Nakamura Yusuke | Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Institute
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概要
- Nakamura Yusukeの詳細を見る
- 同名の論文著者
- Laboratory For Genotyping Riken Snp Research Center C/o Riken Yokohama Instituteの論文著者
関連著者
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Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
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Iida Aritoshi
東京大学医科学研究所ヒトゲノム解析センター
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Iida A
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Iida Aritoshi
理化学研究所遺伝子多型研究センター
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IIDA Aritoshi
Laboratory for Genotyping, SNP Research Center, The Institute of Physical and Chemical Research (RIK
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Akiba Takashi
Department Of Medicine Kidney Center Tokyo Women's Medical University
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SAITO Susumu
Laboratory for Genotyping, SNP Research Center, The Institute of Physical and Chemical Research (RIK
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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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Aritoshi Iida
Laboratory For Pharmacogenetics Snp Research Center The Institute Of Physical And Chemical Research
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Kamatani Naoyuki
Laboratory For Statistical Analysis Center For Genomic Medicine Riken
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SEKINE Akihiro
Laboratory for Genotyping, RIKEN SNP Research Center
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KATAGIRI Toyomasa
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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Tanaka Toshihiro
Laboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN
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Emi Mitsuru
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Kasumi Fujio
Department of Surgery and Pathology, Cancer Institute Hospital
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梶原 哲郎
東京女子医科大学第二病院外科
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梶原 哲郎
Tochigi Cancer Center Hospital
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Sakata Toshiie
山口大学 医学系研究科器官病態内科学
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Sakamoto Goi
Department of Surgery and Pathology, Cancer Institute Hospital
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Tanaka Satoshi
Department Of Nutritional Sciences Faculty Of Nutritional Science Nakamura Gakuen University
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三木 義男
癌研ゲノムセンター
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Ohnishi Yozo
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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Ozaki Kouichi
Laboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN
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SATO Hiroshi
Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine
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HORI Masatsugu
Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine
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Takahashi Atsushi
Laboratory for Statistical Analysis, Center for Genomic Medicine, RIKEN
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IKEGAWA Shiro
Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN
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Tsunoda Tatsuhiko
Laboratory for Medical Informatics, Center for Genomic Medicine, RIKEN
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Kamatani Naoyuki
Laboratory for Statistical Analysis, Center for Genomic Medicine, RIKEN
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Mizuno Kyoichi
日本医科大学 内科学
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OHNISHI Yozo
Laboratory for SNP Analysis, RIKEN Center for Genomic Medicine
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Takei T
Tokyo Metropolitan Univ. Tokyo Jpn
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Suga H
Department Of Cardiovascular Medicine Osaka University Graduate School Of Medicine
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NAKAO Kazuwa
EBM Research Center, Kyoto University Graduate School of Medicine
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Suga Hiroyki
Department Of Systems Physiology Okayama University Graduate School Of Medicine Dentistry And Pharma
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Funahashi Tohru
Division Of Cardiovascular Surgery Department Of Surgery Osaka University Graduate School Of Medicin
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Matsumoto Satoshi
Department Of Pathology Nara Medical University
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Matsuzawa Yuji
熊本大学 医学薬学研究部循環器病態学
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MIZUNO Hiroya
Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine
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NAGAI Ryozo
Department of Cardiovascular Medicine, University of Tokyo
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Mizuno Kyoichi
Division Of Cardiology Hepatology Geriatrics And Integrated Medicine Department Of Internal Medicine
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Matsuda Koichi
Department Of Internal Medicine Tokyo Metropolitan Komagome Hospital
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Kawamoto Manabu
国立医薬品食品衛生研究所
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Kawamoto Manabu
Institute Of Rheumatology Tokyo Women's Medical University
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KAMATANI Naoyuki
Institute of Rheumatology, Tokyo Women's Medical University School of Medicine
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Asaka Takahisa
Cardiovascular Center Yokosuka Kyosai Hospital
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Kamatani Naoyuki
Institute Of Rheumatology Aoyama Hospital Tokyo Women's Medical University
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FUJIOKA Tomoaki
Department of Urology, Iwate Medical University
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MATSUDA Koichi
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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NAKAMURA Takahiro
Laboratory for Mathematics, Premedical Course, National Defense Medical College
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MUSHIRODA Taisei
Laboratory for Pharmacogenetics, RIKEN SNP Research Center
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Kubo Michiaki
Laboratory for Genotyping, Center for Genomic Medicine, RIKEN
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MIKI Tsuneharu
Department of Urology, Kyoto Prefectural University of Medicine Graduate School of Medical Science
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Kawamoto Manabu
Division Of Genomic Medicine Department Of Advanced Biomedical Engineering And Science Tokyo Women&a
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YOKOTA Takashi
Department, of Information Science, Graduate School of Engineering, Utsunomiya University
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Mizuno Kyoichi
First Department Of Internal Medicine Nippon Medical School
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Nakajima Tadahisa
Department Of Metabolic Medicine Osaka University Graduate School Of Medicine
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SHIMIZU Makiko
Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical University
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YAMAZAKI Keiko
Laboratory for Gastrointestinal Diseases, SNP Research Center, The Institute of Physical and Chemica
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MATSUZAWA Yuji
Sumitomo Hospital
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ISOBE Mitsuaki
Department of Cardiovascular Medicine, Tokyo Medical and Dental University
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Matsuda H
Department Of Cardiovascular Surgery Hyogo Medical College
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AOZASA Katsuyuki
Department of Pathology, Osaka University Graduate School of Medicine
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Yoshimatsu Hironobu
Department of Internal Medicine 1, Faculty of Medicine, Oita University
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遠藤 啓吾
群馬大学核医学科
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SAKATA Toshiie
Department of Nutritional Sciences, Faculty of Nutritional Science, Nakamura Gakuen University
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Matsuzawa Yuji
Department of Internal Medicine, Sumitomo Hospital
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NAKAO Kazuwa
Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine
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Yumura Wako
Department of Nephrology, Jichi Medical University
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Nitta Kosaku
Department of Medicine, Kidney Center, Tokyo Womens Medical University
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KAWAGUCHI Yasushi
Institute of Rheumatology, Tokyo Women's Medical University School of Medicine
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Yasutake Masahiro
Division Of Cardiology Department Of Internal Medicine Nippon Medical School
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Morishima Y
Department Of Hematology Kinki University School Of Medicine
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YAMORI Takao
Division of Molecular Pharmacology, Cancer Chemotherapy Center, Japanese Foundation for Cancer Resea
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Funahashi Tohru
Department of Metabolic Medicine, Graduate School of Medicine
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Miyatake Nobuyuki
Okayama Health Foundation Okayama Jpn
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HIRATA KOICHI
First Department of Surgery, Sapporo Medical University School of Medicine
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Maeda Shiro
Laboratory for Diabetic Nephropathy, SNP Research Center, The Institute of Physical and Chemical Res
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Haketa Akira
日本大学 医学部内科学系腎臓高血圧内分泌内科
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Hata Akira
千葉大学 医学研究院公衆衛生学
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MIYAMOTO Yoshinari
Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN
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Kashiwagi Atsunori
滋賀医科大学 内科学講座
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Kashiwagi A
Department Of Medicine Shiga University Of Medical Science
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Kashiwagi Atsunori
Department Of Medicine Shiga University Of Medical Science
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Yasujima Minoru
東北大学 医系研究内部障害学分野
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KAMATANI Yoichiro
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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HOSONO Naoya
Laboratory for Genotyping, SNP Research Center, The Institute of Physical and Chemical Research (RIK
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SAITO Shigeru
Tokushukai Hospital Group
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SHIMOMURA Hideki
Tokushukai Hospital Group
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SUZUKI Takao
Tokushukai Hospital Group
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EBANA Yusuke
Laboratory for Cardiovascular Diseases, SNP Research Center, The Institute of Physical and Chemical
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LWIN Htay
Laboratory for Cardiovascular Diseases, SNP Research Center, The Institute of Physical and Chemical
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ISHII Nobuaki
Laboratory for Cardiovascular Diseases, SNP Research Center, The Institute of Physical and Chemical
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Matsuzawa Y
Department Of Cardiovascular Medicine Graduate School Of Medical Sciences Kumamoto University
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野中 聡
旭川医科大学耳鼻咽喉科・頭頸部外科学講座
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野中 源一郎
九州大学薬学部
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林 達哉
旭川医科大学耳鼻咽喉科・頭頸部外科学講座
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Inoue Katsumi
Department of Cardiology, Kokura Memorial Hospital
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Odashiro Keita
Department of Cardiology, Kokura Memorial Hospital
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Nobuyoshi Masakiyo
Department of Cardiology, Kokura Memorial Hospital
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Horio Masaru
Ehime University
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Matsuda Hikaru
Cardiovascular Division Osaka Polici Hospital
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IKEDA Jun-ichiro
Department of Pathology, Osaka University Graduate School of Medicine
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WATANABE GO
Department of General and Cardiothoracic Surgery, Kanazawa University School of Medicine
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RAKUGI Hiromi
Department of Geriatric Medicine, Osaka University Graduate School of Medicine
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KOHNO Nobuoki
Department of Molecular and Internal Medicine, Graduate School of Biomedical Sciences, Hiroshima Uni
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OHNO Ryuzo
Aichi Cancer Center
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SATO Hitoshi
Department of Clinical and Molecular Pharmacokinetics/Pharmacodynamics, School of Pharmaceutical Sci
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Fukutomi Tatsuya
Department of Cardiology, Nagoya City University Graduate School of Medical Sciences
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MIKI Yoshio
Department of Genetic Diagnosis, the Cancer Institute Hospital of JFCR
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Kikuchi Kenjiro
First Department of Internal Medicine, Asahikawa Medical College
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Yashiro Mayumi
Department of Public Health, Jichi Medical University
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北 徹
Department Of Geriatric Medicine Osaka University Graduate School Of Medicine
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KURIMOTO Masanori
Department of Neurosurgery, Faculty of Medicine, University of Toyama
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ENDO Shunro
Department of Neurosurgery, Faculty of Medicine, University of Toyama
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YAMAMOTO Shinji
Department of Neurosurgery, Kyoto Second Red Cross Hospital
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UEDA Takanori
First Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui
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OIKAWA Shinichi
Division of Endocrinology and Metabolism, Department of Medicine, Nippon Medical School
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MUROHARA Toyoaki
Nagoya University
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OIKAWA Shinichi
Department of Internal Medicine, Nippon Medical School
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Hoshikawa Yoshiko
Div. Of Molecular And Genetic Medicine Dep. Of Genetic Medicine And Regenerative Therapeutics Gradua
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吉川 秀樹
大阪大学大学院医学系研究科器官制御外科学(整形外科)
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Saitoh Satoshi
Division of cardiology, Department of Medicine, Nihon University school of Medicine
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Okawa Akihiko
東京大学医科学研究所
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Okawa Akihiko
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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KATSUYA Tomohiro
Department of Clinical Gene Therapy, Osaka University Graduate School of Medicine, Suita
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SUGIMOTO Ken
Department of Geriatric Medicine, Osaka University Graduate School of Medicine
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OGIHARA Toshio
Department of Geriatric Medicine, Osaka University Graduate School of Medicine
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NAKAGAMI Hironori
Division of Gene Therapy Science, Osaka University Graduate School of Medicine
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YOSHIKAWA Hideki
Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine
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織内 昇
群馬大学大学院医学系研究科
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織内 昇
東京都立保健科学大学放射線学科
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Nakagami Hironori
Division Of Gene Therapy Science Osaka University Graduate School Of Medicine
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Uchida Keiko
Department of Medicine, Kidney Center, Tokyo Womens Medical University
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Nobuyoshi Masakiyo
Kokura Memorial Hospital
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Inoue Katsumi
松江赤十字病院 循環器科
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Morishita Ryuichi
東京大学 先端臨床医学開発講座
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Watanabe Takeshi
Laboratory Of Fish Nutrition Department Of Marine Biosciences Tokyo University Of Marine Sciences An
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Yanagisawa Masao
Department Of Internal Medicine Division Of Cardiology Nippon Medical School Tama-nagayama Hosipital
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Takeda Hiroshi
Department Of Medical Information Science Osaka University Graduate School Of Medicine
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Tatematsu M
Division Of Oncological Pathology Aichi Cancer Center Research Institute
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Takagi Hiromichi
Department Of Medical Information Science Osaka University Graduate School Of Medicine
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KAGAMI Yoshitoyo
Department of Hematology and Cell Therapy, Aichi Cancer Center
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Iwakura K
Cardiovascular Center Sakurabashi Watanabe Hospital
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Takami Yoichi
Department Of Geriatric Medicine And Nephrology Osaka University Graduate School Of Medicine
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Shimamoto K
Department Of Internal Medicine Ii Sapporo Medical University
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Yamamoto Shinji
Department Of Animal Husbandry Faculty Of Agriculture Tohoku University:(present Address) Department
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KANEDA Yasufumi
Division of Gene Therapy Science, Graduate School of Medicine, Osaka University
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Isono Kaichi
Second Department Of Surgery Chiba University School Of Medicine
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Kato Tatsuya
Laboratory of Biotechnology, Faculty of Agriculture, Shizuoka University
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KIMURA YASUTOSHI
First Department of Surgery, Sapporo Medical University School of Medicine
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Koriyama Hiroshi
Department of Geriatric Medicine, Osaka University Medical School
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Yamashita Hidetoshi
Division of Gene Therapy Science, Osaka University Graduate School of Medicine
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Mori Masaki
Division of Gene Therapy Science, Osaka University Graduate School of Medicine
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Hayashi Hiroki
Division of Gene Therapy Science, Osaka University Graduate School of Medicine
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Morishita Ryuichi
Division of Clinical Gene Therapy, Osaka University Graduate School of Medicine
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Haneda Noriyuki
Department of Pediatrics, Shimane Medical University
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HAYAKAWA Toru
Department of Neurosurgery, Osaka University Medical School
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織内 昇
群馬大学
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Tsujita Yasuyuki
Department Of Geriatric Medicine Osaka University Graduate School Of Medicine
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Tabara Yasuharu
国立循環器病センター研究所 疫学部
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Tabara Yasuharu
西予市立野村病院 内科
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Kiyohara Y
Department Of Environmental Medicine Graduate School Of Medical Sciences Kyushu University
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Kiyohara Yutaka
九州大学 医学系学府環境医学
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SASAKI Shin
Department of Physics, Tokyo Metropolitan University
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ARAKI Tsutomu
Department of Cardiology, Kanazawa Cardiovascular Hospital
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YAMADA Yasuaki
Department of Laboratory Medicine, Nagasaki University School of Medicine
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柳川 洋
Department Of Public Health Jichi Medical University
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Kawano Yuhei
国立循環器病センター 高血圧腎臓内科
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Rakugi Hiromi
東北大学 臨床薬学
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Shimamoto Kazuaki
大阪大学 医学系研究科老年内科
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Matsushita Toyoaki
Department Of Cardiology Nagoya University Graduate School Of Medicine
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Shiba T
Department Of Medical Oncology The Cancer Institute Of Japanese Foundation For Cancer Research
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Tokunaga Katsushi
Department Of Clinical Pharmacology And Therapeutics Tohoku University Graduate School Of Pharmaceut
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MISAWA Kazuharu
Research Program for Computational Science, Research and Development Group for Next-Generation Integ
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FUJII Shoogo
Laboratory for Statistical Analysis, RIKEN Center for Genomic Medicine
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YAMAZAKI Toshimasa
Laboratory for Statistical Analysis, RIKEN Center for Genomic Medicine
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TAKASAKI Junichi
Laboratory for Statistical Analysis, RIKEN Center for Genomic Medicine
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OISHI Tetsuya
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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OTSUBO Shigeru
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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USAMI Masayuki
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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TAKEI Takashi
Department of Medicine, Kidney Center, Tokyo Women's Medical University
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TSUCHIYA Ken
Department of Medicine, Kidney Center, Tokyo Women's Medical University
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OHNISI Yozo
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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KOCHI Yuta
Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Resea
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SHIMANE Kenichi
Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Resea
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YAMAMOTO Kazuhiko
Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Resea
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OHISHI Tetsuya
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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OHTSUBO Shigeru
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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CHA Pei-Chieng
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University
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SAITO Satoshi
Division of Cardiology, Department of Medicine, Nihon University School of Medicine
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KIKUCHI Yuka
Laboratory for Pharmacogenetics, SNP Research Center, The Institute of Physical and Chemical Researc
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WANIBUCHI Yasuhiko
Tokushukai Hospital Group
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Matsuzawa Y
Sumitomo Hospital
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Usami Masayuki
東京大学医科学研究所ヒトゲノム解析センター
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Usami Masayuki
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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Uchida Keiko
東京女子医科大学附属腎臓病総合医療センター 腎臓内科
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Uchida Keiko
Department Of Medicine Kidney Center Tokyo Women's Medical University
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Wanibuchi Yasuhiko
Tokushukai Hospital Group Tokyo Jpn
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Shimane Kenichi
Laboratory For Rheumatic Diseases Snp Research Center The Institute Of Physical And Chemical Researc
著作論文
- OE-071 A Genom-Wide Association Study of SNPs in the risk of Atherosclerosis Obliterans(Heart failure, clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- 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
- 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
- Japanese single nucleotide polymorphism database for 267 possible drug-related genes
- A high-throughput SNP typing system for genome-wide association studies
- PJ-152 A functional SNP in the Proteasome Subunit Alpha Type 6 Gene confers Risk of Myocardial Infarction in Japanese Population(Acute myocardial infarction, basic-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-212 Identification of a Novel non-coding RNA, MIAT, that Confers Risk of Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-340 Large-Scale Genetic Association Study of 30 Inflammation-Related Genes for Myocardial Infarction Using Tag SNPs from HapMap Data(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual
- Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene
- Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21
- Genome-wide association study to identify genes related to myocardial infarction
- A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction
- 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
- Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferases
- Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin
- EphA4 receptor, overexpressed in pancreatic ductal adenocarcinoma, promotes cancer cell growth
- Novel tumor marker REG4 detected in serum of patients with resectable pancreatic cancer and feasibility for antibody therapy targeting REG4
- High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis
- Identification of C2orf18, termed ANT2BP (ANT2-binding protein), as one of the key molecules involved in pancreatic carcinogenesis
- Over-expression of cysteine proteinase inhibitor cystatin 6 promotes pancreatic cancer growth
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
- 1P-044 DNAメチル化維持を仲介するSRAドメインのヘミメチル化DNA認識について熱力学的解析(蛋白質・構造機能相関(1),第46回日本生物物理学会年会)
- Prediction of Sensitivity to STI571 among Chronic Myeloid Leukemia Patients by Genome-wide cDNA Microarray Analysis
- Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma : Identification of Genes Related to Disease Progression
- Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
- Isolation of a Novel Gene Showing Reduced Expression in Metastatic Colorectal Carcinoma Cell Lines and Carcinomas
- Distinct pattern of gene expression in pyothorax-associated lymphoma (PAL), a lymphoma developing in long-standing inflammation
- Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1
- Correlation of Allelic Loss with Poor Postoperative Survival in Breast Cancer
- Frequent Allelic Loss at 6q26-27 in Breast Carcinomas of the Solid-tubular Histologic Type
- Detailed Deletion Mapping of Chromosome Arm 3p in Breast Cancers : A 2-cM Region on 3p 14.3-21.1 and a 5-cM Region on 3p 24.3-25.1 Commonly Deleted in Tumors
- Correlation of Allelic Losses and Clinicopathological Factors in Primary Breast Cancers
- Mapping of a Breast Cancer Tumor Suppressor Gene Locus to a 4-cM Interval on Chromosome 18q21
- Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
- Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP)
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Critical roles of T-LAK cell-originated protein kinase in cytokinesis
- Involvement of kinesin family member 2C/mitotic centromere-associated kinesin overexpression in mammary carcinogenesis
- Enhanced SMYD3 expression is essential for the growth of breast cancer cells
- Multiplex Mutation Screening of the BRCA1 Gene in 1000 Japanese Breast Cancers
- Infrequent Mutation of the H-Cadherin Gene on Chromosome 16q24 in Human Breast Cancers
- Non-transmissible Sendai virus encoding granulocyte macrophage colony-stimulating factor is a novel and potent vector system for producing autologous tumor vaccines
- 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
- Identification of candidate predictive markers of anticancer drug sensitivity using a panel of human cancer cell lines
- Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes
- Impact of CYP2D6^*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapy
- Association of genetic polymorphisms in SLCO1B3 and ABCC2 with docetaxel-induced leukopenia
- Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
- No Evidence of Mutation in the Human PTC Gene, Responsible for Nevoid Basal Cell Carcinoma Syndrome, in Human Primary Squamous Cell Carcinomas of the Esophagus and Lung
- Complete cDNA sequence and genomic organization of a human pancreas-specific gene homologous to Caenorhabditis elegans sel-1
- Molecular cloning, expression, and mapping of a novel human cDNA, GRP17, highly homologous to human gadd45 and murine MyD118
- Isolation and characterization of a human cDNA encoding a protein homologous to the 7.2-kDa protein (subunit X) of bovine ubiquinol-cytochrome C reductase
- Loci on murine chromosomes 7 and 13 that modify the phenotype of the NOA mouse, an animal model of atopic dermatitis
- Allelic Loss at 1p34-36 Predicts Poor Prognosis in Node-negative Breast Cancer
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- A Gln/Arg polymorphism at codon 349 of the hBUBR1 gene
- Identification of p53-46F as a super p53 with an enhanced ability to induce p53-dependent apoptosis
- Radioimmunotherapy of solid tumors targeting a cell-surface protein, FZD10 : therapeutic efficacy largely depends on radiosensitivity
- Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
- Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
- Association of the RIP2 Gene with Childhood Atopic Asthma
- Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
- Genomic organization and mapping of the human activin receptor type IIB (hActR-IIB) gene
- Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
- Two Distinct Commonly Deleted Regions on Chromosome 13q Suggest Involvement of BRCA2 and Retinoblastoma Genes in Sporadic Breast Carcinomas
- An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
- Nonrandom Chromosomal Imbalances in Esophageal Squamous Cell Carcinoma Cell Lines : Possible Involvement of the ATF3 and CENPF Genes in the 1q32 Amplicon
- Isolation and Characterization of Human NBL4, a Gene Involved in the β-Catenin/Tcf Signaling Pathway
- Analysis of APCL, a Brain-specific Adenomatous Polyposis Coli Homologue, for Mutations and Expression in Brain Tumors
- High-resolution SNP map in the 55-kb region containing the selectin gene family on chromosome 1q24-q25
- Stanniocalcin 2 overexpression in castration-resistant prostate cancer and aggressive prostate cancer
- Oncogenic role of NALP7 in testicular seminomas
- Novel 5α-steroid reductase (SRD5A3, type-3) is overexpressed in hormone-refractory prostate cancer
- Identification of brain-specific splicing variants of the hDLG1 gene and altered splicing in neuroblastoma cell lines
- Fibroblast growth factor receptor 1 oncogene partner as a novel prognostic biomarker and therapeutic target for lung cancer
- Characterization of SEZ6L2 cell-surface protein as a novel prognostic marker for lung cancer
- Identification of 20 novel SNPs in the guanine nucleotide binding protein alpha 12 gene locus
- Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptors
- Catalog of 178 variations in the Japanese population among eight human genes encoding G protein-coupled receptors (GPCRs)
- Catalog of 680 variations among eight cytochrome P450 (CYP) genes, nine esterase genes, and two other genes in the Japanese population
- Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface
- Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population
- Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes : UGT2A1, UGT2B15, and UGT8
- 906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population
- Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters : ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8
- Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR)
- Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus
- Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population
- Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genes
- Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH : ubiquinone oxidoreductase flavoproteins
- Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families
- Frequent Allelic Loss at 7p14-15 Associated with Aggressive Histologic Types of Breast Cancer
- Mapping of a New Target Region of Allelic Loss to a 2-cM Interval at 22q 13.1 in Primary Breast Cancer
- Inverse correlation of the up-regulation of FZD10 expression and the activation of β-catenin in synchronous colorectal tumors
- A Single Nucleotide Polymorphism in the Matrix Metalloproteinase-1 Promoter in Endometrial Carcinomas
- Characterization of a VNTR polymorphism in the coding region of the CEL gene
- Allelic Loss on Chromosome 1p Is Associated with Progression and Lymph Node Metastasis of Primary Breast Carcinoma
- DINUCLEOTIDE REPEAT POLYMORPHISM ON CHROMOSOME 9q32
- Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes
- Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in children
- Mapping of a gene responsible for dermatitis in NOA (Naruto Research Institute Otsuka Atrichia) mice, an animal model of allergic dermatitis
- ESE-3, an Ets family transcription factor, is up-regulated in cellular senescence
- Expression profiles of two types of human knee-joint cartilage
- Herpes simplex virus-induced, death receptor-dependent apoptosis and regression of transplanted human cancers
- Isolation of p53-target genes and their functional analysis
- Infrequent Replication Errors at Microsatellite Loci in Tumors of Patients with Multiple Primary Cancers of the Esophagus and Various Other Tissues
- Identification of human leukocyte antigen-A24-restricted epitope peptides derived from gene products upregulated in lung and esophageal cancers as novel targets for immunotherapy
- Identification of secernin 1 as a novel immunotherapy target for gastric cancer using the expression profiles of cDNA microarray
- Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene
- 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
- Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population
- Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population
- Molecular Cytogenetic Analysis of 17 Renal Cancer Cell Lines: Increased Copy Number at 5q31-33 in Cell Lines from Nonpapillary Carcinomas
- Identification of novel polymorphisms in the AXIN1 and CDX-2 genes
- Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes (SMC) family
- Detection of novel cancer-testis antigen-specific T-cell responses in TIL, regional lymph nodes, and PBL in patients with esophageal squamous cell carcinoma
- Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
- Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
- Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population
- Orphan receptor tyrosine kinase ROR2 as a potential therapeutic target for osteosarcoma
- Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer
- Involvement of G-patch domain containing 2 overexpression in breast carcinogenesis
- Overexpression of the potential kinase serine/threonine/tyrosine kinase 1 (STYK 1) in castration-resistant prostate cancer
- Serum tumor antigen REG4 as a diagnostic biomarker in pancreatic ductal adenocarcinoma
- Identification of 45 novel SNPs in the 83-kb region containing peptidylarginine deiminase types 1 and 3 loci on chromosomal band 1p36. 13
- Allelic losses as prognostic markers for breast cancers
- Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1-cM Intervals on Genomic Contigs at 6q21 and 6q25.3
- Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3
- Molecular cloning and characterization of two novel genes on chromosome 8p21.3
- Identification of NOL8, a nucleolar protein containing an RNA recognition motif (RRM), which was overexpressed in diffuse-type gastric cancer
- Identification by differential display of eight known genes induced during in vivo intimal hyperplasia
- Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes
- Mutations in Zinc-binding Domains of p53 as a Prognostic Marker of Esophageal-cancer Patients
- Significantly elevated expression of PF4 (platelet factor 4) and eotaxin in the NOA mouse, a model for atopic dermatitis
- Phase I clinical trial using peptide vaccine for human vascular endothelial growth factor receptor 2 in combination with gemcitabine for patients with advanced pancreatic cancer
- Vaccination with multiple peptides derived from novel cancer-testis antigens can induced specific T-cell responses and clinical responses in advanced esophageal cancer
- 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
- Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients : four germline mutations, but no evidence of somatic mutation
- VNTR (variable number of tandem repeat) sequences as transcriptional, translational, or functional regulators
- Detection of Known Missense Mutation of hMLH1 in a Hereditary Non-Polyposis Colorectal Cancer Family Using DNA Extracts from Mouthwash Samples
- Dinucleotide repeat polymorphism in the first intron of the CSR gene
- VNTR sequence on human chromosome 11p15 that affects transcriptional activity
- Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes
- Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease
- Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma
- ALLELIC FREQUENCIES OF TWELVE DINUCLEOTIDE REPEAT MARKER LOCI ON CHROMOSOME 13 IN THE NORMAL JAPANESE POPULATION
- Validation of the histone methyltransferase EZH2 as a therapeutic target for various types of human cancer and as a prognostic marker
- Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene
- Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
- A novel tumor-associated antigen, cell division cycle 45-like can induce cytotoxic T-lymphocytes reactive to tumor cells
- SMYD3 interacts with HTLV-1 Tax and regulates subcellular localization of Tax
- APPLICATION OF DNA MARKERS TO CLINICAL GENETICS
- Cancer genomics
- Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population
- From cancer genomics to thoracic oncology : discovery of new biomarkers and therapeutic targets for lung and esophageal carcinoma
- A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
- Possible involvement of NEDD4 in keloid formation; its critical role in fibroblast proliferation and collagen production
- MRG-binding protein contributes to colorectal cancer development
- Identification of 156 novel SNPs in 29 genes encoding G-protein coupled receptors
- Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
- A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
- 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
- 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
- Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients
- A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma
- Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population
- ISOLATION OF p53-TARGET GENES AND THEIR FUNCTIONAL ANALYSIS
- PKIB expression strongly correlated with phosphorylated Akt expression in breast cancers and also with triple-negative breast cancer subtype
- A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese
- Impact of four loci on serum tamsulosin hydrochloride concentration
- Important and critical scientific aspects in pharmacogenomics analysis: lessons from controversial results of tamoxifen and CYP2D6 studies