Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kodai Matsumoto"'
Autor:
Udai Danyoshi, Kodai Matsumoto, Tomohiro Ryu, Naoyuki Harada, Takeo Nakano, Kiyoshi Miyata, Nobuhiro Yanai, Shigenori Fujikawa, Nobuo Kimizuka
Publikováno v:
Photonic and Phononic Properties of Engineered Nanostructures XIII.
Autor:
Kodai Matsumoto, Udai Danyoshi, Tomohiro Ryu, Junpei Kondo, Takeo Nakano, Kiyoshi Miyata, Nobuhiro Yanai, Shigenori Fujikawa, Nobuo Kimizuka
Publikováno v:
Photonic and Phononic Properties of Engineered Nanostructures XIII.
Publikováno v:
Proceedings of the Combustion Institute.
Publikováno v:
Proceedings of the Combustion Institute. 38:3167-3174
The first combustion experiments aboard the Japanese Experiment Module “Kibo” on the International Space Station, titled “Elucidation of Flame Spread and Group Combustion Excitation Mechanism of Randomly Distributed Droplet Clouds (Group Combus
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
International Conference on Liquid Atomization and Spray Systems (ICLASS). 1
Autor:
Kodai Matsumoto
Publikováno v:
Journal of the Japanese and International Economies. 63:101186
Publikováno v:
Chemistry Letters; Apr2022, Vol. 51 Issue 4, p372-374, 3p
Publikováno v:
HCI International 2019 – Late Breaking Posters ISBN: 9783030307110
HCI (37)
HCI (37)
As part of nursing care, there is physiotherapist’s physical exercise recovery training (walking training, etc.), which is aimed at restoring athletic ability that is called rehabilitation. In rehabilitation for the practitioners, there is a proble
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f69f42f87634813189f5c82410b075f7
https://doi.org/10.1007/978-3-030-30712-7_31
https://doi.org/10.1007/978-3-030-30712-7_31
Publikováno v:
Biochemical and Biophysical Research Communications. 464:1054-1059
Cereblon (CRBN) is encoded by a candidate gene for autosomal recessive nonsyndromic intellectual disability (ID). The nonsense mutation, R419X, causes deletion of 24 amino acids at the C-terminus of CRBN, leading to mild ID. Although abnormal CRBN fu