Investigation of SR-BI gene rs4238001 and rs5888 polymorphisms prevalence and effects on Turkish patients with metabolic syndrome

M Filizfidan, S Pence, B Çaykara… - Turkish Journal of …, 2020 - degruyter.com
Aim Metabolic syndrome (MS) is associated with dyslipidemia such as hypertriglyceridemia
and high-density lipoprotein (HDL) levels. Scavenger receptor BI (SR-BI) is the …

[HTML][HTML] Association of the TTC39B rs581080 SNP and serum lipid levels and the risk of coronary artery disease and ischemic stroke

JH Huang, RX Yin, WJ Li, F Huang… - … Journal of Clinical …, 2017 - ncbi.nlm.nih.gov
The tetratricopeptide repeat domain protein 39B gene (TTC39B) single nucleotide
polymorphism (SNP) of rs581080 has been associated with serum high-density lipoprotein …

[引用][C] 冠心病相关基因多态性的研究进展

岳玉霞, 陈灿 - 中国医药指南, 2014

[PDF][PDF] Relationship between SR-BI genetic polymorphism and coronary heart disease and blood lipid level

HB Wang - International Journal of Clinical and Experimental …, 2016 - e-century.us
To discuss the influence of single nucleotide polymorphism of scavenger receptor class B
type I (SR-BI) exon 1 and intron 5 on blood lipid level and susceptibility to coronary heart …

Hyperhomocysteinemia Is Associated With Lipid Profiles and Lipid Ratio in Patients With Coronary Artery Disease

DF Wu, QC Liao, F Lu, Z Wang, K Yu, JL Deng - 2021 - researchsquare.com
Objective: This study aimed to investigate the correlation of Hyperhomocysteinemia (HHcy)
or serum homocysteine (Hcy) levels with lipid levels and lipid ratios in individuals with …

Scavenger Receptor Class B Type 1 Gene Polymorphism and the Risk of Premature Coronary Artery Disease.

MMA Al Aziz, WES Saad, HAA Sattar… - Egyptian Journal of …, 2018 - search.ebscohost.com
Background: Coronary artery disease (CAD) is one of the greatest causes of morbidity and
mortality worldwide. It is the principal threat to health in countries in Africa and the Middle …

Scavenger Receptor Class B Type 1 Gene rs5888 Single Nucleotide Polymorphism: Association with Risk and Severity of Premature Coronary Artery Disease

WES Saad, MM Abd Al Aziz, MESA Fathi… - The Egyptian Journal …, 2020 - journals.ekb.eg
Background: Many different genetic associations with premature coronary artery disease
(PCAD) have been identified. One exonic single nucleotide polymorphism (SNP) rs5888 of …

[PDF][PDF] Mutational Analysis of Sr-B1 Gene in Relation with Dyslipidemia in Diabetic Patients

T Batool, FA Malik, MR ul Amin, S Hussain… - Medical Forum …, 2021 - medforum.pk
Objective: To find the mutation in scarb1 gene that may be the cause of dyslipidemia in type
2 diabetes mellitus (T2DM). Study Design: A cross-sectional comparative study Place and …

نقش پلی مورفیسم های rs10840293 و rs17087335 در بیماری عروق کرونر در جمعیت ایرانی

M Hesam, M Sadeghi, FS Bitaraf… - مجله دانش و تندرستي در …, 2020‎ - knh.shmu.ac.ir
مقدمه: مطالعات گسترده سراسر ژنومی (GWAS) در گذشته مشخص کرده‌اند که احتمالاً بین
پلی‌مورفیسم ژن‌های SWAP-70 و REST-NOA1 با بیماری عروق کرونر ارتباط وجود دارد. هدف این …

نقش پليمورفيسمهاي rs10840293 و rs17087335 در بيماري عروق كرونر در جمعيت ايراني.

مهدي حسام, مهدي صادقي, فاطمهسادات بيطر&… - … & Health/Dānish va …, 2020‎ - search.ebscohost.com
Introduction: Previous genome-wide association studies (GWASs) have shown an increased
CAD risk associated with single nucleotide polymorphisms (SNPs) in SWAP70 …