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1 rmed with 1-PCPA and mammalian mitochondrial monoamine oxidase B.
2 d selective inhibitor of brain mitochondrial monoamine oxidase B.
3 s formed during the bioactivation of MPTP by monoamine oxidase B.
4 g agent, flecainide, which has no recognized monoamine oxidase B activity, and which has previously b
5 example of a biorelevant synthetic model for monoamine oxidase B activity.
6 amine N-methyl transferase) and disposition (monoamine oxidase B and catechol-O-methyl transferase) o
7 ned most (50-60%) of marker enzyme activity, monoamine oxidase-B and porin proteins, but only about 2
8 ic groups that exist in catalytically active monoamine oxidase B are physically distinct.
9 rkinson's disease based on its inhibition of monoamine oxidase B, but the drug is also a potent state
10            We performed a genomewide scan of monoamine oxidase B for the Collaborative Study on the G
11 trate for the flavin-dependent mitochondrial monoamine oxidase B from bovine liver.
12 a targeting enzyme to disrupt the endogenous monoamine oxidase B gene in human cells.
13 onoamine oxidases with slight preference for monoamine oxidase B in both species.
14  SKF-38393 had no effects either on total or monoamine oxidase B in the striatum.
15   We report the effects of the addition of a monoamine oxidase B inhibitor, rasagiline, to antidepres
16 est placebo-controlled clinical trial of the monoamine oxidase B inhibitor, rasagiline, we examined h
17 2D6 inhibitor, quinidine, and also partly by monoamine oxidase B inhibitors deprenyl and pargyline.
18                                              Monoamine oxidase B inhibitors result in a mild improvem
19 his, a number of highly potent and selective monoamine oxidase B inhibitors were identified.
20 dowed with potent, selective, and reversible monoamine oxidase B inhibitory activity is a clinically
21                    Also, we demonstrate that monoamine oxidase B is an ERRalpha target gene whose exp
22 -deuterium-L-deprenyl ((11)C-DED) to measure monoamine oxidase B located in astrocytes.
23                                              Monoamine oxidase B (MAO B) catalyzes the oxidative deam
24 direct and continuous fluorometric assay for monoamine oxidase B (MAO B) has been developed.
25               The monotopic membrane protein monoamine oxidase B (MAO B) is an important drug target
26                                              Monoamine oxidase B (MAO B) is an integral protein of th
27 al reversible inhibitors selective for human monoamine oxidase B (MAO B) that do not inhibit MAO A ha
28 ture and subunit composition of bovine liver monoamine oxidase B (MAO B) was investigated using size-
29  (AD), i.e., acetylcholinesterase (AChE) and monoamine oxidase B (MAO B), a series of multitarget lig
30 time-dependent, irreversible inactivators of monoamine oxidase B (MAO B).
31  smokers show a 40% decrease in the level of monoamine oxidase B (MAO B; EC 1.4.3.4) relative to non-
32        A set of drugs was further studied in monoamine oxidase B (MAO-B) and cyclooxygenase-1 (COX-1)
33 mine and compare how two monotopic proteins, monoamine oxidase B (MAO-B) and cyclooxygenase-2 (COX-2)
34               Age-related increases in brain monoamine oxidase B (MAO-B) and its ability to produce r
35 l) is a selective, irreversible inhibitor of monoamine oxidase B (MAO-B) at the conventional dose (10
36 enosine receptors (A2AARs) and inhibition of monoamine oxidase B (MAO-B) in the brain are considered
37 mined the effects of GM1 ganglioside and the monoamine oxidase B (MAO-B) inhibitor L-deprenyl, alone
38 llular model of Parkinson's disease in which monoamine oxidase B (MAO-B) is overexpressed and which e
39 evious finding that smokers have lower brain monoamine oxidase B (MAO-B) levels than comparison nonsm
40                                          The monoamine oxidase B (MAO-B) substrate properties and dis
41                                              Monoamine oxidase B (MAO-B) was recently identified as a
42 e, competitive, and reversible inhibitors of monoamine oxidase B (MAO-B).
43 or (NMDAR), acetylcholinesterase (AChE), and monoamine oxidase B (MAO-B).
44 nt inhibitor of the flavin-containing enzyme monoamine oxidase B (MAO-B).
45                                              Monoamine oxidase-B (MAO-B) is a key enzyme in the catab
46                         MPTP is converted by monoamine oxidase-B (MAO-B) to its neurotoxic metabolite
47 diographically in conscious mice without the monoamine oxidase B (MAOB) gene (KO, n=11) and the corre
48 was found to suppress the gene expression of monoamine oxidase B (MAOB) in the brain of wild-type but
49 brane domains from the mitochondrial protein monoamine oxidase B (MaoB) or the endoplasmic reticulum
50 tural comparisons with human metabolites and monoamine oxidase B (MAOB) was identified as the putativ
51 oduce the inhibitory gliotransmitter GABA by monoamine oxidase-B (Maob) and abnormally release GABA t
52 ent complex I inhibitor and the two electron monoamine oxidase B oxidation product of MPTP.
53                                              Monoamine oxidase B, present in the mitochondrial outer
54 ate, decreased benzodiazepine, and increased monoamine oxidase B receptor binding have been reported.
55 nction and these include redox-related genes monoamine oxidase B, ryanodine receptor 2, and glutathio

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