These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis. Yu H; Nasr SZ; Deretic V Infect Immun; 2000 Apr; 68(4):2142-7. PubMed ID: 10722612 [TBL] [Abstract][Full Text] [Related]
9. Mouse models of chronic lung infection with Pseudomonas aeruginosa: models for the study of cystic fibrosis. Stotland PK; Radzioch D; Stevenson MM Pediatr Pulmonol; 2000 Nov; 30(5):413-24. PubMed ID: 11064433 [TBL] [Abstract][Full Text] [Related]
10. Viral-Bacterial Co-infections in the Cystic Fibrosis Respiratory Tract. Kiedrowski MR; Bomberger JM Front Immunol; 2018; 9():3067. PubMed ID: 30619379 [TBL] [Abstract][Full Text] [Related]
11. How mutant CFTR may contribute to Pseudomonas aeruginosa infection in cystic fibrosis. Pier GB; Grout M; Zaidi TS; Goldberg JB Am J Respir Crit Care Med; 1996 Oct; 154(4 Pt 2):S175-82. PubMed ID: 8876538 [TBL] [Abstract][Full Text] [Related]
13. Mucoid Pseudomonas aeruginosa in cystic fibrosis: characterization of muc mutations in clinical isolates and analysis of clearance in a mouse model of respiratory infection. Boucher JC; Yu H; Mudd MH; Deretic V Infect Immun; 1997 Sep; 65(9):3838-46. PubMed ID: 9284161 [TBL] [Abstract][Full Text] [Related]
14. Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections. Pier GB; Grout M; Zaidi TS; Olsen JC; Johnson LG; Yankaskas JR; Goldberg JB Science; 1996 Jan; 271(5245):64-7. PubMed ID: 8539601 [TBL] [Abstract][Full Text] [Related]
15. Airway epithelial control of Pseudomonas aeruginosa infection in cystic fibrosis. Campodónico VL; Gadjeva M; Paradis-Bleau C; Uluer A; Pier GB Trends Mol Med; 2008 Mar; 14(3):120-33. PubMed ID: 18262467 [TBL] [Abstract][Full Text] [Related]
16. Clinical and microbiological characteristics of cystic fibrosis adults never colonized by Pseudomonas aeruginosa: Analysis of the French CF registry. Vongthilath R; Richaud Thiriez B; Dehillotte C; Lemonnier L; Guillien A; Degano B; Dalphin ML; Dalphin JC; Plésiat P PLoS One; 2019; 14(1):e0210201. PubMed ID: 30620748 [TBL] [Abstract][Full Text] [Related]
17. Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation. Ferrari E; Monzani R; Villella VR; Esposito S; Saluzzo F; Rossin F; D'Eletto M; Tosco A; De Gregorio F; Izzo V; Maiuri MC; Kroemer G; Raia V; Maiuri L Cell Death Dis; 2017 Jan; 8(1):e2544. PubMed ID: 28079883 [TBL] [Abstract][Full Text] [Related]
18. Lung and Gut Microbiota Changes Associated with Bacci G; Rossi A; Armanini F; Cangioli L; De Fino I; Segata N; Mengoni A; Bragonzi A; Bevivino A Int J Mol Sci; 2021 Nov; 22(22):. PubMed ID: 34830048 [TBL] [Abstract][Full Text] [Related]