ライフサイエンスコーパス: curare

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

1 e central command influence) using Norcuron (curare).

2 ta (deltaTrp-57) subunits that interact with curare.

3 ine < nicotine < acetylcholine < carbachol < curare.

4 species differences in circuit responses to curare.

5 ocked by alpha-bungarotoxin (0.2 microM) and curare (1 microM).

6 gesting that this residue may be involved in curare-5HT3R interactions.

7 e-field areas, we have exposed the retina to curare, a nicotinic cholinergic antagonist, because spon

8 Within this region of the receptor, curare affinity is reduced by substitution only at Trp-8

9 mitted the first successful entry toward the curare alkaloids (+/-)-tubocurine and (+/-)-curine.

10 in seconds after contact and were blocked by curare and alpha-bungarotoxin, but not by TTX and Cd(2+)

11 ependent synaptic transmission is blocked by curare and by alpha-bungarotoxin (alpha-BTX).

12 The nicotinic antagonists curare and dihydro-beta-erythroidine also up-regulated a

13 he affinity of the 5HT3R for the antagonists curare and granisetron but has little effect on the affi

14 Exposure to cholinergic antagonists, curare and hexamethonium bromide, which block chemical n

15 In Melibe, curare application caused the burst duration of the swim

16 tagonist [alpha-bungarotoxin (alpha-BTX) and curare] binding, these results indicate that mAbs could

17 In both species, replacing the curare-blocked Si3 synapses with artificial synapses usi

18 Application of curare (d-tubocurarine) selectively blocked the Si3 syna

19 structural level, we studied binding of the curare derivatives d-tubocurarine (d-TC) and metocurine

20 pattern to lengthen, whereas in Dendronotus, curare halted bursting altogether.

21 The competitive antagonist d-tubocurarine (curare) has greater potency at mouse than at human 5-hyd

22 mutant receptor, H-K195E,V202I, had the same curare IC50 (133.8 +/- 6.38 nM) as that of the human rec

23 contribute to curare potency, given that the curare IC50's (concentration of drug that produces 50% i

24 (H-K195E or H-V202I) had significantly lower curare IC50's than that of the human receptor.

25 The curare-impaired bursting in Dendronotus was also restore

26 eceptive fields of ganglion cells exposed to curare in hatchlings reared in normal light and dark cyc

27 aneous bursting was chronically blocked with curare in hatchlings, dark-induced expansion of receptiv

28 nanomolar concentrations of d-tubocurarine (curare) in a competitive fashion.

29 title compounds (19, 20ab, and 26) displayed curare-like effects of ultrashort duration in rhesus mon

30 at can be further enhanced by treatment with curare or alpha-BTX, suggesting that muscle paralysis ma

31 line receptor (nAChR)-blocking agents [e.g., curare or alpha-bungarotoxin (alpha-BTX)] prevents the d

32 ke a significant contribution in determining curare potency at the 5-HT3A receptor.

33 significant role in conferring interspecies curare potency differences.

34 ata suggest that loops C and F contribute to curare potency, given that the curare IC50's (concentrat

35 [(3)H]Curare preferentially binds the alpha/gamma interface.

36 nstrate that blocking synaptic activity with curare reduces synaptic neuregulin expression in a dose-

37 approximately 30 degrees degree tilt of the curare scaffold within the binding pocket.

38 This blocking mechanism was tested using curare to demonstrate the open channel nature of the blo

39 Curare was released from Elvax, a slow-release polymer t

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。