コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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
6 amine N-methyl transferase) and disposition (monoamine oxidase B and catechol-O-methyl transferase) o
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
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
20 hydrogen peroxide (H(2)O(2)) originated from monoamine oxidase B in severe reactive astrocytes causes
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
27 2D6 inhibitor, quinidine, and also partly by monoamine oxidase B inhibitors deprenyl and pargyline.
32 dowed with potent, selective, and reversible monoamine oxidase B inhibitory activity is a clinically
34 Results strongly support the presence of monoamine oxidase B-labeled astrogliosis in COVID-DC thr
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
44 smokers show a 40% decrease in the level of monoamine oxidase B (MAO B; EC 1.4.3.4) relative to non-
46 mine and compare how two monotopic proteins, monoamine oxidase B (MAO-B) and cyclooxygenase-2 (COX-2)
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
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
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
68 tural comparisons with human metabolites and monoamine oxidase B (MAOB) was identified as the putativ
70 oduce the inhibitory gliotransmitter GABA by monoamine oxidase-B (Maob) and abnormally release GABA t
73 ate, decreased benzodiazepine, and increased monoamine oxidase B receptor binding have been reported.
75 nction and these include redox-related genes monoamine oxidase B, ryanodine receptor 2, and glutathio