スポンサーリンク
Riken Tokyo Jpn | 論文
- SNP projects in Japan
- High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2
- A case of Mikulicz's disease complicated with severe interstitial nephritis associated with IgG4
- Arterial Stiffness in Patients with Non-Diabetic Chronic Kidney Disease (CKD)
- Low-Dose Losartan Therapy Reduces Proteinuria in Normotensive Patients with Immunoglobulin A Nephropathy
- Clinical assessment of low-dose steroid therapy for patients with IgA nephropathy : a prospective study in a single center
- PJ-224 Primal role of intracellular zinc in PKC-dependent monocyte signalling and adhesive interaction(Atherosclerosis, basic(06)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-363 Functional Impacts of Selectin Haplotypes on Leukocyte-endothelial Interaction(Molecular Biology, Vascular 2 (H) : PJ61)(Poster Session (Japanese))
- Prediction of Sensitivity to STI571 among Chronic Myeloid Leukemia Patients by Genome-wide cDNA Microarray Analysis
- Isolation of a Novel Gene Showing Reduced Expression in Metastatic Colorectal Carcinoma Cell Lines and Carcinomas
- Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- Membrane Localization of Protein-Tyrosine Phosphatase 1B is Essential for its Activation of Sterol Regulatory Element-Binding Protein-1 Gene Expression and Consequent Hypertriglyceridaemia
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
- Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels
- Genetic variations in five genes involved in the excitement of cardiomyocytes
- Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome
- High-density SNP map of human ITR, a gene associated with vascular remodeling
- Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome