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Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of | 論文
- Upregulation of Monocyte Tissue Factor Activity Is Significantly Associated With Low-Grade Chronic Inflammation and Insulin Resistance in Patients With Metabolic Syndrome
- OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
- OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
- Elevated Levels of Both Cardiomyocyte Membrane and Myofibril Damage Markers Predict Adverse Outcomes in Patients With Chronic Heart Failure
- Effects of a Pure α/β-Adrenergic Receptor Blocker on Monocrotaline-Induced Pulmonary Arterial Hypertension With Right Ventricular Hypertrophy in Rats
- 4 Catheter Ablation for the Purkinje-fiber Related Ventricular Tachyarrhythmias Associated with Myocardial Infarction(New Era of Catheter Ablation for Ventricular Arrhythmias,Plenary Session 3 (PL-3) (I),The 73rd Annual Scientific Meeting of The Japanese
- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
- A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
- Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
- 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
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- The characteristics of relapse in adult-onset minimal-change nephrotic syndrome
- Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy
- Left Ventricular Hypertrophy Is Associated with Arterial Stiffness and Vascular Calcification in Hemodialysis Patients
- Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients
- Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy
- Antiphospholipid Syndrome Treated with Prednisolone, Cyclophosphamide and Double-Filtration Plasmapheresis
- Retroperitoneal Fibrosis Associated with Membranous Nephropathy Effectively Treated with Steroids
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