903 results on '"Humphries, S. E."'
Search Results
2. MED-PED: An Integrated Genetic Strategy for Preventing Early Deaths
3. Family History Of Breast Cancer And Cost Of Life Assurance: A Test Case Comparison Of Current Uk Industry Practice
4. Effect of statin treatment for familial hypercholesterolaemia on life assurance: results of consecutive surveys in 1990 and 2002
5. The use of gene probes to investigate the aetiology of arterial diseases
6. Extent Of Underdiagnosis Of Familial Hypercholesterolaemia In Routine Practice: Prospective Registry Study
7. Telomere shortening over 6 years is associated with increased subclinical carotid vascular damage and worse cardiovascular prognosis in the general population
8. Effects of genetic variation on chromatin structure and the transcriptional machinery: analysis of the IL6 gene locus
9. Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies
10. Interleukin-18 genetics and inflammatory disease susceptibility
11. Analysis of the genetic variants associated with circulating levels of sgp130. Results from the IMPROVE study
12. Alcohol consumption in relation to carotid subclinical atherosclerosis and its progression: results from a European longitudinal multicentre study
13. The apolipoprotein A-V genotype and plasma apolipoprotein A-V and triglyceride levels: prospective risk of type 2 diabetes. Results from the Northwick Park Heart Study II
14. APOE polymorphism, socioeconomic status and cognitive function in mid-life: The Whitehall II longitudinal study
15. Novel IL-6 haplotypes and disease association
16. IL-6–174G/C genotype is associated with the bone mineral density response to oestrogen replacement therapy in post-menopausal women
17. High-density lipoprotein cholesterol and abdominal aortic aneurysm -a mendelian randomisation study: O136
18. Variable effects of the APOC3 –482C > T variant on insulin, glucose and triglyceride concentrations in different ethnic groups
19. Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects
20. Review article: pancreatic renin–angiotensin systems in health and disease
21. Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies
22. Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men
23. GENDER-DEPENDENT RISK ASSOCIATIONS OF UCP2,UCP3 AND USF1 GENES FOR CORONARY HEART DISEASE RISK FACTORS: I23
24. Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project
25. P728Subclinical atherosclerosis and its progression are modulated by perilipin-2 through a feed-forward loop between LXR and autophagy
26. Association between the rs1050450 glutathione peroxidise-1 (C>T) gene variant and peripheral neuropathy in two independent samples of subjects with diabetes: A74 (P61)
27. Association between the rs4880 superoxide dismutase 2 (C>T) gene variant with coronary heart disease in diabetes: A73 (P56)
28. Mutation screening in patients for familial hypercholesterolaemia (ADH)
29. Gene–environment interaction in coronary artery disease: apolipoprotein E and smoking and the interleukin-6 gene and inflammation as examples
30. Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia
31. Controversies in familial hypercholesterolaemia: recommendations of the NICE Guideline Development Group for the identification and management of familial hypercholesterolaemia
32. Association between periodontitis and common variants in the promoter of the interleukin-6 gene
33. Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutations
34. Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database
35. Identification of a novel regulatory region in the interleukin-6 gene promoter
36. Relationship between markers of activated coagulation, their correlation with inflammation, and association with coronary heart disease (NPHSII)
37. INSIG2 gene polymorphism is not associated with obesity in Caucasian, Afro-Caribbean and Indian subjects
38. The use of Meta-Analysis Risk Estimates for Candidate Genes in Combination to Predict Coronary Heart Disease Risk
39. Common Adiponectin Gene Variants Show Different Effects on Risk of Cardiovascular Disease and Type 2 Diabetes in European Subjects
40. Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia
41. Cognitive outcome and cyclo-oxygenase-2 gene (−765 G/C) variation in the preterm infant
42. Polymorphisms in the Angiotensin Converting Enzyme Gene and Growth in the First Year of Life
43. European differences in the association between the UCP2 −866G > A common gene variant and markers of body mass and fasting plasma insulin
44. Increase of Plasma Fibrinogen Levels and Variability with Age in a Sample of Middle Aged Healthy Men
45. The Impact of ACE Genotype on Serum ACE Activity in a Black South African Male Population
46. Nat Commun
47. Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
48. Left ventricular growth response to exercise and cigarette smoking: data from LARGE Heart
49. The interleukin-6 gene –174G>C and –572G>C promoter polymorphisms are related to cerebral aneurysms
50. Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: report of the thirty-person/ten-country panel
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.