Bienvenu T - Search Results

1

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: bienvenu t. Respir Res. 2008 May 28;9(1):46. doi: 10.1186/1465-9921-9-46. Respir Res. 2008. PMID: 18507830 Free PMC article.

2

Skipping of exon 9 in CFTR mRNA of human adult and fetal pancreas from non-CF individuals.

Fonknechten N, Bienvenu T, Moriscot C, Beldjord C, Kahn A, Figarella C, Kaplan JC. Fonknechten N, et al. Among authors: bienvenu t. Hum Mol Genet. 1993 Dec;2(12):2141-2. doi: 10.1093/hmg/2.12.2141. Hum Mol Genet. 1993. PMID: 7509229 No abstract available.

3

Identification of a new frameshift mutation (3724 delG) in exon 19 of the CFTR gene.

Bienvenu T, Lenoir G, Fonknechten N, Desclaux-Arramond F, Kaplan JC, Beldjord C. Bienvenu T, et al. Hum Mutat. 1994;3(1):69-70. doi: 10.1002/humu.1380030113. Hum Mutat. 1994. PMID: 7509685 No abstract available.

4

A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patient.

Bienvenu T, Cazeneuve C, Beldjord C, Dusser D, Kaplan JC, Hubert D. Bienvenu T, et al. Hum Mol Genet. 1994 Feb;3(2):365-6. doi: 10.1093/hmg/3.2.365. Hum Mol Genet. 1994. PMID: 7516232 No abstract available.

5

Unexpected inactivation of acceptor consensus splice sequence by a -3 C to T transition in intron 2 of the CFTR gene.

Bienvenu T, Hubert D, Fonknechten N, Dusser D, Kaplan JC, Beldjord C. Bienvenu T, et al. Hum Genet. 1994 Jul;94(1):65-8. doi: 10.1007/BF02272843. Hum Genet. 1994. PMID: 7518409

6

Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect.

Bienvenu T, Lacronique V, Raymondjean M, Cazeneuve C, Hubert D, Kaplan JC, Beldjord C. Bienvenu T, et al. Hum Genet. 1995 Jun;95(6):698-702. doi: 10.1007/BF00209490. Hum Genet. 1995. PMID: 7540587

7

Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotide.

Bienvenu T, Cazeneuve C, Kaplan JC, Beldjord C. Bienvenu T, et al. Hum Mutat. 1995;6(1):23-9. doi: 10.1002/humu.1380060106. Hum Mutat. 1995. PMID: 7550227

8

Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.

Bienvenu T, Bousquet S, Herbulot C, Cartault F, Kaplan JC, Beldjord C. Bienvenu T, et al. Hum Mutat. 1993;2(4):306-8. doi: 10.1002/humu.1380020411. Hum Mutat. 1993. PMID: 7691353

9

A missense mutation (F87L) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene.

Bienvenu T, Petitpretz P, Beldjord C, Kaplan JC. Bienvenu T, et al. Hum Mutat. 1994;3(4):395-6. doi: 10.1002/humu.1380030412. Hum Mutat. 1994. PMID: 8081395 No abstract available.

10

Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Cazeneuve C, Beldjord C, Kaplan JC, Bienvenu T. Cazeneuve C, et al. Among authors: bienvenu t. Ann Genet. 1995;38(4):202-5. Ann Genet. 1995. PMID: 8629807

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