Kumashiro Naoki | Department Of Medicine Metabolism And Endocrinology Juntendo University School Of Medicine
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概要
- KUMASHIRO NAOKIの詳細を見る
- 同名の論文著者
- Department Of Medicine Metabolism And Endocrinology Juntendo University School Of Medicineの論文著者
関連著者
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Kamatani Naoyuki
Laboratory For Statistical Analysis Center For Genomic Medicine Riken
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Kamatani Naoyuki
Laboratory for Statistical Analysis, Center for Genomic Medicine, RIKEN
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Takahashi Atsushi
Laboratory for Statistical Analysis, Center for Genomic Medicine, RIKEN
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Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
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Nakamura Yusuke
東京大学医科学研究所ヒトゲノム解析センター ゲノムシークエンス解析分野
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Asaka Takahisa
Cardiovascular Center Yokosuka Kyosai Hospital
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Akiba Takashi
Department Of Medicine Kidney Center Tokyo Women's Medical University
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Takei Takashi
東京女子医科大学 腎臓病総合医療センター
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Saitoh Satoshi
Laboratory For Genotyping Snp Research Center The Institute Of Physical And Chemical Research (riken
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SAITO Susumu
Laboratory for Genotyping, SNP Research Center, The Institute of Physical and Chemical Research (RIK
著作論文
- 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)
- Association of the MSX2 gene polymorphisms with ankylosing spondylitis in 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
- Lack of association of single nucleotide polymorphism in LRCH1 with knee osteoarthritis susceptibility
- 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
- Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients