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122 related items for PubMed ID: 9684734

  • 1. Molecular basis of an apolipoprotein[a] null allele: a splice site mutation is associated with deletion of a single exon.
    Cox LA, Jett C, Hixson JE.
    J Lipid Res; 1998 Jul; 39(7):1319-26. PubMed ID: 9684734
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  • 3. Molecular cloning of the cDNA encoding the carboxy-terminal domain of chimpanzee apolipoprotein(a): an Asp57 --> Asn mutation in kringle IV-10 is associated with poor fibrin binding.
    Chenivesse X, Huby T, Wickins J, Chapman J, Thillet J.
    Biochemistry; 1998 May 19; 37(20):7213-23. PubMed ID: 9585533
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  • 4. Characterization of the apolipoprotein(a) gene.
    Ichinose A.
    Biochem Biophys Res Commun; 1995 Apr 06; 209(1):365-71. PubMed ID: 7726858
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  • 5. The recurring evolution of lipoprotein(a). Insights from cloning of hedgehog apolipoprotein(a).
    Lawn RM, Boonmark NW, Schwartz K, Lindahl GE, Wade DP, Byrne CD, Fong KJ, Meer K, Patthy L.
    J Biol Chem; 1995 Oct 13; 270(41):24004-9. PubMed ID: 7592597
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  • 6. Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians.
    Ogorelkova M, Gruber A, Utermann G.
    Hum Mol Genet; 1999 Oct 13; 8(11):2087-96. PubMed ID: 10484779
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  • 7. Identification of promoter sequences in the 5' untranslated region of the baboon apolipoprotein[a] gene.
    Hixson JE, Jett C, Birnbaum S.
    J Lipid Res; 1996 Nov 13; 37(11):2324-31. PubMed ID: 8978484
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  • 8. Apolipoprotein(a) (Apo(a)) glycoprotein isoforms result from size differences in Apo(a) mRNA in baboons.
    Hixson JE, Britten ML, Manis GS, Rainwater DL.
    J Biol Chem; 1989 Apr 15; 264(11):6013-6. PubMed ID: 2522926
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  • 9. Baboon lipoprotein(a) binds very weakly to lysine-agarose and fibrin despite the presence of a strong lysine-binding site in apolipoprotein(a) kringle IV type 10.
    Belczewski AR, Ho J, Taylor FB, Boffa MB, Jia Z, Koschinsky ML.
    Biochemistry; 2005 Jan 18; 44(2):555-64. PubMed ID: 15641780
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  • 10. Molecular definition of the extreme size polymorphism in apolipoprotein(a).
    Lackner C, Cohen JC, Hobbs HH.
    Hum Mol Genet; 1993 Jul 18; 2(7):933-40. PubMed ID: 8395942
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  • 11. Molecular basis for "null" lipoprotein(a) phenotypes and the influence of apolipoprotein(a) size on plasma lipoprotein(a) level in the baboon.
    White AL, Hixson JE, Rainwater DL, Lanford RE.
    J Biol Chem; 1994 Mar 25; 269(12):9060-6. PubMed ID: 8132643
    [Abstract] [Full Text] [Related]

  • 12. Intracellular processing of apo(a) in primary baboon hepatocytes.
    White AL, Rainwater DL, Hixson JE, Estlack LE, Lanford RE.
    Chem Phys Lipids; 1994 Jan 25; 67-68():123-33. PubMed ID: 8187206
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  • 13. Multiple members of the plasminogen-apolipoprotein(a) gene family associated with thrombosis.
    Ichinose A.
    Biochemistry; 1992 Mar 31; 31(12):3113-8. PubMed ID: 1554698
    [Abstract] [Full Text] [Related]

  • 14. The baboon apolipoprotein E gene: structure, expression, and linkage with the gene for apolipoprotein C-1.
    Hixson JE, Cox LA, Borenstein S.
    Genomics; 1988 May 31; 2(4):315-23. PubMed ID: 3220472
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  • 15. Detection and quantitation of apolipoprotein(a) mRNA in human liver and its relationship with plasma lipoprotein(a) concentration.
    Wade DP, Knight BL, Harders-Spengel K, Soutar AK.
    Atherosclerosis; 1991 Nov 31; 91(1-2):63-72. PubMed ID: 1839819
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  • 17. Exon 10 skipping caused by intron 10 splice donor site mutation in cholesteryl ester transfer protein gene results in abnormal downstream splice site selection.
    Sakai N, Santamarina-Fojo S, Yamashita S, Matsuzawa Y, Brewer HB.
    J Lipid Res; 1996 Oct 31; 37(10):2065-73. PubMed ID: 8906584
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  • 18. A splice junction mutation causes deletion of a 72-base exon from the mRNA for lysosomal acid lipase in a patient with cholesteryl ester storage disease.
    Klima H, Ullrich K, Aslanidis C, Fehringer P, Lackner KJ, Schmitz G.
    J Clin Invest; 1993 Dec 31; 92(6):2713-8. PubMed ID: 8254026
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  • 19. Aberrant splicing of intron 1 creates a novel null HLA-B*1501 allele.
    Curran MD, Williams F, Little AM, Rima BK, Madrigal JA, Middleton D.
    Tissue Antigens; 1999 Mar 31; 53(3):244-52. PubMed ID: 10203017
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  • 20. Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity.
    Otterness DM, Szumlanski CL, Wood TC, Weinshilboum RM.
    J Clin Invest; 1998 Mar 01; 101(5):1036-44. PubMed ID: 9486974
    [Abstract] [Full Text] [Related]

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