Zobrazeno 1 - 10
of 157
pro vyhledávání: '"Tetsuo Ozawa"'
Autor:
Hideki Hayashi, Rie Saito, Hidetomo Tanaka, Norikazu Hara, Shin Koide, Yosuke Yonemochi, Tetsuo Ozawa, Mariko Hokari, Yasuko Toyoshima, Akinori Miyashita, Osamu Onodera, Kouichirou Okamoto, Takeshi Ikeuchi, Takashi Nakajima, Akiyoshi Kakita
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-6 (2023)
Externí odkaz:
https://doaj.org/article/e672887e1406470b8772e70480138afe
Autor:
Takahiro Nagai, Yoko Sunami, Risa Kato, Megumi Sugai, Makoto Takahara, Kentaro Ohta, Hidehiko Fujinaka, Kiyoe Goto, Osamu Okanura, Takashi Nakajima, Tetsuo Ozawa
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 84-91 (2021)
Spastic paraplegia type 4 (SPG4) is the most common type of hereditary spastic paraplegia (HSP) caused by the mutations in the SPAST gene, which encodes a microtubule-severing protein named spastin. Spastin regulates the number and mobility of microt
Externí odkaz:
https://doaj.org/article/2ce27e00a124430f8f941fa6664ec2f4
Publikováno v:
Molecules, Vol 22, Iss 4, p 548 (2017)
Mitochondria activation factor (MAF) is a high-molecular-weight polyphenol extracted from black tea that stimulates training-induced 5′ adenosine monophosphate-activated protein kinase (AMPK) activation and improves endurance capacity. Originally,
Externí odkaz:
https://doaj.org/article/3c1ea0af424b4794917a2f6ff1acdd70
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69480 (2013)
Aerobic exercise can promote "fast-to-slow transition" in skeletal muscles, i.e. an increase in oxidative fibers, mitochondria, and myoglobin and improvement in glucose and lipid metabolism. Here, we found that mice administered Mitochondria Activati
Externí odkaz:
https://doaj.org/article/6251c11e77844f73894f04c7fca8b06d
Publikováno v:
Internal Medicine
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare progressive neurodegenerative disease caused by either homozygous or compound heterozygous mutations in the SACS gene. The original ARSACS cases found in Quebec showed very
Autor:
Kiyoe Goto, Takashi Nakajima, Megumi Sugai, Yoko Sunami, Kentaro Ohta, Makoto Takahara, Tetsuo Ozawa, Hidehiko Fujinaka, Takahiro Nagai, Osamu Okanura, Risa Kato
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 84-91 (2021)
Case Reports in Neurology
Case Reports in Neurology
Spastic paraplegia type 4 (SPG4) is the most common type of hereditary spastic paraplegia (HSP) caused by the mutations in the SPAST gene, which encodes a microtubule-severing protein named spastin. Spastin regulates the number and mobility of microt
Publikováno v:
Internal Medicine. 59:1309-1313
Homozygous or compound heterozygous mutations in the high-temperature requirement A serine protease 1 gene (HTRA1) cause cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, a very rare hereditary cerebral smal
Autor:
Hidetomo Tanaka, Hiroshi Shimizu, Yosuke Yonemochi, Tetsuo Ozawa, Yasuko Toyoshima, Takashi Nakajima, Akiyoshi Kakita
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 48(4)
Autor:
Xiaofen Wu, Keqin Wang, Jihua Duan, Yinhua Li, Zhonghua Liu, Jianan Huang, Tetsuo Ozawa, Kun Zhu
Publikováno v:
Journal of Food Processing and Preservation. 45
Publikováno v:
Journal of Clinical Neuroscience. 64:106-110
Profound insight into age-related changes in γ-aminobutyric acid type A receptor (GABAA-R) distribution using iodine-123-iomazenil single photon emission computed tomography (IMZ-SPECT) can contribute to accurate in vivo evaluation. We evaluated the