K-I. Nagata, N. Hamada. Pathophysiological mechanism of Munc18-1 mutations in early infantile epilepsies. JOURNAL OF NEUROCHEMISTRY. 2017. 142. 115-115
N. Hamada, H. Ito, H. Tabata, K-I. Nagata. Rbfox1, an autism causal gene, plays an essential role in cortical development. JOURNAL OF NEUROCHEMISTRY. 2015. 134. 253-254
K. Nagata, N. Hamada, H. Ito, I. Iwamoto, R. Morishita, H. Tabata. Abnormal cortical neuron migration by perturbed nucleus-centrosome coupling underlies the pathophysiology of autism with abnormality in RBFOX1/A2BP1 gene. MOLECULAR BIOLOGY OF THE CELL. 2015. 26
K-I. Nagata, N. Hamada, H. Ito, I. Iwamoto, M. Mizuno, R. Morishita, Y. Inaguma, H. Tabata. Biochemical and morphological characterization of an autism-related molecule, A2BP1, in developing cerebral cortex. MOLECULAR BIOLOGY OF THE CELL. 2013. 24