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3 ns of dopamine, and the dopamine metabolites homovanillic acid (HVA) and dihydroxyphenylacetic acid (
4 , 3-4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) and in the DOPAC/dopamine ratio
5 3, 4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) by 76%, 53% and 40%, respectivel
6 s 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in caudate nucleus resulting fro
8 kg i.p.) 15 min prior to sacrifice increased homovanillic acid (HVA) levels in the left medial prefro
9 of greater than 10 points and an increase in homovanillic acid (HVA) or 5-hydroxyindoleacetic acid (5
12 SF concentrations of the dopamine metabolite homovanillic acid (HVA) were determined in 30 recently a
13 ne (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 5-hydroxyindoleacetic acid (5-H
15 triatal tissue punches were analyzed for DA, homovanillic acid (HVA), and DA activity (HVA/DA) using
16 sma levels of fenfluramine, norfenfluramine, homovanillic acid (HVA), cortisol, and prolactin were de
17 SF) concentration of the dopamine metabolite homovanillic acid (HVA), in an extended inbred vervet mo
18 ions of 5-hydroxyindoleacetic acid (5-HIAA), homovanillic acid (HVA), or 3-methoxy-4-hydroxyphenylgyc
19 , 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were elevated over the same tim
20 , 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were found to be decreased by >
24 ites, 3,4-dihydroxyphenylalanine (DOPAC) and homovanillic acid (HVA); norepinephrine (NE) and its met
25 [3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA)] levels and tyrosine hydroxylase
27 alyzed cerebrospinal fluid concentrations of homovanillic acid (the major catabolite of dopamine) and
29 ydroxyindoleacetic acid [5-HIAA]), dopamine (homovanillic acid [HVA]), and norepinephrine (3-methoxy-
31 of tetrahydrobiopterin (BH4), neopterin, and homovanillic acid and low levels of tyrosine hydroxylase
32 30, 1994, were eligible for urinary assay of homovanillic acid and vanillylmandelic acid at 3 weeks a
34 of dopamine, 3,4-dihydroxybenzoic acid, and homovanillic acid in GSHPx knock-out mice than those see
36 stored the decreased content of dopamine and homovanillic acid in the nigrostriatal neurons of the ag
41 ograms and urinary vanillylmandelic acid and homovanillic acid measurements were performed during a 9
42 ystonia during treatment, growth hormone and homovanillic acid measures, psychotic symptom activation
45 catecholamine values, or an increase in the homovanillic acid to vanillylmandelic acid ratio greater
47 of D-cycloserine, relevant amino acids, and homovanillic acid were assayed at baseline and at weeks
48 dopamine, 3,4-dihydroxyphenylacetic acid and homovanillic acid were comparable in the young and aged
49 ine metabolites (5-hydroxyindoleacetic acid, homovanillic acid, and 3-methoxy-4-hydroxyphenethylenegl
50 acetic acid, 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 3-methoxytyramine in addition to
51 the metabolites 3,4-deoxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid were m
52 Aspects of the interaction among thiols, homovanillic acid, and peroxidase are discussed which li
55 CSF measures of 5-hydroxyindoleacetic acid, homovanillic acid, dehydroepiandrosterone, or pregnenolo
57 metabolites, dihydroxyphenylacetic acid and homovanillic acid, increased in the auditory forebrain b
58 bolism to 3,4-dihydroxyphenylacetic acid and homovanillic acid, our results indicate that Met homozyg
59 ds (PCLCs): vanillic acid, isovanillic acid, homovanillic acid, syringic acid, syringaldehyde, feruli
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