A Novel Function for Fragile X Mental Retardation Protein in Translational Activation

Fragile X syndrome, the most frequent form of inherited mental retardation, is due to the absence of Fragile X Mental Retardation Protein (FMRP), an RNA-binding protein involved in several steps of RNA metabolism. To date, two RNA motifs have been found to mediate FMRP/RNA interaction, the G-quartet...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Bechara, Elias G, Didiot, Marie Cecile, Melko, Mireille, Davidovic, Laetitia, Bensaid, Mounia, Martin, Patrick, Castets, Marie, Pognonec, Philippe, Khandjian, Edouard W, Moine, Hervé, Bardoni, Barbara
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2628407/
https://ncbi.nlm.nih.gov/pubmed/19166269
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pbio.1000016
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares