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Journal Abstract Search

209 related items for PubMed ID: 8476605

  • 1. Screening for point mutations by semi-automated DNA sequencing using sequenase and magnetic beads.
    Leren TP, Rødningen OK, Røsby O, Solberg K, Berg K.
    Biotechniques; 1993 Apr; 14(4):618-23. PubMed ID: 8476605
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  • 2. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB).
    Azian M, Hapizah MN, Khalid BA, Khalid Y, Rosli A, Jamal R.
    Malays J Pathol; 2006 Jun; 28(1):7-15. PubMed ID: 17694954
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  • 5. High-resolution melting analysis for detection of familial ligand-defective apolipoprotein B-100 mutations.
    Liyanage KE, Hooper AJ, Defesche JC, Burnett JR, van Bockxmeer FM.
    Ann Clin Biochem; 2008 Mar; 45(Pt 2):170-6. PubMed ID: 18325181
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  • 6. Point mutation analysis in a mammalian gene: rapid preparation of total RNA, PCR amplification of cDNA, and Taq sequencing by a novel method.
    Carothers AM, Urlaub G, Mucha J, Grunberger D, Chasin LA.
    Biotechniques; 1989 May; 7(5):494-6, 498-9. PubMed ID: 2483818
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  • 9. Comparative analysis of human DNA variations by fluorescence-based sequencing of PCR products.
    Kwok PY, Carlson C, Yager TD, Ankener W, Nickerson DA.
    Genomics; 1994 Sep 01; 23(1):138-44. PubMed ID: 7829062
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  • 10. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov 01; 49(4):318-45. PubMed ID: 12553167
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  • 11. Detection of the apolipoprotein B-100 arg(3500) > gl mutation in familial defective apoB-100 by temperature-gradient gel electrophoresis.
    Koch M, Pfohl M, Enderle M, Schnauder G, Seif FJ.
    Z Gastroenterol; 1996 Jun 01; 34 Suppl 3():16-8. PubMed ID: 8767448
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  • 17. Orphan peak analysis: a novel method for detection of point mutations using an automated fluorescence DNA sequencer.
    Hattori M, Shibata A, Yoshioka K, Sakaki Y.
    Genomics; 1993 Feb 01; 15(2):415-7. PubMed ID: 8449509
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  • 20. Two novel mutations 685del 1 and D129G in the low-density lipoprotein receptor gene in a compound heterozygote Chinese family with familial hypercholesterolemia.
    Chen K, Mu YM, Wang BA, Guo QH, Lu ZH, Dou JT, Lu JM.
    Metabolism; 2007 May 01; 56(5):636-40. PubMed ID: 17445538
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