Pathophysiological Mechanism of Neurodevelopmental Disorders—Overview

por Nagata, Koh-ichi
Publicado 2022

Functions of CNKSR2 and Its Association with Neurodevelopmental Disorders

por Ito, Hidenori, Nagata, Koh-ichi
Publicado 2022

Functions of Rhotekin, an Effector of Rho GTPase, and Its Binding Partners in Mammals

por Ito, Hidenori, Morishita, Rika, Nagata, Koh-ichi
Publicado 2018

Physiological significance of WDR45, a responsible gene for β-propeller protein associated neurodegeneration (BPAN), in brain development

por Noda, Mariko, Ito, Hidenori, Nagata, Koh-ichi
Publicado 2021

MUNC18–1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

por Hamada, Nanako, Iwamoto, Ikuko, Tabata, Hidenori, Nagata, Koh-ichi
Publicado 2017

Pathophysiological Mechanisms in Neurodevelopmental Disorders Caused by Rac GTPases Dysregulation: What’s behind Neuro-RACopathies

por Scala, Marcello, Nishikawa, Masashi, Nagata, Koh-ichi, Striano, Pasquale
Publicado 2021

Screening for candidate genes involved in the production of mouse subventricular zone proliferative cells and an estimation of their changes in evolutionary pressure during primate...

por Tabata, Hidenori, Hachiya, Tsuyoshi, Nagata, Koh-ichi, Sakakibara, Yasubumi, Nakajima, Kazunori
Publicado 2013

Impaired Function of PLEKHG2, a Rho-Guanine Nucleotide-Exchange Factor, Disrupts Corticogenesis in Neurodevelopmental Phenotypes

por Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Ueda, Hiroshi, Nagata, Koh-ichi
Publicado 2022

Septin 14 Is Involved in Cortical Neuronal Migration via Interaction with Septin 4

por Shinoda, Tomoyasu, Ito, Hidenori, Sudo, Kaori, Iwamoto, Ikuko, Morishita, Rika, Nagata, Koh-ichi
Publicado 2010

Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

por Hamada, Nanako, Ito, Hidenori, Iwamoto, Ikuko, Morishita, Rika, Tabata, Hidenori, Nagata, Koh-ichi
Publicado 2015

Role of Per3, a circadian clock gene, in embryonic development of mouse cerebral cortex

por Noda, Mariko, Iwamoto, Ikuko, Tabata, Hidenori, Yamagata, Takanori, Ito, Hidenori, Nagata, Koh-ichi
Publicado 2019

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development

por Goto, Naoki, Nishikawa, Masashi, Ito, Hidenori, Noda, Mariko, Hamada, Nanako, Tabata, Hidenori, Kinoshita, Makoto, Nagata, Koh-ichi
Publicado 2023

Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome

por Tabata, Hidenori, Mori, Daisuke, Matsuki, Tohru, Yoshizaki, Kaichi, Asai, Masato, Nakayama, Atsuo, Ozaki, Norio, Nagata, Koh-ichi
Publicado 2023

Roles of Rho-associated Kinase in Cytokinesis; Mutations in Rho-associated Kinase Phosphorylation Sites Impair Cytokinetic Segregation of Glial Filaments

por Yasui, Yoshihiro, Amano, Mutsuki, Nagata, Koh-ichi, Inagaki, Naoyuki, Nakamura, Hideo, Saya, Hideyuki, Kaibuchi, Kozo, Inagaki, Masaki
Publicado 1998

Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development

por Hamada, Nanako, Ito, Hidenori, Nishijo, Takuma, Iwamoto, Ikuko, Morishita, Rika, Tabata, Hidenori, Momiyama, Toshihiko, Nagata, Koh-Ichi
Publicado 2016

Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders

por Goto, Masahide, Mizuno, Makoto, Matsumoto, Ayumi, Yang, Zhiliang, Jimbo, Eriko F., Tabata, Hidenori, Yamagata, Takanori, Nagata, Koh-ichi
Publicado 2017

LIN7A Depletion Disrupts Cerebral Cortex Development, Contributing to Intellectual Disability in 12q21-Deletion Syndrome

por Matsumoto, Ayumi, Mizuno, Makoto, Hamada, Nanako, Nozaki, Yasuyuki, Jimbo, Eriko F., Momoi, Mariko Y., Nagata, Koh-ichi, Yamagata, Takanori
Publicado 2014

Biochemical and Morphological Characterization of a Guanine Nucleotide Exchange Factor ARHGEF9 in Mouse Tissues

por Ibaraki, Kyoko, Mizuno, Makoto, Aoki, Hitomi, Niwa, Ayumi, Iwamoto, Ikuko, Hara, Akira, Tabata, Hidenori, Ito, Hidenori, Nagata, Koh-ichi
Publicado 2018

Septin-mediated RhoA activation engages the exocyst complex to recruit the cilium transition zone

por Safavian, Darya, Kim, Moshe S., Xie, Hong, El-Zeiry, Maha, Palander, Oliva, Dai, Lu, Collins, Richard F., Froese, Carol, Shannon, Rachel, Nagata, Koh-ichi, Trimble, William S.
Publicado 2023

SIL1, a causative cochaperone gene of Marinesco-Sjögren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex

por Inaguma, Yutaka, Hamada, Nanako, Tabata, Hidenori, Iwamoto, Ikuko, Mizuno, Makoto, Nishimura, Yoshiaki V, Ito, Hidenori, Morishita, Rika, Suzuki, Motomasa, Ohno, Kinji, Kumagai, Toshiyuki, Nagata, Koh-ichi
Publicado 2014