A noncanonical RNA-binding domain of the fragile X protein, FMRP, elicits translational repression independent of mRNA G-quadruplexes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference49 articles.
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2. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle;Science,1991
3. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
4. Fragile X genotype characterized by an unstable region of DNA;Yu;Science,1991
5. Autism symptoms in fragile X syndrome;Niu;J. Child Neurol.,2017
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1. Characterization of ribosome stalling and no-go mRNA decay stimulated by the fragile X protein, FMRP;Journal of Biological Chemistry;2024-08
2. Characterization of ribosome stalling and no-go mRNA decay stimulated by the Fragile X protein, FMRP;2024-02-04
3. Peptides and Peptide Derivatives as G‐Quadruplex Targeting Ligands: A Brief Review;ChemistrySelect;2023-09-07
4. Pumping the brakes: A noncanonical RNA-binding domain in FMRP stalls elongating ribosomes;Journal of Biological Chemistry;2023-01
5. In Vitro Analysis of Stalled Ribosomes using Puromycin Incorporation;BIO-PROTOCOL;2023
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