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Journal Abstract Search

248 related items for PubMed ID: 15585207

  • 21. 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]

  • 22. Plasma level and genetic variation of apolipoprotein E in patients with lipoprotein glomerulopathy.
    Zhang B, Liu ZH, Zeng CH, Zheng JM, Chen HP, Zhou H, Li LS.
    Chin Med J (Engl); 2005 Apr 05; 118(7):555-60. PubMed ID: 15820086
    [Abstract] [Full Text] [Related]

  • 23. In vivo metabolism of ApoB, ApoA-I, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the ApoB gene.
    Elias N, Patterson BW, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 2000 May 05; 20(5):1309-15. PubMed ID: 10807747
    [Abstract] [Full Text] [Related]

  • 24. Familial hypobetalipoproteinemia is not associated with low levels of lipoprotein(a).
    Averna M, Marcovina SM, Noto D, Cole TG, Krul ES, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 1995 Dec 05; 15(12):2165-75. PubMed ID: 7489238
    [Abstract] [Full Text] [Related]

  • 25. Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia.
    Katsuda S, Kawashiri MA, Inazu A, Tada H, Tsuchida M, Kaneko Y, Nozue T, Nohara A, Okada T, Kobayashi J, Michishita I, Mabuchi H, Yamagishi M.
    Clin Chim Acta; 2009 Jan 05; 399(1-2):64-8. PubMed ID: 18848826
    [Abstract] [Full Text] [Related]

  • 26. Metabolism of apolipoprotein B-100 in a kindred with familial hypobetalipoproteinemia without a truncated form of apoB.
    Latour MA, Patterson BW, Pulai J, Chen Z, Schonfeld G.
    J Lipid Res; 1997 Mar 05; 38(3):592-9. PubMed ID: 9101440
    [Abstract] [Full Text] [Related]

  • 27. Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.
    Rimbert A, Pichelin M, Lecointe S, Marrec M, Le Scouarnec S, Barrak E, Croyal M, Krempf M, Le Marec H, Redon R, Schott JJ, Magré J, Cariou B.
    Atherosclerosis; 2016 Jul 05; 250():52-6. PubMed ID: 27179706
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. The association of the apolipoprotein E gene promoter polymorphisms and haplotypes with serum lipid and lipoprotein concentrations.
    Viiri LE, Loimaala A, Nenonen A, Islam S, Vuori I, Karhunen PJ, Lehtimäki T.
    Atherosclerosis; 2005 Mar 15; 179(1):161-7. PubMed ID: 15721023
    [Abstract] [Full Text] [Related]

  • 30. Threshold Effects of Circulating Angiopoietin-Like 3 Levels on Plasma Lipoproteins.
    Fazio S, Minnier J, Shapiro MD, Tsimikas S, Tarugi P, Averna MR, Arca M, Tavori H.
    J Clin Endocrinol Metab; 2017 Sep 01; 102(9):3340-3348. PubMed ID: 28633452
    [Abstract] [Full Text] [Related]

  • 31. 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 01; 16(9):1189-96. PubMed ID: 8792774
    [Abstract] [Full Text] [Related]

  • 32. Lengths of truncated forms of apolipoprotein B (apoB) determine their intestinal production.
    Krul ES, Tang J, Kettler TS, Clouse RE, Schonfeld G.
    Biochem Biophys Res Commun; 1992 Dec 15; 189(2):1069-76. PubMed ID: 1472017
    [Abstract] [Full Text] [Related]

  • 33. Frequency of ApoB and ApoE gene mutations as causes of hypobetalipoproteinemia in the framingham offspring population.
    Welty FK, Lahoz C, Tucker KL, Ordovas JM, Wilson PW, Schaefer EJ.
    Arterioscler Thromb Vasc Biol; 1998 Nov 15; 18(11):1745-51. PubMed ID: 9812913
    [Abstract] [Full Text] [Related]

  • 34. Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations.
    Di Leo E, Magnolo L, Bertolotti M, Bourbon M, Carmo Pereira S, Pirisi M, Calandra S, Tarugi P.
    Clin Genet; 2008 Sep 15; 74(3):267-73. PubMed ID: 18492086
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. 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 15; 34(3):501-7. PubMed ID: 8468533
    [Abstract] [Full Text] [Related]

  • 37. PCSK9 dominant negative mutant results in increased LDL catabolic rate and familial hypobetalipoproteinemia.
    Cariou B, Ouguerram K, Zaïr Y, Guerois R, Langhi C, Kourimate S, Benoit I, Le May C, Gayet C, Belabbas K, Dufernez F, Chétiveaux M, Tarugi P, Krempf M, Benlian P, Costet P.
    Arterioscler Thromb Vasc Biol; 2009 Dec 15; 29(12):2191-7. PubMed ID: 19762784
    [Abstract] [Full Text] [Related]

  • 38. Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature.
    Cefalù AB, Norata GD, Ghiglioni DG, Noto D, Uboldi P, Garlaschelli K, Baragetti A, Spina R, Valenti V, Pederiva C, Riva E, Terracciano L, Zoja A, Grigore L, Averna MR, Catapano AL.
    Atherosclerosis; 2015 Mar 15; 239(1):209-17. PubMed ID: 25618028
    [Abstract] [Full Text] [Related]

  • 39. Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.
    Martín-Morales R, García-Díaz JD, Tarugi P, González-Santos P, Saavedra-Vallejo P, Magnolo L, Mesa-Latorre JM, di Leo E, Valdivielso P.
    Gene; 2013 Nov 15; 531(1):92-6. PubMed ID: 24001780
    [Abstract] [Full Text] [Related]

  • 40. 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]

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