Found: 21
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Gender-modulated impact of apolipoprotein A5 gene ( APOA5) −1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 6, p. 778, doi. 10.1515/CCLM.2008.161
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- Article
Association of TLL1 Gene Polymorphism (rs1503298, T > C) with Coronary Heart Disease in PREDICT, UDACS and ED Cohorts.
- Published in:
- Journal of the College of Physicians & Surgeons Pakistan, 2014, v. 24, n. 9, p. 615
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- Publication type:
- Article
A common single-nucleotide variant in T is strongly associated with chordoma.
- Published in:
- Nature Genetics, 2012, v. 44, n. 11, p. 1185, doi. 10.1038/ng.2419
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- Publication type:
- Article
Demonstration of the Presence of the “Deleted” MIR122 Gene in HepG2 Cells.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122471
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- Article
Association of <i>TERC</i> and <i>OBFC1</i> Haplotypes with Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083122
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- Publication type:
- Article
Functional Analysis of Two PLA2G2A Variants Associated with Secretory Phospholipase A2-IIA Levels.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041139
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- Publication type:
- Article
Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and women.
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- Journal of Molecular Medicine, 2006, v. 84, n. 12, p. 1005, doi. 10.1007/s00109-006-0108-7
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- Publication type:
- Article
Functional analysis of four LDLR 5′UTR and promoter variants in patients with familial hypercholesterolaemia.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 790, doi. 10.1038/ejhg.2014.199
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- Publication type:
- Article
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.
- Published in:
- European Heart Journal, 2012, v. 33, n. 3, p. 393, doi. 10.1093/eurheartj/ehr225
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- Publication type:
- Article
Variation in bradykinin receptor genes increases the cardiovascular risk associated with hypertension.
- Published in:
- European Heart Journal, 2003, v. 24, n. 18, p. 1672, doi. 10.1016/S0195-668X(03)00441-X
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- Publication type:
- Article
Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 4, p. 456, doi. 10.1111/j.1469-1809.2011.00654.x
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- Publication type:
- Article
A genome-wide association study identifies multiple loci for variation in human ear morphology.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7500, doi. 10.1038/ncomms8500
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- Article
Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.
- Published in:
- Disease Markers, 2017, p. 1, doi. 10.1155/2017/1096916
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- Publication type:
- Article
Novel Insights Into the Effects of Interleukin 6 Antagonism in Non-ST-Segment-Elevation Myocardial Infarction Employing the SOMAscan Proteomics Platform.
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- 2020
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- Publication type:
- journal article
Identification of the Functional Variant(s) that Explain the Low-Density Lipoprotein Receptor (LDLR) GWAS SNP rs6511720 Association with Lower LDL-C and Risk of CHD.
- Published in:
- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167676
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- Publication type:
- Article
Use of Allele-Specific FAIRE to Determine Functional Regulatory Polymorphism Using Large-Scale Genotyping Arrays.
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- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002908
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- Publication type:
- Article
Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 20, p. 3936, doi. 10.1093/hmg/ddq308
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- Publication type:
- Article
Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2305, doi. 10.1093/hmg/ddp159
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- Publication type:
- Article
Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
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- Human Molecular Genetics, 2004, v. 13, n. 15, p. 1587, doi. 10.1093/hmg/ddh168
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- Publication type:
- Article
Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies.
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- European Heart Journal, 2013, v. 34, n. 13, p. 972, doi. 10.1093/eurheartj/ehs243
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- Publication type:
- Article
Familial lipoprotein lipase (LPL) deficiency: A catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy.
- Published in:
- Human Mutation, 1997, v. 10, n. 6, p. 465, doi. 10.1002/(SICI)1098-1004(1997)10:6<465::AID-HUMU8>3.0.CO;2-C
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- Publication type:
- Article