The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity

Mutations and deletions of the interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene, located on the X chromosome, are associated with intellectual disability (ID) and autism spectrum disorder (ASD). IL1RAPL1 protein is located at the postsynaptic compartment of excitatory synapses and pla...

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Vydáno v:J Neurosci
Hlavní autoři: Montani, Caterina, Ramos-Brossier, Mariana, Ponzoni, Luisa, Gritti, Laura, Cwetsch, Andrzej W., Braida, Daniela, Saillour, Yoann, Terragni, Benedetta, Mantegazza, Massimo, Sala, Mariaelvina, Verpelli, Chiara, Billuart, Pierre, Sala, Carlo
Médium: Artigo
Jazyk:Inglês
Vydáno: Society for Neuroscience 2017
Témata:
Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6596553/
https://ncbi.nlm.nih.gov/pubmed/28576939
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3775-16.2017
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