The Human Fragile X Mental Retardation Protein Inhibits the Elongation Step of Translation through Its RGG and C-Terminal Domains
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0314, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.0c00534
Reference60 articles.
1. Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective
2. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells
3. The Unstable Repeats—Three Evolving Faces of Neurological Disease
4. DNA methylation represses FMR-1 transcription in fragile X syndrome
5. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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