The nuclear isoforms of the Fragile X mental retardation RNA-binding protein associate with genomic DNA bridges

The fragile-X mental retardation protein (FMRP) is a canonical RNA-binding protein whose absence in humans leads to the development of the fragile-X syndrome, characterized by multiple phenotypes including neurodevelopmental disorders, intellectual disability, autism, and macroorchidism. The primary...

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Detalles Bibliográficos
Autores principales: Ledoux, N., Gauthier-Naud, W., Lavoie, O., Watters, V., Hussein, S., Adjibade, P., Mazroui, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2023
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162414/
https://www.ncbi.nlm.nih.gov/pubmed/36884289
http://dx.doi.org/10.1091/mbc.E22-05-0157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162414/
https://www.ncbi.nlm.nih.gov/pubmed/36884289
http://dx.doi.org/10.1091/mbc.E22-05-0157

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