NMDA receptor subunits: function and pharmacology.

By P. Paoletti, J. Neyton. Current opinion in pharmacology (Print), 2007

963 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Spectroscopy

View Paper: https://www.semanticscholar.org/paper/02481fe0249ecfd32f0dcf5cff144f2b4af8e961

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cellular and Molecular Neuroscience

1. Jie Zheng
2. Stephane Oliet
3. P. Maher
4. Jana Lewerenz
5. M. Trudeau

In Molecular Biology

1. Jie Zheng
2. P. Maher
3. Jana Lewerenz
4. M. Trudeau

In Spectroscopy

1. Jie Zheng
2. M. Trudeau

Citations in the corpus

• Chronic Glutamate Toxicity in Neurodegenerative Diseases—What is the Evidence? (2015, background): “NMDA receptors are tetramers containing two NR1 subunits and two NR2 or NR3 subunits (Paoletti and Neyton, 2007).”
• Handbook of ion channels (2015, background): “Other channels, such as the NMDA or GABA receptors, are intrinsically composed of different subunits (99,100).”
• Synaptic and extrasynaptic NMDA receptors are gated by different endogenous coagonists. (2012, methodology): “Conversely, 250 nM of free zinc (Experimental Procedures), a highly specific allosteric inhibitor of GluN2A-NMDARs that acts as a partial antagonist (Paoletti et al., 1997; Paoletti and Neyton, 2007), strongly reduced synaptic NMDAR-fEPSPs (Figure 1C).”