Okamura Ken 岡村賢

Researcher Number	40637229
Other IDs
Affiliation (Current)	2025: 山形大学, 医学部, 講師
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

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

Okamura Ken 岡村 賢

Research Projects

Research Products

Co-Researchers

Establishment of a Vitiligo Model Mouse and Pathological Analysis: Development of a Novel Therapy Focusing on RetrotransposonsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Establishment of an efficient gene testing system for hereditary pigmentation disorders and functional analysis using genome editing technologyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Exhaustive mutation analysis and functional study of hereditary pigmentation disordersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

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

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 62021

Author(s)

Journal Title

DOI

Data Source

[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)

Journal Title

DOI

Data Source

[Journal Article] Impact of a 4-bp deletion variant (rs984225803) in the promoter region of SLC45A2 on color variation among Japanese population2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] NGS‐based targeted resequencing identified rare subtypes of albinism: Providing accurate molecular diagnosis for Japanese patients with albinism2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A 4-bp deletion promoter variant (rs984225803) is associated with mild OCA4 among Japanese patients2018

Author(s)

Journal Title

DOI

Data Source

[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)

Journal Title

DOI

Data Source

[Journal Article] Characterization of melanosomes and melanin in Japanese patients with Hermansky-Pudlak syndrome types 1, 4, 6, and 92017

Author(s)

Journal Title

DOI

Data Source

[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)

Organizer

Data Source

[Presentation] A novel variant in the regulatory region of the SLC45A2 is possibly associated with mild OCA42017

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] Melanin analysis for hair samples from Japanese patients with Hermansky-Pudlak Syndrome types 1, 4, 6, and 92017

Author(s)

Organizer

Data Source

Okamura Ken 岡村賢