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Journal Abstract Search

273 related items for PubMed ID: 18649739

  • 1. Restriction enzyme mining for SNPs in genomes.
    Chuang LY, Yang CH, Tsui KH, Cheng YH, Chang PL, Wen CH, Chang HW.
    Anticancer Res; 2008; 28(4A):2001-7. PubMed ID: 18649739
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  • 2. Prim-SNPing: a primer designer for cost-effective SNP genotyping.
    Chang HW, Chuang LY, Cheng YH, Hung YC, Wen CH, Gu DL, Yang CH.
    Biotechniques; 2009 May; 46(6):421-31. PubMed ID: 19480636
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  • 3. SNP-RFLPing: restriction enzyme mining for SNPs in genomes.
    Chang HW, Yang CH, Chang PL, Cheng YH, Chuang LY.
    BMC Genomics; 2006 Feb 17; 7():30. PubMed ID: 16503968
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  • 5. Software for optimization of SNP and PCR-RFLP genotyping to discriminate many genomes with the fewest assays.
    Gardner SN, Wagner MC.
    BMC Genomics; 2005 May 16; 6():73. PubMed ID: 15904493
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  • 8. A multiplexing single nucleotide polymorphism typing method based on restriction-enzyme-mediated single-base extension and capillary electrophoresis.
    Che Y, Chen X.
    Anal Biochem; 2004 Jun 15; 329(2):220-9. PubMed ID: 15158480
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  • 9. A Novel Teaching-Learning-Based Optimization for Improved Mutagenic Primer Design in Mismatch PCR-RFLP SNP Genotyping.
    Cheng YH.
    IEEE/ACM Trans Comput Biol Bioinform; 2016 Jun 15; 13(1):86-98. PubMed ID: 26886734
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  • 10. Toward genome-wide SNP genotyping.
    Syvänen AC.
    Nat Genet; 2005 Jun 15; 37 Suppl():S5-10. PubMed ID: 15920530
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  • 11. Genotyping of single nucleotide polymorphisms in cytokine genes using real-time PCR allelic discrimination technology.
    Johnson VJ, Yucesoy B, Luster MI.
    Cytokine; 2004 Sep 21; 27(6):135-41. PubMed ID: 15304242
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  • 14. Associate PCR-RFLP assay design with SNPs based on genetic algorithm in appropriate parameters estimation.
    Chuang LY, Cheng YH, Yang CH, Yang CH.
    IEEE Trans Nanobioscience; 2013 Jun 21; 12(2):119-27. PubMed ID: 23722280
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  • 15. Triallelic single nucleotide polymorphisms and genotyping error in genetic epidemiology studies: MDR1 (ABCB1) G2677/T/A as an example.
    Hüebner C, Petermann I, Browning BL, Shelling AN, Ferguson LR.
    Cancer Epidemiol Biomarkers Prev; 2007 Jun 21; 16(6):1185-92. PubMed ID: 17548683
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  • 18. Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia.
    Vuorio AF, Paulin L, Saltevo J, Kontula K.
    Mol Cell Probes; 1999 Dec 21; 13(6):421-4. PubMed ID: 10657146
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  • 19. Comparison of cytochrome P450 2C9 genotyping methods and implications for the clinical laboratory.
    Aquilante CL, Lobmeyer MT, Langaee TY, Johnson JA.
    Pharmacotherapy; 2004 Jun 21; 24(6):720-6. PubMed ID: 15222661
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  • 20. Typing single-nucleotide polymorphisms in Toxoplasma gondii by allele-specific primer extension and microarray detection.
    Su C, Hott C, Brownstein BH, Sibley LD.
    Methods Mol Biol; 2004 Jun 21; 270():249-62. PubMed ID: 15153632
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