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D G Dearborn

Showing results (41-50 of 52) with videos related to

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Protein Science : a Publication of the Protein Society|January 1, 1996
A recombinant peptide model of the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator: comparison of wild-type and delta F508 mutant formsI Yike, J Ye, Y Zhang, et al.
Infection and Immunity|July 1, 1983
In vitro inhibition of lymphocyte proliferation by Pseudomonas aeruginosa phenazine pigmentsR U Sorensen, J D Klinger, H A Cash, et al.
Biopolymers|July 1, 1983
Solution properties of porcine submaxillary mucinR Shogren, A M Jamieson, J Blackwell, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 15, 1994
Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-rJ J Wisnieski, T C Knauss, I Yike, et al.
Pediatric Research|September 1, 1979
Inhibitory effect of cystic fibrosis serum on pseudomonas phagocytosis by rabbit and human alveolar macrophagesM J Thomassen, B Boxerbaum, C A Demko, et al.
The American Review of Respiratory Disease|September 1, 1985
Biochemical and pathologic evidence for proteolytic destruction of lung connective tissue in cystic fibrosisM C Bruce, L Poncz, J D Klinger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1987
Studies on the mechanism of T cell inhibition by the Pseudomonas aeruginosa phenazine pigment pyocyanineJ Nutman, M Berger, P A Chase, et al.
Pediatric Research|May 1, 1980
Ultrastructure and function of alveolar macrophages from cystic fibrosis patientsM J Thomassen, C A Demko, R E Wood, et al.
Journal of Urban Health : Bulletin of the New York Academy of Medicine|March 31, 2000
Evaluation of Stachybotrys chartarum in the house of an infant with pulmonary hemorrhage: quantitative assessment before, during, and after remediationS Vesper, D G Dearborn, I Yike, et al.
The American Review of Respiratory Disease|October 1, 1985
Immune complexes and complement abnormalities in patients with cystic fibrosis. Increased mortality associated with circulating immune complexes and decreased function of the alternative complement pathwayJ J Wisnieski, E W Todd, R K Fuller, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Protein Science : a Publication of the Protein Society|January 1, 1996
A recombinant peptide model of the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator: comparison of wild-type and delta F508 mutant formsI Yike, J Ye, Y Zhang, et al.
Infection and Immunity|July 1, 1983
In vitro inhibition of lymphocyte proliferation by Pseudomonas aeruginosa phenazine pigmentsR U Sorensen, J D Klinger, H A Cash, et al.
Biopolymers|July 1, 1983
Solution properties of porcine submaxillary mucinR Shogren, A M Jamieson, J Blackwell, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 15, 1994
Unique C1 inhibitor dysfunction in a kindred without angioedema. I. A mutant C1 INH that inhibits C1-s but not C1-rJ J Wisnieski, T C Knauss, I Yike, et al.
Pediatric Research|September 1, 1979
Inhibitory effect of cystic fibrosis serum on pseudomonas phagocytosis by rabbit and human alveolar macrophagesM J Thomassen, B Boxerbaum, C A Demko, et al.
The American Review of Respiratory Disease|September 1, 1985
Biochemical and pathologic evidence for proteolytic destruction of lung connective tissue in cystic fibrosisM C Bruce, L Poncz, J D Klinger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1987
Studies on the mechanism of T cell inhibition by the Pseudomonas aeruginosa phenazine pigment pyocyanineJ Nutman, M Berger, P A Chase, et al.
Pediatric Research|May 1, 1980
Ultrastructure and function of alveolar macrophages from cystic fibrosis patientsM J Thomassen, C A Demko, R E Wood, et al.
Journal of Urban Health : Bulletin of the New York Academy of Medicine|March 31, 2000
Evaluation of Stachybotrys chartarum in the house of an infant with pulmonary hemorrhage: quantitative assessment before, during, and after remediationS Vesper, D G Dearborn, I Yike, et al.
The American Review of Respiratory Disease|October 1, 1985
Immune complexes and complement abnormalities in patients with cystic fibrosis. Increased mortality associated with circulating immune complexes and decreased function of the alternative complement pathwayJ J Wisnieski, E W Todd, R K Fuller, et al.
Pageof 6