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Journal Abstract Search

172 related items for PubMed ID: 8468533

  • 1. Four new mutations in the apolipoprotein B gene causing hypobetalipoproteinemia, including two different frameshift mutations that yield truncated apolipoprotein B proteins of identical length.
    Young SG, Pullinger CR, Zysow BR, Hofmann-Radvani H, Linton MF, Farese RV, Terdiman JF, Snyder SM, Grundy SM, Vega GL.
    J Lipid Res; 1993 Mar; 34(3):501-7. PubMed ID: 8468533
    [Abstract] [Full Text] [Related]

  • 2. ApoB-54.8, a truncated apolipoprotein found primarily in VLDL, is associated with a nonsense mutation in the apoB gene and hypobetalipoproteinemia.
    Wagner RD, Krul ES, Tang J, Parhofer KG, Garlock K, Talmud P, Schonfeld G.
    J Lipid Res; 1991 Jun; 32(6):1001-11. PubMed ID: 1940616
    [Abstract] [Full Text] [Related]

  • 3. Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.
    Young SG, Hubl ST, Smith RS, Snyder SM, Terdiman JF.
    J Clin Invest; 1990 Mar; 85(3):933-42. PubMed ID: 2312735
    [Abstract] [Full Text] [Related]

  • 4. A gene-targeted mouse model for familial hypobetalipoproteinemia. Low levels of apolipoprotein B mRNA in association with a nonsense mutation in exon 26 of the apolipoprotein B gene.
    Kim E, Ambroziak P, Véniant MM, Hamilton RL, Young SG.
    J Biol Chem; 1998 Dec 18; 273(51):33977-84. PubMed ID: 9852051
    [Abstract] [Full Text] [Related]

  • 5. Identification and molecular analysis of two apoB gene mutations causing low plasma cholesterol levels.
    Welty FK, Ordovas J, Schaefer EJ, Wilson PW, Young SG.
    Circulation; 1995 Oct 15; 92(8):2036-40. PubMed ID: 7554178
    [Abstract] [Full Text] [Related]

  • 6. ApoB-75, a truncation of apolipoprotein B associated with familial hypobetalipoproteinemia: genetic and kinetic studies.
    Krul ES, Parhofer KG, Barrett PH, Wagner RD, Schonfeld G.
    J Lipid Res; 1992 Jul 15; 33(7):1037-50. PubMed ID: 1431583
    [Abstract] [Full Text] [Related]

  • 7. Dual mechanisms for the low plasma levels of truncated apolipoprotein B proteins in familial hypobetalipoproteinemia. Analysis of a new mouse model with a nonsense mutation in the Apob gene.
    Kim E, Cham CM, Véniant MM, Ambroziak P, Young SG.
    J Clin Invest; 1998 Mar 15; 101(6):1468-77. PubMed ID: 9502790
    [Abstract] [Full Text] [Related]

  • 8. A truncated species of apolipoprotein B (B-38.7) in a patient with homozygous hypobetalipoproteinemia associated with diabetes mellitus.
    Ohashi K, Ishibashi S, Yamamoto M, Osuga J, Yazaki Y, Yukawa S, Yamada N.
    Arterioscler Thromb Vasc Biol; 1998 Aug 15; 18(8):1330-4. PubMed ID: 9714141
    [Abstract] [Full Text] [Related]

  • 9. A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.
    Welty FK, Hubl ST, Pierotti VR, Young SG.
    J Clin Invest; 1991 May 15; 87(5):1748-54. PubMed ID: 2022744
    [Abstract] [Full Text] [Related]

  • 10. Apolipoprotein B-38.9 does not associate with apo[a] and forms two distinct HDL density particle populations that are larger than HDL.
    Groenewegen WA, Averna MR, Pulai J, Krul ES, Schonfeld G.
    J Lipid Res; 1994 Jun 15; 35(6):1012-25. PubMed ID: 8077841
    [Abstract] [Full Text] [Related]

  • 11. Hypobetalipoproteinemia associated with apo B-48.4, a truncated protein only 14 amino acids longer than apo B-48.
    Ruotolo G, Zanelli T, Tettamanti C, Ragogna F, Parlavecchia M, Viganò F, Catapano AL.
    Atherosclerosis; 1998 Mar 15; 137(1):125-31. PubMed ID: 9568744
    [Abstract] [Full Text] [Related]

  • 12. A truncated species of apolipoprotein B, B-83, associated with hypobetalipoproteinemia.
    Farese RV, Garg A, Pierotti VR, Vega GL, Young SG.
    J Lipid Res; 1992 Apr 15; 33(4):569-77. PubMed ID: 1527480
    [Abstract] [Full Text] [Related]

  • 13. The hypobetalipoproteinemias.
    Schonfeld G.
    Annu Rev Nutr; 1995 Apr 15; 15():23-34. PubMed ID: 8527219
    [Abstract] [Full Text] [Related]

  • 14. Homozygous familial hypobetalipoproteinemia. Increased LDL catabolism in hypobetalipoproteinemia due to a truncated apolipoprotein B species, apo B-87Padova.
    Gabelli C, Bilato C, Martini S, Tennyson GE, Zech LA, Corsini A, Albanese M, Brewer HB, Crepaldi G, Baggio G.
    Arterioscler Thromb Vasc Biol; 1996 Sep 15; 16(9):1189-96. PubMed ID: 8792774
    [Abstract] [Full Text] [Related]

  • 15. The molecular basis of truncated forms of apolipoprotein B in a kindred with compound heterozygous hypobetalipoproteinemia.
    Talmud P, King-Underwood L, Krul E, Schonfeld G, Humphries S.
    J Lipid Res; 1989 Nov 15; 30(11):1773-9. PubMed ID: 2614276
    [Abstract] [Full Text] [Related]

  • 16. VLDL and IDL apolipoprotein B-100 kinetics in familial hypercholesterolemia due to impaired LDL receptor function or to defective apolipoprotein B-100.
    Zulewski H, Ninnis R, Miserez AR, Baumstark MW, Keller U.
    J Lipid Res; 1998 Feb 15; 39(2):380-7. PubMed ID: 9507998
    [Abstract] [Full Text] [Related]

  • 17. Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote.
    Hooper AJ, Robertson K, Champain D, Hua J, Song S, Parhofer KG, Barrett PHR, van Bockxmeer FM, Burnett JR.
    Clin Biochem; 2016 Jun 15; 49(9):720-722. PubMed ID: 26916057
    [Abstract] [Full Text] [Related]

  • 18. Dysbetalipoproteinemia in a kindred with hypobetalipoproteinemia due to mutations in the genes for ApoB (ApoB-70.5) and ApoE (ApoE2).
    Groenewegen WA, Krul ES, Averna MR, Pulai J, Schonfeld G.
    Arterioscler Thromb; 1994 Nov 15; 14(11):1695-704. PubMed ID: 7947592
    [Abstract] [Full Text] [Related]

  • 19. Two apolipoprotein B gene defects in a kindred with hypobetalipoproteinemia, one of which results in a truncated variant, apoB-61, in VLDL and LDL.
    Pullinger CR, Hillas E, Hardman DA, Chen GC, Naya-Vigne JM, Iwasa JA, Hamilton RL, Lalouel JM, Williams RR, Kane JP.
    J Lipid Res; 1992 May 15; 33(5):699-710. PubMed ID: 1619363
    [Abstract] [Full Text] [Related]

  • 20. Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation.
    Martín-Campos JM, Roig R, Mayoral C, Martinez S, Martí G, Arroyo JA, Julve J, Blanco-Vaca F.
    Clin Chim Acta; 2012 Mar 22; 413(5-6):552-5. PubMed ID: 22155345
    [Abstract] [Full Text] [Related]

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