スポンサーリンク
Laboratory For Statistical Analysis Snp Research Center Riken | 論文
- Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
- Lack of association of single nucleotide polymorphism in LRCH1 with knee osteoarthritis susceptibility
- High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population
- A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
- Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Patterns in the prevalence of hepatitis C virus infection at the start of hemodialysis in Japan
- Left ventricular apical aneurysm due to unrecognized sarcoidosis
- Impact of Hinge Motion on In-Stent Restenosis After Sirolimus-Eluting Stent Implantation
- Comparison of Contrast Media and Low-Molecular-Weight Dextran for Frequency-Domain Optical Coherence Tomography
- Effect of Direct Renin Inhibitor, Aliskiren, on Peripheral Blood Monocyte Subsets and Myocardial Salvage in Patients With Primary Acute Myocardial Infarction
- Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
- Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography
- A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
- Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women
- Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area
- Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a Japanese population
- A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia