スポンサーリンク
Itami City Hospital | 論文
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
- Lamivudine-to-entecavir switching treatment in type B chronic hepatitis patients without evidence of lamivudine resistance
- SIGNIGICANCE OF VISCERAL FAT ACCUMULATION TO THE DEVELOPMENT OF CORONARY ARTERY DISEASE(CAD)IN NON-OBESE MEN : VISCERAL FAT SYNDROME AS A NEW CLINICAL ENTITY
- 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
- Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
- Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
- Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population