KAMEYA SHUHEI 亀谷修平

… Alternative Names

KAMEYA Shyuhei 亀谷修平

亀谷修平カメヤシュウヘイ

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Researcher Number	30302269
Other IDs
Affiliation (based on the past Project Information) *help	2018 – 2020: 日本医科大学, 医学部, 准教授 2011 – 2013: 日本医科大学, 医学部, 准教授 2007 – 2008: Nippon Medical School, 医学部, 講師 2005 – 2006: Nippon Medical School, Medicine, Research Associate, 医学部, 助手 2003 – 2004: 秋田大学, 医学部, 講師 1999: 秋田大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Ophthalmology / Basic Section 56060:Ophthalmology-related Except Principal Investigator Ophthalmology / Basic Section 56060:Ophthalmology-related / Ophthalmology
Keywords	Principal Investigator Mfrp / Clqtnf5 / C1qtnf5 / エクソーム / DRAM2 / GUCY2D / GNAT1 / POC1B / AO / 補償光学眼底カメラ … More / MIDD / HK1 / rd6マウス / α1-syntrophin / 視神経脊髄炎 / alpha1-syntrophin / neuromyelitis optica / 加齢黄斑変性症 / 遺伝学 / RPE / retinal degeneration / rd6 … More Except Principal Investigator VKH disease / TCR / dendritic cell / 樹状細胞 / Expression / MHC / Tyrosinase / 網膜 / 視神経疾患 / 補償光学 / 画像解析 / 補償光学眼底カメラ / 遺伝子解析 / Speific immune response / Antigen specific for / 特異的抗体 / 特異的免疫反応 / VKHdisease / 特異抗体 / Regulatory dendritic cells / T cells / Antigen presenting cells / TRP1 / in vitro priming / T cell / 抗原提示 / 調節性樹状細胞 / T細胞 / 抗原提示細胞 / Transgenic rats / トランスジェニックラット Less

AOによる遺伝性網膜疾患超早期診断補助法の開発とAOデータベースの作成Principal Investigator
- Principal Investigator
  
  亀谷修平
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  Nippon Medical School
Adaptive optics imaging and electrophysiological analysis of micro cystic macular edema with optic atrophy diseases
- Principal Investigator
  
  後町清子
- Project Period (FY)
  2018 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  Nippon Medical School
Determination of disease causing mechanisms of neuromyelitis optica by analyzing alpha1-syntrophin deficient micePrincipal Investigator
- Principal Investigator
  
  KAMEYA SHUHEI
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Nippon Medical School
Production and analysis of the mouse model of age-related macular degeneration with disruption of C1qtnf5Principal Investigator
- Principal Investigator
  
  KAMEYA Shyuhei
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Nippon Medical School
Development of diagnostic tools and treatment based on the specific immune responses of VKH disease
- Principal Investigator
  
  YAMAKI Kunhiko
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Nippon Medical School
Analysis of interaction among proteins expressed in retinal pigment epitheliumPrincipal Investigator
- Principal Investigator
  
  KAMEYA Shuhei
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Nippon Medical School
Establishment of antigen specific regulatory dendritic cells and treatment of VKH disease with these dendritic cells
- Principal Investigator
  
  YAMAKI Kunihiko
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Nippon Medical School
  Akita University
新規網膜変性遺伝子のMfrpの機能解析Principal Investigator
- Principal Investigator
  
  亀谷修平
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Ophthalmology
- Research Institution
  Akita University
Molecurar immunological study of VKH disease
- Principal Investigator
  
  YAMAKI Kunihiko
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  AKITA UNIVERSITY

All 2021 2020 2019 Other

All Journal Article Presentation Book Other

[Book] 後眼部アトラス2019
- Author(s)
  亀谷修平（共著）
- Total Pages
  430
- Publisher
  総合医学社
- ISBN
  9784883786862
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] A new PDE6A missense variant p.Arg544Gln in rod?cone dystrophy2021
- Author(s)
  Hayashi Takaaki、Mizobuchi Kei、Kameya Shuhei、Yoshitake Kazutoshi、Iwata Takeshi、Nakano Tadashi
- Journal Title
  
  Documenta Ophthalmologica
  
  Volume: online ahead Issue: 1 Pages: 107-114
- DOI
  10.1007/s10633-021-09826-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-21K09756
[Journal Article] Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation2021
- Author(s)
  Oishi Noriko、Kubota Daiki、Nakamoto Kenji、Takeda Yukito、Hayashi Mika、Gocho Kiyoko、Yamaki Kunihiko、Igarashi Tsutomu、Takahashi Hiroshi、Kameya Shuhei
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 41 Issue: 3 Pages: 1-8
- DOI
  10.1080/13816810.2021.1881978
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation2020
- Author(s)
  Kubota Daiki、Matsumoto Kaori、Hayashi Mika、Oishi Noriko、Gocho Kiyoko、Yamaki Kunihiko、Kobayakawa Shinichiro、Igarashi Tsutomu、Takahashi Hiroshi、Kameya Shuhei
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 41 Issue: 6 Pages: 629-638
- DOI
  10.1080/13816810.2020.1810284
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] Tyrosine triple mutated AAV2-BDNF gene therapy in an inner retinal injury model induced by intravitreal injection of N-methyl-D-aspartate (NMDA)2020
- Author(s)
  Asaka Lee Shiozawa, Tsutomu Igarashi, Maika Kobayashi, Kenji Nakamoto, Shuhei Kameya, Shigeto Fujishita, Hiroshi Takahashi, Takashi Okada
- Journal Title
  
  Molecular Vision
  
  Volume: 26 Pages: 409-422
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D-Associated Retinal Disorder2020
- Author(s)
  Liu X, Fujinami K, Kuniyoshi K, Kondo M, Ueno S, Hayashi T, Mochizuki K, Kameya S, Yang L, Fujinami-Yokokawa Y, Arno G, Pontikos N, Sakuramoto H, Kominami T, Terasaki H, Katagiri S, Mizobuchi K, Nakamura N, Yoshitake K, Miyake Y, Li S, Kurihara T, Tsubota K, Iwata T, Tsunoda K; Japan Eye Genetics Consortium
- Journal Title
  
  Transl Vis Sci Technol
  
  Volume: 11 Issue: 6 Pages: 2-2
- DOI
  10.1167/tvst.9.6.2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02954, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-17H06276, KAKENHI-PROJECT-18K09424
[Journal Article] Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency.2020
- Author(s)
  Yang L, Fujinami K, Ueno S, Kuniyoshi K, Hayashi T, Kondo M, Mizota A, Naoi N, Shinoda K, Kameya S, Fujinami-Yokokawa Y, Liu X, Arno G, Pontikos N, Kominami T, Terasaki H, Sakuramoto H, Katagiri S, Mizobuchi K, Nakamura N, Mawatari G, Kurihara T, Tsubota K, Miyake Y, Yoshitake K, Iwata T, Tsunoda K; JEGC study group.
- Journal Title
  
  Sci Rep.
  
  Volume: 10 Issue: 1 Pages: 1-10
- DOI
  10.1038/s41598-020-62119-3
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11430, KAKENHI-PROJECT-18K09399, KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-18H02954, KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11478, KAKENHI-PROJECT-17K19721, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-18K09424, KAKENHI-PROJECT-17H06276
[Journal Article] Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association2020
- Author(s)
  Fujinami-Yokokawa Y, Fujinami K, Kuniyoshi K, Hayashi T, Ueno S, Mizota A, Shinoda K, Arno G, Pontikos N, Yang L, Liu X, Sakuramoto H, Katagiri S, Mizobuchi K, Kominami T, Terasaki H, Nakamura N, Kameya S, Yoshitake K, Miyake Y, Kurihara T, Tsubota K, Miyata H, Iwata T, Tsunoda K; Japan Eye Genetics Consortium.
- Journal Title
  
  Sci Rep
  
  Volume: 12 Issue: 1 Pages: 9531-9531
- DOI
  10.1038/s41598-020-65737-z
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11478, KAKENHI-PROJECT-17K11430, KAKENHI-PROJECT-18K09399, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-17H06276, KAKENHI-PROJECT-18K09424
[Journal Article] RP2-associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype-phenotype association.2020
- Author(s)
  Fujinami K, Liu X, Ueno S, Mizota A, Shinoda K, Kuniyoshi K, Fujinami-Yokokawa Y, Yang L, Arno G, Pontikos N, Kameya S, Kominami T, Terasaki H, Sakuramoto H, Nakamura N, Kurihara T, Tsubota K, Miyake Y, Yoshiake K, Iwata T, Tsunoda K; Japan Eye Genetics Consortium Study Group.
- Journal Title
  
  Am J Med Genet C Semin Med Genet.
  
  Volume: 184 Issue: 3 Pages: 675-693
- DOI
  10.1002/ajmg.c.31830
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11430, KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-17H06276, KAKENHI-PROJECT-18K09424
[Journal Article] Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy2020
- Author(s)
  Kuniyoshi Kazuki、Hayashi Takaaki、Kameya Shuhei、Katagiri Satoshi、Mizobuchi Kei、Tachibana Toshiaki、Kubota Daiki、Sakuramoto Hiroyuki、Tsunoda Kazushige、Fujinami Kaoru、Yoshitake Kazutoshi、Iwata Takeshi、Nakano Tadashi、Kusaka Shunji
- Journal Title
  
  International Journal of Molecular Sciences
  
  Volume: 21 Issue: 4 Pages: 1331-1331
- DOI
  10.3390/ijms21041331
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-17H06276
[Journal Article] Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy2020
- Author(s)
  Hayashi Takaaki、Katagiri Satoshi、Mizobuchi Kei、Yoshitake Kazutoshi、Kameya Shuhei、Matsuura Tomokazu、Iwata Takeshi、Nakano Tadashi
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 41 Issue: 1 Pages: 93-95
- DOI
  10.1080/13816810.2020.1723119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-17H06276
[Journal Article] Novel <i>GUCY2D</i> Variant (E843Q) at Mutation Hotspot Associated with Macular Dystrophy in a Japanese Patient2020
- Author(s)
  Takeda Yukito、Kubota Daiki、Oishi Noriko、Maruyama Kaori、Gocho Kiyoko、Yamaki Kunihiko、Igarashi Tsutomu、Takahashi Hiroshi、Kameya Shuhei
- Journal Title
  
  Journal of Nippon Medical School
  
  Volume: 87 Issue: 2 Pages: 92-99
- DOI
  10.1272/jnms.JNMS.2020_87-207
- NAID
  130007843314
- ISSN
  1345-4676, 1347-3409
- Year and Date
  2020-04-15
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families2020
- Author(s)
  Hayashi Takaaki、Kameya Shuhei、Mizobuchi Kei、Kubota Daiki、Kikuchi Sachiko、Yoshitake Kazutoshi、Mizota Atsushi、Murakami Akira、Iwata Takeshi、Nakano Tadashi
- Journal Title
  
  Scientific Reports
  
  Volume: 10 Issue: 1 Pages: 15883-15883
- DOI
  10.1038/s41598-020-72623-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-17H06276
[Journal Article] Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.2019
- Author(s)
  Maeda-Katahira A, Nakamura N, Hayashi T, Katagiri S, Shimizu S, Ohde H, Matsunaga T, Kaga K, Nakano T, Kameya S, Matsuura T, Fujinami K1, Iwata T, Tsunoda K.
- Journal Title
  
  Molecular Vision
  
  Volume: 25 Pages: 559-573
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Journal Article] Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance2019
- Author(s)
  Kameya Shuhei、Fujinami Kaoru、Ueno Shinji、Hayashi Takaaki、Kuniyoshi Kazuki、Ideta Ryuichi、Kikuchi Sachiko、Kubota Daiki、Yoshitake Kazutoshi、Katagiri Satoshi、Sakuramoto Hiroyuki、Kominami Taro、Terasaki Hiroko、Yang Lizhu、Fujinami-Yokokawa Yu、Liu Xiao、Arno Gavin、Pontikos Nikolas、
- Journal Title
  
  Investigative Opthalmology & Visual Science
  
  Volume: 60 Issue: 10 Pages: 3432-3432
- DOI
  10.1167/iovs.19-26650
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-17K11434
[Journal Article] Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake disease); EAOMD Report No.12019
- Author(s)
  Fujinami Kaoru、Yang Lizhu、Joo Kwangsic、Tsunoda Kazushige、Kameya Shuhei、Hanazono Gen、Fujinami-Yokokawa Yu、Arno Gavin、Kondo Mineo、Nakamura Natsuko、Kurihara Toshihide、Tsubota Kazuo、Zou Xuan、Li Hui、Park Kyu Hyung、Iwata Takeshi、Miyake Yozo、Woo Se Joon、Sui Ruifang
- Journal Title
  
  Ophthalmology
  
  Volume: - Issue: 10 Pages: 1432-1444
- DOI
  10.1016/j.ophtha.2019.04.032
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K16943, KAKENHI-PROJECT-16KK0193, KAKENHI-PROJECT-19K09940, KAKENHI-PROJECT-17K19721, KAKENHI-PROJECT-18K09424
[Journal Article] Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family2019
- Author(s)
  Kubota Daiki、Oishi Noriko、Gocho Kiyoko、Kikuchi Sachiko、Yamaki Kunihiko、Igarashi Tsutomu、Takahashi Hiroshi、Ishida Nobuo、Iwata Takeshi、Mizota Atsushi、Kameya Shuhei
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 40 Issue: 5 Pages: 480-487
- DOI
  10.1080/13816810.2019.1686159
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 非典型的な黄斑病変を示した先天網膜分離症の1例2020
- Author(s)
  永江由季，國吉一樹，林孝彰，近藤千桜里，亀谷修平，岩田岳，日下俊次
- Organizer
  第68回　日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] HK１遺伝子異常を認めた常染色体優性網膜色素変性症一家系のAO解析2020
- Author(s)
  久保田　大紀、大石　典子、後町　清子、五十嵐　勉、山木　邦比古、亀谷　修平、高橋　浩
- Organizer
  第68回　日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 黄斑ジストロフィを呈したm.3243A>G変異によるmaternally inherited diabetes and deafness (MIDD) の１症例2020
- Author(s)
  大石典子、久保田大紀、武田幸人、林美香、後町清子、山木邦比古、小早川信一郎、五十嵐勉、高橋浩、亀谷修平
- Organizer
  第68回　日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] BDNF発現アデノ随伴ウイルスベクターtm-scAAV2-BDNFを用いた網膜内層障害の遺伝子治療2020
- Author(s)
  塩澤朝香、五十嵐勉、小林舞香、中元兼二、亀谷修平、藤下繁人、高橋浩、岡田尚巳
- Organizer
  日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] KCNV2網膜症における中心窩錐体の冗長性2020
- Author(s)
  小柳俊人、上野真治、林孝彰、亀谷修平、後町清子、園田康平、伊藤逸毅
- Organizer
  第68回　日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 全視野ERGで錐体反応良好な黄斑ジストロフィに新規GUCY2D 遺伝子変異を認めた１例2019
- Author(s)
  武田幸人、久保田大紀、後町清子、大石典子、鈴木　界、丸山佳織、山木邦比古、高橋　浩、亀谷修平
- Organizer
  第73回　日本臨床眼科学会総会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] A novel homozygous in-frame deletion of GNAT1 gene cause golden discolouration of the fundus and reduced dark-adapted ERG similar to that of Oguchi disease in a Japanese family2019
- Author(s)
  Shuhei Kameya, Daiki Kubota, Kiyoko Gocho, Sachiko Kikuchi, Kunihiko Yamaki, Tsutomu Igarashi, Hiroshi Takahashi, Nobuo Ishida, Kazutoshi Yoshitake, Takeshi Iwata, Atsushi Mizota
- Organizer
  ISGEDR 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] Functional Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake’s disease); EAOMD Report No.22019
- Author(s)
  Lizhu Yang, Kwangsic Joo, Kazushige Tsunoda, Mineo Kondo, Yu Yokokawa Fujinami, Anthony G. Robson, Toshihide Kurihara, Kazuo Tsubota, Shuhei Kameya, Takeshi Iwata, Xuan Zou, Kyu Hyung Park, Yozo Miyake, Se Joon Woo, Ruifang Sui, Kaoru Fujinami
- Organizer
  ARVO 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] Japan Eye Genetics Consortium: National Cohort Survey and Whole Exome Sequencing Results2019
- Author(s)
  Kaoru Fujinami, Kazutoshi Yoshitake, Takaaki Hayashi, Kazuki Kuniyoshi, Shinji Ueno, Mineo Kondo, Kei Shinoda, Shuhei Kameya, Nobuhisa Nao-i, Hiroyuki Kondo, Yozo Miyake, Takeshi Iwata, Kazushige Tsunoda
- Organizer
  ARVO 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] Rhodopsin（RHO）遺伝子に新規1塩基欠損変異を認めた常染色体優性杆体錐体ジストロフィの1家系2019
- Author(s)
  久保田大紀、後町清子、大石典子、丸山佳織、武田幸人、鈴木界、山木邦比古、高橋浩、亀谷修平
- Organizer
  第67回　日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 眼底動脈壁所見と生活習慣病に関する検討2019
- Author(s)
  山口祐司、岡島史宜、仲村優子、長峯朋子、周東佑樹、久保田大紀、後町清子、亀谷修平、高橋浩、杉原仁、江本直也
- Organizer
  第62回　日本糖尿病学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 「コロイデレミア」シンポジウム2「網脈絡膜ジストロフィの最前線　（JEGCスタディ総括、Part 2）」2019
- Author(s)
  亀谷修平
- Organizer
  第67回日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] A novel homozygous in-frame deletion of GNAT1 gene cause golden discolouration of the fundus and reduced dark-adapted ERG similar to characteristics of Oguchi disease in a Japanese family2019
- Author(s)
  Shuhei Kameya, Daiki Kubota, Kiyoko Gocho, Sachiko Kikuchi, Kunihiko Yamaki, Tsutomu Igarashi, Hiroshi Takahashi, Nobuo Ishida, Kazutoshi Yoshitake, Takeshi Iwata, Atsushi Mizota
- Organizer
  ARVO 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09940
[Presentation] 眼底動脈壁所見と生活習慣病に関する検討2019
- Author(s)
  山口祐司、岡島史宜、仲村優子、長峯朋子、周東佑樹、久保田大紀、後町清子、亀谷修平、高橋浩、杉原仁、江本直也
- Organizer
  第51回　日本動脈硬化学会
- Data Source
  KAKENHI-PROJECT-19K09940
[]

1. YAMAKI Kunihiko (20125751)

# of Collaborated Projects: 6 results

# of Collaborated Products: 0 results
2. GOTO Yoko (80277524)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
3. SUZUKI Yuko (00342931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. TAKAHASHI Hisatomo (10445801)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. KONNO Seiki (00312710)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. SAKURAGI Shozo (80006767)

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7. HAYAKAWA Kouchi (80312700)

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8. 近藤功 (50234927)

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9. 原宏二 (60375251)

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10. 後町清子 (20333940)

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11. 久保田大紀 (20763155)

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12. 近藤峰生

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13. 篠田啓

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14. 藤波優

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15. 林孝彰

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KAMEYA SHUHEI 亀谷 修平

KAMEYA Shyuhei 亀谷 修平

亀谷 修平 カメヤ シュウヘイ

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AOによる遺伝性網膜疾患超早期診断補助法の開発とAOデータベースの作成Principal Investigator

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Adaptive optics imaging and electrophysiological analysis of micro cystic macular edema with optic atrophy diseases

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Determination of disease causing mechanisms of neuromyelitis optica by analyzing alpha1-syntrophin deficient micePrincipal Investigator

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Production and analysis of the mouse model of age-related macular degeneration with disruption of C1qtnf5Principal Investigator

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Development of diagnostic tools and treatment based on the specific immune responses of VKH disease

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Analysis of interaction among proteins expressed in retinal pigment epitheliumPrincipal Investigator

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Establishment of antigen specific regulatory dendritic cells and treatment of VKH disease with these dendritic cells

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新規網膜変性遺伝子のMfrpの機能解析Principal Investigator

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Molecurar immunological study of VKH disease

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[Book] 後眼部アトラス2019

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[Journal Article] A new PDE6A missense variant p.Arg544Gln in rod?cone dystrophy2021

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[Journal Article] Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation2021

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[Journal Article] High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation2020

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KAMEYA SHUHEI 亀谷修平

KAMEYA Shyuhei 亀谷修平

亀谷修平カメヤシュウヘイ