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Items: 1 to 20 of 21


Role of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.

Ribeiro CM, Lubamba BA.

Int J Mol Sci. 2017 Jan 9;18(1). pii: E118. doi: 10.3390/ijms18010118. Review.


"TRP inflammation" relationship in cardiovascular system.

Numata T, Takahashi K, Inoue R.

Semin Immunopathol. 2016 May;38(3):339-56. doi: 10.1007/s00281-015-0536-y. Epub 2015 Oct 19. Review.


Hypertrophic scar contracture is mediated by the TRPC3 mechanical force transducer via NFkB activation.

Ishise H, Larson B, Hirata Y, Fujiwara T, Nishimoto S, Kubo T, Matsuda K, Kanazawa S, Sotsuka Y, Fujita K, Kakibuchi M, Kawai K.

Sci Rep. 2015 Jun 25;5:11620. doi: 10.1038/srep11620.


Increased NF-κB Activity and Decreased Wnt/β-Catenin Signaling Mediate Reduced Osteoblast Differentiation and Function in ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mice.

Le Henaff C, Mansouri R, Modrowski D, Zarka M, Geoffroy V, Marty C, Tarantino N, Laplantine E, Marie PJ.

J Biol Chem. 2015 Jul 17;290(29):18009-17. doi: 10.1074/jbc.M115.646208. Epub 2015 Jun 9.


Abnormal n-6 fatty acid metabolism in cystic fibrosis is caused by activation of AMP-activated protein kinase.

Umunakwe OC, Seegmiller AC.

J Lipid Res. 2014 Jul;55(7):1489-97. doi: 10.1194/jlr.M050369. Epub 2014 May 24.


Implication of NADPH oxidases in the early inflammation process generated by cystic fibrosis cells.

Pongnimitprasert N, Hurtado M, Lamari F, El Benna J, Dupuy C, Fay M, Foglietti MJ, Bernard M, Gougerot-Pocidalo MA, Braut-Boucher F.

ISRN Inflamm. 2012 Jul 5;2012:481432. doi: 10.5402/2012/481432. eCollection 2012.


CFTR activity and mitochondrial function.

Valdivieso AG, Santa-Coloma TA.

Redox Biol. 2013 Feb 5;1:190-202. doi: 10.1016/j.redox.2012.11.007. Review.


Digitoxin induces apoptosis in cancer cells by inhibiting nuclear factor of activated T-cells-driven c-MYC expression.

Yang QF, Dalgard CL, Eidelman O, Jozwik C, Pollard BS, Srivastava M, Pollard HB.

J Carcinog. 2013 May 20;12:8. doi: 10.4103/1477-3163.112268. Print 2013.


Effect of allergy and inflammation on eicosanoid gene expression in CFTR deficiency.

Bickford JS, Mueller C, Newsom KJ, Barilovits SJ, Beachy DE, Herlihy JD, Keeler B, Flotte TR, Nick HS.

J Cyst Fibros. 2013 May;12(3):258-65. doi: 10.1016/j.jcf.2012.08.014. Epub 2012 Sep 15.


Inhibiting NF-κB in the developing lung disrupts angiogenesis and alveolarization.

Iosef C, Alastalo TP, Hou Y, Chen C, Adams ES, Lyu SC, Cornfield DN, Alvira CM.

Am J Physiol Lung Cell Mol Physiol. 2012 May 15;302(10):L1023-36. doi: 10.1152/ajplung.00230.2011. Epub 2012 Feb 24.


CFTR and Ca Signaling in Cystic Fibrosis.

Antigny F, Norez C, Becq F, Vandebrouck C.

Front Pharmacol. 2011 Oct 25;2:67. doi: 10.3389/fphar.2011.00067. eCollection 2011.


The Pseudomonas aeruginosa autoinducer 3O-C12 homoserine lactone provokes hyperinflammatory responses from cystic fibrosis airway epithelial cells.

Mayer ML, Sheridan JA, Blohmke CJ, Turvey SE, Hancock RE.

PLoS One. 2011 Jan 31;6(1):e16246. doi: 10.1371/journal.pone.0016246.


Restoration of chloride efflux by azithromycin in airway epithelial cells of cystic fibrosis patients.

Saint-Criq V, Rebeyrol C, Ruffin M, Roque T, Guillot L, Jacquot J, Clement A, Tabary O.

Antimicrob Agents Chemother. 2011 Apr;55(4):1792-3. doi: 10.1128/AAC.01403-10. Epub 2011 Jan 10.


Mechanisms of action and clinical application of macrolides as immunomodulatory medications.

Kanoh S, Rubin BK.

Clin Microbiol Rev. 2010 Jul;23(3):590-615. doi: 10.1128/CMR.00078-09. Review.


Lack of CFTR in skeletal muscle predisposes to muscle wasting and diaphragm muscle pump failure in cystic fibrosis mice.

Divangahi M, Balghi H, Danialou G, Comtois AS, Demoule A, Ernest S, Haston C, Robert R, Hanrahan JW, Radzioch D, Petrof BJ.

PLoS Genet. 2009 Jul;5(7):e1000586. doi: 10.1371/journal.pgen.1000586. Epub 2009 Jul 31.


Dysfunctional cystic fibrosis transmembrane conductance regulator inhibits phagocytosis of apoptotic cells with proinflammatory consequences.

Vandivier RW, Richens TR, Horstmann SA, deCathelineau AM, Ghosh M, Reynolds SD, Xiao YQ, Riches DW, Plumb J, Vachon E, Downey GP, Henson PM.

Am J Physiol Lung Cell Mol Physiol. 2009 Oct;297(4):L677-86. doi: 10.1152/ajplung.00030.2009. Epub 2009 Jul 24.


Mechanisms of the noxious inflammatory cycle in cystic fibrosis.

Rottner M, Freyssinet JM, Martínez MC.

Respir Res. 2009 Mar 13;10:23. doi: 10.1186/1465-9921-10-23. Review.


Abnormal spatial diffusion of Ca2+ in F508del-CFTR airway epithelial cells.

Antigny F, Norez C, Cantereau A, Becq F, Vandebrouck C.

Respir Res. 2008 Oct 30;9:70. doi: 10.1186/1465-9921-9-70.


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. doi: 10.2353/ajpath.2008.070310. Epub 2008 Mar 27.


Heart failure drug digitoxin induces calcium uptake into cells by forming transmembrane calcium channels.

Arispe N, Diaz JC, Simakova O, Pollard HB.

Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2610-5. doi: 10.1073/pnas.0712270105. Epub 2008 Feb 12.

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