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

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

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

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

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