Watanabe Atsushi 渡邉淳

… Alternative Names

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

渡邉淳ワタナベアツシ

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Researcher Number	10307952
Affiliation (Current)	2025: 金沢大学, 附属病院, 特任教授
Affiliation (based on the past Project Information) *help	2018 – 2024: 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 2007 – 2008: Nippon Medical School, 医学部, Assistant Professor … More 2007: 日本医科大学, 医学部, 助教 2002 – 2006: 日本医科大学, 医学部, 助手 1999 – 2000: 日本医科大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Applied health science / Thoracic surgery / 医療における生命倫理 / Pathological medical chemistry Except Principal Investigator Pediatrics / Basic Section 56010:Neurosurgery-related / Science education / Basic Section 58070:Lifelong developmental nursing-related / Basic Section 59020:Sports sciences-related … More / Basic Section 09080:Science education-related / Human genetics / Otorhinolaryngology / Plastic surgery Less
Keywords	Principal Investigator penetration peptide uniting enzyme / glucocerebrosidase / Gaucher diseas / TAT融合蛋白 / 血液脳関門 / 膜透過ペプチド / 神経型Gaucher病 / 膜透過ペプチド融合酵素 / グルコセレブロシデース / Gaucher病 … More / 一般市民 / 中等教育 / 遺伝リテラシー / コラーゲン / 血管型エーラス・ダンロス症候群 / COL3A1 / RNAi / 変異型 / 血管型エーラス・ダンロス症候群 / 家族性大動脈瘤 / 心臓大血管外科学 / 臨床遺伝教育プログラム / 遺伝情報 / 生命倫理 / 医学教育 / 遺伝学 / 臨床遺伝教育 / ミスマッチ修復遺伝子 / トリプレット病 … More Except Principal Investigator 遺伝子治療 / 遺伝子 / 血管狭窄 / RNF213 / 脳動脈瘤 / 内頸動脈 / もやもや病 / 健康教育 / Gene therapy / Cochlin / 遺伝子解析 / 遺伝看護 / 遺伝学的検査 / 生命倫理 / 教科横断的学習 / 教科等横断型学習 / 初等・中等教育 / 参加型プログラム / 遺伝教育 / 中大脳動脈 / ＮＧＳの2次所見 / アスリート遺伝リテラシー / クリスパーキャス / RNA-seq / 遺伝子ドーピング検出法 / ｃｆＤＮＡ / リキッドバイオプシー / 遺伝子ドーピング / 食育 / 運動 / 児童 / 幼児 / コンピテンス基盤型教育 / STEAM教育 / 内頸動脈狭窄 / RNF / 内頸動脈瘤 / もやもや病 / ミスセンス / モヤモヤ病 / 動脈瘤 / 遺伝子変異 / 内頸動脈閉塞症 / 脳血管障害 / 脳神経外科 / 学際的幼児教育プログラム / 科学教育カリキュラム / 科学教育 / 生物の共通性と多様性 / 日本文化 / 怪我 / 歯 / 生物の多様性と共通性 / 幼児教育プログラム / 生命科学教育 / アルカリフォスファターゼ / 低フォスファターゼ症 / アルカリホスファターゼ / レンチウイルスベクター / 骨格筋芽細胞 / 造血幹細胞 / 骨髄幹細胞 / 低ホスファターゼ症 / 再生・細胞医療 / 国際情報交換 / 全エクソーム解析 / 候補遺伝子解析 / 次世代シーケンス / 結合組織疾患 / 新規病型 / エーラスダンロス症候群 / ゲノムリテラシー / 中等教育 / ヒトの遺伝教育 / Metachromatic leukodystrophy / Mannose-6 phosp[hate receptor / Lysosomal diseases / Blood brain barrier / Viral vector / トランスサイトーシス / マンノース6リン酸 / アリルスルファターゼ / 異染性白質ジストロフィー / マンノース-6-リン酸受容体 / リソゾーム病 / 血液脳関門 / ウイルスベクター / isoform / Inner ear specific / Coch gene / アイソフォーム / 内耳特異的 / COCH遺伝子 / 一塩基多型 / SNP / IL-6 / ＳＮＰ / ＩＬ－６ / ケロイド / 遺伝病 Less

脳動脈瘤の臨床表現型に着目したRNF213の網羅的解析
- Principal Investigator
  
  村井保夫
- Project Period (FY)
  2022 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56010:Neurosurgery-related
- Research Institution
  Nippon Medical School
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
- Principal Investigator
  
  石沢順子
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 09080:Science education-related
- Research Institution
  Shirayuri University
In search of analytical method for genetic testing
- Principal Investigator
  
  TAKEKOSHI KAZUHIRO
- 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
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
- 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
Identification of expression mechanism by comprehensive gene analysis of Moyamoya disease analogous vascular stenosis
- Principal Investigator
  
  Murai Yasuo
- 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
Development of the interdisciplinary early childhood life science education programs based on Japanese culture
- Principal Investigator
  
  Ohnuki Asami
- 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] 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] 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] 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] 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] 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] 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
[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
[Journal Article] FOCUS 認定遺伝カウンセラー®(CGC)2022
- Author(s)
  渡邉淳、池田和美、関屋智子
- Journal Title
  
  検査と技術
  
  Volume: 50 Issue: 4 Pages: 418-421
- DOI
  10.11477/mf.1543208651
- ISSN
  0301-2611, 1882-1375
- Year and Date
  2022-04-01
- Data Source
  KAKENHI-PROJECT-23K20349
[Journal Article] 「跳ぶ」能力を育む教科等横断型学習を支援する保育者・教育者養成に向けた取り組み2022
- Author(s)
  石沢順子，大貫麻美，椎橋げんき，佐々木玲子，原口るみ，奈良典子，稲田結美，渡邉淳
- Journal Title
  
  白百合女子大学初等教育学科紀要　保育・教育の実践と研究
  
  Volume: 7 Pages: 9-18
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K03258
[Journal Article] 出生前診断に関わる遺伝教育プログラムの試みー高校生を対象としてー2021
- Author(s)
  森藤香奈子, 宮田海香子, 松本正, 高尾真未, 宮原春美, 渡邊淳, 平岡さゆり, 武田右子, 佐々木規子
- Journal Title
  
  日本遺伝カウンセリング学会誌
  
  Volume: 42(3) Pages: 289-298
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K20349
[Journal Article] Proof of Gene Doping in a Mouse Model with a Human Erythropoietin Gene Transferred Using an Adenoviral Vector2021
- Author(s)
  Sugasawa Takehito、Nakano Takuro、Fujita Shin-ichiro、Matsumoto Yuki、Ishihara Genki、Aoki Kai、Yanazawa Koki、Ono Seiko、Tamai Shinsuke、Manevich Lev、Ueda Haruna、Ishibashi Noriyo、Tamai Kenshirou、Kanki Yasuharu、Yoshida Yasuko、Watanabe Koichi、Takemasa Tohru、Kawakami Yasushi、Takekoshi Kazuhiro
- Journal Title
  
  Genes
  
  Volume: 12 Issue: 8 Pages: 1249-1249
- DOI
  10.3390/genes12081249
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H03432, KAKENHI-PROJECT-20H04062
[Journal Article] 2020年度健康教育におけるコンピテンスの検討に関する全体協議会（オンライン）実施報告2021
- Author(s)
  石沢順子，大貫麻美，椎橋げんき，稲田結美，渡邉淳，佐々木玲子，奈良典子，原口るみ，鍜治礼子
- Journal Title
  
  白百合女子大学初等教育学科紀要　保育・教育の実践と研究
  
  Volume: 6 Pages: 71-76
- NAID
  120007115678
- Open Access
- Data Source
  KAKENHI-PROJECT-20K03258
[Journal Article] A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A.2021
- Author(s)
  Matano F(1), Murai Y(1), Watanabe A(2), Shirokane K(1), Igarashi
- Journal Title
  
  Front Endocrinol (Lausanne)
  
  Volume: 12 Pages: 703410-703410
- DOI
  10.3389/fendo.2021.703410
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K09008, KAKENHI-PROJECT-22K16671
[Journal Article] RNF213 c.14576G>A Is Associated with Intracranial Internal Carotid Artery Saccular Aneurysms.2021
- Author(s)
  Murai Y(1), Ishisaka E(1), Watanabe A(2)(3), Sekine T(4), Shirokane K(1), Matano F(1), Nakae R(5), Tamaki T(6), Koketsu K(1), Morita A(1).
- Journal Title
  
  Genes (Basel).
  
  Volume: 23 Issue: 10 Pages: 1468-1468
- DOI
  10.3390/genes12101468
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K09008, KAKENHI-PROJECT-21K07686
[Journal Article] Ring finger protein 213 c.14576G>A mutation is not involved in internal carotid artery and middle cerebral artery dysplasia.2021
- Author(s)
  Murai Y(1), Ishisaka E(2), Watanabe A(3)(4), Sekine T(5), Shirokane K(2), Matano F(2), Nakae R(6), Tamaki T(7), Koketsu K(2), Morita A(2).
- Journal Title
  
  Sci Rep.
  
  Volume: 11 Issue: 1 Pages: 22163-22163
- DOI
  10.1038/s41598-021-01623-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K09008, KAKENHI-PROJECT-21K07686
[Journal Article] 看護基礎教育課程への遺伝医学・遺伝看護学教育の普及に向けた活動報告2021
- Author(s)
  野間口千香穂, 中込さと子, 北村千章, 沓脱小枝子, 佐々木規子, 鈴木智恵子, 渡邉淳, 協力者, 西垣昌和, 関屋智子, 柊中智恵子
- Journal Title
  
  日本遺伝看護学会誌
  
  Volume: 19(2) Pages: 20-29
- Data Source
  KAKENHI-PROJECT-23K20349
[Journal Article] Role of RNF213 polymorphism in defining quasi-moyamoya disease and definitive moyamoya disease.2021
- Author(s)
  Ishisaka E(1), Watanabe A(2)(3), Murai Y(1), Shirokane K(4), Matano F(1), Tsukiyama A(1), Baba E(1), Nakagawa S(1), Tamaki T(4), Mizunari T(5), Tanikawa R(6), Morita A(1).
- Journal Title
  
  Neurosurg Focus.
  
  Volume: 51 Issue: 3 Pages: E2-E2
- DOI
  10.3171/2021.5.focus21182
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K09008
[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] Treatment of hypophosphatasia by muscle-directed expression of bone-targeted alkaline phosphatase 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
  
  Molecular Therapy- Methods & Clinical Development
  
  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] 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] 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] 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 Issue: 12 Pages: 801-12
- DOI
  10.1089/hum.2015.078
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09604, KAKENHI-PROJECT-26461596, KAKENHI-PROJECT-25461564
[Journal Article] Perinatal hypophosphatasia caused by uniparental isodisomy.2014
- 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, J.L., Fukunaga, Y., Shimada, T.
- Journal Title
  
  Hum. Gene Ther.
  
  Volume: 23 Pages: 399-406
- Data Source
  KAKENHI-PROJECT-22390212
[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 JL, Fukunaga Y, Shimada T.
- Journal Title
  
  Hum Gene Ther
  
  Volume: 23 Pages: 399-406
- Data Source
  KAKENHI-PROJECT-22591554
[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] 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] 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] 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] 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 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] 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] 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] 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
- 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] 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、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] 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] 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] 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-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 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] 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] 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] 遺伝性神経難病の看護をテーマとしたオンラインセミナーの評価と課題2023
- Author(s)
  須坂洋子, 宮田海香子, 鴨川七重, 森屋宏美, 野正佳余, 関屋智子, 青木美紀子, 中込さと子, 村上裕美, 浦野真理, 柊中智恵子, 酒井規夫, 佐々木規子, 佐藤智佳, 玉置知子, 御手洗幸子, 渡邉淳, 川目裕
- Organizer
  日本遺伝看護学会第22回学術大会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 成人前教育における「ヒトの遺伝」導入に向けた課題の検討がん教育担当者への調査を通して2023
- Author(s)
  池田和美, 松本恵, 森藤香奈子, 佐々木規子, 福田令, 河野久美子, 渡邉淳
- Organizer
  第47回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 初心者向け「家系図の意義並びに作成法と活用法に関する学習プログラム」の開発と評価2023
- Author(s)
  佐々木規子, 佐藤智佳, 村上裕美, 浦野真理, 渡邉淳, 玉置知子, 中込さと子, 青木美紀子, 柊中智惠子, 酒井規夫, 御手洗幸子, 川目裕
- Organizer
  第47回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 本邦における「ヒトの遺伝」教育・啓発コンテンツ確認シートの作成2023
- Author(s)
  佐々木規子, 秋山奈々, 鳥嶋雅子, 宮崎幸子, 森屋宏美, 鈴木美慧, 十川麗美, 内山正登, 佐々木元子, 森藤香奈子, 櫻井晃洋, 渡邉淳
- Organizer
  第47回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 難病をもつ患者・家族が有する遺伝的課題・遺伝医療への要望に関する実態調査2022
- Author(s)
  関屋智子、渡邉淳
- Organizer
  日本遺伝カウンセリング学会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 遺伝看護委員会による第2回遺伝の初歩セミナーの開催報告2022
- Author(s)
  佐々木規子、中込さと子、村上裕美、青木美紀子、浦野真理、柊中智恵子、酒井規夫、佐藤智佳、玉置知子、御手洗幸子、渡邉淳、川目裕
- Organizer
  第46回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 本邦における「ヒトの遺伝」に関する教育・啓発コンテンツの活用状況アンケート調査2021
- Author(s)
  佐々木規子, 鈴木美慧, 巽純子, 滝澤公子, 西垣昌和, 秋山奈々, 中山智祥, 水島純子, 櫻井晃洋, 渡邉淳
- Organizer
  第45回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] 初心者向け遺伝・ゲノム医療教育セミナー「遺伝の初歩セミナー」の報告2021
- Author(s)
  中込さと子, 村上裕美, 佐藤智佳, 玉置知子, 大川恵, 佐々木規子, 浦野真理, 山下浩美, 渡邊淳, 青木美紀子, 川目裕, 福嶋義光, 小杉眞司
- Organizer
  第45回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] もやもや病関連遺伝子変異 RNF213（c.14576G>A）の頭蓋内内頸動脈嚢状動脈瘤における検討2021
- Author(s)
  村井保夫1,石坂栄太郎2,渡邉淳3,4,白銀一貴5,亦野文宏1,纐纈健太6,玉置智規5,水成隆之6,森田明夫1
- Organizer
  日本医科大学医学会総会
- Data Source
  KAKENHI-PROJECT-18K09008
[Presentation] 看護基礎教育課程における遺伝医学・遺伝看護学教育の実態調査2020
- Author(s)
  佐々木規子、沓脱小枝子、鈴木智恵子、北村千章、渡邊淳、野間口千香穂、中込さと子
- Organizer
  日本遺伝看護学会第19回学術大会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] ゲノム医療における二次的所見の取り扱いに関する実態調査-遺伝医療専門家を対象とした質問票調査より　倫理問題検討委員会報告2020
- Author(s)
  土屋実央、山田崇弘、赤石理奈、井本逸勢、梅村啓史、清水健司、浜之上はるか、平沢晃、吉田晶子、吉橋博史、四元淳子、渡邊淳、小杉真司
- Organizer
  第44回日本遺伝カウンセリング学会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] K大学病院における遺伝カウンセリングでの看護師の関わり2020
- Author(s)
  関屋智子、池田和美、渡邊淳
- Organizer
  日本遺伝看護学会第19回学術大会
- Data Source
  KAKENHI-PROJECT-23K20349
[Presentation] NIPTを題材とした高校生向け遺伝教育プログラムの開発および評価2020
- Author(s)
  森藤香奈子、松本正、佐藤信二、宮田海香子、高尾真未、渡邊淳、武田右子、宮原春美、佐々木規子
- Organizer
  第44回日本遺伝カウンセリング学会
- Data Source
  KAKENHI-PROJECT-23K20349
[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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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: 19 results
2. MIYAKE Koichi (90267211)

# of Collaborated Projects: 3 results

# of Collaborated Products: 14 results
3. MIGITA Makoto (50256963)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
4. Ohnuki Asami (40531166)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
5. Murai Yasuo (30287750)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
6. 亦野文宏 (70557511)

# of Collaborated Projects: 2 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
16. FUKUSHIMA Yoshimitsu (70273084)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. HATAMOCHI Atsushi (90172923)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. MATSUMOTO Naomichi (80325638)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. MIYAYE Noriko (40523494)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
20. WAKUI Keiko (50324249)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. MORISAKI Hiroko (40311451)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
22. Iijima Osamu (40466206)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
23. TAKEKOSHI KAZUHIRO (40261804)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. 塙秀樹 (10256977)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. 久安早苗 (00089616)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. 石上七鞘 (10151359)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. 瀧上豊 (40206909)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. 鈴木誠 (60322856)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. 白鳥信義 (80720846)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
30. 古金悦子 (90592410)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
31. 石沢順子 (40310445)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
32. 稲田結美 (30585633)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
33. 椎橋元貴 (10788938)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
34. 佐々木玲子 (80178673)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
35. 奈良典子 (40844840)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
36. 原口るみ (60445468)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
37. 渡部厚一 (30447247)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
38. 菅澤威仁 (60821840)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
39. 竹村瑞穂 (70634351)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
40. 森藤香奈子 (70404209)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
41. 宮原春美 (00209933)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
42. 平間理子 (40979952)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
43. 本多直子 (50746617)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
44. 佐々木規子 (90315268)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
45. 高尾真未 (90882465)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
46. 渡名喜海香子 (10818321)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
47. MIYAKE HIDEHIKO

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
48. TAKIZAWA KIMIKO

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
49. KIMURA MIDORI

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
50. KANKI Yasuharu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
51. 前田規子

# of Collaborated Projects: 0 results

# of Collaborated Products: 11 results
52. 宮田海香子

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
53. 平井幸彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Watanabe Atsushi 渡邉 淳

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

渡邉 淳 ワタナベ アツシ

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

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An investigation for tasks and development of self-study materials for effective educational programs of clinical geneticsPrincipal Investigator

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Watanabe Atsushi 渡邉淳

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

渡邉淳ワタナベアツシ

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

[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] 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