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1 smarinic acid and luteolin in the microwaved basil.
2 d as a primary trigger for CI in postharvest basil.
3 homeolog-phased chromosome-level genome for basil.
4 the seed mucilage films of quince, flax, and basil.
5 ing JA-elicited basil instead of the control basil.
6 pentacyclic triterpene biosynthesis in sweet basil.
7 ices, beers, tomato sauces, olives and dried basil.
8 or the formation of methylcinnamate in sweet basil.
9 Angioplasty for Severe Ischaemia of the Leg (BASIL)-2 was an open-label, pragmatic, multicentre, phas
13 ng analysis of the recombinant sheep CRF-BP (Basil 7) expressed in CHO cells revealed that it binds h
17 We studied transcriptional changes in sweet basil after methyl jasmonate (MeJA) treatment, which is
19 ng the secondary metabolic pathways of sweet basil and developing metabolic engineering strategies fo
21 colonize the roots of Arabidopsis and sweet basil and form a biofilm as observed by scanning electro
27 aily light integral is > 12 mol m(-2) d(-1), basil and petunia yield and quality is acceptable for co
28 ite concentrations were determined for sweet basil and scallions over 24h to determine if time of sam
33 was the only pathogenic strain toward sweet basil, and PAO214 biofilm appeared comparable with biofi
36 the potential anti-inflammatory activity of basil anthocyanins was observed after treatment with eac
45 vitro activity and bioaccessibility of sweet basil, cinnamon basil, red rubin basil, and lemon basil
46 indings highlight the need for evaluation of basil cultivars and postharvest preservation methods reg
49 is expressed in glands but not in leaves of basil cv Sweet Dani, whose glands contain geraniol and c
50 ng power of the drinks show that the roselle-basil drink may serve as health drink and addition of sw
52 o identify key metabolites involved in CI of basil during cold storage to better understand the under
53 was to investigate the effect of addition of basil elicited with jasmonic acid (JA) on the biological
54 tion of isoeugenol, and an Ocimum basilicum (basil) enzyme, eugenol synthase 1 (ObEGS1), that produce
58 study, it can be concluded that JA-elicited basil (especially elicited with 100microM jasmonic acid)
59 late-almond gum (WA) coacervates loaded with basil essential oil (BEO) were compared for encapsulatio
62 also influenced the chemical composition of basil essential oils - 100muM JA increased the linalool,
63 eugenol, possess an enzyme homologous to the basil eugenol-forming enzyme that also uses coniferyl ac
64 ed from shoeblack leaves, okra, and seeds of basil, fenugreek, and flax, which were identified as SBM
67 ribe the volatile profile of three different basil genotypes (Genovese and Green and Purple Iranian),
68 t potential of the essential oils (EO) of 24 basil genotypes was assessed by 4 distinct in vitro eval
76 ds (guacamole, virgin olive oil, tortellini, basil hummus, creamed spinach, vegetable pasta, green te
80 elle calyces (Hibiscus sabdariffa) and sweet basil leaves (Ocimum basilicum L) may provide therapeuti
81 creased with the addition of the dried sweet basil leaves and samples kept at a higher temperature of
82 creased with the addition of the dried sweet basil leaves and samples kept at a higher temperature of
87 serve as health drink and addition of sweet basil leaves up to 5% may be suitable to produce roselle
94 eomes of the glandular trichomes of the four basil lines shared many similarities they were also each
95 late, respectively, in the peltate glands of basil lines SW (which produces essentially only eugenol)
98 ase Ca content of baby leaf vegetables (BLV: basil, mizuna, tatsoi and endive), as fresh-cut products
100 tulsi (O. tenuiflorum), and African or clove basil (O. gratissimum) have traditionally been used for
103 ein extracts from peltate trichomes of sweet basil (Ocimum basilicum L.) cultivars readily hydroxylat
105 idative activity of anthocyanins from purple basil (Ocimum basilicum L.) leaves induced by arachidoni
106 h isolated trichomes of four different sweet basil (Ocimum basilicum L.) lines possessing very differ
107 of the flavone 8-hydroxylase (F8H) in sweet basil (Ocimum basilicum L.) trichomes as a Rieske-type o
108 ssinolide (EBL) and l-phenylalanine on sweet basil (Ocimum basilicum L.) were studied to determine th
109 n sequence is approximately 40% identical to basil (Ocimum basilicum) and Clarkia breweri phenylprope
111 oterpene fraction of the lemon-scented sweet basil (Ocimum basilicum) cv Sweet Dani consists mostly o
114 pressed sequence tag database for four sweet basil (Ocimum basilicum) lines afforded identification o
116 ributed throughout the aerial parts of sweet basil (Ocimum basilicum) produce and store monoterpene,
118 e obtained from the glandular trichomes of a basil (Ocimum basilicum) variety that produces high leve
119 (Helianthus annuus), linden (Tilia cordata), basil (Ocimum basilicum), buckwheat (Fagopyrum esculentu
120 oils of basil herbs such as nyazbo or sweet basil (Ocimum basilicum), holy basil or tulsi (O. tenuif
121 infecting the roots of Arabidopsis and sweet basil (Ocimum basilicum), in vitro and in the soil, and
122 show here that glandular trichomes of sweet basil (Ocimum basilicum), which synthesize and accumulat
123 osella), roselle (Hibiscus sabdariffa), tree basil (Ocimum gratissimum), Barbados Gooseberry (Pereski
128 azbo or sweet basil (Ocimum basilicum), holy basil or tulsi (O. tenuiflorum), and African or clove ba
129 acid p-coumaroyl transferase is expressed in basil peltate glands that are actively producing eugenol
130 al hydroxylase activities were identified in basil peltate glands that convert p-coumaroyl 4-hydroxyp
131 he content, activity and bioaccessibility of basil phytochemicals varied depending on the cultivar as
132 of phenolic compounds and in the dry mass of basil plants (O. basilicum L.) grown in a hydroponic sys
134 not active in glands of noneugenol-producing basil plants, suggesting that the levels of this activit
135 , and cadmium promoted a stress condition in basil plants, which resulted in the reduction of the dry
139 tested cakes was increased after addition of basil, proportionally to the amount of the additive.
140 maleic acid were negatively associated with basil quality, while increased levels of secondary metab
142 nd bioaccessibility of sweet basil, cinnamon basil, red rubin basil, and lemon basil were investigate
143 cally added to foodstuffs: citronella, dill, basil, red thyme, thyme, rosemary, oregano, clove and ci
146 contrast, induction of RA secretion by sweet basil roots and exogenous supplementation of Arabidopsis
148 mum inhibitory concentration levels in sweet basil's root exudates before P. aeruginosa formed a biof
153 ographical properties significantly affected basil saturated FA and just unsaturated linoleic acid.
154 ds, and phenylpropanoids revealed changes in basil secondary metabolism under CMS, which appear to be
158 ng to amplify signal with isobaric labeling (BASIL) strategy increased the overall number of quantifi
160 els of synteny were observed between the two basil subgenomes but comparisons to Salvia rosmarinus sh
164 sed the amount of essential oils produced by basil - the highest oil yield (0.78+/-0.005mL/100gdw) wa
166 ncept experiment demonstrated the ability of BASIL to distinguish acute myeloid leukemia cells based
167 Calcium bioaccessibility ranged from 25% (basil) to 40% (endive) but the biofortified vegetables s
169 cteristics of the plant and essential oil of basil, two landraces, Purple and Green, were dried in su
170 ons and phenolic acid levels in eight purple basil varieties and examined the relationship between an
172 se (EOMT) cDNAs were isolated from the sweet basil variety EMX-1 using a biochemical genomics approac
173 tral, and not in glands or leaves of another basil variety that makes other monoterpenes but not gera
175 tems, as they were able to emit many typical basil volatiles with very low amounts of phenylpropanoid
177 This experiment pointed out that microwaved basil wastes could be re-used in the food, pharmacy and/
178 s supplemented with the control and elicited basil were characterized by satisfactory consumer accept
179 Volatiles from different parts of lemon basil were evaluated to determine the parts that influen
181 antimicrobial and antioxidant activities of basil were studied, along with its characterization in p
182 enolic and total flavonoid contents of sweet basils were determined by a spectrophotometer, and indiv
185 te-dependent flavone demethylase activity in basil, which explains the accumulation of 7-O-demethylat