Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila
SUMMARY Fragile X syndrome (FXS), the most common inherited determinant of intellectual disability and autism spectrum disorders, is caused by loss of the fragile X mental retardation 1 (FMR1) gene product (FMRP), an mRNA-binding translational repressor. A number of conserved FMRP targets have been...
Main Authors: | Samuel H. Friedman, Neil Dani, Emma Rushton, Kendal Broadie |
---|---|
Format: | Article |
Language: | English |
Published: |
The Company of Biologists
2013-11-01
|
Series: | Disease Models & Mechanisms |
Online Access: | http://dmm.biologists.org/content/6/6/1400 |
Similar Items
-
Fragile X Mental Retardation Protein Regulates Activity-Dependent Membrane Trafficking and Trans-Synaptic Signaling Mediating Synaptic Remodeling
by: James C. Sears, et al.
Published: (2018-01-01) -
Temporal requirements of the fragile X mental retardation protein in modulating circadian clock circuit synaptic architecture
by: Cheryl L Gatto, et al.
Published: (2009-08-01) -
The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neurons
by: Charles R. Tessier, et al.
Published: (2011-01-01) -
Neuron class-specific requirements for Fragile X Mental Retardation Protein in critical period development of calcium signaling in learning and memory circuitry
by: Caleb A. Doll, et al.
Published: (2016-05-01) -
Fragile X mental retardation protein and synaptic plasticity
by: Sidorov, Michael Samuel, et al.
Published: (2013)