Literature DB >> 7683952

Identification of 12 novel mutations in the CFTR gene.

M P Audrézet1, B Mercier, H Guillermit, I Quéré, C Verlingue, G Rault, C Férec.   

Abstract

Over 200 mutations, besides the deletion delta F508, have been identified in the CFTR gene and are known to cause CF. In order to characterize the molecular defects of non delta F508 CF chromosomes of various French origin, we have combined the techniques of denaturing gradient gel electrophoresis (DGGE) and direct sequencing to screen for mutations in the whole coding sequence of the CFTR gene corresponding to the 27 exons and their exon-intron boundaries. This approach enabled us to identify 12 novel mutations which are described here. We have systematically tested a large number of other nucleotide changes distributed in the 27 exons, each of them was clearly detected. These data support the notion that the DGGE conditions we have defined for screening coding sequence of the CFTR gene allows the identification of most of, if not all, the CFTR gene mutations.

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Year:  1993        PMID: 7683952     DOI: 10.1093/hmg/2.1.51

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  18 in total

1.  Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

Authors:  M Cheung; M H Akabas
Journal:  Biophys J       Date:  1996-06       Impact factor: 4.033

2.  Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis.

Authors:  J Sarles; S Barthellemy; C Férec; J Iovanna; M Roussey; J P Farriaux; A Toutain; J Berthelot; N Maurin; J P Codet; P Berthézène; J C Dagorn
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1999-03       Impact factor: 5.747

3.  Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations.

Authors:  V Brancolini; L Cremonesi; E Belloni; E Pappalardo; R Bordoni; M Seia; S Russo; R Padoan; A Giunta; M Ferrari
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

4.  Validation of high-resolution DNA melting analysis for mutation scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Authors:  Marie-Pierre Audrezet; Aurélia Dabricot; Cédric Le Marechal; Claude Ferec
Journal:  J Mol Diagn       Date:  2008-08-07       Impact factor: 5.568

5.  Mutations at arginine 352 alter the pore architecture of CFTR.

Authors:  Guiying Cui; Zhi-Ren Zhang; Andrew R W O'Brien; Binlin Song; Nael A McCarty
Journal:  J Membr Biol       Date:  2008-04-18       Impact factor: 1.843

6.  Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses.

Authors:  C Férec; C Verlingue; P Parent; J F Morin; J P Codet; G Rault; M Dagorne; A Lemoigne; H Journel; M Roussey
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

7.  Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patients.

Authors:  M P Audrézet; N Canki-Klain; B Mercier; D Bracar; C Verlingue; C Férec
Journal:  Hum Genet       Date:  1994-06       Impact factor: 4.132

8.  Association of 1078 del T cystic fibrosis mutation with severe disease.

Authors:  P Moullier; M Jéhanne; M P Audrézet; B Mercier; C Verlingue; I Quéré; H Guillermit; O Raguénès; V Storni; G Rault
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

9.  Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosis.

Authors:  C Verlingue; B Mercier; I Lecoq; M P Audrézet; D Laroche; G Travert; C Férec
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

10.  Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.

Authors:  T Casals; L Bassas; J Ruiz-Romero; M Chillón; J Giménez; M D Ramos; G Tapia; H Narváez; V Nunes; X Estivill
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

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