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Journal Abstract Search

209 related items for PubMed ID: 8476605

  • 21. Direct cycle sequencing of mutated alleles detected by PCR single-strand conformation polymorphism analysis.
    Mok SC, Lo KW, Tsao SW.
    Biotechniques; 1993 May; 14(5):790-4. PubMed ID: 8512704
    [Abstract] [Full Text] [Related]

  • 22. Double-stranded DNA sequencing by linear amplification with Taq DNA polymerase.
    Wang B, Fang Q, Williams WV, Weiner DB.
    Biotechniques; 1992 Oct; 13(4):527-30. PubMed ID: 1476718
    [No Abstract] [Full Text] [Related]

  • 23. A rapid and simple method for labeling short DNA fragments using Taq polymerase.
    Mizobuchi M, Frohman LA.
    Biotechniques; 1992 Mar; 12(3):350-4. PubMed ID: 1571140
    [Abstract] [Full Text] [Related]

  • 24. Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia.
    Baron H, Fung S, Aydin A, Bähring S, Luft FC, Schuster H.
    Nat Biotechnol; 1996 Oct; 14(10):1279-82. PubMed ID: 9631093
    [Abstract] [Full Text] [Related]

  • 25. Mutation analysis in familial hypercholesterolemia patients of different ancestries: identification of three novel LDLR gene mutations.
    Callis M, Jansen S, Thiart R, de Villiers JN, Raal FJ, Kotze MJ.
    Mol Cell Probes; 1998 Jun; 12(3):149-52. PubMed ID: 9664576
    [Abstract] [Full Text] [Related]

  • 26. Screening for mutations in exon 4 of the LDL receptor gene in Thai subjects with primary hypercholesterolemia: detection of a novel mutation D151Y by PCR-CFLP.
    Pongrapeeporn KU, Sutthikhum V, Likidlilid A, Poldee S, Futrakul A, Yamwong P, Amornrattana A, Ong-Ajyooth S.
    J Med Assoc Thai; 2000 Nov; 83 Suppl 2():S66-73. PubMed ID: 11194025
    [Abstract] [Full Text] [Related]

  • 27. Screening for mutations in the LDL receptor gene and apolipoprotein B-100 gene in 218 patients with severe hypercholesterolemia.
    Geisel J, Holzem G, Schleifenbaum T, Oette K.
    Z Gastroenterol; 1996 Jun; 34 Suppl 3():14-5. PubMed ID: 8767447
    [Abstract] [Full Text] [Related]

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  • 29. [Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].
    Lin J, Wang LY, Liu S, Pan XD, Du LP, Shi FR, Qin YW, Zhao Q, Guo HY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):14-8. PubMed ID: 14767901
    [Abstract] [Full Text] [Related]

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  • 31. Improved detection of p53 point mutations by dideoxyfingerprinting (ddF).
    Martincic D, Whitlock JA.
    Oncogene; 1996 Nov 07; 13(9):2039-44. PubMed ID: 8934553
    [Abstract] [Full Text] [Related]

  • 32. Sequencing reactions for the applied biosystems 373A Automated DNA Sequencer.
    Halloran N, Du Z, Wilson RK.
    Methods Mol Biol; 1993 Nov 07; 23():297-315. PubMed ID: 8220762
    [No Abstract] [Full Text] [Related]

  • 33. Detection of ciprofloxacin resistance mutations in Campylobacter jejuni gyrA by nonradioisotopic single-strand conformation polymorphism and direct DNA sequencing.
    Charvalos E, Peteinaki E, Spyridaki I, Manetas S, Tselentis Y.
    J Clin Lab Anal; 1996 Nov 07; 10(3):129-33. PubMed ID: 8731499
    [Abstract] [Full Text] [Related]

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  • 36. Serial processing of biological reactions using flow-through microfluidic devices: coupled PCR/LDR for the detection of low-abundant DNA point mutations.
    Hashimoto M, Barany F, Xu F, Soper SA.
    Analyst; 2007 Sep 07; 132(9):913-21. PubMed ID: 17710267
    [Abstract] [Full Text] [Related]

  • 37. [The improvement of a direct DNA sequencing method by devising the primer design: detection of lipoprotein lipase gene aberrations].
    Mori A, Takagi A, Ikeda Y, Yamamoto A.
    Rinsho Byori; 1996 Oct 07; 44(10):983-90. PubMed ID: 8937192
    [Abstract] [Full Text] [Related]

  • 38. [Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100].
    Krapivner SR, Malyshev PP, Rozhkova TA, Potaraus AB, Kukharchuk VV, Bochkov VN.
    Ter Arkh; 2000 Oct 07; 72(4):9-12. PubMed ID: 10833789
    [Abstract] [Full Text] [Related]

  • 39. [A rapid and simple detection of DNA fragment with point mutation by capillary electrophoresis].
    Jing H, Liu J, Ru Q, Deng Y, Luo G, Huang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Aug 07; 18(4):317-21. PubMed ID: 11484177
    [Abstract] [Full Text] [Related]

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