146 related articles for article (PubMed ID: 11404242)
1. Antioxidant imbalance in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice.
Velsor LW; van Heeckeren A; Day BJ
Am J Physiol Lung Cell Mol Physiol; 2001 Jul; 281(1):L31-8. PubMed ID: 11404242
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Hypertonic saline increases lung epithelial lining fluid glutathione and thiocyanate: two protective CFTR-dependent thiols against oxidative injury.
Gould NS; Gauthier S; Kariya CT; Min E; Huang J; Brian DJ
Respir Res; 2010 Aug; 11(1):119. PubMed ID: 20799947
[TBL] [Abstract][Full Text] [Related]
4. A role for CFTR in the elevation of glutathione levels in the lung by oral glutathione administration.
Kariya C; Leitner H; Min E; van Heeckeren C; van Heeckeren A; Day BJ
Am J Physiol Lung Cell Mol Physiol; 2007 Jun; 292(6):L1590-7. PubMed ID: 17369290
[TBL] [Abstract][Full Text] [Related]
5. Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation.
Hudson VM
Free Radic Biol Med; 2001 Jun; 30(12):1440-61. PubMed ID: 11390189
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial oxidative stress in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice.
Velsor LW; Kariya C; Kachadourian R; Day BJ
Am J Respir Cell Mol Biol; 2006 Nov; 35(5):579-86. PubMed ID: 16763223
[TBL] [Abstract][Full Text] [Related]
7. Glutathione levels and BAX activation during apoptosis due to oxidative stress in cells expressing wild-type and mutant cystic fibrosis transmembrane conductance regulator.
Jungas T; Motta I; Duffieux F; Fanen P; Stoven V; Ojcius DM
J Biol Chem; 2002 Aug; 277(31):27912-8. PubMed ID: 12023951
[TBL] [Abstract][Full Text] [Related]
8. Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challenge.
Trudel S; Kelly M; Fritsch J; Nguyen-Khoa T; Thérond P; Couturier M; Dadlez M; Debski J; Touqui L; Vallée B; Ollero M; Edelman A; Brouillard F
PLoS One; 2009 Jun; 4(6):e6075. PubMed ID: 19562038
[TBL] [Abstract][Full Text] [Related]
9. CFTR is the primary known apical glutathione transporter involved in cigarette smoke-induced adaptive responses in the lung.
Gould NS; Min E; Martin RJ; Day BJ
Free Radic Biol Med; 2012 Apr; 52(7):1201-6. PubMed ID: 22266045
[TBL] [Abstract][Full Text] [Related]
10. Impaired defenses of neonatal mouse alveolar macrophage with
Gauthier TW; Grunwell JR; Ping XD; Harris FL; Brown LA
Physiol Rep; 2017 Mar; 5(6):. PubMed ID: 28325787
[TBL] [Abstract][Full Text] [Related]
11. Effect of lentivirus-mediated CFTR overexpression on oxidative stress injury and inflammatory response in the lung tissue of COPD mouse model.
Xu X; Huang H; Yin X; Fang H; Shen X
Biosci Rep; 2020 Jan; 40(1):. PubMed ID: 31894837
[TBL] [Abstract][Full Text] [Related]
12. GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models.
Kelly-Aubert M; Trudel S; Fritsch J; Nguyen-Khoa T; Baudouin-Legros M; Moriceau S; Jeanson L; Djouadi F; Matar C; Conti M; Ollero M; Brouillard F; Edelman A
Hum Mol Genet; 2011 Jul; 20(14):2745-59. PubMed ID: 21518732
[TBL] [Abstract][Full Text] [Related]
13. Abnormal glutathione transport in cystic fibrosis airway epithelia.
Gao L; Kim KJ; Yankaskas JR; Forman HJ
Am J Physiol; 1999 Jul; 277(1):L113-8. PubMed ID: 10409237
[TBL] [Abstract][Full Text] [Related]
14. Aberrant GSH reductase and NOX activities concur with defective CFTR to pro-oxidative imbalance in cystic fibrosis airways.
de Bari L; Favia M; Bobba A; Lassandro R; Guerra L; Atlante A
J Bioenerg Biomembr; 2018 Apr; 50(2):117-129. PubMed ID: 29524019
[TBL] [Abstract][Full Text] [Related]
15. Extracellular oxidation in cystic fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity.
Stolarczyk M; Veit G; Schnúr A; Veltman M; Lukacs GL; Scholte BJ
Am J Physiol Lung Cell Mol Physiol; 2018 Apr; 314(4):L555-L568. PubMed ID: 29351448
[TBL] [Abstract][Full Text] [Related]
16. New insights into the pathogenesis of cystic fibrosis: pivotal role of glutathione system dysfunction and implications for therapy.
Hudson VM
Treat Respir Med; 2004; 3(6):353-63. PubMed ID: 15658882
[TBL] [Abstract][Full Text] [Related]
17. Cystic fibrosis transmembrane conductance regulator controls lung proteasomal degradation and nuclear factor-kappaB activity in conditions of oxidative stress.
Boncoeur E; Roque T; Bonvin E; Saint-Criq V; Bonora M; Clement A; Tabary O; Henrion-Caude A; Jacquot J
Am J Pathol; 2008 May; 172(5):1184-94. PubMed ID: 18372427
[TBL] [Abstract][Full Text] [Related]
18. Resistance to Pseudomonas aeruginosa chronic lung infection requires cystic fibrosis transmembrane conductance regulator-modulated interleukin-1 (IL-1) release and signaling through the IL-1 receptor.
Reiniger N; Lee MM; Coleman FT; Ray C; Golan DE; Pier GB
Infect Immun; 2007 Apr; 75(4):1598-608. PubMed ID: 17283089
[TBL] [Abstract][Full Text] [Related]
19. CFTR prevents neuronal apoptosis following cerebral ischemia reperfusion via regulating mitochondrial oxidative stress.
Zhang YP; Zhang Y; Xiao ZB; Zhang YB; Zhang J; Li ZQ; Zhu YB
J Mol Med (Berl); 2018 Jul; 96(7):611-620. PubMed ID: 29761302
[TBL] [Abstract][Full Text] [Related]
20. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.
Blanchard E; Marie S; Riffault L; Bonora M; Tabary O; Clement A; Jacquot J
Biochem Biophys Res Commun; 2011 Aug; 411(3):471-6. PubMed ID: 21723850
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]