Showing results (81-90 of 163) with videos related to
Sort By:
Pageof 17
British Journal of Sports Medicine|October 25, 2008
Biomechanical variables associated with Achilles tendinopathy in runnersL B Azevedo, M I Lambert, C L Vaughan, et al.Gamete Research|March 1, 1989
Protein carboxyl methyltransferase activity specific for age-modified aspartyl residues in mouse testes and ovaries: evidence for translation during spermiogenesisC M O'Connor, B J Germain, K M Guthrie, et al.American Journal of Respiratory Cell and Molecular Biology|May 26, 1999
Migration of neutrophils across human pulmonary endothelial cells is not blocked by matrix metalloproteinase or serine protease inhibitorsA J Mackarel, D C Cottell, K J Russell, et al.Insect Biochemistry and Molecular Biology|January 1, 1997
Structural organization and developmental expression of the protein isoaspartyl methyltransferase gene from Drosophila melanogasterM B O'Connor, A Galus, M Hartenstine, et al.American Journal of Respiratory and Critical Care Medicine|September 1, 1994
Neutrophil collagenase in sputum from patients with cystic fibrosisC Power, C M O'Connor, D MacFarlane, et al.Matrix Biology : Journal of the International Society for Matrix Biology|October 12, 1999
Ultrastructure of lung elastin and collagen in mouse models of spontaneous emphysemaM D O'Donnell, C M O'Connor, M X FitzGerald, et al.The American Review of Respiratory Disease|December 1, 1993
alpha 1-Proteinase inhibitor, elastase activity, and lung disease severity in cystic fibrosisC M O'Connor, K Gaffney, J Keane, et al.American Heart Journal|March 29, 2001
Evaluation Study of Congestive Heart Failure and Pulmonary Artery Catheterization Effectiveness (ESCAPE): design and rationaleM R Shah, C M O'Connor, G Sopko, et al.Thorax|June 1, 1996
Effect of nebulised recombinant DNase on neutrophil elastase load in cystic fibrosisC M Costello, C M O'Connor, G A Finlay, et al.European Journal of Human Genetics : EJHG|April 21, 2001
An alpha1-antitrypsin enhancer polymorphism is a genetic modifier of pulmonary outcome in cystic fibrosisM T Henry, S Cave, J Rendall, et al.Pageof 17