Detection of the ΔF508 (F508del) mutation of the cystic fibrosis gene by surface plasmon resonance and biosensor technology
暂无分享,去创建一个
R Gambari | R. Gambari | N. Bianchi | C. Mischiati | G. Feriotto | N Bianchi | C Mischiati | G Feriotto | M. Lucci | M Lucci
[1] R Gambari,et al. Biosensor technology and surface plasmon resonance for real-time detection of HIV-1 genomic sequences amplified by polymerase chain reaction. , 1997, Clinical and diagnostic virology.
[2] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA , 1989, Science.
[3] 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.
[4] J. Clegg,et al. Detection of the Factor V Leiden Mutation Using Whole Blood PCR , 1996, Thrombosis and Haemostasis.
[5] R. Karlsson,et al. Surface plasmon resonance detection and multispot sensing for direct monitoring of interactions involving low-molecular-weight analytes and for determination of low affinities. , 1995, Analytical biochemistry.
[6] P. Nilsson,et al. Real-time monitoring of DNA manipulations using biosensor technology. , 1995, Analytical biochemistry.
[7] K. Mullis,et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.
[8] J. Harper,et al. CLINICAL EXPERIENCE WITH PREIMPLANTATION GENETIC DIAGNOSIS OF CYSTIC FIBROSIS (ΔF508) , 1996 .
[9] S. Antonarakis. Recommendations for a nomenclature system for human gene mutations , 1998 .
[10] R. Gambari,et al. Use of an automated laboratory workstation for isolation of genomic DNA suitable for PCR and allele-specific hybridization. , 1993, BioTechniques.
[11] D. Fink,et al. Rapid construction of deleted DNA fragments for use as internal standards in competitive PCR. , 1994, PCR methods and applications.
[12] R. Gibbs,et al. PCR test for cystic fibrosis deletion , 1990, Nature.
[13] M. Uhlén,et al. Detection of mutations in PCR products from clinical samples by surface plasmon resonance , 1997, Journal of molecular recognition : JMR.
[14] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.
[15] F. Collins,et al. Two frameshift mutations in the cystic fibrosis gene. , 1991, American journal of human genetics.
[16] S. Wood. DNA-DNA Hybridization in Real Time Using BIAcore , 1993 .
[17] D. Garling,et al. Rapid cycle DNA amplification: time and temperature optimization. , 1991, BioTechniques.
[18] R. Karlsson,et al. Real-time biospecific interaction analysis using surface plasmon resonance and a sensor chip technology. , 1991, BioTechniques.
[19] C. Férec,et al. Detection of over 98% cystic fibrosis mutations in a Celtic population , 1992, Nature Genetics.
[20] L. Tsui,et al. Methods for analysis of multiple cystic fibrosis mutations , 1991, Human Genetics.
[21] Michael Dean,et al. A frame-shift mutation in the cystic fibrosis gene , 1990, Nature.
[22] J. Wall,et al. Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening , 1992, Human Genetics.
[23] Magnus Malmqvist,et al. Biospecific interaction analysis using biosensor technology , 1993, Nature.
[24] R. Gambari,et al. Polymerase-chain reaction: analysis of DNA/DNA hybridization by capillary electrophoresis. , 1993, Nucleic acids research.
[25] C. Coutelle,et al. Identification of three novel mutations in the CFTR gene using temperature-optimized non-radioactive conditions for SSCP analysis , 1994, Human Genetics.
[26] P. Pignatti,et al. Screening of 62 mutations in a cohort of cystic fibrosis patients from north eastern Italy: Their incidence and clinical features of defined genotypes , 1993, Human mutation.
[27] B. Kerem,et al. Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease. , 1992, American journal of human genetics.
[28] B. Dallapiccola,et al. Molecular characterization of a frameshift mutation in exon 19 of the CFTR gene , 1993, Human mutation.
[29] L. Tsui,et al. Rapid nonradioactive detection of the major cystic fibrosis mutation. , 1990, American journal of human genetics.
[30] F. Collins,et al. Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[31] Pankaj Vadgama,et al. Biosensors: recent trends. A review , 1992 .
[32] M. Uhlén,et al. Rapid colorimetric quantification of PCR-amplified DNA. , 1991, BioTechniques.
[33] M. White,et al. A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death. , 1991, Genomics.
[34] K. Klinger,et al. Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs. , 1993, Human molecular genetics.