Literature DB >> 1551658

Screening for cystic fibrosis gene mutations by multiplex DNA amplification.

L Picci1, F Anglani, M Scarpa, F Zacchello.   

Abstract

We have developed a simple rapid DNA screening test that allows us simultaneously to analyze seven CF mutations (delta F508, R347P, S549N, G551D, R553X, R334W, 444delA) that together account for about 60% of all CF mutations in the Italian population. It consists of three steps: multiplex polymerase chain reaction (PCR) amplification of exons 4, 7, 10 and 11; restriction endonuclease digestion of the PCR products; and vertical polyacrylamide gel electrophoresis analysis. We have used our multiplex assay for analyzing 15 CF chromosomes (non delta F508) and have found 3 cases of the R553X mutation; the latter have been confirmed by amplification and digestion of exon 11.

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Year:  1992        PMID: 1551658     DOI: 10.1007/bf00219343

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  12 in total

1.  Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.

Authors:  B S Kerem; J Zielenski; D Markiewicz; D Bozon; E Gazit; J Yahav; D Kennedy; J R Riordan; F S Collins; J M Rommens
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

2.  The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

Authors:  P Gasparini; V Nunes; A Savoia; M Dognini; N Morral; A Gaona; A Bonizzato; M Chillon; F Sangiuolo; G Novelli
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

3.  Identification of the cystic fibrosis gene: genetic analysis.

Authors:  B Kerem; J M Rommens; J A Buchanan; D Markiewicz; T K Cox; A Chakravarti; M Buchwald; L C Tsui
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

4.  Statement from the National Institutes of Health workshop on population screening for the cystic fibrosis gene.

Authors: 
Journal:  N Engl J Med       Date:  1990-07-05       Impact factor: 91.245

5.  A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.

Authors:  G R Cutting; L M Kasch; B J Rosenstein; J Zielenski; L C Tsui; S E Antonarakis; H H Kazazian
Journal:  Nature       Date:  1990-07-26       Impact factor: 49.962

6.  Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT).

Authors:  M B White; L J Krueger; D S Holsclaw; B C Gerrard; C Stewart; L Quittell; G Dolganov; V Baranov; T Ivaschenko; N I Kapronov
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

7.  Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families.

Authors:  R A Gibbs; P N Nguyen; A Edwards; A B Civitello; C T Caskey
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

8.  Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification.

Authors:  A Ballabio; J E Ranier; J S Chamberlain; M Zollo; C T Caskey
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

9.  Silver stain for detecting 10-femtogram quantities of protein after polyacrylamide gel electrophoresis.

Authors:  K Ohsawa; N Ebata
Journal:  Anal Biochem       Date:  1983-12       Impact factor: 3.365

10.  Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.

Authors:  J S Chamberlain; R A Gibbs; J E Ranier; P N Nguyen; C T Caskey
Journal:  Nucleic Acids Res       Date:  1988-12-09       Impact factor: 16.971

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