97 related articles for article (PubMed ID: 30732491)
1. Novel cystamine-core dendrimer-formulation rescues ΔF508-CFTR and inhibits Pseudomonas aeruginosa infection by augmenting autophagy.
Faraj J; Bodas M; Pehote G; Swanson D; Sharma A; Vij N
Expert Opin Drug Deliv; 2019 Feb; 16(2):177-186. PubMed ID: 30732491
[TBL] [Abstract][Full Text] [Related]
2. Dendrimer-based selective autophagy-induction rescues ΔF508-CFTR and inhibits Pseudomonas aeruginosa infection in cystic fibrosis.
Brockman SM; Bodas M; Silverberg D; Sharma A; Vij N
PLoS One; 2017; 12(9):e0184793. PubMed ID: 28902888
[TBL] [Abstract][Full Text] [Related]
3. Targeting autophagy as a novel strategy for facilitating the therapeutic action of potentiators on ΔF508 cystic fibrosis transmembrane conductance regulator.
Luciani A; Villella VR; Esposito S; Gavina M; Russo I; Silano M; Guido S; Pettoello-Mantovani M; Carnuccio R; Scholte B; De Matteis A; Maiuri MC; Raia V; Luini A; Kroemer G; Maiuri L
Autophagy; 2012 Nov; 8(11):1657-72. PubMed ID: 22874563
[TBL] [Abstract][Full Text] [Related]
4. Towards a rational combination therapy of cystic fibrosis: How cystamine restores the stability of mutant CFTR.
Villella VR; Esposito S; Maiuri MC; Raia V; Kroemer G; Maiuri L
Autophagy; 2013 Sep; 9(9):1431-4. PubMed ID: 23800975
[TBL] [Abstract][Full Text] [Related]
5. Nano-based rescue of dysfunctional autophagy in chronic obstructive lung diseases.
Vij N
Expert Opin Drug Deliv; 2017 Apr; 14(4):483-489. PubMed ID: 27561233
[TBL] [Abstract][Full Text] [Related]
6. The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability.
Moreau-Marquis S; Bomberger JM; Anderson GG; Swiatecka-Urban A; Ye S; O'Toole GA; Stanton BA
Am J Physiol Lung Cell Mol Physiol; 2008 Jul; 295(1):L25-37. PubMed ID: 18359885
[TBL] [Abstract][Full Text] [Related]
7. ERp29 regulates DeltaF508 and wild-type cystic fibrosis transmembrane conductance regulator (CFTR) trafficking to the plasma membrane in cystic fibrosis (CF) and non-CF epithelial cells.
Suaud L; Miller K; Alvey L; Yan W; Robay A; Kebler C; Kreindler JL; Guttentag S; Hubbard MJ; Rubenstein RC
J Biol Chem; 2011 Jun; 286(24):21239-53. PubMed ID: 21525008
[TBL] [Abstract][Full Text] [Related]
8. Restoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutation.
De Stefano D; Villella VR; Esposito S; Tosco A; Sepe A; De Gregorio F; Salvadori L; Grassia R; Leone CA; De Rosa G; Maiuri MC; Pettoello-Mantovani M; Guido S; Bossi A; Zolin A; Venerando A; Pinna LA; Mehta A; Bona G; Kroemer G; Maiuri L; Raia V
Autophagy; 2014; 10(11):2053-74. PubMed ID: 25350163
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of autophagy inducers in epithelial cells carrying the ΔF508 mutation of the cystic fibrosis transmembrane conductance regulator CFTR.
Zhang S; Stoll G; Pedro JMBS; Sica V; Sauvat A; Obrist F; Kepp O; Li Y; Maiuri L; Zamzami N; Kroemer G
Cell Death Dis; 2018 Feb; 9(2):191. PubMed ID: 29415993
[TBL] [Abstract][Full Text] [Related]
10. Activation of 3-phosphoinositide-dependent kinase 1 (PDK1) and serum- and glucocorticoid-induced protein kinase 1 (SGK1) by short-chain sphingolipid C4-ceramide rescues the trafficking defect of ΔF508-cystic fibrosis transmembrane conductance regulator (ΔF508-CFTR).
Caohuy H; Yang Q; Eudy Y; Ha TA; Xu AE; Glover M; Frizzell RA; Jozwik C; Pollard HB
J Biol Chem; 2014 Dec; 289(52):35953-68. PubMed ID: 25384981
[TBL] [Abstract][Full Text] [Related]
11. Does the F508-CFTR mutation induce a proinflammatory response in human airway epithelial cells?
Hampton TH; Ballok AE; Bomberger JM; Rutkowski MR; Barnaby R; Coutermarsh B; Conejo-Garcia JR; O'Toole GA; Stanton BA
Am J Physiol Lung Cell Mol Physiol; 2012 Sep; 303(6):L509-18. PubMed ID: 22821996
[TBL] [Abstract][Full Text] [Related]
12. Defective CFTR induces aggresome formation and lung inflammation in cystic fibrosis through ROS-mediated autophagy inhibition.
Luciani A; Villella VR; Esposito S; Brunetti-Pierri N; Medina D; Settembre C; Gavina M; Pulze L; Giardino I; Pettoello-Mantovani M; D'Apolito M; Guido S; Masliah E; Spencer B; Quaratino S; Raia V; Ballabio A; Maiuri L
Nat Cell Biol; 2010 Sep; 12(9):863-75. PubMed ID: 20711182
[TBL] [Abstract][Full Text] [Related]
13. Deleterious impact of Pseudomonas aeruginosa on cystic fibrosis transmembrane conductance regulator function and rescue in airway epithelial cells.
Trinh NT; Bilodeau C; Maillé É; Ruffin M; Quintal MC; Desrosiers MY; Rousseau S; Brochiero E
Eur Respir J; 2015 Jun; 45(6):1590-602. PubMed ID: 25792634
[TBL] [Abstract][Full Text] [Related]
14. DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.
Rowe SM; Pyle LC; Jurkevante A; Varga K; Collawn J; Sloane PA; Woodworth B; Mazur M; Fulton J; Fan L; Li Y; Fortenberry J; Sorscher EJ; Clancy JP
Pulm Pharmacol Ther; 2010 Aug; 23(4):268-78. PubMed ID: 20226262
[TBL] [Abstract][Full Text] [Related]
15. Cystic fibrosis transmembrane conductance regulator-mRNA delivery: a novel alternative for cystic fibrosis gene therapy.
Bangel-Ruland N; Tomczak K; Fernández Fernández E; Leier G; Leciejewski B; Rudolph C; Rosenecker J; Weber WM
J Gene Med; 2013; 15(11-12):414-26. PubMed ID: 24123772
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A truncated CFTR protein rescues endogenous DeltaF508-CFTR and corrects chloride transport in mice.
Cormet-Boyaka E; Hong JS; Berdiev BK; Fortenberry JA; Rennolds J; Clancy JP; Benos DJ; Boyaka PN; Sorscher EJ
FASEB J; 2009 Nov; 23(11):3743-51. PubMed ID: 19620404
[TBL] [Abstract][Full Text] [Related]
18. Augmentation of S-Nitrosoglutathione Controls Cigarette Smoke-Induced Inflammatory-Oxidative Stress and Chronic Obstructive Pulmonary Disease-Emphysema Pathogenesis by Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function.
Bodas M; Silverberg D; Walworth K; Brucia K; Vij N
Antioxid Redox Signal; 2017 Sep; 27(7):433-451. PubMed ID: 28006950
[TBL] [Abstract][Full Text] [Related]
19. Pseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cells.
Swiatecka-Urban A; Moreau-Marquis S; Maceachran DP; Connolly JP; Stanton CR; Su JR; Barnaby R; O'toole GA; Stanton BA
Am J Physiol Cell Physiol; 2006 Mar; 290(3):C862-72. PubMed ID: 16236828
[TBL] [Abstract][Full Text] [Related]
20. Does ivacaftor interfere with the antimicrobial activity of commonly used antibiotics against Pseudomonas aeruginosa?-Results of an in vitro study.
Millar BC; Rendall JC; Downey DG; Moore JE
J Clin Pharm Ther; 2018 Dec; 43(6):836-843. PubMed ID: 29959786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]