Viel M - Search Results

1

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.

Saillour Y, Cossée M, Leturcq F, Vasson A, Beugnet C, Poirier K, Commere V, Sublemontier S, Viel M, Letourneur F, Barbot JC, Deburgrave N, Chelly J, Bienvenu T. Saillour Y, et al. Among authors: viel m. Hum Mutat. 2008 Sep;29(9):1083-90. doi: 10.1002/humu.20829. Hum Mutat. 2008. PMID: 18683213

2

Could a defective epithelial sodium channel lead to bronchiectasis.

Fajac I, Viel M, Sublemontier S, Hubert D, Bienvenu T. Fajac I, et al. Among authors: viel m. Respir Res. 2008 May 28;9(1):46. doi: 10.1186/1465-9921-9-46. Respir Res. 2008. PMID: 18507830 Free PMC article.

3

Characterization of SLC26A9 in patients with CF-like lung disease.

Bakouh N, Bienvenu T, Thomas A, Ehrenfeld J, Liote H, Roussel D, Duquesnoy P, Farman N, Viel M, Cherif-Zahar B, Amselem S, Taam RA, Edelman A, Planelles G, Sermet-Gaudelus I. Bakouh N, et al. Among authors: viel m. Hum Mutat. 2013 Oct;34(10):1404-14. doi: 10.1002/humu.22382. Epub 2013 Aug 13. Hum Mutat. 2013. PMID: 24272871

4

Spectrum of CFTR mutations on Réunion Island: impact on neonatal screening.

Bienvenu T, Viel M, Leroy C, Cartault F, Lesure JF, Renouil M. Bienvenu T, et al. Among authors: viel m. Hum Biol. 2005 Oct;77(5):705-14. doi: 10.1353/hub.2006.0002. Hum Biol. 2005. PMID: 16596947

5

A novel missense mutation A1081P in the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a Laotian patient with congenital bilateral absence of the vas deferens.

Ngukam A, Jacquemont ML, Souville I, Viel M, Beldjord C, Hubert D, Hughes JN, Bienvenu T. Ngukam A, et al. Among authors: viel m. J Trop Pediatr. 2004 Aug;50(4):239-40. doi: 10.1093/tropej/50.4.239. J Trop Pediatr. 2004. PMID: 15357566

6

A frequent large rearrangement in the CFTR gene in cystic fibrosis patients from Reunion Island.

Nectoux J, Audrezet MP, Viel M, Leroy C, Raguenes O, Ferec C, Lesure JF, Davy N, Renouil M, Cartault F, Bienvenu T. Nectoux J, et al. Among authors: viel m. Genet Test. 2006 Fall;10(3):208-14. doi: 10.1089/gte.2006.10.208. Genet Test. 2006. PMID: 17020473

7

ENaCbeta and gamma genes as modifier genes in cystic fibrosis.

Viel M, Leroy C, Hubert D, Fajac I, Bienvenu T. Viel M, et al. J Cyst Fibros. 2008 Jan;7(1):23-9. doi: 10.1016/j.jcf.2007.04.003. Epub 2007 Jun 7. J Cyst Fibros. 2008. PMID: 17560176 Free article.

8

DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.

Viel M, Hubert D, Burgel PR, Génin E, Honoré I, Martinez B, Gaitch N, Chapron J, Kanaan R, Dusser D, Girodon E, Bienvenu T. Viel M, et al. Clin Respir J. 2016 Nov;10(6):777-783. doi: 10.1111/crj.12288. Epub 2015 Apr 15. Clin Respir J. 2016. PMID: 25763772

9

Novel length variant of the polypyrimidine tract within the splice acceptor site in intron 8 of the CFTR gene: consequences for genetic testing using standard assays.

Viel M, Leroy C, Des Georges M, Claustres M, Bienvenu T. Viel M, et al. Eur J Hum Genet. 2005 Feb;13(2):136-8. doi: 10.1038/sj.ejhg.5201261. Eur J Hum Genet. 2005. PMID: 15562283 No abstract available.

10

Combination of ENaC and CFTR mutations may predispose to cystic fibrosis-like disease.

Fajac I, Viel M, Gaitch N, Hubert D, Bienvenu T. Fajac I, et al. Among authors: viel m. Eur Respir J. 2009 Sep;34(3):772-3. doi: 10.1183/09031936.00057309. Eur Respir J. 2009. PMID: 19720813 Free article. No abstract available.

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