Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ryutaro Akiba"'
Autor:
Take Matsuyama, Hung-Ya Tu, Jianan Sun, Tomoyo Hashiguchi, Ryutaro Akiba, Junki Sho, Momo Fujii, Akishi Onishi, Masayo Takahashi, Michiko Mandai
Publikováno v:
iScience, Vol 24, Iss 8, Pp 102866- (2021)
Summary: ESC/iPSC-retinal sheet transplantation, which supplies photoreceptors as well as other retinal cells, has been shown to be able to restore visual function in mice with end-stage retinal degeneration. Here, by introducing a novel type of gene
Externí odkaz:
https://doaj.org/article/a66400a246a743b58dabb3fdb6bb53fd
Autor:
Ryutaro Akiba, Take Matsuyama, Hung-Ya Tu, Tomoyo Hashiguchi, Junki Sho, Shuichi Yamamoto, Masayo Takahashi, Michiko Mandai
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Quantitative and qualitative evaluation of synapses is crucial to understand neural connectivity. This is particularly relevant now, in view of the recent advances in regenerative biology and medicine. There is an urgent need to evaluate synapses to
Externí odkaz:
https://doaj.org/article/6011b284d0a44b4e9670446ab4da9302
Autor:
Ryutaro Akiba, Hirotaka Yokouchi, Masahiro Mori, Toshiyuki Oshitari, Takayuki Baba, Setsu Sawai, Satoshi Kuwabara, Shuichi Yamamoto
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0167473 (2016)
Previous studies of neuromyelitis optica spectrum disorder (NMOSD) using spectral domain optical coherence tomography (SD-OCT) showed that the outer nuclear layer (ONL) in eyes without a history of optic neuritis (ON) was thinner than that of healthy
Externí odkaz:
https://doaj.org/article/acc96a2a0e274c2fa9552a9b560a2834
Cellular and circuit remodeling of the primate foveal midget pathway after acute photoreceptor loss.
Autor:
Ryutaro Akiba, Boniec, Shane Lind, Knecht, Sharm, Hirofumi Uyama, Hung-Ya Tu, Takayuki Baba, Masayo Takahashi, Michiko Mandai, Wong, Rachel O.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 9/10/2024, Vol. 121 Issue 37, p1-10, 20p
Publikováno v:
Japanese Journal of Ophthalmology. 67:119-128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85a9b5f78c64881535430ee6be66643e
https://doi.org/10.1007/s10384-022-00974-5
https://doi.org/10.1007/s10384-022-00974-5
Autor:
Masayo Takahashi, Junki Sho, Jianan Sun, Take Matsuyama, Tomoyo Hashiguchi, Akishi Onishi, Momo Fujii, Ryutaro Akiba, Michiko Mandai, Hung-Ya Tu
Publikováno v:
iScience
iScience, Vol 24, Iss 8, Pp 102866-(2021)
iScience, Vol 24, Iss 8, Pp 102866-(2021)
Summary ESC/iPSC-retinal sheet transplantation, which supplies photoreceptors as well as other retinal cells, has been shown to be able to restore visual function in mice with end-stage retinal degeneration. Here, by introducing a novel type of genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18368e9880a633ef18cbe64324858f14
https://pubmed.ncbi.nlm.nih.gov/34409267
https://pubmed.ncbi.nlm.nih.gov/34409267
Autor:
Take Matsuyama, Hung-Ya Tu, Michiko Mandai, Momo Fujii, Masayo Takahashi, Junki Sho, Tomoyo Hashiguchi, Jianan Sun, Ryutaro Akiba, Akishi Onishi
ES/iPS-retinal sheet transplantation, which supplies photoreceptors as well as other retinal cells, has been shown able to restore visual function in mice with end-stage retinal degeneration. Here, by introducing a novel type of genetically engineere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9ca6634bea679ee4c0b706aaebbd4bd
https://doi.org/10.1101/2020.12.23.424068
https://doi.org/10.1101/2020.12.23.424068
Publikováno v:
Nihon yakurigaku zasshi. Folia pharmacologica Japonica. 155(2)
Retinitis pigmentosa (RP) is a group of hereditary diseases that involve loss of photoreceptors. There has been no established treatment for RP, and it is now the 2nd leading cause of blindness in Japan. Previous clinical researches using human fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::571e116c7ce6a2a7b674a69a9cfbc700
https://pubmed.ncbi.nlm.nih.gov/32115485
https://pubmed.ncbi.nlm.nih.gov/32115485
Autor:
Masayo Takahashi, Ryoji Fujiki, Yasuo Kurimoto, Seiji Takagi, Akiko Yoshida, Osamu Ohara, Akira Inaba, Kanako Kawai, Ryutaro Akiba, Akiko Maeda, Yuki Arai, Yasuhiko Hirami
Publikováno v:
Japanese Journal of Ophthalmology. 62:451-457
Retinitis Pigmentosa (RP) is the most common form of inherited retinal dystrophy caused by different genetic variants. More than 60 causative genes have been identified to date. The establishment of cost-effective molecular diagnostic tests with high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0a9df2a90b092bab224ab6b5f59b11
https://doi.org/10.1007/s10384-018-0601-x
https://doi.org/10.1007/s10384-018-0601-x
Publikováno v:
Neuro-Ophthalmology. 39:30-33
Neuromyelitis optica spectrum disorder (NMO-SD) is an autoimmune inflammatory disorder associated with the anti-aquaporin-4 (AQP4) antibody. Over 90% of NMO-SD patients have poor prognosis, and pregnancy is a disease-worsening factor. The authors rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41d5b47e8e5bfc4720fdbcb16e3146c7
https://doi.org/10.3109/01658107.2014.971188
https://doi.org/10.3109/01658107.2014.971188