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M R Knowles

Showing results (41-50 of 109) with videos related to

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Progress in Clinical and Biological Research|January 1, 1987
Is cystic fibrosis respiratory epithelium characterized by a single defect (Cl-) or multiple ion transport defects?R C Boucher, C U Cotton, M J Stutts, et al.
Experimental Lung Research|May 17, 2000
Prolonged airway retention of insoluble particles in cystic fibrosis versus primary ciliary dyskinesiaJ A Regnis, K L Zeman, P G Noone, et al.
Pediatric Research|December 1, 1984
Cl- permeabilities in red blood cells and peripheral blood lymphocytes from cystic fibrosis and control subjectsR C Boucher, D W Ross, M R Knowles, et al.
The American Review of Respiratory Disease|July 1, 1982
Measurements of transepithelial electric potential differences in the trachea and bronchi of human subjects in vivoM R Knowles, W H Buntin, P A Bromberg, et al.
The American Review of Respiratory Disease|October 1, 1981
Measurements of nasal transepithelial electric potential differences in normal human subjects in vivoM R Knowles, J L Carson, A M Collier, et al.
Human Pathology|June 1, 1990
Ultrastructure of airway epithelial cell membranes among patients with cystic fibrosisJ L Carson, A M Collier, T M Gambling, et al.
The Journal of Clinical Investigation|January 1, 1987
Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysisC U Cotton, M J Stutts, M R Knowles, et al.
The Journal of Physiology|November 1, 1988
Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell culturesR C Boucher, C U Cotton, J T Gatzy, et al.
Toxicology and Applied Pharmacology|February 1, 1986
Effects of formaldehyde on bronchial ion transportM J Stutts, J T Gatzy, M R Knowles, et al.
The Journal of Pediatrics|March 20, 1998
Comparison of the clinical manifestations of cystic fibrosis in black and white patientsA Hamosh, S C FitzSimmons, M Macek, et al.
Pageof 11

Showing results (41-50 of 109) with videos related to

Sort By:
Pageof 11
Progress in Clinical and Biological Research|January 1, 1987
Is cystic fibrosis respiratory epithelium characterized by a single defect (Cl-) or multiple ion transport defects?R C Boucher, C U Cotton, M J Stutts, et al.
Experimental Lung Research|May 17, 2000
Prolonged airway retention of insoluble particles in cystic fibrosis versus primary ciliary dyskinesiaJ A Regnis, K L Zeman, P G Noone, et al.
Pediatric Research|December 1, 1984
Cl- permeabilities in red blood cells and peripheral blood lymphocytes from cystic fibrosis and control subjectsR C Boucher, D W Ross, M R Knowles, et al.
The American Review of Respiratory Disease|July 1, 1982
Measurements of transepithelial electric potential differences in the trachea and bronchi of human subjects in vivoM R Knowles, W H Buntin, P A Bromberg, et al.
The American Review of Respiratory Disease|October 1, 1981
Measurements of nasal transepithelial electric potential differences in normal human subjects in vivoM R Knowles, J L Carson, A M Collier, et al.
Human Pathology|June 1, 1990
Ultrastructure of airway epithelial cell membranes among patients with cystic fibrosisJ L Carson, A M Collier, T M Gambling, et al.
The Journal of Clinical Investigation|January 1, 1987
Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysisC U Cotton, M J Stutts, M R Knowles, et al.
The Journal of Physiology|November 1, 1988
Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell culturesR C Boucher, C U Cotton, J T Gatzy, et al.
Toxicology and Applied Pharmacology|February 1, 1986
Effects of formaldehyde on bronchial ion transportM J Stutts, J T Gatzy, M R Knowles, et al.
The Journal of Pediatrics|March 20, 1998
Comparison of the clinical manifestations of cystic fibrosis in black and white patientsA Hamosh, S C FitzSimmons, M Macek, et al.
Pageof 11