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1 oester, which then serves as a substrate for chalcone synthase.
2 ion of CHLOROPHYLL A/B BINDING PROTEIN 3 and CHALCONE SYNTHASE.
3 the first enzyme in flavonoid biosynthesis, chalcone synthase.
4 oid pathway, phenylalanine ammonia-lyase and chalcone synthase.
5 s related to beta-ketoacyl-CoA synthases and chalcone synthases.
6 petunia plants can result in degradation of chalcone synthase A RNAs and loss of chalcone synthase,
8 e pathway branch for flavonoid biosynthesis (chalcone synthase), a key enzyme in medicarpin biosynthe
9 sion of a reporter driven by the promoter of CHALCONE SYNTHASE, a gene encoding a flavonol biosynthet
10 de anther-specific proteins with homology to chalcone synthase, a key flavonoid biosynthesis enzyme.
12 tion of chalcone synthase A RNAs and loss of chalcone synthase, a process called cosuppression or pos
14 psis F3H gene is coordinately expressed with chalcone synthase and chalcone isomerases is seedlings,
15 ype, lactofen caused enhanced expressions of chalcone synthase and chalcone reductase genes, mainly i
17 nous biosynthetic genes (c2 and a1, encoding chalcone synthase and flavanone/dihydroflavonol reductas
18 arent testa4-2, which has a null mutation in CHALCONE SYNTHASE and therefore synthesizes no flavonol
19 he heterologous phenylalanine ammonia lyase, chalcone synthase, and DRR206 promoter-beta-glucuronidas
21 pression levels (most notably those of NDL1, CHALCONE SYNTHASE, and MYB DOMAIN PROTEIN44) in plants c
22 ne after hormone induction, whereas only the chalcone synthase (c2) and flavanone/dihydroflavonol red
23 omatized coumaryl-trione intermediate of the chalcone synthase-catalyzed cyclization of the fully ext
26 ain protein that regulates the expression of chalcone synthase, chalcone isomerase and dihydroflavono
28 also did not inhibit the accumulation of the chalcone synthase, chalcone isomerase, or flavanone-3-hy
29 ys further demonstrated interactions between chalcone synthase, CHI, and flavonol 3-hydroxylase in ly
30 it ripening is accompanied by an increase in CHALCONE SYNTHASE (CHS) activity and flavonoid biosynthe
32 The cellular and subcellular locations of chalcone synthase (CHS) and chalcone isomerase (CHI), th
33 ncoding L-phenylalanine ammonia-lyase (PAL), chalcone synthase (CHS) and chalcone reductase (CHR) wer
37 ctures and floral pigmentation patterns from chalcone synthase (chs) co-suppression among 47 Petunia
40 trefoil) were transformed with an antisense chalcone synthase (CHS) gene construct made using a stre
43 s of the I locus in Glycine max silence nine chalcone synthase (CHS) genes to inhibit function of the
46 coding the key flavonoid biosynthesis enzyme chalcone synthase (CHS) is regulated by several environm
51 gmentation patterns were scored in 185 sense Chalcone synthase (Chs) transgenotes and 85 antisense Ch
52 Crystallographic and functional studies of chalcone synthase (CHS), a plant-specific PKS, indicate
54 that simultaneous RNAi silencing of HCT and chalcone synthase (CHS), an enzyme essential for flavono
55 cS), the gene family that encodes the enzyme chalcone synthase (Chs), and the gene family that encode
56 ties with C. microcarpa ACS, Medicago sativa chalcone synthase (CHS), and the previously reported Aeg
57 examining phenylalanine ammonia-lyase (PAL), chalcone synthase (CHS), chalcone isomerase (CHI), and d
58 istent with previous studies indicating that chalcone synthase (CHS), chalcone isomerase (CHI), flava
59 re well illustrated by the genes that encode chalcone synthase (CHS), the first committed step in fla
61 ], 4-coumarate coenzyme A:ligase [4-CL], and chalcone synthase [CHS]) are conserved in the t-CAH prom
63 stilbene backbone, seem to have evolved from chalcone synthases (CHSs) several times independently in
65 the introduction of a heterologous antisense chalcone synthase construct into L. corniculatus resulte
66 ile element dynamics in seven alleles of the chalcone synthase D locus (CHS-D) of the common morning
68 PqsD is structurally similar to the FabH and chalcone synthase families of fatty acid and polyketide
70 P-glucose pyrophosphorylase gene (APL3), and chalcone synthase gene (CHS), whereas the mybs2 mutant e
73 vergence times based on sequence data of the chalcone synthase gene are congruent with comparative pa
74 e 3' splice acceptor site in the Arabidopsis chalcone synthase gene completely disrupts synthesis of
75 ontrolled post-transcriptional regulation of chalcone synthase gene expression by influencing the sur
77 C2-Idf is a stable dominant mutation of the chalcone synthase gene, c2, which encodes the first dedi
80 nd Glycine max chalcone synthase1 (Gmachs1), chalcone synthase, involved in phytoalexin production.
81 N), which is biosynthesized in bacteria by a chalcone synthase-like (CS-like) type III polyketide syn
82 s, we disrupted a mas-like gene, msl7, and a chalcone synthase-like gene, pks10, with phage-mediated
84 al roots under the Pi- Suc- condition in the chalcone synthase mutant (tt4-2) indicated a potential r
85 the H-box (CCTACC) element in the bean CHS15 chalcone synthase promoter was purified, and internal pe
87 ved from an evolutionarily related member of chalcone synthase superfamily by mere substitution of tw
88 ch have a null mutation in the gene encoding chalcone synthase, the first enzyme in flavonoid synthes
90 n (a commonly reported derailment product of chalcone synthase), while similar in vitro analyses usin
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