The peptidylglycine-α-amidating monooxygenase (PAM) gene rs13175330 A>G polymorphism is associated with hypertension in a Korean population
暂无分享,去创建一个
Minkyung Kim | Minjoo Kim | J. H. Lee | J. Chae | Sang-Hyun Lee | H. Yoo
[1] H. J. Yoo,et al. Estrogen-related receptor γ gene (ESRRG) rs1890552 A>G polymorphism in a Korean population: Association with urinary prostaglandin F2α concentration and impaired fasting glucose or newly diagnosed type 2 diabetes. , 2017, Diabetes & metabolism.
[2] Minkyung Kim,et al. Influence of estrogen-related receptor γ (ESRRG) rs1890552 A > G polymorphism on changes in fasting glucose and arterial stiffness , 2017, Scientific Reports.
[3] S. Choi,et al. Introns: The Functional Benefits of Introns in Genomes , 2015, Genomics & informatics.
[4] Tubao Yang,et al. GRK5 Intronic (CA)n Polymorphisms Associated with Type 2 Diabetes in Chinese Hainan Island , 2014, PloS one.
[5] Kari Stefansson,et al. Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes , 2014, Nature Genetics.
[6] S. Visvikis-Siest,et al. Genetic biomarkers of hypertension and future challenges integrating epigenomics. , 2012, Clinica chimica acta; international journal of clinical chemistry.
[7] Alan D. Lopez,et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010 , 2012, The Lancet.
[8] J. Mi,et al. Physical activity modifies the associations between genetic variants and hypertension in the Chinese children. , 2012, Atherosclerosis.
[9] Tom R. Gaunt,et al. Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk , 2011, Nature.
[10] W. Sadee,et al. Intronic polymorphism in CYP3A4 affects hepatic expression and response to statin drugs , 2011, The Pharmacogenomics Journal.
[11] A. Dominiczak,et al. GENOME WIDE ASSOCIATION STUDY OF BLOOD PRESSURE EXTREMES IDENTIFIES VARIANT IN UMOD ASSOCIATED WITH HYPERTENSION: 6B.01 , 2010 .
[12] M. Nagarkatti,et al. Unique SNP in CD44 intron 1 and its role in breast cancer development. , 2010, Anticancer research.
[13] Andrew D. Johnson,et al. Genome-wide association study of blood pressure and hypertension , 2009, Nature Genetics.
[14] S. Roth. Genetics Primer for Exercise Science and Health , 2007 .
[15] J. Witteman,et al. Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes , 2007, Journal of hypertension.
[16] J. Mehta,et al. Oxidative stress in diabetes: a mechanistic overview of its effects on atherogenesis and myocardial dysfunction. , 2006, The international journal of biochemistry & cell biology.
[17] R. Mains,et al. Deletion of peptide amidation enzymatic activity leads to edema and embryonic lethality in the mouse. , 2005, Developmental biology.
[18] N. Bäck,et al. Peptidylglycine-α-amidating monooxygenase and pro-atrial natriuretic peptide constitute the major membrane-associated proteins of rat atrial secretory granules , 2003 .
[19] T. Teramoto,et al. Assessment of LDL particle size by triglyceride/HDL-cholesterol ratio in non-diabetic, healthy subjects without prominent hyperlipidemia. , 2003, Journal of atherosclerosis and thrombosis.
[20] G. Sagnella. Atrial natriuretic peptide mimetics and vasopeptidase inhibitors. , 2001, Cardiovascular research.
[21] W. Sadee,et al. CYP3A4 intronic SNP rs35599367 (CYP3A4*22) alters RNA splicing. , 2016, Pharmacogenetics and genomics.
[22] F. Amiri,et al. Regulation of natriuretic peptide secretion by the heart. , 1999, Annual review of physiology.
[23] D. Steinberg,et al. Role of oxidised low density lipoprotein in atherogenesis. , 1993, British heart journal.