Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
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Carbamazepine potentiates the effectiveness of morphine in a rodent model of neuropathic painVolatile anesthetics inhibit sodium channels without altering bulk lipid bilayer properties.Chimeric Glutamate Receptor Subunits Reveal the Transmembrane Domain Is Sufficient for NMDA Receptor Pore Properties but Some Positive Allosteric Modulators Require Additional Domains.Biphasic voltage-dependent inactivation of human NaV 1.3, 1.6 and 1.7 Na+ channels expressed in rodent insulin-secreting cells.
P2860
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 06 December 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@en
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@nl
type
label
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@en
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@nl
prefLabel
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@en
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@nl
P2860
P356
P1476
Sidedness of carbamazepine accessibility to voltage-gated sodium channels.
@en
P2093
Bruce P Bean
Sooyeon Jo
P2860
P304
P356
10.1124/MOL.113.090472
P577
2013-12-06T00:00:00Z