Kono Michihirro 河野通浩

… Alternative Names

河野通浩コウノミチヒロ

MICHIHIRO Kono 河野通浩

KONO Michihiro 河野道浩

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Researcher Number	60319324
Other IDs
Affiliation (Current)	2025: 秋田大学, 医学系研究科, 教授
Affiliation (based on the past Project Information) *help	2018 – 2023: 秋田大学, 医学系研究科, 教授 2017: 名古屋大学, 医学系研究科, 准教授 2011 – 2015: 名古屋大学, 医学(系)研究科(研究院), 講師 2013: 名古屋大学, 医学系研究科, 講師 2009 – 2011: 名古屋大学, 医学系研究科, 講師 … More 2008 – 2011: 名古屋大学, 大学院・医学系研究科, 講師 2007: 名古屋大学, 医学系研究科, 講師 2007: Nagoya University, Graduate School of Medicine Department of dermatology, Assistant Professor 2007: 名古屋大学, 医学部附属病院, 助教 2006: 名古屋大学, 医学部附属病院, 助手 2002: 名大, 医学部附属病院, 助手 2001: 名古屋大学, 医学部・附属病院, 助手 2000: 愛知医科大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Dermatology / Basic Section 53050:Dermatology-related / Dermatology Except Principal Investigator Dermatology / Basic Section 53050:Dermatology-related / Dermatology
Keywords	Principal Investigator モデルマウス / 遺伝性対側性色素異常症 / 遺伝性色素異常症 / ADAM10 / 網状肢端色素沈着症 / ADAR1 / 色素細胞 / RNA編集 / メラノソーム / 原因遺伝子 … More / オートファジー / POFUT1 / Dowling-Degos病 / 常染色体優性遺伝形式 / Dowling-Degos disease / 皮膚科学 / 遺伝子診断 / 治療 / DSH / dyschromatosis / メラノサイト / SCF / ノックアウトマウス / 色素細胞学 / MART-1 / チロシナーゼ / 角化細胞 / 画像解析 / 補助的診断法 / ブラックライト / ゲノムプロジェクト / ポジショナルクローニング … More Except Principal Investigator 眼皮膚白皮症 / 遺伝子 / 魚鱗癬 / メラニン / ADAR1 / 色素異常症 / 全身性エリテマトーデス / 疾患モデルマウス / 炎症性ミオパチー / 自己抗体 / 皮膚筋炎 / 間質性肺炎 / 魚燐癬 / 表皮脂質 / 皮膚バリア / 表皮 / 角化 / 脂質 / proteome analysis / gene diagnosis / hereditary pigment disorders / melanosome / melanin / Hermansky-Pudlak syndrome / oculocutaneous albinism / 遺伝病 / プロテオーム / 遺伝学 / プロテオーム解析 / 遺伝子診断 / 遺伝性色素異常症 / メラノソーム / ヘルマンスキー・パドラック症候群 / 遺伝子治療 / マウスモデル / フィラグリン / ABCA12 / 角化異常症 / 皮膚病理学 / メラノサイト初代培養 / モデルマウス / 遺伝性対側性色素異常症 / Hermansky-Pudlak症候群 / 色素細胞学 / メラノサイト / 白斑 / 遺伝性疾患 / SNP / マイクロアレイ法 / オリゴアレイ法 Less

Understanding the pathogenesis of pigmentary disorders focusing on autophagy and the establishment of novel inherited pigmentary disorders.Principal Investigator
- Principal Investigator
  
  河野通浩
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Akita University
The comprehensivve elucidation of pathogenesis and the establishment of therapeutic agent with model mouse for Dowling-Degos diseasePrincipal Investigator
- Principal Investigator
  
  Kono Michihirro
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Akita University
皮膚筋炎におけるRNA編集酵素ADAR1の自己免疫応答ともたらす病態
- Principal Investigator
  
  室慶直
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Nagoya University
Elucidation of pathogenic mechanisms of ichthyosis due to epidermal lipid abnormalities and development of novel therapeutic agents
- Principal Investigator
  
  AKIYAMA Masashi
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Nagoya University
comprehensive elucidation of pathophysiology of reticulate acropigmentation of Kitamura and development of therapeutic agents using model mice and antibody arraysPrincipal Investigator
- Principal Investigator
  
  Kono Michihiro
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Akita University
  Nagoya University
The development of new non-invasive therapeutic strategy of dyschromatosis symmetrica hereditaria with topical agentPrincipal Investigator
- Principal Investigator
  
  Kono Michihiro
- Project Period (FY)
  2012 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Innovation of novel treatments for various phenotypes of ichthyosis by restoration of ABCA12 lipid transporter gene expression
- Principal Investigator
  
  AKIYAMA Masashi
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Study on regulatory mechanism of melanin synthesis clarified by elucidation of molecular pathology on pigmentary disorders
- Principal Investigator
  
  SAWADA Masaki
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Elucidation of pathogenesis of DSH with the model mouse that melanocyte is distributed in epidermisPrincipal Investigator
- Principal Investigator
  
  KONO Michihiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya 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
イノシン特異的mRNA切断によるADAR1基質同定と遺伝性対側性色素異常症病態解明Principal Investigator
- Principal Investigator
  
  河野通浩
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
Functional analyses of the genes in which mutations cause oculocutaneous albinisms
- 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
色素異常症における発現遺伝子プロファイリングの差異による新規関連遺伝子の検索Principal Investigator
- Principal Investigator
  
  河野通浩
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University
新ゲノム解析オリゴアレイ法による遺伝性対側性色素異常症の病因遺伝子の解明
- Principal Investigator
  
  YASUSHI Tomita
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Dermatology
- Research Institution
  Nagoya University

[Book] 今日の治療指針2014年度版「酒さ様皮膚炎・口囲皮膚炎」2014
- Author(s)
  河野通浩、戸倉新樹、新谷陽一、天野正宏、川田暁、海老原全、高山かおる、浅野善英、神戸直智、片桐一元、村田哲、佐伯秀久、三原祥嗣、室田浩之、佐藤貴浩、石黒直子、末木博彦、相原道子、赤坂江美子、照井正、他
- Total Pages
  2052
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-24591646
[Book] Dyschromatosis symmetrica hereditaria and RNA editing enzyme. in the book "Current Genetics in Dermatology"2013
- Author(s)
  Michihiro Kono, Masashi Akiyama.
- Total Pages
  213
- Publisher
  InTech
- Data Source
  KAKENHI-PROJECT-24591646
[Book] 皮膚科診療カラーアトラス大系第3巻(色調異常/水庖性疾患・膿疱症)「遺伝性対側性色素異常症(遠山)」2009
- Author(s)
  河野通浩
- Total Pages
  186
- Publisher
  講談社
- Data Source
  KAKENHI-PROJECT-21591460
[Book] 皮膚科診療カラーアトラス大系第3巻(色調異常/水疱性疾患・膿疱症)2009
- Author(s)
  河野通浩
- Publisher
  講談社
- Data Source
  KAKENHI-PROJECT-21591459
[Book] 「遺伝性対側性色素異常症(遠山)」皮膚科診療カラーアトラス大系第3巻(色調異常/水疱性疾患・膿疱症)2009
- Author(s)
  河野通浩
- Total Pages
  182
- Publisher
  東京、講談社
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] SDR9C7 catalyzes critical dehydrogenation of acylceramides for skin barrier formation2020
- Author(s)
  Takeichi T, Hirabayashi T, Miyasaka Y, Kawamoto A, Okuno Y, Taguchi S, Tanahashi K, Murase C, Takama H, Tanaka K, Boeglin WE, Calcutt MW, Watanabe D, Kono M, Muro Y, Ishikawa J, Ohno T, Brash AR, Akiyama M
- Journal Title
  
  J Clin Invest
  
  Volume: 130 Issue: 2 Pages: 890-903
- DOI
  10.1172/jci130675
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K06978, KAKENHI-PROJECT-18H02832
[Journal Article] Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1.2020
- Author(s)
  Muro Y, Ogawa-Momohara M, Takeichi T, Fukaya S, Yasuoka H, Kono M, Akiyama M.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 100 Issue: 1 Pages: 82-84
- DOI
  10.1016/j.jdermsci.2020.08.008
- NAID
  120007146027
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08688
[Journal Article] Recurrent KRT10 variant in ichthyosis with confetti.2020
- Author(s)
  Takeichi T, Suga Y, Mizuno T, Okuno Y, Ichikawa D, Kono M, Lee JYW, McGrath JA, Akiyama M.
- Journal Title
  
  Acta Dermato-Venereol
  
  Volume: 100 Issue: 14 Pages: adv00209-adv00209
- DOI
  10.2340/00015555-3570
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19540, KAKENHI-PROJECT-18H02832
[Journal Article] Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutations.2018
- Author(s)
  Takeichi T, Honda A, Okuno Y, Kojima D, Kono M, Nakamura Y, Tohyama M, Tanaka T, Aoyama Y, Akiyama M.
- Journal Title
  
  Br J Dermatol.
  
  Volume: 179 Issue: 5 Pages: 1186-1188
- DOI
  10.1111/bjd.16823
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19717, KAKENHI-PROJECT-15H04887, KAKENHI-PROJECT-18H02832
[Journal Article] Reduction of stratum corneum ceramides in Neu-Laxova syndrome caused by phosphoglycerate dehydrogenase deficiency.2018
- Author(s)
  Reduction of stratum corneum ceramides in Neu-Laxova syndrome caused by phosphoglycerate dehydrogenase deficiency.
- Journal Title
  
  Journal of lipid research
  
  Volume: 59 Issue: 12 Pages: 2413-1420
- DOI
  10.1194/jlr.p087536
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K08301, KAKENHI-PROJECT-16K10165, KAKENHI-PROJECT-16K19717, KAKENHI-PROJECT-15H04887, KAKENHI-PROJECT-18H02832
[Journal Article] IgE-independent pathophysiology of severe atopic dermatitis demonstrated in an IgE-deficient patient.2016
- Author(s)
  Ogawa Y, Kono M, Tsujikawa M, Tsujiuchi H, Akiyama M.
- Journal Title
  
  J Dermatol Sci.
  
  Volume: - Issue: 2 Pages: 139-141
- DOI
  10.1016/j.jdermsci.2016.01.008
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26461657
[Journal Article] Hyper-IgE syndrome with a novel mutation of the STAT3 gene.2016
- Author(s)
  Minakawa S, Tanaka H, Kaneko T, Matsuzaki Y, Kono M, Akiyama M, Minegishi Y, Sawamura D.
- Journal Title
  
  Clin Exp Dermatol.
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Angiofibroma of soft tissue in the cheek: diagnosis confirmed by gene rearrangement in NCOA2.2016
- Author(s)
  Jeong JW, Kono M, Hasegawa-Murakami Y, Motoi T, Yokota K, Matsumoto T, Kaibuchi-Ando K, Kato Y, Tada T, Akiyama M.
- Journal Title
  
  Acta Derm Venereol.
  
  Volume: -
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Reticulate acropigmentation of Kitamura with a novel ADAM10 mutation: a case report.2016
- Author(s)
  Tsutsumi M, Kono M, Akiyama M, Katoh N, Nakai N.
- Journal Title
  
  J Dermatol
  
  Volume: - Issue: 8 Pages: 1-2
- DOI
  10.1111/1346-8138.13308
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26461698
[Journal Article] Unilateral generalized linear porokeratosis with nail dystrophy.2016
- Author(s)
  Kono M, Yokoyama N, Ogawa Y, Takama H, Sugiura K, Akiyama M.
- Journal Title
  
  J Dermatol
  
  Volume: 43 Issue: 3 Pages: 286-7
- DOI
  10.1111/1346-8138.13204
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26670526
[Journal Article] Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.2016
- Author(s)
  Okamura K, Araki Y, Abe Y, Shigyou A, Fujiyama T, Baba A, Kanekura T, Chinen Y, Kono M, Niizeki H, Tsubota A, Konno T, Hozumi Y, Suzuki T.
- Journal Title
  
  J Dermatol Sci.
  
  Volume: 81 Issue: 2 Pages: 140-2
- DOI
  10.1016/j.jdermsci.2015.10.014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-25461702
[Journal Article] Dyschromatosis symmetrica hereditaria and Aicardi-Goutires syndrome 6 are phenotypic variants caused by ADAR1 mutations.2016
- Author(s)
  Kono M, Matsumoto F, Suzuki Y, Suganuma M, Saitsu H, Ito Y, Fujiwara S, Matsumoto K, Moriwaki S, Matsumoto N, Tomita Y, Sugiura K, Akiyama M.
- Journal Title
  
  J Invest Dermatol.
  
  Volume: 136 Issue: 4 Pages: 875-8
- DOI
  10.1016/j.jid.2015.12.034
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-16K15546, KAKENHI-PROJECT-15H04886
[Journal Article] Hyperpigmentation over the metacarpophalangeal joints and the malleoli in a case of hyaline fibromatosis syndrome with ANTXR2 mutations.2016
- Author(s)
  Sugiura K, Ohno A, Kono M, Kitoh H, Itomi K, Akiyama M.
- Journal Title
  
  J Eur Acad Dermatol Venereol.
  
  Volume: - Issue: 10 Pages: 44-46
- DOI
  10.1111/jdv.13290
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-15K15548, KAKENHI-PROJECT-16K15546, KAKENHI-PROJECT-15H04886
[Journal Article] A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.2016
- Author(s)
  Kono M, Fukai K, Omura R, Sugawara K, Tsuruta D, K Sugiura K, Akiyama M.
- Journal Title
  
  J Eur Acad Dermatol Venereol.
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] A 45-year-old woman with Ehlers-Danlos syndrome caused by dermatan 4-O-sulfotransferase-1 deficiency: implications of dermatan sulfate depletion on early aging.2016
- Author(s)
  Kono M, Hasegawa-Murakami Y, Sugiura K, Ono M, Toriyama K, Miyake N, Hatamochi A, Kamei Y, Kosho T, Akiyama M.
- Journal Title
  
  Acta Derm Venereol.
  
  Volume: - Pages: 1-2
- DOI
  10.2340/00015555-2390
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-25460405, KAKENHI-PROJECT-25461675, KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-16K15546, KAKENHI-PROJECT-15H04886
[Journal Article] Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.2015
- Author(s)
  Kono M, Suganuma M, Takama H, Zarzoso I, Saritha M, Bodet D, Aboobacker S, Kaliaperumal K, Suzuki T, Tomita Y, Sugiura K, Akiyama M.
- Journal Title
  
  Br J Dermatol
  
  Volume: 173 Issue: 2 Pages: 584-6
- DOI
  10.1111/bjd.13702
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26670526
[Journal Article] Large epidermal cleft formation in verrucous-keratotic malignant melanoma on the heel2015
- Author(s)
  Takaaki Matsumoto, Kenji Yokota, Masaki Sawada, Yoshie Hasegawa, Aya Takeuchi, Michihiro Kono, Masashi Akiyama
- Journal Title
  
  J Am Acad Dermatol.
  
  Volume: 72 Issue: 1 Pages: e37-e38
- DOI
  10.1016/j.jaad.2014.09.044
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] アトピー性皮膚炎とフィラグリン遺伝子2015
- Author(s)
  河野通浩, 秋山真志
- Journal Title
  
  チャイルドヘルス
  
  Volume: 18 Pages: 660-2
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Lymphatic flow is mostly preserved after sentinel lymph node biopsy in primary cutaneous malignant melanoma.2015
- Author(s)
  Yokota K, Sawada M, Matsumoto T, Hasegawa Y, Kono M, Akiyama M.
- Journal Title
  
  J Dermatol Sci.
  
  Volume: 78 Issue: 2 Pages: 101-7
- DOI
  10.1016/j.jdermsci.2015.02.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Annular Elastolytic Giant Cell Granuloma Successfully Treated with Minocycline Hydrochloride.2015
- Author(s)
  Nanbu A, Sugiura K, Kono M, Muro Y, Akiyama M.
- Journal Title
  
  Acta Derm Venereol.
  
  Volume: in press Issue: 6 Pages: 756-7
- DOI
  10.2340/00015555-2056
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-26670526
[Journal Article] Porokeratotic eccrine ostial and dermal duct nevus with a somatic homozygous or monoallelic variant of connexin 26.2015
- Author(s)
  Noda K, Sugiura K, Kono M, Akiyama M.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 80 Issue: 1 Pages: 74-6
- DOI
  10.1016/j.jdermsci.2015.07.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26670526
[Journal Article] 色素失調症の男児例2015
- Author(s)
  清水奈美, 深井和吉, 小澤俊幸, 新宅治夫, 河野通浩, 鶴田大輔
- Journal Title
  
  日本小児皮膚科学会雑誌
  
  Volume: 34 Pages: 113-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Buruli ulcer successfully treated with negative-pressure wound therapy.2015
- Author(s)
  Murase C, Kono M, Nakanaga K, Ishii N, Akiyama M.
- Journal Title
  
  JAMA Dermatol.
  
  Volume: 151 Issue: 10 Pages: 1137-9
- DOI
  10.1001/jamadermatol.2015.1567
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Impetigo herpetiformis with IL36RN mutations in a Chinese patient: A founder haplotype of c.115+6T>C in East Asia.2015
- Author(s)
  Sugiura K, Nakasuka A, Kono H, Kono M, Akiyama M.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 79 Issue: 3 Pages: 319-20
- DOI
  10.1016/j.jdermsci.2015.06.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K15414, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-26670526
[Journal Article] 頭頂部のVascular Eccrine Spiradenomaの1例2014
- Author(s)
  安達明子, 横田憲二, 河野通浩, 澤田昌樹, 松本高明, 長谷川佳恵, 山中直樹, 室慶直, 秋山真志
- Journal Title
  
  皮膚科の臨床
  
  Volume: 56 Pages: 835-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Revertant Mutation Releases Confined Lethal Mutation, Opening Pandora' s Box : A Novel Genetic Pathogenesis2014
- Author(s)
  Ogawa Y, Takeichi T, Kono M, Hamajima N, Yamamoto T, Sugiura K, Akiyama M
- Journal Title
  
  PLoS Genet
  
  Volume: 10(5) Issue: 5 Pages: e1004276-e1004276
- DOI
  10.1371/journal.pgen.1004276
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-25670342, KAKENHI-PROJECT-25670502, KAKENHI-PROJECT-26461657, KAKENHI-PROJECT-26670526, KAKENHI-PROJECT-24405017
[Journal Article] Spindle cell angiosarcoma almost exclusively made up of spindle cells.2014
- Author(s)
  Makita S, Kono M, Yamada M, Suzuki N, Karasawa T, Tanahashi C, Akiyama M.
- Journal Title
  
  Eur J Dermatol
  
  Volume: 24 Issue: 1 Pages: 106-7
- DOI
  10.1684/ejd.2013.2224
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Spindle cell carcinoma of the breast in a patient with neurofibromatosis type 1.2014
- Author(s)
  Nogimori M, Yokota K, Sawada M, Matsumoto T, Kono M, Akiyama M.
- Journal Title
  
  Eur J Dermatol.
  
  Volume: 24 Issue: 3 Pages: 397-8
- DOI
  10.1684/ejd.2014.2329
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations2014
- Author(s)
  Kono M, Nomura T, Ohguchi Y, Mizuno O, Suzuki S, Tsujiuchi H, Hamajima N, McLean WH, Shimizu H, Akiyama M.
- Journal Title
  
  Allergy
  
  Volume: 69(4) Issue: 4 Pages: 537-540
- DOI
  10.1111/all.12369
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390152, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-25670494
[Journal Article] 【網状を呈する皮膚疾患】topics 網状肢端色素沈着症　原因遺伝子の解明.2014
- Author(s)
  河野通浩
- Journal Title
  
  皮膚病診療
  
  Volume: 36 Pages: 206-12
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Urticaria pigmentosa complicated with esophageal eosinophilia2014
- Author(s)
  Rirei Nin-Asai, Michihiro Kono, Masashi Akiyama
- Journal Title
  
  J Am Acad Dermatol.
  
  Volume: 71 Issue: 5 Pages: e207-e208
- DOI
  10.1016/j.jaad.2014.05.037
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Proposed classification of longitudinal melanonychia based on clinical and dermoscopic criteria.2014
- Author(s)
  Sawada M, Yokota K, Matsumoto T, Shibata S, Yasue S, Sakakibara A, Kono M, Akiyama M
- Journal Title
  
  Int J Dermatol.
  
  Volume: 53 Pages: 581-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations2014
- Author(s)
  Tanahashi K, Sugiura K, Kono M, Takama H, Hamajima N, Akiyama M
- Journal Title
  
  PLoS ONE
  
  Volume: 9(2) Issue: 2 Pages: e89261-e89261
- DOI
  10.1371/journal.pone.0089261
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease2013
- 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 Pages: 3524-3533
- Data Source
  KAKENHI-PROJECT-23249058
[Journal Article] Extraordinarily large, giant spider angioma in an alcoholic cirrhotic patient.2013
- Author(s)
  Hane H, Yokota K, Kono M, Muro Y, Akiyama M.
- Journal Title
  
  Int J Dermatol
  
  Volume: 53 Issue: 2
- DOI
  10.1111/j.1365-4632.2012.05548.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?2013
- Author(s)
  Kono M, Akiyama M, Suganuma M, Sanchez-Valle A, Tomita Y
- Journal Title
  
  Int J Dermatol
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Novel ADAR1 mutations including single amino acid deletion in the deaminase domain underly dyschromatosis symmetrica hereditaria in Japanese families2013
- Author(s)
  Kono M, Suganuma M, Ito Y, Ujiie H, Morimoto K, Akiyama M
- Journal Title
  
  Int J Dermatol
  
  Volume: 印刷中 Issue: 3
- DOI
  10.1111/j.1365-4632.2012.05765.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] Novel ABCA12 splice site deletion mutation and ABCA12 mRNA analysis of pulled hair samples in harlequin ichthyosis2013
- Author(s)
  Takeichi T, Sugiura K, Matsuda K, Kono M, Akiyama M
- Journal Title
  
  J Dermatol Sci
  
  Volume: 69 Pages: 259-261
- Data Source
  KAKENHI-PROJECT-23249058
[Journal Article] Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?2013
- Author(s)
  Kono M, Akiyama M, Suganuma M, Sanchez-Valle A, Tomita Y.
- Journal Title
  
  Int J Dermatol
  
  Volume: 52 Issue: 12 Pages: 1582-4
- DOI
  10.1111/j.1365-4632.2011.05372.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[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] The majority of generalized pusular psoriasis without psoriasis vulgaris is caused by deficiency of interleukin-36 receptor antagonist2013
- Author(s)
  Sugiura K, Takemoto A, Yamaguchi M, Takahashi H, Shoda Y, Mitsuma T, Tsuda K, Nishida E, Togawa Y, Nakajima K, Sakakibara A, Kawachi S, Shimizu M, Ito Y, Takeichi T, Kono M, Ogawa Y, Muro Y, Ishida-Yamamoto A, Sano S, Matsue H, Morita A, Mizutani H, Iizuka H, Muto M, Akiyama M
- Journal Title
  
  J Invest Dermatol
  
  Volume: 133 Pages: 2514-2521
- Data Source
  KAKENHI-PROJECT-23249058
[Journal Article] Clinico-pathologic Analysis of 66 Japanese Thin Melanomas with Metastasis of Sentinel or Regional Lymph Node.2013
- Author(s)
  Mori M, Sugiura M, Kono M et al
- Journal Title
  
  J Cutan Pathol.
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?2013
- Author(s)
  Kono M, Akiyama M et al.
- Journal Title
  
  Int J Dermatol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Novel ABCA12 splice site deletion mutation and ABCA12 mRNA analysis of pulled hair samples in harlequin ichthyosis2013
- Author(s)
  Takeichi T, Sugiura K, et al.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 69 Issue: 3 Pages: 259-261
- DOI
  10.1016/j.jdermsci.2012.11.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-23659546, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] The majority of generalized pusular psoriasis without psoriasis vulgaris is caused by deficiency of interleukin-36 receptor antagonist.2013
- Author(s)
  Sugiura K, Takemoto A, Yamaguchi M, Takahashi H, Shoda Y, Mitsuma T, Tsuda K, Nishida E, Togawa Y, Nakajima K, Sakakibara A, Kawachi S, Shimizu M, Ito Y, Takeichi T, Kono M, Ogawa Y, Muro Y, Ishida-Yamamoto A, Sano S, Matsue H, Morita A, Mizutani H, Iizuka H, Muto M, Akiyama M.
- Journal Title
  
  J Invest Dermatol
  
  Volume: 133 Issue: 11 Pages: 2514-2521
- DOI
  10.1038/jid.2013.230
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526, KAKENHI-PROJECT-25461695
[Journal Article] Sporadic VACTERL association in a Japanese family with Sjogren-Larsson syndrome.2013
- Author(s)
  Takeichi T, Sugiura K, Arai H, Ishii K, Kono M, Akiyama M.
- Journal Title
  
  Acta Dermato-Venereol
  
  Volume: 93 Issue: 5 Pages: 579-580
- DOI
  10.2340/00015555-1526
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591628, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] 皮膚病理へのいざない(第1回)　総論および皮膚腫瘍(Part I)　表皮系良性腫瘍(疣贅を含む)と有棘細胞癌(前駆症を含む)(解説)2013
- Author(s)
  河野通浩
- Journal Title
  
  日本皮膚科学会雑誌
  
  Volume: 123 Pages: 2621-2624
- Data Source
  KAKENHI-PROJECT-24591646
[Journal Article] Clinico-pathologic Analysis of 66 Japanese Thin Melanomas with Metastasis of Sentinel or Regional Lymph Node.2013
- Author(s)
  Mori M, Sugiura M, Kono M, Matsumoto T, Sawada M, Yokota K, Yasue S, Shibata S, Sakakibara A, Nakamura S, Tomita Y, Akiyama M.
- Journal Title
  
  J Cutan Pathol
  
  Volume: 40 Issue: 12 Pages: 1027-34
- DOI
  10.1111/cup.12222
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526, KAKENHI-PROJECT-24791150
[Journal Article] Severe chilblain lupus is associated with heterozygous missense mutations of catalytic amino acids or their adjacent in the exonuclease domains of 3' -repair exonuclease 12012
- Author(s)
  Sugiura K, Takeichi T, Kono M, Ito Y, Ogawa Y, Muro Y, Akiyama M
- Journal Title
  
  J Invest Dermatol
  
  Volume: 132 Pages: 2855-2857
- Data Source
  KAKENHI-PROJECT-23249058
[Journal Article] Oculocutaneous albinism 1 minimal pigment type: A case report on the analysis of genotype of an OCA1MP patient.2012
- Author(s)
  Kono M et al.
- Journal Title
  
  Br J Dermatol.
  
  Volume: 166(4) Pages: 896-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] A novel IL36RN/IL1F5 homozygous nonsense mutation, p. Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis2012
- Author(s)
  Sugiura K, Takeichi T, Kono M, Ogawa Y, Shimoyama Y, Muro Y, Akiyama M
- Journal Title
  
  Br J Dermatol
  
  Volume: 167 Pages: 699-701
- Data Source
  KAKENHI-PROJECT-23249058
[Journal Article] Severe chilblain lupus is associated with heterozygous missense mutations of catalytic amino acids or their adjacent in the exonuclease domains of 3'-repair exonuclease 12012
- Author(s)
  Sugiura K
- Journal Title
  
  J Invest Dermatol
  
  Volume: 132 Issue: 12 Pages: 2855-2857
- DOI
  10.1038/jid.2012.210
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-23591618, KAKENHI-PROJECT-23659546, KAKENHI-PROJECT-23689054, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: report of a novel ADAR1 mutation.2012
- Author(s)
  Kantaputra PN, Chinadet W, Ohazama A, Kono M.
- Journal Title
  
  Am J Med Genet A.
  
  Volume: 158A Issue: 9 Pages: 2258-65
- DOI
  10.1002/ajmg.a.35488
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591646
[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] Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria2012
- Author(s)
  Kono M, Akiyama M, Kondo T, Suzuki T, Suganuma M, Wataya-Kaneda M, Lam J, Shibaki A, Tomita Y
- Journal Title
  
  J Dermatol
  
  Volume: 39 Issue: 9 Pages: 819-21
- DOI
  10.1111/j.1346-8138.2011.01385.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460, KAKENHI-PROJECT-23659546, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis2012
- Author(s)
  Sugiura K
- Journal Title
  
  Br J Dermatol
  
  Volume: 167 Issue: 3 Pages: 699-701
- DOI
  10.1111/j.1365-2133.2012.10953.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23249058, KAKENHI-PROJECT-23591617, KAKENHI-PROJECT-23591618, KAKENHI-PROJECT-23659546, KAKENHI-PROJECT-23689054, KAKENHI-PROJECT-24591646, KAKENHI-PROJECT-24659526
[Journal Article] Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria.2012
- Author(s)
  Kono M, Akiyama M et al.
- Journal Title
  
  J Dermatol.
  
  Volume: 39(9) Pages: 819-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Detection of Merkel cell polyomavirus in cutaneous squamous cell carcinoma prior to occurrence of Merkel cell carcinoma.2011
- Author(s)
  Kaibuchi-Noda K, … Kono M et al
- Journal Title
  
  J Am Acad Dermatol
  
  Volume: 65(5)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] 遺伝子解析より眼皮膚白皮症4型と考えられた1例2011
- Author(s)
  小島知子, 馬渕智生, 梅澤慶紀, 松山孝, 小澤明, 近藤泰輔, 河野通浩, 富田靖, 鈴木民夫
- Journal Title
  
  日本皮膚科学会雑誌
  
  Volume: 121(2) Pages: 1707-13
- NAID
  10031164950
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Detection of Merkel cell polyomavirus in cutaneous squamous cell carcinoma before occurrence of Merkel cell carcinoma2011
- Author(s)
  Kaibuchi-Noda K, Yokota K, Matsumoto T, Sawada M, Sakakibara A, Kono M, et al
- Journal Title
  
  J Am Acad Dermatol.
  
  Volume: 65
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 遺伝子解析より眼皮膚白皮症4型と考えられた1例2011
- Author(s)
  小島知子,馬渕智生, 梅澤慶紀, 松山孝, 小澤明, 近藤泰輔, 河野通浩, 富田靖, 鈴木民夫
- Journal Title
  
  日本皮膚科学会雑誌
  
  Volume: 121(2) Pages: 1707-13
- NAID
  10031164950
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients2010
- Author(s)
  Sakakibara A, Kamijima M, Shibata S, Yasue S, Kono M, Tomita Y
- Journal Title
  
  J Dermatol
  
  Volume: 37 Pages: 316-22
- NAID
  10027066531
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] 遺伝子解析より眼皮膚白皮症4型と考えられた1例2010
- Author(s)
  小島知子, 馬渕智生, 梅澤慶紀, 松山孝, 小澤明, 近藤泰輔, 河野通浩, 富田靖, 鈴木民夫
- Journal Title
  
  日本皮膚科学会雑誌
  
  Volume: 52 Pages: 1707-1713
- NAID
  10031164950
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] 遺伝子解析より眼皮膚白皮症4型と考えられた1例2010
- Author(s)
  小島知子, 馬渕智生, 梅澤慶紀, 松山孝, 小澤明, 近藤泰輔, 河野通浩, 富田靖, 鈴木民夫
- Journal Title
  
  日本皮膚科学会雑誌
  
  Volume: 52 Pages: 1707-1713
- NAID
  10031164950
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Demoscopic evaluation of vascular structures of various skin tumors in Japanese patients2010
- Author(s)
  Sakakibara A, Kamijima M, Shibata S, Yasue S, Kono M, Tomita Y
- Journal Title
  
  J Dermatol
  
  Volume: 37 Pages: 316-22
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients.2010
- Author(s)
  Akihiro Sakakibara, Michihiro Kamijima, Shinichi Shibata, Satoshi Yasue, Michihiro Kono, Yasushi Tomita.
- Journal Title
  
  J Dermatol
  
  Volume: 37(4) Pages: 316-322
- NAID
  10027066531
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Interval sentinel lymph nodes in patients with cutaneous melanoma : a single-institution study in Japan2010
- Author(s)
  Matsumoto T, Shibata S, Yasue S, Sakakibara A, Yokota K, Sawada M, Kono M, Kato K, Shimoyama Y, Tomita Y
- Journal Title
  
  J Dermatol
  
  Volume: 37 Pages: 629-34
- NAID
  10026637323
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 【治療にてこずる皮膚疾患】尋常性白斑被覆化粧品・医薬部外品2010
- Author(s)
  河野通浩
- Journal Title
  
  皮膚科の臨床
  
  Volume: 52(11) Pages: 1707-1713
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Interval sentinel lymph nodes in patients with cutaneous melanoma : A single-institution study in Japan2010
- Author(s)
  Takaaki Matsumoto, Shinichi Shibata, Satoshi Yasue, Akihiro Sakakibara, KenjiYokota, Masaki Sawada, Michihiro Kono, Katsuhiko Kato, Yoshie Shimoyama, Yasushi Tomita.
- Journal Title
  
  J Dermatol
  
  Volume: 37(7) Pages: 629-634
- NAID
  10026637323
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Interval sentinel lymph nodes in patients with cutaneous melanoma: A single-institution study in Japan2010
- Author(s)
  Takaaki Matsumoto, Shinichi Shibata, Satoshi Yasue, Akihiro Sakakibara, Kenji Yokota, Masaki Sawada, Michihiro Kono, Katsuhiko Kato, Yoshie Shimoyama, Yasushi Tomita.
- Journal Title
  
  J Dermatol
  
  Volume: 37(7) Pages: 629-634
- NAID
  10026637323
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients2010
- Author(s)
  Akihiro Sakakibara, Michihiro Kamijima, Shinichi Shibata, Satoshi Yasue, Michihiro Kono, Yasushi Tomita
- Journal Title
  
  Japanese patients
  
  Volume: 37(4) Pages: 316-322
- NAID
  10027066531
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 【治療にてこずる皮膚疾患】尋常性白斑被覆化粧品・医薬部外品2010
- Author(s)
  河野通浩
- Journal Title
  
  皮膚科の臨床
  
  Volume: 52(11) Pages: 1707-1713
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Interval sentinel lymph nodes in patients with cutaneous melanoma : a single-institution study in Japan2010
- Author(s)
  Matsumoto T, Shibata S, Yasue S, Sakakibara A, Yokota K, Sawada M, Kono M, Kato K, Shimoyama Y, Tomita Y
- Journal Title
  
  J Dermatol
  
  Volume: 37 Pages: 629-34
- NAID
  10026637323
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Establishment of a screening system for chemicals that up regulate a melanoma antigen2009
- Author(s)
  Hai Zhen Song, Michihiro Kono, Yasushi Tomita.
- Journal Title
  
  Melan-A/MART-1 Tohoku J Exp Med
  
  Volume: 217(3) Pages: 231-237
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.2009
- Author(s)
  Ichidai Murata, Yutaka Hozumi, Masakazu Kawaguchi, Yoshiyuki Katagiri, Shinichiro Yasumoto, Yoshiaki Kubo, Wataru Fujimoto, Tatsuya Horikawa, Taisuke Kondo, Michihiro Kono, Yasushi Tomita, Tamio Suzuki.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 53(1) Pages: 76-77
- NAID
  10025332183
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[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] Establishment of a screening system for chemicals that upregulate a melanoma antigen, Melan-A/MART-1.2009
- Author(s)
  Hai Zhen Song, Michihiro Kono, Yasushi Tomita.
- Journal Title
  
  Tohoku J Exp Med
  
  Volume: 217(3) Pages: 231-237
- NAID
  10025105371
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2.2009
- Author(s)
  Takayuki Konno, Yuko Abe, Masakazu Kawaguchi, Katrien Storm, Martine Biervliet, Winnie Courtens, Michihiro Kono, Yasushi Tomita, Tamio Suzuki.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 149A(8) Pages: 1773-1776
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria2009
- Author(s)
  Ichidai Murata, Yutaka Hozumi, Masakazu Kawaguchi, Yoshiyuki Katagiri, Shinichiro Yasumoto, Yoshiaki Kubo, Wataru Fujimoto, Tatsuya Horikawa, Taisuke Kondo, Michihiro Kono, Yasushi Tomita, Tamio Suzuki.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 53(1) Pages: 76-77
- NAID
  10025332183
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 陰茎に生じた環状肉芽腫の1例2009
- Author(s)
  吉田紫、正木貞男、河野通浩, 富田靖
- Journal Title
  
  臨床皮膚科
  
  Volume: 63 Pages: 747-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] 遺伝子解析により診断されたHermansky-Pudlak症候群の女児例2009
- Author(s)
  近藤泰輔、鈴木民夫、河野通浩、中澤満、富田靖
- Journal Title
  
  皮膚病診療
  
  Volume: 31(3) Pages: 333-336
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 遺伝性対側性色素異常症病因遺伝子の変異部位はADAR1酵素のp150アイソフォームの欠損を示す2009
- Author(s)
  河野通浩、近藤泰輔、鈴木民夫、鈴木教之、富田靖
- Journal Title
  
  皮膚病診療
  
  Volume: 31(3) Pages: 309-312
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Oculocutaneous albinism type IV : A boy of Moroccan descent with a novel mutation in SLC45A2.2009
- Author(s)
  Konno T, Abe Y, Kawaguchi M, Storm K, Biervliet M, Courtens W, Kono M, Tomita Y, Suzuki T.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 149A Pages: 1773-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] 遺伝性対側性色素異常症病因遺伝子の変異部位は ADAR1 酵素の p150 アイソフォームの欠損を示す2009
- Author(s)
  河野通浩、近藤泰輔、鈴木民夫、鈴木教之、富田靖
- Journal Title
  
  皮膚病診療
  
  Volume: 31(3) Pages: 309-312
- Data Source
  KAKENHI-PROJECT-21591460
[Journal Article] Oculocutaneous albinism type IV : A boy of Moroccan descent with a novel mutation inSLC45A22009
- Author(s)
  Takayuki Konno, Yuko Abe, Masakazu Kawaguchi, Katrien Storm, Martine Biervliet, Winnie Courtens, MichihiroKono, Yasushi Tomita, Tamio Suzuki.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 149A(8) Pages: 1773-1776
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] 遺伝子解析により診断された Hermansky -Pudlak 症候群の女児例2009
- Author(s)
  近藤泰輔、鈴木民夫、河野通浩、中澤満、富田靖
- Journal Title
  
  皮膚病診療
  
  Volume: 31(3) Pages: 333-336
- Data Source
  KAKENHI-PROJECT-21591460
[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] 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] 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 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] 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] 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] Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis : ahidden link?
- Author(s)
  Kono M, Akiyama M, et al.(5人中1番目)
- Journal Title
  
  Int J Dermatol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Clinico-pathologic Analysis of66 Japanese Thin Melanomas with Metastasis of Sentinel or Regional Lymph Node
- Author(s)
  Mori M, Sugiura M, Kono M, et al.(12人中3番目)
- Journal Title
  
  J Cutan Pathol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Four novel ADAR1 gene mutations inpatients with dyschromatosis symmetrica hereditaria
- Author(s)
  Kono M, Akiyama M, et al.(9人中1番目)
- Journal Title
  
  J Dermatol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria
- Author(s)
  Kono M, Akiyama M, et al
- Journal Title
  
  J Dermatol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Oculocutaneous albinism 1 minimal pigment type : A case report on the analysis of genotype of an OCA1MP patient
- Author(s)
  Kono M, et al
- Journal Title
  
  Br J Dermatol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Detection of Merkel cell polyomavirus in cutaneous squamous cell carcinoma prior to occurrence of Merkel cell carcinoma
- Author(s)
  Kaibuchi-Noda K, …Kono M, et al.(11人中5番目)
- Journal Title
  
  J Am Acad Dermatol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Journal Article] Oculocutaneous albinism 1 minimal pigment type : A case report on the analysis of genotype of an OCA1MP patient
- Author(s)
  Kono M, et al.(7人中1番目)
- Journal Title
  
  Br J Dermatol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591459
[Patent] 悪性黒色腫抗原の発現上昇剤およびその用途2007
- Inventor(s)
  河野通浩、富田靖
- Filing Date
  2007-11-28
- Overseas
- Data Source
  KAKENHI-PROJECT-19390294
[Patent] 悪性黒色腫抗原の発現上昇剤およびその用途2007
- Inventor(s)
  河野通浩, 富田靖
- Industrial Property Rights Holder
  国立大学法人名古屋大学
- Filing Date
  2007-11-28
- Overseas
- Data Source
  KAKENHI-PROJECT-19390294
[Presentation] 遺伝性対側性色素異常症と Aicardi-Goutieres症候群6はADAR1遺伝子変異による表現型バリアントである.2016
- Author(s)
  河野通浩、松本文博、鈴木保宏、菅沼睦美、才津浩智、伊藤康友、藤原作平、森脇真一、松本和彦、松本直通、富田靖、杉浦一充、秋山真志.
- Organizer
  第9回自己炎症疾患研究会
- Place of Presentation
  東京都千代田区（フクラシア東京ステーション）
- Year and Date
  2016-02-06
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 第15回浜名湖皮膚病理研究会「左頬部皮下結節の一例」の経過と最終診断.2016
- Author(s)
  Jeong Jin-Wook、長谷川佳恵、河野通浩、秋山真志、加藤陽一.
- Organizer
  第16回浜名湖皮膚病理研究会
- Place of Presentation
  静岡県浜松市（TPK 浜松アクトタワーカンファレンスセンター）
- Year and Date
  2016-02-13
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] アトピー性皮膚炎（ＡＤ）と好酸球性胃腸炎患者におけるフィラグリン（FLG）遺伝子変異の検討.2016
- Author(s)
  皆川智子、金子高英、松﨑康司、中野　創、澤村大輔、平賀寛人、櫻庭裕丈、河野通浩、秋山真志.
- Organizer
  第79回日本皮膚科学会東京・東部支部合同学術大会
- Place of Presentation
  東京都新宿区（京王プラザホテル）
- Year and Date
  2016-02-20
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 同一家系内に見られた滴状脱色素斑.2015
- Author(s)
  江上将平、本田治樹、横山知明、杉浦丹、河野通浩、秋山真志.
- Organizer
  第114回日本皮膚科学会総会
- Place of Presentation
  神奈川県横浜市（パシフィコ横浜）
- Year and Date
  2015-05-29
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 左第5趾足底部の腫瘤.2015
- Author(s)
  渡邊直樹、河野通浩、横田憲二、松本高明、村上佳恵、秋山真志、下山芳江.
- Organizer
  第14回東海皮膚病理研究会
- Place of Presentation
  愛知県名古屋市（ウインクあいち）
- Year and Date
  2015-08-08
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Filaggrin gene mutations are significantly associated with food allergy in Japanese primary school children.2015
- Author(s)
  Kono M, Akiyama M, Nomura T, McLean WHI, Shimizu H, Sugiura K, Hata A, Okamoto Y, Inoue Y, Suzuki Y, Shimojo N.
- Organizer
  第40回日本研究皮膚科学会
- Place of Presentation
  岡山県岡山市（岡山コンベンションセンター）
- Year and Date
  2015-12-11
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Epidermolytic ichthyosisの一例.2015
- Author(s)
  大村玲奈, 深井和吉, 菅原弘二, 鶴田大輔, 永尾淳, 河野通浩, 秋山真志.
- Organizer
  第39回小児皮膚科学会学術大会
- Place of Presentation
  鹿児島県鹿児島市（かごしま県民交流センター）
- Year and Date
  2015-07-18
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 網状肢端色素沈着症の1例.2015
- Author(s)
  堤美穂、中井章淳、加藤則人、河野通浩.
- Organizer
  第440回日本皮膚科学会京滋地方会
- Place of Presentation
  京都府京都市（京都大学）
- Year and Date
  2015-06-06
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 日本におけるブルーリ潰瘍の疫学と新規治療法の提唱.2015
- Author(s)
  村瀬千晶、河野通浩、松本高明、横田憲二、長谷川佳恵、中永和枝、石井則久、秋山真志.
- Organizer
  第114回日本皮膚科学会総会
- Place of Presentation
  神奈川県横浜市（パシフィコ横浜）
- Year and Date
  2015-05-29
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 左頬皮下結節の1例.2015
- Author(s)
  Jeong Jin-Wook、長谷川佳恵、河野通浩、加藤陽一、秋山真志.
- Organizer
  第13回東海皮膚病理研究会
- Place of Presentation
  愛知県名古屋市（名古屋ルーセントタワー）
- Year and Date
  2015-04-02
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] NCOA2遺伝子再構成陽性の顔のangiofibroma of soft tissue.2015
- Author(s)
  Jeong Jin-Wook、村上佳恵、河野通浩、加藤陽一、小沢広明、元井亨、多田豊曠、秋山真志.
- Organizer
  第274回日本皮膚科学会東海地方会
- Place of Presentation
  愛知県名古屋市（大正製薬(株)名古屋支店）
- Year and Date
  2015-12-06
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Hyperpigmentation over the metacarpophalangeal joints and the malleoli in a case of hyaline fibromatosis syndrome with ANTXR2 mutations.2015
- Author(s)
  Sugiura K, Ohno A, Kono M, Kitoh H, Itomi K, Akiyama M.
- Organizer
  第40回日本研究皮膚科学会
- Place of Presentation
  岡山県岡山市（岡山コンベンションセンター）
- Year and Date
  2015-12-11
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 左臀部の黒色結節の一例.2015
- Author(s)
  森章一郎、村上佳恵、河野通浩、大城宏治、中黒匡人、秋山真志.
- Organizer
  第15回東海皮膚病理研究会
- Place of Presentation
  愛知県名古屋市（エーザイ株式会社名古屋コミュニケーションオフィス）
- Year and Date
  2015-12-05
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 網状肢端色素沈着症はADAM10の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64回　日本皮膚科学会中部支部学術総会
- Place of Presentation
  名古屋国際会議場、名古屋市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 右臀部の腫瘤2013
- Author(s)
  長谷川佳恵、横田憲二、河野通浩、澤田昌樹、秋山真志
- Organizer
  第29回　日本皮膚病理組織学会
- Place of Presentation
  石垣記念ホール、東京都港区
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 尋常性乾癬を伴わない汎発性膿疱性乾癬の大半はIL-36RN欠損症(DITRA)である2013
- Author(s)
  杉浦一充, 武市拓也, 河野通浩, 小川靖, 室慶直, 秋山真志, 武藤正彦
- Organizer
  第77回　日本皮膚科学会東部支部学術総会
- Place of Presentation
  大宮ソニックシティ、大宮市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 免疫抑制状態にある子宮頚癌術後患者に発症したBowen様丘疹症の一例2013
- Author(s)
  澤田昌樹、河野通浩, 秋山真志
- Organizer
  第64回　日本皮膚科学会中部支部学術総会
- Place of Presentation
  名古屋国際会議場、名古屋市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] [教育講演] 皮膚病理へのいざない(第1回)　総論および皮膚腫瘍(Part I)　表皮系良性腫瘍(疣贅を含む)と有棘細胞癌(前駆症を含む)2013
- Author(s)
  河野通浩
- 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-24591646
[Presentation] 常性乾癬を伴わない汎発性膿疱性乾癬の大半はIL-36RN欠損症(DITRA)である2013
- Author(s)
  杉浦一充, 武市拓也, 河野通浩, 小川靖, 室慶直, 武藤正彦, 秋山真志
- Organizer
  第64回　日本皮膚科学会中部支部学術総会
- Place of Presentation
  名古屋国際会議場、名古屋市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 網状肢端色素沈着症はADAM10の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
  大阪大学銀杏会館、吹田市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 臀部粉瘤より発生した有棘細胞癌の一例2013
- Author(s)
  長谷川佳恵, 横田憲二, 河野通浩, 澤田昌樹, 松本高明, 秋山真志
- Organizer
  第29回　日本皮膚悪性腫瘍学会学術大会
- Place of Presentation
  甲府富士屋ホテル、甲府市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 網状肢端色素沈着症はADAM10の遺伝子変異によって発症する2013
- Author(s)
  河野通浩, 杉浦一充, 富田靖, 秋山真志, 林昌浩, 鈴木民夫, 高間弘道, 松永佳世子
- Organizer
  第77回　日本皮膚科学会東部支部学術総会
- Place of Presentation
  大宮ソニックシティ、大宮市
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 頭部腫瘍の一例2012
- Author(s)
  牧田澄子、山田元人、鈴木教之、唐沢卓生、前田松喜、河野通浩、秋山真志
- Organizer
  第28回　日本皮膚病理組織学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] 教育講演　皮膚病理へのいざない「上皮系腫瘍」2012
- Author(s)
  河野通浩
- Organizer
  第111回　日本皮膚科学会総会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Novel ADAR1 mutations including single amino acid deletion in the deaminase domain underly dyschromatosis symmetrica hereditaria2012
- Author(s)
  Michihiro Kono, Yasutomo Ito, Hideyuki Ujiie, Kenichi Morimoto, Masashi Akiyama
- Organizer
  The 36th Annual Meeting of the Japanese Society for Investigative Dermatology
- Place of Presentation
  那覇
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Oculo cutaneous albinism 1 minimal pigment type ; a case report on the analysis of genotype-phenotype correlation2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Shiro Ito, Tamio Suzuki, Kazumasa Wakamatsu, ShosukeIto, Yasushi Tomita
- Organizer
  XXIst International Pigment Cell Conference
- Place of Presentation
  Bordeaux, France
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Two novel ADAR1 mutations in dyschromatosis symmetrica hereditaria suggest haploinsufficiency as pathomechanisms of the disease2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Yasushi Tomita, Masashi Akiyama
- Organizer
  The 36th Annual Meeting of the Japanese Society for Investigative Dermatology
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Oculocutaneous albinism 1 minimal pigment type; a case report on the analysis of genotype-phenotype correlation2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Shiro Ito, Tamio Suzuki, Kazumasa Wakamatsu, Shosuke Ito, Yasushi Tomita
- Organizer
  XXIst International Pigment Cell Conference.
- Place of Presentation
  Bordeaux, France.
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Two novel ADAR1 mutations in dyschromatosis symmetrica hereditaria suggest haploinsufficiency as pathomechanisms of the disease.2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Yasushi Tomita, Masashi Akiyama
- Organizer
  The 36th Annual Meeting of the Japanese Society for Investigative Dermatology.
- Place of Presentation
  国立京都国際会館（京都）
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Oculocutaneous albinism 1 minimal pigment type ; a case report on the analysis of genotype-phenotype correlation2011
- Author(s)
  Kono M, et al
- Organizer
  XXIst International Pigment Cell Conference
- Place of Presentation
  Bordeaux, France
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Two novel ADAR1 mutations in dyschromatosis symmetrica hereditaria suggest haploinsufficiency as pathomechanisms of the disease2011
- Author(s)
  Kono M, et al
- Organizer
  The 36 th Annual Meeting of the Japanese Society for Investigative Dermatology
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Oculocutaneous albinism 1 minimal pigment type; a case report on the analysis of genotype-phenotype correlation.2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Shiro Ito, Tamio Suzuki, Kazumasa Wakamatsu, Shosuke Ito, Yasushi Tomita
- Organizer
  XXIst International Pigment Cell Conference
- Place of Presentation
  Bordeaux, France
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Two novel ADAR1 mutations in dyschromatosis symmetrica hereditaria suggest haploinsufficiency as pathomechanisms of the disease2011
- Author(s)
  Michihiro Kono, Taisuke Kondo, Yasushi Tomita, Masashi Akiyama
- Organizer
  The 36th Annual Meeting of the Japanese Society for Investigative Dermatology.
- Place of Presentation
  Kyoto, Japan.
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Five novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a known mutation in a patient developing her skin manifestation after viral encephalitis2010
- Author(s)
  Michihiro Kono, Taisuke Kondo, Tamio Suzuki, Mari Kaneda, Sakuhei Fujiwara, Akihiko Shibaki, Amarillis Sanchez-Valle, Hirotaka Akita, Joseph Lam, Yasushi Tomita
- Organizer
  第23回日本色素細胞学会
- Place of Presentation
  東京
- Year and Date
  2010-11-27
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Four novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a mutation in patient associated with encephalitis2010
- Author(s)
  Kono M, Kondo T, Suzuki T, Kaneda M, Shibaki A, Sanchez-Valle A, Akita H, Tomita Y
- Organizer
  日本研究皮膚科学会第35回年次学術大会・総会
- Place of Presentation
  和歌山県民文化会館(和歌山)
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Four novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a mutation in patient associated with encephalitis2010
- Author(s)
  Michihiro Kono, Taisuke Kondo, Tamio Suzuki, Mari Kaneda, Akihiko Shibaki, Amarillis Sanchez-Valle, Hirotaka Akita, Yasushi Tomita
- Organizer
  The 35th Annual Meeting of the Japanese Society for Investigative Dermatology
- Place of Presentation
  和歌山
- Year and Date
  2010-12-03
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Five novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a known mutation in a patient developing her skin manifestati on after viral encephalitis2010
- Author(s)
  Michihiro Kono, Taisuke Kondo, Tamio Suzuki, Mari Kaneda, Sakuhei Fujiwara, Akihiko Shibaki, Amarillis Sanchez-Valle, Hirotaka Akita, Joseph Lam, Yasushi Tomita
- Organizer
  第23回日本色素細胞学会
- Place of Presentation
  東京
- Year and Date
  2010-11-27
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Four novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a mutation in patient associated with ence phalitis2010
- Author(s)
  Michihiro Kono, Taisuke Kondo, Tamio Suzuki, Mari Kaneda, Akihiko Shibaki, Amarillis Sanchez-Valle, Hirotaka Akita, Yasushi Tomita
- Organizer
  The 35th Annual Meeting of the Japanese Society for Investigative Dermatology
- Place of Presentation
  和歌山
- Year and Date
  2010-12-03
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Four novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a mutation in patient associated with encephalitis2010
- Author(s)
  Kono M, Kondo T, Suzuki T, Kaneda M, Shibaki A, Sanchez-Valle A, Akita H, Tomita Y
- Organizer
  日本研究皮膚科学会第35回年次学術大会・総会
- Place of Presentation
  和歌山
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Five novel ADAR1 mutations in patients with dyschromatosis symmetrica hereditaria and a known mutation in a patient developing her skin manifestation after viral encephalitis2010
- Author(s)
  Kono M, Kondo T, Suzuki T, Kaneda M, Fujiwara S, Shibaki A, Sanchez-Valle A, Akita H, Lam J, Tomita Y
- Organizer
  第23回日本色素細胞学会
- Place of Presentation
  東京慈恵会医科大学(東京)
- Year and Date
  2010-11-27
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] Knockdown of ADAR1 gene expression in cultured melanocytes by si RNA2009
- Author(s)
  Michihiro Kono, Tamio Suzuki, Yasushi, Tomita
- Organizer
  第34回日本研究皮膚科学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] 遺伝性対側性色素異常症の病因遺伝子ADAR1のヒト培養メラノサイトでの働きについて2009
- Author(s)
  河野通浩、近藤泰輔、鈴木民夫、富田靖
- Organizer
  第15回分子皮膚科学フォーラム
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] 遺伝性対側性色素異常症の病因遺伝子 ADAR1の分化段階の異なるマウスメラノサイトでの働きの検討2009
- Author(s)
  河野通浩、鈴木民夫、富田靖
- Organizer
  第16回分子皮膚科学フォーラム
- Place of Presentation
  札幌
- Year and Date
  2009-11-20
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] Knockdown of ADAR1 gene expression in cultured melanocytes by siRNA2009
- Author(s)
  Michihiro Kono, Tamio Suzuki, Yasushi Tomita
- Organizer
  第34回日本研究皮膚科学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] 遺伝性対側性色素異常症の病因遺伝子ADAR1の分化段階の異なるマウスメラノサイトでの働きの検討2009
- Author(s)
  河野通浩、鈴木民夫、富田靖
- Organizer
  第22回日本色素細胞学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] 遺伝性対側性色素異常症の病因遺伝子 ADAR1の分化段階の異なるマウスメラノサイトでの働きの検討2009
- Author(s)
  河野通浩、鈴木民夫、富田靖
- Organizer
  第22回日本色素細胞学会学術大会
- Place of Presentation
  福岡
- Year and Date
  2009-12-05
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] 遺伝性対側性色素異常症の病因遺伝子ADAR1の分化段階の異なるマウスメラノサイトでの働きの検討2009
- Author(s)
  河野通浩、鈴木民夫、富田靖
- Organizer
  第16回分子皮膚科学フォーラム
- Place of Presentation
  札幌
- Year and Date
  2009-11-20
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] 遺伝子解析から眼皮膚白皮症4型と考えられた1例2009
- Author(s)
  小島知子、馬渕智生、梅澤慶紀、松山孝、小澤明、近藤泰輔、河野通浩、富田靖、鈴木民夫
- Organizer
  第108回日本皮膚科学会総会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-21591460
[Presentation] 遺伝性対側性色素異常症の病因遺伝子ADAR1の分化段階の異なるマウスメラノサイトでの働きの検討2009
- Author(s)
  河野通浩、鈴木民夫、富田靖
- Organizer
  第22回日本色素細胞学会学術大会
- Place of Presentation
  福岡
- Year and Date
  2009-12-05
- Data Source
  KAKENHI-PROJECT-21591459
[Presentation] 遺伝子解析から眼皮膚白皮症4型と考えられた1例2009
- Author(s)
  小島知子、馬渕智生、梅澤慶紀、松山孝、小澤明、近藤泰輔、河野通浩、富田靖、鈴木民夫
- Organizer
  第108回日本皮膚科学会総会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-21591459
[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] Aphidicolin as a possible modulating agent for melanoma antigen expression in melanoma immunity2008
- Author(s)
  Michihiro Kono,Hai Zheng Song, Yasushi Tomita
- Organizer
  International Investigative Dermatology
- Place of Presentation
  京都市
- Year and Date
  2008-05-06
- Data Source
  KAKENHI-PROJECT-19390294
[Presentation] 特発性脳内石灰化症を合併した遺伝性対側性色素異常症の1例2007
- Author(s)
  近藤泰輔、河野通浩, ら
- Organizer
  第21回日本色素細胞学会年次学術大会
- Place of Presentation
  名古屋、日本
- Year and Date
  2007-12-09
- Data Source
  KAKENHI-PROJECT-18790784
[Presentation] 塩基特異的mRNA切断法を用いたADAR1酵素の基質遺伝子の同定および遺伝性対側性色素異常症の病態解明2007
- Author(s)
  河野通浩
- Organizer
  第105回日本皮膚科学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18390312
[Presentation] 新規遺伝子変異を認めた遺伝性対側性色素異常症の4例2007
- Author(s)
  近藤泰輔, 鈴木民夫, 伊藤史朗, 秋田浩章, 河野通浩, ら
- Organizer
  第106回日本皮膚科学会総会
- Place of Presentation
  横浜、日本
- Year and Date
  2007-04-21
- Data Source
  KAKENHI-PROJECT-18790784
[Presentation] Dowling-Degos disease is genetically and clinico-pathologically distinct from reticulate acropigmentation of Kitamura, further confirmation.
- Author(s)
  Michihiro Kono, Mutsumi Suganuma, Kazumitsu Sugiura, Hiromichi Takama, Tamio Suzuki, Kayoko Matsunaga, Yasushi Tomita and Masashi Akiyama
- Organizer
  第39回日本研究皮膚科学会
- Place of Presentation
  ホテル阪急エキスポパーク（大阪府吹田市）
- Year and Date
  2014-12-12 – 2014-12-14
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.
- Author(s)
  河野通浩
- Organizer
  第113回日本皮膚科学会総会
- Place of Presentation
  京都国際会議場（京都府京都市）
- Year and Date
  2014-05-30 – 2014-06-01
- Invited
- Data Source
  KAKENHI-PROJECT-24591646
[Presentation] Reticulate acropigmentation of Kitamura and Dowling-Degos disease are genetically independent disorders distinct from each other; further confirmation
- Author(s)
  Michihiro Kono, Kazumitsu Sugiura, Mutsumi Suganuma, Hiromichi Takama, Tamio Suzuki, Kayoko Matsunaga, Yasushi Tomita and Masashi Akiyama
- Organizer
  XXII International Pigment Cell Conference
- Place of Presentation
  Singapore, Singapore
- Year and Date
  2014-09-04 – 2014-09-07
- Data Source
  KAKENHI-PROJECT-24591646

1. YOSHINAO Muro (80270990)

# of Collaborated Projects: 4 results

# of Collaborated Products: 5 results
2. AKIYAMA Masashi (60222551)

# of Collaborated Projects: 4 results

# of Collaborated Products: 58 results
3. TAMIO Suzuki (30206502)

# of Collaborated Projects: 3 results

# of Collaborated Products: 10 results
4. SAWADA Masaki (80467315)

# of Collaborated Projects: 3 results

# of Collaborated Products: 5 results
5. YASUSHI Tomita (70108512)

# of Collaborated Projects: 2 results

# of Collaborated Products: 8 results
6. KUNISADA Takahiro (30205108)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. MATSUMOTO Takaaki (70508944)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
8. OGAWA Yasushi (10567754)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
9. ABE Riichiro (60344511)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. SUGIURA Kazumitsu (70335032)

# of Collaborated Projects: 1 results

# of Collaborated Products: 17 results
11. 宮村佳典 (50272034)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 安江敬 (40335039)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 武市拓也 (30754931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
15. KONDO Taisuke

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
16. NOMURA Toshifumi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. WAKAMATSU Kazumasa

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 平林哲也

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 清水宏

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
20. 伊藤祥輔

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kono Michihirro 河野 通浩

河野 通浩 コウノ ミチヒロ

MICHIHIRO Kono 河野 通浩

KONO Michihiro 河野 道浩

Research Projects

Research Products

Co-Researchers

Understanding the pathogenesis of pigmentary disorders focusing on autophagy and the establishment of novel inherited pigmentary disorders.Principal Investigator

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The comprehensivve elucidation of pathogenesis and the establishment of therapeutic agent with model mouse for Dowling-Degos diseasePrincipal Investigator

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皮膚筋炎におけるRNA編集酵素ADAR1の自己免疫応答ともたらす病態

Principal Investigator

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Elucidation of pathogenic mechanisms of ichthyosis due to epidermal lipid abnormalities and development of novel therapeutic agents

Principal Investigator

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Review Section

Research Institution

comprehensive elucidation of pathophysiology of reticulate acropigmentation of Kitamura and development of therapeutic agents using model mice and antibody arraysPrincipal Investigator

Principal Investigator

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Research Institution

The development of new non-invasive therapeutic strategy of dyschromatosis symmetrica hereditaria with topical agentPrincipal Investigator

Principal Investigator

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Innovation of novel treatments for various phenotypes of ichthyosis by restoration of ABCA12 lipid transporter gene expression

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Study on regulatory mechanism of melanin synthesis clarified by elucidation of molecular pathology on pigmentary disorders

Principal Investigator

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Elucidation of pathogenesis of DSH with the model mouse that melanocyte is distributed in epidermisPrincipal Investigator

Principal Investigator

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Study on regulatory mechanism of melanin synthesis clarified by elucidation of molecular pathology on pigmentary disorders

Principal Investigator

Project Period (FY)

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Research Institution

イノシン特異的mRNA切断によるADAR1基質同定と遺伝性対側性色素異常症病態解明Principal Investigator

Principal Investigator

Project Period (FY)

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Research Institution

Functional analyses of the genes in which mutations cause oculocutaneous albinisms

Principal Investigator

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Research Institution

色素異常症における発現遺伝子プロファイリングの差異による新規関連遺伝子の検索Principal Investigator

Kono Michihirro 河野通浩

河野通浩コウノミチヒロ

MICHIHIRO Kono 河野通浩

KONO Michihiro 河野道浩

[Book] 皮膚科診療カラーアトラス大系第3巻(色調異常/水庖性疾患・膿疱症)「遺伝性対側性色素異常症(遠山)」2009

[Book] 「遺伝性対側性色素異常症(遠山)」皮膚科診療カラーアトラス大系第3巻(色調異常/水疱性疾患・膿疱症)2009

[Journal Article] Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutations.2018