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Journal Abstract Search

215 related items for PubMed ID: 9888384

  • 1. From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms.
    Syvänen AC.
    Hum Mutat; 1999; 13(1):1-10. PubMed ID: 9888384
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. Arrayed primer extension reaction for genotyping on oligonucleotide microarray.
    Pullat J, Metspalu A.
    Methods Mol Biol; 2008; 444():161-7. PubMed ID: 18425479
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  • 5. The single-nucleotide primer extension (SNuPE) method for the multiplex detection of various DNA sequences: from detection of point mutations to microbial ecology.
    Nikolausz M, Chatzinotas A, Táncsics A, Imfeld G, Kästner M.
    Biochem Soc Trans; 2009 Apr; 37(Pt 2):454-9. PubMed ID: 19290881
    [Abstract] [Full Text] [Related]

  • 6. High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise.
    Bray MS, Boerwinkle E, Doris PA.
    Hum Mutat; 2001 Apr; 17(4):296-304. PubMed ID: 11295828
    [Abstract] [Full Text] [Related]

  • 7. A gel-free SNP genotyping method: bioluminometric assay coupled with modified primer extension reactions (BAMPER) directly from double-stranded PCR products.
    Zhou GH, Shirakura H, Kamahori M, Okano K, Nagai K, Kambara H.
    Hum Mutat; 2004 Aug; 24(2):155-63. PubMed ID: 15241797
    [Abstract] [Full Text] [Related]

  • 8. Genotyping of single-nucleotide polymorphisms by primer extension reaction in a dry-reagent dipstick format.
    Litos IK, Ioannou PC, Christopoulos TK, Traeger-Synodinos J, Kanavakis E.
    Anal Chem; 2007 Jan 15; 79(2):395-402. PubMed ID: 17222001
    [Abstract] [Full Text] [Related]

  • 9. Rapid identification of single nucleotide polymorphisms by fluorescence-based capillary electrophoresis.
    Bernat M, Titos E, Clària J.
    Genet Mol Res; 2002 Mar 31; 1(1):72-8. PubMed ID: 14963815
    [Abstract] [Full Text] [Related]

  • 10. A novel human leucocyte antigen-DRB1 genotyping method based on multiplex primer extension reactions.
    Jaakkola E, Herzberg I, Crane AM, Pointon JJ, Laiho K, Kauppi M, Kaarela K, Wordsworth BP, Tuomilehto J, Brown MA.
    Tissue Antigens; 2004 Jul 31; 64(1):88-95. PubMed ID: 15191530
    [Abstract] [Full Text] [Related]

  • 11. Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification.
    Ye F, Li MS, Taylor JD, Nguyen Q, Colton HM, Casey WM, Wagner M, Weiner MP, Chen J.
    Hum Mutat; 2001 Apr 31; 17(4):305-16. PubMed ID: 11295829
    [Abstract] [Full Text] [Related]

  • 12. SNP genotyping using multiplex single base primer extension assays.
    Podini D, Vallone PM.
    Methods Mol Biol; 2009 Apr 31; 578():379-91. PubMed ID: 19768606
    [Abstract] [Full Text] [Related]

  • 13. Multiplex high-throughput solid-phase minisequencing by capillary electrophoresis and liquid core waveguide fluorescence detection.
    Curcio M, Stålhandske P, Lindberg P, Roeraade J.
    Electrophoresis; 2002 May 31; 23(10):1467-72. PubMed ID: 12116157
    [Abstract] [Full Text] [Related]

  • 14. Allele-specific PCR in SNP genotyping.
    Gaudet M, Fara AG, Beritognolo I, Sabatti M.
    Methods Mol Biol; 2009 May 31; 578():415-24. PubMed ID: 19768609
    [Abstract] [Full Text] [Related]

  • 15. Proofreading genotyping assays and electrochemical detection of SNPs.
    King GC, Di Giusto DA, Wlassoff WA, Giesebrecht S, Flening E, Tyrelle GD.
    Hum Mutat; 2004 May 31; 23(5):420-5. PubMed ID: 15108272
    [Abstract] [Full Text] [Related]

  • 16. A new technology for mutation detection.
    Shackelford W, Deng S, Murayama K, Wang J.
    Ann N Y Acad Sci; 2004 Jun 31; 1022():257-62. PubMed ID: 15251970
    [Abstract] [Full Text] [Related]

  • 17. SNP genotyping by multiplexed solid-phase amplification and fluorescent minisequencing.
    Shapero MH, Leuther KK, Nguyen A, Scott M, Jones KW.
    Genome Res; 2001 Nov 31; 11(11):1926-34. PubMed ID: 11691857
    [Abstract] [Full Text] [Related]

  • 18. Towards automatic detection of point mutations: use of scintillating microplates in solid-phase minisequencing.
    Ihalainen J, Siitari H, Laine S, Syvänen AC, Palotie A.
    Biotechniques; 1994 May 31; 16(5):938-43. PubMed ID: 8068351
    [Abstract] [Full Text] [Related]

  • 19. Multiplex detection of mutations.
    Perlin DS, Balashov S, Park S.
    Methods Mol Biol; 2008 May 31; 429():23-31. PubMed ID: 18695956
    [Abstract] [Full Text] [Related]

  • 20. Multiplex PCR-single-base extension genotyping of multiple glutathione S-transferase polymorphisms.
    Faber A, Ferreira GN, Silva SN, Rueff J, Gaspar J.
    Biotechnol Appl Biochem; 2005 Feb 31; 41(Pt 1):9-15. PubMed ID: 15182232
    [Abstract] [Full Text] [Related]

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