New X-chromosomal interactors of dFMRP regulate axonal and synaptic morphology of brain neurons in Drosophila melanogaster

Fragile X syndrome is a neuro-developmental disease caused by transcriptional inactivation of the gene FMR1 (fragile X mental retardation 1) and loss of its protein product FMRP. FMRP has multiple neuronal functions which are implemented together with other proteins. To better understand these funct...

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Detalles Bibliográficos
Autores principales: Georgieva, Dimitrina, Dimitrov, Roumen, Kitanova, Meglena, Genova, Ginka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Article; Medical Biotechnology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684054/
https://www.ncbi.nlm.nih.gov/pubmed/26740770
http://dx.doi.org/10.1080/13102818.2014.937897

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684054/
https://www.ncbi.nlm.nih.gov/pubmed/26740770
http://dx.doi.org/10.1080/13102818.2014.937897

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