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東京大学医科学研究所ヒトゲノム解析センター | 論文
- ゲノム解析を基盤としたがんペプチドワクチン療法の開発と展望
- 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
- 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
- 巻頭対談 21世紀のライフライン 日本の医療 崩壊を招いた構造と再生への提言 : 患者さんに「希望」を提供する医療を実現するために : 中村祐輔氏 シカゴ大学医学部血液・腫瘍内科教授 東京大学医科学研究所ヒトゲノム解析センター教授 上昌広氏 東京大学医科学研究所特任教授
- 線形計画法による遺伝情報解析のためのスコア関数の学習
- Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population
- Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population
- Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome
- Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis
- Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes
- Making a haplotype catalog with estimated frequencies based on SNP homozygotes
- Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population
- Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression
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