Zobrazeno 1 - 10
of 667
pro vyhledávání: '"Yu-Ichi Goto"'
Autor:
Yuka Shirakawa, Heng Li, Yuki Inoue, Hitomi Izumi, Yoshimi Kaga, Yu-ichi Goto, Ken Inoue, Masumi Inagaki
Publikováno v:
IBRO Neuroscience Reports, Vol 16, Iss , Pp 67-77 (2024)
The homozygous Bronx waltzer (bv) mouse, which shows hearing impairment, also exhibits anxiety accompanied by a reduction in cortical parvalbumin (PV)-positive GABAergic interneurons. Recently, a mutation in splicing factor Ser/Arg repetitive matrix
Externí odkaz:
https://doaj.org/article/9c5f8e64c1b4417a8e422f050ea28339
Autor:
Keiya Iijima, Hiroyuki Fujii, Fumio Suzuki, Kumiko Murayama, Yu-ichi Goto, Yuko Saito, Terunori Sano, Hiroyoshi Suzuki, Hajime Miyata, Yukio Kimura, Takuma Nakashima, Hiromichi Suzuki, Masaki Iwasaki, Noriko Sato
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionLow-grade epilepsy-associated tumors are the second most common histopathological diagnoses in cases of drug-resistant focal epilepsy. However, the connection between neuroimaging features and genetic alterations in these tumors is unclea
Externí odkaz:
https://doaj.org/article/ffdfde74e10e4215bbcbe99475285cd0
Autor:
Takako Enokida, Nanako Yoshida, Megumi Tatsumi, Shinsuke Hidese, Yu-ichi Goto, Mikio Hoshino, Hiroshi Kunugi, Kotaro Hattori
Publikováno v:
Heliyon, Vol 10, Iss 10, Pp e30695- (2024)
Schizophrenia is a syndrome with multiple etiologies, one of which is the potential for an autoimmune disease of the brain such as N-methyl-d-aspartate receptor (NMDAR) encephalitis, which can induce psychosis resembling schizophrenia. Here, we exami
Externí odkaz:
https://doaj.org/article/f736d50effdd4f5c99ec7025bc13bb77
Autor:
Yoshinori Aoki, Hongmei Dai, Fumika Furuta, Tomohisa Akamatsu, Takuya Oshima, Naoto Takahashi, Yu-ichi Goto, Akira Oka, Masayuki Itoh
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-13 (2023)
Abstract Background Microglial cells play an important role in the immune system in the brain. Activated microglial cells are not only injurious but also neuroprotective. We confirmed marked lectin-like oxidized low-density lipoprotein receptor-1 (LO
Externí odkaz:
https://doaj.org/article/c601080a670f43a59035a34ea080107a
Autor:
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, Takaaki Hayashi, Shinji Ueno, Takeshi Iwata, Hatsue Ishibashi-Ueda, Tsutomu Tomita, Michio Noguchi, Ayako Takahashi, Yu-ichi Goto, Sumiko Yoshida, Kotaro Hattori, Ryo Matsumura, Aritoshi Iida, Yutaka Maruoka, Hiroyuki Gatanaga, Masaya Sugiyama, Satoshi Suzuki, Kengo Miyo, Yoichi Matsubara, Akihiro Umezawa, Kenichiro Hata, Tadashi Kaname, Kouichi Ozaki, Haruhiko Tokuda, Hiroshi Watanabe, Shumpei Niida, Eisei Noiri, Koji Kitajima, Reiko Miyahara, Hideyuki Shimanuki
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101843- (2024)
Purpose: Achromatopsia (ACHM) is an early-onset cone dysfunction caused by 5 genes with cone-specific functions (CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H) and by ATF6, a transcription factor with ubiquitous expression. To improve the relatively low vari
Externí odkaz:
https://doaj.org/article/a0a40200ace245f49c062e5cf42c6c3b
Autor:
Yosuke Kawai, Yusuke Watanabe, Yosuke Omae, Reiko Miyahara, Seik-Soon Khor, Eisei Noiri, Koji Kitajima, Hideyuki Shimanuki, Hiroyuki Gatanaga, Kenichiro Hata, Kotaro Hattori, Aritoshi Iida, Hatsue Ishibashi-Ueda, Tadashi Kaname, Tatsuya Kanto, Ryo Matsumura, Kengo Miyo, Michio Noguchi, Kouichi Ozaki, Masaya Sugiyama, Ayako Takahashi, Haruhiko Tokuda, Tsutomu Tomita, Akihiro Umezawa, Hiroshi Watanabe, Sumiko Yoshida, Yu-Ichi Goto, Yutaka Maruoka, Yoichi Matsubara, Shumpei Niida, Masashi Mizokami, Katsushi Tokunaga
Publikováno v:
PLoS Genetics, Vol 19, Iss 12, p e1010625 (2023)
The Japanese archipelago is a terminal location for human migration, and the contemporary Japanese people represent a unique population whose genomic diversity has been shaped by multiple migrations from Eurasia. We analyzed the genomic characteristi
Externí odkaz:
https://doaj.org/article/687445c603e447609e3532d4d0fb3522
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Background X-linked methyl-CpG-binding protein 2 (MECP2) duplication syndrome is prevalent in approximately 1% of X-linked intellectual disabilities. Accumulating evidence has suggested that MECP2 is the causative gene of MECP2 duplication s
Externí odkaz:
https://doaj.org/article/796b026aed4a4860bb93951ff4dbfd91
Autor:
Koki Ibayashi, Yoshihisa Fujino, Masakazu Mimaki, Kenji Fujimoto, Shinya Matsuda, Yu-ichi Goto
Publikováno v:
Journal of Epidemiology, Vol 33, Iss 2, Pp 68-75 (2023)
Background: To provide a better healthcare system for patients with mitochondrial diseases, it is important to understand the basic epidemiology of these conditions, including the number of patients affected. However, little information about them ha
Externí odkaz:
https://doaj.org/article/038877c7154b4288bf811e68572d95ef
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-6 (2022)
Biobanks: Japanese network promotes research collaboration Japan’s National Center Biobank Network (NCBN) has standardized the collection and storage of high-quality disease-related data and samples, offering collaboration opportunities in basic an
Externí odkaz:
https://doaj.org/article/a1e80815abb14fce965241fe91618bfb
Publikováno v:
Brain Disorders, Vol 8, Iss , Pp 100057- (2022)
We report a female patient with typical chronic progressive external ophthalmoplegia (CPEO) presented with central neurogenic hyperventilation (CNH), which is characterized by sustained hyperventilation during awake and sleep. CNH is usually caused b
Externí odkaz:
https://doaj.org/article/a7fdb18979b8447f93309d77084752c7