Asano Takashi | First Department Of Internal Medicine School Of Medicine Fukuoka University

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著作論文

Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
Japanese single nucleotide polymorphism database for 267 possible drug-related genes
A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13-p12 in Japanese
Association Between Circulating Monocyte Subsets and In-Stent Restenosis After Coronary Stent Implantation in Patients With ST-Elevation Myocardial Infarction
Assessment by Optical Coherence Tomography of Stent Struts Across Side Branch : Comparison of Bare-Metal Stents and Drug-Eluting Stents
Clinical Characteristics of Patients With Kawasaki Disease and Levels of Peripheral Endothelial Progenitor Cells and Blood Monocyte Subpopulations
Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyriod disease in the Japanese
Left ventricular apical aneurysm due to unrecognized sarcoidosis
Hypotensive Response to Angiotensin II Analogue and Angiotensin I Converting Enzyme Inhibitor in Pseudo-Bartters Syndrome
Insulin Delivery Rate in Response to Glucose Infusion in Normal and Diabetic Subjects
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
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population
Optical Coherence Tomography-Derived Anatomical Criteria for Functionally Significant Coronary Stenosis Assessed by Fractional Flow Reserve
Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms
Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis
Application of Optical Coherence Tomography in Percutaneous Coronary Intervention
Circulating CD14^+CD16^+ Monocyte Subsets as Biomarkers of the Severity of Coronary Artery Disease in Patients With Stable Angina Pectoris
Hunting for genes for hypertension : the Millennium Genome Project for Hypertension

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