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Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
Author(s) -
Nisha Raj,
Zachary T. McEachin,
William Harousseau,
Ying Zhou,
Feiran Zhang,
Megan E. Merritt-Garza,
J. Matthew Taliaferro,
Magdalena Kalinowska,
Samuele Marro,
Chadwick M. Hales,
Elizabeth BerryKravis,
Marisol WolfOchoa,
Verónica MartínezCerdeño,
Marius Wernig,
Lu Chen,
Eric Klann,
Stephen T. Warren,
Peng Jin,
Zhexing Wen,
Gary J. Bassell
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.108991
Subject(s) - neurogenesis , neural stem cell , fmr1 , fragile x syndrome , biology , translation (biology) , microbiology and biotechnology , pi3k/akt/mtor pathway , induced pluripotent stem cell , cell growth , progenitor cell , neurosphere , gene silencing , rna binding protein , cellular differentiation , stem cell , messenger rna , signal transduction , embryonic stem cell , genetics , adult stem cell , gene , fragile x

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