ライフサイエンスコーパス: leucine enkephalin

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1 ity limit of 8 fmol has been established for leucine enkephalin.

2 a transmitters gastrin-releasing peptide and leucine-enkephalin.

3 des tested, only N, N-dibenzyl[Phe(p-NCS)(4)]leucine enkephalin (2) exhibited wash-resistant inhibiti

4 ne exception was N, N-dibenzyl[Phe(p-NCS)(4)]leucine enkephalin (2) which exhibited a 2-fold increase

5 Dilator responses to leucine enkephalin and dynorphin, endogenous delta and k

6 Leucine enkephalin and dynorphin-induced pial artery dil

7 milar inhibition by NOC/oFQ was observed for leucine enkephalin and dynorphin.

8 d as the biologically active conformation of leucine enkephalin and its methyl ester in the nonpolar

9 An equimolar mixture of leucine enkephalin and maltopentaose was studied to veri

10 molecules in droplets containing bradykinin, leucine enkephalin and myoglobin, but loss of the heme g

11 In this study Tyr residues of both leucine enkephalin and salmon calcitonin (sCT) were targ

12 FPI attenuated PACAP, methionine enkephalin, leucine enkephalin, and dynorphin induced elevations in

13 Leucine enkephalin- and dynorphin-induced dilation and a

14 Using leucine enkephalin as a diagnostic molecule, the fragmen

15 Mass spectra of leucine enkephalin, bradykinin, substance P, and polylys

16 A leucine enkephalin-coated surface demonstrated good line

17 s opiate receptor to the agonist D-alanine-5-leucine-enkephalin (DADLE) in wild-type and T149A mutant

18 ons of the opioids methionine enkephalin and leucine enkephalin during hypoxia in the newborn pig.

19 The transport of radiolabeled leucine enkephalin exhibits saturable kinetics, with a K

20 Here we present SID of leucine enkephalin, fibrinopeptide A, melittin, insulin

21 ine enkephalin and N,N-diallyl[Aib(2),Aib(3)]leucine enkephalin (ICI-174, 864) were substituted with

22 ion as shown by Perls' iron stain as well as leucine-enkephalin immunoreactivity, both markers for th

23 rijuana, releases endogenous dynorphin A and leucine enkephalin in the production of analgesia.

24 port, and chromatographic data indicate that leucine enkephalin is not hydrolyzed in the extracellula

25 Methionine-enkephalin (M-ENK) and leucine-enkephalin (L-ENK) are small endogenous opioid p

26 e also dually labeled for the opioid peptide leucine-enkephalin (L-ENK).

27 The delta-OPR agonist leucine-enkephalin (LE, 10(-8) mol/L) markedly inhibited

28 er methionine enkephalin (met-enkephalin) or leucine enkephalin (leu-enkephalin), we observed enkepha

29 stigated the effect of exposure to exogenous leucine-enkephalin (Leu-Enk), methionine-enkephalin (Met

30 ion in levels of the endogenous DOR peptide, leucine enkephalin, normally seen during SH, thus protec

31 Under these conditions, leucine-enkephalin present at concentrations as low as 1

32 tapeptides, including the endogenous opioids leucine enkephalin (Tyr-Gly-Gly-Phe-Leu) and methionine

33 res produced more methionine enkephalin than leucine enkephalin under basal conditions.

34 ptimal derivatization conditions for 1microM leucine-enkephalin were achieved when 10mM cysteine and

35 Somatostatin and leucine-enkephalin were homogeneously distributed throug

36 glycine and the fluorescamine derivative of leucine enkephalin, with the peak excitation cross secti

37 h of the five different residues of (Ala(2))-leucine enkephalin (YAGFL).

38 ed protonated C-terminally methyl esterified leucine enkephalin [YGGFL-OMe+H](+).

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