Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Takuma Mori"'
Autor:
Mengyun Zhou, Wen Qiu, Nobuhiko Ohashi, Lihao Sun, Marie-Louis Wronski, Emi Kouyama-Suzuki, Yoshinori Shirai, Toru Yanagawa, Takuma Mori, Katsuhiko Tabuchi
Publikováno v:
Cells, Vol 13, Iss 3, p 275 (2024)
Cigarette smoking during pregnancy is known to be associated with the incidence of attention-deficit/hyperactive disorder (ADHD). Recent developments in deep learning algorithms enable us to assess the behavioral phenotypes of animal models without c
Externí odkaz:
https://doaj.org/article/e9b82716e535484b9dbc10fb3663dab9
Publikováno v:
Genes, Vol 14, Iss 8, p 1656 (2023)
CASK-related disorders are a form of rare X-linked neurological diseases and most of the patients are females. They are characterized by several symptoms, including microcephaly with pontine and cerebellar hypoplasia (MICPCH), epilepsy, congenital ny
Externí odkaz:
https://doaj.org/article/7c40cd7798444552aeda0a96f838feca
Autor:
Chie Satou, Rachael L Neve, Hassana K Oyibo, Pawel Zmarz, Kuo-Hua Huang, Estelle Arn Bouldoires, Takuma Mori, Shin-ichi Higashijima, Georg B Keller, Rainer W Friedrich
Publikováno v:
eLife, Vol 11 (2022)
The zebrafish is an important model in systems neuroscience but viral tools to dissect the structure and function of neuronal circuitry are not established. We developed methods for efficient gene transfer and retrograde tracing in adult and larval z
Externí odkaz:
https://doaj.org/article/953084a35d814ae0a44b105f74d5fa17
Autor:
Qi Guo, Emi Kouyama-Suzuki, Yoshinori Shirai, Xueshan Cao, Toru Yanagawa, Takuma Mori, Katsuhiko Tabuchi
Publikováno v:
Cells, Vol 12, Iss 8, p 1177 (2023)
Microcephaly with pontine and cerebellar hypoplasia (MICPCH) syndrome is a neurodevelopmental disorder caused by the deficiency of the X-chromosomal gene CASK. However, the molecular mechanisms by which CASK deficiency causes cerebellar hypoplasia in
Externí odkaz:
https://doaj.org/article/65c5aa1e4d2b4023b26efdea77ba4b13
Autor:
Moataz Badawi, Takuma Mori, Taiga Kurihara, Takahiro Yoshizawa, Katsuhiro Nohara, Emi Kouyama-Suzuki, Toru Yanagawa, Yoshinori Shirai, Katsuhiko Tabuchi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Six mutations in the salt-inducible kinase 1 (SIK1)-coding gene have been identified in patients with early infantile epileptic encephalopathy (EIEE-30) accompanied by autistic symptoms. Two of the mutations are non-sense mutations that truncate the
Externí odkaz:
https://doaj.org/article/0cbf8869133e44c0a1fbcc13dc8af473
Autor:
Bo Pang, Takuma Mori, Moataz Badawi, Mengyun Zhou, Qi Guo, Emi Suzuki-Kouyama, Toru Yanagawa, Yoshinori Shirai, Katsuhiko Tabuchi
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 14, p 7927 (2022)
Six mutations in the salt-inducible kinase 1 (SIK1) have been identified in developmental and epileptic encephalopathy (DEE-30) patients, and two of the mutations are nonsense mutations that truncate the C-terminal region of SIK1. In a previous study
Externí odkaz:
https://doaj.org/article/c98c37b5dfd94221bfe09a3eb6cdca0f
Autor:
Anuradha Mehta, Yoshinori Shirai, Emi Kouyama-Suzuki, Mengyun Zhou, Takahiro Yoshizawa, Toru Yanagawa, Takuma Mori, Katsuhiko Tabuchi
Publikováno v:
Cells, Vol 10, Iss 10, p 2724 (2021)
IQSEC2 is a guanine nucleotide exchange factor (GEF) for ADP-ribosylation factor 6 (Arf6), of which protein is exclusively localized to the postsynaptic density of the excitatory synapse. Human genome studies have revealed that the IQSEC2 gene is ass
Externí odkaz:
https://doaj.org/article/af3ccf3d4aba45d0ae46509d05901c3a
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 04, Pp e372-e375 (2019)
Abstract Objective Here, we report a case of fetal sick sinus syndrome (SSS) caused by pulmonary stenosis regurgitation (PSR) that spontaneously resolved during pregnancy. Case Report A 29-year-old woman was referred to our hospital at 21 weeks o
Externí odkaz:
https://doaj.org/article/1f53f9fa568d499eb8fca98da9e74f08
Autor:
Norio Yukawa, Makoto Takahashi, Kazuyoshi Sasaki, Takuma Mori, Ayumi Matsuo, Kuniyasu Ito, Hiroyuki Kirikoshi, Kiyoshi Ohya, Nobuyuki Wada, Yasushi Rino, Munetaka Masuda
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Extrahepatic portal vein aneurysm is a rare disorder. From 1956 to 2008, we found only 43 published English-language reports, including 67 cases, using Pub Med. We report a case of a 77-year-old woman who had complaints of lower abdominal fullness an
Externí odkaz:
https://doaj.org/article/6f452c2b9c35474d96f8d97c7c6d99df
Autor:
Syou Maki, Seiichi Tanaka, Kohta Miyagi, Takuma Mori, Yuki Isaka, Masayuki Hagiwara, Seiji Fujiwara
Publikováno v:
Experimental Heat Transfer. :1-17