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2. Gene Ontology annotations and resources

4. Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits

5. Replication and characterization of association between ABO SNPs and red blood cell traits by meta-analysis in Europeans

6. Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis

7. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

8. blood pressure loci identified with a gene-centricarray

9. The Gene Ontology in 2010: extensions and refinements

10. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

12. APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis

13. New genetic loci link adipose and insulin biology to body fat distribution.

14. New genetic loci link adipose and insulin biology to body fat distribution

15. Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study

17. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

18. Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425))

20. Association of TERC and OBFC1 Haplotypes with Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease

21. Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data

22. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

23. Lipoprotein Lipase Variants D9N and N291S are associated with Increased Plasma Triglyceride and Lower High-Density Lipoprotein Cholesterol concentrations. Studies in the Fasting and Postprandial States. The European Atherosclerosis Research Studies

24. The cholesterol ester transfer protein (CETP) TaqIB variant, HDL cholesterol levels, cardiovascular risk and the efficacy of pravastatin treatment – an individual patient meta-analisis of 13,677 subjects

25. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

28. Characterization of recombinant wild type and site-directed mutations of apolipoprotein C-III: Lipid binding, displacement of ApoE, and inhibition of lipoprotein lipase

30. Familial lipoprotein lipase (LPL) deficiency: a catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy

33. Human Apolipoprotein-b Signal Sequence Variants Confer a Secretion-defective Phenotype When Expressed in Yeast

35. SERPINA1 11478G→A variant, serum α1-antitrypsin, exacerbation frequency and FEV1 decline in COPD.

37. ADIPOQ gene polymorphism rs1501299 interacts with fibre intake to affect adiponectin concentration in children: the GENe-Diet Attica Investigation on childhood obesity.

38. Inflammatory biomarkers and the prediction of coronary events among people at intermediate risk: the EPIC-Norfolk prospective population study.

41. Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies

43. Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries

44. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

45. The Gene Ontology: enhancements for 2011

46. Association of a sequence variant in DAB2IP with coronary heart disease

47. Genetic studies of body mass index yield new insights for obesity biology

48. New genetic loci link adipose and insulin biology to body fat distribution

49. Improving Interpretation of Cardiac Phenotypes and Enhancing Discovery With Expanded Knowledge in the Gene Ontology.

50. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

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