Zobrazeno 1 - 2
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pro vyhledávání: '"Lital Gildin"'
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 16; Pages: 9278
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c9dc8f42b82747e38a59e53f8c75283
https://doi.org/10.3390/ijms23169278
https://doi.org/10.3390/ijms23169278
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; Volume 23; Issue 4; Pages: 2048
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c38d0116bad711fb2fca27287df9a9
https://doi.org/10.3390/ijms23042048
https://doi.org/10.3390/ijms23042048