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Journal Abstract Search

169 related items for PubMed ID: 15251970

  • 21. 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
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  • 26. Mutation detection and typing of polymorphic loci through double-strand conformation analysis.
    Argüello JR, Little AM, Pay AL, Gallardo D, Rojas I, Marsh SG, Goldman JM, Madrigal JA.
    Nat Genet; 1998 Feb 15; 18(2):192-4. PubMed ID: 9462755
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  • 27. 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 15; 37(Pt 2):454-9. PubMed ID: 19290881
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  • 28. Detection of single-base DNA mutations by enzyme-amplified electronic transduction.
    Patolsky F, Lichtenstein A, Willner I.
    Nat Biotechnol; 2001 Mar 15; 19(3):253-7. PubMed ID: 11231559
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  • 29. 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 15; 16(5):938-43. PubMed ID: 8068351
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  • 32. Restriction enzyme analysis of PCR products.
    Ota M, Asamura H, Oki T, Sada M.
    Methods Mol Biol; 2009 May 15; 578():405-14. PubMed ID: 19768608
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  • 34. High sensitive approach for point mutation detection based on electrochemiluminescence.
    Zhu D, Xing D, Shen X, Liu J, Chen Q.
    Biosens Bioelectron; 2004 Oct 15; 20(3):448-53. PubMed ID: 15494224
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  • 35. Analytical evaluation of the PapilloCheck test, a new commercial DNA chip for detection and genotyping of human papillomavirus.
    Dalstein V, Merlin S, Bali C, Saunier M, Dachez R, Ronsin C.
    J Virol Methods; 2009 Mar 15; 156(1-2):77-83. PubMed ID: 19041893
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  • 36. Rapid and reliable genotyping procedure for detection of alleles with mutations, deletion, or/and duplication of the CYP2D6 gene.
    Arneth B, Shams M, Hiemke C, Härtter S.
    Clin Biochem; 2009 Aug 15; 42(12):1282-90. PubMed ID: 19393232
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  • 37. PCR-based detection of minority point mutations.
    Mike Makrigiorgos G.
    Hum Mutat; 2004 May 15; 23(5):406-12. PubMed ID: 15108270
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  • 38. High performance DNA sequencing, and the detection of mutations and polymorphisms, on the Clipper sequencer.
    Yager TD, Baron L, Batra R, Bouevitch A, Chan D, Chan K, Darasch S, Gilchrist R, Izmailov A, Lacroix JM, Marchelleta K, Renfrew J, Renfrew J, Rushlow D, Steinbach E, Ton C, Waterhouse P, Zaleski H, Dunn JM, Stevens J.
    Electrophoresis; 1999 Jun 15; 20(6):1280-300. PubMed ID: 10380769
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  • 39. A novel diagnostic test detects a low frequency of the hemicentin Gln5345Arg variant among Northern Irish age related macular degeneration patients.
    McKay GJ, Clarke S, Hughes A, McConnell V, Schultz DW, Klein ML, Silvestri G, Simpson DA.
    Mol Vis; 2004 Sep 24; 10():682-7. PubMed ID: 15467524
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