Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Naoto Nishimura"'
Autor:
Saishu YOSHIDA, Hideaki YURINO, Masaaki KOBAYASHI, Naoto NISHIMURA, Kentaro YANO, Ken FUJIWARA, Shin-ichi HASHIMOTO, Takako KATO, Yukio KATO
Publikováno v:
The Journal of Reproduction and Development, Vol 68, Iss 3, Pp 225-231 (2022)
Pituitary endocrine cells are supplied by Sox2-expressing stem/progenitor cells in the anterior lobe of the adult pituitary gland. These SOX2-positive cells are maintained in two types of microenvironments (niches): the marginal cell layer (MCL)-nich
Externí odkaz:
https://doaj.org/article/2548dae6ac2947539fcc89b79dfdda54
Autor:
Saishu Yoshida, Naoto Nishimura, Hiroki Ueharu, Naoko Kanno, Masashi Higuchi, Kotaro Horiguchi, Takako Kato, Yukio Kato
Publikováno v:
Stem Cell Research, Vol 17, Iss 2, Pp 318-329 (2016)
Recent studies have demonstrated that Sox2-expressing stem/progenitor cells play roles in the pituitary cell turnover. Two types of niches have been proposed for stem/progenitor cells, the marginal cell layer (MCL) and the dense cell clusters in the
Externí odkaz:
https://doaj.org/article/90ef5d0eab4342a7bacdf440999add57
Autor:
Saishu Yoshida, Naoto Nishimura, Hideaki Yurino, Masaaki Kobayashi, Kotaro Horiguchi, Kentaro Yano, Shin-Ichi Hashimoto, Takako Kato, Yukio Kato
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0196029 (2018)
Pituitary endocrine cells are supplied by Sox2-expressing stem/progenitor cells in the anterior lobe of the adult pituitary. In relation to their microenvironment ("niche"), SOX2-positive cells exist in two types of niches; the marginal cell layer-ni
Externí odkaz:
https://doaj.org/article/b7836e26b275443788c269075dc12267
Dissertation/ Thesis
Autor:
西村 直登, Naoto Nishimura
本論文は、1923年9月に発生した関東大震災における朝鮮人虐殺事件を経験し生き延びた朝鮮人にとって、関東大震災朝鮮人虐殺がどのような出来事だったのかについて実証的に明らかに
Autor:
Minako Takagi, Shin Ono, Tatsuro Kumaki, Naoto Nishimura, Hiroaki Murakami, Yumi Enomoto, Takuya Naruto, Hideaki Ueda, Kenji Kurosawa
Publikováno v:
American Journal of Medical Genetics Part A. 191:882-892
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d3de73b61b427931af5d96de8806b2
https://doi.org/10.1002/ajmg.a.63089
https://doi.org/10.1002/ajmg.a.63089
Autor:
Yandejia SONG, Tadatsugu HOSOYA, Akito YASUDA, Yuki ASHIZUKA, Takayuki KOBAYASHI, Naoto NISHIMURA, Mariko NISHIKITANI
Publikováno v:
Japanese Journal of Zoo and Wildlife Medicine. 27:119-125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69e2742819bd8e075a6bee7b114f1d00
https://doi.org/10.5686/jjzwm.27.119
https://doi.org/10.5686/jjzwm.27.119
Autor:
Naoto Nishimura, Yumi Enomoto, Tatsuro Kumaki, Hiroaki Murakami, Azusa Ikeda, Tomohide Goto, Kenji Kurosawa
Publikováno v:
Molecular Syndromology. 13:221-225
Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS) and genitopatellar syndrome (GPS) are caused by variants of lysine acetyltransferase 6B (KAT6B). These variants tend to occur in the terminal exons of KAT6B. Here, we report a patient with global d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::989a90f980ef66c29833c03ab88e3bcf
https://doi.org/10.1159/000520134
https://doi.org/10.1159/000520134
Autor:
Yusuke Hirose, Naoto Nishimura, Kentaro Enoki, Fuminori Honda, Tetsuya Takeuchi, Kiyohiro Sugiyama, Masayuki Hagiwara, Koichi Kindo, Rikio Settai, Yoshichika Ōnuki
Publikováno v:
Journal of the Physical Society of Japan. 92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fddeaf561a7f4dbee133e0e44ce2652
https://doi.org/10.7566/jpsj.92.018001
https://doi.org/10.7566/jpsj.92.018001
Autor:
Yukiko Kuroda, Mizuki Asano, Noriko Aida, Hiroaki Murakami, Kenjiro Kosaki, Tatsuro Kumaki, Naoto Nishimura, Kenji Kurosawa, Tomoko Uehara, Yumi Enomoto
Publikováno v:
Mol Syndromol
Okur-Chung neurodevelopmental syndrome is a rare autosomal dominant disorder caused by pathogenic variants in CSNK2A1, which encodes the alpha 1 catalytic subunit of casein kinase II. This syndrome is characterized by intellectual disability, devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5ba8f053a71ddecefd475035e5e741d
https://doi.org/10.1159/000517977
https://doi.org/10.1159/000517977
Autor:
Katsuaki Toyoshima, Kenji Kurosawa, Kaoru Katsumata, Hiroaki Murakami, Yumi Enomoto, Naoto Nishimura, Tatsuro Kumaki
Publikováno v:
Human Genome Variation, Vol 7, Iss 1, Pp 1-4 (2020)
Human Genome Variation
Human Genome Variation
Variants of GRIN1, which encodes GluN1, are associated with developmental delay, epilepsy, and cortical malformation. Here, we report a case of arthrogryposis multiplex congenita with polymicrogyria and infantile encephalopathy caused by a heterozygo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b36082b5f10a9634d43c7d81d6991c
http://link.springer.com/article/10.1038/s41439-020-00116-8
http://link.springer.com/article/10.1038/s41439-020-00116-8