Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 79

1.

CFTR, mucins, and mucus obstruction in cystic fibrosis.

Kreda SM, Davis CW, Rose MC.

Cold Spring Harb Perspect Med. 2012 Sep 1;2(9):a009589. doi: 10.1101/cshperspect.a009589. Review.

2.

Cystic fibrosis: an inherited disease affecting mucin-producing organs.

Ehre C, Ridley C, Thornton DJ.

Int J Biochem Cell Biol. 2014 Jul;52:136-45. doi: 10.1016/j.biocel.2014.03.011. Epub 2014 Mar 28. Review.

3.

Unplugging Mucus in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.

Mall MA.

Ann Am Thorac Soc. 2016 Apr;13 Suppl 2:S177-85. doi: 10.1513/AnnalsATS.201509-641KV. Review.

PMID:
27115954
4.
5.
6.

Role of CFTR in airway disease.

Pilewski JM, Frizzell RA.

Physiol Rev. 1999 Jan;79(1 Suppl):S215-55. Review.

7.

Therapeutic options for hydrating airway mucus in cystic fibrosis.

Tildy BE, Rogers DF.

Pharmacology. 2015;95(3-4):117-32. doi: 10.1159/000377638. Epub 2015 Mar 19. Review.

8.

Regulation of mucin genes in chronic inflammatory airway diseases.

Voynow JA, Gendler SJ, Rose MC.

Am J Respir Cell Mol Biol. 2006 Jun;34(6):661-5. Epub 2006 Feb 2. Review.

PMID:
16456183
9.
10.

[Early bronchial inflammation in cystic fibrosis].

Puchelle E.

J Soc Biol. 2002;196(1):29-35. Review. French.

PMID:
12134630
11.

Cystic Fibrosis and the Nervous System.

Reznikov LR.

Chest. 2017 May;151(5):1147-1155. doi: 10.1016/j.chest.2016.11.009. Epub 2016 Nov 19. Review.

12.

Lumacaftor and ivacaftor in the management of patients with cystic fibrosis: current evidence and future prospects.

Kuk K, Taylor-Cousar JL.

Ther Adv Respir Dis. 2015 Dec;9(6):313-26. doi: 10.1177/1753465815601934. Epub 2015 Sep 28. Review.

PMID:
26416827
13.

Structure and function of the cystic fibrosis transmembrane conductance regulator.

Morales MM, Capella MA, Lopes AG.

Braz J Med Biol Res. 1999 Aug;32(8):1021-8. Review.

14.

Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis.

Quinton PM.

Am J Physiol Cell Physiol. 2010 Dec;299(6):C1222-33. doi: 10.1152/ajpcell.00362.2010. Epub 2010 Oct 6. Review.

15.

HCO3- transport in relation to mucus secretion from submucosal glands.

Joo NS, Krouse ME, Wu JV, Saenz Y, Jayaraman S, Verkman AS, Wine JJ.

JOP. 2001 Jul;2(4 Suppl):280-4. Review.

16.

Terminal glycosylation in cystic fibrosis.

Scanlin TF, Glick MC.

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

17.

Does epithelial sodium channel hyperactivity contribute to cystic fibrosis lung disease?

Hobbs CA, Da Tan C, Tarran R.

J Physiol. 2013 Sep 15;591(18):4377-87. doi: 10.1113/jphysiol.2012.240861. Epub 2013 Jul 22. Review.

18.

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
19.

Early pulmonary inflammation and lung damage in children with cystic fibrosis.

Schultz A, Stick S.

Respirology. 2015 May;20(4):569-78. doi: 10.1111/resp.12521. Epub 2015 Mar 30. Review.

20.

Airway mucus: the good, the bad, the sticky.

Evans CM, Koo JS.

Pharmacol Ther. 2009 Mar;121(3):332-48. doi: 10.1016/j.pharmthera.2008.11.001. Epub 2008 Nov 18. Review.

PMID:
19059283

Supplemental Content

Support Center