Emi Mitsuru | Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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概要
- Emi Mitsuruの詳細を見る
- 同名の論文著者
- Department of Molecular Biology, Institute of Gerontology, Nippon Medical Schoolの論文著者
関連著者
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Emi Mitsuru
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Emi M
Department Of Neurology Hematology Metabolism Endocrinology And Diabetes Yamagata University School
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Emi Mitsuru
東京都老人医療センター
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Emi Mitsuru
山形大学 医学部循環･呼吸･腎臓内科学
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Emi Mitsuru
日本医科大学 第2生化
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Nagai Hisaki
日本医科大学老人病研究所
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Nagai H
Department Of Surgery Tokyo Women's Medical University Daini Hospital
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Nagai Hisaki
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Nagai Hisaki
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Nagai H
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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NAKAJIMA Toshiaki
Department of Molecular Biology-Institute of Gerontology, Nippon Medical School
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Nakajima Toshiaki
Department Of Ischemic Circulatory Physiology University Of Tokyo
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EZURA Yoichi
Department of Molecular Biology-Institute of Gerontology, Nippon Medical School
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Ezura Yoichi
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Nakajima T
Department Of Orthopedic Surgery University Of Occupational And Environmental Health
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江面 陽一
日本医科大学老人病研究所分子生物学教室
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Ezura Yoichi
日本医科大学老人病研究所 分子生物学
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Ezura Yoichi
日本医科大学 内科学第2
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Sakamoto Goi
Department of Surgery and Pathology, Cancer Institute Hospital
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Kasumi Fujio
Department of Surgery and Pathology, Cancer Institute Hospital
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Nakamura Yusuke
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of T
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Saito Yasushi
千葉大学 臨床遺伝子応用医学
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HOSOI Takayuki
Department of Advanced Medicine, National Center for Geriatrics and Gerontology
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Onda Masahiko
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Nakajima Toshiaki
東京医科歯科大学 疾患生命科学研究部ゲノム多様性
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三木 義男
癌研ゲノムセンター
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Akiyama Fumihiro
Human Genome Center The Institute Of Medical Science University Of Tokyo
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Inoue Satoshi
Department of Geriatric Medicine, University of Tokyo
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Matsumoto Satoshi
Department Of Pathology Nara Medical University
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Harada Haruhito
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Harada Haruhito
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Harada Haruhito
日本医科大学老人病研究所
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Harada Haruhito
Division Of Cardiovascular Disease Kurume University Medical Center
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Nagahata T
Nippon Medical School Kawasaki Jpn
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Nagahata Takemitsu
日本医科大学老人病研究所
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Nagahata Takemitsu
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Nagahata Takemitsu
東レ
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Nagahata Takemitsu
The Institute Of Molecular And Cellular Biology Osaka University
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SHIRAKI Masataka
Research Institute and Practice for Involutional Diseases
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UTADA Yoshihito
Department of Surgery, Tokyo Women's Medical University Daini Hospital.
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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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Aritoshi Iida
Laboratory For Pharmacogenetics Snp Research Center The Institute Of Physical And Chemical Research
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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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TAKADA Daisuke
Department of Molecular Biology-Institute of Gerontology and Department of Internal Medicine II, Nip
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Katagiri Toyomasa
京都大学 医学部外科学
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Tsuruo T
Division Of Experimental Chemotherapy Cancer Chemotherapy Center Japanese Foundation For Cancer Rese
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ARAKI Tsutomu
Department of Cardiology, Kanazawa Cardiovascular Hospital
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FUJITA Yuko
Department of Internal Medicine, Divisions of Neurology, Nephrology, and Rheumatology, Nippon Medica
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Takada Daisuke
日本医科大学老人病研究所 分子生物学
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Fujita Yuko
Department Of Internal Medicine Divisions Of Neurology Nephrology And Rheumatology Nippon Medical Sc
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Takada Daisuke
Nippon Medical School Tokyo Jpn
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Koyano Satoru
山形大学 医学部生命情報内科学分野
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Koyano Satoru
Department Of Neurology Hematology Metabolism Endocrinology And Diabetes Yamagata University School
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Koyano Satoru
山形大学 医学部消化器病態制御内科
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HUNT Steven
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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HOPKINS Paul
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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ONDA Masamitsu
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Kodama Tetsuro
栃木県立がんセンター研究所 がん遺伝子研究室
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HAGA Shunsuke
Department of Surgery, Tokyo Women's Medical University Daini Hospital.
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IINO Yasuhiko
Department of Internal Medicine, Divisions of Neurology, Nephrology, and Rheumatology, Nippon Medica
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KATAYAMA Yasuo
Department of Internal Medicine, Divisions of Neurology, Nephrology, and Rheumatology, Nippon Medica
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Iino Yasuhiko
日本医科大学 第二内科学教室
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Iino Yasuhiko
Department Of Internal Medicine Divisions Of Neurology Nephrology And Rheumatology Nippon Medical Sc
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Iino Yasuhiko
日本医科大学 内科学第1
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Tomino Yasuhiko
Department Of Nephrology Nippon Medical School
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Iino Y
Department Of Molecular Biology-institute Of Gerontology And Department Of Internal Medicine Ii Nipp
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Katayama Y
Department Of Internal Medicine Divisions Of Neurology Nephrology And Rheumatology Nippon Medical Sc
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Katayama Yasuo
日本医科大学 第二内科学教室
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NOBE Yukiko
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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WU Lily
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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STEPHENSON Susan
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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NAGAHATA Takemitsu
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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KONISHI Noboru
Department of Pathology, Nara Medical University
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Konishi N
Department Of Pathology Nara Medical University School Of Medicine
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Konishi Noboru
日本医科大学老人病研究所
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Tsuneizumi Michiko
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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SAITO Yasushi
Department of Clinical Cell Biology Graduate School of Medicine, Chiba University
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UMEMURA Satoshi
Yokohama City University
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BUJO Hideaki
Department of Genome Research and Clinical Application, Chiba University Graduate School of Medicine
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OUCHI Yasuyoshi
Department of Geriatric Medicine, University of Tokyo
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梶原 哲郎
Tochigi Cancer Center 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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Bujo Hideaki
筑波大学 人間総合科学研究科内分泌代謝･糖尿病内科
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Bujo Hideaki
Department Of Genome Research & Clinical Application Chiba University Graduate School Of Medicin
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Bujo Hideaki
Department Of Genome Research And Clinical Application And Department Of Clinical Cell Biology Chiba
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Shiba T
Department Of Medical Oncology The Cancer Institute Of Japanese Foundation For Cancer Research
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Ishigami Tomoaki
Department Of Medical Science And Cardiorenal Medicine Yokohama City University School Of Medicine
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KAMIMURA Kouhei
Awa Medical Association Hospital
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Kamimura K
Awa Medical Association Hospital
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Kamimura Kouhei
日本医科大学 第二内科学教室
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Emi Mitsuru
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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TERADA Yoshie
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Terada Y
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Terada Yoshie
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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SHIMIZU KAZUO
Department of Surgery, Cardiovascular Surgery, Nippon Medical School
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OGAWA OSAMU
Department of Urology, Faculty of Medicine, Kyoto University
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HABUCHI TOMONORI
Departments of Urology, Kyoto University Graduate School of Medicine
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YOKOTA Takashi
Department, of Information Science, Graduate School of Engineering, Utsunomiya University
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Ishigami Tomoaki
Department Of Cardiology Yokohama City University Hospital
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TAKAHASHI Kaneo
Awa Medical Association Hospital
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Takahashi Kaneo
Second Department Of Internal Medicine Nippon Medical School
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Kaneko Tomohiro
Nippon Medical School Tokyo Jpn
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XIN Yuanpei
Cardiovascular Genetics Research Clinic, University of Utah, Health Science Center
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TAJIRI Takashi
Department of Surgery I, Nippon Medical School
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KATO Takeo
Department of Neurology, Hematology, Metabolism, Endocrinology and Diabetology, Yamagata University
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HATTORI Hiroaki
Department of Advanced Technology and Development, BML, Inc.
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SHIMADA Takashi
Department of Applied Physics, The University of Tokyo
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KAWATA Sumio
Department of Gastroenterology, Yamagata University School of Medicine
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TERAMOTO Akira
Departments of Neurosurgery, Nippon Medical School
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Umemura Satoshi
Second Department of Internal Medicine, Yokohama City University Hospital
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Araki Kazuhiro
千葉大学フロンティアメディカル工学研究開発センター
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Tsubakio-yamamoto Kazumi
大阪大学 医学系研究科循環器内科学
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Nishida Makoto
Health Care Center Osaka University
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Ishigami Tomoaki
横浜市立大学 医学部第二内科学教室
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SATO Keiko
Department of Molecular Biology-Institute of Gerontology and Department of Internal Medicine II, Nip
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ONO Shuji
Department of Molecular Biology, Institute of Gerontology,Nippon Medical School
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ISHIGAMI Tomoaki
Second Department of Internal Medicine, Yokohama City University School of Medicine
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Ono S
Nippon Medical School Kawasaki Jpn
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Ono Shuji
日本医科大学老人病研究所
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Ishigami Tomoaki
Second Department Of Internal Medicine Yokohama City University School Of Medicine
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SUZUKI Hiroyoshi
Department of Urology, Graduate School of Medicine, Chiba University
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Nakamura Yusuke
Human genome center
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Umemura S
Department Of Internal Medicine And Cardiorenal Medicine Yokohama City University Graduate School Of
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YABE Aya
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Nagane Yutaka
Department Of Urology Sanai Hospital
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Nakazawa Ichiro
Department Of Regenerative Medicine
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Yabe Aya
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Kajiwara Tetsuro
Tochigi Cancer Center Hospital
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KUBOTA Isao
Department of Cardiology, Pulmonology and Nephrology, Yamagata University of School of Medicine
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Hattori Hiroaki
京都大学 医学研究科加齢医学
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Tanaka Shigeo
Department Of Disease Control And Homeostasis Kanazawa University
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OGAWA Sumito
Department of Geriatric Medicine, Graduate School of Medicine, University of Tokyo
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Umemura Satoshi
Department of medical science and cardiorenal medcine, Yokohama City University Graduate School of M
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Ishigami Tomoaki
Department of Cardiorenal Medicine, Yokohama City University Graduate School of Medicien
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EGASHIRA Tohru
Department of Advanced Technology and Development, BML, Inc.
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HATA Akira
Department of Public Health, Graduate School of Medicine, Chiba University
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Inagaki Miwako
大阪大学 医学系研究科循環器内科学
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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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Bujo H
Department Of Genome Research And Clinical Application Chiba University Graduate School Of Medicine
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Hata Akira
千葉大学 医学研究院公衆衛生学
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Katagiri T
Univ. Tokyo Tokyo Jpn
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KOMIYA Akira
Department of Urology, Graduate School of Medicine and Pharmaceutical Sciences for Research, Univers
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XIN Yunpei
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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LARRINAGA-SHUM Stacey
Cardiovascular Genetics Research Clinic, University of Utah Heart Science Center
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LARRINGA-SHUM Stacey
Cardiovascular Genetics Research Clinic, University of Utah, Health Science Center
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BABA Masaru
Department of Internal Medicine III, Mie University School of Medicine
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Baba Masaru
日本医科大学老人病研究所
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Baba Masaru
Department Of Internal Medicine Iii Mie University School Of Medicine
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Takahashi Hiroshi
Department of Cardiology, Nagoya Kyoritsu Hospital
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SATO Takaaki
Department of Biotechnology, The University of Tokyo
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Nagano M
Health Care Center Osaka University
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Egashira T
Department Of Advanced Medical Technology And Development Bml Inc.
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Egashira Tohru
京都大学 医学研究科加齢医学
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Egashira Tohru
Research Department R & D Center Bml Inc.
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Hiroaki Hattori
Department Of Cardiology Sumitomo Hospital
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Hattori Hiroaki
信州大学 院臓器発生制御学
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Sato Akira
Department of Cardiology, Yokosuka Kyosai Hospital
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Kazui Teruhisa
First Department of Surgery, Humamatsu University School of Medicine
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Nakamura Yusuke
Institute of Medical Science, University of Tokyo
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MIKI Yoshio
Department of Genetic Diagnosis, the Cancer Institute Hospital of JFCR
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Fujino Takahiro
The Second Department Of Internal Medicine Nihon University School Of Medicine
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SHIMADA Kazuyuki
Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical School
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HORIBE Hiroshi
Keisen Clinic
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Ishiwata Isamu
Ishiwata Obstetrics and Gynecology Hospital
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MAKINO Naohiko
Department of Gastroenterology, Yamagata University School of Medicine
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荒木 勉
大阪大学大学院 基礎工学研究科
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Ito Isao
Department Of Respiratory Medicine Graduate School Of Medicine Kyoto University
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TAKAHASHI Satoru
Department of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Me
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Ishigami Masato
Department Of Biomedical Informatics Division Of Health Sciences Osaka University Graduate School Of
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Tokunaga Katsushi
Department Of Clinical Pharmacology And Therapeutics Tohoku University Graduate School Of Pharmaceut
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KATAGIRI Toyomasa
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University
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MII Akiko
Department of Internal Medicine, Divisions of Neurology, Nephrology, and Rheumatology, Nippon Medica
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SATO Keiko
Second Department of Internal Medicine, Yokohama City University School of Medicine
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UEMURA Kouhei
Awa Medical Association Hospital
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Uemura Kouhei
Second Department Of Internal Medicine Nippon Medical School
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Katagiri Toyomasa
Laboratory Of Molecular Biosignal Research Center Kobe University School Of Medicine
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UEDA TAKESHI
Department of Urology, Chiba University
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ITO HARUO
Department of Urology, Chiba University
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AKIMOTO Susumu
Department of Urology, Chiba University School of Medicine
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NAGANO MAKOTO
Department of Gene Science, BML, Inc.
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KAWAMURA Katsumi
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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NOPKINS Paul
Cardiovascular Genetics Research Clinic, University of Utah, Health Science Center
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MINEGISHI Masaharu
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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HORIGUCHI Maya
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School
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Akiyama Fumihiro
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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Nakazawa Ichirou
日本医科大学老人病研究所
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Horiguchi Maya
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Minegishi Masaharu
Department Of Molecular Biology Institute Of Gerontology Nippon Medical School
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Kasugai Tsutomu
東京大学医科学研究所ヒトゲノム解析センター 分子医学
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SAITO Takafumi
Department of Gastroenterology, Yamagata University of School of Medicine
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TORIYAMA Sayumi
HuBit genomix Research Institute
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ISHII Miho
HuBit genomix Research Institute
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HATTORI Hiroaki
Research Department, R & D Center, BML, Inc.
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Kohro Takahide
Department of Translational Research for Healthcare and Clinical Science, The University of Tokyo
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KOBAYASHI Kenichi
The 1st Department of Internal Medicine, Kanazawa University School of Medicine
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Takahashi Masafumi
Department Of Cardiovascular Medicine Shinshu University Graduate School Of Medicine
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Kohro Takahide
Laboratory For System Biology And Medicine Rcast The University Of Tokyo
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Kohro Takahide
Department Of Cardiology Tokyo University School Of Medicine
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IKEDA Uichi
Department of Cardiovascular Medicine, Shinshu University Graduate School of Medicine
著作論文
- Overrepresentation of the EBAG9 Gene at 8q23 Associated with Early-Stage Breast Cancers
- Down-regulation of members of glycolipid-enriched membrane raft gene family, MAL and BENE, in cervical squamous cell cancers
- Genetic Association of Low-Density Lipoprotein Receptor-Related Protein 2 (LRP2) with Plasma Lipid Levels
- Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia
- Hypercholesterolemia associated with splice-junction variation of inter-α-trypsin inhibitor heavy chain 4 (ITIH4) gene
- A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia
- Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene
- G-substrate gene promoter SNP (-1323T>C) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia : Intra-familial association study in an eight-generation hyperlipidemic kindred
- Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia : intrafamilial association study in an eight-generation hyperlipidemic kindred
- Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter : molecular study in a 1135-member familial hypercholesterolemia kindred
- Characterization of liver-cirrhosis nodules by analysis of gene-expression profiles and patterns of allelic loss
- Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity
- Three Distinct Commonly Deleted Regions of Chromosome Arm 16q in Human Primary and Metastatic Prostate Cancers
- Localization of a Tumor Suppressor Gene Associated With Progression of Human Prostate Cancer Within a 1.2 Mb Region of 8p22-p21.3
- A 3-Mb Physical Map of the Chromosome Region 8p21.3-p22,Including a 600-kb Region Commonly Deleted in Human Hepatocellular Carcinoma, Colorectal Cancer, and Non-Small Cell Lung Cancer
- Clinical variant of Tangier disease in Japan : mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis
- Allelic Losses of Loci at 3p25.1,8p22,13q12,17p13.3,and 22q13 Correlate with Postoperative Recurrence in Breast Cancer
- Segmental Copy Number Loss of SFMBT1 Gene in Elderly Individuals with Ventriculomegaly: A Community-Based Study
- Genetic mapping of allelic loss on chromosome 6q within heterogeneous prostate carcinoma
- Identification of a 1-Mb Common Region at 16q24.1-24.2 Deleted in Hepatocellular Carcinoma
- Allelic Loss at 1p34,13q12,17p13.3,and 17q21.1 Correlates With Poor Postoperative Prognosis in Breast Cancer
- Identification of a 1-cM Region of Common Deletion on 4q35 Associated With Progression of Hepatocellular Carcinoma
- Correlation of Allelic Loss with Poor Postoperative Survival in Breast Cancer
- PTEN/MMAC1 Mutations in Hepatocellular Carcinomas: Somatic Inactivation of Both Alleles in Tumors
- 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
- Expression profiling to predict postoperative prognosis for estrogen receptor-negative breast cancers by analysis of 25,344 genes on a cDNA microarray
- Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers
- Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers
- Upregulation and Overexpression of Human X-box Binding Protein 1 (hXBP-1) Gene in Primary Breast Cancers
- Amplification, up-regulation and over-expression of DVL-1, the human counterpart of the Drosophila disheveled gene, in primary breast cancers
- Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in Japan
- Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
- Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer
- Association of common missense changes in ELAC2 (HPC2) with prostate cancer in a Japanese case-control series
- Genomic Structure and Mapping of Human Orphan Receptor LXR Alpha : Upregulation of LXRa mRNA During Monocyte to Macrophage Differentiation
- Genetic Association between Aldehyde Dehydrogenase 2 (ALDH2) Variation and High-Density Lipoprotein Cholesterol (HDL-C) Among Non-Drinkers in Two Large Population Samples in Japan
- Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations
- Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients
- Correlation of Allelic Losses and Clinicopathological Factors in 504 Primary Breast Cancers
- Association of Allelic Losses at 3p25.1, 13q12, or 17p13.3 with Poor Prognosis in Breast Cancers with Lymph Node Metastasis
- Allelic Loss at 1p34-36 Predicts Poor Prognosis in Node-negative Breast Cancer
- DNA alterations during multi-step development of human hepatocellular carcinomas revealed by laser capture microdissection
- Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase : comparison of exon/intron organization of sterol-sensing domains among four related genes
- Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene
- Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers
- Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line
- Two Target Regions of Allelic Loss on Chromosome 9 in Urinary-bladder Cancer
- Mapping of a New Target Region of Allelic Loss to a 6-cM Interval at 21q21 in Primary Breast Cancers
- Hypermethylation associated with inactivation of the SOCS-1 gene, a JAK/STAT inhibitor, in human hepatoblastomas
- Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
- Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women
- Association of a single-nucleotide polymorphism in the promoter region of leukemia inhibitory factor receptor gene with low bone mineral density in adult women
- Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene
- Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density
- Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women
- Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women
- Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss
- Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals
- Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene
- Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene
- Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus
- Two Distinct Commonly Deleted Regions on Chromosome 13q Suggest Involvement of BRCA2 and Retinoblastoma Genes in Sporadic Breast Carcinomas
- PRLTS Gene Alterations in Human Prostate Cancer
- A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density
- Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus
- Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis
- Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women
- The important role for βVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptor
- Down-regulation in Multiple Human Cancers of a Novel Gene, DMHC, from 17q25.1 That Encodes an Integral Membrane Protein
- Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers
- Genomic organization and chromosomal mapping of ELKS, a gene rearranged in a papillary thyroid carcinoma
- Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japa
- Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia : A Molecular Study in an Eight-generation Hyperlipidemic Family
- Three Aberrant Splicing Variants of the HMGIC Gene Transcribed in Uterine Leiomyomas
- 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
- Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene
- Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene
- Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene
- Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene
- Familial Hypercholesterolemia with Cholesteryl Ester Traansfer Protein Deficiency
- Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure
- Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locus
- Fusion of a Novel Gene, ELKS, to RET Due to Translocation t(10;12)(q11;p13) in a Papillary Thyroid Carcinoma
- Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities
- A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia
- Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes : genomic structure and seven polymorphisms of the FAP-1 gene
- Genomic structure and eight novel exonic polymorphisms of the human N-cadherin gene
- Allelic Loss on Chromosome 1p Is Associated with Progression and Lymph Node Metastasis of Primary Breast Carcinoma
- Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method
- Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene
- The c-Jun NH_2-terminal kinase3 (JNK3) gene : genomic structure, chromosomal assignment, and loss of expression in brain tumors
- Nine novel single-nucleotide polymorphisms in the integrin β4 (ITGB4) gene in the Japanese population
- Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene
- Human calcitonin receptor-like receptor for adrenomedullin : genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis
- Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability
- Frameshift Mutations and a Length Polymorphism in the hMSH3 Gene and the Spectrum of Microsatellite Instability in Sporadic Colon Cancer
- A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus
- Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus
- Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus
- A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFAα) locus
- Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus
- Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus
- A polymorphic CA repeat sequence at the human calcitonin locus
- Fusion of a Sequence from HEI10 (14q11) to the HMGIC Gene at 12ql5 in a Uterine Leiomyoma
- Allelic losses as prognostic markers for breast cancers
- Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas
- Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenoposal Japanese women
- Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1-cM Intervals on Genomic Contigs at 6q21 and 6q25.3
- Somatic Mutations of the PTEN/MMAC1 Gene in Fifteen Japanese Endometrial Cancers : Evidence for Inactivation of Both Alleles
- Localization of a Target Region of Allelic Loss to a 1-cM Interval on Chromosome 16p.13.13 in Hepatocellular Carcinoma
- Two single nucleotide polymorphisms of the hSNF5/INI1 gene
- A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene
- Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients : four germline mutations, but no evidence of somatic mutation
- A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene
- Association of amino acid variation (Trp64Arg) in the beta3-adrenergic receptor gene with bone mineral density
- Ethnic difference in contribution of alleles of the interleukin-1 receptor antagonist gene to predisposition to osteoporosis