S. Yamashita

Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome

K. Yamakawa, T. Nakahata, H. Hosoi, 2016, Journal of Human Genetics.

Luteolin attenuates interleukin-6-mediated astrogliosis in human iPSC-derived neural aggregates: A candidate preventive substance for maternal immune activation-induced abnormalities

H. Hosoi, M. Morimoto, K. Ono, 2017, Neuroscience Letters.

Longitudinal change in white matter in preterm infants without magnetic resonance imaging abnormalities: Assessment of serial diffusion tensor imaging and their relationship to neurodevelopmental outcomes

Kei Yamada, H. Hosoi, M. Morimoto, 2016, Brain and Development.

Low-grade intraventricular hemorrhage disrupts cerebellar white matter in preterm infants: evidence from diffusion tensor imaging

Kei Yamada, H. Hosoi, M. Morimoto, 2015, Neuroradiology.

Mislocalization of syntaxin‐1 and impaired neurite growth observed in a human iPSC model for STXBP1‐related epileptic encephalopathy

N. Matsumoto, T. Nakahata, H. Hosoi, 2016, Epilepsia.

[Successful treatment with levetiracetam in a case of Ohtahara syndrome caused by STXBP1 mutation].

H. Hosoi, H. Saitsu, M. Morimoto, 2013, No to hattatsu = Brain and development.

From heterogeneous morphogenetic fields to homogeneous regions as a step towards understanding complex tissue dynamics.

François Graner, S. Yamashita, Boris Guirao, 2021, Development.

Impaired neuronal activity and differential gene expression in STXBP1 encephalopathy patient iPSC-derived GABAergic neurons.

Mami Shibata, H. Okano, M. Morimoto, 2021, Human molecular genetics.