Suzuki Tamio 鈴木民夫

… Alternative Names

SUZUKI Tamio 鈴木民夫

TAMIO Suzuki 鈴木民夫

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Researcher Number	30206502
Other IDs
External Links
Affiliation (Current)	2025: 山形大学, 医学部, 名誉教授
Affiliation (based on the past Project Information) *help	2016 – 2023: 山形大学, 医学部, 教授 2010 – 2014: 山形大学, 医学部, 教授 2006 – 2008: Yamagata University School of Medicine, Professor, 医学部, 教授 2004 – 2005: 名古屋大学, 大学院・医学系研究科, 助教授 2002 – 2003: 名古屋大学, 医学部附属病院, 講師 2002: 名古屋大学, 医学部付属病院, 講師 1988 – 1990: 山形大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Dermatology / Basic Section 53050:Dermatology-related / Biological Sciences Except Principal Investigator Dermatology / 代謝生物化学 / Dermatology / Basic Section 58020:Hygiene and public health-related: including laboratory approach
Keywords	Principal Investigator メラニン / 遺伝性対側性色素異常症 / 遺伝性色素異常症 / 眼皮膚白皮症 / melanin / メンブレントラフィック / 白皮症 / メラノソーム / 遺伝学 / hereditary pigment disorders … More / melanosome / Hermansky-Pudlak syndrome / 遺伝子診断 / 色素細胞 / ヘルマンスキーパドラック症候群 / 眼皮膚白皮症4型 / 細胞死 / ｘCT / CDH13 / マウスモデル / 化学白斑 / pigmentation / mouse / inflammation / melanocyte / ヒスタミン / 肥満細胞 / 炎症後色素沈着 / マクロファージ / メラニン代謝 / アトピー性皮膚炎 / モデルマウス / 化学物質 / 機能解析 / ロドデノール / 感受性遺伝子 / 化学物質誘発性白斑 / 尋常性白斑 / proteome analysis / gene diagnosis / oculocutaneous albinism / 遺伝病 / プロテオーム / 遺伝子 / プロテオーム解析 / ヘルマンスキー・パドラック症候群 / membrane traffic / Dyschromatosis symmetrica hereditaria / albino / Oculocutaneous albinism / 色素異常症 / 蒙古斑 / 色素脱出 / 色素沈着 / 遺伝性 / 色素異常 / 遺伝子変異 / 新規遺伝子変異 / 常染色体優性遺伝 / 遺伝子解析 / ノッチシグナル経路 / アールエヌエー編集 / ヘルマンスキーパドラック症候 … More Except Principal Investigator SNP / ADAR1 / メチル化 / モザイク / targeting factor / DSRAD / アデノシン脱アミノ化酵素 / 細胞質因子 / ミトコンドリア / 延長ペプチド / ミトコンドリア蛋白質前駆体 / メラニン / 白斑 / 色素異常症 / ダイレクトシークエンス / ダイレクトシーケンス / 遺伝性対側性色素異常症 / polymorphism / 飲酒 / バイオマーカー / メラノーシス / メラノーマ / アセトアルデヒド / エタノール / 発がん / アルデヒド / 遺伝子多型 / ALDH2 / 尋常性白斑 / eQTL / 一塩基多型 / 発症リスク / HLA-A / mitochondrial outermembrane / receptor for precursor proteins / Import of mitochondrial proteins / precursor of mitochondrial proteins / cytosolic factor / オルニチンアミノ基転移酵素 / 熱ショック蛋白質 / 蛋白質輸入機構 / 前駆体受容体 / ミトコンドリア蛋白質の輸入 / RNA editing / Dyschromatosis / adenosine deaminase / RNA編集 / Adenosine deaminase / Direct Sequence / Positional cloning / Dyschoromatosis / 候補領域 / SUP / ポジショナルクローニング法 / mitochondria / bypass-import / translocation machinery / contact site / import machinery / presequence / mitochondrial protein precursor / 前駆体蛋白質 / 前駆体蛋白質受容体 / バイパス輸送 / 膜透過装置 / コンタクトサイト / 輸送装置 / メラノサイト / 眼皮膚白皮症 / 遺伝性疾患 Less

Comprehensive analyses of the pathogenesis of chemical vitiligo, a form of vitiligo, and development of new treatment methodsPrincipal Investigator
- Principal Investigator
  
  鈴木民夫
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Yamagata University
Alcohol and rs671 on melanoma development: an experimental approach
- Principal Investigator
  
  松本明子
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 58020:Hygiene and public health-related: including laboratory approach
- Research Institution
  Saga University
A mouse model for postinflammatory hyperpigmentation: an analysis of molecular, and histological traits, and an establishment of effective treatment.Principal Investigator
- Principal Investigator
  
  Suzuki Tamio
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Yamagata University
Investigation of the role of HLA-A in the pathogenesis of autoimmune vitiligo and regulatory mechanism of HLA-A expression
- Principal Investigator
  
  HAYASHI MASAHIRO
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Identification and functional analyzes of chemical-induced vitiligo susceptibility genes.Principal Investigator
- Principal Investigator
  
  Suzuki Tamio
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Identification and functional analysis of responsible gene(s) for Mongolian blue spotPrincipal Investigator
- Principal Investigator
  
  SUZUKI Tamio
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Functional analyses of the genes responsible for hereditary pigment disordersPrincipal Investigator
- Principal Investigator
  
  SUZUKI Tamio
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Study on regulatory mechanism of melanin synthesis clarified by elucidation of molecular pathology on pigmentary disorders
- Principal Investigator
  
  YASUSHI Tomita
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
アールエヌエー編集障害により発症する遺伝性対側性色素異常症の病態解析Principal Investigator
- Principal Investigator
  
  鈴木民夫
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Functional analyses of the genes in which mutations cause oculocutaneous albinismsPrincipal Investigator
- Principal Investigator
  
  SUZUKI Tamio
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
ヘルマンスキー・パドラック症候群および眼皮膚白皮症の病因遺伝子産物の機能解析Principal Investigator
- Principal Investigator
  
  鈴木民夫
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Nagoya University
皮疹の形を規定する表皮モザイクと遺伝子メチル化の研究
- Principal Investigator
  
  榊原章浩
- Project Period (FY)
  2004
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Study on pathomechanism of Dyschromatosis Symmetrica Hereditaria caused by gene mutation of RNA editing enzyme, DSRAD
- Principal Investigator
  
  TOMITA Yasushi
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Functional analyses of the genes in which mutations cause hereditary pigment disordersPrincipal Investigator
- Principal Investigator
  
  SUZUKI Tamio
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
発疹の分布に関与する表皮モザイクと遺伝子メチル化の研究
- Principal Investigator
  
  榊原章浩
- Project Period (FY)
  2003
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
表皮におけるモザイク的遺伝子制御の解明
- Principal Investigator
  
  榊原章浩
- Project Period (FY)
  2002
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Positional cloning of the gene causing Dyschromatosis Symmetrica Hereditaria
- Principal Investigator
  
  TOMITA Yasushi
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Molecular mechanism of recognition of mitochondrial protein precursor by mitochondria
- Principal Investigator
  
  ONO Hideyu, TUBOI Syozo
- Project Period (FY)
  1990 – 1991
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  代謝生物化学
- Research Institution
  Yamagata University
Research for molecular mechanism of import of mitochondrial proteins into mitochondrial
- Principal Investigator
  
  TUBOI Syozo
- Project Period (FY)
  1988 – 1989
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  代謝生物化学
- Research Institution
  Yamagata University School of Medicine

[Book] Fitzpatrick’s Dermatology 9th Edi.2019
- Author(s)
  Masahiro Hayashi, Tamio Suzuki
- Total Pages
  3951
- Publisher
  Mc Graw Hill Education
- ISBN
  9780071837798
- Data Source
  KAKENHI-PROJECT-16K10123
[Book] 皮膚疾患最新の治療2015‐20162015
- Author(s)
  鈴木民夫他
- Total Pages
  303
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-25670498
[Book] 今日の治療指針2015私はこう治療している2015
- Author(s)
  鈴木民夫他
- Total Pages
  1973
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-25670498
[Book] 皮膚疾患最新の治療2013‐2014(滝川雅浩ら編)2013
- Author(s)
  鈴木民夫
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 今日の治療指針2013私はこう治療している2013
- Author(s)
  鈴木民夫
- Total Pages
  1067
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-25670498
[Book] 今日の治療指針20132013
- Author(s)
  鈴木民夫
- Total Pages
  1067
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 皮膚疾患最新の治療2013‐20142013
- Author(s)
  鈴木民夫
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-25670498
[Book] 皮膚疾患最新の治療2013‐20142013
- Author(s)
  鈴木民夫
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 皮膚科臨床アセット20忘れてはならない皮膚科症候群，第20巻2013
- Author(s)
  大磯直毅、鈴木民夫
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-25670498
[Book] 今日の治療指針 2013私はこう治療している(山口徹ら編)2013
- Author(s)
  鈴木民夫
- Total Pages
  1067
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 匠に学ぶ皮膚科外用療法(上出良一編)2012
- Author(s)
  林昌浩、鈴木民夫
- Publisher
  全日本病院出版会
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 今日の皮膚疾患治療指針第4版(塩原哲夫ら編)2012
- Author(s)
  鈴木民夫
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 今日の皮膚疾患治療指針第4版、びまん性色素沈着をきたす疾患2012
- Author(s)
  鈴木民夫
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-22591236
[Book] 今日の治療指針 2011私はこう治療している(山口徹ら編)2012
- Author(s)
  鈴木民夫
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-22591236
[Book] Oculocutaneous albinism in Asians. Asian Skin and Skin Diseases(Edited by HC Eun, SC Kim, and WS Lee)2011
- Author(s)
  Suzuki T., et al.
- Total Pages
  6
- Publisher
  Medrang Inc., Seoul
- Data Source
  KAKENHI-PROJECT-22591236
[Book] からだと光の事典(太陽紫外線防御研究委員会編)2010
- Author(s)
  鈴木民夫
- Publisher
  朝倉書店
- Data Source
  KAKENHI-PROJECT-22591236
[Book] スキンケア最前線、3色素細胞を知る2008
- Author(s)
  鈴木民夫
- Total Pages
  4
- Publisher
  メデイカルレビュー社
- Data Source
  KAKENHI-PROJECT-18659322
[Book] スキンケア最前線、3色素細胞を知る2008
- Author(s)
  鈴木民夫
- Total Pages
  4
- Publisher
  メデイカルレビュー社
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Recent Advances in Clinical Research on Rare Intractable Hereditary Skin Diseases in Japan2025
- Author(s)
  Akiyama Masashi、Takeichi Takuya、Ikeda Shigaku、Ishiko Akira、Kurosawa Michiko、Murota Hiroyuki、Shimomura Yutaka、Suzuki Tamio、Tamai Katsuto、Tanaka Akio、Terui Tadashi、Amagai Masayuki
- Journal Title
  
  The Keio Journal of Medicine
  
  Volume: 74 Issue: 1 Pages: 11-20
- DOI
  10.2302/kjm.2023-0008-IR
- ISSN
  0022-9717, 1880-1293
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K07779, KAKENHI-PROJECT-18K10075
[Journal Article] Worldwide expert recommendations for the diagnosis and management of vitiligo: Position statement from the International Vitiligo Task Force Part 1: towards a new management algorithm.2023
- Author(s)
  van Geel N, Speeckaert R, Taieb A, Ezzedine K, Lim HW, et al
- Journal Title
  
  J Eur Acad Dermatol Venereol .
  
  Volume: 37 Issue: 11 Pages: 2173-2184
- DOI
  10.1111/jdv.19451
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08409, KAKENHI-PROJECT-23K07779
[Journal Article] Copper chelation by d-penicillamine alleviates melanocyte death induced by rhododendrol without inhibiting tyrosinase2023
- Author(s)
  Nagatani Kei、Abe Yuko、Homma Takujiro、Fujii Junichi、Suzuki Tamio
- Journal Title
  
  Biochemical and Biophysical Research Communications
  
  Volume: 663 Pages: 71-77
- DOI
  10.1016/j.bbrc.2023.04.062
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K15388, KAKENHI-PROJECT-23K07779, KAKENHI-PROJECT-21K06850
[Journal Article] JAK Inhibitors in the Treatment of Vitiligo2023
- Author(s)
  井上紳太郎、鈴木民夫、佐野栄紀、片山一朗
- Journal Title
  
  The Japanese Journal of Dermatology
  
  Volume: 133 Issue: 12 Pages: 2837-2848
- DOI
  10.14924/dermatol.133.2837
- ISSN
  0021-499X, 1346-8146
- Year and Date
  2023-11-20
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K07779
[Journal Article] Not Follicular but Dermal Melanocyte Precursors Are Histopathologically Retained in Vitiligo2023
- Author(s)
  Tanemura Atsushi、Kawabe Ryoko、Sudo Yuka、Yokoi Kazunori、Kabasawa Takanobu、Futakuchi Mitsuru、Suzuki Tamio、Fujimoto Manabu
- Journal Title
  
  Journal of Cosmetics, Dermatological Sciences and Applications
  
  Volume: 13 Issue: 01 Pages: 38-44
- DOI
  10.4236/jcdsa.2023.131004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K07779
[Journal Article] Worldwide expert recommendations for the diagnosis and management of vitiligo: Position statement from the international Vitiligo Task Force-Part 2: Specific treatment recommendations2023
- Author(s)
  Huggins R, Oh SH, Harris JE, Hamzavi IH, Gupta S, Grimes P, et al
- Journal Title
  
  J Eur Acad Dermatol Venereol.
  
  Volume: 37 Issue: 11 Pages: 2185-2195
- DOI
  10.1111/jdv.19450
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08409, KAKENHI-PROJECT-23K07779
[Journal Article] Establishment of a mouse model for post‐inflammatory hyperpigmentation2020
- Author(s)
  Nakano Shoko、Abe Yuko、Nakajima Kimiko、Sano Shigetoshi、Yamamoto Osamu、Wakamatsu Kazumasa、Ito Shosuke、Hayashi Masahiro、Suzuki Tamio
- Journal Title
  
  Pigment Cell & Melanoma Research
  
  Volume: 34 Issue: 1 Pages: 101-110
- DOI
  10.1111/pcmr.12911
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08742
[Journal Article] Development and validation of the Vitiligo Extent Score for a Target Area (VESTA) to assess the treatment response of a target lesion.2019
- Author(s)
  Bae JM, Oh SH, Kang HY, Ryoo YW, Lan CE, Xiang LH, Kim KH, Suzuki T, Katayama I, Lee SC; East Asia Vitiligo Association.
- Journal Title
  
  Pigment Cell Melanoma Res.
  
  Volume: 32 Issue: 2 Pages: 315-319
- DOI
  10.1111/pcmr.12730
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08267, KAKENHI-PROJECT-16K10123
[Journal Article] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mouse model of rhododendrol-induced vitiligo.2019
- Author(s)
  Hayashi M, Okamura K, Abe Y, Hozumi Y, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 46 Issue: 6 Pages: 548-550
- DOI
  10.1111/1346-8138.14879
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10228
[Journal Article] Leukoderma induced by rhododendrol is different from leukoderma of vitiligo in pathogenesis: A novel comparative morphological study.2019
- Author(s)
  Tsutsumi R, Sugita K, Abe Y, Hozumi Y, Suzuki T, Yamada N, Yoshida Y, Yamamoto O
- Journal Title
  
  J Cutan Pathol.
  
  Volume: 46 Issue: 2 Pages: 123-129
- DOI
  10.1111/cup.13396
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10123
[Journal Article] Spectrophotometer is useful for assessing vitiligo and chemical leukoderma severity by quantifying color difference with surrounding normally pigmented skin.2018
- Author(s)
  Hayashi M, Okamura K, Araki Y, Suzuki M, Tanaka T, Abe Y, Nakano S, Yoshizawa J, Hozumi Y, Inoie M, Suzuki T
- Journal Title
  
  Skin Res Technol.
  
  Volume: 24 Issue: 2 Pages: 175-179
- DOI
  10.1111/srt.12410
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10123
[Journal Article] Microsatellite polymorphism located immediately upstream of the phosphatidylinositol glycan, class K gene (PIGK) affects its expression, which correlates with tyrosinase activity in human melanocytes.2017
- Author(s)
  129.Okamura K, Hayashi M, Abe Y, Araki Y, Hozumi Y, Suzuki T
- Journal Title
  
  J Dermatol Sci.
  
  Volume: 85 Issue: 2 Pages: 131-134
- DOI
  10.1016/j.jdermsci.2016.10.012
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K10123
[Journal Article] Positive selection with diversity in oculocutaneous albinisms type 2 gene (OCA2) among Japanese.2015
- Author(s)
  Shimanuki M, Abe Y, Tamiya G, Ueki M, Hozumi Y, Suzuki T.
- Journal Title
  
  Pigment Cell Melanoma Res
  
  Volume: 28 Issue: 2 Pages: 233-5
- DOI
  10.1111/pcmr.12337
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25460403, KAKENHI-PROJECT-25670498, KAKENHI-PROJECT-25870074
[Journal Article] Oculocutaneous albinism (OCA) in Japanese patients: five novel mutations.2014
- Author(s)
  Okamura K, Yoshizawa J, Abe Y, Hanaoka K, Higashi N, Togawa Y, Nakagawa S, Kambe N, Funasaka Y, Ohko K, Hozumi Y, Suzuki T
- Journal Title
  
  J Dermatol Sci
  
  Volume: 74 Issue: 2 Pages: 173-174
- DOI
  10.1016/j.jdermsci.2013.12.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] Gene expression and in situ localization of ADAM17 during skin wound healing.2014
- Author(s)
  Kawaguchi M, Suzuki T
- Journal Title
  
  Int J Dermatol
  
  Volume: 53 Issue: 3
- DOI
  10.1111/ijd.12119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] A case of Hermansky-Pudlak syndrome 1 (HPS1) patient with milder symptoms in Japanese.2014
- Author(s)
  Takeuchi S, Abe Y, Yamada T, Kawano S, Hozumi Y, Ito S, Suzuki T, Nishigori C
- Journal Title
  
  J Dermatology
  
  Volume: 41 Issue: 3 Pages: 268-270
- DOI
  10.1111/1346-8138.12390
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] ADAM17 is involved in the regulation of chemokine expression in keratinocytes.2014
- Author(s)
  Kawaguchi M, Suzuki T
- Journal Title
  
  Int J Dermatol
  
  Volume: 53 Issue: 3
- DOI
  10.1111/ijd.12090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] Variants in melanogenesis-related genes associate with skin cancer risk among Japanese populations.2014
- Author(s)
  Yoshizawa J, Abe Y, Oiso N, Fukai K, Hozumi Y, Nakamura T, Narita T, Motokawa T, Wakamatsu K, Ito S, Kawada A, Tamiya G, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 41 Issue: 4 Pages: 296-302
- DOI
  10.1111/1346-8138.12432
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-24112702, KAKENHI-PROJECT-24500450, KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25460403, KAKENHI-PROJECT-25670498, KAKENHI-PROJECT-25670504
[Journal Article] Hermansky-Pudlak Syndrome Type 4 with a novel mutation.2014
- Author(s)
  Araki Y, Ishii Y, Abe Y, Yoshizawa J, Okamoto F, Hozumi Y, Suzuki T
- Journal Title
  
  J Dermatology
  
  Volume: 41 Issue: 2 Pages: 186-187
- DOI
  10.1111/1346-8138.12386
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] An Intractable Case of Hermansky-Pudlak Syndrome2014
- Author(s)
  Kanazu M, Arai T, Sugimoto C, Kitaichi M, Akira M, Abe Y, Hozumi Y, Suzuki T, Inoue Y
- Journal Title
  
  Intern. Med.
  
  Volume: 53 Issue: 22 Pages: 2629-2634
- DOI
  10.2169/internalmedicine.53.2446
- NAID
  130004713242
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.2013
- Author(s)
  Kono M, Sugiura K, Suganuma M, Hayashi M, Takama H, Suzuki T, Matsunaga K, Tomita Y, Akiyama M.
- Journal Title
  
  Hum Mol Genet
  
  Volume: 22 Issue: 17 Pages: 3524-3533
- DOI
  10.1093/hmg/ddt207
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526, KAKENHI-PROJECT-25670498
[Journal Article] Association of melanogenesis genes with skin color variation among Japanese females2013
- Author(s)
  Abe Y, Tamiya G, Nakamura T, Hozumi Y, and Suzuki T
- Journal Title
  
  J Dermatol Sci
  
  Volume: 69 Pages: 167-172
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] A patient with dyschromatosis symmetrica hereditaria treated with mini punch grafting, followed by excimer light therapy.2013
- Author(s)
  Kawakami T, Otaguchi R, Kyoya M, Soma Y, Suzuki T.
- Journal Title
  
  Journal of Dermatology
  
  Volume: 40 Issue: 9 Pages: 771-772
- DOI
  10.1111/1346-8138.12205
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591658, KAKENHI-PROJECT-25670498
[Journal Article] Case of a Mongolian child with extensive Mongolian spots in Mucopolysaccharidosis type VI: Identification of a novel mutation in the arylsulfatase B gene.2013
- Author(s)
  Okamura K, Munkhbat B, Bachimeg B, Tamiya G, Hozumi Y, Suzuki T.
- Journal Title
  
  J Dermatol
  
  Volume: 40 Issue: 9 Pages: 758-759
- DOI
  10.1111/1346-8138.12237
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-24112702, KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25460403, KAKENHI-PROJECT-25670498
[Journal Article] Agminated pigmented matricoma: a case of a unique tumor with a multifocal appearance composed of neoplastic matrical cells with a significant component of melanocyte.2013
- Author(s)
  Nikaido M, Yamada M, Konno T, Hara K, Yamamoto T, Suzuki T
- Journal Title
  
  J Cutan Pathol
  
  Volume: 40 Issue: 9 Pages: 823-828
- DOI
  10.1111/cup.12185
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25670498
[Journal Article] Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.2012
- Author(s)
  Arase N, Wataya-Kaneda M, Oiso N, Tanemura A, Kawada A, Suzuki T, Katayama I
- Journal Title
  
  J Dermatol Sci.
  
  Volume: 64(2) Issue: 2 Pages: 147-9
- DOI
  10.1016/j.jdermsci.2011.08.006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591219, KAKENHI-PROJECT-22591236
[Journal Article] Lipocalin-type prostaglandin D synthase as a marker for the growth potential of melanocyte-linage cells in the human skin2012
- Author(s)
  Shimanuki M, Takeda K, Kawaguchi M, Suzuki T, and Shibahara S
- Journal Title
  
  J Dermatol
  
  Volume: 39 Issue: 8 Pages: 699-704
- DOI
  10.1111/j.1346-8138.2011.01485.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Reduced GNG2 expression levels in mouse malignant melanomas and human melanoma cell lines2012
- Author(s)
  Yajima I, Kumasaka MY, Suzuki T, Kato M et al.
- Journal Title
  
  Am J Can Res
  
  Volume: 2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature2012
- Author(s)
  Rice GI, Kasher PR, Suzuki T, Crow YJ, et al.
- Journal Title
  
  Nat Genet
  
  Volume: 44 Issue: 11 Pages: 1243-1248
- DOI
  10.1038/ng.2414
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria2012
- Author(s)
  Kawaguchi M, Hayashi M, Suzuki T et al.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 66 Issue: 3 Pages: 245-246
- DOI
  10.1016/j.jdermsci.2012.01.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Oculocutaneous albinism 1 minimal pigment type : a case report on the analysis of genotype of an OCA1MP patient2012
- Author(s)
  Kono, M., Kondo, T., Ito, S., Suzuki, T., Wakamatsu, K, et al
- Journal Title
  
  Br.J.Dermatol.
  
  Volume: 166 Issue: 4 Pages: 896-898
- DOI
  10.1111/j.1365-2133.2011.10690.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21500358, KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-24591646
[Journal Article] Dyschromatosis symmetrica hereditaria: a case report from Turkey, a new association and a novel gene mutation2012
- Author(s)
  Bilen N, Akturk AS, Kawaguchi M, Suzuki T et al.
- Journal Title
  
  J Dermatol
  
  Volume: 39 Issue: 10 Pages: 857-858
- DOI
  10.1111/j.1346-8138.2012.01575.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Blaschkitis-like eruptions with hypodontia and low IκB kinase gamma expression2012
- Author(s)
  Oiso N, Kimura M, Suzuki T, et al
- Journal Title
  
  J Dermatol
  
  Volume: 39 Issue: 11 Pages: 941-943
- DOI
  10.1111/j.1346-8138.2011.01493.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Pediatric case report: clinical profile of a patient with PCWH with p.Q377X nonsense mutation in the SOX10 gene2012
- Author(s)
  Oshimo T, Fukai K, Suzuki T, et al
- Journal Title
  
  J Dermatol
  
  Volume: 39 Issue: 12 Pages: 1022-1025
- DOI
  10.1111/j.1346-8138.2012.01671.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] その他:尋常性白斑診療ガイドライン2012
- Author(s)
  鈴木民夫、金田眞理、種村篤
- Journal Title
  
  日皮会誌
  
  Volume: 122 Pages: 1725-1740
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] on behalf of the Vitiligo Global Issue Consensus Conference panelists: Revised classification/nomenclature of vitiligo and related issues: The Vitiligo Global Issues Consensus Conference2011
- Author(s)
  Ezzedine K, Lim HW , Suzuki T, et al.
- Journal Title
  
  Pigment Cell Melanoma Res
  
  Volume: 25 Issue: 3 Pages: 84-87
- DOI
  10.1111/j.1755-148x.2012.00997.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Oculocutaneous Albinism Type 3: a Japanese Girl With Novel Mutations in TYRP1 gene2011
- Author(s)
  Yamada M, Hayashi M, Suzuki T et al.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 64 Issue: 3 Pages: 217-222
- DOI
  10.1016/j.jdermsci.2011.09.005
- NAID
  10030893699
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Generalized Vitiligo and Associated Autoimmune Diseases in Japanese Patients and Their Families2011
- Author(s)
  Narita T, Oiso N, Suzuki T et al.
- Journal Title
  
  Allergol. Int.
  
  Volume: 60 Issue: 4 Pages: 505-508
- DOI
  10.2332/allergolint.11-OA-0303
- NAID
  130004477112
- ISSN
  1323-8930, 1440-1592
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Dyschromatosis symmetrica hereditaria with acral hypertrophy2011
- Author(s)
  Murata T, Yagi Y, Tanioka M, Suzuki T, et al.
- Journal Title
  
  Euro J Dermatol
  
  Volume: 21 Issue: 4 Pages: 649-650
- DOI
  10.1684/ejd.2011.1486
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Two children with a mild or moderate piebaldism phenotype and a father with no leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT2011
- Author(s)
  Narita T, Oiso N, Suzuki T et al.
- Journal Title
  
  Euro J Dermatol
  
  Volume: 21 Issue: 3 Pages: 446-447
- DOI
  10.1684/ejd.2011.1350
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Dermoscopic features of dyschromatosis symmetrica hereditaria2011
- Author(s)
  Oiso N, Murata I, Suzuki T,et al.
- Journal Title
  
  J Dermatol
  
  Volume: 38 Issue: 1 Pages: 91-93
- DOI
  10.1111/j.1346-8138.2010.01110.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Mutation Analysis of Patients with Dyschromatosis Symmetrica Hereditaria: Five Novel Mutations of the ADAR1 Gene2010
- Author(s)
  Murata I, Hayashi M, Suzuki T et al.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 58 Issue: 3 Pages: 218-220
- DOI
  10.1016/j.jdermsci.2010.04.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236
[Journal Article] Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria2009
- Author(s)
  Michihiro Kono, Yasushi Tomita, Tamio Suzuki (他9名11番目)
- Journal Title
  
  J Dermatol Sci. 53
  
  Pages: 76-77
- NAID
  10025332183
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria : Histological observation and comparison of genotypes and clinical phenotypes2008
- Author(s)
  Taisuke Kondo, Tamio Suzuki, Yoshihiko Mitsuhashi, Shiro Ito, Michihiro Kono, Mayumi Komine, Hirotaka Akita, Yasushi Tomita
- Journal Title
  
  J Dermatol 35
  
  Pages: 395-406
- NAID
  10024297257
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] Segmental lentiginosis and cafe au lait spots within naevoid hypopigmentation2008
- Author(s)
  Kabashima K, Tokura Y, Takahashi K, Suzuki T, and Miyachi Y
- Journal Title
  
  J Eur Acad Dermatol Venereol 22:5. 5
  
  Pages: 397-398
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Dyschromatosis symmetrica hereditaria associated with neurological disorders2008
- Author(s)
  Taisuke Kondo, Tamio Suzuki, Shiro Ito, Michihiro Kono, Tamiko Negoro, Yasushi Tomita
- Journal Title
  
  J Dermatol 35
  
  Pages: 661-665
- NAID
  10023919239
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] Oculocutaneous albinism types 2 and 4 in the Japanese population2008
- Author(s)
  Tamio Suzuki, Yasushi Tomita
- Journal Title
  
  J Dermatol Sci 51
  
  Pages: 1-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with…2007
- Author(s)
  N. Suzuki, et al
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] Ten Novel Mutations of the ADAR01 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria.2007
- Author(s)
  Noriyuki, Suzuki
- Journal Title
  
  J. Invest Dermatol 127
  
  Pages: 309-311
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria2007
- Author(s)
  N Suzuki, et al.
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Ten Novel Mutations of the ADARI Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria2007
- Author(s)
  Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Horikawa T, Fujiwara S, Ishiko A, Matsunaga K, Aoyama Y, Tosaki-Ichikawa H, and Tomita Y
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Ten Novel Mutations of the ADARI Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria.2007
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria2007
- Author(s)
  Tamio Suzuki, Michihiro Kono, Yasushi Tomita (他9名12番目)
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19390294
[Journal Article] 遺伝子異常から見た色素異常症2007
- Author(s)
  鈴木民夫
- Journal Title
  
  日本皮膚科学会雑誌 117
  
  Pages: 2180-2185
- NAID
  10027062503
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria2007
- Author(s)
  N.Suzuki, et al.
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Ten Novel Mutations of the ADARl Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria.2007
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol 127
  
  Pages: 309-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18659322
[Journal Article] Hermansky-Pudlak syndrome2006
- Author(s)
  鈴木民夫
- Journal Title
  
  臨床皮膚科 60
  
  Pages: 23-26
- NAID
  40007274667
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Two novel mutations detected in Japanese patients with oculocutaneous albinism2006
- Author(s)
  Ito S, Suzuki T, Inagaki K, Suzuki N, Kono M, Iwamoto T, Mochizuki S, and Tomita Y
- Journal Title
  
  J Dermatol Sci 44
  
  Pages: 116-118
- NAID
  10020548360
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] 遺伝性対側性色素異常症における新規遺伝子変異の同定2006
- Author(s)
  鈴木教之
- Journal Title
  
  日本皮膚科学会雑誌 116
  
  Pages: 2230-2233
- NAID
  10027062243
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Oculocutaneous albinism type 4 : six novel mutations in the membrane-associated transporter protein gene(SLC45A2) and their phenotype2006
- Author(s)
  Inagaki K, Suzuki T, Ito S, Suzuki N, Adachi K, Okuyama T, Nakata Y, Shimizu H, Matsuura H, Oono T, Iwamatsu H, Kono M, and Tomita Y
- Journal Title
  
  Pigment Cell Res 19
  
  Pages: 451-453
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Dystonia in a Family with Dyschromatosis Symmetriia Hereditaria2006
- Author(s)
  Tojo K, Sekijima Y, Suzuki T, Suzuki N, Tomita Y, Yoshida K, Hashimoto T, and Ikeda S
- Journal Title
  
  Movement disorders 21
  
  Pages: 1510-1513
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Mutation Analysis of the ADAR1 gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.2005
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol 124
  
  Pages: 1186-1192
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.2005
- Author(s)
  Tamio Suzuki
- Journal Title
  
  Br J Dermatol 152
  
  Pages: 174-175
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.2005
- Author(s)
  Tamio Suzuki
- Journal Title
  
  Br J Dermatol 152
  
  Pages: 174-175
- Data Source
  KAKENHI-PROJECT-16044221
[Journal Article] 遺伝性対側性色素異常症の病因遺伝子の発見とその病態について2005
- Author(s)
  鈴木教之, 他
- Journal Title
  
  臨床皮膚科 59
  
  Pages: 54-59
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis2005
- Author(s)
  N Suzuki, et al.
- Journal Title
  
  J Invest Dermatol 124
  
  Pages: 1186-1192
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene.2005
- Author(s)
  Tamio Suzuki et al.
- Journal Title
  
  Br J Dermatol 152
  
  Pages: 174-175
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Identification of pathological gene causing Dyschromatosis Symmetrica Hereditaria and its molecular pathology2005
- Author(s)
  N Suzuki, et al.
- Journal Title
  
  RINSHOU HIFUKA 59
  
  Pages: 54-59
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Mutation Analysis of the ADAR1 gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.2005
- Author(s)
  Noriyuki Suzuki et al.
- Journal Title
  
  J Invest Dermatol 124
  
  Pages: 1186-1192
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Mutation Analysis of the ADARI Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis2005
- Author(s)
  N.Suzuki, et al.
- Journal Title
  
  J Invest Dermatol 124
  
  Pages: 1186-1192
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic・・・2005
- Author(s)
  Suzuki 他
- Journal Title
  
  J.Invest.Dermatol 124
  
  Pages: 1186-1192
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Mutation Analysis of the ADARI gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.2005
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol 124
  
  Pages: 1186-1192
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Genetics of Pigmentary Disorders.2004
- Author(s)
  Yasushi Tomita, Tamio Suzuki
- Journal Title
  
  Am J Med Genet 131C
  
  Pages: 75-81
- NAID
  120000975148
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Investigation on the IVS5 +5G→A Splice Site Mutation of HPS1 Gene Found in Japanese Patients with Hermansky-Pudlak Syndrome.2004
- Author(s)
  Tamio Suzuki
- Journal Title
  
  J Dermatol Sci 36
  
  Pages: 106-108
- NAID
  10016185356
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Investigation on the IVS5 +5G→A Splice Site Mutation of HPS1 Gene Found in Japanese Patients with Hermansky-Pudlak Syndrome.2004
- Author(s)
  Tamio Suzuki
- Journal Title
  
  J Dermatol Sci 36
  
  Pages: 106-108
- NAID
  10016185356
- Data Source
  KAKENHI-PROJECT-16044221
[Journal Article] Investigation on the IVS5+5G→A Splice Site Mutation of HPS1 Gene Found in Japanese Patients with Hermansky-Pudlak Syndrome.2004
- Author(s)
  Tamio Suzuki et al.
- Journal Title
  
  J Dermatol Sci 36
  
  Pages: 106-108
- NAID
  10016185356
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Genetics of Pigmentary Disorders2004
- Author(s)
  Y.Tomita, T.Suzuki
- Journal Title
  
  Am J Med Genet (Semin Med Genet) 131C
  
  Pages: 75-81
- NAID
  120000975148
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Investigation on the IVS5+5G…2004
- Author(s)
  Suzuki et al.
- Journal Title
  
  J Dermatol Sci 36
  
  Pages: 106-108
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Mutation Analysis of the ADAR1 gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol in press
- Data Source
  KAKENHI-PROJECT-16591095
[Journal Article] Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
- Author(s)
  Tamio Suzuki
- Journal Title
  
  J Dermatol Sci (In press)
- NAID
  10024119255
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
- Author(s)
  Tamio, Suzuki
- Journal Title
  
  J. Dermatol Sci. (In press)
- NAID
  10024119255
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
- Author(s)
  Suzuki T, and Tomita Y
- Journal Title
  
  J Dermatol Sci (in press)
- NAID
  10024119255
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Journal Article] Mutation Analysis of the ADAR1 gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis.
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol in press
- Data Source
  KAKENHI-PROJECT-16044221
[Journal Article] Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
- Author(s)
  Tamio Suzuki
- Journal Title
  
  J Dermatol Sci
- NAID
  10024119255
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18659322
[Journal Article] Mutation analysis of the ADAR1 gene…
- Author(s)
  Suzuki et al.
- Journal Title
  
  J Invest Dermatol in press
- Data Source
  KAKENHI-PROJECT-16390315
[Journal Article] Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria.
- Author(s)
  Noriyuki Suzuki
- Journal Title
  
  J Invest Dermatol (In press)
- Data Source
  KAKENHI-PROJECT-18659322
[Patent] ケラチノサイトのメラノソーム取り込み輸送の検出方法2011
- Inventor(s)
  鈴木民夫, ら
- Industrial Property Rights Holder
  鈴木民夫, ら
- Industrial Property Number
  2010-081487
- Filing Date
  2011-01-17
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Special aspects of vitiligo in the Far East: chemical-induced vitiligo.2023
- Author(s)
  Tamio Suzuki, Yuko Abe, Ken Okamura,
- Organizer
  25th World Congress of Dermatology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K07779
[Presentation] Suicide substrate properties of rhododendrol are responsible for tyrosinase inactivation and melanocyte death.2023
- Author(s)
  Kei Nagatani, Yuko Abe, Junichi Fujii, Tamio Suzuki
- Organizer
  1st International Societies for Investigative Dermatology Meeting
- Data Source
  KAKENHI-PROJECT-23K07779
[Presentation] 色素異常症に関わる最近の話題：色白、白斑、色素斑2021
- Author(s)
  鈴木民夫
- Organizer
  日本皮膚科学会長崎地方会第345回例会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08742
[Presentation] 炎症後色素沈着症のモデル動物の確立2020
- Author(s)
  中野祥子、阿部優子、中島喜美子、佐野栄紀、山元修、若松一雅、伊藤祥輔、林昌浩、鈴木民夫
- Organizer
  第50回日本皮膚免疫アレルギー学会総会学術大会
- Data Source
  KAKENHI-PROJECT-19K08742
[Presentation] Establishment of a mouse model for post-inflammatory pigmentation (PIH)2019
- Author(s)
  Shoko Nakano, Yuko Abe, Yutaka Hozumi, Tamio Suzuki, Kimiko Nakajima, Shigetoshi Sano, Osamu Yamamoto
- Organizer
  The 44th annual meeting of the Japanese Society for investigative Dermatology
- Data Source
  KAKENHI-PROJECT-19K08742
[Presentation] 48.Analysis of post-inflammatory hyperpigmentation (PIH) using a new model mouse.2019
- Author(s)
  Tamio Suzuki
- Organizer
  20th Hamchun Dermatology Symposium,
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08742
[Presentation] Chemical vitiligo: instructive evidence that we have learned from Rhododenol-induced leukoderma.2018
- Author(s)
  Tamio Suzuki
- Organizer
  The 70th KDA Annual Autumn Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10123
[Presentation] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mice model of rhododendrol-induced leukoderma2018
- Author(s)
  Masahiro Hayashi, Ken Okamura, Yuko Abe, Yutaka Hozumi, Imi Saito,Tamio Suzuki
- Organizer
  International Investigative Dermatology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10228
[Presentation] Repigmentation in a vitiligo mouse model.2018
- Author(s)
  Tamio Suzuki , Yuko Abe , Ken Okamura , Yutaka Hozumi , Kazumasa Wakamatsu, Shosuke Ito
- Organizer
  The 2nd EAVA meeting Annual Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10123
[Presentation] Rhododendrol-induced leukoderma analyzed with a model mouse.2016
- Author(s)
  11.Tamio Suzuki, Yuko Abe, Ken Okamura, Yutaka Hozumi, Hitomi Aoki, Takahiro Kunisada, Shosuke Ito, Kazumasa Wakamatsu
- Organizer
  VITILIGO INTERNATIONAL SYMPOSIUM 2016
- Place of Presentation
  the hotel NH Vittorio Veneto, Roma
- Year and Date
  2016-12-02
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10123
[Presentation] ロドデノール配合化粧品使用者にみられた白斑に関する検討2013
- Author(s)
  阿部優子, 吉澤順子, 大江倫太郎, 穂積豊, 山川光徳, 鈴木民夫
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] ADAM protease inhibitor regulates chemokine expression in human keratinocytes, and modulates melanogenesis in human melanocytes2013
- Author(s)
  M. Kawaguchi, Y. Hozumi, T. Suzuki
- Organizer
  International Investigative Dermatology 2013
- Place of Presentation
  Edinburgh International Conference Centre, Edinburgh, UK
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] 『わかりやすい色素異常症』正常日本人の皮膚色決定因子2013
- Author(s)
  鈴木民夫､阿部優子､穂積豊
- Organizer
  第112回日本皮膚科学会総会
- Place of Presentation
  パシフィコ横浜、横浜市
- Invited
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] ADAMﾌﾟﾛﾃｱｰｾﾞ阻害剤はﾋﾄﾒﾗﾉｻｲﾄのmelanogenesisを調節する2013
- Author(s)
  川口雅一, 穂積豊, 鈴木民夫
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] Association of melanogenesis genes with skin color variation and risk factor for skin cancers among Japanese population2013
- Author(s)
  Suzuki T, Abe Y, Yoshizawa J, Shimanuki M, Hozumi Y, Tamiya G
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Invited
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] 眼皮膚白皮症における皮膚がん発症ﾘｽｸについての文献的考察2013
- Author(s)
  深井和吉, 安水真規子, 鶴田大輔, 大磯直毅, 鈴木民夫
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] Genetic studies in Japanese patients with oculocutaneous albinism (OCA)2013
- Author(s)
  T. Suzuki, J. Yoshizawa, Y. Abe, Y. Hozumi, M. Hayashi
- Organizer
  International Investigative Dermatology 2013
- Place of Presentation
  Edinburgh International Conference Centre, Edinburgh, UK
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] 網状肢端色素沈着症はADAM10遺伝子変異によって発症する2013
- Author(s)
  河野通浩, 杉浦一充, 林昌浩, 高間弘道, 鈴木民夫, 松永佳世子, 富田靖, 秋山真志
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] Extensive Mongolian Spots in Mucopolysaccharidosis Type VI2013
- Author(s)
  Okamura K, Munkhbat B, Batchimeg B, Tamiya G, Hozumi Y, Suzuki T
- Organizer
  第25回日本色素細胞学会学術大会
- Place of Presentation
  大阪大学吹田キャンパス銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] 皮膚科領域の遺伝子検査2012
- Author(s)
  鈴木民夫
- Organizer
  第57回日本人類遺伝学会
- Place of Presentation
  京王プラザホテル（東京都新宿区）
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] 遺伝性対側性色素異常症について2012
- Author(s)
  鈴木民夫
- Organizer
  第111回日本皮膚科学会総会
- Place of Presentation
  国立京都国際会館(京都府京都市）
- Invited
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Genetic variants in pigmentation genes, skin color, and risk of skin cancer in Japanese2012
- Author(s)
  T. Suzuki
- Organizer
  62th Annual Meeting of The American Society of Human Genetics
- Place of Presentation
  Moscone Center(San Francisco, USA)
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Recent proceedings in hereditary hypopigmentary disorders2012
- Author(s)
  T. Suzuki
- Organizer
  第24回日本色素細胞学会
- Place of Presentation
  長浜バイオ大学(滋賀県長浜市)
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Genetic variants in pigmentation genes, skin color, and risk of skin cancer in Japanese2012
- Author(s)
  T. Suzuki , Y. Abe, J. Yoshizawa, Y. Hozumi, T. Nakamura, G. Tamiya
- Organizer
  62th Annual Meeting of The American Society of Human Genetics
- Place of Presentation
  Moscone Center, San Francisco, USA
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] What's new in albinism among Japanese 20112011
- Author(s)
  T. Suzuki
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux, Bordeaux, France
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Hypopigmentary disorders: a better understanding from a genetic view2011
- Author(s)
  T. Suzuki
- Organizer
  The 9th International Symposium of the Cutaneous Biology Research Institute
- Place of Presentation
  Yonsei University, Seoul, Korea
- Year and Date
  2011-10-01
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Albinochip: a universal genetic diagnosis for all known mutations associated to albinism2011
- Author(s)
  E. Molto, A. Fernandez, C. Phillips, M. Torres, O. Maronas, B. Arveiler, F. Morice-Picard, A. Taieb, R. Aquaron, V. Schiaffino, M. Hayashi, T. Suzuki, M. Martinez, M. J. Trujillo, C. Ayuso, A. Carracedo, L. Montoliu
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux, Bordeaux, France
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Oculocutaneous albinism 1 minimal pigment type; a case report on the analysis of genotype-phenotype correlation2011
- Author(s)
  M. Kono, T. Kondo, S. Ito, T. Suzuki, K. Wakamatsu, S. Ito, Y. Tomita
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux, Bordeaux, France
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Association of the melanogenesis genes with Japanese skin color2011
- Author(s)
  Y.Abe, Y.Hozumi, G Tamia, T. Suzuki
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux,Bordeaux, France
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] A Case of epidermolytic palmoplantar keratoderma with knuckle pads2011
- Author(s)
  Hayashi M, Nakano H, Sawamura D, T. Suzuki
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  COEX Convention and Exhibition Center, Seoul, Korea
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Hereditary hypo-pigmentary disorders2011
- Author(s)
  Suzuki T., et al.
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  Seoul, Korea(招待講演)
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] What's new in albinism among Japanese 20112011
- Author(s)
  Suzuki T., et al.
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Bordeaux, France(招待講演)
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Generalized vitiligo and related autoimmune disorders in Japanese patients and their families2011
- Author(s)
  N. Oiso, K. Fukai, T. Narita, K. Kabashima, A. Kawada, T. Suzuki
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux,Bordeaux, France
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Hypopigmentary disorders : a better understanding from a genetic view2011
- Author(s)
  Suzuki T.
- Organizer
  The 9th International Symposium of the Cutaneous Biology Research Institute
- Place of Presentation
  Seoul, Korea(招待講演)
- Year and Date
  2011-10-01
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Hereditary hypo-pigmentary disorders2011
- Author(s)
  T. Suzuki, M. Hayashi
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  COEX Convention and Exhibition Center, Seoul, Korea
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Dermal lobular capillary hemangioma2010
- Author(s)
  M Hayashi, T. Suzuki
- Organizer
  The 1st Eastern Asia Dermatology Congress
- Place of Presentation
  Hotel New Otani Hakata, Fukuoka, Japan
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Nephrogenic systemic fibrosis; Two includes clinically different phenotypes; A study on Japanese patients2010
- Author(s)
  N. Abe, Y. Matsumoto, Y. Mitsuhashi, F. Momma, T. Suzuki, R. Tsuboi
- Organizer
  The 1st Eastern Asia Dermatology Congress
- Place of Presentation
  Hotel New Otani Hakata,Fukuoka, Japan
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] 遺伝性色素異常症の最近の話題2010
- Author(s)
  鈴木民夫
- Organizer
  日本皮膚科学会第353回福岡地方会
- Place of Presentation
  久留米大学筑水会館
- Year and Date
  2010-07-11
- Data Source
  KAKENHI-PROJECT-22591236
[Presentation] Dyschromatosis symmetrica hereditaria:Gene and morphological2008
- Author(s)
  Taisuke Kondo, Tamio Suzuki, Michihiro Kono, Yasushi Tomita (他5名)
- Organizer
  International Investigative Dermatology
- Place of Presentation
  京都市
- Year and Date
  2008-05-06
- Data Source
  KAKENHI-PROJECT-19390294
[Presentation] Oculocutaneous albinism and dyschromatosis symmetrica hereditaria2008
- Author(s)
  Yasushi Tomita, Taisuke Kondo, Michihiro Kono, Tamio Suzuki
- Organizer
  The 20^<th> International Pigment Cell Conference
- Place of Presentation
  札幌市
- Year and Date
  2008-05-09
- Data Source
  KAKENHI-PROJECT-19390294
[Presentation] Dyschromatosis symmetrica hereditaria associated with neurological disorders2008
- Author(s)
  Taisuke Kondo, Tamio Suzuki, Shiro Ito, Michihiro Kono, Tamiko Negoro, Yasutomo Ito, Yasushi Tomita
- Organizer
  The 20^<th> International Pigment Cell Conference
- Place of Presentation
  札幌市
- Year and Date
  2008-05-09
- Data Source
  KAKENHI-PROJECT-19390294
[Presentation] モロッコ系ベルギー人で初めて確認された眼皮膚白皮症4型患者で見つかった新規遺伝子変異の機能解析2007
- Author(s)
  鈴木民夫
- Organizer
  日本研究皮膚科学会第32回年次学術大会
- Place of Presentation
  横浜
- Year and Date
  2007-04-19
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] 色素細胞の生物学遺伝子異常から見た色素異常症2007
- Author(s)
  鈴木民夫
- Organizer
  第105回日本皮膚科学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] Hermansky-Pudlak Syndrome Detected Among Japanese Albino Patients2007
- Author(s)
  Tamio Suzuki
- Organizer
  2nd Conference of The Asian Society for Pigment Cell Research
- Place of Presentation
  Singapore
- Data Source
  KAKENHI-PROJECT-18659322
[Presentation] やさしい分子遺伝学入門〜美白遺伝子など〜2007
- Author(s)
  鈴木民夫
- Organizer
  第71回日本皮膚科学会東部支部学術大会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] Hermansky-Pudalk Syndrome Detected Among Japanese Albino Patients2007
- Author(s)
  Tamio, Suzuki
- Organizer
  2nd Conference of The Asian Society for Pigment Cell Research
- Place of Presentation
  Singapore
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] 色素細胞の生物学遺伝子異常から見た色素異常症2007
- Author(s)
  鈴木民夫
- Organizer
  第105回日本皮膚科学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18659322
[Presentation] モロッコ系ベルギ-人で初めて確認された眼皮膚白皮症4型患者で見つかった新規遺伝子変異の機能解析2007
- Author(s)
  鈴木民夫
- Organizer
  日本研究皮膚科学会第32回年次学術大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] やさしい分子遺伝学入門〜美白遺伝子など〜2007
- Author(s)
  鈴木民夫
- Organizer
  第71回日本皮膚科学会東部支部学術大会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-18659322
[Presentation] Hermansky-Pudlak Syndrome Detected Among Japanese Albino Patients2007
- Author(s)
  T. Suzuki, S. Ito, T. Kondo, Y. Tomita
- Organizer
  2nd Conference of The Asian Society for Pigment Cell Research
- Place of Presentation
  Singapore
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] モロッコ系ベルギー人で初めて確認された眼皮膚白皮症4型患者で見つかった新規遺伝子変異の機能解析2007
- Author(s)
  鈴木民夫
- Organizer
  日本研究皮膚科学会第32回年次学術大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18659322
[Presentation] 日本人白皮症患者におけるHermansky-Pudlak症候群1型遺伝子の解析2006
- Author(s)
  鈴木民夫
- Organizer
  日本研究皮膚科学会第31回年次学術大会
- Place of Presentation
  京都
- Year and Date
  2006-05-31
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] Oculocutaneous albinism type 4:three novel mutations in the MATP gene and their genotype-phenotype correlation2006
- Author(s)
  Tamio, Suzuki
- Organizer
  35th Annual Meeting of The European Society for Dermatological Research
- Place of Presentation
  Paris, France
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] Oculocutaneous albinism type 4 : three novel mutations in the MATP gene and their genotype-phenotype correlation2006
- Author(s)
  T. Suzuki, K. Inagaki, S. Ito, N. Suzuki, K. Adachi, T. Oono, Y. Tomita
- Organizer
  35th Annual Meeting of The European Society for Dermatological Research
- Place of Presentation
  Paris, France
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] Positive selection with diversity in oculocutaneous
- Author(s)
  Shimanuki M, Tamiya G, Abe Y, Hozumi Y, Suzuki T
- Organizer
  39th Annual Meeting fo the Japanese Society for Investigative Dermatology
- Place of Presentation
  エキスポホテル(伊丹市)
- Year and Date
  2014-12-13 – 2014-12-14
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] Positive selection with diversity in oculocutaneous albinisms type 2 gene (OCA2) among Japanese.
- Author(s)
  Shimanuki M, Tamiya G, Abe Y, Hozumi Y, Suzuki T
- Organizer
  12th international pigment cell conference
- Place of Presentation
  Shangri-La Hotel, Singapore
- Year and Date
  2014-09-04 – 2014-09-07
- Data Source
  KAKENHI-PROJECT-25670498
[Presentation] Association of melanogenesis genes with skin color variation and risk factor for skin cancers among Japanese population.
- Author(s)
  T. Suzuki, Y. Abe, J. Yoshizawa, N. Oiso, Y. Hozumi, T. Nakamura, G. Tamiya
- Organizer
  3rd EADC 2014
- Place of Presentation
  済州国際センター（韓国、済州島）
- Year and Date
  2014-09-24 – 2014-09-26
- Invited
- Data Source
  KAKENHI-PROJECT-25670498

1. YASUSHI Tomita (70108512)

# of Collaborated Projects: 8 results

# of Collaborated Products: 10 results
2. MIYAMURA Yoshinori (50272034)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
3. ONO Hideyu (40160915)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
4. 榊原章浩 (50313995)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
5. HOZUMI Yutaka

# of Collaborated Projects: 3 results

# of Collaborated Products: 21 results
6. OKAMOTO Ken

# of Collaborated Projects: 3 results

# of Collaborated Products: 6 results
7. MICHIHIRO Kono (60319324)

# of Collaborated Projects: 2 results

# of Collaborated Products: 11 results
8. TUBOI Syozo (70004554)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
9. YASUE Takashi (40335039)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
10. ARAKI Yuua

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
11. YOSHINAO Muro (80270990)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. KUNISADA Takahiro (30205108)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. YOSHIDA Tadashi (10004673)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. HAYASHI MASAHIRO (30396569)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
15. 杉浦光洋 (60378031)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 松本明子 (10330979)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 伊藤祥輔 (70121431)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
18. 若松一雅 (80131259)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
19. 辻田忠志 (20622046)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 原俊哉 (70274602)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. KONDO Taisuke

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
22. ABE Yuko

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
23. KANEDA Mari

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 片山一朗

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 杉浦一充

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 秋山真志

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 本間拓二郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 川上民裕

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 田宮元

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results

Suzuki Tamio 鈴木 民夫

SUZUKI Tamio 鈴木 民夫

TAMIO Suzuki 鈴木 民夫

Research Projects

Research Products

Co-Researchers

Comprehensive analyses of the pathogenesis of chemical vitiligo, a form of vitiligo, and development of new treatment methodsPrincipal Investigator

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A mouse model for postinflammatory hyperpigmentation: an analysis of molecular, and histological traits, and an establishment of effective treatment.Principal Investigator

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Identification and functional analyzes of chemical-induced vitiligo susceptibility genes.Principal Investigator

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Identification and functional analysis of responsible gene(s) for Mongolian blue spotPrincipal Investigator

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Functional analyses of the genes responsible for hereditary pigment disordersPrincipal Investigator

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アールエヌエー編集障害により発症する遺伝性対側性色素異常症の病態解析Principal Investigator

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Functional analyses of the genes in which mutations cause oculocutaneous albinismsPrincipal Investigator

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ヘルマンスキー・パドラック症候群および眼皮膚白皮症の病因遺伝子産物の機能解析Principal Investigator

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Functional analyses of the genes in which mutations cause hereditary pigment disordersPrincipal Investigator

Suzuki Tamio 鈴木民夫

SUZUKI Tamio 鈴木民夫

TAMIO Suzuki 鈴木民夫