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Items: 1 to 20 of 167

1.

Altered terminal glycosylation and the pathophysiology of CF lung disease.

Rhim AD, Stoykova LI, Trindade AJ, Glick MC, Scanlin TF.

J Cyst Fibros. 2004 Aug;3 Suppl 2:95-6.

2.

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell.

Rhim AD, Stoykova L, Glick MC, Scanlin TF.

Glycoconj J. 2001 Sep;18(9):649-59. Review.

PMID:
12386452
3.

Hyperacidification in cystic fibrosis: links with lung disease and new prospects for treatment.

Poschet J, Perkett E, Deretic V.

Trends Mol Med. 2002 Nov;8(11):512-9. Review.

PMID:
12421684
4.

Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells.

Glick MC, Kothari VA, Liu A, Stoykova LI, Scanlin TF.

Biochimie. 2001 Aug;83(8):743-7.

PMID:
11530206
5.

Terminal glycosylation in cystic fibrosis.

Scanlin TF, Glick MC.

Biochim Biophys Acta. 1999 Oct 8;1455(2-3):241-53. Review.

6.

Alpha1,3fucosyltransferases in cystic fibrosis airway epithelial cells.

Stoykova LI, Liu A, Scanlin TF, Glick MC.

Biochimie. 2003 Mar-Apr;85(3-4):363-7.

PMID:
12770774
7.

Role of airway surface liquid and submucosal glands in cystic fibrosis lung disease.

Verkman AS, Song Y, Thiagarajah JR.

Am J Physiol Cell Physiol. 2003 Jan;284(1):C2-15. Review.

8.

An immunocytochemical assay to detect human CFTR expression following gene transfer.

Davidson H, Wilson A, Gray RD, Horsley A, Pringle IA, McLachlan G, Nairn AC, Stearns C, Gibson J, Holder E, Jones L, Doherty A, Coles R, Sumner-Jones SG, Wasowicz M, Manvell M, Griesenbach U, Hyde SC, Gill DR, Davies J, Collie DD, Alton EW, Porteous DJ, Boyd AC.

Mol Cell Probes. 2009 Dec;23(6):272-80. doi: 10.1016/j.mcp.2009.07.001. Epub 2009 Jul 15.

PMID:
19615439
9.

Gene expression profile study in CFTR mutated bronchial cell lines.

Gambardella S, Biancolella M, D'Apice MR, Amati F, Sangiuolo F, Farcomeni A, Chillemi G, Bueno S, Desideri A, Novelli G.

Clin Exp Med. 2006 Dec;6(4):157-65.

PMID:
17191107
10.

Effects of cystic fibrosis transmembrane conductance regulator and DeltaF508CFTR on inflammatory response, ER stress, and Ca2+ of airway epithelia.

Hybiske K, Fu Z, Schwarzer C, Tseng J, Do J, Huang N, Machen TE.

Am J Physiol Lung Cell Mol Physiol. 2007 Nov;293(5):L1250-60. Epub 2007 Sep 7.

11.

Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression.

Leir SH, Parry S, Palmai-Pallag T, Evans J, Morris HR, Dell A, Harris A.

Am J Respir Cell Mol Biol. 2005 May;32(5):453-61. Epub 2005 Jan 27.

PMID:
15677769
12.

Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.

LeSimple P, Goepp J, Palmer ML, Fahrenkrug SC, O'Grady SM, Ferraro P, Robert R, Hanrahan JW.

Am J Respir Cell Mol Biol. 2013 Oct;49(4):511-6. doi: 10.1165/rcmb.2012-0419RC.

PMID:
23742042
13.

Sildenafil (Viagra) corrects DeltaF508-CFTR location in nasal epithelial cells from patients with cystic fibrosis.

Dormer RL, Harris CM, Clark Z, Pereira MM, Doull IJ, Norez C, Becq F, McPherson MA.

Thorax. 2005 Jan;60(1):55-9.

14.

Airway epithelial cells--hyperabsorption in CF?

Kunzelmann K, Schreiber R.

Int J Biochem Cell Biol. 2012 Aug;44(8):1232-5. doi: 10.1016/j.biocel.2012.04.012. Epub 2012 Apr 21. Review.

PMID:
22542896
15.

Spontaneous rescue from cystic fibrosis in a mouse model.

Charizopoulou N, Wilke M, Dorsch M, Bot A, Jorna H, Jansen S, Stanke F, Hedrich HJ, de Jonge HR, T├╝mmler B.

BMC Genet. 2006 Mar 29;7:18.

16.
17.

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.

18.

Hyperinflammation in airways of cystic fibrosis patients: what's new?

Jacquot J, Tabary O, Clement A.

Expert Rev Mol Diagn. 2008 Jul;8(4):359-63. doi: 10.1586/14737159.8.4.359. Review. No abstract available.

PMID:
18598217
19.

Terminal glycosylation of cystic fibrosis airway epithelial cells.

Rhim AD, Kothari VA, Park PJ, Mulberg AE, Glick MC, Scanlin TF.

Glycoconj J. 2000 Jun;17(6):385-91.

PMID:
11294504
20.

Developmental paradigm for early features of cystic fibrosis.

Larson JE, Cohen JC.

Pediatr Pulmonol. 2005 Nov;40(5):371-7. Review.

PMID:
15830387

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