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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                                              Phenylethanolamine N-methyltransferase (PNMT) is a criti
19 chain reaction, we detected a single form of phenylethanolamine N-methyltransferase (PNMT) mRNA in hy
20                                              Phenylethanolamine N-methyltransferase (PNMT) promoter-l
21  the most potent and selective inhibitors of phenylethanolamine N-methyltransferase (PNMT) reported t
22 mone epinephrine through its biosynthesis by phenylethanolamine N-methyltransferase (PNMT) via PNMT g
23 es (3-methyl-THIQs) are potent inhibitors of phenylethanolamine N-methyltransferase (PNMT), but are n
24            We report for the first time that phenylethanolamine N-methyltransferase (PNMT), proteasom
25 tional inhibitory activity of finasteride on phenylethanolamine N-methyltransferase (PNMT), the limit
26 n of the genes Tyrosine Hydroxylase (Th) and Phenylethanolamine N-methyltransferase (Pnmt), which als
27 re highly potent and selective inhibitors of phenylethanolamine N-methyltransferase (PNMT).
28                                   The enzyme phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2
29 -substituted-THIQs) are potent inhibitors of phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2
30 M, selectivity (alpha2 Ki/PNMT Ki) = 6.0) of phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2
31 9661, 1) is a potent inhibitor of the enzyme phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.2
32  -759 and -773 bp in the promoter of the rat phenylethanolamine N-methyltransferase (PNMT; EC 2.1.1.2
33 e synthesized and evaluated as inhibitors of phenylethanolamine N-methyltransferase (PNMT; EC 2.1.1.2
34 NK) and the epinephrine synthesizing enzyme, phenylethanolamine-N-methyltransferase (PNMT) in the sam
35          In the VMM and RVLM, immunoreactive phenylethanolamine-N-methyltransferase (PNMT) neurons we
36 mber of dopamine-beta-hydroxylase (DBH)- and phenylethanolamine-N-methyltransferase (PNMT)-positive n
37 reactive for tyrosine hydroxylase [TH-ir] or phenylethanolamine N-methyltransferase [PNMT-ir]).
38 pa decarboxylase, dopamine beta-hydroxylase, phenylethanolamine-N-methyltransferase, tryptophan hydro
39 in which the epinephrine-synthesizing enzyme phenylethanolamine N-methyltransferase was knocked out (
40 ne hydroxylase, dopamine ss-hydroxylase, and phenylethanolamine N-methyltransferase, we used coimmuno
41 e synthetic enzymes tyrosine hydroxylase and phenylethanolamine-N-methyltransferase were assayed.