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Structural and Functional Characterization of a Novel α-Conotoxin Mr1.7 from Conus marmoreus Targeting Neuronal nAChR α3β2, α9α10 and α6/α3β2β3 Subtypes.TRPing on the pore phenomenon: what do we know about transient receptor potential ion channel-related pore dilation up to now?Bivalent ligand that activates mu opioid receptor and antagonizes mGluR5 receptor reduces neuropathic pain in mice.
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description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 23 February 2012
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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
Receptor and channel heteromers as pain targets.
@en
Receptor and channel heteromers as pain targets.
@nl
type
label
Receptor and channel heteromers as pain targets.
@en
Receptor and channel heteromers as pain targets.
@nl
prefLabel
Receptor and channel heteromers as pain targets.
@en
Receptor and channel heteromers as pain targets.
@nl
P2093
P2860
P356
P1433
P1476
Receptor and channel heteromers as pain targets.
@en
P2093
Amol M Patwardhan
Armen N Akopian
Kelly A Berg
P2860
P304
P356
10.3390/PH5030249
P577
2012-02-23T00:00:00Z