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1 and defense enzymes (polyphenol oxidase and phenylalanine ammonia-lyase).
2 M would resemble the well known plant enzyme phenylalanine ammonia lyase.
3 alase, superoxide dismutase, peroxidase, and phenylalanine ammonia lyase.
4 the activities of tyrosine ammonia-lyase and phenylalanine ammonia-lyase.
5 peroxide dismutase, ascorbate peroxidase and phenylalanine ammonia-lyase.
6 gulated in either cinnamate 4-hydroxylase or phenylalanine ammonia-lyase.
7 e encP gene indeed encodes a novel bacterial phenylalanine ammonia-lyase.
8 that contains three AC elements, the minimal PHENYLALANINE AMMONIA-LYASE 2 (PAL2) promoter from Phase
9 ines, while the expression of PR-1, PR-2 and phenylalanine ammonia-lyase 3 (PAL3) did not change sign
12 in the dark, as does the cellular content of phenylalanine ammonia-lyase, a light-inducible enzyme in
14 lignin deposition, pigment accumulation, and phenylalanine ammonia lyase activity, but does not disru
16 eatment induced significant decreases in the phenylalanine ammonia-lyase activity and significantly i
17 ocyanins, total phenolics, antioxidants, and phenylalanine ammonia-lyase activity, and lower levels o
19 and the phenylpropanoid biosynthesis genes L-PHENYLALANINE AMMONIA LYASE and PHENYLACETALDEHYDE SYNTH
21 es of the phenolic compound pathway, such as phenylalanine ammonia-lyase and O-methyltransferase, ind
23 igher endogenous phenolics and activities of phenylalanine-ammonia lyase and shikimate dehydrogenase.
24 eroxide dismutase), LOX (lipoxygenase), PAL (phenylalanine ammonia lyase), and PR-1 (pathogenesis rel
25 conjugated various enzymes (glucose oxidase, phenylalanine ammonia-lyase, and beta-lactamase) with pH
26 tively with the increase in the activity, of phenylalanine ammonia-lyase, and cytochrome P450 enzymes
28 o the TATA box of the rice pal gene encoding phenylalanine ammonia-lyase, caused DNA bending, and enh
30 nducible expression of several pea PR genes: phenylalanine ammonia lyase, chalcone synthase, and DRR2
31 uced when plants containing the heterologous phenylalanine ammonia lyase, chalcone synthase, and DRR2
32 thway was induced, and transcript levels for phenylalanine ammonia lyase, cinnamate 4-hydroxylase, p-
33 s (bean) phenylalanine ammonia-lyase (PAL; L-phenylalanine ammonia-lyase, EC 4.3.1.5) gene, modified
35 fied with multiwalled carbon nanotubes where phenylalanine ammonia-lyase enzyme was immobilized using
36 NAE 14:0, but not myristic acid, activated phenylalanine ammonia lyase expression at submicromolar
39 has been developed using mutant variants of phenylalanine ammonia-lyase from Arabidopsis thaliana (A
40 lyethylene glycol (and in some cases against phenylalanine ammonia lyase), future studies are needed
44 Exogenous NAE 14:0 induced expression of phenylalanine ammonia lyase in a manner similar to funga
45 white campion flowers were treated with the phenylalanine ammonia lyase inhibitor 2-aminoindan-2-pho
50 hylene production, respiration, weight loss, phenylalanine ammonia lyase (PAL) activity and ion leaka
52 ed with a novel one-pot approach by coupling phenylalanine ammonia lyase (PAL) amination with a chemo
54 cal and clinical investigations suggest that phenylalanine ammonia lyase (PAL) could be an effective
55 mus" is carried out by the novel prokaryotic phenylalanine ammonia lyase (PAL) EncP, which converts t
56 H2O2 accumulation was concurrent with higher phenylalanine ammonia lyase (PAL) enzyme activity leadin
57 ynthetic and therapeutic relevance, five new phenylalanine ammonia lyase (PAL) enzymes were discovere
58 the metabolic disorder phenylketonuria with phenylalanine ammonia lyase (PAL) from Rhodosporidium to
59 as a result of down-regulation (1.4-fold) in phenylalanine ammonia lyase (PAL) gene expression and a
60 result from a down-regulation (1.4-fold) of phenylalanine ammonia lyase (PAL) gene expression and a
61 The first three-dimensional structure of phenylalanine ammonia lyase (PAL) has been determined at
62 xpressing a nahG transgene or treated with a phenylalanine ammonia lyase (PAL) inhibitor showed enhan
63 e, is derived from chorismate via either the phenylalanine ammonia lyase (PAL) or the isochorismate s
64 known pathways of plant SA biosynthesis, the phenylalanine ammonia lyase (PAL) pathway is more ancien
66 und treatment at 25 and 29W, the activity of phenylalanine ammonia lyase (PAL) was increased signific
67 strain expresses the Phe-metabolizing enzyme phenylalanine ammonia lyase (PAL), catalyzing the deamin
68 defense enzymes, such as beta-1,3-glucanase, phenylalanine ammonia lyase (PAL), peroxidase (POX), pol
69 tic xylem clearly show the downregulation of phenylalanine ammonia lyase (PAL), the enzyme catalyzing
70 riptional regulator of CaPAL1, which encodes phenylalanine ammonia lyase (PAL), the regulatory, gatek
71 -3-methylglutaryl CoA reductase (HMGR) and l-phenylalanine ammonia lyase (PAL), two defense genes enc
77 n existing literature such as alterations in phenylalanine ammonia-lyase (PAL) activity and glutathio
78 aves was followed by a transient increase in phenylalanine ammonia-lyase (PAL) activity in the petiol
79 nic acid (5-CQA), total carotenoids, AC, and phenylalanine ammonia-lyase (PAL) activity of five comme
83 gher anthocyanin concentration due to higher phenylalanine ammonia-lyase (PAL) and lower polyphenol o
84 pruning triggered a transient expression of phenylalanine ammonia-lyase (PAL) and stilbene synthase
88 B46, encoding a transcriptional activator of PHENYLALANINE AMMONIA-LYASE (PAL) genes which are requir
89 ized pathogenesis-related protein (PR-1) and phenylalanine ammonia-lyase (PAL) genes, we propose that
90 ant activity, and the activity of the enzyme phenylalanine ammonia-lyase (PAL) in caper berries treat
98 AE 14:0) resulted in an increase in relative phenylalanine ammonia-lyase (PAL) transcript abundance w
100 development and adaptation, and depends on L-phenylalanine ammonia-lyase (PAL), an enzyme catalyzing
101 ctivities of shikimate dehydrogenase (SKDH), phenylalanine ammonia-lyase (PAL), catalase (CAT), super
102 ation of flavonoid biosynthesis by examining phenylalanine ammonia-lyase (PAL), chalcone synthase (CH
104 eterminations of hydroxyproline, peroxidase, phenylalanine ammonia-lyase (PAL), phenol, and lignin co
105 of the kinases activated has a known target, phenylalanine ammonia-lyase (PAL), which has an importan
110 bed by introduction of a heterologous (bean) phenylalanine ammonia-lyase (PAL; L-phenylalanine ammoni
111 otprints in early phenylpropanoid promoters (phenylalanine ammonia lyase [PAL], 4-coumarate coenzyme
116 efficacy of recombinant Anabaena variabilis phenylalanine ammonia lyase (produced in Escherichia col
118 NAs encoded the first enzyme in the pathway (phenylalanine ammonia-lyase), the first in the pathway b
119 transient increases in the SaB4H, SaBIS, and phenylalanine ammonia lyase transcript levels preceded p
120 e of several carbohydrate-active enzymes and phenylalanine ammonia-lyases was also altered in transge
121 sually those with milder PKU), and pegylated phenylalanine ammonia lyase, which requires daily subcut
122 that initiate the degradation of the enzyme phenylalanine ammonia-lyase, which catalyzes the first s