Искусственные генетические системы. Том 1 - Патрушев Л.И.
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299. Lyamichev V., Brow M.A., Dahlberg J.E. Structure specific endonucleolytic cleavage of nucleic acids by eubacterial DNA polymerases // Science. Vol. 260. 1993. P. 778-783.
300. Heid C.A., Stevens J., Livak K.J., Williams P.M. Real time quantitative PCR // Genome Research. 1996. Vol. 6. P. 986-994.
301. Livak KJ., Flood S.J., Marmaro J. et al. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization // PCR Methods and Applications. 1995. Vol. 4. P. 357-362.
302. Sun C.-F., Lee C.-H., Cheng S.-W. et al. Real-time quantitative PCR analysis for a-thalassemia-1 of Southeast Asian type deletion in Taiwan. Clin. Genet. 2001. Vol. 60. P. 305-309.
303. Glazer A.N., Mathies R.A. Energy-transfer fluorescent reagents for DNA analyses // Curr. Opin. Biotechnol. 1997. Vol. 8. P. 94-102.
304. Wittwer C.T., Herrmann M.G., Moss A .A., Rasmussen R.P. Continuous fluorescence monitoring of rapid cycle DNA amplification // Biotechniques.
1997. Vol. 22. P. 130-131, 134-138.
305. Tyagi S., Bratu D.P., Kramer F.R. Multicolor molecular beacons for allele discrimination // Nature Biotechnol. 1998. Vol. 16. P. 49-53.
306. Antony Т., Subramaniam V. Molecular beacons: Nucleic acid hybridization and emerging applications // J. Biomol. Struct. Dynamics. 2001. Vol. 19. P. 497-504.
307. Tyagi S., Landegren U., Tazi M. et. al. Extremely sensitive, background-free gene detection using binary probes and beta replicase // Proc. Nat. Acad. Sci. USA. 1996. Vol. 93. P. 5395-5400.
308. Morrison T.B., Weis JJ., Wittwer C.T. Quantification of low-copy transcripts by continuous SYBR Green I monitoring during amplification. Biotechniques // 1998. Vol. 24. P. 954-962.
309. Whitcombe D., TheakerJ., Guy S.P. et al. Detection of PCR products using self-probing amplicons and fluorescence // Nature Biotechnology. 1999. Vol. 17. P. 804-807.
310. Thelwell N., Millington S., Solinas A. et al. Mode of action and application of Scorpion primers to mutation detection // Nucl. Acids Res. 2000. Vol. 28. P. 3752-3761.
311. Cantor C.R., Smith CL. // Genomics: The science and technology behind the human genome project. N.Y. Wiley: 1999. P. 98-130.
312. Riley J., Butler R., Olgivie D. et al. A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones // Nucl. Acids Res. 1990. Vol. 18. P. 2887-2890.
313. Triglia Т., Peterson M.G., Kemp DJ. A procedure for in vivo amplification of DNA segments that lie outside the boundaries of known sequences // Ibid. 1988. Vol. 16. P. 8186.
314. Cantor C.R., Smith CL. I I Genomics: The science and technology behind the human genome project. N.Y. Wiley: 1999. P. 112-113.
315. Mudge J., Anderson W.R., Kehrer R.L., Fairbanks DJ. A RAPD genetic map of Saccharum officinarum // Crop Sci. 1996. Vol. 36. P. 1362-1366
316. Zarlenga D.S., Higgins J. PCR as a diagnostic and quantitative technique in veterinary parasitology //Veterinary Parasitol. 2001. Vol. 101. P. 215-230.
317. Zhang L., Cui X., Schmitt K. et al. Whole genome amplification from a single cell: Implications for genetic analysis // Proc. Nat. Acad. Sci. USA.
1992. Vol. 89. P. 5847-5851.
318. Cheung V.G., Nelson S.F. Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA // Ibid. 1996. Vol. 93. Vol. 14676-14679.
319. Grothues D., Cantor C.R., Smith CL. PCR amplification of megabase DNA with tagged random primers (T-PCR) // Nucl. Acids Res. 1993. Vol. 21. P. 1321-1322.
320. Samura O., Pertl B., Sohda S. et al. Female fetal cells in maternal blood:
Use of DNA polymorphisms to prove origin // Hum. Genet. 2000. Vol. 107. P. 28-32.
321. Hahn S., Zhong X.Y., Troeger C. et al. Current applications of single-cell PCR // Cell. Mol. Life Sci. 2000. Vol. 57. P. 96-10.
322. Barany F. Genetic disease detection and DNA amplification using cloned thermostable ligase // Proc. Nat. Acad. Sci. USA. 1991. Vol. 98. P. 189-193.
323. Jarvius J. et al. Oligonucleotide ligation assay // Meth. Mol. Biol. 2003. Vol. 212. P. 215-228.
324. Fahy E., Kwoh D.Y., Gingeras T.R. Self-sustained sequence replication (3SR): An isothermal transcription-based amplification system alternative to PCR // PCR Meth. and Appl. 1991. Vol. 1. P. 25-33.
325. Schweitzer B., Kingsmore S. Combining nucleic acid amplification and detection // Curr. Opin. Biotechnol. 2001. Vol. 12. P. 21-27.
326. Walker G.T., Little М., Nadeau J.G., Shank D.D. Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system // Proc. Nat. Acad. Sci. USA. 1992. Vol. 89. P. 392-396.
327. Little М., Andrews J., Moore R. et al. Strand displacement amplification and homogeneous real-time detection incorporated in a second-generation DNA probe system, BDProbeTecET // Clin. Chem. 1999. Vol. 45. P. 777-784.
328. Westin L., Xu X., Miller C. et al. Anchored multiplex amplification on a microelectronic chip array // Nature Biotechnol. 2000. Vol. 18. P. 199-204.
