Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Nozomu, Yoshioka"'
Autor:
Hiroaki Oizumi, Yuki Miyamoto, Chika Seiwa, Masahiro Yamamoto, Nozomu Yoshioka, Seiichi Iizuka, Tomohiro Torii, Katsuya Ohbuchi, Kazushige Mizoguchi, Junji Yamauchi, Hiroaki Asou
Publikováno v:
iScience, Vol 26, Iss 10, Pp 107448- (2023)
Summary: Multiple sclerosis (MS) is a leading disease that causes disability in young adults. We have previously shown that a DEAD-box RNA helicase Ddx54 binds to mRNA and protein isoforms of myelin basic protein (MBP) and that Ddx54 siRNA blocking a
Externí odkaz:
https://doaj.org/article/63a42a4946ca499fb147b3974ca292f5
Autor:
Dang Minh Tran, Nozomu Yoshioka, Norihisa Bizen, Yukiko Mori-Ochiai, Masato Yano, Shogo Yanai, Junya Hasegawa, Satoshi Miyashita, Mikio Hoshino, Junko Sasaki, Takehiko Sasaki, Hirohide Takebayashi
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 7 (2023)
Externí odkaz:
https://doaj.org/article/5cbc1fa65ddd426cb8b5ad38b16b23e3
Autor:
Nozomu Yoshioka, Masayuki Kurose, Masato Yano, Dang Minh Tran, Shujiro Okuda, Yukiko Mori-Ochiai, Masao Horie, Toshihiro Nagai, Ichizo Nishino, Shinsuke Shibata, Hirohide Takebayashi
Publikováno v:
eLife, Vol 11 (2022)
Dystonin (DST), which encodes cytoskeletal linker proteins, expresses three tissue-selective isoforms: neural DST-a, muscular DST-b, and epithelial DST-e. DST mutations cause different disorders, including hereditary sensory and autonomic neuropathy
Externí odkaz:
https://doaj.org/article/cabcf3fd073e457ba5cfb5ea34742533
Autor:
Nozomu Yoshioka1,2, Masayuki Kurose3,4, Hiromi Sano5,6,7, Dang Minh Tran1, Satomi Chiken5,6, Kazuki Tainaka8, Kensuke Yamamura4, Kenta Kobayashi9, Atsushi Nambu5,6, Hirohide Takebayashi1,10 takebaya@med.niigata-u.ac.jp
Publikováno v:
Science Advances. 7/26/2024, Vol. 10 Issue 30, p1-16. 16p.
Autor:
Nozomu Yoshioka, Yudai Kabata, Momona Kuriyama, Norihisa Bizen, Li Zhou, Dang M. Tran, Masato Yano, Atsushi Yoshiki, Tatsuo Ushiki, Thomas J. Sproule, Riichiro Abe, Hirohide Takebayashi
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 5 (2020)
Loss-of-function mutations in dystonin (DST) can cause hereditary sensory and autonomic neuropathy type 6 (HSAN-VI) or epidermolysis bullosa simplex (EBS). Recently, DST-related diseases were recognized to be more complex than previously thought beca
Externí odkaz:
https://doaj.org/article/1be9fe63694c464d9f7dca7326f58544
Autor:
Shigeki Kato, Ryoji Fukabori, Kayo Nishizawa, Kana Okada, Nozomu Yoshioka, Masateru Sugawara, Yuko Maejima, Kenju Shimomura, Masahiro Okamoto, Satoshi Eifuku, Kazuto Kobayashi
Publikováno v:
Cell Reports, Vol 22, Iss 9, Pp 2370-2382 (2018)
Summary: Learning processes contributing to appropriate selection and flexible switching of behaviors are mediated through the dorsal striatum, a key structure of the basal ganglia circuit. The major inputs to striatal subdivisions are provided from
Externí odkaz:
https://doaj.org/article/caa4716990a0496eb494a3cb5b2d7257
Autor:
Nozomu Yoshioka, Shinji Miyata, Atsushi Tamada, Yumi Watanabe, Asami Kawasaki, Hiroshi Kitagawa, Keizo Takao, Tsuyoshi Miyakawa, Kosei Takeuchi, Michihiro Igarashi
Publikováno v:
Molecular Brain, Vol 10, Iss 1, Pp 1-10 (2017)
Abstract Chondroitin sulfate (CS) is an important glycosaminoglycan and is mainly found in the extracellular matrix as CS proteoglycans. In the brain, CS proteoglycans are highly concentrated in perineuronal nets (PNNs), which surround synapses and m
Externí odkaz:
https://doaj.org/article/340fb9df62194890b434151f3709a398
Autor:
Katsuya Miyajima, Yusuke Sudo, Sho Sanechika, Yoshitaka Hara, Mieko Horiguchi, Feng Xu, Minori Suzuki, Satoshi Hara, Koichi Tanda, Ken‐ichi Inoue, Masahiko Takada, Nozomu Yoshioka, Hirohide Takebayashi, Masayo Mori‐Kojima, Masahiro Sugimoto, Chiho Sumi‐Ichinose, Kazunao Kondo, Keizo Takao, Tsuyoshi Miyakawa, Hiroshi Ichinose
Publikováno v:
Journal of neurochemistry. 161(Issue 2):129-145
Increasing evidence suggests the involvement of peripheral amino acid metabolism in the pathophysiology of neuropsychiatric disorders, whereas the molecular mechanisms are largely unknown. Tetrahydrobiopterin (BH4) is a cofactor for enzymes that cata
Autor:
Youichi Shinozaki, Alex Leung, Kazuhiko Namekata, Sei Saitoh, Huy Bang Nguyen, Akiko Takeda, Yosuke Danjo, Yosuke M. Morizawa, Eiji Shigetomi, Fumikazu Sano, Nozomu Yoshioka, Hirohide Takebayashi, Nobuhiko Ohno, Takahiro Segawa, Kunio Miyake, Kenji Kashiwagi, Takayuki Harada, Shin-ichi Ohnuma, Schuichi Koizumi
Publikováno v:
Science advances. 8(44)
Astrocyte abnormalities have received great attention for their association with various diseases in the brain but not so much in the eye. Recent independent genome-wide association studies of glaucoma, optic neuropathy characterized by retinal gangl
Autor:
Nozomu Yoshioka, Masayuki Kurose, Masato Yano, Dang Minh Tran, Shujiro Okuda, Yukiko Mori-Ochiai, Masao Horie, Toshihiro Nagai, Ichizo Nishino, Shinsuke Shibata, Hirohide Takebayashi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d47db89d5a60818932a4aac25c39498a
https://doi.org/10.7554/elife.78419.sa2
https://doi.org/10.7554/elife.78419.sa2