The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B.
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From molecular phylogeny towards differentiating pharmacology for NMDA receptor subtypesAntagonistic action on NMDA/GluN2B mediated currents of two peptides that were conantokin-G structure-based designedConantokins derived from the Asprella clade impart conRl-B, an N-methyl d-aspartate receptor antagonist with a unique selectivity profile for NR2B subunits.Probing NMDA receptor GluN2A and GluN2B subunit expression and distribution in cortical neurons.Pharmacology of triheteromeric N-Methyl-D-Aspartate Receptors.Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.
P2860
The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B.
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2009 nî lūn-bûn
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2009年の論文
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name
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@en
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@nl
type
label
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@en
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@nl
prefLabel
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@en
The selectivity of conantokin- ...... dues in the S2 region of NR2B.
@nl
P2093
P2860
P1433
P1476
The selectivity of conantokin- ...... idues in the S2 region of NR2B
@en
P2093
Francis J Castellino
Mary Prorok
Zhenyu Sheng
Zhong Liang
P2860
P304
P356
10.1016/J.NEUROPHARM.2009.04.014
P577
2009-05-08T00:00:00Z