Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Masahiro, Kono"'
Autor:
Sergei Balashov, Ella Imasheva, Saurav Misra, Masahiro Kono, Suyi Liu, Jie Liang, Govindjee Govindjee, Thomas G. Ebrey
Publikováno v:
LS- International Journal of Life Sciences. 12:1-14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1de11a4f20f81109b0aa9ec835d428fd
https://doi.org/10.5958/2319-1198.2023.00001.5
https://doi.org/10.5958/2319-1198.2023.00001.5
Autor:
Masahiro Kono, Keiichi Okai, Akiyoshi Masaki, Tomoya Kogirima, Tetsuya Sato, Junichi Kazawa, Daisaku Masaki
Publikováno v:
AEROSPACE TECHNOLOGY JAPAN, THE JAPAN SOCIETY FOR AERONAUTICAL AND SPACE SCIENCES. 22:11-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcc10b366bd9e85f1829b860a627f9c8
https://doi.org/10.2322/astj.22.11
https://doi.org/10.2322/astj.22.11
Autor:
Akiyoshi Masaki, Tetsuya Sato, Keiichi Okai, Daisaku Masaki, Masahiro Kono, Junichi Kazawa, Seiya Mizutori
Publikováno v:
AIAA Propulsion and Energy 2021 Forum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43920a64bdcb5e66e0f0376dc321b73e
https://doi.org/10.2514/6.2021-3552
https://doi.org/10.2514/6.2021-3552
Publikováno v:
Photochem Photobiol Sci
Retinal, the vitamin A aldehyde, is a potent photosensitizer that plays a major role in light-induced damage to vertebrate photoreceptors. 11-Cis retinal is the light-sensitive chromophore of rhodopsin, the photopigment of vertebrate rod photorecepto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b4dcc05e6654688d3c244d814068adf
https://europepmc.org/articles/PMC7559207/
https://europepmc.org/articles/PMC7559207/
Autor:
John E. Oatis, Masahiro Kono, Rikard Frederiksen, King Wai Yau, Li-Hui Cao, Dong Gen Luo, M. Carter Cornwall, Rajan Adhikari, Daniel Silverman
Publikováno v:
SSRN Electronic Journal.
Retinal rod and cone photoreceptors mediate vision in dim and bright light, respectively, by transducing absorbed photons into electrical signals. Their phototransduction mechanisms are essentially identical. However, one distinct difference between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1fb264650ead63b0c1cdeb2f7c12b35
https://doi.org/10.2139/ssrn.3600548
https://doi.org/10.2139/ssrn.3600548
Publikováno v:
Nihon Gekakei Rengo Gakkaishi (Journal of Japanese College of Surgeons). 42:1063-1066
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::685ce5b7b79701b67ae81506e46501f9
https://doi.org/10.4030/jjcs.42.1063
https://doi.org/10.4030/jjcs.42.1063
Autor:
Masahiro KONO, Atsushi AKISAWA
Publikováno v:
The Proceedings of the Symposium on Environmental Engineering. :420
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ceb1e209f429a535cb3ac72b8902465
https://doi.org/10.1299/jsmeenv.2021.31.420
https://doi.org/10.1299/jsmeenv.2021.31.420
Autor:
Daniel Silverman, Rajan Adhikari, Masahiro Kono, Dong Gen Luo, M. Carter Cornwall, Li Hui Cao, King Wai Yau, Rikard Frederiksen, John E. Oatis
Publikováno v:
Curr Biol
Retinal rod and cone photoreceptors mediate vision in dim and bright light, respectively, by transducing absorbed photons into neural electrical signals. Their phototransduction mechanisms are essentially identical. However, one difference is that, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cc8dbfa9dc1027301fde92187196287
https://doi.org/10.1016/j.cub.2020.09.062
https://doi.org/10.1016/j.cub.2020.09.062
Publikováno v:
Transactions of the American Ophthalmological Society. 115
To test the hypothesis that delayed dark adaptation in patients with macular degeneration is due to an excess of free unliganded opsin (apo-opsin) and a deficiency of the visual chromophore, 11A total of 50 human autopsy eyes were harvested from dono
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7438e5bac36dd2e98fb4041fdbc67f6b
https://pubmed.ncbi.nlm.nih.gov/28900371
https://pubmed.ncbi.nlm.nih.gov/28900371
Publikováno v:
The Journal of Neuroscience. 34:13336-13348
Retinitis pigmentosa (RP) is an inherited neurodegenerative disease involving progressive vision loss, and is often linked to mutations in the rhodopsin gene. Mutations that abolish N-terminal glycosylation of rhodopsin (T4K and T17M) cause sector RP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50d020c35da09de6cacab650825315f
https://doi.org/10.1523/jneurosci.1655-14.2014
https://doi.org/10.1523/jneurosci.1655-14.2014