Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR gene
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Milan Macek | Ada Hamosh | Bernard Mercier | A. Hamosh | M. Macek | C. Férec | B. Mercier | Garry R. Cutting | Claude Férec | Alice Macková | Patrice Weiner Miller | Garry R Cutting | Alice Macková | Patrice Weiner Miller | Patrice W. Miller
[1] R. Kelley,et al. Smith-Lemli-Opitz syndrome: prenatal diagnosis by quantification of cholesterol precursors in amniotic fluid. , 1995, American journal of medical genetics.
[2] L. Tsui,et al. Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family , 1995, Clinical genetics.
[3] B. Kemper,et al. Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[4] C. Férec,et al. Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: Identification of three novel alleles , 1995, Human mutation.
[5] M. Claustres,et al. Novel missense mutation in the first transmembrane segment of the CFTR gene (Q98R) identified in a male adult , 1995, Human mutation.
[6] J. Crawford,et al. A splicing mutation (1898 + 1G→T) in the CFTR gene causing cystic fibrosis , 1995, Human mutation.
[7] C. Cazeneuve,et al. Mutation heterogeneity of cystic fibrosis in France: Screening by denaturing gradient gel electrophoresis using psoralen‐modified oligonucleotide , 1995, Human mutation.
[8] G. Efremov,et al. Identification of two new mutations (711 +3A-->G and V1397E) in CF chromosomes of Albanian and Macedonian origin. , 1994, Human molecular genetics.
[9] G. Thomas,et al. Relative efficiency of denaturing gradient gel electrophoresis and single strand conformation polymorphism in the detection of mutations in exons 5 to 8 of the p53 gene. , 1994, Oncogene.
[10] E. Girodon,et al. Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. , 1994, Genomics.
[11] T. Meitinger,et al. A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis. , 1994, The Journal of clinical investigation.
[12] J. Cheadle,et al. Population variation of common cystic fibrosis mutations , 1994 .
[13] J. Kaplan,et al. A missense mutation (F87L) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene , 1994, Human mutation.
[14] M. Goossens,et al. Exhaustive analysis of the P53 gene coding sequence by denaturing gradient gel electrophoresis: Application to the detection of point mutations in acute leukemias , 1994, Human mutation.
[15] Riccardo Fodde,et al. Mutation detection by denaturing gradient gel electrophoresis (DGGE) , 1994, Human mutation.
[16] H. Scheffer,et al. A novel mutation (G1249R) in exon 20 of the CFTR gene , 1994, Human mutation.
[17] P. Gasparini,et al. Development of RNA‐SSCP protocols for the identification and screening of CFTR mutations: Identification of two new mutations , 1994, Human mutation.
[18] D J Prockop,et al. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[19] M. Grompe,et al. The rapid detection of unknown mutations in nucleic acids , 1993, Nature genetics.
[20] G. Thomas,et al. Efficient screening of p53 mutations by denaturing gradient gel electrophoresis in colorectal tumors. , 1993, Oncogene.
[21] B. Dallapiccola,et al. Identification of eight novel mutations in a collaborative analysis of a part of the second transmembrane domain of the CFTR gene. , 1993, Genomics.
[22] G. Cutting. Spectrum of mutations in cystic fibrosis , 1993, Journal of bioenergetics and biomembranes.
[23] J. Littlewood,et al. Cystic fibrosis in Asians. , 1993, Archives of disease in childhood.
[24] C. Férec,et al. Identification of 12 novel mutations in the CFTR gene. , 1993, Human molecular genetics.
[25] R. Eeles,et al. Detection of point mutations in the p53 gene: Comparison of single‐strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques , 1993, Human mutation.
[26] R. Saiki,et al. Genetic analysis using polymerase chain reaction-amplified DNA and immobilized oligonucleotide probes: reverse dot-blot typing. , 1993, Methods in enzymology.
[27] J. Capeau,et al. Detection of sequence variations in the human insulin‐receptor gene by parallel denaturing gradient gel electrophoresis , 1993, Human mutation.
[28] F. Nicholas,et al. Temperature gradient gel electrophoresis : detection of a single base substitution in the cattle β-lactoglobulin gene , 2009 .
[29] H. Sasaki,et al. Delta F508 mutation of cystic fibrosis gene is not found in chronic bronchitis with severe obstruction in Japan. , 1992, The American review of respiratory disease.
[30] M. Vidaud,et al. Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions. , 1992, Genomics.
[31] C. Férec,et al. Detection of over 98% cystic fibrosis mutations in a Celtic population , 1992, Nature Genetics.
[32] S. O’Brien,et al. Detecting single base substitutions as heteroduplex polymorphisms. , 1992, Genomics.
[33] M. Devoto,et al. A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A----G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene. , 1992, Genomics.
[34] A. Hamosh,et al. Identification of a novel nonsense mutation (L88X) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene in a native Korean cystic fibrosis chromosome , 1992, Human mutation.
[35] P. Gasparini,et al. Identification of a new splicing mutation (406‐1 G‐C) in the CFTR gene , 1992, Human mutation.
[36] G. Cutting,et al. Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians. , 1992, American journal of human genetics.
[37] D. Charnock-Jones,et al. New protocols for DNA sequencing with dye terminators. , 1992, DNA sequence : the journal of DNA sequencing and mapping.
[38] M. Devoto,et al. Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypes , 1992, Human mutation.
[39] M. Zasloff,et al. A cross-species analysis of the cystic fibrosis transmembrane conductance regulator. Potential functional domains and regulatory sites. , 1991, The Journal of biological chemistry.
[40] S. Antonarakis,et al. Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[41] J. Mattick,et al. 'Touchdown' PCR to circumvent spurious priming during gene amplification. , 1991, Nucleic acids research.
[42] M. Devoto,et al. Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy. , 1991, American journal of human genetics.
[43] L. Tsui,et al. Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. , 1991, Genomics.
[44] A. Ganguly,et al. Detection of single-base mutations by reaction of DNA heteroduplexes with a water-soluble carbodiimide followed by primer extension: application to products from the polymerase chain reaction , 1990, Nucleic Acids Res..
[45] S. Antonarakis,et al. Use of denaturing gradient gel electrophoresis to detect point mutations in the factor VIII gene. , 1990, Genomics.
[46] B. Theophilus,et al. Comparison of RNase A, a chemical cleavage and GC-clamped denaturing gradient gel electrophoresis for the detection of mutations in exon 9 of the human acid beta-glucosidase gene. , 1989, Nucleic acids research.
[47] T. Sekiya,et al. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[48] R. D. Campbell,et al. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[49] Val C. Sheffield,et al. Detection of single base changes in DNA: ribonuclease cleavage and denaturing gradient gel electrophoresis. , 1988 .
[50] R. Myers,et al. Detection and localization of single base changes by denaturing gradient gel electrophoresis. , 1987, Methods in enzymology.
[51] L. Lerman,et al. Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. , 1987, Methods in enzymology.
[52] R. Myers,et al. Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes. , 1985, Science.
[53] R. Myers,et al. Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis. , 1985, Nucleic acids research.
[54] L. Lerman,et al. Sequence-determined DNA separations. , 1984, Annual review of biophysics and bioengineering.
[55] D. Rushton,et al. Cystic fibrosis in 3 Pakistani children. , 1974, Archives of disease in childhood.
[56] J. Yamazaki,et al. Cystic fibrosis in an Oriental child. , 1968, The New England journal of medicine.
[57] N. Morton,et al. Genetic studies on cystic fibrosis in Hawaii. , 1968, American journal of human genetics.