Animal model for cystic fibrosis: pulmonary clearance of Staphylococcus aureus in mice treated with reserpine.
暂无分享，去创建一个
[1] D. Sordelli,et al. Pulmonary Clearance of Staphylococcus aureus in Mutant Mice with Some Hereditary Alterations Resembling Cystic Fibrosis , 1977, Pediatric Research.
[2] B. Pleuvry,et al. A comparison of the effects of morphine and pethidine upon body temperature and the reversal of reserpine's effects upon body temperature in the mouse , 1976, The Journal of pharmacy and pharmacology.
[3] P. di Sant'Agnese,et al. Research in cystic fibrosis (second of three parts). , 1976, The New England journal of medicine.
[4] R. Stitzel. The biological fate of reserpine. , 1976, Pharmacological reviews.
[5] D. Quissell,et al. The Chronically Reserpinized Rat as a Possible Animal Model for Cystic Fibrosis. IV. The Protein Composition of Pulmonary Lavage Fluid , 1976, Pediatric Research.
[6] G. Barbero,et al. The Chronically Reserpinized Rat as a Possible Model for Cystic Fibrosis. I. Submaxillary Gland Morphology and Ultrastructure , 1975, Pediatric Research.
[7] K. C. Richardson,et al. A new effect of reserpine: accumulation of glycoprotein in the submaxillary gland. , 1967, The Journal of pharmacology and experimental therapeutics.
[8] E. Kass,et al. FACTORS INFLUENCING THE CLEARANCE OF BACTERIA BY THE LUNG. , 1964, The Journal of clinical investigation.