BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 27206937)

  • 1. 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; 10(3):505-511.e1. PubMed ID: 27206937
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 11(6):1329-1337.e3. PubMed ID: 28951076
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain.
    Lamiquiz-Moneo I; Blanco-Torrecilla C; Bea AM; Mateo-Gallego R; Pérez-Calahorra S; Baila-Rueda L; Cenarro A; Civeira F; de Castro-Orós I
    Lipids Health Dis; 2016 Apr; 15():82. PubMed ID: 27108409
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 429():61-8. PubMed ID: 24291057
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 10(6):e0129488. PubMed ID: 26079787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 272(2):185-96. PubMed ID: 22239554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 412(23-24):2194-8. PubMed ID: 21846464
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Compound but non-linked heterozygous p.W14X and p.L279 V LPL gene mutations in a Chinese patient with long-term severe hypertriglyceridemia and recurrent acute pancreatitis.
    Li X; Yang Q; Shi X; Chen W; Pu N; Li W; Li J
    Lipids Health Dis; 2018 Jun; 17(1):144. PubMed ID: 29921298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Additive effects of LPL, APOA5 and APOE variant combinations on triglyceride levels and hypertriglyceridemia: results of the ICARIA genetic sub-study.
    Ariza MJ; Sánchez-Chaparro MA; Barón FJ; Hornos AM; Calvo-Bonacho E; Rioja J; Valdivielso P; Gelpi JA; González-Santos P
    BMC Med Genet; 2010 Apr; 11():66. PubMed ID: 20429872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 28(10):1866-71. PubMed ID: 18635818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and functional characterization of a novel heterozygous missense variant in the LPL associated with recurrent hypertriglyceridemia-induced acute pancreatitis in pregnancy.
    Shi XL; Yang Q; Pu N; Li XY; Chen WW; Zhou J; Li G; Tong ZH; Férec C; Cooper DN; Chen JM; Li WQ
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1048. PubMed ID: 31962008
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A promoter variant of the APOA5 gene increases atherogenic LDL levels and arterial stiffness in hypertriglyceridemic patients.
    Kim M; Kim M; Yoo HJ; Lee E; Chae JS; Lee SH; Lee JH
    PLoS One; 2017; 12(12):e0186693. PubMed ID: 29211729
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extreme hypertriglyceridemia: Genetic diversity, pancreatitis, pregnancy, and prevalence.
    Chyzhyk V; Kozmic S; Brown AS; Hudgins LC; Starc TJ; Davila AD; Blevins TC; Diffenderfer MR; He L; Geller AS; Rush C; Hegele RA; Schaefer EJ
    J Clin Lipidol; 2019; 13(1):89-99. PubMed ID: 30352774
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypertriglyceridemic acute pancreatitis in emergency department: Typical clinical features and genetic variants.
    Chen WJ; Sun XF; Zhang RX; Xu MJ; Dou TH; Zhang XB; Zhong M; Yang WQ; Liu L; Lu XY; Zhu CQ
    J Dig Dis; 2017 Jun; 18(6):359-368. PubMed ID: 28548292
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Clinical Case of a Homozygous Deletion in the
    Vasiluev PA; Ivanova ON; Semenova NA; Strokova TV; Taran NN; Chubykina UV; Ezhov MV; Zakharova EY; Dadli EL; Kutsev SI
    Genes (Basel); 2022 Jun; 13(6):. PubMed ID: 35741823
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE.
    Abedi AH; Yıldırım Şimşir I; Bayram F; Onay H; Özgür S; Mcintyre AD; Toth PP; Hegele RA
    Turk Kardiyol Dern Ars; 2023 Jan; 51(1):10-21. PubMed ID: 36689289
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Significant but partial lipoprotein lipase functional loss caused by a novel occurrence of rare LPL biallelic variants.
    Hu Y; Chen JM; Zuo H; Pu N; Zhang G; Duan Y; Li G; Tong Z; Li W; Li B; Yang Q
    Lipids Health Dis; 2024 Apr; 23(1):92. PubMed ID: 38561841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The East Asian-specific LPL p.Ala288Thr (c.862G > A) missense variant exerts a mild effect on protein function.
    Hu Y; Zhang G; Yang Q; Pu N; Li K; Li B; Cooper DN; Tong Z; Li W; Chen JM
    Lipids Health Dis; 2023 Aug; 22(1):119. PubMed ID: 37550668
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variation in apolipoprotein A-V in hypertriglyceridemia.
    Perera SD; Hegele RA
    Curr Opin Lipidol; 2024 Apr; 35(2):66-77. PubMed ID: 38117614
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.