Ionotropic and metabotropic glutamate receptor structure and pharmacology
By J. Kew, J. Kemp. Psychopharmacology, 2005
800 citations recorded by the source corpus.
Subfields: Biochemistry, Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/722300b1366ce5db0ea574c79dab39abb459ae54
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biochemistry
In Cellular and Molecular Neuroscience
In Molecular Biology
Citations in the corpus
- NMDA receptor subunits: function and pharmacology. (2007, background): “They are usually conformationally constrained amino acid derivatives containing an v-phosphonic group [21].”
- Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo (2006, background): “Of note, systemic delivery of LY367385 was not attempted due to its poor penetration across the blood-brain barrie”
- Glutamate and dopamine in schizophrenia: an update for the 21st century (2015, background): “Ionotropic glutamate receptors are named after the agonists originally found to selectively activate them: a-amino-3-hydroxy-5-methyl-4-isoazolepropionic acid (AMPA), kainate and N-methyl-D-aspartate (NMDA) (Dingledine et al., 1999; Kew and Kemp, 2005).”