51 results on '"Humphries, S.E."'
Search Results
2. Lp-PLA2 activity and PLA2G7 A379V genotype in patients with diabetes mellitus
3. Adiponectin and its gene variants as risk factors for insulin resistance, the metabolic syndrome and cardiovascular disease
4. EPCR Ser219Gly: Elevated sEPCR, prothrombin F1+2, risk for coronary heart disease, and increased sEPCR shedding in vitro
5. Interaction between the C-260T polymorphism of the CD14 gene and the plasma IL-6 concentration on the risk of myocardial infarction: the HIFMECH study
6. Non-coronary heart disease mortality and risk of fatal cancer in patients with treated heterozygous familial hypercholesterolaemia: a prospective registry study
7. The −629C>A polymorphism in the CETP gene does not explain the association of TaqIB polymorphism with risk and age of myocardial infarction in Icelandic men
8. The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study
9. Effect of apo E phenotype on plasma postprandial triglyceride levels in young male adults with and without a familial history of myocardial infarction: the EARS II study
10. A novel common variant −181 G insertion in the promoter of the gene for phospholipid transfer protein
11. MS443 THE ARG399GLN VARIANT IN THE DNA REPAIR ENZYME XRCC1 IS ASSOCIATED WITH INCREASED GENETIC INSTABILITY IN PATIENTS WITH ATHEROSCLEROSIS
12. MS194 THE INFLUENCE OF APOLIPOPROTEIN E GENETIC VARIANTS ON SERUM LIPIDS AND INSULIN RESISTANCE IN TARF STUDY
13. P156 PLA2G2A, PLA2G5 AND PLA2G10 VARIANTS, SPLA2 ACTIVITY AND MASS AND CHD RISK: RESULTS FROM GRACE AND EPIC-NORFOLK
14. P84 THE UCL LDLR, PCSK9 & LDLRAP1 VARIANT DATABASES: UPDATE, ANALYSIS & OVERVIEW OF THREE PUBLICLY AVAILABLE FAMILIAL HYPERCHOLESTEROLEMIA GENE DATABASES
15. P69 RAPID AND ACCURATE GENETIC DIAGNOSIS BY LIPOCHIP® IN UK FH PATIENTS
16. W56 TELOMERES ARE SHORTER IN PATIENTS WITH POLYGENIC AND MONOGENIC FORMS OF CORONARY HEART DISEASE
17. IS FH CASCADE TESTING FEASIBLE AND COST-EFFECTIVE IN THE UK?
18. DEVELOPMENT OF AN AFFORDABLE, SENSITIVE AND RAPID SCREENING METHOD FOR MUTATION DETECTION IN UK FH SUBJECTS
19. ASSOCIATION OF LP-PLA2 ACTIVITY AND PAF-AH ALA379VAL GENOTYPE AND EARLY ATHEROSCLEROSIS. RESULTS FROM THE CYPRUS STUDY
20. UPDATE AND ANALYSIS OF THE UCL LOW DENSITY LIPOPROTEIN RECEPTOR GENE (LDLR) FAMILIAL HYPERCHOLESTEROLEMIA (FH) DATABASE
21. CRITICAL APPRAISAL OF THE UTILITY OF CRP MEASUREMENT IN THE PREDICTION OF CARDIOVASCULAR EVENTS
22. ANGPTL4 VARIANTS ARE ASSOCIATED WITH LOWER PLASMA TRIGLYCERIDE LEVELS AND IMPROVED POSTPRANDIAL RESPONSES
23. What training and education is required to implement cascade testing for FH?
24. Update and analysis of the UCL low density lipoprotein receptor gene familial hypercholesterolemia database
25. Significant factors in implementing cascade testing for familial hypercholesterolaemia
26. We-W45:6 Apolipoprotein AV, triglycerides and risk of future coronary artery disease in apparently healthy men and women; the EPIC-Norfolk population study
27. We-W35:3 A variant in the thrombomodulin promoter leads to impaired expression in response to inflammatory cytokines; previous CHD-risk association explained
28. We-W35:2 Inherited and acquired risk factors for juvenile myocardial infarction in an European cohort
29. We-W33:5 An interleukin-18 (IL-18) haplotype is associated with higher BMI and inflammatory markers in subjects with diabetes and coronary heart disease
30. We-PL3:3 Can candidate gene genotypes improve estimation of CHD risk over-and above conventional risk factors in healthy UK men?
31. Mo-P6:451 Single-strand conformation polymorphisms for the mutation scanning of proprotein convertase subtilisin Kexin 9 in familial hypercholesterolaemia
32. Mo-P6:420 Two novel APOA5 missense mutations in patients with severe hypertriglyceridemia
33. Mo-P6:389 Ace insertion/deletion polymorphism interaction associated with regional incidence of myocardial infarction (MI) in Europe
34. W14-P-004 A thrombomodulin haplotype (V/DELTT),associated with risk of coronary heart disease, does not influence plasma levels of soluble thrombomodulin
35. W14-O-001 EPCR genotype 6936A>G (SER219GLY): Reduced apc generation in GLY homozygotes with type 2 diabetes
36. W06-IS-001 Resolution of the functionality of APOA5 common variants
37. W05-IS-001 Pharmacogenetics: Progress, pitfalls and clinical potential
38. W01-O-001 Gene expression in atherosclerotic plaques categorised by their echodensity
39. W14.345 Mutation scanning of LDLR in the whole population
40. 3WS17-6 Genetic risk factors for stroke: Insights into patho-physiology from candidate gene approaches
41. 1FS04-3 Genetic determinants of plasma triglycerides and CHD risk
42. Increased PAI activity and PAI-1 antigen occurring with an oral fat load: associations with PAI-1 genotype and plasma active TGF- β levels
43. The association between free fatty acid concentrations and triglyceride-rich lipoproteins in the post-prandial state is altered by a common deletion polymorphism of the apo B signal peptide
44. Association between the LPL-D9N mutation in the lipoprotein lipase gene and plasma lipid traits in myocardial infarction survivors from the ECTIM study
45. Gene-environment interactions determining the risk of thrombosis
46. Interaction between genotype and environmental factors in the development of atherosclerotic-thrombotic disease
47. Effect on plasma lipid levels of different classes of mutations in the LDL receptor gene in patients with familial hypercholesterolemia (FH)
48. Angiotensin converting enzyme (ACE) gene polymorphism and the course of angiographically defined coronary artery disease
49. Effect of acetyl-LDL on monocyte/macrophage expression of matrix metalloproteinases
50. Common variation in genes coding for apolipoproteins B and C-III and lipoprotein lipase modulates postprandial lipoprotein metabolism: a pilot study
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