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Okamura Ken  岡村 賢

ORCIDConnect your ORCID iD *help
Researcher Number 40637229
Other IDs
Affiliation (Current) 2025: 山形大学, 医学部, 助教
Affiliation (based on the past Project Information) *help 2024: 山形大学, 医学部, 助教
2021: 山形大学, 医学部, 助教
2016 – 2019: 山形大学, 医学部, 助教
Review Section/Research Field
Principal Investigator
Basic Section 53050:Dermatology-related / Dermatology
Keywords
Principal Investigator
DSH / HPS / OCA / 眼皮膚白皮症 / 遺伝性色素異常症 / HIV / レトロトランスポゾン / モデルマウス / 自己免疫性疾患 / 白斑 … More / MITF / SASH1 / targeted resequencing / NGS / ターゲットシークエンス / CRISPR/Cas9 / ゲノム編集 / 医療・福祉 / ゲノム / 遺伝子 / 電子顕微鏡 / メラニン / genome editing / pigmentation disorder / melanin / exome / 次世代シークエンサー / エクソーム解析 / ワールデンブルグ症候群 / 遺伝性汎発性色素異常症 / 遺伝性対側性色素異常症 / アルビノ Less
  • Research Projects

    (3 results)
  • Research Products

    (11 results)
  • Co-Researchers

    (3 People)
  •  Establishment of a Vitiligo Model Mouse and Pathological Analysis: Development of a Novel Therapy Focusing on RetrotransposonsPrincipal Investigator

    • Principal Investigator
      岡村 賢
    • Project Period (FY)
      2024 – 2026
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 53050:Dermatology-related
    • Research Institution
      Yamagata University
  •  Establishment of an efficient gene testing system for hereditary pigmentation disorders and functional analysis using genome editing technologyPrincipal Investigator

    • Principal Investigator
      Okamura Ken
    • Project Period (FY)
      2020 – 2021
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 53050:Dermatology-related
    • Research Institution
      Yamagata University
  •  Exhaustive mutation analysis and functional study of hereditary pigmentation disordersPrincipal Investigator

    • Principal Investigator
      Okamura Ken
    • Project Period (FY)
      2016 – 2017
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Dermatology
    • Research Institution
      Yamagata University

All 2022 2021 2019 2018 2017

All Journal Article Presentation

  • [Journal Article] Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease2022

    • Author(s)
      Matsuyuki Keigo、Ide Mizuki、Houjou Keishirou、Shima Saho、Tanaka Seiji、Watanabe Yoriko、Tomino Hiroyuki、Egashira Tomoko、Takayanagi Toshimitsu、Tashiro Katsuya、Okamura Ken、Suzuki Tamio、Miyamoto Takayuki、Shibata Hirofumi、Yasumi Takahiro、Nishikomori Ryuta
    • Journal Title

      Pediatric Allergy and Immunology

      Volume: 33 Issue: 2 Pages: 1-4

    • DOI

      10.1111/pai.13748

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K16046
  • [Journal Article] Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 62021

    • Author(s)
      Saito Toru、Okamura Ken、Kosaki Rika、Wakamatsu Kazumasa、Ito Shosuke、Nakajima Osamu、Yamashita Hidetoshi、Hozumi Yutaka、Suzuki Tamio
    • Journal Title

      Pigment Cell & Melanoma Research

      Volume: 35 Issue: 2 Pages: 212-219

    • DOI

      10.1111/pcmr.13024

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K16046
  • [Journal Article] Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT5.2019

    • Author(s)
      Okamura K, Fukushima S, Yamashita J, Abe Y, Hayashi M, Hozumi Y, Ihn H, Suzuki T
    • Journal Title

      The Journal of dermatology

      Volume: 印刷中 Issue: 7

    • DOI

      10.1111/1346-8138.14788

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K08301, KAKENHI-PROJECT-18K16046, KAKENHI-PROJECT-16K10165
  • [Journal Article] Impact of a 4-bp deletion variant (rs984225803) in the promoter region of SLC45A2 on color variation among Japanese population2019

    • Author(s)
      Ken Okamuraa, Yuko Abea, Masahiro Hayashia, Toru Saitoa, Kei Nagatania, Toshihide Tanoueb, Mari Wataya-Kaneda, Yutaka Hozumia, and Tamio Suzukia
    • Journal Title

      J Dermatol.

      Volume: - Issue: 8 Pages: 295-296

    • DOI

      10.1111/1346-8138.14831

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K10155, KAKENHI-PROJECT-18K16046
  • [Journal Article] NGS‐based targeted resequencing identified rare subtypes of albinism: Providing accurate molecular diagnosis for Japanese patients with albinism2019

    • Author(s)
      Okamura Ken、Hayashi Masahiro、Abe Yuko、Kono Michihiro、Nakajima Kimiko、Aoyama Yumi、Nishigori Chikako、Ishimoto Hiroshi、Ishimatsu Yuji、Nakajima Mika、Hozumi Yutaka、Suzuki Tamio
    • Journal Title

      Pigment Cell & Melanoma Research

      Volume: 32 Issue: 6 Pages: 848-853

    • DOI

      10.1111/pcmr.12800

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K16046
  • [Journal Article] A 4-bp deletion promoter variant (rs984225803) is associated with mild OCA4 among Japanese patients2018

    • Author(s)
      Okamura Ken、Hayashi Masahiro、Nakajima Osamu、Kono Michihiro、Abe Yuko、Hozumi Yutaka、Suzuki Tamio
    • Journal Title

      Pigment Cell & Melanoma Research

      Volume: 32 Issue: 1 Pages: 79-84

    • DOI

      10.1111/pcmr.12727

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K16046
  • [Journal Article] Waardenburg syndrome type IIE in a Japanese patient caused by a novel non-frame-shift duplication mutation in the SOX10 gene2017

    • Author(s)
      Hemmi Ami、Okamura Ken、Tazawa Ryushi、Abe Yuko、Hayashi Masahiro、Izumi Shuji、Tohyama Jun、Shimomura Yutaka、Hozumi Yutaka、Suzuki Tamio
    • Journal Title

      J Dermatol.

      Volume: in press Issue: 5

    • DOI

      10.1111/1346-8138.14151

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K19704
  • [Journal Article] Characterization of melanosomes and melanin in Japanese patients with Hermansky-Pudlak syndrome types 1, 4, 6, and 92017

    • Author(s)
      Okamura Ken、Abe Yuko、Araki Yuta、Wakamatsu Kazumasa、Seishima Mariko、Umetsu Takafumi、Kato Atsushi、Kawaguchi Masakazu、Hayashi Masahiro、Hozumi Yutaka、Suzuki Tamio
    • Journal Title

      Pigment Cell Melanoma Res.

      Volume: 31 Issue: 2 Pages: 267-276

    • DOI

      10.1111/pcmr.12662

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K19704
  • [Presentation] 遺伝性色素異常症の遺伝子解析システムの確立およびゲノム編集技術を用いた機能解析2019

    • Author(s)
      岡村 賢
    • Organizer
      日本皮膚科学会総会
    • Data Source
      KAKENHI-PROJECT-18K16046
  • [Presentation] A novel variant in the regulatory region of the SLC45A2 is possibly associated with mild OCA42017

    • Author(s)
      Ken Okamura
    • Organizer
      76th Annual meeting of Society for Investigative Dematology
    • Place of Presentation
      Oregon Convention Center (Portland, USA)
    • Year and Date
      2017-04-26
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K19704
  • [Presentation] Melanin analysis for hair samples from Japanese patients with Hermansky-Pudlak Syndrome types 1, 4, 6, and 92017

    • Author(s)
      Ken Okamura
    • Organizer
      The 23th International Pigment Cell Conference
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K19704
  • 1.  FUKUSHIMA Satoshi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 2.  KANEDA Mari
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 3.  尹 浩信
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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