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1 ock (0.35 mA) on Day 5 after approaching the spout.
2 rcement after a tone (CS+) and to ignore the spout after a different tone (CS-).
3 ced with a water reward but responses to the spout after a negative conditional stimulus (CS-) were n
4  prepolymer reagents, is entrained in a thin spout along with the oil.
5 rtheless, most biological assays of vascular spouting are conducted in a static mechanical milieu.
6                      For coffee roasted in a spouted bed reactor, the summation of the 16 PAHs ranged
7  in nonessential behaviors (e.g., licking on spouts beyond the period of reward delivery) and were sl
8 Belize, Central America, has yielded several spouted ceramic vessels that contain residues from the p
9 residue homodimeric protein belonging to the SPOUT class of methyltransferases.
10 ry similar to the conserved core fold of the SPOUT-class methyltransferases but contains a novel exte
11 valent to the cofactor-binding site in other SPOUT-class methyltransferases.
12 ossessing the trefoil knot characteristic of SPOUT enzymes, Trm10 does not share the same quaternary
13  (such as cabbage, cauliflower, and brussels spouts), exhibits antitumor effects through poorly defin
14 e or key sequences with other members of the SPOUT family, suggesting a novel mechanism of catalysis.
15 that YOR021C is the first known MTase with a SPOUT fold that methylates a substrate other than RNA (p
16 e Trm10 family displays a typical SpoU-TrmD (SPOUT) fold.
17 imbic areas as rabbits learned to approach a spout for water reinforcement after a tone (CS+) and to
18 Here we show that mice trained to lick a dry spout in order to receive intra-gastric infusions of a f
19 The entrained particles eventually cause the spout interface to break, producing a thin coat of contr
20 rther distinguishing it from the other known SPOUT m1G methyltransferase, TrmD.
21  L30e-like amino-terminal domain (NTD) and a SPOUT methyltransferase family catalytic carboxyl-termin
22 et)-dependent alpha/beta-knot superfamily of SPOUT methyltransferases (MTases), with a high structura
23        Our findings suggest a wider role for SPOUT methyltransferases in nature.
24 erestingly, Yor021c belongs to the family of SPOUT methyltransferases that, to date, have only been s
25 member of the alpha/beta-knot superfamily of SPOUT MTases in the RlmH or COG1576 family with bound Ad
26 ily to omit their prepotent responses to the spout on CS- trials.
27         Similarly, NBQX&NRP/GRP induced more spouting, regeneration or sparing of descending projecti
28                                    Nep1 is a SPOUT RNA methyltransferase, and can catalyze methylatio
29 sented on disks attached to the tubes' metal spouts so the rats could only smell them.
30 er in solution, whereas other members of the SPOUT superfamily all function as homodimers.
31                   The smallest member of the SPOUT superfamily of methyltransferases, RlmH lacks the
32 ferase (Trm10) is a member of the SpoU-TrmD (SPOUT) superfamily of methyltransferases, and Trm10 homo
33 ponses yielding oral contact with a drinking spout that was inserted into the conditioning chamber af
34 aracteristics and structures of the original spouting vessels (stalks) from the choroid, polypoidal s
35     Transanal resection of an elongated IPAA spout was performed on 58 patients; abdominoperineal mob
36 n was apparent, and after 4 weeks, extensive spouting was observed throughout the entire dorsal horn,
37                 Rats trained to drink from a spout were given a footshock (0.35 mA) on Day 5 after ap
38 ch task, ferrets were rewarded for licking a spout when they heard a target tone amid a sequence of r

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