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pro vyhledávání: '"Lital Gildin"'
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 16, p 9278 (2022)
Fragile X Syndrome (FXS) is the main genetic reason for intellectual disability and is caused by the silencing of fragile X mental retardation protein (FMRP), an RNA-binding protein regulating the translation of many neuronal mRNAs. Neural differenti
Externí odkaz:
https://doaj.org/article/07bc99503a9144cb82004383ca9f4b33
Autor:
Lital Gildin, Rossana Rauti, Ofir Vardi, Liron Kuznitsov-Yanovsky, Ben M. Maoz, Menahem Segal, Dalit Ben-Yosef
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 4, p 2048 (2022)
Fragile X syndrome (FXS), the most common form of inherited intellectual disability, is caused by a developmentally regulated silencing of the FMR1 gene, but its effect on human neuronal network development and function is not fully understood. Here,
Externí odkaz:
https://doaj.org/article/5549077711264e5baf7bc5c2ce49e4de