A carregar...
Fmr1 deletion enhances and ultimately desensitizes CB(1) signaling in autaptic hippocampal neurons
Fragile X Syndrome (FXS) is a heritable form of mental retardation caused by a non-coding trinucleotide expansion of the FMR1 gene leading to loss of expression of this RNA binding protein. Mutations in this gene are strongly linked to enhanced Group I metabotropic glutamate receptor (mGluR) signali...
Na minha lista:
| Main Authors: | , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3702050/ https://ncbi.nlm.nih.gov/pubmed/23578490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2013.04.002 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|