Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ryosuke, Kowada"'
Autor:
Ryosuke Kowada, Atsushi Kodani, Hiroyuki Ida, Masamitsu Yamaguchi, Im-Soon Lee, Yasushi Okada, Hideki Yoshida
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Synthesis of cytochrome c oxidase (Scox) is a Drosophila homolog of human SCO2 encoding a metallochaperone that transports copper to cytochrome c, and is an essential protein for the assembly of cytochrome c oxidase in the mitochondrial resp
Externí odkaz:
https://doaj.org/article/bef9fe10e70545db80da7348ac66ab91
Publikováno v:
IBRO Reports, Vol 8, Iss , Pp 65-75 (2020)
Various mutations in the SLC25A46 gene have been reported in mitochondrial diseases that are sometimes classified as type 2 Charcot-Marie-Tooth disease, optic atrophy, and Leigh syndrome. Although human SLC25A46 is a well-known transporter that acts
Externí odkaz:
https://doaj.org/article/f30c379a724045a6bd5d5b1173e52df0
Publikováno v:
IBRO Reports, Vol 8, Iss, Pp 65-75 (2020)
IBRO Reports
IBRO Reports
Highlights • Neuron-specific dSLC25A46a knockdown resulted in reduced mobility in larvae as well as adults. • Neuron-specific dSLC25A46a knockdown induced an aberrant morphology for NMJ and learning disability. • Neuron-specific dSLC25A46a knoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96062f6d45c7d6731f58c10301910b28
http://www.sciencedirect.com/science/article/pii/S2451830120300054
http://www.sciencedirect.com/science/article/pii/S2451830120300054
Autor:
Atsushi Kodani, Ryosuke Kowada, Hideki Yoshida, Im-Soon Lee, Yasushi Okada, Masamitsu Yamaguchi, Hiroyuki Ida
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Synthesis of cytochrome c oxidase (Scox) is a Drosophila homolog of human SCO2 encoding a metallochaperone that transports copper to cytochrome c, and is an essential protein for the assembly of cytochrome c oxidase in the mitochondrial respiratory c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac42f564c485226525085062c902204
https://doi.org/10.1038/s41598-021-00663-2
https://doi.org/10.1038/s41598-021-00663-2
Autor:
Yasuhide, Yoshioka, Keisuke, Anzai, Ryosuke, Kowada, Ken, Hiratsuka, Teppei, Hirayabu, Masashi, Yasuda, Yasuyuki, Ohkawa, Tetsuya, Sato, Mikita, Suyama, Hideki, Yoshida, Masamitsu, Yamaguchi
Publikováno v:
Experimental Cell Research. 420:113307
The CCAAT motif-binding factor NF-Y consists of three different subunits, NF-YA, NF-YB, and NF-YC. Although it is suggested that NF-Y activity is essential for normal tissue homeostasis, survival, and metabolic function, its precise role in lipid met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::890fc045fe96a6151a589c2771209a4a
https://doi.org/10.1016/j.yexcr.2022.113307
https://doi.org/10.1016/j.yexcr.2022.113307
Autor:
Ryosuke Kowada, Atsushi Nikaido, Hiroshi Kimura, Yuuka Muraoka, Hideki Yoshida, Masamitsu Yamaguchi
Publikováno v:
NeuroReport.
Mutations in the factor-induced-gene 4 (FIG 4) gene are associated with multiple disorders, including Charcot-Marie-Tooth disease (CMT), epilepsy with polymicrogyria, Yunis-Varón syndrome and amyotrophic lateral sclerosis. The wide spectrum of disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b607b7024d83935df0841a6f58d4e20
https://doi.org/10.1097/wnr.0000000000001636
https://doi.org/10.1097/wnr.0000000000001636