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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 the activities of tyrosine ammonia-lyase and phenylalanine ammonia-lyase.
4 gulated in either cinnamate 4-hydroxylase or phenylalanine ammonia-lyase.
5 e encP gene indeed encodes a novel bacterial phenylalanine ammonia-lyase.
6 that contains three AC elements, the minimal PHENYLALANINE AMMONIA-LYASE 2 (PAL2) promoter from Phase
7 ines, while the expression of PR-1, PR-2 and phenylalanine ammonia-lyase 3 (PAL3) did not change sign
10 in the dark, as does the cellular content of phenylalanine ammonia-lyase, a light-inducible enzyme in
12 lignin deposition, pigment accumulation, and phenylalanine ammonia lyase activity, but does not disru
14 eatment induced significant decreases in the phenylalanine ammonia-lyase activity and significantly i
19 o the TATA box of the rice pal gene encoding phenylalanine ammonia-lyase, caused DNA bending, and enh
21 nducible expression of several pea PR genes: phenylalanine ammonia lyase, chalcone synthase, and DRR2
22 uced when plants containing the heterologous phenylalanine ammonia lyase, chalcone synthase, and DRR2
23 thway was induced, and transcript levels for phenylalanine ammonia lyase, cinnamate 4-hydroxylase, p-
24 s (bean) phenylalanine ammonia-lyase (PAL; L-phenylalanine ammonia-lyase, EC 4.3.1.5) gene, modified
26 fied with multiwalled carbon nanotubes where phenylalanine ammonia-lyase enzyme was immobilized using
27 NAE 14:0, but not myristic acid, activated phenylalanine ammonia lyase expression at submicromolar
29 lyethylene glycol (and in some cases against phenylalanine ammonia lyase), future studies are needed
33 Exogenous NAE 14:0 induced expression of phenylalanine ammonia lyase in a manner similar to funga
34 white campion flowers were treated with the phenylalanine ammonia lyase inhibitor 2-aminoindan-2-pho
39 ed with a novel one-pot approach by coupling phenylalanine ammonia lyase (PAL) amination with a chemo
41 cal and clinical investigations suggest that phenylalanine ammonia lyase (PAL) could be an effective
42 mus" is carried out by the novel prokaryotic phenylalanine ammonia lyase (PAL) EncP, which converts t
43 H2O2 accumulation was concurrent with higher phenylalanine ammonia lyase (PAL) enzyme activity leadin
44 ynthetic and therapeutic relevance, five new phenylalanine ammonia lyase (PAL) enzymes were discovere
45 the metabolic disorder phenylketonuria with phenylalanine ammonia lyase (PAL) from Rhodosporidium to
46 as a result of down-regulation (1.4-fold) in phenylalanine ammonia lyase (PAL) gene expression and a
47 result from a down-regulation (1.4-fold) of phenylalanine ammonia lyase (PAL) gene expression and a
48 The first three-dimensional structure of phenylalanine ammonia lyase (PAL) has been determined at
49 xpressing a nahG transgene or treated with a phenylalanine ammonia lyase (PAL) inhibitor showed enhan
50 e, is derived from chorismate via either the phenylalanine ammonia lyase (PAL) or the isochorismate s
51 und treatment at 25 and 29W, the activity of phenylalanine ammonia lyase (PAL) was increased signific
52 -3-methylglutaryl CoA reductase (HMGR) and l-phenylalanine ammonia lyase (PAL), two defense genes enc
55 aves was followed by a transient increase in phenylalanine ammonia-lyase (PAL) activity in the petiol
56 nic acid (5-CQA), total carotenoids, AC, and phenylalanine ammonia-lyase (PAL) activity of five comme
58 pruning triggered a transient expression of phenylalanine ammonia-lyase (PAL) and stilbene synthase
62 ized pathogenesis-related protein (PR-1) and phenylalanine ammonia-lyase (PAL) genes, we propose that
68 AE 14:0) resulted in an increase in relative phenylalanine ammonia-lyase (PAL) transcript abundance w
70 development and adaptation, and depends on L-phenylalanine ammonia-lyase (PAL), an enzyme catalyzing
71 ation of flavonoid biosynthesis by examining phenylalanine ammonia-lyase (PAL), chalcone synthase (CH
73 eterminations of hydroxyproline, peroxidase, phenylalanine ammonia-lyase (PAL), phenol, and lignin co
74 of the kinases activated has a known target, phenylalanine ammonia-lyase (PAL), which has an importan
78 bed by introduction of a heterologous (bean) phenylalanine ammonia-lyase (PAL; L-phenylalanine ammoni
79 otprints in early phenylpropanoid promoters (phenylalanine ammonia lyase [PAL], 4-coumarate coenzyme
83 efficacy of recombinant Anabaena variabilis phenylalanine ammonia lyase (produced in Escherichia col
84 NAs encoded the first enzyme in the pathway (phenylalanine ammonia-lyase), the first in the pathway b
85 transient increases in the SaB4H, SaBIS, and phenylalanine ammonia lyase transcript levels preceded p
86 e of several carbohydrate-active enzymes and phenylalanine ammonia-lyases was also altered in transge
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