NMDA receptor function in inhibitory neurons
Neuropharmacology, ISSN: 0028-3908, Vol: 196, Page: 108609
2021
- 18Citations
- 44Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations18
- Citation Indexes18
- 18
- CrossRef13
- Captures44
- Readers44
- 44
Review Description
N -methyl- d -aspartate receptors (NMDARs) are present in the majority of brain circuits and play a key role in synaptic information transfer and synaptic plasticity. A key element of many brain circuits are inhibitory GABAergic interneurons that in themselves show diverse and cell-type-specific NMDAR expression and function. Indeed, NMDARs located on interneurons control cellular excitation in a synapse-type specific manner which leads to divergent dendritic integration properties amongst the plethora of interneuron subtypes known to exist. In this review, we explore the documented diversity of NMDAR subunit expression in identified subpopulations of interneurons and assess the NMDAR subtype-specific control of their function. We also highlight where knowledge still needs to be obtained, if a full appreciation is to be gained of roles played by NMDARs in controlling GABAergic modulation of synaptic and circuit function. This article is part of the 'Special Issue on Glutamate Receptors – NMDA receptors'.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0028390821001635; http://dx.doi.org/10.1016/j.neuropharm.2021.108609; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85108299791&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34000273; https://linkinghub.elsevier.com/retrieve/pii/S0028390821001635; https://dx.doi.org/10.1016/j.neuropharm.2021.108609
Elsevier BV
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