[1] Travers ME, Mackay DJ, Dekker Nitert M, et al. Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets[J]. Diabetes, 2013, 62(3):987-992. [2] Martini S, Nair V, Patel SR, et al. From SNP to transcriptional mechanism:a model for FRMD3 in diabetic nephropathy[J]. Diabetes, 2013, 62(7):2605-2612. [3] 唐立群, 肖层林, 王伟平. SNP分子标记的研究及其应用进展[J]. 中国农学通报, 2012, 28(12):154-158. [4] Ugozzoli L, Wallace RB. Allele-specific polymerase chain reaction[J]. Methods, 1991, 2:42-48. [5] Billadeau D, Blackstadt M, Greipp P, et al. Analysis of B-lymphoid malignancies using allele-specific polymerase chain reaction:a technique for sequential quantitation of residual disease[J]. Blood, 1991 78(11):3021-3029. [6] Liu AH, Guan GQ, Liu JL, et al. Polymorphism analysis of Chinese theileria sergenti using allele-specific polymerase chain reaction of the major piroplasm surface protein gene[J]. J Parasitol, 2011, 97(1):116-121. [7] Zhang LR, Zhang W, Yin ZK, et al. Genetie polymor phisms of drug-metabolizing enzymes CYP2C9, NAT2 and TPMT in Han Chinese populaton from He-nan area[J]. Chinese Journal of New Drugs and Clinical Remedies, 2006, 25(8):561-564. [8] Corless CL, Harrell P, Lacouture M, et al. Allele-specific polymerase chain reaction for the imatinib-resistant KIT D816V and D816F mutations in mastocytosis and acute myelogenous leukemia[J]. Journal of Molecular Diagnostics, 2006, 8(5):604-612. [9] Bassam L, Amal A. Detection of the NQO1 C609T polymorphism by a simple one step Tri-primer amplificatification Refractory Mutation System-PCR method[J]. Am J Biomed Sci, 2011, 3(2):77-83. [10] Hamajima N. PCR-CTPP:a new genotyping technique in the era of genetic epidemiology[J]. Expert Revi Mole Diagn, 2001, 1(1):119-123. [11] Ye S, Dhillon S, Ke XY, et al. An effi-cient procedure for genotyping single nucleotide polymorphisms[J]. Nucleic Acids Research, 2001, 29(17):E88. [12] Stephan S, Cécile R, Isabelle T, et al. A comparison of restriction fragment length polymorphism, tetra primer ampli?cation refractory mutation system PCR and unlabeled probe melting analysis for LTA+252 CNT SNP genotyping[J]. Clinica Chimica Acta, 2011, 412:430-434. [13] 刘兴顺, 程牛亮, 梁小波, 等.四引物扩增受阻突变体系聚合酶链反应在SNP 基因分型中的研究[J]. 山西医科大学学报, 2008, 39(6):483-485. [14] 卜莹, 古卓良, 张晓丹, 等.四引物PCR扩增反应的单管SNP快速测定法[J].中国生物化学与分子生物学报, 2004, 20(2):252-256. [15] 卜莹, 张晓丹, 马涛, 等.五引物单管聚合酶链反应(PCR)扩增法快速测定人CYP2D6﹡10等位基因的类型[J].分析化学, 2005, 33(2):155-160. [16] Yang HY, Diao Y, Zhou GH, et al. Genotyping three single nucleotide polymorphisms associated with risk of gout by improved tri-primer PCR[C]// Progress on Post-Genome Technologies and Modern Natural products, Proceedings of the 7th international forum on post-genome technologies and China-Japan-Korea summit on natural products, Chongqing, 2010. Nanjing:Southeast university press, 2010:310-312. [17] Piccioli P, Serra M, Gismondi V, et al. Multiplex tetra-primer amplification refractory mutation system PCR to detect 6 common germline mutations of the MUTYH gene associated with polyposis and colorectal cancer[J]. Clin Chem, 2006, 52(4):739-743. [18] Rees WA, Yager TD, Korte J, et al. Betaine can eliminate the base pair composition dependence of DNA melting[J]. Biochemistry, 1993, 32(1):137-144. [19] Lajin B, Alachkar A, Sakur AA. Triplex tetra-primer ARMS-PCR method for the simultane ous detection of MTHFR c.677C >T and c.1298A>C, and MTRR c.6 6A >G Polymorphisms of the folate homocysteine metabolic pathway[J]. Molecular and Cellular Probes, 2012, 26(1):16-20. [20] Lajin B, Alachkar A, Alhaj Sakur A. Betaine significantly improves multiplex tetra-primer ARMS-PCR methods[J]. Molecular Biotechnology, 2013, 54(3):977-982. [21] 刘颖, 张晨, 马学军, 等.多重嵌合引物对四引物扩增受阻突变体系PCR的改进及在卵巢癌相关位点中的应用[J].暨南大学学报:医学版, 2012, 3(22):152-155. [22] 张建勇, 王清印, 王伟继, 等.四引物扩增受阻突变体系PCR技术在中国明对虾SNP基因分型中的研究[J].中国水产科学, 2011, 18(4):751-759. [23] 孙晓如, 卜莹, 丁新生, 等.应用基于适配器连接介导的等位基因特异性扩增法检测LRRK2基因的单核苷酸多态性[J].现代生物医学进展, 2009, 14:2716-2720. [24] Zhang J, Yin LH, Lian GY, et al. Detection of CYP2E1, a genetic biomarker of susceptibility to benzene metabolism toxicity in immortal human lymphocytes derived from the Han Chinese population[J]. Biomed Environ Sci, 2010, 24(3):300-309. [25] Pollegioni P, Van der Linden G, Belisario A, et al. Mechanisms governing the responses to anthracnose pathogen in Juglans spp[J]. J Biotechnol, 2012, 159(4):251-264. [26] Choi JY, Kim YT, Byun JY, et al. An integrated allele-specific polymerase chain reaction-microarray chip for multiplex single nucleotide polymorphism typing[J]. Lab on a Chip, 2012, 12(24):5146-5154. [27] Choi JY, Kim YT, Ahn J, et al. Integrated allele-specific polymerase chain reaction-capillary electrophoresis microdevice for single nucleotide polymorphism genotyping[J].Biosensors Bioelectronics, 2012, 35(1):327-334. [28] Chen T, Liu Q, Jiang L, Liu C, et al. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree[J]. Genetic Testing and Molecular Biomarkers, 2013, 17(2):122-130. [29] Liao HW, Tsai IL, Chen GY, et al. Simultaneous detection of single nucleotide polymorphisms and copy number variations in the CYP2D6 gene by multiplex polymerase chain reaction combined with capillary electrophoresis[J]. Analytica Chimica Acta, 2013, 763:67-75. [30] Al-Soud WA, R? dstr?m P. Purification and characterization of PCR-inhibitory components in blood cells[J]. Journal of Clinical Microbiology, 2001, 39(2):485-493. [31] Akane A, Matsubara K, Nakamura H, et al. Identification of the heme compound copurified with deoxyribonucleic acid(DNA)from bloodstains, a major inhibitor of polymerase chain reaction(PCR)amplification[J]. J Forensic Sci, 1994, 39(2):362-372. [32] Ding M, Bullotta A, Caruso L, et al. An optimized sensitive method for quantitation of DNA/RNA viruses in heparinized and cryopreserved plasma[J]. J Virol Methods, 2011, 176(1-2):1-8. [33] Sharma R, Virdi AS, Singh P. A novel method for whole blood PCR without pretreatment[J]. Gene, 2012, 501(1):85-88. [34] Zhang Z, Kermekchiev MB, Barnes WM. Direct DNA amplification from crude clinical samples using a PCR enhancer cocktail and novel mutants of Taq[J]. J Mol Diagn, 2010, 12(2):152-161. [35] Katarina D, Efremov GD. Influence of salts and PCR inhibitions on the amplification capacity of three thermostable DNA polymerases[J]. Macedonian Journal of Chemistry and Chemical Engineering, 2010, 29(1):57-62. [36] Kreader CA. Relief of Amplification Inhibition in PCR with Bovine Serum Albumin or T4 Gene 32 protein[J]. Applied and Environmental Microbiology, 1996, 62(3):1102-1106. [37] Chua AL, Elina HT, Lim BH, et al. Development of a dry reagent-based triplex PCR for the detection of toxigenic and non-toxigenic Vibrio cholerae [J]. J Med Microbiol, 2011, 60:481-485. [38] Horáková H, Polakovi?ová I, Shaik GM, et al. 1, 2-propanediol-trehalose mixture as a potent quantitative real- time PCR enhancer [J]. BMC Biotechnology, 2011, 11:41. [39] Fuehrer HP, Fally MA, Habler VE, et al. Novel nested direct PCR technique for malaria diagnosis using filter paper samples[J]. Journal of Clinical Microbiology, 2011, 49(4):1628-1630. [40] 游玉权, 王清瑶, 许超尘, 等.福建省泉州地区人群SLC2A9 SLC17A3 ABCG2基因单核苷酸多态性与痛风易感性的研究[J].中华风湿病学杂志, 2013, 17(22):114-118. [41] 杨会勇, 许超尘, 王清瑶, 等.ABCG2基因单核苷酸多态性与闽南地区人群原发性痛风相关性研究[J].风湿病与关节炎, 2013, 2(1):24-28. [42] Zhu JJ, Chen LX, Mao Y, et al. Multiplex allele-specific amplifica-tion from whole blood for detecting multiple polymorphisms simultaneously. genetic testing and molecular biomarkers[J]. Genet Metabolism, 2012, 106(2):175-188. [43] Rottinghaus E, Bile E, Modukanele M, et al. Comparison of ahlstrom grade 226, munktell TFN, and whatman 903 filter papers for dried blood spot specimen collection and subsequent HIV-1 load and drug resistance genotyping analysis[J]. Journal of Clinical Microbiology, 2013, 51(1):55-60. [44] Ross RS, Stambouli O, Grüner N, et al. Detection of infections with hepatitis B virus, hepatitis C virus, and human immunodeficiency virus by analyses of dried blood spots--performance characteristics of the ARCHITECT system and two commercial assays for nucleic acid amplification[J]. Virol J, 2013, 10:72. [45] Aubry M, Roche C, Dupont-Rouzeyrol M, et al. Use of serum and blood samples on filter paper to improve the surveillance of dengue in Pacific Island Countries[J]. Journal of Clinical Virology, 2012, 55(1):23-29. [46] Andresen BS, Lund AM, Hougaard DM, et al. MCAD deficiency in Denmark[J]. Molecular, 2012, 17(1):10-15. [47] Casado-Díaz A, Cuenca-Acevedo R, Quesada JM, et al. Individual single tube genotyping and DNA pooling by allele-specific PCR to uncover associations of polymorphisms with complex diseases[J]. Clinica Chimoca Acta, 2007, 376(1-2):155-162. [48] Takagi S, Omae R, Makanga JO, et al. Simple and rapid detection method for the mutations in SLC22A12 that cause hypouricemia by allele-specific real-time polymerase chain reaction[J]. Clinica Chimica Acta, 2013, 415:330-333. |