Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis

por Raj, Nisha, McEachin, Zachary T., Harousseau, William, Zhou, Ying, Zhang, Feiran, Merritt-Garza, Megan E., Taliaferro, J. Matthew, Kalinowska, Magdalena, Marro, Samuele G., Hales, Chadwick M., Berry-Kravis, Elizabeth, Wolf-Ochoa, Marisol W., Martinez-Cerdeño, Veronica, Wernig, Marius, Chen, Lu, Klann, Eric, Warren, Stephen T., Jin, Peng, Wen, Zhexing, Bassell, Gary J.
Publicado 2021