Donaldson SH - Search Results

1

Airway Mucus Hyperconcentration in Non-Cystic Fibrosis Bronchiectasis.

Ramsey KA, Chen ACH, Radicioni G, Lourie R, Martin M, Broomfield A, Sheng YH, Hasnain SZ, Radford-Smith G, Simms LA, Burr L, Thornton DJ, Bowler SD, Livengood S, Ceppe A, Knowles MR, Noone PG Sr, Donaldson SH, Hill DB, Ehre C, Button B, Alexis NE, Kesimer M, Boucher RC, McGuckin MA. Ramsey KA, et al. Among authors: donaldson sh. Am J Respir Crit Care Med. 2020 Mar 15;201(6):661-670. doi: 10.1164/rccm.201906-1219OC. Am J Respir Crit Care Med. 2020. PMID: 31765597 Free PMC article.

2

Regulation of the epithelial sodium channel by serine proteases in human airways.

Donaldson SH, Hirsh A, Li DC, Holloway G, Chao J, Boucher RC, Gabriel SE. Donaldson SH, et al. J Biol Chem. 2002 Mar 8;277(10):8338-45. doi: 10.1074/jbc.M105044200. Epub 2001 Dec 26. J Biol Chem. 2002. PMID: 11756432 Free article.

3

Secreted and cell-associated adenylate kinase and nucleoside diphosphokinase contribute to extracellular nucleotide metabolism on human airway surfaces.

Donaldson SH, Picher M, Boucher RC. Donaldson SH, et al. Am J Respir Cell Mol Biol. 2002 Feb;26(2):209-15. doi: 10.1165/ajrcmb.26.2.4650. Am J Respir Cell Mol Biol. 2002. PMID: 11804872

4

Update on pathogenesis of cystic fibrosis lung disease.

Donaldson SH, Boucher RC. Donaldson SH, et al. Curr Opin Pulm Med. 2003 Nov;9(6):486-91. doi: 10.1097/00063198-200311000-00007. Curr Opin Pulm Med. 2003. PMID: 14534400 Review.

5

Mucus clearance and lung function in cystic fibrosis with hypertonic saline.

Donaldson SH, Bennett WD, Zeman KL, Knowles MR, Tarran R, Boucher RC. Donaldson SH, et al. N Engl J Med. 2006 Jan 19;354(3):241-50. doi: 10.1056/NEJMoa043891. N Engl J Med. 2006. PMID: 16421365 Free article. Clinical Trial.

6

Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia.

Tarran R, Trout L, Donaldson SH, Boucher RC. Tarran R, et al. Among authors: donaldson sh. J Gen Physiol. 2006 May;127(5):591-604. doi: 10.1085/jgp.200509468. J Gen Physiol. 2006. PMID: 16636206 Free PMC article.

7

Sodium channels and cystic fibrosis.

Donaldson SH, Boucher RC. Donaldson SH, et al. Chest. 2007 Nov;132(5):1631-6. doi: 10.1378/chest.07-0288. Chest. 2007. PMID: 17998363 Review.

8

A biophysical basis for mucus solids concentration as a candidate biomarker for airways disease.

Hill DB, Vasquez PA, Mellnik J, McKinley SA, Vose A, Mu F, Henderson AG, Donaldson SH, Alexis NE, Boucher RC, Forest MG. Hill DB, et al. Among authors: donaldson sh. PLoS One. 2014 Feb 18;9(2):e87681. doi: 10.1371/journal.pone.0087681. eCollection 2014. PLoS One. 2014. PMID: 24558372 Free PMC article.

9

Hypertonic saline for cystic fibrosis: worth its salt?

Goralski JL, Donaldson SH. Goralski JL, et al. Among authors: donaldson sh. Expert Rev Respir Med. 2014 Jun;8(3):267-9. doi: 10.1586/17476348.2014.896203. Epub 2014 Mar 26. Expert Rev Respir Med. 2014. PMID: 24666113

10

Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.

Henderson AG, Ehre C, Button B, Abdullah LH, Cai LH, Leigh MW, DeMaria GC, Matsui H, Donaldson SH, Davis CW, Sheehan JK, Boucher RC, Kesimer M. Henderson AG, et al. Among authors: donaldson sh. J Clin Invest. 2014 Jul;124(7):3047-60. doi: 10.1172/JCI73469. Epub 2014 Jun 2. J Clin Invest. 2014. PMID: 24892808 Free PMC article.

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