检索结果 - Takeshi Iwata

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  1. 1
    A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos

    A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos 由 Takeshi Iwata

    出版 2000
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  2. 2
    Suppression of Drusen Formation by Compstatin, a Peptide Inhibitor of Complement C3 activation, on Cynomolgus Monkey with Early-Onset Macular Degeneration

    Suppression of Drusen Formation by Compstatin, a Peptide Inhibitor of Complement C3 activation, on Cynomolgus Monkey with Early-Onset Macular Degeneration 由 Zai‐Long Chi, Tsunehiko Yoshida, John D. Lambris, Takeshi Iwata

    出版 2010
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  3. 3
    Modeling Retinal Degeneration Using Patient-Specific Induced Pluripotent Stem Cells

    Modeling Retinal Degeneration Using Patient-Specific Induced Pluripotent Stem Cells 由 Zi‐Bing Jin, Satoshi Okamoto, Fumitaka Osakada, Kohei Homma, Juthaporn Assawachananont, Yasuhiko Hirami, Takeshi Iwata, Masayo Takahashi

    出版 2011
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  4. 4
    Processing of Optineurin in Neuronal Cells

    Processing of Optineurin in Neuronal Cells 由 Xiang Shen, Hongyu Ying, Ye Qiu, Jeong‐Seok Park, Rajalekshmy Shyam, Zai‐Long Chi, Takeshi Iwata, Jianbo Yue

    出版 2010
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  5. 5
    VAV2 and VAV3 as Candidate Disease Genes for Spontaneous Glaucoma in Mice and Humans

    VAV2 and VAV3 as Candidate Disease Genes for Spontaneous Glaucoma in Mice and Humans 由 Keiko Fujikawa, Takeshi Iwata, Kaoru Inoue, Masakazu Akahori, Hanako Kadotani, Masahiro Fukaya, Masahiko Watanabe, Qing Chang, Edward M. Barnett, Wojciech Swat

    出版 2010
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  6. 6
    Enhanced optineurin E50K–TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma

    Enhanced optineurin E50K–TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma 由 Yuriko Minegishi, Daisuke Iejima, Hiroaki Kobayashi, Zai-Long Chi, Kazuhide Kawase, Tetsuya Yamamoto, Tomohisa Seki, Shinsuke Yuasa, Keiichi Fukuda, Takeshi Iwata

    出版 2013
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  7. 7
    Mitochondrial pathogenic mechanism and degradation in optineurin E50K mutation-mediated retinal ganglion cell degeneration

    Mitochondrial pathogenic mechanism and degradation in optineurin E50K mutation-mediated retinal ganglion cell degeneration 由 Myoung Sup Shim, Yuji Takihara, Keunyoung Kim, Takeshi Iwata, Jianbo Yue, Masaru Inatani, Robert N. Weinreb, Guy Perkins, Won‐Kyu Ju

    出版 2016
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  8. 8
    Correction: Corrigendum: Mitochondrial pathogenic mechanism and degradation in optineurin E50K mutation-mediated retinal ganglion cell degeneration

    Correction: Corrigendum: Mitochondrial pathogenic mechanism and degradation in optineurin E50K mutation-mediated retinal ganglion cell degeneration 由 Myoung Sup Shim, Yuji Takihara, Keunyoung Kim, Takeshi Iwata, Jianbo Yue, Masaru Inatani, Robert N. Weinreb, Guy Perkins, Won‐Kyu Ju

    出版 2017
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  9. 9
    Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques

    Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques 由 Yu Fujinami‐Yokokawa, Nikolas Pontikos, Lizhu Yang, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Hiroaki Miyata, Kaoru Fujinami, on behalf of Japan Eye Genetics Consortium

    出版 2019
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  10. 10
    Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy

    Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy 由 Kamron Khan, Melissa Kasilian, Omar A. Mahroo, Preena Tanna, Angelos Kalitzeos, Anthony G. Robson, Kazushige Tsunoda, Takeshi Iwata, Anthony T. Moore, Kaoru Fujinami, Michel Michaelides

    出版 2018
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  11. 11
    Dominant Mutations in RP1L1 Are Responsible for Occult Macular Dystrophy

    Dominant Mutations in RP1L1 Are Responsible for Occult Macular Dystrophy 由 Masakazu Akahori, Kazushige Tsunoda, Yozo Miyake, Y. Fukuda, Hiroyuki Ishiura, Shoji Tsuji, Tomoaki Usui, Tetsuhisa Hatase, Makoto Nakamura, Hisao Ohde, Takeshi Itabashi, H. Okamoto, Yuichiro Takada, Takeshi Iwata

    出版 2010
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  12. 12
    CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability

    CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability 由 Yuriko Minegishi, Xunlun Sheng, Kazutoshi Yoshitake, Yuri V. Sergeev, Daisuke Iejima, Yoshio Shibagaki, Norikazu Monma, Kazuho Ikeo, Masaaki Furuno, Wenjun Zhuang, Yani Liu, Weining Rong, Seisuke Hattori, Takeshi Iwata

    出版 2016
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  13. 13
    Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population

    Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population 由 Asako Goto, Masakazu Akahori, H. Okamoto, M. Minami, N. Terauchi, Y. Haruhata, Minoru Obazawa, Toru Noda, Miki Honda, Atsushi Mizota, Minoru Tanaka, Takaaki Hayashi, Masaki Tanito, Naoko Ogata, Takeshi Iwata

    出版 2009
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  14. 14
    Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice

    Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice 由 Zai‐Long Chi, Masakazu Akahori, Minoru Obazawa, M. Minami, Toru Noda, Naoki Nakaya, Stanislav I. Tomarev, Kazuhide Kawase, Tetsuya Yamamoto, Setsuko Noda, Masaki Sasaoka, Atsushi Shimazaki, Yuichiro Takada, Takeshi Iwata

    出版 2010
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  15. 15
    Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa

    Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa 由 Satoshi Katagiri, Masakazu Akahori, Yuri V. Sergeev, Kazutoshi Yoshitake, Kazuho Ikeo, Masaaki Furuno, Takaaki Hayashi, Mineo Kondo, Shinji Ueno, Kazushige Tsunoda, Kei Shinoda, Kazuki Kuniyoshi, Yoshinori Tsurusaki, Naomichi Matsumoto, Hiroshi Tsuneoka, Takeshi Iwata

    出版 2014
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  16. 16
    Ablation of Htra1 leads to sub-RPE deposits and photoreceptor abnormalities

    Ablation of Htra1 leads to sub-RPE deposits and photoreceptor abnormalities 由 Pooja Biswas, DaNae R. Woodard, TJ Hollingsworth, Naheed W. Khan, Danielle Lazaro, Anne Marie Berry, Manisha Dagar, Yang Pan, Donita Garland, Peter X. Shaw, Chio Oka, Takeshi Iwata, Monica M. Jablonski, Radha Ayyagari

    出版 2025
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  17. 17
    The Association Between Complement Component 2/Complement Factor B Polymorphisms and Age-related Macular Degeneration: A HuGE Review and Meta-Analysis

    The Association Between Complement Component 2/Complement Factor B Polymorphisms and Age-related Macular Degeneration: A HuGE Review and Meta-Analysis 由 Ammarin Thakkinstian, Mark McEvoy, Usha Chakravarthy, Subhabrata Chakrabarti, Gareth J. McKay, Euijung Ryu, Giuliana Silvestri, Inderjeet Kaur, Peter J. Francis, Takeshi Iwata, Masakazu Akahori, Astrid Arning, Albert O. Edwards, Johanna M. Seddon, John Attia

    出版 2012
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    Revisão
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  18. 18
    Biological Magnetic Resonance Data Bank

    Biological Magnetic Resonance Data Bank 由 Jeffrey C. Hoch, Kumaran Baskaran, Harrison Burr, John Chin, Hamid R. Eghbalnia, Toshimichi Fujiwara, Michael R. Gryk, Takeshi Iwata, Chojiro Kojima, Genji Kurisu, Dmitri Maziuk, Yohei Miyanoiri, Jonathan R. Wedell, Colin W. Wilburn, Hongyang Yao, Masashi Yokochi

    出版 2022
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  19. 19
    Novel<i>RP1L1</i>Variants and Genotype–Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy

    Novel<i>RP1L1</i>Variants and Genotype–Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy 由 Kaoru Fujinami, Shuhei Kameya, Sachiko Kikuchi, Shinji Ueno, Mineo Kondo, Takaaki Hayashi, Kei Shinoda, Shigeki Machida, Kazuki Kuniyoshi, Yuichi Kawamura, Masakazu Akahori, Kazutoshi Yoshitake, Satoshi Katagiri, Ayami Nakanishi, Hiroyuki Sakuramoto, Yoko Ozawa, Kazuo Tsubota, Kunihiko Yamaki, Atsushi Mizota, Hiroko Terasaki, Yozo Miyake, Takeshi Iwata, Kazushige Tsunoda

    出版 2016
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  20. 20
    Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing

    Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing 由 Akiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kaoru Fujinami, Yozo Miyake, Kazuki Kuniyoshi, Takaaki Hayashi, Kei Mizobuchi, Shinji Ueno, Hiroko Terasaki, Taro Kominami, Nobuhisa Nao‐i, Go Mawatari, Atsushi Mizota, Kei Shinoda, Mineo Kondo, Kumiko Kato, Tetsuju Sekiryu, Makoto Nakamura, Sentaro Kusuhara, Hiroyuki Yamamoto, Shuji Yamamoto, Kiyofumi Mochizuki, Hiroyuki Kondo, Itsuka Matsushita, Shuhei Kameya, Takeo Fukuchi, Tetsuhisa Hatase, Masayuki Horiguchi, Yoshiaki Shimada, Atsuhiro Tanikawa, Shuichi Yamamoto, Gen Miura, Nana Ito, Akira Murakami, Takuro Fujimaki, Yoshihiro Hotta, Koji Tanaka, Takeshi Iwata

    出版 2022
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