Similar articles for PMID: 15028554

Year	Number of Results
1992	4
1993	2
1994	3
1995	3
1996	5
1997	5
1998	4
1999	8
2000	12
2001	13
2002	12
2003	5
2004	11
2005	12
2006	9
2007	10
2008	18
2009	15
2010	28
2011	22
2012	39
2013	26
2014	16
2015	9
2016	11
2017	2
2018	4
2019	6
2020	9
2021	12
2022	12
2023	3
2024	0

1

A domain mimic increases DeltaF508 CFTR trafficking and restores cAMP-stimulated anion secretion in cystic fibrosis epithelia.

Clarke LL, Gawenis LR, Hwang TC, Walker NM, Gruis DB, Price EM. Clarke LL, et al. Am J Physiol Cell Physiol. 2004 Jul;287(1):C192-9. doi: 10.1152/ajpcell.00337.2003. Epub 2004 Mar 17. Am J Physiol Cell Physiol. 2004. PMID: 15028554 Free article.

2

Endogenous surface expression of ΔF508-CFTR mediates cAMP-stimulated Cl(-) current in CFTR(ΔF508/ΔF508) pig thyroid epithelial cells.

Li Y, Ganta S, Fong P. Li Y, et al. Exp Physiol. 2012 Jan;97(1):115-24. doi: 10.1113/expphysiol.2011.060756. Epub 2011 Sep 23. Exp Physiol. 2012. PMID: 21948195 Free PMC article.

3

Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.

Wang F, Zeltwanger S, Hu S, Hwang TC. Wang F, et al. J Physiol. 2000 May 1;524 Pt 3(Pt 3):637-48. doi: 10.1111/j.1469-7793.2000.00637.x. J Physiol. 2000. PMID: 10790148 Free PMC article.

4

SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.

Grubb BR, Gabriel SE, Mengos A, Gentzsch M, Randell SH, Van Heeckeren AM, Knowles MR, Drumm ML, Riordan JR, Boucher RC. Grubb BR, et al. Am J Respir Cell Mol Biol. 2006 Mar;34(3):355-63. doi: 10.1165/rcmb.2005-0286OC. Epub 2005 Nov 11. Am J Respir Cell Mol Biol. 2006. PMID: 16284361 Free PMC article.

5

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.

Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC. Mall M, et al. Gastroenterology. 2004 Jan;126(1):32-41. doi: 10.1053/j.gastro.2003.10.049. Gastroenterology. 2004. PMID: 14699484

6

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. Rowe SM, et al. Pulm Pharmacol Ther. 2010 Aug;23(4):268-78. doi: 10.1016/j.pupt.2010.02.001. Epub 2010 Mar 10. Pulm Pharmacol Ther. 2010. PMID: 20226262 Free PMC article.

7

Trafficking of GFP-tagged DeltaF508-CFTR to the plasma membrane in a polarized epithelial cell line.

Loffing-Cueni D, Loffing J, Shaw C, Taplin AM, Govindan M, Stanton CR, Stanton BA. Loffing-Cueni D, et al. Am J Physiol Cell Physiol. 2001 Dec;281(6):C1889-97. doi: 10.1152/ajpcell.2001.281.6.C1889. Am J Physiol Cell Physiol. 2001. PMID: 11698247 Free article.

8

Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: potential use as a biomarker of ΔF508 cystic fibrosis transmembrane conductance regulator rescue.

Pyle LC, Fulton JC, Sloane PA, Backer K, Mazur M, Prasain J, Barnes S, Clancy JP, Rowe SM. Pyle LC, et al. Am J Respir Cell Mol Biol. 2010 Nov;43(5):607-16. doi: 10.1165/rcmb.2009-0281OC. Epub 2009 Dec 30. Am J Respir Cell Mol Biol. 2010. PMID: 20042712 Free PMC article.

9

Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function.

Ko YH, Delannoy M, Pedersen PL. Ko YH, et al. Biochemistry. 1997 Apr 22;36(16):5053-64. doi: 10.1021/bi9630265. Biochemistry. 1997. PMID: 9125527

10

Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells.

Costa de Beauregard MA, Edelman A, Chesnoy-Marchais D, Tondelier D, Lapillonne A, El Marjou F, Robine S, Louvard D. Costa de Beauregard MA, et al. Eur J Cell Biol. 2000 Nov;79(11):795-802. doi: 10.1078/0171-9335-00116. Eur J Cell Biol. 2000. PMID: 11139142

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