Zahm JM - Search Results

1

Ion composition and rheology of airway liquid from cystic fibrosis fetal tracheal xenografts.

Baconnais S, Tirouvanziam R, Zahm JM, de Bentzmann S, Péault B, Balossier G, Puchelle E. Baconnais S, et al. Among authors: zahm jm. Am J Respir Cell Mol Biol. 1999 Apr;20(4):605-11. doi: 10.1165/ajrcmb.20.4.3264. Am J Respir Cell Mol Biol. 1999. PMID: 10100991

2

Technical approaches to analyze the in vivo ion composition of airway surface liquid.

Zahm JM, Baconnais S, Balossier G, Puchelle E. Zahm JM, et al. Methods Mol Med. 2002;70:563-72. doi: 10.1385/1-59259-187-6:563. Methods Mol Med. 2002. PMID: 11917551 No abstract available.

3

Salmeterol restores secretory functions in cystic fibrosis airway submucosal gland serous cells.

Delavoie F, Molinari M, Milliot M, Zahm JM, Coraux C, Michel J, Balossier G. Delavoie F, et al. Among authors: zahm jm. Am J Respir Cell Mol Biol. 2009 Apr;40(4):388-97. doi: 10.1165/rcmb.2008-0037OC. Epub 2008 Oct 17. Am J Respir Cell Mol Biol. 2009. PMID: 18931328 Free PMC article.

4

[Effect of rhDNase on rheologic properties and transport capacity of mucus in cystic fibrosis].

Puchelle E, Zahm JM. Puchelle E, et al. Among authors: zahm jm. Arch Pediatr. 1995 Jul;2(7):670-3. doi: 10.1016/0929-693x(96)81224-3. Arch Pediatr. 1995. PMID: 7663658 French.

5

Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches.

Puchelle E, de Bentzmann S, Zahm JM. Puchelle E, et al. Among authors: zahm jm. Respiration. 1995;62 Suppl 1:2-12. doi: 10.1159/000196486. Respiration. 1995. PMID: 7792436 Review.

6

Effect of extracellular ATP and UTP on fluid transport by human nasal epithelial cells in culture.

Benali R, Pierrot D, Zahm JM, de Bentzmann S, Puchelle E. Benali R, et al. Among authors: zahm jm. Am J Respir Cell Mol Biol. 1994 Apr;10(4):363-8. doi: 10.1165/ajrcmb.10.4.8136152. Am J Respir Cell Mol Biol. 1994. PMID: 8136152

7

Revisited physicochemical and transport properties of respiratory mucus in genotyped cystic fibrosis patients.

Deneuville E, Perrot-Minot C, Pennaforte F, Roussey M, Zahm JM, Clavel C, Puchelle E, de Bentzmann S. Deneuville E, et al. Among authors: zahm jm. Am J Respir Crit Care Med. 1997 Jul;156(1):166-72. doi: 10.1164/ajrccm.156.1.9606123. Am J Respir Crit Care Med. 1997. PMID: 9230742

8

Improvement of cystic fibrosis airway mucus transportability by recombinant human DNase is related to changes in phospholipid profile.

Zahm JM, Galabert C, Chaffin A, Chazalette JP, Grosskopf C, Puchelle E. Zahm JM, et al. Am J Respir Crit Care Med. 1998 Jun;157(6 Pt 1):1779-84. doi: 10.1164/ajrccm.157.6.9706036. Am J Respir Crit Care Med. 1998. PMID: 9620905

9

X-ray microanalysis of airway surface liquid collected in cystic fibrosis mice.

Zahm JM, Baconnais S, Davidson DJ, Webb S, Dorin J, Bonnet N, Balossier G, Puchelle E. Zahm JM, et al. Am J Physiol Lung Cell Mol Physiol. 2001 Aug;281(2):L309-13. doi: 10.1152/ajplung.2001.281.2.L309. Am J Physiol Lung Cell Mol Physiol. 2001. PMID: 11435203 Free article.

10

Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells.

Baconnais S, Delavoie F, Zahm JM, Milliot M, Terryn C, Castillon N, Banchet V, Michel J, Danos O, Merten M, Chinet T, Zierold K, Bonnet N, Puchelle E, Balossier G. Baconnais S, et al. Among authors: zahm jm. Exp Cell Res. 2005 Oct 1;309(2):296-304. doi: 10.1016/j.yexcr.2005.06.010. Exp Cell Res. 2005. PMID: 16051214

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