BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 21875686)

  • 1. Increased risk of coronary artery disease in Caucasians with extremely low HDL cholesterol due to mutations in ABCA1, APOA1, and LCAT.
    Tietjen I; Hovingh GK; Singaraja R; Radomski C; McEwen J; Chan E; Mattice M; Legendre A; Kastelein JJ; Hayden MR
    Biochim Biophys Acta; 2012 Mar; 1821(3):416-24. PubMed ID: 21875686
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism.
    Abd El-Aziz TA; Mohamed RH; Hagrass HA
    J Clin Lipidol; 2014; 8(4):381-9. PubMed ID: 25110219
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans.
    Singaraja RR; Tietjen I; Hovingh GK; Franchini PL; Radomski C; Wong K; vanHeek M; Stylianou IM; Lin L; Wang L; Mitnaul L; Hubbard B; Winther M; Mattice M; Legendre A; Sherrington R; Kastelein JJ; Akinsanya K; Plump A; Hayden MR
    J Lipid Res; 2014 Aug; 55(8):1693-701. PubMed ID: 24891332
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol.
    Tietjen I; Hovingh GK; Singaraja RR; Radomski C; Barhdadi A; McEwen J; Chan E; Mattice M; Legendre A; Franchini PL; Dubé MP; Kastelein JJ; Hayden MR
    PLoS One; 2012; 7(8):e37437. PubMed ID: 22952570
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of antioxidant/anti-inflammatory properties and apoA-I-containing subpopulations of HDL from family subjects with monogenic low HDL disorders.
    Daniil G; Phedonos AA; Holleboom AG; Motazacker MM; Argyri L; Kuivenhoven JA; Chroni A
    Clin Chim Acta; 2011 Jun; 412(13-14):1213-20. PubMed ID: 21420943
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited disorders of HDL metabolism and atherosclerosis.
    Hovingh GK; de Groot E; van der Steeg W; Boekholdt SM; Hutten BA; Kuivenhoven JA; Kastelein JJ
    Curr Opin Lipidol; 2005 Apr; 16(2):139-45. PubMed ID: 15767853
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Plasma levels of 27-hydroxycholesterol in humans and mice with monogenic disturbances of high density lipoprotein metabolism.
    Karuna R; Holleboom AG; Motazacker MM; Kuivenhoven JA; Frikke-Schmidt R; Tybjaerg-Hansen A; Georgopoulos S; van Eck M; van Berkel TJ; von Eckardstein A; Rentsch KM
    Atherosclerosis; 2011 Feb; 214(2):448-55. PubMed ID: 21130455
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increased prevalence of clinical and subclinical atherosclerosis in patients with damaging mutations in ABCA1 or APOA1.
    Abdel-Razek O; Sadananda SN; Li X; Cermakova L; Frohlich J; Brunham LR
    J Clin Lipidol; 2018; 12(1):116-121. PubMed ID: 29150341
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
    Conca P; Pileggi S; Simonelli S; Boer E; Boscutti G; Magnolo L; Tarugi P; Penco S; Franceschini G; Calabresi L; Gomaraschi M
    J Clin Lipidol; 2012; 6(3):244-50. PubMed ID: 22658148
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple rare alleles contribute to low plasma levels of HDL cholesterol.
    Cohen JC; Kiss RS; Pertsemlidis A; Marcel YL; McPherson R; Hobbs HH
    Science; 2004 Aug; 305(5685):869-72. PubMed ID: 15297675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism.
    Karuna R; Park R; Othman A; Holleboom AG; Motazacker MM; Sutter I; Kuivenhoven JA; Rohrer L; Matile H; Hornemann T; Stoffel M; Rentsch KM; von Eckardstein A
    Atherosclerosis; 2011 Dec; 219(2):855-63. PubMed ID: 21944699
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Premature atherosclerosis, extremely low HDL-cholesterol and concurrent defects in APOA1 and ABCA1 genes: a family case report.
    Koopal C; Visseren FL; Kastelein JJ; Westerink J
    Int J Cardiol; 2014 Nov; 177(1):e19-21. PubMed ID: 25127959
    [No Abstract]   [Full Text] [Related]  

  • 13. Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations.
    Mott S; Yu L; Marcil M; Boucher B; Rondeau C; Genest J
    Atherosclerosis; 2000 Oct; 152(2):457-68. PubMed ID: 10998475
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in APOA-I and ABCA1 in Norwegians with low levels of HDL cholesterol.
    Berge KE; Leren TP
    Clin Chim Acta; 2010 Dec; 411(23-24):2019-23. PubMed ID: 20800056
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.
    Holleboom AG; Daniil G; Fu X; Zhang R; Hovingh GK; Schimmel AW; Kastelein JJ; Stroes ES; Witztum JL; Hutten BA; Tsimikas S; Hazen SL; Chroni A; Kuivenhoven JA
    Arterioscler Thromb Vasc Biol; 2012 Dec; 32(12):3066-75. PubMed ID: 23023370
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels.
    Trigueros-Motos L; van Capelleveen JC; Torta F; Castaño D; Zhang LH; Chai EC; Kang M; Dimova LG; Schimmel AWM; Tietjen I; Radomski C; Tan LJ; Thiam CH; Narayanaswamy P; Wu DH; Dorninger F; Yakala GK; Barhdadi A; Angeli V; Dubé MP; Berger J; Dallinga-Thie GM; Tietge UJF; Wenk MR; Hayden MR; Hovingh GK; Singaraja RR
    Arterioscler Thromb Vasc Biol; 2017 Nov; 37(11):2147-2155. PubMed ID: 28882873
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional LCAT is not required for macrophage cholesterol efflux to human serum.
    Calabresi L; Favari E; Moleri E; Adorni MP; Pedrelli M; Costa S; Jessup W; Gelissen IC; Kovanen PT; Bernini F; Franceschini G
    Atherosclerosis; 2009 May; 204(1):141-6. PubMed ID: 18922527
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.
    Clee SM; Kastelein JJ; van Dam M; Marcil M; Roomp K; Zwarts KY; Collins JA; Roelants R; Tamasawa N; Stulc T; Suda T; Ceska R; Boucher B; Rondeau C; DeSouich C; Brooks-Wilson A; Molhuizen HO; Frohlich J; Genest J; Hayden MR
    J Clin Invest; 2000 Nov; 106(10):1263-70. PubMed ID: 11086027
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High density lipoprotein as a source of cholesterol for adrenal steroidogenesis: a study in individuals with low plasma HDL-C.
    Bochem AE; Holleboom AG; Romijn JA; Hoekstra M; Dallinga-Thie GM; Motazacker MM; Hovingh GK; Kuivenhoven JA; Stroes ESG
    J Lipid Res; 2013 Jun; 54(6):1698-1704. PubMed ID: 23511897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.
    Tobar HE; Cataldo LR; González T; Rodríguez R; Serrano V; Arteaga A; Álvarez-Mercado A; Lagos CF; Vicuña L; Miranda JP; Pereira A; Bravo C; Aguilera CM; Eyheramendy S; Uauy R; Martínez Á; Gil Á; Francone O; Rigotti A; Santos JL
    Lipids Health Dis; 2019 Jun; 18(1):132. PubMed ID: 31164121
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.