A carregar...
Fragile X Mental Retardation Protein Interactions with a G quadruplex structure in the 3′-Untranslated Region of NR2B mRNA
Fragile X syndrome, the most common cause of inherited intellectual disability, is caused by a trinucleotide CGG expansion in the 5′-untranslated region of the FMR1 gene, which leads to the loss of expression of the fragile X mental retardation protein (FMRP). FMRP, an RNA-binding protein that regul...
Na minha lista:
| Publicado no: | Mol Biosyst |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4643373/ https://ncbi.nlm.nih.gov/pubmed/26412477 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c5mb00423c |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|