about
Ion channels as drug targets in central nervous system disordersBeyond classical benzodiazepines: novel therapeutic potential of GABAA receptor subtypes.The Concise Guide to PHARMACOLOGY 2013/14: G protein-coupled receptorsCurcumol allosterically modulates GABA(A) receptors in a manner distinct from benzodiazepines.GAT-1 mediated GABA uptake in rat oligodendrocytes.Benzodiazepines revisited--will we ever learn?Alleviation of pain in painful diabetic neuropathy.The enantiomers of syn-2,3-difluoro-4-aminobutyric acid elicit opposite responses at the GABA(C) receptor.Welcome to 'GABAergic drugs'.Agonists of the γ-aminobutyric acid type B (GABAB) receptor derived from β-hydroxy and β-amino difluoromethyl ketones.Drugging the undruggable: gabapentin, pregabalin and the calcium channel α2δ subunit.
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
An historical perspective on GABAergic drugs.
@en
An historical perspective on GABAergic drugs.
@nl
type
label
An historical perspective on GABAergic drugs.
@en
An historical perspective on GABAergic drugs.
@nl
prefLabel
An historical perspective on GABAergic drugs.
@en
An historical perspective on GABAergic drugs.
@nl
P2860
P356
P1476
An historical perspective on GABAergic drugs.
@en
P2093
Wolfgang Froestl
P2860
P304
P356
10.4155/FMC.10.285
P577
2011-02-01T00:00:00Z