Cystic Fibrosis Research Today is a free monthly online journal that collates and summarizes the latest research about Cystic Fibrosis, including details on symptoms, genetics, treatment, information.

Volume 4 (2007), Issue 5 (May)

1. Plasma fatty acids and lipid hydroperoxides increase after antibiotic therapy in cystic fibrosis.
   Eur Respir J, 29(5): 958-64. [Abstract] [Full-text]
2. Selection of nitrogen-fixing deficient Burkholderia vietnamiensis strains by cystic fibrosis patients: involvement of nif gene deletions and auxotrophic mutations.
   Environ Microbiol, 9(5): 1176-85. [Abstract] [Full-text]
3. Molecular epidemiology of Mycobacterium abscessus, with focus on cystic fibrosis.
   J Clin Microbiol, 45(5): 1497-504. [Abstract] [Full-text]
4. Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X.
   J Med Genet, 44(5): 341-6. [Abstract] [Full-text]
5. Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes.
   Pediatr Pulmonol, 42(6): 533-41. [Abstract] [Full-text]
6. Predictors of mortality in adults with cystic fibrosis.
   Pediatr Pulmonol, 42(6): 525-32. [Abstract] [Full-text]
7. Amiloride-insensitive nasal potential difference varies with the menstrual cycle in cystic fibrosis.
   Pediatr Pulmonol, 42(6): 519-24. [Abstract] [Full-text]
8. Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function.
   Pediatr Pulmonol, 42(6): 513-8. [Abstract] [Full-text]
9. Heritability of lung disease severity in cystic fibrosis.
   Am J Respir Crit Care Med, 175(10): 1036-43. [Abstract] [Full-text]
10. Exceptionally high representation of Burkholderia cepacia among B. cepacia complex isolates recovered from the major Portuguese cystic fibrosis center.
    J Clin Microbiol, 45(5): 1628-33. [Abstract] [Full-text]
11. Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis.
    J Appl Physiol, 102(5): 1969-75. [Abstract] [Full-text]
12. Role of IKK and ERK pathways in intrinsic inflammation of cystic fibrosis airways.
    Biochem Pharmacol, 73(12): 1982-94. [Abstract] [Full-text]
13. Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients.
    Mol Microbiol, 64(2): 512-33. [Abstract] [Full-text]
14. Inhalation of Moli1901 in patients with cystic fibrosis.
    Chest, 131(5): 1461-6. [Abstract] [Full-text]
15. Induction of IL-6 gene expression in a CF bronchial epithelial cell line by Pseudomonas aeruginosa is dependent on transcription factors belonging to the Sp1 superfamily.
    Biochem Biophys Res Commun, 357(4): 977-83. [Abstract] [Full-text]
16. Beta-2-adrenergic receptor polymorphisms in cystic fibrosis.
    Pharmacogenet Genomics, 17(6): 425-30. [Abstract] [Full-text]
17. Abdominal dystocia in a case of undetected intrauterine meconium peritonitis due to cystic fibrosis.
    Congenit Anom (Kyoto), 47(2): 72-3. [Abstract] [Full-text]
18. Burkholderia cenocepacia, B. multivorans, B. ambifaria and B. vietnamiensis isolates from cystic fibrosis patients have different profiles of exoenzyme production.
    APMIS, 115(4): 311-8. [Abstract] [Full-text]
19. Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association.
    J Pediatr, 150(6): 656-8, 658.e1. [Abstract] [Full-text]
20. RSV mediates Pseudomonas aeruginosa binding to cystic fibrosis and normal epithelial cells.
    Pediatr Res, 61(4): 398-403. [Abstract] [Full-text]
21. Sweat testing practice in Swiss hospitals.
    Swiss Med Wkly, 137(13): 192-8. [Abstract] [Full-text]
22. Survey of acute renal failure in patients with cystic fibrosis in the UK.
    Thorax, 62(6): 541-5. [Abstract] [Full-text]
23. Pseudomembranous colitis in four patients with cystic fibrosis following lung transplantation.
    Thorax, 62(6): 554-6. [Abstract] [Full-text]
24. Educational practice for inhaled treatments in French cystic fibrosis care centers.
    J Aerosol Med, 20(2): 105-11. [Abstract] [Full-text]

© 2004-2010 Cystic Fibrosis Research Today. All Rights Reserved.