosi MF, Dearborn DG and Doring G: Complement receptor expression on neutrophils at an inflammatory site, the pseudomonas-infected lung in cystic fibrosis. J Clin Invest 1989, 84:1302-1313.
-
(1989)
J. Clin. Invest.
, vol.84
, pp. 1302-1313
-
-
Berger, M.1
Sorensen, R.U.2
Tosi, M.F.3
Dearborn, D.G.4
Doring, G.5
-
96
-
-
0028240276
-
Protease-antiprotease imbalance in the lungs of children with cystic fibrosis
-
Birrer P, McElvaney NG, Rudeberg A, Sommer CW, Liechti-Gallati S, Kraemer R, Hubbard R and Crystal RG: Protease-antiprotease imbalance in the lungs of children with cystic fibrosis. Am J Respir Crit Care Med 1994, 150:207-213.
-
(1994)
Am. J. Respir. Crit. Care Med.
, vol.150
, pp. 207-213
-
-
Birrer, P.1
McElvaney, N.G.2
Rudeberg, A.3
Sommer, C.W.4
Liechti-Gallati, S.5
Kraemer, R.6
Hubbard, R.7
Crystal, R.G.8
-
97
-
-
0034816784
-
Antioxidant imbalance in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice
-
Velsor LW, van Heeckeren A and Day BJ: Antioxidant imbalance in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice. Am J Physiol Lung Cell Mol Physiol 2001, 281:L31-L38.
-
(2001)
Am. J. Physiol. Lung Cell Mol. Physiol.
, vol.281
-
-
Velsor, L.W.1
van Heeckeren, A.2
Day, B.J.3
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