590 results on '"Humphries, S.E."'
Search Results
152. W56 TELOMERES ARE SHORTER IN PATIENTS WITH POLYGENIC AND MONOGENIC FORMS OF CORONARY HEART DISEASE
153. P84 THE UCL LDLR, PCSK9 & LDLRAP1 VARIANT DATABASES: UPDATE, ANALYSIS & OVERVIEW OF THREE PUBLICLY AVAILABLE FAMILIAL HYPERCHOLESTEROLEMIA GENE DATABASES
154. APOE, CETP and LPL genes show strong association with lipid levels in Greek children
155. A proposal to redefine familial combined hyperlipidaemia -- third workshop on FCHL held in Barcelona from 3 to 5 May 2001, during the scientific sessions of the European Society for Clinical Investigation.
156. Cost-effectiveness analysis of the use of a high-intensity statin compared to a low-intensity statin in the management of patients with familial hypercholesterolaemia
157. ANGPTL3 VARIATION IN TYPE 2 DIABETES
158. ALL-CAUSE AND CARDIOVASCULAR MORTALITY IN TREATED PATIENTS WITH SEVERE HYPERTRIGLYCERIDAEMIA: A LONG-TERM PROSPECTIVE REGISTRY STUDY
159. IDENTIFICATION OF GENES ASSOCIATED WITH QT INTERVAL USING THE 50K CARDIO-METABOLIC SNP CHIP: RESULTS FROM THE WHITEHALL II STUDY
160. ASSOCIATION OF TELOMERE LENGTH WITH TYPE 2 DIABETES, OXIDATIVE STRESS AND UCP2 GENE VARIATION
161. PRO-PROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE9 (PCSK9) VARIANT DATABASE: PRELIMINARY ANALYSIS
162. DOWN-REGULATION OF ACE EXPRESSION IN HUVECS USING siRNA RESULTS IN DOWN-REGULATION OF UCP2 EXPRESSION: A POTENTIAL MECHANISM OF THE CLINICAL BENEFIT OF ACE-INHIBITORS?
163. EXPLORING THE GENETIC ARCHITECTURE OF LIPID TRAITS IN WHITEHALL II HEALTHY MEN AND WOMEN USING THE 50K-SNP CARDIO-METABOLIC CHIP
164. FUNCTIONAL ANALYSIS OF REGULATORY LPL SNPS
165. THE COMMON FUNCTIONAL ARG399GLN VARIANT IN THE DNA REPAIR ENZYME XRCC1 IS ASSOCIATED WITH ELEVATED LEVELS OF MICRONUCLEUS CHROMOSOMAL DNA DAMAGE AND SHORTER TELOMERE LENGTH IN PATIENT WITH ATHEROSCLEROSIS
166. LRP5 VARIANTS ARE ASSOCIATED WITH TRIGLYCERIDE LEVELS AND TYPE 2 DIABETES
167. ANGPTL4 E40K AND T266M: EFFECTS ON PLASMA TRIGLYCERIDE AND HDL LEVELS, ANGPTL4 LEVELS AND CHD RISK
168. GENOTYPES AT MATRIX METALLOPROTINASE (MMP) LOCI FOR MMP7, MMP9 AND MMP12 ARE ASSOCIATED WITH CAROTID IMT AND PRESENCE OF PLAQUES
169. PLASMA PCSK9 LEVELS ARE LOW IN HEALTHY SUBJECTS CARRYING THE PCSK9 P.R46L VARIANT AND IN P.D374Y FAMILIAL HYPERCHOLESTEROL-EMIA PATIENTS
170. Effects of Six APOA5 Variants, Identified in Patients With Severe Hypertriglyceridemia, on In Vitro Lipoprotein Lipase Activity and Receptor Binding
171. Mutation detection rate and spectrum in definite (DFH) and possible (PFH) patients from the department of health (DH) pilot project
172. IS FH CASCADE TESTING FEASIBLE AND COST-EFFECTIVE IN THE UK?
173. ASSOCIATION OF LP-PLA2 ACTIVITY AND PAF-AH ALA379VAL GENOTYPE AND EARLY ATHEROSCLEROSIS. RESULTS FROM THE CYPRUS STUDY
174. DEVELOPMENT OF AN AFFORDABLE, SENSITIVE AND RAPID SCREENING METHOD FOR MUTATION DETECTION IN UK FH SUBJECTS
175. UPDATE AND ANALYSIS OF THE UCL LOW DENSITY LIPOPROTEIN RECEPTOR GENE (LDLR) FAMILIAL HYPERCHOLESTEROLEMIA (FH) DATABASE
176. ANGPTL4 VARIANTS ARE ASSOCIATED WITH LOWER PLASMA TRIGLYCERIDE LEVELS AND IMPROVED POSTPRANDIAL RESPONSES
177. CRITICAL APPRAISAL OF THE UTILITY OF CRP MEASUREMENT IN THE PREDICTION OF CARDIOVASCULAR EVENTS
178. Candidate Gene Association Studies in Abdominal Aortic Aneurysm Disease: A Review and Meta-Analysis
179. Association of Plasminogen Activator Inhibitor (PAI)-1 (SERPINE1) SNPs With Myocardial Infarction, Plasma PAI-1, and Metabolic Parameters
180. What training and education is required to implement cascade testing for FH?
181. Update and analysis of the UCL low density lipoprotein receptor gene familial hypercholesterolemia database
182. Significant factors in implementing cascade testing for familial hypercholesterolaemia
183. PAI-1 GENE HAPLOTYPES ARE ASSOCIATED WITH MYOCARDIAL INFARCTION OCCURRENCE IN NON SMOKERS: THE HIFMECH STUDY
184. PO2-52 AMINO ACIDS 140–148 OF APOAV PLAY A CRUCIAL ROLE IN LPL ACTIVATION
185. PO3-83 THE EFFECT OF APOA5 AND APOC3 VARIANTS ON LIPID PARAMETERS IN EUROPEAN WHITES, INDIAN ASIANS AND AFRO-CARIBBEANS WITH TYPE 2 DIABETES
186. WO12-OR-5 THE EFFECT OF THE WNT5B IVS3C>G VARIATION ON THE SUSCEPTIBILITY TO TYPE 2 DIABETES IN UK CAUCASIAN SUBJECTS
187. PO5-127 THE R46L VARIANT IN THE PCSK9 GENE IS ASSOCIATED WITH PLASMA LIPID LEVELS AND LOWER CARDIOVASCULAR RISK IN UK MEN
188. PO11-309 ARTERIAL WALL REMODELLING AND THE RAS. IMPLICATED IN AAA DISEASE
189. PO5-142 VARIATION WITHIN IL18 BUT NOT IL18BP INFLUENCES FREE IL-18 LEVELS AT BASELINE AND DURING POST-OPERATIVE STRESS
190. PO5-140 THE UCP3-55C/T POLYMORPHISM EFFECTS BLOOD PRESSURE LEVELS IN THE TURKISH ADULT RISK FACTOR (TARF) STUDY
191. PO5-139 GENES AND HDL-C ASSOCIATION IN THE ADULT TURKISH POPULATION
192. WO7-OR-5 FUNCTIONAL IL6 POLYMORPHISM IS ASSOCIATED WITH IL-6 SERUM LEVELS BUT NOT CVD
193. PO5-138 ENDOTHELIAL NITRIC OXIDE SYNTHASE G894T GENE POLYMORPHISM, BLOOD PRESSURE AND HYPERTENSION IN THE TURKISH ADULT RISK FACTOR STUDY
194. PO16-445 HOW DOES THE PREVALENCE OF FAMILY HISTORY OF EARLY CARDIOVASCULAR DISEASE COMPARE IN PATIENTS WITH AND WITHOUT FAMILIAL HYPERCHOLESTEROLEMIA?
195. We-W45:6 Apolipoprotein AV, triglycerides and risk of future coronary artery disease in apparently healthy men and women; the EPIC-Norfolk population study
196. We-W35:2 Inherited and acquired risk factors for juvenile myocardial infarction in an European cohort
197. 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
198. Mo-P6:451 Single-strand conformation polymorphisms for the mutation scanning of proprotein convertase subtilisin Kexin 9 in familial hypercholesterolaemia
199. We-PL3:3 Can candidate gene genotypes improve estimation of CHD risk over-and above conventional risk factors in healthy UK men?
200. Mo-P6:389 Ace insertion/deletion polymorphism interaction associated with regional incidence of myocardial infarction (MI) in Europe
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