Cytoplasmic Polyadenylation Element-Binding Protein 1 Post-transcriptionally Regulates Fragile X Mental Retardation 1 Expression Through 3′ Untranslated Region in Central Nervous System Neurons

Fragile X syndrome (FXS) is an inherited intellectual disability caused by a deficiency in Fragile X mental retardation 1 (Fmr1) gene expression. Recent studies have proposed the importance of cytoplasmic polyadenylation element-binding protein 1 (CPEB1) in FXS pathology; however, the molecular inte...

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Detalles Bibliográficos
Autores principales: Oe, Souichi, Hayashi, Shinichi, Tanaka, Susumu, Koike, Taro, Hirahara, Yukie, Seki-Omura, Ryohei, Kakizaki, Rio, Sakamoto, Sumika, Nakano, Yosuke, Noda, Yasuko, Yamada, Hisao, Kitada, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051318/
https://www.ncbi.nlm.nih.gov/pubmed/35496917
http://dx.doi.org/10.3389/fncel.2022.869398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051318/
https://www.ncbi.nlm.nih.gov/pubmed/35496917
http://dx.doi.org/10.3389/fncel.2022.869398

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