RareAPOA5promoter variants associated with paradoxical HDL cholesterol decrease in response to fenofibric acid therapy
出版年份 2013 全文链接
标题
RareAPOA5promoter variants associated with paradoxical HDL cholesterol decrease in response to fenofibric acid therapy
作者
关键词
-
出版物
JOURNAL OF LIPID RESEARCH
Volume 54, Issue 7, Pages 1980-1987
出版商
American Society for Biochemistry & Molecular Biology (ASBMB)
发表日期
2013-05-01
DOI
10.1194/jlr.m034132
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The paradox of ApoA5 modulation of triglycerides: Evidence from clinical and basic research
- (2012) Mahdi Garelnabi et al. CLINICAL BIOCHEMISTRY
- Prevalence of lipid abnormalities in the United States: The National Health and Nutrition Examination Survey 2003–2006
- (2012) Peter P. Tóth et al. Journal of Clinical Lipidology
- LPLgene variants affect apoC-III response to combination therapy of statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia
- (2012) Ariel Brautbar et al. JOURNAL OF LIPID RESEARCH
- Interaction between SNPs in theRXRAand nearANGPTL3gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia
- (2012) Li Ma et al. JOURNAL OF LIPID RESEARCH
- Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia
- (2011) Ariel Brautbar et al. ATHEROSCLEROSIS
- Genetic Variant of the Scavenger Receptor BI in Humans
- (2011) Menno Vergeer et al. NEW ENGLAND JOURNAL OF MEDICINE
- Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
- (2010) Alkes L. Price et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarction
- (2010) Raffaele De Caterina et al. ATHEROSCLEROSIS
- Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies
- (2010) LANCET
- Biological, clinical and population relevance of 95 loci for blood lipids
- (2010) Tanya M. Teslovich et al. NATURE
- Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
- (2010) Christopher T Johansen et al. NATURE GENETICS
- The −1131T>C SNP of the APOA5 gene modulates response to fenofibrate treatment in patients with the metabolic syndrome: A postprandial study
- (2009) Fernando Cardona et al. ATHEROSCLEROSIS
- Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the Genetics of Lipid-Lowering Drugs and Diet Network study
- (2009) Yongjun Liu et al. Pharmacogenetics and Genomics
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
- (2009) Bo Eskerod Madsen et al. PLoS Genetics
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Evaluation of a New Formulation of Fenofibric Acid, ABT-335, Co-Administered with Statins
- (2008) Peter H Jones et al. CLINICAL DRUG INVESTIGATION
- Common variants at 30 loci contribute to polygenic dyslipidemia
- (2008) Sekar Kathiresan et al. NATURE GENETICS
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started