HOSONO Katsuhiro 細野克博

Researcher Number	60402260
Other IDs
Affiliation (based on the past Project Information) *help	2022: 浜松医科大学, 医学部, 助教 2009 – 2019: 浜松医科大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Ophthalmology / Basic Section 56060:Ophthalmology-related Except Principal Investigator Ophthalmology
Keywords	Principal Investigator 遺伝子診断 / EYS / 遺伝子変異解析 / 網膜色素変性 / テーラーメード医療 / 眼遺伝学 / レーバー先天盲 / 次世代シークエンサー / 遺伝子解析 / Leber先天盲 … More / 先天性視覚障害 / EYS遺伝子 / 常染色体劣性遺伝 / 遺伝子変異 / 遺伝学 … More Except Principal Investigator 遺伝子診断 / 次世代シークエンサー / 生体計測 / 遺伝性眼疾患 / 遺伝子変異探索 / 早発型発達緑内障 / 先天白内障 / 先天緑内障 / ミトコンドリア異常 / 外眼筋麻痺 / ミトコンドリア / ミトコンドリアDNA / 慢性進行性外眼筋麻痺 / 遺伝子解析 / 未診断眼疾患 / 未診断眼疾患患者 / ターゲットシークエンス解析 / 変異解析 / 希少眼疾患 / 遺伝性網膜変性 / 遺伝子変異解析 / 網膜色素変性 / 感受性 / 1塩基多型 / アポトーシス / ラット / 戻し交配 / 加齢黄斑変性 / 多型解析 / モリス水迷路 / 連続戻し交配 / 網膜光障害 / 生体分子 / プロテオーム / 神経科学 / シグナル伝達 / 遺伝子 / 相互作用タンパク / 緑内障 Less

小児期に発症する網膜ジストロフィの分子遺伝学的基盤の構築に関する研究Principal Investigator
- Principal Investigator
  
  細野克博
- Project Period (FY)
  2022 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  Hamamatsu University School of Medicine
Construction of a comprehensive regional medical system and development of diagnostic method for rare and undiagnosed eye disease patients in Japan
- Principal Investigator
  
  Hotta Yoshihiro
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Development of the simple diagnostic method for the patients with chronic progressive external ophthalmoplegia and the construction of the database
- Principal Investigator
  
  Hikoya Akiko
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Development of diagnosis program and clinical application with congenital visual impairment patients for tailor-made medicinePrincipal Investigator
- Principal Investigator
  
  Hosono Katsuhiro
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
3D-analysis using biometric technology and the database construction for elucidating the pathological mechanism with congenital cataract
- Principal Investigator
  
  Tachibana Nobutaka
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Development of genetic diagnosis for Japanese Retinitis Pigmentosa patients using next generation sequencer
- Principal Investigator
  
  Hotta Yoshihiro
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
The development and clinical application of EYS gene mutation diagnosis in Japanese Retinitis pigmentosa patientsPrincipal Investigator
- Principal Investigator
  
  HOSONO Katsuhiro
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Genotype-phenotype analysis and prevalence study of disease-causing mutations in the EYS gene among Japanese patients with retinitis pigmentosaPrincipal Investigator
- Principal Investigator
  
  HOSONO Katsuhiro
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Identification of candidate genes responsible for an increased susceptibility of age-related macular degeneration using an animal model and its application to gene diagnosis.
- Principal Investigator
  
  OHISHI Kentaro
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Molecular analysis of glaucoma-developing mechanism : Investigation of an OPTN-interacting protein
- Principal Investigator
  
  OHTSUBO Masafumi
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine

All 2019 2018 2017 2016 2015 2014 2012 2011 2010 2009 Other

All Journal Article Presentation Book Patent

[Book] あたらしい眼科2019
- Author(s)
  堀田喜裕、細野克博、倉田健太郎
- Total Pages
  9
- Publisher
  メディカル葵出版
- Data Source
  KAKENHI-PROJECT-17K11447
[Book] RETINA Medicine　ゲノムと網膜関連疾患の関与を探る　網膜色素変性2014
- Author(s)
  堀田喜裕、細野克博
- Total Pages
  94
- Publisher
  先端医学社
- Data Source
  KAKENHI-PROJECT-26462659
[Book] RETINA Medicine　ゲノムと網膜関連疾患の関与を探る　網膜色素変性2014
- Author(s)
  堀田喜裕、細野克博
- Total Pages
  94
- Publisher
  先端医学社
- Data Source
  KAKENHI-PROJECT-25861626
[Book] 眼科　眼と遺伝　2.網膜色素変性2014
- Author(s)
  細野克博、堀田喜裕
- Total Pages
  112
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-25861626
[Journal Article] Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.2019
- Author(s)
  Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH.
- Journal Title
  
  Jounal of Medical Genetics
  
  Volume: 56 Issue: 10 Pages: 662-670
- DOI
  10.1136/jmedgenet-2018-105691
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-17K11447
[Journal Article] Phenotypic features of Oguchi disease and retinitis pigmentosa in patients with SAG mutations. A long-term follow-up study2019
- Author(s)
  Nishiguchi KM, Ikeda Y, Fujita K, Kunikata H, Akiho M, Hashimoto K, Hosono K, Kurata K, Koyanagi Y, Akiyama M, Suzuki T, Kawasaki R, Wada Y, Hotta Y, Sonoda K-H, Murakami A, Nakazawa M, Nakazawa T, Abe T.
- Journal Title
  
  Ophthalmology
  
  Volume: 126 Issue: 11 Pages: 1557-1565
- DOI
  10.1016/j.ophtha.2019.05.027
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09926, KAKENHI-PROJECT-17K11447
[Journal Article] 診断にＲＥＴｅｖａｌが有用であった発達障害を伴うＬｅｂｅｒ先天盲の一例2019
- Author(s)
  瀧伶、鈴木寛子、倉田健太郎、古森美和、細野克博、彦谷明子、佐藤美保、堀田喜裕
- Journal Title
  
  眼臨紀
  
  Volume: 12(1) Pages: 49-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11284
[Journal Article] Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations2019
- Author(s)
  Miyamichi Daisuke、Nishina Sachiko、Hosono Katsuhiro、Yokoi Tadashi、Kurata Kentaro、Sato Miho、Hotta Yoshihiro、Azuma Noriyuki
- Journal Title
  
  Human Genome Variation
  
  Volume: 6 Issue: 1 Pages: 1-1
- DOI
  10.1038/s41439-019-0064-8
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K10004, KAKENHI-PROJECT-17K11447
[Journal Article] 特集第72回日本臨床眼科学会講演集[1] 原著 RDH12遺伝子変異による網膜色素変性症の1例2019
- Author(s)
  武田優, 倉田健太郎, 細野克博, 堀田喜裕
- Journal Title
  
  臨床眼科
  
  Volume: 73 Issue: 3 Pages: 307-314
- DOI
  10.11477/mf.1410213074
- ISSN
  0370-5579, 1882-1308
- Year and Date
  2019-03-15
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11447
[Journal Article] A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants.2019
- Author(s)
  Haque MN, Kurata K, Hosono K, Ohtsubo M, Ohishi K, Sato M, Minoshima S, Hotta Y
- Journal Title
  
  Hum Genome Var
  
  Volume: 6:18 Issue: 1
- DOI
  10.1038/s41439-019-0048-8
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11447
[Journal Article] 診断にＲＥＴｅｖａｌが有用であった発達障害を伴うＬｅｂｅｒ先天盲の一例2019
- Author(s)
  瀧伶、鈴木寛子、倉田健太郎、古森美和、細野克博、彦谷明子、佐藤美保、堀田喜裕
- Journal Title
  
  眼臨紀
  
  Volume: 12(1) Pages: 49-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11479
[Journal Article] 診断にＲＥＴｅｖａｌが有用であった発達障害を伴うＬｅｂｅｒ先天盲の一例2019
- Author(s)
  瀧伶、鈴木寛子、倉田健太郎、古森美和、細野克博、彦谷明子、佐藤美保、堀田喜裕
- Journal Title
  
  眼臨紀
  
  Volume: 12(1) Pages: 49-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11447
[Journal Article] X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers2019
- Author(s)
  Kurata Kentaro、Hosono Katsuhiro、Hayashi Takaaki、Mizobuchi Kei、Katagiri Satoshi、Miyamichi Daisuke、Nishina Sachiko、Sato Miho、Azuma Noriyuki、Nakano Tadashi、Hotta Yoshihiro
- Journal Title
  
  International Journal of Molecular Sciences
  
  Volume: 20 Issue: 6 Pages: 1518-1518
- DOI
  10.3390/ijms20061518
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-19K10004, KAKENHI-PROJECT-15H04998, KAKENHI-PROJECT-19H03810, KAKENHI-PROJECT-17K11434
[Journal Article] Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.2018
- Author(s)
  Katagiri S, Iwasa M, Hayashi T, Hosono K, Yamashita T, Kuniyoshi K, Ueno S, Kondo M, Ueyama H, Ogita H, Shichida Y, Inagaki H, Kurahashi H, Kondo H, Ohji M, Hotta Y, Nakano T.
- Journal Title
  
  Sci Rep
  
  Volume: 8 Issue: 1 Pages: 11507-11507
- DOI
  10.1038/s41598-018-29891-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K19721, KAKENHI-PROJECT-16H02515, KAKENHI-PROJECT-18H02954, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-16K07437, KAKENHI-PROJECT-16K11284
[Journal Article] Long-term clinical course of two Japanese patients with PRPF31-related retinitis pigmentosa2018
- Author(s)
  10.1007/s10384-017-0560-7
- Journal Title
  
  Jpn. J. Ophthalmol .
  
  Volume: 62(2) Issue: 2 Pages: 186-193
- DOI
  10.1007/s10384-017-0560-7
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-17K11447
[Journal Article] Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants2018
- Author(s)
  Katagiri S, Hosono K, Hayashi T, Kurata K, Mizobuchi K, Matsuura T, Yoshitake K, Iwata T, Nakano T, Hotta Y
- Journal Title
  
  Molecular Vision
  
  Volume: 24 Pages: 286-296
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11447
[Journal Article] Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants2018
- Author(s)
  Katagiri S, Hosono K, Hayashi T, Kurata K, Mizobuchi K, Matsuura T, Yoshitake K, Iwata T, Nakano T, Hotta Y
- Journal Title
  
  Molecular Vision
  
  Volume: 24 Pages: 286-296
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K11284
[Journal Article] Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono Katsuhiro、Nishina Sachiko、Yokoi Tadashi、Katagiri Satoshi、Saitsu Hirotomo、Kurata Kentaro、Miyamichi Daisuke、Hikoya Akiko、Mizobuchi Kei、Nakano Tadashi、Minoshima Shinsei、Fukami Maki、Kondo Hiroyuki、Sato Miho、Hayashi Takaaki、Azuma Noriyuki、Hotta Yoshihiro
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 8279-8279
- DOI
  10.1038/s41598-018-26524-z
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11441, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K11479, KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-16K11309
[Journal Article] Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa2018
- Author(s)
  Kurata Kentaro、Hosono Katsuhiro、Hotta Yoshihiro
- Journal Title
  
  Documenta Ophthalmologica
  
  Volume: 137 Issue: 1 Pages: 47-56
- DOI
  10.1007/s10633-018-9649-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-16K11284
[Journal Article] Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations2018
- Author(s)
  Kurata Kentaro、Hosono Katsuhiro、Hikoya Akiko、Kato Akihiko、Saitsu Hirotomo、Minoshima Shinsei、Ogata Tsutomu、Hotta Yoshihiro
- Journal Title
  
  Japanese Journal of Ophthalmology
  
  Volume: 62 Issue: 4 Pages: 458-466
- DOI
  10.1007/s10384-018-0591-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K11479, KAKENHI-PROJECT-17H04204, KAKENHI-PROJECT-16K11284
[Journal Article] Long-term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness2017
- Author(s)
  Kurata K, Hosono K and Hotta Y.
- Journal Title
  
  Case Rep. Ophthalmol.
  
  Volume: 8(1) Issue: 1 Pages: 237-244
- DOI
  10.1159/000462961
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-17K11447
[Journal Article] ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISC REGION2017
- Author(s)
  Yokoi T, Katagiri S, Hiraoka M, Nakayama Y, Hosono K, Hotta Y, Nishina S, Azuma N
- Journal Title
  
  RETINA
  
  Volume: 印刷中 Issue: 8 Pages: 1-1
- DOI
  10.1097/iae.0000000000001779
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-16K11309, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-15H02566, KAKENHI-PROJECT-17K16996
[Journal Article] Retinitis pigmentosa in Japanese population2017
- Author(s)
  Hosono K, Minoshima S, Hotta Y
- Journal Title
  
  Essentials in Ophthalmology Advances in Vision Research
  
  Volume: volume I Pages: 111-128
- DOI
  10.1007/978-4-431-56511-6_11
- ISBN
  9784431565093, 9784431565116
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-17K11447
[Journal Article] Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations2017
- Author(s)
  Nagase Y, Kurata K, Hosono K, Suto K, Hikoya A, Nakanishi H, Mizuta K, Mineta K, Minoshima S and Hotta Y
- Journal Title
  
  Semin. Ophthalmol.
  
  Volume: 印刷中 Issue: 4 Pages: 560-565
- DOI
  10.1080/08820538.2017.1340487
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K11479
[Journal Article] Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy.2016
- Author(s)
  Wang C, Hosono K, Kachi S, Suto K, Nakamura M, Terasaki H, Miyake Y, Hotta Y, Minoshima S.
- Journal Title
  
  Hum Genome Var.
  
  Volume: 3 Issue: 1 Pages: 16011-16011
- DOI
  10.1038/hgv.2016.11
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04994, KAKENHI-PROJECT-26462659, KAKENHI-PROJECT-16K11284
[Journal Article] Genotype-phenotype correlation of the PAX6 gene mutations in aniridia2016
- Author(s)
  Yokoi T, Nishina S, Fukami M, Ogata T, Hosono K, Hotta Y, Azuma N.
- Journal Title
  
  Human Genome Variation
  
  Volume: 3 Issue: 1 Pages: 15052-15052
- DOI
  10.1038/hgv.2015.52
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462659, KAKENHI-PROJECT-15H02566, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25462767, KAKENHI-PROJECT-15K15640, KAKENHI-PROJECT-16K11309
[Journal Article] Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism.2016
- Author(s)
  *Miyamichi D, Asahina M, Nakajima J, Sato M, Hosono K, Nomura T, Negishi T, Miyake N, Hotta Y, Ogata T, Matsumoto N.
- Journal Title
  
  J Hum Genet.
  
  Volume: 61(9) Issue: 9 Pages: 839-842
- DOI
  10.1038/jhg.2016.56
- NAID
  40020938230
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-26462659, KAKENHI-PROJECT-16K11264, KAKENHI-PROJECT-16K11284
[Journal Article] Novel GUCY2D gene mutations in Japanese male twins with Leber congenital amaurosis2015
- Author(s)
  Hosono K, Harada Y, Kurata K, Hikoya A, Sato M, Minoshima S, Hotta Y.
- Journal Title
  
  J. Ophthalmol.
  
  Volume: 693468 Pages: 1-10
- DOI
  10.1155/2015/693468
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462659
[Journal Article] Interaction between optineurin and the bZIP transcription factor NRL2014
- Author(s)
  Wang C, Hosono K, Ohtsubo M, Ohishi K, Gao J, Nakanishi N, Hikoya A, Sato M, Hotta Y, Minoshima S.
- Journal Title
  
  Cell Biol. Int.
  
  Volume: 38(1) Issue: 1 Pages: 16-25
- DOI
  10.1002/cbin.10174
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592561, KAKENHI-PROJECT-23592562, KAKENHI-PROJECT-24592622, KAKENHI-PROJECT-25462708, KAKENHI-PROJECT-25861626
[Journal Article] The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.2014
- Author(s)
  Yang Zhao, Katsuhiro Hosono, Kimiko Suto, Chie Ishigami, Yuki Arai, Akiko Hikoya, Yasuhiko Hirami, Masafumi Ohtsubo, Shinji Ueno, Hiroko Terasaki, Miho Sato, Hiroshi Nakanishi, Shiori Endo, Kunihiro Mizuta, Hiroyuki Mineta, Mineo Kondo, Masayo Takahashi, Shinsei Minoshima, Yoshihiro Hotta.
- Journal Title
  
  J Hum Genet.
  
  Volume: 59 Issue: 9 Pages: 521-528
- DOI
  10.1038/jhg.2014.65
- NAID
  40020198536
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25861626, KAKENHI-PROJECT-26462659, KAKENHI-PROJECT-26462683
[Journal Article] Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in the EYS Gene2014
- Author(s)
  Suto K, Hosono K, Takahashi M, Hirami Y, Arai Y, Nagase Y, Ueno S, Terasaki H, Minoshima S, Kondo M, Hotta Y.
- Journal Title
  
  Ophthalmic Genet.
  
  Volume: 35(1) Issue: 1 Pages: 25-34
- DOI
  10.3109/13816810.2013.768673
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592561, KAKENHI-PROJECT-23592603, KAKENHI-PROJECT-25861626
[Journal Article] Genetic diagnosis from buccal mucousmembrane in cases of chronic progress ophthalmoplegia2012
- Author(s)
  Kaoruko Torii, Takashi Negishi, Katsuhiro Hosono, Mayu Sawada, Akiko Hikoya, Miho Sato, Yoshihiro Hotta
- Journal Title
  
  Jpn.J.Clin.Ophthalmol
  
  Volume: 66(10) Pages: 1497-1502
- Data Source
  KAKENHI-PROJECT-23791975
[Journal Article] Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population.2012
- Author(s)
  Nakanishi H, Ueno S, Yokoi T, Hikoya A, Fujita T, Zhao Y, Nishina S, Shin JP, Kim IT, Yamamoto S, Azuma N, Terasaki H, Sato M, Kondo M, Minoshima M, Hotta Y.
- Journal Title
  
  PLoS One
  
  Volume: 7(2) Issue: 2 Pages: e31036-e31036
- DOI
  10.1371/journal.pone.0031036
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390327, KAKENHI-PROJECT-22591975, KAKENHI-PROJECT-23390401, KAKENHI-PROJECT-23592561, KAKENHI-PROJECT-23592562, KAKENHI-PROJECT-23592603, KAKENHI-PROJECT-23791975, KAKENHI-PROJECT-24659770
[Journal Article] Genetic diagnosis from buccal mucous membrane in cases of chronic progress ophthalmoplegia2012
- Author(s)
  Torii K, Negishi T, Hosono K, Sawada M, Hikoya A, Sato M, Hotta Y
- Journal Title
  
  Japanese Journal of Clinical Ophthalmology
  
  Volume: 66(19) Pages: 32-34
- NAID
  40019462659
- Data Source
  KAKENHI-PROJECT-23791975
[Journal Article] 眼白子が疑われた姉妹例2012
- Author(s)
  野村隆仁、佐藤美保、細野克博、彦谷明子、根岸貴志、澤田麻友、堀田喜裕
- Journal Title
  
  臨床眼科紀要
  
  Volume: 5(4) Pages: 367-372
- Data Source
  KAKENHI-PROJECT-23791975
[Journal Article] 眼白子が疑われた姉妹例2012
- Author(s)
  野村隆仁、佐藤美保、細野克博、彦谷明子、根岸貴志、澤田麻友、堀田喜裕
- Journal Title
  
  眼臨紀
  
  Volume: 5(4) Pages: 367-372
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791975
[Journal Article] Clinical features of a Japanese case with Bothnia dystrophy2012
- Author(s)
  Nojima K, Hosono K, Zhao Y, Toshiba T, Hikoya A, Asai T, Kato M. Kondo M, Minoshima S, Hotta Y
- Journal Title
  
  Ophthalmic Genet
  
  Volume: 33(2) Issue: 2 Pages: 83-88
- DOI
  10.3109/13816810.2011.634877
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592561, KAKENHI-PROJECT-23592562, KAKENHI-PROJECT-23592603, KAKENHI-PROJECT-23791975
[Patent] 遺伝子の変異を検出するためのプライマー、プローブ、マイクロアレイ、及び、これらを備える検出キット、並びに、網膜色素変性症原因遺伝子変異の検査方法、網膜色素変性症への遺伝的感受性の検査方法2010
- Inventor(s)
  細野克博、堀田喜裕
- Industrial Property Rights Holder
  国立大学法人浜松医科大学
- Industrial Property Number
  2010-294236
- Filing Date
  2010-12-28
- Overseas
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] 浜松医科大学を受診した網膜芽細胞腫2例の遺伝子検査2019
- Author(s)
  山﨑智幸、細野克博、坂口公祥、小松和幸、川上領太、清水大輔、彦谷明子、倉田健太郎、才津浩智、蓑島伸生、佐藤美保、緒方勤、堀田喜裕
- Organizer
  第73回静岡県眼科医会集談会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] Chronic progressive external ophthalmoplegia associated with proptosis: A report of two cases.2019
- Author(s)
  Takeda Y, Suzuki H, Iimori H, Hosono K, Hikoya A, Sato M, Hotta Y
- Organizer
  AAPOS/RANZO/APSPOS 2019 Joing
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] 不均衡型転座により6p25モノソミーと18p11トリソミーをもつ続発小児緑内障の1例2019
- Author(s)
  細野克博、川瀬和秀、倉田健太郎、新美裕介、才津浩智、蓑島伸生、大西秀典、山本崇裕、彦谷明子、立花信貴、深尾敏幸、山本哲也、堀田喜裕
- Organizer
  第40回東海緑内障の会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] 眼球突出を主訴に受診し慢性進行性外眼筋麻痺と診断された２症例2019
- Author(s)
  武田優、鈴木寛子、飯森宏仁、細野克博、彦谷明子、堀田喜裕、佐藤美保
- Organizer
  第75回日本弱視斜視学会総会第44回日本小児眼科学会合同学会総会合同学会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] Fine analysis of IKBKG in a Japanese boy and 3 girls with incontinentia pigmenti2019
- Author(s)
  ハックムハンマドナズムール、大坪正史、仁科幸子、中尾志郎、細野克博、倉田健太郎、大石健太郎、佐藤美保、堀田喜裕、蓑島伸生、東範行
- Organizer
  第123回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] SAG変異を病院とする小口病と網膜色素変性の臨床表現型比較2019
- Author(s)
  西口康二、池田康博、細野克博、和田裕子、園田康平、堀田喜裕、村上晶、中澤満、中澤徹、阿部俊明
- Organizer
  第67回日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Molecular diagnosis of 34 Japanese families with Leber congenital amaurosis using targeted next generation sequencing2019
- Author(s)
  細野克博、東範行、堀田喜裕
- Organizer
  第75回日本弱視斜視学会総会第44回日本小児眼科学会合同学会総会合同学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 日本人X連鎖性網膜色素変性症の遺伝型と臨床像の検討2019
- Author(s)
  倉田健太郎、細野克博、溝渕圭、片桐聡、宮道大督、仁科幸子、東範行、中野匡、林孝彰、堀田喜裕
- Organizer
  第123回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 浜松医科大学を受診した網膜芽細胞腫2例の遺伝子検査2019
- Author(s)
  山﨑智幸、細野克博、坂口公祥、小松和幸、川上領太、清水大輔、彦谷明子、倉田健太郎、才津浩智、蓑島伸生、佐藤美保、緒方勤、堀田喜裕
- Organizer
  第75回日本弱視斜視学会総会第44回日本小児眼科学会合同学会総会合同学会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation2019
- Author(s)
  Hosono K, Kawase K, Kurata K, Niimi Y, Saitsu H, Minoshima S, Ohnishi H, Yamamoto T, Hikoya A, Tachibana N, Fukao T, Yamamoto T, Hotta Y
- Organizer
  2019 Joint Meeting of the ISGRDR and DOG Genetics
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] Targeted resequencing of 83 causative genes in 1,204 Japanese patients with retinitis pigmentosa2019
- Author(s)
  Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda K
- Organizer
  The 19th EURETINA Congress
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] X連鎖性レーバー先天盲2症例の臨床像2019
- Author(s)
  仁科幸子、細野克博、横井匡、倉田健太郎、吉田朋世、深見真紀、堀田喜裕、東範行
- Organizer
  第123回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] RPE65 変異により重度網膜視機能障害および斑点を認めた網膜ジストロフィ2018
- Author(s)
  林孝彰、細野克博、片桐聡、倉田健太郎、溝渕圭、月花環、岩田岳、中野匡、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Resequencing of 83 causative genes in 1,204 Japanese patients with retinitis pigmentosa2018
- Author(s)
  Koyanagi Y, Akiyama M, Nishiguchi K, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda K
- Organizer
  The 11th Joint Meeting of Japan-China-Korea Ophthalmologists
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 日本人錐体桿体ジストロフィー家系から検出された新規変異と文献情報を併用した遺伝子型-表現型関連解析2018
- Author(s)
  Nazmul Haque、大坪正史、細野克博、倉田健太郎、大石健太郎、佐藤美保、蓑島伸生、堀田喜裕
- Organizer
  第25回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] FOXC1遺伝子を含む6p25領域に欠失が示唆された早発型発達緑内障の１例2018
- Author(s)
  新美佑介、川瀬和秀、山本哲也、山本崇裕、倉田健太郎、立花信貴、細野克博、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] BBS10遺伝子変異によるBardet-Biedl syndromeの1例2018
- Author(s)
  倉田健太郎、細野克博、彦谷明子、加藤明彦、才津浩智、蓑島伸生、緒方勤、堀田喜裕
- Organizer
  第43回日本小児眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] RDH12遺伝子変異による網膜色素変性症の１例2018
- Author(s)
  武田優、倉田健太郎、細野克博、堀田喜裕
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] GNAT1変異を認めた優性遺伝性先天停在性夜盲の1家系2018
- Author(s)
  林孝彰、細野克博、片桐聡、溝渕圭、倉田健太郎、中野匡、堀田喜裕
- Organizer
  第66回日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 本邦における網膜色素変性1,204例の次世代シークエンスから得られた遺伝的特徴2018
- Author(s)
  小栁俊人、秋山雅人、西口康二、桃沢幸秀、鎌谷洋一郎、高田定暁、稲井智栄、岩崎雄介、村上祐介、熊野美香子、面高宗子、阿部俊明、小森汐里、高丹、平形寿彬、倉田健太郎、細野克博、上野真治、堀田喜裕、村上晶、寺﨑浩子、和田裕子、中澤徹、池田康博、久保充明、園田康平
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Molecular Analysis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya　A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  日本人類遺伝学会第63回大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] FOXC1遺伝子を含む6p25領域に欠失が示唆された早発型発達緑内障の１例2018
- Author(s)
  新美佑介、川瀬和秀、山本哲也、山本崇裕、倉田健太郎、立花信貴、細野克博、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Kurata K, Miyamichi D, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  ARVO2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] FOXC1遺伝子を含む6p25領域に欠失が示唆された早発型発達緑内障の1例2018
- Author(s)
  新美佑介、川瀬和秀、山本哲也、山本崇裕、倉田健太郎、立花信貴、細野克博、堀田喜裕
- Organizer
  第122回日本眼科学会
- Data Source
  KAKENHI-PROJECT-15K20253
[Presentation] RP1遺伝子変異による常染色体劣性網膜色素変性症の1例2018
- Author(s)
  倉田健太郎，細野克博，堀田喜裕
- Organizer
  第437回東海眼科学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Molecular Analysis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya　A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  日本人類遺伝学会第63回大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] 日本人錐体桿体ジストロフィー家系から検出された新規変異と文献情報を併用した遺伝子型-表現型関連解析2018
- Author(s)
  Nazmul Haque、大坪正史、細野克博、倉田健太郎、大石健太郎、佐藤美保、蓑島伸生、堀田喜裕
- Organizer
  第25回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] CDHR1遺伝子に新規変異を認めた日本人錐体杆体ジストロフィー成人発症兄妹例2018
- Author(s)
  Nazmul Haque、倉田健太郎、細野克博、大坪正史、大石健太郎、佐藤美保、蓑島伸生、堀田喜裕
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Long-term clinical course of Japanese patients with retinitis pigmenosa caused by mutations in pre-mRNA splicing gene2018
- Author(s)
  Kurata K, Hosono K, Hotta Y
- Organizer
  ARVO2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Long-Term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness2018
- Author(s)
  Hideki Iida, Kentaro Kurata, Katsuhiro Hosono, Yoshihiro Hotta
- Organizer
  APAO
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Six cases with Leber congenital amaurosis associated with Coats-like vasculopathy2018
- Author(s)
  Ogawa H, Nishina S, Yokoi T, Tanaka S, Nakao S, Yoshida T, Fukami M, Hosono K, Hotta Y, Azuma N
- Organizer
  第57回日本網膜硝子体学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 日本人Leber先天盲の次世代シークエンサーによる遺伝子変異解析2018
- Author(s)
  細野克博、仁科幸子、林孝彰、倉田健太郎、横井匡、片桐聡、宮道大督、溝渕圭、佐藤美保、蓑島伸生、深見真紀、中野匡、近藤寛之、東範行、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 次世代シークエンサーを用いた日本人Leber先天盲の遺伝子変異解析2018
- Author(s)
  細野克博、東範行、堀田喜裕
- Organizer
  第66回日本臨床視覚電気生理学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 次世代シークエンサーを用いた日本人Leber先天盲の遺伝子変異解析2018
- Author(s)
  細野克博、東範行、堀田喜裕
- Organizer
  第66回日本臨床視覚電気生理学会
- Invited
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] 日本人Leber先天盲の次世代シークエンサーによる遺伝子変異解析2018
- Author(s)
  細野克博、仁科幸子、林孝彰、倉田健太郎、横井匡、片桐聡、宮道大督、溝渕圭、佐藤美保、蓑島伸生、深見真紀、中野匡、近藤寛之、東範行、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Kurata K, Miyamichi D, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  ARVO2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] GNAT1変異を認めた優性遺伝性先天停在性夜盲の1家系2018
- Author(s)
  林孝彰、細野克博、片桐聡、溝渕圭、倉田健太郎、中野匡、堀田喜裕
- Organizer
  第66回日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Long-Term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness2018
- Author(s)
  Hideki Iida, Kentaro Kurata, Katsuhiro Hosono, Yoshihiro Hotta
- Organizer
  APAO
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] RDH12遺伝子変異による網膜色素変性症の１例2018
- Author(s)
  武田優、倉田健太郎、細野克博、堀田喜裕
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Resequencing of 83 causative genes in 1,204 Japanese patients with retinitis pigmentosa2018
- Author(s)
  Koyanagi Y, Akiyama M, Nishiguchi K, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda K
- Organizer
  The 11th Joint Meeting of Japan-China-Korea Ophthalmologists
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] CDHR1遺伝子に新規変異を認めた日本人錐体杆体ジストロフィー成人発症兄妹例2018
- Author(s)
  Nazmul Haque、倉田健太郎、細野克博、大坪正史、大石健太郎、佐藤美保、蓑島伸生、堀田喜裕
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 本邦における網膜色素変性1,204例の次世代シークエンスから得られた遺伝的特徴2018
- Author(s)
  小栁俊人、秋山雅人、西口康二、桃沢幸秀、鎌谷洋一郎、高田定暁、稲井智栄、岩崎雄介、村上祐介、熊野美香子、面高宗子、阿部俊明、小森汐里、高丹、平形寿彬、倉田健太郎、細野克博、上野真治、堀田喜裕、村上晶、寺﨑浩子、和田裕子、中澤徹、池田康博、久保充明、園田康平
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Molecular Analysis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya　A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  日本人類遺伝学会第63回大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] RP1遺伝子変異による常染色体劣性網膜色素変性症の1例2018
- Author(s)
  倉田健太郎，細野克博，堀田喜裕
- Organizer
  第437回東海眼科学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] CACNA1F遺伝子変異を同定したレーバー先天盲の１例2018
- Author(s)
  仁科幸子、細野克博、横井匡、吉田朋世、深見真紀、堀田喜裕、東範行
- Organizer
  第57回日本網膜硝子体学会総会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] RDH12遺伝子変異による網膜色素変性症の1例2018
- Author(s)
  武田優、倉田健太郎、細野克博、堀田喜裕
- Organizer
  第71回静岡県眼科医会集談会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] レーバー先天盲の日本人患者に対する次世代シークエンサーを用いた遺伝子診断2017
- Author(s)
  細野克博、仁科幸子、倉田健太郎、宮道大督、横井匡、蓑島伸生、深見真紀、佐藤美保、近藤寛之、堀田喜裕
- Organizer
  第121回日本眼科学会
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] 次世代シークエンサーの登場により遺伝性網膜変性の変異解析は大きく進歩した2017
- Author(s)
  細野克博、蓑島伸生、堀田喜裕
- Organizer
  第121回日本眼科学会
- Invited
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Changes in Macular Structure and Retinal Function in Patients with Leber Congenital Amaurosis with RPGRIP1 Mutations2017
- Author(s)
  Daisuke Miyamichi, Sachiko Nishina, Katsuhiro Hosono, Tadashi Yokoi, Kentaro Kurata, Miho Sato, Shinsei Minoshima, Maki Fukami, Yoshihiro Hotta, Noriyuki Azuma
- Organizer
  ARVO
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Changes in Macular Structure and Retinal Function in Patients with Leber Congenital Amaurosis with RPGRIP1 Mutations2017
- Author(s)
  Daisuke Miyamichi, Sachiko Nishina, Katsuhiro Hosono, Tadashi Yokoi, Kentaro Kurata, Miho Sato, Shinsei Minoshima, Maki Fukami, Yoshihiro Hotta, Noriyuki Azuma
- Organizer
  ARVO
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Long-Term Clinical Course In A Patient With Complete Congenital Stationary Night Blindness2017
- Author(s)
  Kentaro Kurata, Katsuhiro Hosono, Yoshihiro Hotta
- Organizer
  ISGEDR
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Leber先天盲の1家系3症例のターゲットシークエンス解析2017
- Author(s)
  堀田喜裕、仁科幸子、細野克博、宮道大督、横井匡、倉田健太郎、彦谷明子、佐藤美保、深見真紀、蓑島伸生、東範行
- Organizer
  第24回日本遺伝子診療学会
- Data Source
  KAKENHI-PROJECT-17K11479
[Presentation] Leber先天盲の1家系3症例のターゲットシークエンス解析2017
- Author(s)
  堀田喜裕、仁科幸子、細野克博、宮道大督、横井匡、倉田健太郎、彦谷明子、佐藤美保、深見真紀、蓑島伸生、東範行
- Organizer
  第24回日本遺伝子診療学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 次世代シークエンサーを用いたレーバー先天盲の1家系3症例の遺伝子変異解析とその臨床像2017
- Author(s)
  細野克博、仁科幸子、宮道大督、横井匡、倉田健太郎、彦谷明子、蓑島伸生、佐藤美保、深見真紀、堀田喜裕、東範行
- Organizer
  第22回浜松医科学シンポジウム
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Long-Term Clinical Course In A Patient With Complete Congenital Stationary Night Blindness2017
- Author(s)
  Kentaro Kurata, Katsuhiro Hosono, Yoshihiro Hotta
- Organizer
  ISGEDR
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] Fine genomic analysis of deletion mutations in the locus control region of OPN1LW/OPN1MW genes in 2 Japanese families with blue cone monochromacy2016
- Author(s)
  Katsuhiro Hosono, Chunxia Wang, Shu Kachi, Kentaro Kurata, Kimiko Suto, Makoto Nakamura, Hiroko Terasaki, Yozo Miyake, Yoshihiro Hotta, Shinsei Minoshima
- Organizer
  XXII Biennial Meeting of the International Society for Eye Research
- Place of Presentation
  東京
- Year and Date
  2016-09-25
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] Fine genomic analysis of deletion mutations in the locus control region of OPN1LW/OPN1MW genes in 2 Japanese families with blue cone monochromacy2016
- Author(s)
  Katsuhiro Hosono, Chunxia Wang, Shu Kachi, Kentaro Kurata, Kimiko Suto, Makoto Nakamura, Hiroko Terasaki, Yozo Miyake, Yoshihiro Hotta, Shinsei Minoshima
- Organizer
  XXII Biennial Meeting of the International Society for Eye Research
- Place of Presentation
  東京
- Year and Date
  2016-09-25
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] A novel homozygous c.636delT mutation in SAG in a Japanese patient with retinal dystrophy2016
- Author(s)
  Kentaro Kurata, Nobutaka Tachibana, Takahiro Matsuoka, Katuhiro Hosono, Akiko Hikoya, Yuuki Ohashi, Miho Sato, Masayo Takahashi, Yoshihiro Hotta
- Organizer
  XVIIth International Symposium on Retinal Degeneration
- Place of Presentation
  京都
- Year and Date
  2016-09-19
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] A novel homozygous c.636delT mutation in SAG in a Japanese patient with retinal dystrophy2016
- Author(s)
  Kentaro Kurata, Nobutaka Tachibana, Takahiro Matsuoka, Katuhiro Hosono, Akiko Hikoya, Yuuki Ohashi, Miho Sato, Masayo Takahashi, Yoshihiro Hotta
- Organizer
  XVIIth International Symposium on Retinal Degeneration
- Place of Presentation
  京都
- Year and Date
  2016-09-19
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K20253
[Presentation] 長期間のフォローが可能であった完全型先天停在性夜盲の1例2016
- Author(s)
  倉田健太郎，細野克博，堀田喜裕
- Organizer
  第64回日本臨床視覚電気生理学会
- Place of Presentation
  三重
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] 次世代シークエンサーを用いたレーバー先天盲の1家系3症例の遺伝子変異解析2016
- Author(s)
  細野克博、仁科幸子、宮道大督、横井匡、彦谷明子、佐藤美保、蓑島伸生、深見真紀、東範行、堀田喜裕
- Organizer
  第41回日本小児眼科学会
- Place of Presentation
  横浜
- Year and Date
  2016-06-24
- Data Source
  KAKENHI-PROJECT-16K11284
[Presentation] 次世代シークエンサーを用いたレーバー先天盲の1家系3症例の遺伝子変異解析2016
- Author(s)
  細野克博、仁科幸子、宮道大督、横井匡、彦谷明子、佐藤美保、蓑島伸生、深見真紀、東範行、堀田喜裕
- Organizer
  第41回日本小児眼科学会
- Place of Presentation
  横浜
- Year and Date
  2016-06-24
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] RPGRIP1遺伝子異常によるレーバー先天盲の1家系3症例の臨床像2016
- Author(s)
  宮道大督、仁科幸子、細野克博、横井匡、倉田健太郎、彦谷明子、蓑島伸生、佐藤美保、深見真紀、堀田喜裕、東範行
- Organizer
  第55回日本網膜硝子体学会総会
- Place of Presentation
  東京
- Year and Date
  2016-12-02
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] 全エキソーム解析からHPS6遺伝子異常を同定できた眼白日証の姉妹例2015
- Author(s)
  宮道大督、朝比奈美輝、中島隼也、佐藤美保、細野克博、野村隆仁、根岸貴志、今川英里、三宅紀子、堀田喜裕、緒方勤、松本直道
- Organizer
  第69回日本臨床眼科学会
- Place of Presentation
  名古屋
- Year and Date
  2015-10-22
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] SAG遺伝子の636delT をホモ接合体で持つ網膜ジストロフィの１例2015
- Author(s)
  松岡貴大、細野克博、立花信貴、彦谷明子、荒井優気、佐藤美保、高橋　政代、堀田喜裕
- Organizer
  第69回日本臨床眼科学会
- Place of Presentation
  名古屋
- Year and Date
  2015-10-22
- Data Source
  KAKENHI-PROJECT-15K20253
[Presentation] レーバー先天盲の（二卵性）双生児の次世代シークエンサーを用いた遺伝子変異解析2015
- Author(s)
  細野克博、佐藤美保、原田祐子、倉田健太郎、彦谷明子、蓑島伸生、堀田喜裕
- Organizer
  第71回日本弱視斜視学会総会/第40回日本小児眼科学会総会
- Place of Presentation
  神戸
- Year and Date
  2015-07-03
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] 常染色体劣性網膜色素変性患者におけるEYS遺伝子各エキソンのコピー数変異解析2015
- Author(s)
  細野克博、蓑島伸生、彦谷明子、佐藤美保、堀田喜裕
- Organizer
  第119回日本眼科学会総会
- Place of Presentation
  札幌
- Year and Date
  2015-04-16
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] SAG遺伝子の636delT をホモ接合体で持つ網膜ジストロフィの１例2015
- Author(s)
  松岡貴大、細野克博、立花信貴、彦谷明子、荒井優気、佐藤美保、高橋　政代、堀田喜裕
- Organizer
  第69回日本臨床眼科学会
- Place of Presentation
  名古屋
- Year and Date
  2015-10-22
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] Visual Outcomes of Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations2015
- Author(s)
  Suto K, Hosono K, Nagase Y, Nakanishi H, Mizuta K, Minoshima S, Hotta Y
- Organizer
  ARVO 2015
- Place of Presentation
  Denver
- Year and Date
  2015-05-03
- Invited
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] EYS(Eye sShut Homolog)遺伝子の変異解析2012
- Author(s)
  細野　克博
- Organizer
  第116回日本眼科学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] ラット網膜光障害感受性の遺伝解析:加齢黄斑変性の易罹患性の原因遺伝子の同定に向けて2012
- Author(s)
  大石健太郎、細野克博、尾花明、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第23回眼科酸化ストレス研究会
- Place of Presentation
  神戸
- Year and Date
  2012-07-28
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] An Adenine Insertion between Nucleotide Positions 4957 and 4958 in the EYS Gene Is a Possible Major Cause of arRP in the Japanese Population2012
- Author(s)
  Katsuhiro Hosono, Chie Ishigami, Masayo Takahashi, Yasuhiko Hirami, Shinji Ueno, Noriyuki Azuma, Hiroko Terasaki, Mineo Kondo, Shinsei Minoshima, YoshihiroHotta
- Organizer
  ARVO
- Place of Presentation
  Fort Lauderdale
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] わが国の網膜色素変性患者の遺伝子解析2012
- Author(s)
  細野克博
- Organizer
  第66回日本臨床眼科学会
- Place of Presentation
  京都
- Invited
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] ラット網膜光障害感受性の責任遺伝子領域の限局化2012
- Author(s)
  大石健太郎、細野克博、尾花明、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第116回日本眼科学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] 本邦網膜色素変性患者のEYS(Eyes ShutHomolog)遺伝子の変異解析2012
- Author(s)
  細野克博、石上智愛、高橋政代、平見恭彦、上野真治、山本修一、東範行、寺崎浩子、佐藤美保、近藤峰生、蓑島伸生、堀田喜裕
- Organizer
  第116回日本眼科学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] Establishing a mouse cell line from a brain tumor developed with SV40 Large T antigen driven by a photoreceptor-specific gene promoter.2011
- Author(s)
  Hosono K, Ohishi K, Yamamoto S, Nakanishi H, Yamaguchi Y, Kudoh J, Shimizu N, Hotta Y, Minoshima S.
- Organizer
  ARVO
- Place of Presentation
  Fort Lauderdale
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] Genetic Analysis of Rat Strain-dependent Difference in the Susceptibility to Retinal Photic Injury and Mapping Possible Susceptibility Loci2011
- Author(s)
  Ohishi, K., Hosono, K., Obana, A., Hotta, Y., Hiramitsu, T., Minoshima, T
- Organizer
  4th International Conference on Health and Longevity Sciences (ICHALS)
- Place of Presentation
  Shizuoka
- Year and Date
  2011-10-21
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] Clinical features of a Japanese patient with Bothnia dystrophy.2011
- Author(s)
  Nojima K, Hosono K, Zhao Y, Toshiba T, Asai T, Kato M, Minoshima S, Hotta Y.
- Organizer
  ARVO
- Place of Presentation
  Fort Lauderdale
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] 本邦症例における網膜色素変性原因遺伝子EYSの寄与と原因変異解析2011
- Author(s)
  細野克博、中西啓、彦谷明子、藤田太一、須藤希実子、趙洋、佐藤美保、蓑島伸生、堀田喜裕
- Organizer
  第5回浜松医科学シンポジウム(招待講演)
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] ラット網膜光障害の行動学的解析法の妥当性の検証:病理組織観察結果との相関解析2011
- Author(s)
  大石健太郎、細野克博、尾花明、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第115回日本眼科学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] 視細胞特異的プロモーターとSV40LargeT抗原によるマウス培養細胞株の樹立2011
- Author(s)
  細野克博、大石健太郎、山口良考、工藤純、清水信義、堀田喜裕、蓑島伸生
- Organizer
  第115回日本眼科学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23791975
[Presentation] 視細胞特異的プロモーターとSV40LargeT抗原によるマウス培養細胞株の樹立2011
- Author(s)
  細野克博
- Organizer
  第115回日本眼科学会総会
- Place of Presentation
  東京
- Year and Date
  2011-05-13
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] ラット網膜光障害感受性の責任遺伝子探索:連続戻し交配による領域の限局化2010
- Author(s)
  大石健太郎、細野克博、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第33回日本分子生物学会年会
- Place of Presentation
  神戸
- Year and Date
  2010-12-10
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] 緑内障原因遺伝子オプチニュリンによるタンパク品質管理系の制御の可能性の検討(The possibility for protein maintenance by glaucoma-causative gene OPTN)2010
- Author(s)
  大坪正史、細野克博、高潔、Mary K. Wirtz、堀田喜裕、蓑島伸生
- Organizer
  第33回日本分子生物学会・第83回日本生化学会合同大会(BMB2010)
- Place of Presentation
  神戸ポートアイランド(兵庫県)
- Year and Date
  2010-12-10
- Data Source
  KAKENHI-PROJECT-21592223
[Presentation] マイクロサテライト多型解析によるラット網膜光障害感受性の遺伝学的解析2010
- Author(s)
  大石健太郎、細野克博、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第21回眼科酸化ストレス研究会
- Place of Presentation
  東京
- Year and Date
  2010-07-31
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] ラット網膜光障害感受性の遺伝学的解析:加齢黄斑変性の発症機序解明に向けて.2010
- Author(s)
  大石健太郎、細野克博、堀田喜裕、平光忠久、蓑島伸生
- Organizer
  第114回日本眼科学会総会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-22591939
[Presentation] Isolation of proteins interacting with optineurin, a glaucoma-causative gene product(緑内障原因遺伝子産物オプチニュリンと相互作用するタンパクの同定)2009
- Author(s)
  大坪正史、Thanseem Ismail、細野克博、堀田喜裕、蓑島伸生
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-12-12
- Data Source
  KAKENHI-PROJECT-21592223
[Presentation] Isolation of proteins interacting with optineurin, a product protein of glaucoma-causative gene2009
- Author(s)
  大坪正史(Masafumi Ohtsubo), Thanseem Ismail,細野克博(Katsuhiro Hosono), Ryo Asaoka, Chunxia Wang, Hiroshi Nakanishi, Hiroyuki Mineta, Yoshihiro Hotta, Shinsei Minoshima
- Organizer
  第9回慶北-浜松合同医学シンポジウム
- Place of Presentation
  慶北医科大学(中国)
- Year and Date
  2009-09-25
- Data Source
  KAKENHI-PROJECT-21592223
[Presentation] The first USH2A mutation analysis of Japanese Autosomal Recessive Retinitis Pigmentosa patients: A totally different mutation profile with the lack of frequent mutations found in Caucasian patients
- Author(s)
  Katsuhiro Hosono, Yang Zhao, Kimiko Suto, Chie Ishigami, Yuuki Arai, Akiko Hikoya, Yasuhiko Hirami, Masafumi Ohtsubo, Shinji Ueno, Hiroko Terasaki, Miho Sato, Hiroshi Nakanishi, Shiori Endo, Kunihiro Mizuta, Hiroyuki Mineta, Mineo Kondo, Masayo Takahashi, Shinsei Minoshima, and Yoshihiro Hotta
- Organizer
  XVIth International Symposium on Retinal Degeneration
- Place of Presentation
  California
- Year and Date
  2014-07-13 – 2014-07-18
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] 常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析
- Author(s)
  堀田喜裕、細野克博、趙洋、須藤希実子、石上智愛、荒井優気、彦谷明子、平見恭彦、大坪正史、上野真治、寺﨑浩子、佐藤美保、中西啓、遠藤志織、水田邦博、峯田周幸、近藤峰生、高橋政代、蓑島伸生
- Organizer
  日本人類遺伝学会第59回大会・日本遺伝子診療学会第21回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-19 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] わが国の網膜色素変性患者の遺伝子解析の現状と近未来の可能性
- Author(s)
  細野克博
- Organizer
  第61回日本臨床視覚電気生理学会
- Place of Presentation
  大阪
- Year and Date
  2013-10-04 – 2013-10-05
- Invited
- Data Source
  KAKENHI-PROJECT-25861626
[Presentation] Molecular Genetics of Retinitis Pigmentosa in East Asian Populations
- Author(s)
  Katsuhiro Hosono
- Organizer
  WOC2014
- Place of Presentation
  Tokyo
- Year and Date
  2014-04-02 – 2014-04-06
- Invited
- Data Source
  KAKENHI-PROJECT-25861626
[Presentation] Mutation Analysis of the USH2A Gene in Japanese Patients with Autosomal Recessive Retinitis Pigmentosa
- Author(s)
  Katsuhiro Hosono, Yang Zhao, Chie Ishigami, Shinji Ueno, Hiroshi Nakanishi, Hiroko Terasaki, Mineo Kondo, Masayo Takahashi, Shinsei Minoshima, and Yoshihiro Hotta
- Organizer
  ARVO2014
- Place of Presentation
  Orland
- Year and Date
  2014-05-05 – 2014-05-08
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] 常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析
- Author(s)
  細野克博、石上智愛、須藤希実子、荒井優気、趙洋、水田邦博、峯田周幸、上野真治、寺﨑浩子、近藤峰生、高橋政代、蓑島伸生、堀田喜裕
- Organizer
  第118回日本眼科学会総会
- Place of Presentation
  東京
- Year and Date
  2014-04-02 – 2014-04-06
- Data Source
  KAKENHI-PROJECT-25861626
[Presentation] A twin with Leber congenital amaurosis possibly caused by the GUCY2D gene mutation
- Author(s)
  Yuko Harada, Katsuhiro Hosono, , Akiko Hikoya, Shinsei Minoshima, Miho Sato, Yoshihiro Hotta
- Organizer
  AAPOS-JAPO-JASA Joint Meeting
- Place of Presentation
  京都
- Year and Date
  2014-11-30 – 2014-12-01
- Data Source
  KAKENHI-PROJECT-26462659
[Presentation] The first USH2A mutation analysis of Japanese Autosomal Recessive Retinitis Pigmentosa patients: A totally different mutation profile with the lack of frequent mutations found in Caucasian patients
- Author(s)
  Katsuhiro Hosono, Yang Zhao, Kimiko Suto, Chie Ishigami, Yuuki Arai, Akiko Hikoya, Yasuhiko Hirami, Masafumi Ohtsubo, Shinji Ueno, Hiroko Terasaki, Miho Sato, Hiroshi Nakanishi, Shiori Endo, Kunihiro Mizuta, Hiroyuki Mineta, Mineo Kondo, Masayo Takahashi, Shinsei Minoshima, and Yoshihiro Hotta
- Organizer
  XVIth International Symposium on Retinal Degeneration
- Place of Presentation
  California
- Year and Date
  2014-07-13 – 2014-07-18
- Data Source
  KAKENHI-PROJECT-25861626
[Presentation] Mutation Analysis of the USH2A Gene in Japanese Patients with Autosomal Recessive Retinitis Pigmentosa
- Author(s)
  Katsuhiro Hosono, Yang Zhao, Chie Ishigami, Shinji Ueno, Hiroshi Nakanishi, Hiroko Terasaki, Mineo Kondo, Masayo Takahashi, Shinsei Minoshima, and Yoshihiro Hotta
- Organizer
  ARVO2014
- Place of Presentation
  Orland
- Year and Date
  2014-05-04 – 2014-05-08
- Data Source
  KAKENHI-PROJECT-25861626
[Presentation] 網膜色素変性と関連疾患におけるEYS遺伝子の2種類の変異の分子遺伝学的解析
- Author(s)
  細野克博、石上智愛、高橋政代、朴東浩、上野真治、萩原章、山本修一、佐藤美保、寺﨑浩子、金仁澤、東範行、近藤峰生、蓑島伸生、堀田喜裕
- Organizer
  第117回日本眼科学会総会
- Place of Presentation
  東京
- Year and Date
  2013-04-04 – 2013-04-07
- Data Source
  KAKENHI-PROJECT-25861626

1. HOTTA Yoshihiro (90173608)

# of Collaborated Projects: 8 results

# of Collaborated Products: 117 results
2. MINOSHIMA Shinsei (90181966)

# of Collaborated Projects: 3 results

# of Collaborated Products: 34 results
3. TAKAHASHI Masayo (80252443)

# of Collaborated Projects: 3 results

# of Collaborated Products: 13 results
4. YAMAMOTO Shuichi (20230550)

# of Collaborated Projects: 3 results

# of Collaborated Products: 3 results
5. AZUMA Noriyuki (10159395)

# of Collaborated Projects: 3 results

# of Collaborated Products: 23 results
6. OHISHI Kentarou (80345826)

# of Collaborated Projects: 2 results

# of Collaborated Products: 7 results
7. KONDO Mineo (80303642)

# of Collaborated Projects: 2 results

# of Collaborated Products: 9 results
8. 佐藤美保 (50252242)

# of Collaborated Projects: 2 results

# of Collaborated Products: 17 results
9. 近藤寛之 (40268991)

# of Collaborated Projects: 2 results

# of Collaborated Products: 7 results
10. 仁科幸子 (40237954)

# of Collaborated Projects: 2 results

# of Collaborated Products: 10 results
11. KURATA KENTARO

# of Collaborated Projects: 2 results

# of Collaborated Products: 8 results
12. OHTSUBO Masafumi (10327653)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
13. OBANA Akira (40194625)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
14. Hikoya Akiko (80464113)

# of Collaborated Projects: 1 results

# of Collaborated Products: 10 results
15. Tachibana Nobutaka (80647397)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
16. 寺崎浩子 (40207478)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
17. 横井匡 (80514025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
18. SAITSU hirotomo

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
19. FUKAMI maki

# of Collaborated Projects: 1 results

# of Collaborated Products: 8 results
20. NAKANO tadashi

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
21. HAYASHI takaaki

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
22. UENO Shinji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. NAKANISHI Hiroshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 扇田久和

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 中澤満

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 阿部俊明

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 松本直通

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 三宅紀子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

HOSONO Katsuhiro 細野 克博

Research Projects

Research Products

Co-Researchers

小児期に発症する網膜ジストロフィの分子遺伝学的基盤の構築に関する研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Construction of a comprehensive regional medical system and development of diagnostic method for rare and undiagnosed eye disease patients in Japan

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Development of the simple diagnostic method for the patients with chronic progressive external ophthalmoplegia and the construction of the database

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Development of diagnosis program and clinical application with congenital visual impairment patients for tailor-made medicinePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

3D-analysis using biometric technology and the database construction for elucidating the pathological mechanism with congenital cataract

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Development of genetic diagnosis for Japanese Retinitis Pigmentosa patients using next generation sequencer

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The development and clinical application of EYS gene mutation diagnosis in Japanese Retinitis pigmentosa patientsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Genotype-phenotype analysis and prevalence study of disease-causing mutations in the EYS gene among Japanese patients with retinitis pigmentosaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of candidate genes responsible for an increased susceptibility of age-related macular degeneration using an animal model and its application to gene diagnosis.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular analysis of glaucoma-developing mechanism : Investigation of an OPTN-interacting protein

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] あたらしい眼科2019

Author(s)

Total Pages

Publisher

Data Source

[Book] RETINA Medicine ゲノムと網膜関連疾患の関与を探る 網膜色素変性2014

Author(s)

Total Pages

Publisher

Data Source

[Book] RETINA Medicine ゲノムと網膜関連疾患の関与を探る 網膜色素変性2014

Author(s)

Total Pages

Publisher

Data Source

[Book] 眼科 眼と遺伝 2.網膜色素変性2014

HOSONO Katsuhiro 細野克博

[Book] RETINA Medicine　ゲノムと網膜関連疾患の関与を探る　網膜色素変性2014

[Book] RETINA Medicine　ゲノムと網膜関連疾患の関与を探る　網膜色素変性2014

[Book] 眼科　眼と遺伝　2.網膜色素変性2014

[Journal Article] 特集第72回日本臨床眼科学会講演集[1] 原著 RDH12遺伝子変異による網膜色素変性症の1例2019