참고문헌
- Bowtell, D. and Sambrook, J. (2002) Mutation detection and SNPgenotyping; in A Molecular Cloning Manual: DNA Microarray,1st ed., pp. 400-401, Cold Spring Harbor Laboratory Press,New York, USA.
- Drake, J. W., Allen, E. F., Forsberg, S. A. and Greening, E. O.(1969) Spontaneous mutation. Genetic control of mutation ratesin bacterophage T4. Nature 221, 1128-1131. https://doi.org/10.1038/2211128a0
- Goodman, M. F. and Fygenson, D. K. (1998) DNA polymerase fidelity: from genetics toward a biochemical understanding.Genetics 148, 1475-1482.
- Huang, M. M., Arnheim, N. and Goodman, M. F. (1992)Extension of base mispairs by Taq DNA polymerase:implications for single nucleotide discrimination in PCR.Nucleic Acids Res. 20, 4567-4573. https://doi.org/10.1093/nar/20.17.4567
- Kwok, S., Kellogg, D. E., McKinney, N., Spasic, D., Goda, L.,Levenson, C. and Sninsky, J. J. (1990) Effects of primer-templatemismatches on the polymerase chain reaction: humanimmunodeficiency virus type 1 model studies. Nucleic AcidsRes. 18, 995-1005.
- Li, K. and Zhang, J. (2001) ISIS-3521 (ISIS Pharmaceutics). Curr.Opin. Investig. Drug 2, 1454-1461.
- Morshed, M., Khan, H., Akhteruzzaman S. (2002) Associationbetween angiotensin I-converting enzyme gene polymorphismand hypertension in selected individuals of the bangladeshipopulation. J. Biochem. Mol. Biol. 35, 251-254. https://doi.org/10.5483/BMBRep.2002.35.3.251
- Nedelcheva Kristensen, V., Kelefiotis, D., Kristensen, T. andBorresen-Dale, A. (2001) High-throughput method fordetection of genetic variation. Biotechniques 30, 318-332.
- Salisbury, B. A., Pungliya, M., Choi J. Y., Jiang, R., Sun, X. J.,Stephens, J. C. (2003) SNP and haplotype variation in thehuman genome. Mutat. Res. 526, 53-61. https://doi.org/10.1016/S0027-5107(03)00014-9
- Zhang, J. Liao, D. F., Chen, L. L., Zhang, X., Li, K. (2003b)Application of DNA polymerase with 3' exonuclease in SNPassay. J. Nanhua Univ. 31, 128-131.
- Zhang, J. and Li, K. (2001) The 3' terminal labeled primerextension: A new method of high throughput screening forSNP analysis. Curr. Drug Disc. 9, 21-24.
- Zhang, J., Li, K., Deng, Z., Liao, D., Fang, W. and Zhang, X.(2003a) Efficient mutagenesis method for producing thetemplates of single nucleotide polymorphisms. Mol. Biotechnol.24, 105-110. https://doi.org/10.1385/MB:24:2:105
피인용 문헌
- Proofreading genotyping assays mediated by high fidelity exo+ DNA polymerases vol.23, pp.2, 2005, https://doi.org/10.1016/j.tibtech.2004.12.009
- Molecular diagnosis of HIV and relevant novel technologies in mutation analysis vol.26, pp.5, 2008, https://doi.org/10.1016/j.biotechadv.2008.04.007
- Discrimination of A1555G and C1494T Point Mutations in the Mitochondrial 12S rRNA Gene by On/Off Switch vol.166, pp.1, 2012, https://doi.org/10.1007/s12010-011-9419-4
- Exo+ proofreading polymerases mediate genetic analysis and its application in biomedical studies1 vol.26, pp.3, 2005, https://doi.org/10.1111/j.1745-7254.2005.00056.x