Background A genome-wide association study has recognized C6orf10-BTNL2
polymorphism in coronary artery disease. The goal of this study was to explore the potential …

Background The pathological basis of coronary heart disease (CHD) is atherosclerosis.
BTNL2 can inhibit the activation of T cells. We aimed to explore the association between …

OBJECTIVE: We have performed a genome-wide association study (GWAS) to identify
genetic variants that confer susceptibility to myocardial infarction (MI) in Japanese and …

Diabet. Med. 28, 1381–1387 (2011) Abstract Aims We previously showed that the C→ T
polymorphism (rs6929846) of BTN2A1 was significantly associated with myocardial …

Background: Dilated cardiomyopathy (DCM) is one type of primary myocardial disease,
partly caused by immunity dysfunctions. BTNL2 (butyrophilin-like 2) has already been …

We have previously shown that the C→ T polymorphism (rs6929846) of the butyrophilin,
subfamily 2, member A1 gene (BTN2A1) was significantly associated with myocardial …

We previously identified rs6929846 of the butyrophilin, subfamily 2, member A1 gene
(BTN2A1) as a susceptibility locus for myocardial infarction in Japanese individuals by a …

Dyslipidemia is an important risk factor for myocardial infarction (MI). We previously showed
that gene polymorphisms associated with MI differed among individuals with different lipid …

Recent evidence suggests that genetic variants that confer susceptibility to myocardial
infarction (MI) may differ between men and women or between individuals with or without …

Background The authors previously showed that the C→ T polymorphism (rs6929846) of
butyrophilin, subfamily 2, member A1 gene (BTN2A1) was significantly associated with …