Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kazumi Shimaoka"'
Autor:
Kunihiko Yamashiro, Kei Hori, Esther S.K. Lai, Ryo Aoki, Kazumi Shimaoka, Nariko Arimura, Saki F. Egusa, Asami Sakamoto, Manabu Abe, Kenji Sakimura, Takaki Watanabe, Naofumi Uesaka, Masanobu Kano, Mikio Hoshino
Publikováno v:
iScience, Vol 23, Iss 12, Pp 101820- (2020)
Summary: Autism susceptibility candidate 2 (AUTS2), a risk gene for autism spectrum disorders (ASDs), is implicated in telencephalon development. Because AUTS2 is also expressed in the cerebellum where defects have been linked to ASDs, we investigate
Externí odkaz:
https://doaj.org/article/4df5afb623654ec88f01000b92c476e3
Autor:
Kei Hori, Kunihiko Yamashiro, Taku Nagai, Wei Shan, Saki F. Egusa, Kazumi Shimaoka, Hiroshi Kuniishi, Masayuki Sekiguchi, Yasuhiro Go, Shoji Tatsumoto, Mitsuyo Yamada, Reika Shiraishi, Kouta Kanno, Satoshi Miyashita, Asami Sakamoto, Manabu Abe, Kenji Sakimura, Masaki Sone, Kazuhiro Sohya, Hiroshi Kunugi, Keiji Wada, Mitsuhiko Yamada, Kiyofumi Yamada, Mikio Hoshino
Publikováno v:
iScience, Vol 23, Iss 6, Pp 101183- (2020)
Summary: Impairments in synapse development are thought to cause numerous psychiatric disorders. Autism susceptibility candidate 2 (AUTS2) gene has been associated with various psychiatric disorders, such as autism and intellectual disabilities. Alth
Externí odkaz:
https://doaj.org/article/549c93a6eb7d439aace1a24299f58f6e
Publikováno v:
Cells, Vol 11, Iss 1, p 11 (2021)
Neurodevelopmental disorders (NDDs), including autism spectrum disorders (ASD) and intellectual disability (ID), are a large group of neuropsychiatric illnesses that occur during early brain development, resulting in a broad spectrum of syndromes aff
Externí odkaz:
https://doaj.org/article/583032551e824dbf8d66ddc1539b4700
Autor:
Yukiko U. Inoue, Yuki Morimoto, Mayumi Yamada, Ryosuke Kaneko, Kazumi Shimaoka, Shinji Oki, Mayuko Hotta, Junko Asami, Eriko Koike, Kei Hori, Mikio Hoshino, Itaru Imayoshi, Takayoshi Inoue
Publikováno v:
Cells, Vol 10, Iss 5, p 1076 (2021)
Fluorescent reporter mouse lines and Cre/Flp recombinase driver lines play essential roles in investigating various molecular functions in vivo. Now that applications of the CRISPR/Cas9 genome-editing system to mouse fertilized eggs have drastically
Externí odkaz:
https://doaj.org/article/55a6df81cf8e4f539542750ba586a3e0
Publikováno v:
Cells, Vol 11, Iss 11, p 11 (2022)
Cells
Cells
Neurodevelopmental disorders (NDDs), including autism spectrum disorders (ASD) and intellectual disability (ID), are a large group of neuropsychiatric illnesses that occur during early brain development, resulting in a broad spectrum of syndromes aff
Autor:
Reika Shiraishi, Shoji Tatsumoto, Kazumi Shimaoka, Saki F. Egusa, Taku Nagai, Masaki Sone, Manabu Abe, Wei Shan, Kazuhiro Sohya, Kunihiko Yamashiro, Satoshi Miyashita, Hiroshi Kunugi, Yasuhiro Go, Mitsuyo Yamada, Hiroshi Kuniishi, Mikio Hoshino, Masayuki Sekiguchi, Kenji Sakimura, Asami Sakamoto, Keiji Wada, Mitsuhiko Yamada, Kouta Kanno, Kiyofumi Yamada, Kei Hori
Publikováno v:
iScience, Vol 23, Iss 6, Pp 101183-(2020)
iScience
iScience
Summary Impairments in synapse development are thought to cause numerous psychiatric disorders. Autism susceptibility candidate 2 (AUTS2) gene has been associated with various psychiatric disorders, such as autism and intellectual disabilities. Altho
Autor:
Naofumi Uesaka, Kunihiko Yamashiro, Manabu Abe, Nariko Arimura, Kenji Sakimura, Kei Hori, Saki F. Egusa, Mikio Hoshino, Masanobu Kano, Takaki Watanabe, Kazumi Shimaoka, Asami Sakamoto, Esther S.K. Lai, Ryo Aoki
Publikováno v:
iScience
iScience, Vol 23, Iss 12, Pp 101820-(2020)
iScience, Vol 23, Iss 12, Pp 101820-(2020)
Summary Autism susceptibility candidate 2 (AUTS2), a risk gene for autism spectrum disorders (ASDs), is implicated in telencephalon development. Because AUTS2 is also expressed in the cerebellum where defects have been linked to ASDs, we investigated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2699ab1f2599317d4a1e3a3d3c8452f
https://doi.org/10.1101/2020.01.24.917989
https://doi.org/10.1101/2020.01.24.917989
Autor:
Kunihiko Yamashiro, Kiyofumi Yamada, Mitsuyo Yamada, Kouta Kanno, Hiroshi Kunugi, Yasuhiro Go, Kenji Sakimura, Masaki Sone, Taku Nagai, Saki F. Egusa, Manabu Abe, Mikio Hoshino, Kei Hori, Reika Shiraishi, Kazuhiro Sohya, Shoji Tatsumoto, Wei Shan, Kazumi Shimaoka, Satoshi Miyashita, Asami Sakamoto
Impairments in synapse development are thought to cause numerous psychiatric disorders.Autism susceptibility candidate 2(AUTS2) gene has been associated with various psychiatric disorders, such as autism and intellectual disabilities. Although roles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d32d24c4563e70fbfe194de384e16e4
Autor:
Takayoshi Inoue, Nariko Arimura, Ken Ichi Dewa, Mikio Hoshino, Tomoki Nishioka, Satoshi Miyashita, Mako Okada, Akiko Tsuzuki, Kazumi Shimaoka, Hirotomo Uetake, Koichi Hashizume, Yuchio Yanagawa, Shinichiro Taya, Yukiko U. Inoue, Kozo Kaibuchi, Kazuhiro Yamakawa, Saki F. Egusa
Publikováno v:
Science Advances
DSCAM regulates neuronal delamination from the ventricular surface by suppressing RapGEF2/Rap1 and N-cadherin.
For normal neurogenesis and circuit formation, delamination of differentiating neurons from the proliferative zone must be precisely c
For normal neurogenesis and circuit formation, delamination of differentiating neurons from the proliferative zone must be precisely c
Publikováno v:
Zoological science. 34(2)
Xenopus vasa-like gene 1 (XVLG1), a DEAD-Box Helicase 4 (DDX4) gene identified as a vertebrate vasa homologue, is required for the formation of primordial germ cells (PGCs). However, it remains to be clarified when and how XVLG1 functions in the form