Synapse assembly and neurodevelopmental disorders
- PMID: 24990427
- PMCID: PMC4262893
- DOI: 10.1038/npp.2014.163
Synapse assembly and neurodevelopmental disorders
Abstract
In this review we examine the current understanding of how genetic deficits associated with neurodevelopmental disorders may impact synapse assembly. We then go on to discuss how the critical periods for these genetic deficits will shape the nature of future clinical interventions.
Figures
References
-
- Ahmari SE, Buchanan J, Smith SJ (2000). Assembly of presynaptic active zones from cytoplasmic transport packets. Nat Neurosci 3: 445–451. - PubMed
-
- Aldinger KA, Plummer JT, Qiu S, Levitt P (2011). SnapShot: genetics of autism. Neuron 72: 418–418 e411. - PubMed
-
- Auerbach BD, Osterweil EK, Bear MF (2011). Mutations causing syndromic autism define an axis of synaptic pathophysiology. Nature 480: 63–68 In this study, crosses of Fmr1 and Tsc2 mutant mice to each other demonstrate antagonistic roles for these genes in metabotropic glutamate receptor-dependent LTD that cancel each other out. - PMC - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
