スポンサーリンク
Laboratory For Genotyping The Snp Research Center The Institute Of Physical And Chemical Research (riken) | 論文
- Identification of 197 genetic variations in six human methyltransferase genes in the Japanese population
- High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene
- Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population
- Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes
- Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population
- 5αDH-DOC (5α-dihydro-deoxycorticosterone) activates androgen receptor in castration-resistant prostate cancer
- Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes
- Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
- Usefulness of endoscopic biopsy using FOXP3^+ Treg up-regulation in the duodenal papilla in the differential diagnosis between autoimmune pancreatitis and pancreatic cancer
- Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population
- Novel Findings for the Development of Drug Therapy for Various Liver Diseases : Liver Microsomal Triglyceride Transfer Protein Activator May Be a Possible Therapeutic Agent in Non-alcoholic Steatohepatitis
- Platelet count for predicting fibrosis in nonalcoholic fatty liver disease
- Semaphorin 4D, a lymphocyte semaphorin, enhances tumor cell motility through binding its receptor, plexinB1, in pancreatic cancer
- Prevalence and associated metabolic factors of nonalcoholic fatty liver disease in the general population from 2009 to 2010 in Japan : a multicenter large retrospective study
- 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