These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 27403930)

  • 1. Type 1 Hyperlipoproteinemia Due to Compound Heterozygous Rare Variants in GCKR.
    Shetty S; Xing C; Garg A
    J Clin Endocrinol Metab; 2016 Nov; 101(11):3884-3887. PubMed ID: 27403930
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. A case of severe acquired hypertriglyceridemia in a 7-year-old girl.
    Lilley JS; Linton MF; Kelley JC; Graham TB; Fazio S; Tavori H
    J Clin Lipidol; 2017; 11(6):1480-1484. PubMed ID: 28916403
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia.
    Caddeo A; Mancina RM; Pirazzi C; Russo C; Sasidharan K; Sandstedt J; Maurotti S; Montalcini T; Pujia A; Leren TP; Romeo S; Pingitore P
    Nutr Metab Cardiovasc Dis; 2018 Feb; 28(2):158-164. PubMed ID: 29288010
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Type 1 hyperlipoproteinemia in a child with large homozygous deletion encompassing GPIHBP1.
    Patni N; Brothers J; Xing C; Garg A
    J Clin Lipidol; 2016; 10(4):1035-1039.e2. PubMed ID: 27578137
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Targeted sequencing of candidate genes of dyslipidemia in Punjabi Sikhs: Population-specific rare variants in GCKR promote ectopic fat deposition.
    Sanghera DK; Hopkins R; Malone-Perez MW; Bejar C; Tan C; Mussa H; Whitby P; Fowler B; Rao CV; Fung KA; Lightfoot S; Frazer JK
    PLoS One; 2019; 14(8):e0211661. PubMed ID: 31369557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Type 1 hyperlipoproteinemia due to a novel deletion of exons 3 and 4 in the GPIHBP1 gene.
    Berge KE; Retterstøl K; Romeo S; Pirazzi C; Leren TP
    Atherosclerosis; 2014 May; 234(1):30-3. PubMed ID: 24589565
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.
    Rabacchi C; Pisciotta L; Cefalù AB; Noto D; Fresa R; Tarugi P; Averna M; Bertolini S; Calandra S
    Atherosclerosis; 2015 Jul; 241(1):79-86. PubMed ID: 25966443
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis.
    Jin JL; Sun D; Cao YX; Zhang HW; Guo YL; Wu NQ; Zhu CG; Gao Y; Dong QT; Liu G; Dong Q; Li JJ
    EBioMedicine; 2018 Dec; 38():171-177. PubMed ID: 30420299
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Type 1 hyperlipoproteinemia and recurrent acute pancreatitis due to lipoprotein lipase antibody in a young girl with Sjogren's syndrome.
    Ashraf AP; Beukelman T; Pruneta-Deloche V; Kelly DR; Garg A
    J Clin Endocrinol Metab; 2011 Nov; 96(11):3302-7. PubMed ID: 21880794
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New rare genetic variants of LMF1 gene identified in severe hypertriglyceridemia.
    Serveaux Dancer M; Di Filippo M; Marmontel O; Valéro R; Piombo Rivarola MDC; Peretti N; Caussy C; Krempf M; Vergès B; Mahl M; Marçais C; Moulin P; Charrière S
    J Clin Lipidol; 2018; 12(5):1244-1252. PubMed ID: 30037590
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants.
    Kassner U; Salewsky B; Wühle-Demuth M; Szijarto IA; Grenkowitz T; Binner P; März W; Steinhagen-Thiessen E; Demuth I
    Eur J Hum Genet; 2015 Sep; 23(9):1259-61. PubMed ID: 25585702
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variants of Lipid-Related Genes in Adult Japanese Patients with Severe Hypertriglyceridemia.
    Matsunaga A; Nagashima M; Yamagishi H; Saku K
    J Atheroscler Thromb; 2020 Dec; 27(12):1264-1277. PubMed ID: 32115487
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes.
    Rees MG; Ng D; Ruppert S; Turner C; Beer NL; Swift AJ; Morken MA; Below JE; Blech I; ; Mullikin JC; McCarthy MI; Biesecker LG; Gloyn AL; Collins FS
    J Clin Invest; 2012 Jan; 122(1):205-17. PubMed ID: 22182842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency.
    Rodríguez-Gutiérrez PG; Colima-Fausto AG; Zepeda-Olmos PM; Hernández-Flores TJ; González-García JR; Magaña-Torres MT
    Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36613909
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early gene-diet interaction between glucokinase regulatory protein (GCKR) polymorphism, vegetable and fish intakes in modulating triglyceride levels in healthy adolescents.
    Tam CH; Wang Y; Lee HM; Luk AO; Tong PC; Chan MH; Ozaki R; Kong AP; So WY; Chan JC; Ma RC
    Nutr Metab Cardiovasc Dis; 2015 Oct; 25(10):951-8. PubMed ID: 26234566
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic bases of hypertriglyceridemic phenotypes.
    Johansen CT; Hegele RA
    Curr Opin Lipidol; 2011 Aug; 22(4):247-53. PubMed ID: 21519249
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.