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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                   Harmol or a combination of monoamine oxidase B and GABA-A receptor modulators exten
8  results reveal that peripheral targeting of monoamine oxidase B and GABA-A receptor, common antidepr
9 ned most (50-60%) of marker enzyme activity, monoamine oxidase-B and porin proteins, but only about 2
10 ltaneous modulation of the targets of harmol monoamine-oxidase B and GABA-A receptor reproduces harmo
11 ic groups that exist in catalytically active monoamine oxidase B are physically distinct.
12 rkinson's disease based on its inhibition of monoamine oxidase B, but the drug is also a potent state
13  volume ([(11)C]SL25.1188 V(T)), an index of monoamine oxidase B density and a marker of astrogliosis
14            We performed a genomewide scan of monoamine oxidase B for the Collaborative Study on the G
15 trate for the flavin-dependent mitochondrial monoamine oxidase B from bovine liver.
16 a targeting enzyme to disrupt the endogenous monoamine oxidase B gene in human cells.
17                        Off-target binding to monoamine oxidase B has been overcome, as demonstrated b
18 elective, and reversible inhibitors of human monoamine oxidase B (hMAO-B).
19 onoamine oxidases with slight preference for monoamine oxidase B in both species.
20 hydrogen peroxide (H(2)O(2)) originated from monoamine oxidase B in severe reactive astrocytes causes
21  SKF-38393 had no effects either on total or monoamine oxidase B in the striatum.
22 ng 18F-flortaucipir scanning to test whether monoamine oxidase B inhibition blocked flortaucipir bind
23   We report the effects of the addition of a monoamine oxidase B inhibitor, rasagiline, to antidepres
24 est placebo-controlled clinical trial of the monoamine oxidase B inhibitor, rasagiline, we examined h
25 ploratory subpopulations of PASADENA: use of monoamine oxidase B inhibitors at baseline (yes versus n
26 cipants who were diffuse malignant or taking monoamine oxidase B inhibitors at baseline).
27 2D6 inhibitor, quinidine, and also partly by monoamine oxidase B inhibitors deprenyl and pargyline.
28                                              Monoamine oxidase B inhibitors result in a mild improvem
29 his, a number of highly potent and selective monoamine oxidase B inhibitors were identified.
30                                              Monoamine oxidase-B inhibitors and dopamine agonists can
31                                 In contrast, monoamine oxidase-B inhibitors improved both depressive
32 dowed with potent, selective, and reversible monoamine oxidase B inhibitory activity is a clinically
33                    Also, we demonstrate that monoamine oxidase B is an ERRalpha target gene whose exp
34     Results strongly support the presence of monoamine oxidase B-labeled astrogliosis in COVID-DC thr
35 -deuterium-L-deprenyl ((11)C-DED) to measure monoamine oxidase B located in astrocytes.
36                                              Monoamine oxidase B (MAO B) catalyzes the oxidative deam
37 direct and continuous fluorometric assay for monoamine oxidase B (MAO B) has been developed.
38               The monotopic membrane protein monoamine oxidase B (MAO B) is an important drug target
39                                              Monoamine oxidase B (MAO B) is an integral protein of th
40 al reversible inhibitors selective for human monoamine oxidase B (MAO B) that do not inhibit MAO A ha
41 ture and subunit composition of bovine liver monoamine oxidase B (MAO B) was investigated using size-
42  (AD), i.e., acetylcholinesterase (AChE) and monoamine oxidase B (MAO B), a series of multitarget lig
43 time-dependent, irreversible inactivators of monoamine oxidase B (MAO B).
44  smokers show a 40% decrease in the level of monoamine oxidase B (MAO B; EC 1.4.3.4) relative to non-
45        A set of drugs was further studied in monoamine oxidase B (MAO-B) and cyclooxygenase-1 (COX-1)
46 mine and compare how two monotopic proteins, monoamine oxidase B (MAO-B) and cyclooxygenase-2 (COX-2)
47               Age-related increases in brain monoamine oxidase B (MAO-B) and its ability to produce r
48 l) is a selective, irreversible inhibitor of monoamine oxidase B (MAO-B) at the conventional dose (10
49 enosine receptors (A2AARs) and inhibition of monoamine oxidase B (MAO-B) in the brain are considered
50 mined the effects of GM1 ganglioside and the monoamine oxidase B (MAO-B) inhibitor L-deprenyl, alone
51 ine agonists (Frequency ratio 1.4, p=0.058), monoamine oxidase B (MAO-B) inhibitors (Frequency ratio
52 llular model of Parkinson's disease in which monoamine oxidase B (MAO-B) is overexpressed and which e
53 evious finding that smokers have lower brain monoamine oxidase B (MAO-B) levels than comparison nonsm
54                                          The monoamine oxidase B (MAO-B) substrate properties and dis
55                                              Monoamine oxidase B (MAO-B) was recently identified as a
56              Illudinine was found to inhibit monoamine oxidase B (MAO-B) with an IC(50) of 18 +/- 7.1
57 e, competitive, and reversible inhibitors of monoamine oxidase B (MAO-B).
58 or (NMDAR), acetylcholinesterase (AChE), and monoamine oxidase B (MAO-B).
59 nt inhibitor of the flavin-containing enzyme monoamine oxidase B (MAO-B).
60 novel radiotracer, [(11)C]SL25.1188, targets monoamine oxidase-B (MAO-B) enzyme, found primarily in a
61 itors of brain carbonic anhydrases (CAs) and monoamine oxidase-B (MAO-B) for the management of Alzhei
62                                              Monoamine oxidase-B (MAO-B) is a key enzyme in the catab
63                         MPTP is converted by monoamine oxidase-B (MAO-B) to its neurotoxic metabolite
64 diographically in conscious mice without the monoamine oxidase B (MAOB) gene (KO, n=11) and the corre
65 was found to suppress the gene expression of monoamine oxidase B (MAOB) in the brain of wild-type but
66 brane domains from the mitochondrial protein monoamine oxidase B (MaoB) or the endoplasmic reticulum
67 known factors in Alzheimer's disease such as monoamine oxidase B (MAOB) protein.
68 tural comparisons with human metabolites and monoamine oxidase B (MAOB) was identified as the putativ
69     Here, we demonstrated elevated levels of monoamine oxidase B (MAOB), a mitochondrial enzyme that
70 oduce the inhibitory gliotransmitter GABA by monoamine oxidase-B (Maob) and abnormally release GABA t
71 ent complex I inhibitor and the two electron monoamine oxidase B oxidation product of MPTP.
72                                              Monoamine oxidase B, present in the mitochondrial outer
73 ate, decreased benzodiazepine, and increased monoamine oxidase B receptor binding have been reported.
74                                        Since monoamine oxidase B receptors are expressed by astrocyte
75 nction and these include redox-related genes monoamine oxidase B, ryanodine receptor 2, and glutathio
76                                    Measuring monoamine oxidase-B with neuroimaging and glial fibrilla