The fragile X mental retardation protein is associated with ribosomes
- 1 January 1996
- journal article
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 12 (1), 91-93
- https://doi.org/10.1038/ng0196-91
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- FMR1 Protein: Conserved RNP Family Domains and Selective RNA BindingScience, 1993
- The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationNature Genetics, 1993
- The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding proteinCell, 1993
- Characterization and localization of the FMR-1 gene product associated with fragile X syndromeNature, 1993
- Regulation of Translation in Eukaryotic SystemsAnnual Review of Cell Biology, 1992
- DNA methylation represses FMR-1 transcription in fragile X syndromeHuman Molecular Genetics, 1992
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nScience, 1991
- Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X SyndromeScience, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 1991