ライフサイエンスコーパス: spout

1 ions (i.e., licking either a left or a right spout).

2 citric acid, quinine, and water) from a lick spout.

3 monitored by a capacitive touch-sensor water spout.

4 ock (0.35 mA) on Day 5 after approaching the spout.

5 gue kinematics in mice drinking from a water spout.

6 resulted in hypometric licks that missed the spout.

7 rcement after a tone (CS+) and to ignore the spout after a different tone (CS-).

8 ced with a water reward but responses to the spout after a negative conditional stimulus (CS-) were n

9 nd the ratio of air flow rate to the minimum spouting air flow rate (Q)) on the residual enzyme activ

10 prepolymer reagents, is entrained in a thin spout along with the oil.

11 rtheless, most biological assays of vascular spouting are conducted in a static mechanical milieu.

12 In this study, the spouted bed dryer was utilized for drying the garden rad

13 Overall, the results confirmed that a spouted bed reactor can be used as a promising method fo

14 For coffee roasted in a spouted bed reactor, the summation of the 16 PAHs ranged

15 re considerably improved after drying by the spouted bed.

16 in nonessential behaviors (e.g., licking on spouts beyond the period of reward delivery) and were sl

17 In a multi-spout brief-access consumption task, mice displayed lick

18 mesolimbic dopamine signals during the multi-spout brief-access task that display strong correlations

19 Belize, Central America, has yielded several spouted ceramic vessels that contain residues from the p

20 residue homodimeric protein belonging to the SPOUT class of methyltransferases.

21 ry similar to the conserved core fold of the SPOUT-class methyltransferases but contains a novel exte

22 valent to the cofactor-binding site in other SPOUT-class methyltransferases.

23 submovements, as well as errors in predicted spout contact.

24 with a deep trefoil knot in their catalytic (SPOUT) domain.

25 Herein, we describe current knowledge of SPOUT enzyme structure, domain architecture, and key ele

26 the process of substrate recognition by the SPOUT enzymes will be critical for defining many facets

27 ossessing the trefoil knot characteristic of SPOUT enzymes, Trm10 does not share the same quaternary

28 (such as cabbage, cauliflower, and brussels spouts), exhibits antitumor effects through poorly defin

29 e or key sequences with other members of the SPOUT family, suggesting a novel mechanism of catalysis.

30 that YOR021C is the first known MTase with a SPOUT fold that methylates a substrate other than RNA (p

31 e Trm10 family displays a typical SpoU-TrmD (SPOUT) fold.

32 rant box for a brief time before moving to a spout for reward collection.

33 imbic areas as rabbits learned to approach a spout for water reinforcement after a tone (CS+) and to

34 Here we show that mice trained to lick a dry spout in order to receive intra-gastric infusions of a f

35 e obtain a sugar water reward if they lick a spout in the presence of the rewarded odorant and avoid

36 The entrained particles eventually cause the spout interface to break, producing a thin coat of contr

37 rther distinguishing it from the other known SPOUT m1G methyltransferase, TrmD.

38 L30e-like amino-terminal domain (NTD) and a SPOUT methyltransferase family catalytic carboxyl-termin

39 s and the discovery of the dependence of one SPOUT methyltransferase on metal ion binding for catalys

40 th a new sequence alignment that divides the SPOUT methyltransferase superfamily into four major clad

41 The SpoU-TrmD (SPOUT) methyltransferase superfamily was designated when

42 et)-dependent alpha/beta-knot superfamily of SPOUT methyltransferases (MTases), with a high structura

43 SPOUT methyltransferases are found in all domains of lif

44 Our findings suggest a wider role for SPOUT methyltransferases in nature.

45 Modifications placed by SPOUT methyltransferases play diverse roles in regulatin

46 erestingly, Yor021c belongs to the family of SPOUT methyltransferases that, to date, have only been s

47 member of the alpha/beta-knot superfamily of SPOUT MTases in the RlmH or COG1576 family with bound Ad

48 ily to omit their prepotent responses to the spout on CS- trials.

49 Similarly, NBQX&NRP/GRP induced more spouting, regeneration or sparing of descending projecti

50 SPOUT1/CENP-32 encodes a putative SPOUT RNA methyltransferase previously identified as a m

51 Nep1 is a SPOUT RNA methyltransferase, and can catalyze methylatio

52 sented on disks attached to the tubes' metal spouts so the rats could only smell them.

53 er in solution, whereas other members of the SPOUT superfamily all function as homodimers.

54 The smallest member of the SPOUT superfamily of methyltransferases, RlmH lacks the

55 ferase (Trm10) is a member of the SpoU-TrmD (SPOUT) superfamily of methyltransferases, and Trm10 homo

56 ingual kinematics as mice drank from a water spout that unexpectedly changed position during licking,

57 ponses yielding oral contact with a drinking spout that was inserted into the conditioning chamber af

58 However, these vessels-which include a spout through which liquid could be poured-have also bee

59 MD neurons in mice allowed to freely lick a spout to obtain different tastes.

60 or fatty acids of residues from three small, spouted vessels that were found in Bronze and Iron Age g

61 aracteristics and structures of the original spouting vessels (stalks) from the choroid, polypoidal s

62 Transanal resection of an elongated IPAA spout was performed on 58 patients; abdominoperineal mob

63 n was apparent, and after 4 weeks, extensive spouting was observed throughout the entire dorsal horn,

64 Rats trained to drink from a spout were given a footshock (0.35 mA) on Day 5 after ap

65 ch task, ferrets were rewarded for licking a spout when they heard a target tone amid a sequence of r

66 to associate tastants sampled from a central spout with different actions (i.e., licking either a lef