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182 related items for PubMed ID: 16531747

  • 1. APOA5 and triglyceride metabolism, lesson from human APOA5 deficiency.
    Calandra S, Priore Oliva C, Tarugi P, Bertolini S.
    Curr Opin Lipidol; 2006 Apr; 17(2):122-7. PubMed ID: 16531747
    [Abstract] [Full Text] [Related]

  • 2. Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene.
    Priore Oliva C, Carubbi F, Schaap FG, Bertolini S, Calandra S.
    J Intern Med; 2008 Apr; 263(4):450-8. PubMed ID: 18324930
    [Abstract] [Full Text] [Related]

  • 3. Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia.
    Priore Oliva C, Pisciotta L, Li Volti G, Sambataro MP, Cantafora A, Bellocchio A, Catapano A, Tarugi P, Bertolini S, Calandra S.
    Arterioscler Thromb Vasc Biol; 2005 Feb; 25(2):411-7. PubMed ID: 15591215
    [Abstract] [Full Text] [Related]

  • 4. Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.
    Marçais C, Verges B, Charrière S, Pruneta V, Merlin M, Billon S, Perrot L, Drai J, Sassolas A, Pennacchio LA, Fruchart-Najib J, Fruchart JC, Durlach V, Moulin P.
    J Clin Invest; 2005 Oct; 115(10):2862-9. PubMed ID: 16200213
    [Abstract] [Full Text] [Related]

  • 5. Molecular analysis of chylomicronemia in a clinical laboratory setting: diagnosis of 13 cases of lipoprotein lipase deficiency.
    Martín-Campos JM, Julve J, Roig R, Martínez S, Errico TL, Martínez-Couselo S, Escolà-Gil JC, Méndez-González J, Blanco-Vaca F.
    Clin Chim Acta; 2014 Feb 15; 429():61-8. PubMed ID: 24291057
    [Abstract] [Full Text] [Related]

  • 6. Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding.
    Dorfmeister B, Zeng WW, Dichlberger A, Nilsson SK, Schaap FG, Hubacek JA, Merkel M, Cooper JA, Lookene A, Putt W, Whittall R, Lee PJ, Lins L, Delsaux N, Nierman M, Kuivenhoven JA, Kastelein JJ, Vrablik M, Olivecrona G, Schneider WJ, Heeren J, Humphries SE, Talmud PJ.
    Arterioscler Thromb Vasc Biol; 2008 Oct 15; 28(10):1866-71. PubMed ID: 18635818
    [Abstract] [Full Text] [Related]

  • 7. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia.
    Chokshi N, Blumenschein SD, Ahmad Z, Garg A.
    J Clin Lipidol; 2014 Oct 15; 8(3):287-95. PubMed ID: 24793350
    [Abstract] [Full Text] [Related]

  • 8. Genetic Variants Associated with Gestational Hypertriglyceridemia and Pancreatitis.
    Xie SL, Chen TZ, Huang XL, Chen C, Jin R, Huang ZM, Zhou MT.
    PLoS One; 2015 Oct 15; 10(6):e0129488. PubMed ID: 26079787
    [Abstract] [Full Text] [Related]

  • 9. Modulation of phenotypic expression of APOA5 Q97X and L242P mutations.
    Charrière S, Cugnet C, Guitard M, Bernard S, Groisne L, Charcosset M, Pruneta-Deloche V, Merlin M, Billon S, Delay M, Sassolas A, Moulin P, Marçais C.
    Atherosclerosis; 2009 Nov 15; 207(1):150-6. PubMed ID: 19447388
    [Abstract] [Full Text] [Related]

  • 10. Rare and common variants in LPL and APOA5 in Thai subjects with severe hypertriglyceridemia: A resequencing approach.
    Khovidhunkit W, Charoen S, Kiateprungvej A, Chartyingcharoen P, Muanpetch S, Plengpanich W.
    J Clin Lipidol; 2016 Nov 15; 10(3):505-511.e1. PubMed ID: 27206937
    [Abstract] [Full Text] [Related]

  • 11. Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride.
    Buonuomo PS, Rabacchi C, Macchiaiolo M, Trenti C, Fasano T, Tarugi P, Bartuli A, Bertolini S, Calandra S.
    J Clin Lipidol; 2017 Nov 15; 11(6):1329-1337.e3. PubMed ID: 28951076
    [Abstract] [Full Text] [Related]

  • 12. APOA5 deficiency causes hypertriglyceridemia by reducing amounts of lipoprotein lipase in capillaries.
    Yang Y, Konrad RJ, Ploug M, Young SG.
    J Lipid Res; 2024 Jul 15; 65(7):100578. PubMed ID: 38880127
    [Abstract] [Full Text] [Related]

  • 13. Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia.
    Pisciotta L, Fresa R, Bellocchio A, Guido V, Priore Oliva C, Calandra S, Bertolini S.
    Clin Chim Acta; 2011 Nov 20; 412(23-24):2194-8. PubMed ID: 21846464
    [Abstract] [Full Text] [Related]

  • 14. Functional importance of apolipoprotein A5 185G in the activation of lipoprotein lipase.
    Huang YJ, Lin YL, Chiang CI, Yen CT, Lin SW, Kao JT.
    Clin Chim Acta; 2012 Jan 18; 413(1-2):246-50. PubMed ID: 22008704
    [Abstract] [Full Text] [Related]

  • 15. Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.
    Surendran RP, Visser ME, Heemelaar S, Wang J, Peter J, Defesche JC, Kuivenhoven JA, Hosseini M, Péterfy M, Kastelein JJ, Johansen CT, Hegele RA, Stroes ES, Dallinga-Thie GM.
    J Intern Med; 2012 Aug 18; 272(2):185-96. PubMed ID: 22239554
    [Abstract] [Full Text] [Related]

  • 16. Resequencing the apolipoprotein A5 (APOA5) gene in patients with various forms of hypertriglyceridemia.
    Evans D, Aberle J, Beil FU.
    Atherosclerosis; 2011 Dec 18; 219(2):715-20. PubMed ID: 21993410
    [Abstract] [Full Text] [Related]

  • 17. Clinical features and genetic analysis of three patients with severe hypertriglyceridaemia.
    Hooper AJ, Kurtkoti J, Hamilton-Craig I, Burnett JR.
    Ann Clin Biochem; 2014 Jul 18; 51(Pt 4):485-9. PubMed ID: 24591733
    [Abstract] [Full Text] [Related]

  • 18. Is apolipoprotein A5 a novel regulator of triglyceride-rich lipoproteins?
    Jakel H, Nowak M, Helleboid-Chapman A, Fruchart-Najib J, Fruchart JC.
    Ann Med; 2006 Jul 18; 38(1):2-10. PubMed ID: 16448983
    [Abstract] [Full Text] [Related]

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  • 20. Rare APOA5 mutations--clinical consequences, metabolic and functional effects: an ENID review.
    Talmud PJ.
    Atherosclerosis; 2007 Oct 18; 194(2):287-92. PubMed ID: 17222847
    [Abstract] [Full Text] [Related]

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