Denamur E - Search Results

1

Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients.

Verlingue C, Vuillaumier S, Mercier B, Le Gac M, Elion J, Férec C, Denamur E. Verlingue C, et al. Among authors: denamur e. J Med Genet. 1998 Feb;35(2):137-40. doi: 10.1136/jmg.35.2.137. J Med Genet. 1998. PMID: 9507393 Free PMC article.

2

Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations.

Messaoud T, Verlingue C, Denamur E, Pascaud O, Quéré I, Fattoum S, Elion J, Férec C. Messaoud T, et al. Among authors: denamur e. Eur J Hum Genet. 1996;4(1):20-4. doi: 10.1159/000472165. Eur J Hum Genet. 1996. PMID: 8800923

3

Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.

Vuillaumier S, Dixmeras I, Messaï H, Lapouméroulie C, Lallemand D, Gekas J, Chehab FF, Perret C, Elion J, Denamur E. Vuillaumier S, et al. Among authors: denamur e. Biochem J. 1997 Nov 1;327 ( Pt 3)(Pt 3):651-62. doi: 10.1042/bj3270651. Biochem J. 1997. PMID: 9581539 Free PMC article.

4

Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index case.

Muller F, Dommergues M, Simon-Bouy B, Ferec C, Oury JF, Aubry MC, Bessis R, Vuillard E, Denamur E, Bienvenu T, Serre JL. Muller F, et al. Among authors: denamur e. J Med Genet. 1998 Aug;35(8):657-60. doi: 10.1136/jmg.35.8.657. J Med Genet. 1998. PMID: 9719372 Free PMC article.

5

Complexity of Pseudomonas aeruginosa infection in cystic fibrosis: combined results from esterase electrophoresis and rDNA restriction fragment length polymorphism analysis.

Denamur E, Picard B, Goullet P, Bingen E, Lambert N, Elion J. Denamur E, et al. Epidemiol Infect. 1991 Jun;106(3):531-9. doi: 10.1017/s0950268800067595. Epidemiol Infect. 1991. PMID: 1675610 Free PMC article.

6

Denaturing gradient gel electrophoresis analysis for the detection of point mutations in the Chlamydia trachomatis major outer-membrane protein gene.

Sayada C, Denamur E, Grandchamp B, Orfila J, Elion J. Sayada C, et al. Among authors: denamur e. J Med Microbiol. 1995 Jul;43(1):14-25. doi: 10.1099/00222615-43-1-14. J Med Microbiol. 1995. PMID: 7608950

7

Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient.

Gouya L, Pascaud O, Munck A, Elion J, Denamur E. Gouya L, et al. Among authors: denamur e. Hum Mutat. 1997;10(1):86-7. doi: 10.1002/(SICI)1098-1004(1997)10:1<86::AID-HUMU15>3.0.CO;2-W. Hum Mutat. 1997. PMID: 9222768 No abstract available.

8

CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblasts.

Dixméras I, Lapouméroulie C, Tallec LP, Bens M, Elion J, Vandewalle A, Denamur E. Dixméras I, et al. Among authors: denamur e. Biochem Biophys Res Commun. 1998 Sep 18;250(2):328-34. doi: 10.1006/bbrc.1998.9292. Biochem Biophys Res Commun. 1998. PMID: 9753629

9

A combined analysis of the cystic fibrosis transmembrane conductance regulator: implications for structure and disease models.

Chen JM, Cutler C, Jacques C, Boeuf G, Denamur E, Lecointre G, Mercier B, Cramb G, Férec C. Chen JM, et al. Among authors: denamur e. Mol Biol Evol. 2001 Sep;18(9):1771-88. doi: 10.1093/oxfordjournals.molbev.a003965. Mol Biol Evol. 2001. PMID: 11504857

10

Phylogenetic analysis of cystic fibrosis transmembrane conductance regulator gene in mammalian species argues for the development of a rabbit model for cystic fibrosis.

Vuillaumier S, Kaltenboeck B, Lecointre G, Lehn P, Denamur E. Vuillaumier S, et al. Among authors: denamur e. Mol Biol Evol. 1997 Apr;14(4):372-80. doi: 10.1093/oxfordjournals.molbev.a025773. Mol Biol Evol. 1997. PMID: 9100367

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