Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Akane Kyotani"'
Autor:
Yukie Kushimura, Yumiko Azuma, Takahiko Tokuda, Yuuka Muraoka, Akane Kyotani, Masamitsu Yamaguchi, Toshiki Mizuno, Hideki Yoshida, Ikuko Mizuta
Publikováno v:
NeuroReport. 29:856-862
Charcot-Marie-Tooth disease (CMT) is the most common hereditary neuropathy, and more than 80 CMT-causing genes have been identified to date. CMT4J is caused by a loss-of-function mutation in the Factor-Induced-Gene 4 (FIG4) gene, the product of which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c130c98625a3a7c8e4b70afc6efa73
https://doi.org/10.1097/wnr.0000000000001044
https://doi.org/10.1097/wnr.0000000000001044
Autor:
Ikuko Mizuta, Masanori Nakagawa, Hideki Yoshida, Itaru Yamamoto, Takahiko Tokuda, Akane Kyotani, Toshiki Mizuno, Yumiko Azuma, Masamitsu Yamaguchi
Publikováno v:
Experimental Neurology. 277:86-95
Mutations in Factor-Induced-Gene 4 (FIG4) gene have been identified in Charcot-Marie-Tooth disease type 4J (CMT4J), Yunis-Varon syndrome and epilepsy with polymicrogyria. FIG4 protein regulates a cellular abundance of phosphatidylinositol 3,5-bisphos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15294ebee1c34023b82515ac26f60e93
https://doi.org/10.1016/j.expneurol.2015.12.011
https://doi.org/10.1016/j.expneurol.2015.12.011
Autor:
Tomokatsu Yoshida, Toshiki Mizuno, Takahiko Tokuda, Masanori Nakagawa, Mai Shimamura, Yumiko Azuma, Akane Kyotani, Thanh Binh Nguyen, Ikuko Mizuta, Hideki Yoshida, Masamitsu Yamaguchi
Publikováno v:
Experimental Cell Research. 326:36-45
Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease that causes progressive muscular weakness. Fused in Sarcoma (FUS) that has been identified in familial ALS is an RNA binding protein that is normally localized in the nucleus. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab3dc0c1c4a5ff2a2f8e41df2ce86c61
https://doi.org/10.1016/j.yexcr.2014.06.004
https://doi.org/10.1016/j.yexcr.2014.06.004
Autor:
Nobuhiro Fujikake, Tomokatsu Yoshida, Akane Kyotani, Yoshitaka Nagai, Toshiki Mizuno, Morio Ueyama, Ikuko Mizuta, Yumiko Azuma, Masanori Nakagawa, Masamitsu Yamaguchi, Hiroshi Sasayama, Mai Shimamura, Takahiko Tokuda
Publikováno v:
Human molecular genetics. 23(13)
In humans, mutations in the fused in sarcoma (FUS) gene have been identified in sporadic and familial forms of amyotrophic lateral sclerosis (ALS). Cabeza (Caz) is the Drosophila ortholog of human FUS. Previously, we established Drosophila models of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ebd3557bc609c0868479ba13d94bac1
https://pubmed.ncbi.nlm.nih.gov/24497576
https://pubmed.ncbi.nlm.nih.gov/24497576