Birnbaum, R., Weinberger, D.R., 2017. Genetic insights into the neurodevelopmental
origins of schizophrenia. Nat. Rev. Neurosci. 18 (12), 727–740.
Nakagawa, M., Taniguchi, Y., Senda, S., Takizawa, N., Ichisaka, T., Asano, K.,
Morizane, A., Doi, D., Takahashi, J., Nishizawa, M., Yoshida, Y., Toyoda, T.,
Osafune, K., Sekiguchi, K., Yamanaka, S., 2014. A novel efficient feeder-free culture
system for the derivation of human induced pluripotent stem cells. Sci. Rep. 4, 3594.
Okita, K., Yamakawa, T., Matsumura, Y., Sato, Y., Amano, N., Watanabe, A.,
Goshima, N., Yamanaka, S., 2013. An efficient nonviral method to generate
integration-free human-induced pluripotent stem cells from cord blood and
peripheral blood cells. Stem Cells 31, 458–466.
Tamminga, C.A., Holcomb, H.H., 2005. Phenotype of schizophrenia: a review and
formulation. Mol. Psychiatry 10 (1), 27–39.
4.6. Flow cytometry analysis
iPSCs were treated with Accumax (Innovative Cell Technologies, San
Diego, CA, US) and dissociated into single cells. Then, the cells were
incubated at 1.0 × 106 cells/ml concentration in PBS containing 2% FBS
and 20 µl SSEA-4 APC conjugated monoclonal antibody (BD Biosciences,
Franklin Lakes, NJ, US) for 30 min at 4 ◦ C. The cells were washed twice
with PBS containing 2% FBS and analyzed by FACSAria (BD
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