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Items: 1 to 20 of 179

1.

Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.

Carbone A, Castellani S, Favia M, Diana A, Paracchini V, Di Gioia S, Seia M, Casavola V, Colombo C, Conese M.

J Cell Mol Med. 2014 Aug;18(8):1631-43. doi: 10.1111/jcmm.12303. Epub 2014 Jun 3.

2.

Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cells.

Paracchini V, Carbone A, Colombo F, Castellani S, Mazzucchelli S, Gioia SD, Degiorgio D, Seia M, Porretti L, Colombo C, Conese M.

J Biomed Biotechnol. 2012;2012:575471. doi: 10.1155/2012/575471. Epub 2012 Jan 22.

3.

The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.

Varelogianni G, Hussain R, Strid H, Oliynyk I, Roomans GM, Johannesson M.

Cell Biol Int. 2013 Nov;37(11):1149-56. doi: 10.1002/cbin.10146. Epub 2013 Jul 23.

PMID:
23765701
4.

NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway.

Castellani S, Guerra L, Favia M, Di Gioia S, Casavola V, Conese M.

Lab Invest. 2012 Nov;92(11):1527-40. doi: 10.1038/labinvest.2012.123. Epub 2012 Sep 10.

5.

CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium.

Zhang L, Button B, Gabriel SE, Burkett S, Yan Y, Skiadopoulos MH, Dang YL, Vogel LN, McKay T, Mengos A, Boucher RC, Collins PL, Pickles RJ.

PLoS Biol. 2009 Jul;7(7):e1000155. doi: 10.1371/journal.pbio.1000155. Epub 2009 Jul 21.

6.

Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.

Gianotti A, Melani R, Caci E, Sondo E, Ravazzolo R, Galietta LJ, Zegarra-Moran O.

Am J Respir Cell Mol Biol. 2013 Sep;49(3):445-52. doi: 10.1165/rcmb.2012-0408OC.

PMID:
23600628
7.

Paracellular transport through healthy and cystic fibrosis bronchial epithelial cell lines--do we have a proper model?

Molenda N, Urbanova K, Weiser N, Kusche-Vihrog K, Günzel D, Schillers H.

PLoS One. 2014 Jun 19;9(6):e100621. doi: 10.1371/journal.pone.0100621. eCollection 2014.

8.

CFTR and tight junctions in cultured bronchial epithelial cells.

Nilsson HE, Dragomir A, Lazorova L, Johannesson M, Roomans GM.

Exp Mol Pathol. 2010 Feb;88(1):118-27. doi: 10.1016/j.yexmp.2009.09.018. Epub 2009 Oct 8.

PMID:
19818767
9.

Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.

Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, Jayle C, Becq F, Vandebrouck C.

Am J Respir Cell Mol Biol. 2011 Jan;44(1):83-90. doi: 10.1165/rcmb.2009-0347OC. Epub 2010 Mar 4.

PMID:
20203293
10.

Anoctamin 1 dysregulation alters bronchial epithelial repair in cystic fibrosis.

Ruffin M, Voland M, Marie S, Bonora M, Blanchard E, Blouquit-Laye S, Naline E, Puyo P, Le Rouzic P, Guillot L, Corvol H, Clement A, Tabary O.

Biochim Biophys Acta. 2013 Dec;1832(12):2340-51. doi: 10.1016/j.bbadis.2013.09.012. Epub 2013 Sep 27.

11.

The effect of NO-donors on chloride efflux, intracellular Ca(2+) concentration and mRNA expression of CFTR and ENaC in cystic fibrosis airway epithelial cells.

Oliynyk I, Hussain R, Amin A, Johannesson M, Roomans GM.

Exp Mol Pathol. 2013 Jun;94(3):474-80. doi: 10.1016/j.yexmp.2013.03.003. Epub 2013 Mar 21.

PMID:
23523754
12.

Adult stem cells from bone marrow stroma differentiate into airway epithelial cells: potential therapy for cystic fibrosis.

Wang G, Bunnell BA, Painter RG, Quiniones BC, Tom S, Lanson NA Jr, Spees JL, Bertucci D, Peister A, Weiss DJ, Valentine VG, Prockop DJ, Kolls JK.

Proc Natl Acad Sci U S A. 2005 Jan 4;102(1):186-91. Epub 2004 Dec 22.

13.

Low temperature and chemical rescue affect molecular proximity of DeltaF508-cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial sodium channel (ENaC).

Qadri YJ, Cormet-Boyaka E, Rooj AK, Lee W, Parpura V, Fuller CM, Berdiev BK.

J Biol Chem. 2012 May 11;287(20):16781-90. doi: 10.1074/jbc.M111.332031. Epub 2012 Mar 22.

14.

Improvement of defective cystic fibrosis airway epithelial wound repair after CFTR rescue.

Trinh NT, Bardou O, Privé A, Maillé E, Adam D, Lingée S, Ferraro P, Desrosiers MY, Coraux C, Brochiero E.

Eur Respir J. 2012 Dec;40(6):1390-400. doi: 10.1183/09031936.00221711. Epub 2012 Apr 10.

15.

Unimpaired lysosomal acidification in respiratory epithelial cells in cystic fibrosis.

Haggie PM, Verkman AS.

J Biol Chem. 2009 Mar 20;284(12):7681-6. doi: 10.1074/jbc.M809161200. Epub 2009 Jan 9.

16.

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.

Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.

Hepatology. 1999 Jun;29(6):1624-34.

PMID:
10347100
17.

The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.

Gentzsch M, Dang H, Dang Y, Garcia-Caballero A, Suchindran H, Boucher RC, Stutts MJ.

J Biol Chem. 2010 Oct 15;285(42):32227-32. doi: 10.1074/jbc.M110.155259. Epub 2010 Aug 13.

18.

Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice.

Dhooghe B, Noël S, Bouzin C, Behets-Wydemans G, Leal T.

PLoS One. 2013 Oct 24;8(10):e77314. doi: 10.1371/journal.pone.0077314. eCollection 2013.

19.

Modeling Cystic Fibrosis Using Pluripotent Stem Cell-Derived Human Pancreatic Ductal Epithelial Cells.

Simsek S, Zhou T, Robinson CL, Tsai SY, Crespo M, Amin S, Lin X, Hon J, Evans T, Chen S.

Stem Cells Transl Med. 2016 May;5(5):572-9. doi: 10.5966/sctm.2015-0276. Epub 2016 Mar 31.

PMID:
27034411
20.

Adenovirus 5-fiber 35 chimeric vector mediates efficient apical correction of the cystic fibrosis transmembrane conductance regulator defect in cystic fibrosis primary airway epithelia.

Granio O, Ashbourne Excoffon KJ, Henning P, Melin P, Norez C, Gonzalez G, Karp PH, Magnusson MK, Habib N, Lindholm L, Becq F, Boulanger P, Zabner J, Hong SS.

Hum Gene Ther. 2010 Mar;21(3):251-69. doi: 10.1089/hum.2009.056.

PMID:
19788389
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