Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis.
Raj N, McEachin ZT, Harousseau W, Zhou Y, Zhang F, Merritt-Garza ME, Taliaferro JM, Kalinowska M, Marro SG, Hales CM, Berry-Kravis E, Wolf-Ochoa MW, Martinez-Cerdeño V, Wernig M, Chen L, Klann E, Warren ST, Jin P, Wen Z, Bassell GJ.
Raj N, et al. Among authors: wolf ochoa mw.
Cell Rep. 2021 Apr 13;35(2):108991. doi: 10.1016/j.celrep.2021.108991.
Cell Rep. 2021.
PMID: 33852833
Free PMC article.