Watanabe Atsushi 渡邉淳

… Alternative Names

Researcher Number	10307952
Affiliation (Current)	2020: 金沢大学, 附属病院, 特任教授
Affiliation (based on the past Project Information) *help	2020: 金沢大学, 附属病院, 特任教授 2018: 金沢大学, 附属病院, 特任教授 2017: 日本医科大学, 医学部, 助手 2011 – 2017: 日本医科大学, 医学部, 准教授 2010: 日本医科大学, 医学部, 講師 … More
Review Section/Research Field	Principal Investigator Pathological medical chemistry / 医療における生命倫理 / Thoracic surgery / Applied health science / Pediatrics Except Principal Investigator Pediatrics / Science education / Plastic surgery / Otorhinolaryngology / Human genetics … More
Keywords	Principal Investigator トリプレット病 / ミスマッチ修復遺伝子 / 臨床遺伝教育 / 遺伝学 / 医学教育 / 生命倫理 / 遺伝情報 / 臨床遺伝教育プログラム / 心臓大血管外科学 / 家族性大動脈瘤 … More Except Principal Investigator 遺伝子治療 / 遺伝子 / Cochlin / Gene therapy / 健康教育 / 遺伝病 / ケロイド / ＩＬ－６ / ＳＮＰ / 遺伝子解析 / IL-6 / SNP / 一塩基多型 / COCH遺伝子 / 内耳特異的 / アイソフォーム / Coch gene / Inner ear specific / isoform / ウイルスベクター / 血液脳関門 / リソゾーム病 / マンノース-6-リン酸受容体 / 異染性白質ジストロフィー / アリルスルファターゼ / マンノース6リン酸 / トランスサイトーシス / Viral vector / Blood brain barrier / Lysosomal diseases / Mannose-6 phosp[hate receptor / Metachromatic leukodystrophy / ヒトの遺伝教育 / 中等教育 / ゲノムリテラシー / エーラスダンロス症候群 / 新規病型 / 結合組織疾患 / 次世代シーケンス / 候補遺伝子解析 / 全エクソーム解析 / 国際情報交換 / 再生・細胞医療 / 低ホスファターゼ症 / 骨髄幹細胞 / 造血幹細胞 / 骨格筋芽細胞 / レンチウイルスベクター / アルカリホスファターゼ / 低フォスファターゼ症 / アルカリフォスファターゼ / 生命科学教育 / 幼児教育プログラム / 生物の多様性と共通性 / 生物の共通性と多様性 / 科学教育 / 科学教育カリキュラム / 学際的幼児教育プログラム / モヤモヤ病 / 内頸動脈瘤 / RNF / 内頸動脈狭窄 / もやもや病 / RNF213 / 血管狭窄 / 遺伝教育 / 遺伝看護 / 遺伝子ドーピング / リキッドバイオプシー / クリスパーキャス / アスリート遺伝リテラシー / ＮＧＳの2次所見 / STEAM教育 / コンピテンス基盤型教育 / 幼児 / 児童 Less

初等・中等教育における遺伝学を用いた命の学習プログラム開発と導入に向けた検討Ongoing
- Principal Investigator
  
  森藤香奈子
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 58070:Lifelong developmental nursing-related
- Research Institution
  Nagasaki University
In search of analytical method for genetic testingOngoing
- Principal Investigator
  
  竹越一博
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 59020:Sports sciences-related
- Research Institution
  University of Tsukuba
幼少期から自らの健康を保持・増進できるコンピテンスを育むSTEAM教育の検討Ongoing
- Principal Investigator
  
  石沢順子
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 09080:Science education-related
- Research Institution
  Shirayuri College
Identification of expression mechanism by comprehensive gene analysis of Moyamoya disease analogous vascular stenosisOngoing
- Principal Investigator
  
  村井保夫
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56010:Neurosurgery-related
- Research Institution
  Nippon Medical School
新しい生命科学教育の根幹を担う日本独自の学際的幼児教育プログラムの開発Ongoing
- Principal Investigator
  
  大貫麻美
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Science education
- Research Institution
  Shirayuri College
Clarification of issues and measures for introducing "human genetics" to school education
- Principal Investigator
  
  SASAKI MOTOKO
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Science education
- Research Institution
  Ochanomizu University
  Nippon Medical School
Investigations for tasks toward development of literacy for human genetics to a citizen and making programsPrincipal Investigator
- Principal Investigator
  
  WATANABE ATSUSHI
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Applied health science
- Research Institution
  Nippon Medical School
Clinical and molecular investigation for new forms of Ehlers-Danlos syndrome
- Principal Investigator
  
  KOSHO Tomoki
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University
Development of regenerative medicine and cell therapy for inherited metabolic diseases using hypophosphatasia mice
- Principal Investigator
  
  Iijima Osamu
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Nippon Medical School
A polymorphysm in the IL-6 promotor region associated with the keloid in the Japanease population
- Principal Investigator
  
  MAMIKO Tosa
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Plastic surgery
- Research Institution
  Nippon Medical School
Perinatal gene therapy for severe genetic diseases
- Principal Investigator
  
  SHIMADA Takashi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Nippon Medical School
Development and classification of therapeutic method for vascularEhlers-Danlos syndrome by mutation typesPrincipal Investigator
- Principal Investigator
  
  WATANABE Atsushi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Thoracic surgery
- Research Institution
  Nippon Medical School
An investigation for tasks and development of self-study materials for effective educational programs of clinical geneticsPrincipal Investigator
- Principal Investigator
  
  WATANABE Atsushi
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  医療における生命倫理
- Research Institution
  Nippon Medical School
Non-invasive gene therapy for inherited neurodegenerative disorders (How to cross the BBB?)
- Principal Investigator
  
  SHIMADA Takashi
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Nippon Medical School
Analysis of shift in brain with film penetration peptide uniting enzyme for nerve type Gaucher disease treatmentPrincipal Investigator
- Principal Investigator
  
  WATANABE Atsushi
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Nippon Medical School
Inner ear specifc gene therapy using COCH promoter
- Principal Investigator
  
  IKEZONO Tetsuo
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Nippon Medical School
トリプレット病におけるミスマッチ修復遺伝子の関与及び治療に関する研究Principal Investigator
- Principal Investigator
  
  渡邉淳
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Nippon Medical School

[Book] 【最新遺伝医学研究と遺伝カウンセリング(シリーズ3)　最新多因子遺伝性疾患研究と遺伝カウンセリング】 (第5章)多因子疾患の遺伝情報と社会　社会における遺伝リテラシー向上2018
- Author(s)
  渡邉　淳
- Total Pages
  6
- Publisher
  メディカルドゥ
- ISBN
  4944157266
- Data Source
  KAKENHI-PROJECT-15K12395
[Book] 診療・研究にダイレクトにつながる遺伝医学2017
- Author(s)
  渡邉　淳
- Total Pages
  245
- Publisher
  羊土社
- Data Source
  KAKENHI-PROJECT-26560385
[Book] コルフ臨床遺伝医学2014
- Author(s)
  渡邉　淳　（櫻井晃洋編）
- Total Pages
  320
- Publisher
  丸善出版
- Data Source
  KAKENHI-PROJECT-26560385
[Book] Ehlers-Danlos 症候群.先天代謝異常ハンドブック遠藤文夫(総編集)2013
- Author(s)
  渡邉淳,島田隆
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22591554
[Book] Ehlkers-Danlos 症候群　（分担）先天代謝異常ハンドブック2013
- Author(s)
  渡邉淳
- Total Pages
  440
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22591554
[Book] Prenatal diagnosis of severe perinatal (lethal) hypophosphatasia.2012
- Author(s)
  Watanabe, A., Orimo, H., Takeshita, T., Shimada, T.
- Publisher
  Prenatal Diagnosis - Morphology Scan and Invasive Methods (Edited by Richard Choy) InTech.
- Data Source
  KAKENHI-PROJECT-22390212
[Book] 遺伝情報を診療で活用するための課題, 生命倫理(玉井真理子、大谷いづみ(編))2009
- Author(s)
  渡邉淳
- Publisher
  有斐閣2009(in press)
- Data Source
  KAKENHI-PROJECT-19602005
[Book] 生命倫理遺伝情報を診療で活用するための課題.2009
- Author(s)
  渡邉淳(玉井真理子, 大谷いづみ, 他編集)
- Publisher
  知泉書館(In press)
- Data Source
  KAKENHI-PROJECT-19602005
[Book] トンプソン&トンプソン遺伝医学, 第3章ヒトゲノム : 遺伝子の構造と機能(福嶋義光監訳)2009
- Author(s)
  渡邉淳(訳)
- Publisher
  メディカル・サイエンス・インターナショナル, 東京
- Data Source
  KAKENHI-PROJECT-19602005
[Book] 血管型 Ehlers-Danlos症候群の遺伝診療とその課題, 遺伝診療をとりまく社会(吉田雅幸, 小笹由香(編))2007
- Author(s)
  渡邉淳、島田隆
- Publisher
  ブレーン出版
- Data Source
  KAKENHI-PROJECT-19602005
[Book] 遺伝診療をとりまく社会その科学的・倫理的アプローチ2007
- Author(s)
  渡邉淳(吉田雅幸他編集)
- Total Pages
  181
- Publisher
  ブレーン出版
- Data Source
  KAKENHI-PROJECT-19602005
[Journal Article] 学校教育における「ヒトの遺伝・遺伝学」導入の実践2018
- Author(s)
  渡邉淳、市石博、巽純子、中川奈保子、松田雅代、米田勝将、武田正道、大野智久、菅野治虫、佐々木元子、田村和朗、櫻井晃洋
- Journal Title
  
  生物の科学「遺伝」
  
  Volume: 72 Pages: 86-92
- Data Source
  KAKENHI-PROJECT-15K12395
[Journal Article] 希少疾患の児童との向き合い方2017
- Author(s)
  渡邉淳
- Journal Title
  
  こどもと保健
  
  Volume: 95 Pages: 10-11
- Data Source
  KAKENHI-PROJECT-15K12395
[Journal Article] 衛生検査所における遺伝子関連検査・染色体検査の受託状況.2016
- Author(s)
  藤本英也, 渡邉淳, 堤正好, 山口敏和, 伊藤尚志, 権藤延久, 神山誠, 菅野康吉, 野村文夫
- Journal Title
  
  日本遺伝カウンセリング学会誌
  
  Volume: 37 Pages: 143-148
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26560385
[Journal Article] Treatment of Hypophosphatasia by muscle-directed expression of bone-targeted alkaline phosphatasia via self-complementary AAV8 vector.2016
- Author(s)
  Nakamura-Takahashi,A., Miyake,K., Watanabe, A., Hirai, Y., Iijima, O., Miyake, N., Adachi K.,, Nitahara-Kasahara, Y., Kinoshita, H., Noguchi, T., Abe, S., Narisawa, S., Millán, J. L., Shimada, T.,Okada, T.
- Journal Title
  
  Mol Ther Methods Clin Dev.
  
  Volume: 3 Pages: 15059-15059
- DOI
  10.1038/mtm.2015.59
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-25460407, KAKENHI-PROJECT-25461564, KAKENHI-PROJECT-26293328
[Journal Article] 遺伝学的検査を扱う際に知っておくべきガイドラインの概要2015
- Author(s)
  渡邉淳，武田（岡崎）恵利，佐々木元子
- Journal Title
  
  遺伝子医学MOOK
  
  Volume: 28 Pages: 222-227
- Data Source
  KAKENHI-PROJECT-15K12395
[Journal Article] Prevention of Lethal Murine Hypophosphatasia by Neonatal Ex Vivo Gene Therapy Using Lentivirally Transduced Bone Marrow Cells.2015
- Author(s)
  Iijima O, Miyake K, Watanabe A, Miyake N, Igarashi T, Kanokoda C, Nakamura-Takahashi A, Kinoshita H, Noguchi T, Abe S, Narisawa S, Millán JL, Okada T, Shimada T.
- Journal Title
  
  Hum Gene Ther.
  
  Volume: 26 Pages: 801-12
- DOI
  10.1089/hum.2015.078
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09604, KAKENHI-PROJECT-26461596, KAKENHI-PROJECT-25461564
[Journal Article] 第4章遺伝カウンセリングとその周辺　１．遺伝学的検査を扱う際に知っておくべきガイドラインの概要．2015
- Author(s)
  渡邉淳，武田（岡崎）恵利，佐々木元子.
- Journal Title
  
  遺伝子医学MOOK
  
  Volume: 28 Pages: 222-7
- Data Source
  KAKENHI-PROJECT-26560385
[Journal Article] Perinatal hypophosphatasia caused by uniparental isodisomy2014
- Author(s)
  Watanabe A, Satoh S, Fujita A, Naing BT, Orimo H, Shimada T.
- Journal Title
  
  Bone
  
  Volume: 60 Pages: 93-97
- DOI
  10.1016/j.bone.2013.12.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461564, KAKENHI-PROJECT-26560385
[Journal Article] Successful gene therapy in utero for lethal murine hypophosphatasia.2012
- Author(s)
  Sugano H, Matsumoto T, Miyake K, Watanabe A, Iijima O, Migita M, Narisawa S, Millan JL, Fukunaga Y, Shimada T.
- Journal Title
  
  Hum Gene Ther
  
  Volume: 23 Pages: 399-406
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Banyar ThanNaing, Shimada T, Fujimoto W, NinomiyaS, Ueda Y, Kondo E, Yamanouchi Y, Ouchi K, Kuroki Y. Ehlers-Danlos Syndrome, Vascular Type: A Novel Missense Mutation in COL3A1 Gene.2012
- Author(s)
  Masuno M, Watanabe A
- Journal Title
  
  Congenit Anom
  
  Volume: 52 Pages: 207-210
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Successful gene therapy in utero for lethal murine hypophosphatasia.2012
- Author(s)
  Sugano, H., Matsumoto, T., Miyake, K., Watanabe, A., Iijima, O., Migita, M., Narisawa, S., Millan, J.L., Fukunaga, Y., Shimada, T.
- Journal Title
  
  Hum. Gene Ther.
  
  Volume: 23 Pages: 399-406
- Data Source
  KAKENHI-PROJECT-22390212
[Journal Article] Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers.2011
- Author(s)
  Watanabe A, Karasugi T, Sawai H, Banyar Tang Naing, Ikegawa S, Orimo H, Shimada S.
- Journal Title
  
  J Hum Genet
  
  Volume: 56 Pages: 166-168
- NAID
  10030658012
- Data Source
  KAKENHI-PROJECT-22390212
[Journal Article] Ehlers-Danlos 症候群の基礎2011
- Author(s)
  渡邉淳 , 島田隆
- Journal Title
  
  日本胸部臨床
  
  Volume: 70 Pages: 319-328
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] A novel mutation screening system for Ehlers-Danlos Syndrome, vascular type by high-resolution melting curve analysis in combination with small amplicon genotyping using genomic DNA.2011
- Author(s)
  Banyar Than Naing, Watanabe A, Shimada T
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: 405 Pages: 368-372
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypopho sphatasia in Japanese and effects of the mutation on heterozygous carriers.2011
- Author(s)
  Watanabe, A.
- Journal Title
  
  J Hum Genet.
  
  Volume: 56 Pages: 166-168
- NAID
  10030658012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390212
[Journal Article] Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers2011
- Author(s)
  Watanabe A.
- Journal Title
  
  J Hum Genet
  
  Volume: 56 Pages: 166-168
- NAID
  10030658012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390212
[Journal Article] Ehlers-Danlos症候群の基礎2011
- Author(s)
  渡邉淳
- Journal Title
  
  日本胸部臨床
  
  Volume: 70 Pages: 319-328
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] 難治性疾患克服事業による血管型エーラスダンロス症候群の実態調査2010
- Author(s)
  古庄知己, 渡邉淳 ,森崎裕子,福嶋義光,籏持淳
- Journal Title
  
  日本遺伝カウンセリング学会誌
  
  Volume: 31 Pages: 157-161
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Targeted gene delivery to selected liver segments via isolated hepatic perfusion.2010
- Author(s)
  Kinoshita H, Watanabe A, Hisayasu S, Suzuki S, Shimada T
- Journal Title
  
  J Surg Res
  
  Volume: 160 Pages: 47-51
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Pleuropulmonary pathology of vascular Ehlers-Danlos syndrome: Laceration, haematoma, and fibrous nodules.2010
- Author(s)
  Kawabata Y, Watanabe A, Yamaguchi S, Aoshima M, Shiraki A, Hatamochi A, Kawamura T, Uchiyama T, Watanabe A, Fukuda Y
- Journal Title
  
  Histopathology
  
  Volume: 56 Pages: 944-950
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Too friable to treat?2010
- Author(s)
  Kimura K, Sakai-Kimura M, Takahashi R, Watanabe A, Mukai M, Noma S, Fukuda K
- Journal Title
  
  Lancet
  
  Volume: 375 Pages: 1578-1578
- Data Source
  KAKENHI-PROJECT-22591554
[Journal Article] Global Diffuse Distribution in the Brain and Efficient Gene Delivery to the Dorsal Root Ganglia by Intrathecal Injection of AAV1 Vector2009
- Author(s)
  Iwamoto, N., Watanabe, A., Yamamoto, M., Miyake, N., Kurai, T., Teramoto, A., Shimada, T.
- Journal Title
  
  J.Gene Med. (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] 医学部における臨床遺伝教育-日本医科大学の試み-2007
- Author(s)
  渡邉淳、浅野ありさ、三宅秀彦、右田真、平井幸彦、志村俊郎、島田隆
- Journal Title
  
  医学教育 38
  
  Pages: 245-250
- NAID
  10019965543
- Data Source
  KAKENHI-PROJECT-19602005
[Journal Article] The establishment of an ethics consultation system in clinical genetics Trial at the Nippon Medical School Main Hospital2007
- Author(s)
  Watanabe A, Shimada T
- Journal Title
  
  Journal of Philosophy and Ethics in Health Care and Medicine 2
  
  Pages: 66-82
- Data Source
  KAKENHI-PROJECT-19602005
[Journal Article] 医学部における臨床遺伝教育-日本医科大学の試み-2007
- Author(s)
  渡邉淳
- Journal Title
  
  医学教育 38
  
  Pages: 245-250
- NAID
  10019965543
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19602005
[Journal Article] The establishment of an ethics consultation system in clinical genetics Trial at the Nippon Medical School Main Hospital2007
- Author(s)
  A Watanabe
- Journal Title
  
  Journal of Philosophy and Ethics in Health Care and Medicine 2
  
  Pages: 66-82
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19602005
[Journal Article] Mutations of the p53 cDNA sequence introduced by the retroviral vector2006
- Author(s)
  Su, S., Watanabe, A., Yamamoto, M., Nakajima, E., Miyake, K., Shimada, T.
- Journal Title
  
  Biochem.Biophys.Res.Commun. 340
  
  Pages: 567-572
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Mutations of the p53 cDNA sequence introduced by the retroviral vector2006
- Author(s)
  Su, S., Watanabe, A., et al
- Journal Title
  
  Biochem. Biophys. Res. Commun. 340
  
  Pages: 567-572
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Targeted gene delivery to selected liver segments via isolated hepatic perfusion2006
- Author(s)
  Kinoshita, H., Watanabe, A., et al
- Journal Title
  
  J. Surg. Res. in press
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Adeno-associated virus 2-mediated intratumoral prostate cancer gene therapy : long-term maspin expression efficiently suppresses tumor growth.2005
- Author(s)
  Watanabe,M., et al.
- Journal Title
  
  Hum Gene Ther. 16
  
  Pages: 699-710
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Adeno-associated virus-mediated human IL-10 gene transfer suppresses the development of experimental autoimmune orchitis.2005
- Author(s)
  Watanabe,M., et al.
- Journal Title
  
  Gene Ther. 12
  
  Pages: 1126-1132
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Adeno-associated virus-mediated human IL-10 gene transfer suppresses the development of experimental autoimmune orchitis2005
- Author(s)
  Watanabe, M., Kashiwakura, Y., Kusumi, N., Tamayose, K., Nasu, Y., Nagai, A., Shimada, T., Daida, H., Kumon, H.
- Journal Title
  
  Gene Ther. 12
  
  Pages: 1126-1132
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Adeno-associated virus 2-mediated intratumoral prostate cancer gene therapy : long-term maspin expression efficiently suppresses tumor growth2005
- Author(s)
  Watanabe, M., Nasu, Y., Kashiwakura, Y., Kusumi, N., Tamayose, K., Nagai, A., Sasano, T., Shimada, T., Daida, H., Kumon, H.
- Journal Title
  
  Hum Gene Ther. 16
  
  Pages: 699-710
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17390305
[Journal Article] Identification of a novel Cochlin isoform in the perilymph : insights to Cochlin function and the pathogenesis of DFNA9.2004
- Author(s)
  Ikezono T, Shindo S, Li L, Omori A, Ichinose S, Watanabe A, Kobayashi T, Pawankar R, Yagi T.
- Journal Title
  
  Biochem Biophys Res Commun. 314(2)
  
  Pages: 440-446
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14571644
[Journal Article] Identification of the protein product of the Coch gene- hereditary deafness gene - as the major component of bovine inner ear protein.2001
- Author(s)
  Ikezono T, Omori A, Ichinose S, Pawankar R, Watanabe A, Yagi T.
- Journal Title
  
  Biochimica Biophysica Acta-Molecular Basis of Disease 1535(3)
  
  Pages: 258-265
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14571644
[Patent] 家族性大動脈瘤の遺伝子変異スクリーニング方法に関する特許1件2011
- Inventor(s)
  渡邉淳、島田隆
- Industrial Property Rights Holder
  日本医科大学
- Acquisition Date
  2011-03-17
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] 中等教育（中学校・高校）での取り組み（３）―遺伝カウンセラーと教員の2つの視点から―2018
- Author(s)
  佐々木元子、渡邉淳
- Organizer
  第41回日本遺伝カウンセリング学会学術集会　市民公開講座『学校教育における「ヒトの遺伝・遺伝学」導入の実践―初等・中等教育において「ヒトの遺伝」をどのように導入するか』
- Invited
- Data Source
  KAKENHI-PROJECT-15K12395
[Presentation] Genetic Education for Undergraduate Medical Students in Japan2016
- Author(s)
  Atsushi WATANABE
- Organizer
  13th International Congress of Human Genetics in 2016 (ICHG2016)
- Place of Presentation
  Kyoto
- Year and Date
  2016-04-07
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26560385
[Presentation] 認定遺伝カウンセラーとしての役割2016
- Author(s)
  佐々木元子、渡邉淳
- Organizer
  第23回日本遺伝子診療学会シンポジウム「遺伝学的検査情報に関連する臨床現場の情報フローについて」
- Place of Presentation
  東京
- Year and Date
  2016-10-06
- Invited
- Data Source
  KAKENHI-PROJECT-15K12395
[Presentation] 中等教育担当者との協働活動の取り組み2015
- Author(s)
  渡邉淳
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京都
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-15K12395
[Presentation] Rescue of lethal murine hypophosphatasia using genetically modified bone marrow cells expressing bone-targeted tissue non-specific alkaline phosphatase.2015
- Author(s)
  Iijima O, Miyake K, Watanabe A, Miyake N, Igarashi T, Kanokoda C, Nakamura-Takahashi A, Kinoshita H, Noguchi T, Abe S, Narisawa S, Millan JL, Okada T, Shimada T.
- Organizer
  第11回ALPS研究会
- Place of Presentation
  日本女子大学（東京都）
- Year and Date
  2015-07-18
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] Natural history of dermatan 4-O-sulfotransferase 1 (D4ST1)-deficient Ehlers-Danlos Syndrome (DDEDS): from an international collaborative clinical study by the International Consortium for EDS.2015
- Author(s)
  Kosho T, Syx D, Van Damme T, Morisaki H, Kawame H, Sonoda T, Hilhorst-Hofstee Y, Maugeri A, Voermans N, Mendoza-Londono R, Wierenga K, Jayakar P, Ishikawa K, Kobayashi T, Aoki Y, Watanabe S, Ohura T, Kono M, Mochida K, Morisaki T, Miyake N, Malfait F.
- Organizer
  American Society of Human Genetics 65nd Annual Meeting, Baltimore
- Place of Presentation
  Baltimore Convention Center（米国）
- Year and Date
  2015-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460405
[Presentation] Prolonged Survival and Improved Phenotypes of Lethal Hypophosphatasia Model Mice By Adeno-Associated Virus Mediated Muscle Transduction of Bone-Targeted Alkaline Phosphatase.2015
- Author(s)
  Nakamura A, Miyake K, Watanabe A, Hirai Y, Miyake N, Iijima O, Adachi K, Kinoshita H, Noguchi T, Abe S, Shimada T, Okada T.
- Organizer
  18th American Society of Gene and Cell Therapy Annual Meeting
- Place of Presentation
  Hyatt Regency New Orleans（New Orleans, LA）
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] Gene therapy to rescue lethal hypophosphatasia model mice by adeno-associated virus-mediated muscle transduction of bone-targeted alkaline phosphatase.2015
- Author(s)
  Nakamura A, Miyake K, Watanabe A, Hirai Y, Iijima O, Miyake N, Adachi K, Nitahara-Kasahara Y, Kinoshita H, Noguchi T, Abe S, Narisawa S, Millan JL, Shimada T, Okada T.
- Organizer
  第21回日本遺伝子治療学会学術集会
- Place of Presentation
  大阪国際会議場（大阪府）
- Year and Date
  2015-07-23
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] Long-term enzyme replacement therapy for hypophosphatasia by muscle-directed expression of bone targeted alkaline phosphatase using self-complementary AAV8 vector.2015
- Author(s)
  Nakamura-Takahashi A, Miyake K, Watanabe A, Hirai Y, Iijima O, Miyake N, Adachi K, Nitahara-Kasahara Y, Kinoshita H, Noguchi T, Abe S, Narisawa S, Millan JL, Shimada T, Okada T.
- Organizer
  第11回ALPS研究会
- Place of Presentation
  日本女子大学（東京都）
- Year and Date
  2015-07-18
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] 中等教育担当者との協働活動の取り組み．遺伝関連学会合同シンポジウム「ヒトの遺伝教育の充実に向けて」2015
- Author(s)
  渡邉淳
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京
- Year and Date
  2015-10-14
- Invited
- Data Source
  KAKENHI-PROJECT-26560385
[Presentation] ヒトの遺伝リテラシー向上を目指した遺伝医学関連学会の取組「初等・中等教育家課程における『ヒトの遺伝学』教育の課題と推進方策」2014
- Author(s)
  渡邉　淳
- Organizer
  日本学術会議第二部会主催公開シンポジウム
- Place of Presentation
  お茶の水女子大学
- Year and Date
  2014-09-06
- Data Source
  KAKENHI-PROJECT-26560385
[Presentation] Bone marrow cell based enzyme replacement prolongs survival and improves disease phenotypes in a mouse model of lethal hypophosphatasia2013
- Author(s)
  Iijima O, Miyake K, Nakamura A, Igarashi T, Kanokoda C, Watanabe A, Shimada T
- Organizer
  55th American Society of Hematology Annual Meeting and Exposition
- Place of Presentation
  Ernest N. Morial Convention Center (New Orleans, LA, USA)
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] ケロイド患者におけるIL-6関連遺伝子多型パターンと臨床像との関連について2013
- Author(s)
  土佐眞美子、渡邉　淳、村上正洋、ガジザデ・モハマッド
- Organizer
  第56回日本形成外科学会総会
- Place of Presentation
  京王プラザホテル
- Data Source
  KAKENHI-PROJECT-24592723
[Presentation] 低フォスファターゼ症マウスに対するex vivo遺伝子治療法の検討2013
- Author(s)
  飯島　修、三宅弘一、中村有希、鹿子田千津、五十嵐勉、渡邉　淳、島田　隆
- Organizer
  第58回日本人類遺伝学会
- Place of Presentation
  江陽グランドホテル（宮城県仙台市）
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] n intronic mutation affecting pre-mRNA splicing in the COL3A1 gene as novel mechanisms causing vascular Ehlres-Danlos syndrome.2012
- Author(s)
  A. Watanabe
- Organizer
  Annual meeting of American Society of Human Genetics
- Place of Presentation
  サンフランシスコ
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Phenotype differences in patients with nonsense mutations of COL3A1 causing nonsense-medicated mRNA decay in vascular Ehlers-Danlos Syndrome.2012
- Author(s)
  Naing BT,Watanabe A, Hatamochi A, Morisaki H , Shimada T.
- Organizer
  First International Symposium on the Ehlers-Danlos Syndrome.
- Place of Presentation
  Ghent, Belgium
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] A novel gene therapy strategy for vascular Ehlers-Danlos syndrome.2012
- Author(s)
  Watanabe A, Naing BT, Shimada T.
- Organizer
  First International Symposium on the Ehlers-Danlos Syndrome
- Place of Presentation
  Ghent, Belgium
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Hypermobility Syndrome in Japan.2012
- Author(s)
  Watanabe A, Hatakeyama M, Tsunoda R, Matsumoto K, Kawame H, Shimada T
- Organizer
  First International Symposium on the Ehlers-Danlos Syndrome
- Place of Presentation
  Ghent, Belgium
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] A novel gene therapy strategy for vascular Ehlers-Danlos syndrome2012
- Author(s)
  A. Watanabe
- Organizer
  First International Symposium on the Ehlers-Danlos Syndrome
- Place of Presentation
  ゲント, ベルギー
- Invited
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Phenotype differences in patients with nonsense mutations of COL3A1 causing nonsense-medicated mRNA decay in vascular Ehlers-Danlos Syndrome2012
- Author(s)
  A. Watanabe
- Organizer
  First International Symposium on the Ehlers-Danlos Syndrome
- Place of Presentation
  ゲント, ベルギー
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] An intronic mutation affecting pre-mRNA splicing in the COL3A1 gene as novel mechanisms causing vascular Ehlres-Danlos syndrome.2012
- Author(s)
  Watanabe A, Naing K,. Kosaihira BT Sasaki S, Gemma M, Akutsu A, Shimada T
- Organizer
  AmericanSociety of Human Genetics Meeting 2012 San Francisco
- Place of Presentation
  CA, USA
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] The first case of Tenascin-X deficient type Ehlers-Danlos syndrome in Japan.2012
- Author(s)
  Watanabe A, Hatakeyama M, Tsunoda R, Matsumoto K, Kawame H, Shimada T.
- Organizer
  European Human Genetics Conference2012
- Place of Presentation
  Nuremberg, Germany
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] 日本における周産期型低フォスファターゼ症高頻度変異部位1559delTと周産期時期からのfollow upの重要性2011
- Author(s)
  渡邉淳
- Organizer
  第29回日本骨代謝学会学術集会
- Place of Presentation
  大阪(ポスター)
- Data Source
  KAKENHI-PROJECT-22390212
[Presentation] イントロンの塩基置換から新規スプライシングを来した血管型 Ehlers-Danlos 症候群の 1 例2011
- Author(s)
  Banyar Than Naing, 渡邉淳 ,佐々木元子,圷宏一,小齊平聖治,弦間昭彦,島田隆
- Organizer
  日本人類遺伝学会第56回大会
- Place of Presentation
  於幕張メッセ
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] COL3A1 遺伝子新規ミスセンス変異による血管型Ehlers-Danlos 症候群の一例2011
- Author(s)
  升野光雄,渡邉淳,藤本亘,二宮伸介,上田恭典,近藤英生,山内泰子,尾内一信,黒木良和
- Organizer
  日本人類遺伝学会第56回大会
- Place of Presentation
  於幕張メッセ
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Fetal Gene Therapy for Lethal Murine Hypophosphatasia.2011
- Author(s)
  Sugano, H., Matsumoto, T., Miyake, K., Watanabe, A., Narisawa, S.,Millan, J.L., Fukunaga, Y., Shimada, T.
- Organizer
  14th Annual Meeting of the American Society of Gene & Cell Therapy.
- Place of Presentation
  Seattle, WA
- Data Source
  KAKENHI-PROJECT-22390212
[Presentation] Banyar Than Naing, SHIMADAT. a novel mutation screening system FOR vascular type Ehlers-Danlossyndrome (vEDS, EDS type IV) using highresolution melting curve analysis(hrMCA).2011
- Author(s)
  WATANABE A
- Organizer
  9^<th> Asia Pacific Conference onHuman Genetics
- Place of Presentation
  HongKong
- Year and Date
  2011-12-11
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] 日本エーラスダンロス症候群協会(友の会).日本におけるエーラス・ダンロス症候群の現状と課題患者会と協働で行ったアンケート調査を踏まえて2010
- Author(s)
  渡辺淳,古庄知己,鈴木由美
- Organizer
  第34回日本遺伝カウンセリング学会学術集会
- Place of Presentation
  於東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] COL3A1 遺伝子にナンセンス変異を同定した血管型 Ehlers-Danlos 症候群2症例.2010
- Author(s)
  Banyar Than Naing, 渡邉淳森崎裕子,K,. Kosaihira S, Gemma A, Shimada T. An菅野美紀,船越美由紀,籏持淳,島田隆
- Organizer
  日本人類遺伝学会第55回大会
- Place of Presentation
  於さいたま
- Year and Date
  2010-10-22
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Nonsense mutations of COL3A1 genecausing nonsense-mediated mRNA decay in two Japanese patients with Vasculartype of Ehlers-Danlos Syndrome.2010
- Author(s)
  Banyar Than Naing,WATANABE A,HATAMOCHI A, MORISAKI M, SHIMADA T.
- Organizer
  60^<th> Annual meeting of Amercan Society of Human Genetics ASHG
- Place of Presentation
  ワシントン DC
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Ehlers-Danlos 症候群の一例.日本人類高解像度融解曲線分析法を用いた血管型 Ehlers-Danlos 症候群(vEDS, EDS type IV)の新規遺伝子変異スクリーニングシステムの開発2010
- Author(s)
  バニャータンナイン, 渡邉淳島田隆
- Organizer
  第42回日本結合組織学会学術大会
- Place of Presentation
  於秋田
- Year and Date
  2010-08-22
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] Genotype frequency of 1559T deletion (1559delT) in the TNSALP gene and clinical significance of hypophoshatasia in Japan.2010
- Author(s)
  Watanabe A, Naing BT, Sawai H, Karasugi T, Kondo H, Ikegawa S, Orimo H, Shimada T.
- Organizer
  2010 ACMG Annual Clinical Genetics Meeting.
- Place of Presentation
  Albuquerque, NM
- Data Source
  KAKENHI-PROJECT-22390212
[Presentation] A NOVEL MUTATION SCREENING SYSTEM FOR VASCULAR TYPEEHLERS-DANLOS SYNDROME (VEDS, EDS TYPE IV) USING HIGH RESOLUTION MELTING CURVE ANALYSIS (HRMCA)2010
- Author(s)
  Atsushi Watanabe
- Organizer
  9^<th> Asia Pacific Conference on Human Genetics
- Place of Presentation
  HongKong
- Year and Date
  2010-12-01
- Data Source
  KAKENHI-PROJECT-22591554
[Presentation] How does ncreased medical knwledge affect medical communication skills?2008
- Author(s)
  Hirotaka Onishi, Hirono Ishikawa, Yasutomo Oda, Toshiro Shimura, Naomi Sugimoto, Rika Moriya, Motohumi Yoshida, Atsushi Watanabe, Ryoko Aso
- Organizer
  The 13th Ottawa International Conference on Clinical Competence
- Year and Date
  2008-03-05
- Data Source
  KAKENHI-PROJECT-19602005
[Presentation] 医学生に向けた臨床遺伝教育に関する内容・手法の検討2007
- Author(s)
  渡邉淳
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  東京京王プラザホテル
- Year and Date
  2007-09-15
- Data Source
  KAKENHI-PROJECT-19602005
[Presentation] Improvement of hypophosphatasia model mice by muscle specific expression of bone targeted alkaline phosphatase using self-complementary AAV8 vector.
- Author(s)
  Nakamura A, Iijima O, Miyake K, Watanabe A, Hirai Y, Kinoshita H, Noguchi T, Abe S, Okada T, Shimada T.
- Organizer
  日本遺伝子治療学会学術集会（第20回）
- Place of Presentation
  東京慈恵会医科大学（東京都）
- Year and Date
  2014-08-06 – 2014-08-08
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] A novel gene therapy strategy for vascular Ehlers-Danlos syndrome.
- Author(s)
  Watanabe A.
- Organizer
  First International symposium on Ehlers-Danlos syndrome Ghent Belgium.
- Place of Presentation
  Ghent,Belgium
- Data Source
  KAKENHI-PROJECT-22390212
[Presentation] Rescue of lethal hypophosphatasia model mice by adeno-associated virus mediated muscle specific expression of bone targeted alkaline phosphatase.
- Author(s)
  Nakamura A, Iijima O, Miyake K, Watanabe A, Hirai Y, Kinoshita H, Noguchi T, Abe S, Okada T, Shimada T.
- Organizer
  American Society of Human Genetics Annual Meeting (64th)
- Place of Presentation
  San Diego Convention Center（San Diego, CA）
- Year and Date
  2014-10-18 – 2014-10-22
- Data Source
  KAKENHI-PROJECT-25461564
[Presentation] 中等教育における『ヒトの遺伝』の導入に向けた取り組み
- Author(s)
  渡邉　淳、市石　博、中村雅浩、鈴木恵子、白石直樹、佐々木元子、櫻井晃洋
- Organizer
  日本人類遺伝学会（第59回）
- Place of Presentation
  タワーホール船堀
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-26560385
[Presentation] Hypermobility Syndrome in Japan.
- Author(s)
  Watanabe A.
- Organizer
  First International symposium on Ehlers-Danlos syndrome Ghent Belgium.
- Place of Presentation
  Ghent,Belgium
- Data Source
  KAKENHI-PROJECT-22390212
[Presentation] IL-6 promoter polymorphisms and keloid susceptibility in the Japanese population.
- Author(s)
  M. Ghazizadeh, M. Tosa, Atsushi. Watanabe, S. Egawa, H. Murakami.
- Organizer
  第6回日本創傷治癒外科学会総会
- Place of Presentation
  高松市
- Year and Date
  2014-07-24 – 2014-07-25
- Data Source
  KAKENHI-PROJECT-24592723
[Presentation] Neonatal transplantation of lentivirally transduced bone marrow cells for the treatment of lethal hypophosphatasia mice.
- Author(s)
  Iijima O, Miyake K, Watanabe A, Nakamura A, Igarashi T, Kanokoda C, Kinoshita H, Noguchi T, Abe S, Okada T, Shimada T.
- Organizer
  日本遺伝子治療学会学術集会（第20回）
- Place of Presentation
  東京慈恵会医科大学（東京都）
- Year and Date
  2014-08-06 – 2014-08-08
- Data Source
  KAKENHI-PROJECT-25461564

1. SHIMADA Takashi (20125074)

# of Collaborated Projects: 4 results

# of Collaborated Products: 21 results
2. MIYAKE Koichi (90267211)

# of Collaborated Projects: 3 results

# of Collaborated Products: 15 results
3. MIGITA Makoto (50256963)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
4. 大貫麻美 (40531166)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. TAMAI Mariko (80283274)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. MORIYA Rika (80220094)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. DOUZONO Toshihiko (90396705)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. MAMIKO Tosa (30301568)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. GHAZIZADEH M (30190979)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
10. IKEZONO Tetsuo (80277491)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
11. MOCHIZUKI Hideki (90230044)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. SASAKI MOTOKO (90725665)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
13. KOSHO Tomoki (90276311)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
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Watanabe Atsushi 渡邉 淳

渡邉 淳 ワタナベ アツシ

WATANABE Atsushi 渡邉 淳

渡邊 淳 ワタナベ アツシ

渡辺 淳 ワタナベ アツシ

Research Projects

Research Products

Co-Researchers

初等・中等教育における遺伝学を用いた命の学習プログラム開発と導入に向けた検討Ongoing

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In search of analytical method for genetic testingOngoing

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幼少期から自らの健康を保持・増進できるコンピテンスを育むSTEAM教育の検討Ongoing

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Identification of expression mechanism by comprehensive gene analysis of Moyamoya disease analogous vascular stenosisOngoing

Principal Investigator

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新しい生命科学教育の根幹を担う日本独自の学際的幼児教育プログラムの開発Ongoing

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Clarification of issues and measures for introducing "human genetics" to school education

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Investigations for tasks toward development of literacy for human genetics to a citizen and making programsPrincipal Investigator

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Clinical and molecular investigation for new forms of Ehlers-Danlos syndrome

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Development of regenerative medicine and cell therapy for inherited metabolic diseases using hypophosphatasia mice

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A polymorphysm in the IL-6 promotor region associated with the keloid in the Japanease population

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Perinatal gene therapy for severe genetic diseases

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Development and classification of therapeutic method for vascularEhlers-Danlos syndrome by mutation typesPrincipal Investigator

Principal Investigator

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Watanabe Atsushi 渡邉淳

渡邉淳ワタナベアツシ

WATANABE Atsushi 渡邉淳

渡邊淳ワタナベアツシ

渡辺淳ワタナベアツシ

[Book] 【最新遺伝医学研究と遺伝カウンセリング(シリーズ3)　最新多因子遺伝性疾患研究と遺伝カウンセリング】 (第5章)多因子疾患の遺伝情報と社会　社会における遺伝リテラシー向上2018

[Book] 診療・研究にダイレクトにつながる遺伝医学2017

[Book] Ehlers-Danlos 症候群.先天代謝異常ハンドブック遠藤文夫(総編集)2013

[Book] Ehlkers-Danlos 症候群　（分担）先天代謝異常ハンドブック2013

[Book] 生命倫理遺伝情報を診療で活用するための課題.2009

[Book] トンプソン&トンプソン遺伝医学, 第3章ヒトゲノム : 遺伝子の構造と機能(福嶋義光監訳)2009