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Journal Abstract Search

248 related items for PubMed ID: 15894400

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  • 6. Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation.
    Pulai JI, Zakeri H, Kwok PY, Kim JH, Wu J, Schonfeld G.
    Am J Med Genet; 1998 Nov 16; 80(3):218-20. PubMed ID: 9843041
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  • 7. Absence of fatty liver in familial hypobetalipoproteinemia linked to chromosome 3p21.
    Yue P, Tanoli T, Wilhelm O, Patterson B, Yablonskiy D, Schonfeld G.
    Metabolism; 2005 May 16; 54(5):682-8. PubMed ID: 15877300
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  • 8. Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
    Yue P, Yuan B, Gerhard DS, Neuman RJ, Isley WL, Harris WS, Schonfeld G.
    Hum Mutat; 2002 Aug 16; 20(2):110-6. PubMed ID: 12124991
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  • 9. Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum.
    Tarugi P, Averna M.
    Adv Clin Chem; 2011 Aug 16; 54():81-107. PubMed ID: 21874758
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  • 11. Decreased production rates of VLDL triglycerides and ApoB-100 in subjects heterozygous for familial hypobetalipoproteinemia.
    Elias N, Patterson BW, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 1999 Nov 16; 19(11):2714-21. PubMed ID: 10559016
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  • 12. Familial hypobetalipoproteinemia: genetics and metabolism.
    Schonfeld G, Lin X, Yue P.
    Cell Mol Life Sci; 2005 Jun 16; 62(12):1372-8. PubMed ID: 15818469
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  • 13. Genetic variation of apolipoprotein B can produce both low and high levels of apoB-containing lipoproteins in plasma.
    Schonfeld G.
    Can J Cardiol; 1995 Oct 16; 11 Suppl G():86G-92G. PubMed ID: 7585299
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  • 14. A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5).
    Tarugi P, Lonardo A, Ballarini G, Erspamer L, Tondelli E, Bertolini S, Calandra S.
    J Hepatol; 2000 Sep 16; 33(3):361-70. PubMed ID: 11019990
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  • 15. Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.
    Noto D, Cefalù AB, Valenti V, Fayer F, Pinotti E, Ditta M, Spina R, Vigna G, Yue P, Kathiresan S, Tarugi P, Averna MR.
    Arterioscler Thromb Vasc Biol; 2012 Mar 16; 32(3):805-9. PubMed ID: 22247256
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  • 16. 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 16; 250():52-6. PubMed ID: 27179706
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  • 17. Recurrent familial hypobetalipoproteinemia-induced nonalcoholic fatty liver disease after living donor liver transplantation.
    Harada N, Soejima Y, Taketomi A, Yoshizumi T, Uchiyama H, Ikegami T, Saibara T, Nishizaki T, Maehara Y.
    Liver Transpl; 2009 Jul 16; 15(7):806-9. PubMed ID: 19562718
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  • 20. The hypobetalipoproteinemias.
    Schonfeld G.
    Annu Rev Nutr; 1995 Jul 16; 15():23-34. PubMed ID: 8527219
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