Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator
- 28 February 1995
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 126 (2), 230-233
- https://doi.org/10.1016/s0022-3476(95)70549-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Pseudomonas aeruginosa pili bind to asialoGM1 which is increased on the surface of cystic fibrosis epithelial cells.Journal of Clinical Investigation, 1993
- Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosisCell, 1993
- Prognostic implications of initial oropharyngeal bacterial flora in patients with cystic fibrosis diagnosed before the age of two yearsThe Journal of Pediatrics, 1993
- Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosisThe Lancet, 1993
- Defective acidification of intracellular organelles in cystic fibrosisNature, 1991
- Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutationThe Lancet, 1991
- The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF508)New England Journal of Medicine, 1990
- Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosaThe Journal of Pediatrics, 1990
- Many pulmonary pathogenic bacteria bind specifically to the carbohydrate sequence GalNAc beta 1-4Gal found in some glycolipids.Proceedings of the National Academy of Sciences, 1988
- Long-Term Study of One Hundred Five Patients with Cystic FibrosisA.M.A. Journal of Diseases of Children, 1958