ライフサイエンスコーパス: gamma-aminobutyric acid receptor

1 cient synaptic inhibition upon activation of gamma-aminobutyric acid receptors.

2 also includes the metabotropic glutamate and gamma-aminobutyric acid receptors.

3 dopamine and muscarinic cholinergic, but not gamma-aminobutyric acid receptors.

4 by picrotoxin, an antagonist of the GABA(A) (gamma-aminobutyric acid) receptor.

5 entiate neuronal inhibition through GABA(A) (gamma-aminobutyric acid) receptors.

6 onal cell-surface antibodies, mainly against gamma-aminobutyric acid receptors (53% vs 11%; P < .001)

7 ethyl-d-aspartate receptor in 4 patients and gamma-aminobutyric acid receptor A in 1 patient of 111 p

8 In the A-type gamma-aminobutyric acid receptor, a threonine residue in

9 Gamma-aminobutyric acid receptor agonist medications are

10 piramate-a glutamate receptor antagonist and gamma-aminobutyric acid receptor agonist-would result in

11 he known subunit stoichiometry of the A-type gamma-aminobutyric acid receptor allowed us to create re

12 acts as a non-competitive antagonist of the gamma-aminobutyric acid receptor and has shown prolonged

13 enhance inhibitory transmission mediated by gamma-aminobutyric acid receptors and have anticonvulsan

14 Incubation with the gamma-aminobutyric acid receptor antagonist bicuculline

15 hreshold dose of picrotoxin, a use-dependent gamma-aminobutyric acid receptor antagonist, reduces cor

16 Ionotropic gamma-aminobutyric acid receptors are primary ligand-gat

17 ter-operated ion channels, such as the GABA (gamma-aminobutyric acid) receptor, are important in fast

18 le-associated protein 1 light chain 3 (LC3), gamma-aminobutyric acid receptor-associated protein (GAB

19 The gamma-aminobutyric acid receptor-associated protein (GAB

20 of reduced lysosomal degradation of RhoB in Gamma-aminobutyric acid receptor-associated protein (GAB

21 Baclofen, a gamma-aminobutyric acid receptor(B) agonist, is used to

22 Six markers for five genes, gamma-aminobutyric acid receptor beta3 (Gabrb3), syntaxi

23 by disinhibition because local antagonism of gamma-aminobutyric acid receptors blocked responses to C

24 etylcholine receptor for neonicotinoids, the gamma-aminobutyric acid receptor/chloride channel for po

25 and pharmacological evidence that ionotropic gamma-aminobutyric acid receptors contribute to fluid tr

26 +/- 9% enhancement) than it was at enhancing gamma-aminobutyric acid receptor current (3 +/- 3% enhan

27 n N-methyl-D-aspartate receptor currents and gamma-aminobutyric acid receptor currents within the sam

28 E cells juxtaposed next to cohorts of normal gamma-aminobutyric acid receptor expressing secretory ce

29 Novel gamma-aminobutyric acid receptor (GABA(A)R) ligands stru

30 nscriptional control of the mammalian type A gamma-aminobutyric acid receptor (GABA(A)R) subunit gene

31 The regulated expression of type A gamma-aminobutyric acid receptor (GABA(A)R) subunit gene

32 amic activation process for the metabotropic gamma-aminobutyric acid receptor (GABA(B)R) based on ext

33 Metabotropic gamma-aminobutyric acid receptor (GABA(B)R), a class C G

34 the Ca(2+)-sensing receptor (CaR) and type B gamma-aminobutyric acid receptor (GABA-B-R) from human e

35 xpression of delta-subunit containing type A gamma-aminobutyric acid receptors (GABA(A)(delta)R) incr

36 Gamma-aminobutyric acid receptors (GABA(A)R) are the maj

37 Changes in the function of type A gamma-aminobutyric acid receptors (GABA(A)Rs) are associ

38 Type A gamma-aminobutyric acid receptors (GABA(A)Rs) are pentam

39 Type A gamma-aminobutyric acid receptors (GABA(A)Rs) are the pr

40 Type A gamma-aminobutyric acid receptors (GABA(A)Rs) represent

41 which drive neuronal excitation, and type A gamma-aminobutyric acid receptors (GABA(A)Rs), which are

42 ized populations of extrasynaptic receptors, gamma-aminobutyric acid receptors (GABA(A)Rs).

43 Metabotropic gamma-aminobutyric acid receptors (GABA(B)) are involved

44 cently become appreciated that activation of gamma-aminobutyric acid receptors (GABA-Rs) on ss-cells

45 Type A GABA (gamma-aminobutyric acid) receptors (GABA(A) receptors) m

46 oxication causes changes in the rodent brain gamma-aminobutyric acid receptor (GABAAR) subunit compos

47 receptor in the central nervous system, the gamma-aminobutyric acid receptor (GABAAR).

48 stsynaptic potentials mediated by ionotropic gamma-aminobutyric acid receptors (GABAARs) and glycine

49 Type-A gamma-aminobutyric acid receptors (GABAARs) are the prin

50 The accumulation of gamma-aminobutyric acid receptors (GABAARs) at the appro

51 Mechanisms controlling the metabotropic gamma-aminobutyric acid receptor (GABAB) cell surface st

52 t rapid antidepressants cause a shift in the gamma-aminobutyric acid receptor (GABABR) signaling path

53 Upon activation by agonist, the type A gamma-aminobutyric acid receptor (GABAR) 'gates', allowi

54 ange the type of excitability: a depolarized gamma-Aminobutyric acid receptor (GABAR) reversal potent

55 A single point mutation in the insect gamma-aminobutyric acid receptor (GABAR)-encoding gene (

56 dentified, including one disrupting multiple gamma-aminobutyric acid receptor genes.

57 ciation with variants of the enthoprotin and gamma-aminobutyric acid receptor genes.

58 peptide (AgRP) neurons because inhibition of gamma-aminobutyric acid receptor in the ARC did not prev

59 igated the role of regionally discrete GABA (gamma-aminobutyric acid) receptors in the sedative respo

60 n of unknown function isolated previously as gamma-aminobutyric acid receptor-interacting factor 1 (G

61 Here, we report a novel function of gamma-aminobutyric acid receptors involving alveolar flu

62 macologically distinct ionotropic receptors: gamma-aminobutyric acid receptors, levamisole-sensitive

63 The effect is caused by a decrease in type A gamma-aminobutyric acid receptor-mediated inhibition of

64 IPSPs were comprised of GABAA and GABAB (gamma-aminobutyric acid) receptor-mediated components.

65 sed by cocaine-induced reduction of GABA(A) (gamma-aminobutyric acid) receptor-mediated inhibition of

66 Neither inhibitors of gamma-aminobutyric acid receptors nor an inhibitor of pr

67 ated the expression of functional ionotropic gamma-aminobutyric acid receptors on the apical plasma m

68 Reduction of the gamma-aminobutyric acid receptor pi subunit using RNA in

69 ministration model, we studied glutamate and gamma-aminobutyric acid receptor regulation in the synap

70 Type A GABA (gamma-aminobutyric acid) receptors represent a diverse p

71 lar endothelial growth factor, integrin, and gamma-aminobutyric acid receptor signaling cascades, plu

72 s, and behavioral results suggest that local gamma-aminobutyric acid receptor signaling mediates the

73 g amylin's effects on energy balance through gamma-aminobutyric acid receptor signaling.

74 ficant association with polymorphisms in the gamma-aminobutyric acid receptor subunit B3 gene (GABRB3

75 on chromosome 15 to an area surrounding the gamma-aminobutyric acid-receptor subunit genes, in AutD,

76 e identified with differential expression of gamma-aminobutyric acid receptor subunits and transporte

77 ved from studies of anesthetic resistance in gamma aminobutyric acid receptors, tandem pore potassium

78 inactivation of BLA by microinfusion of the gamma-aminobutyric acid receptor type A agonist muscimol

79 physiological studies have demonstrated that gamma-aminobutyric acid receptors type A (GABA(A)) media

80 steroids on neural transmission mediated by gamma-aminobutyric acid receptors within forebrain neuro