ライフサイエンスコーパス: phenylethanolamine N-methyltransferase

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1 tained for c-Fos, dopamine beta-hydroxylase, phenylethanolamine-N-methyltransferase, and glucagon-lik

2 ownregulated B2AR, tyrosine hydroxylase, and phenylethanolamine-N-methyltransferase expression, but p

3 The X-ray structure of human phenylethanolamine N-methyltransferase (hPNMT) complexed

4 tent of the epinephrine synthesizing enzyme, phenylethanolamine N-methyltransferase, immunohistochemi

5 s labeled with biotinamide were examined for phenylethanolamine N-methyltransferase immunoreactivity

6 nes for nicotinamide N-methyltransferase and phenylethanolamine N-methyltransferase in several specie

7 nes for nicotinamide N-methyltransferase and phenylethanolamine N-methyltransferase in several specie

8 lase, and dopamine beta-hydroxylase, but not phenylethanolamine-N-methyltransferase, indicating inner

9 Interestingly, phenylethanolamine N-methyltransferase KO did not change

10 sine hydroxylase, dopamine beta-hydroxylase, phenylethanolamine-N-methyltransferase, neuronal nitric

11 -fluoromethyl-THIQs) was proposed, and their phenylethanolamine N-methyltransferase (PNMT) and alpha(

12 s synthesized and evaluated as inhibitors of phenylethanolamine N-methyltransferase (PNMT) and as inh

13 abeling experiments using antibodies against phenylethanolamine N-methyltransferase (PNMT) and cholin

14 The rat phenylethanolamine N-methyltransferase (PNMT) gene promo

15 combinase under the chromaffin cell-specific phenylethanolamine N-methyltransferase (PNMT) gene promo

16 introduced into murine cells expressing the Phenylethanolamine n-methyltransferase (Pnmt) gene, whic

17 21) were synthesized and evaluated for their phenylethanolamine N-methyltransferase (PNMT) inhibitory

18 chain reaction, we detected a single form of phenylethanolamine N-methyltransferase (PNMT) mRNA in hy

19 Phenylethanolamine N-methyltransferase (PNMT) promoter-l

20 the most potent and selective inhibitors of phenylethanolamine N-methyltransferase (PNMT) reported t

21 mone epinephrine through its biosynthesis by phenylethanolamine N-methyltransferase (PNMT) via PNMT g

22 es (3-methyl-THIQs) are potent inhibitors of phenylethanolamine N-methyltransferase (PNMT), but are n

23 We report for the first time that phenylethanolamine N-methyltransferase (PNMT), proteasom

24 n of the genes Tyrosine Hydroxylase (Th) and Phenylethanolamine N-methyltransferase (Pnmt), which als

25 re highly potent and selective inhibitors of phenylethanolamine N-methyltransferase (PNMT).

26 -substituted-THIQs) are potent inhibitors of phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2

27 M, selectivity (alpha2 Ki/PNMT Ki) = 6.0) of phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2

28 9661, 1) is a potent inhibitor of the enzyme phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2

29 -759 and -773 bp in the promoter of the rat phenylethanolamine N-methyltransferase (PNMT; EC 2.1.1.2

30 e synthesized and evaluated as inhibitors of phenylethanolamine N-methyltransferase (PNMT; EC 2.1.1.2

31 NK) and the epinephrine synthesizing enzyme, phenylethanolamine-N-methyltransferase (PNMT) in the sam

32 In the VMM and RVLM, immunoreactive phenylethanolamine-N-methyltransferase (PNMT) neurons we

33 mber of dopamine-beta-hydroxylase (DBH)- and phenylethanolamine-N-methyltransferase (PNMT)-positive n

34 reactive for tyrosine hydroxylase [TH-ir] or phenylethanolamine N-methyltransferase [PNMT-ir]).

35 pa decarboxylase, dopamine beta-hydroxylase, phenylethanolamine-N-methyltransferase, tryptophan hydro

36 in which the epinephrine-synthesizing enzyme phenylethanolamine N-methyltransferase was knocked out (

37 ne hydroxylase, dopamine ss-hydroxylase, and phenylethanolamine N-methyltransferase, we used coimmuno

38 e synthetic enzymes tyrosine hydroxylase and phenylethanolamine-N-methyltransferase were assayed.

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