Molecular beacons: a new approach for semiautomated mutation analysis.
暂无分享,去创建一个
H. Blom | J. Vet | F. Trijbels | J A Vet | H J Blom | F J Trijbels | S Tyagi | E J Mensink | B. Giesendorf | S. Tyagi | E. Mensink | B A Giesendorf | Jacqueline A. M. Vet | Belinda A. J. Giesendorf | Sanjay Tyagi | Ewald J. M. G. Mensink | Frans J.M. Trijbels | Henk J. Blom | Frans J. M. Trijbels
[1] M. Malinow. Homocyst(e)ine and arterial occlusive diseases , 1994, Journal of internal medicine.
[2] R. Matthews,et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase , 1995, Nature Genetics.
[3] M. den Heyer,et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida , 1995, The Lancet.
[4] Fred Russell Kramer,et al. Multicolor molecular beacons for allele discrimination , 1998, Nature Biotechnology.
[5] K. Itakura,et al. Dissociation kinetics of 19 base paired oligonucleotide-DNA duplexes containing different single mismatched base pairs. , 1987, Nucleic acids research.
[6] G. Omenn,et al. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. , 1995, JAMA.
[7] Sanjay Tyagi,et al. Molecular Beacons: Probes that Fluoresce upon Hybridization , 1996, Nature Biotechnology.
[8] K. Livak,et al. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. , 1995, PCR methods and applications.
[9] H. Blom,et al. Maternal hyperhomocysteinemia: a risk factor for neural-tube defects? , 1994, Metabolism: clinical and experimental.
[10] P. Frosst,et al. Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. , 1996, American journal of human genetics.