187 related articles for article (PubMed ID: 22314624)
1. Role of CD95 in pulmonary inflammation and infection in cystic fibrosis.
Becker KA; Henry B; Ziobro R; Tümmler B; Gulbins E; Grassmé H
J Mol Med (Berl); 2012 Sep; 90(9):1011-23. PubMed ID: 22314624
[TBL] [Abstract][Full Text] [Related]
2. Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis.
Teichgräber V; Ulrich M; Endlich N; Riethmüller J; Wilker B; De Oliveira-Munding CC; van Heeckeren AM; Barr ML; von Kürthy G; Schmid KW; Weller M; Tümmler B; Lang F; Grassme H; Döring G; Gulbins E
Nat Med; 2008 Apr; 14(4):382-91. PubMed ID: 18376404
[TBL] [Abstract][Full Text] [Related]
3. Interferon regulatory factor 8 regulates expression of acid ceramidase and infection susceptibility in cystic fibrosis.
Gardner AI; Wu Y; Verhaegh R; Liu Y; Wilker B; Soddemann M; Keitsch S; Edwards MJ; Haq IJ; Kamler M; Becker KA; Brodlie M; Gulbins E
J Biol Chem; 2021; 296():100650. PubMed ID: 33839155
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Pseudomonas aeruginosa-induced apoptosis is defective in respiratory epithelial cells expressing mutant cystic fibrosis transmembrane conductance regulator.
Cannon CL; Kowalski MP; Stopak KS; Pier GB
Am J Respir Cell Mol Biol; 2003 Aug; 29(2):188-97. PubMed ID: 12878584
[TBL] [Abstract][Full Text] [Related]
6. CFTR-dependent susceptibility of the cystic fibrosis-host to Pseudomonas aeruginosa.
Grassmé H; Becker KA; Zhang Y; Gulbins E
Int J Med Microbiol; 2010 Dec; 300(8):578-83. PubMed ID: 20951085
[TBL] [Abstract][Full Text] [Related]
7. Acid sphingomyelinase inhibitors normalize pulmonary ceramide and inflammation in cystic fibrosis.
Becker KA; Riethmüller J; Lüth A; Döring G; Kleuser B; Gulbins E
Am J Respir Cell Mol Biol; 2010 Jun; 42(6):716-24. PubMed ID: 19635928
[TBL] [Abstract][Full Text] [Related]
8. Critical modifier role of membrane-cystic fibrosis transmembrane conductance regulator-dependent ceramide signaling in lung injury and emphysema.
Bodas M; Min T; Mazur S; Vij N
J Immunol; 2011 Jan; 186(1):602-13. PubMed ID: 21135173
[TBL] [Abstract][Full Text] [Related]
9. Ceramide in Pseudomonas aeruginosa infections and cystic fibrosis.
Becker KA; Grassmé H; Zhang Y; Gulbins E
Cell Physiol Biochem; 2010; 26(1):57-66. PubMed ID: 20502005
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Invariant natural killer T (iNKT) cells prevent autoimmunity, but induce pulmonary inflammation in cystic fibrosis.
Siegmann N; Worbs D; Effinger F; Bormann T; Gebhardt M; Ulrich M; Wermeling F; Müller-Hermelink E; Biedermann T; Tighe M; Edwards MJ; Caldwell C; Leadbetter E; Karlsson MC; Becker KA; Gulbins E; Döring G
Cell Physiol Biochem; 2014; 34(1):56-70. PubMed ID: 24977481
[TBL] [Abstract][Full Text] [Related]
12. Role for cystic fibrosis transmembrane conductance regulator protein in a glutathione response to bronchopulmonary pseudomonas infection.
Day BJ; van Heeckeren AM; Min E; Velsor LW
Infect Immun; 2004 Apr; 72(4):2045-51. PubMed ID: 15039325
[TBL] [Abstract][Full Text] [Related]
13. Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.
Pier GB
Proc Natl Acad Sci U S A; 2000 Aug; 97(16):8822-8. PubMed ID: 10922041
[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. IL-17 primes airway epithelial cells lacking functional Cystic Fibrosis Transmembrane conductance Regulator (CFTR) to increase NOD1 responses.
Roussel L; Rousseau S
Biochem Biophys Res Commun; 2010 Jan; 391(1):505-9. PubMed ID: 19931506
[TBL] [Abstract][Full Text] [Related]
16. Nutritional effects on host response to lung infections with mucoid Pseudomonas aeruginosa in mice.
van Heeckeren AM; Schluchter M; Xue L; Alvarez J; Freedman S; St George J; Davis PB
Infect Immun; 2004 Mar; 72(3):1479-86. PubMed ID: 14977953
[TBL] [Abstract][Full Text] [Related]
17. Fenretinide corrects newly found ceramide deficiency in cystic fibrosis.
Guilbault C; De Sanctis JB; Wojewodka G; Saeed Z; Lachance C; Skinner TA; Vilela RM; Kubow S; Lands LC; Hajduch M; Matouk E; Radzioch D
Am J Respir Cell Mol Biol; 2008 Jan; 38(1):47-56. PubMed ID: 17656682
[TBL] [Abstract][Full Text] [Related]
18. The role of the CFTR in susceptibility to Pseudomonas aeruginosa infections in cystic fibrosis.
Goldberg JB; Pier GB
Trends Microbiol; 2000 Nov; 8(11):514-20. PubMed ID: 11121762
[TBL] [Abstract][Full Text] [Related]
19. Regulation of the inflammasome by ceramide in cystic fibrosis lungs.
Grassmé H; Carpinteiro A; Edwards MJ; Gulbins E; Becker KA
Cell Physiol Biochem; 2014; 34(1):45-55. PubMed ID: 24977480
[TBL] [Abstract][Full Text] [Related]
20. Accumulation of ceramide in the trachea and intestine of cystic fibrosis mice causes inflammation and cell death.
Becker KA; Tümmler B; Gulbins E; Grassmé H
Biochem Biophys Res Commun; 2010 Dec; 403(3-4):368-74. PubMed ID: 21078296
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]