ライフサイエンスコーパス: leafy

1 on of the floral meristem-identity gene LFY (LEAFY).

2 ulation and floral fate synergistically with LEAFY.

3 tables were grouped into green-leafy and non-leafy.

4 on of SINGLE LEAFLET1 (SGL1), an ortholog of LEAFY.

5 ivation of the floral meristem-identity gene LEAFY.

6 loral identity, such as the Arabidopsis gene LEAFY.

7 FT and impairing activation of APETALA1 and LEAFY.

8 xpression of onion FLOWERING LOCUS T (AcFT), LEAFY (AcLFY) and GIBBERELLIN-3 OXIDASE (GA3ox1) during

9 lin catabolism gene; consequently, increased LEAFY activity causes reduced gibberellin levels.

10 vations contrast with previous findings that LEAFY acts as a direct activator of floral homeotic gene

11 The Arabidopsis transcription factor LEAFY acts upstream of homeotic genes such as AGAMOUS to

12 is involved as well as the floral regulators LEAFY and AGAMOUS.

13 correlated with the floral-regulatory genes, LEAFY and APETALA1, RNA levels.

14 types of two floral meristem identity genes, LEAFY and APETALA1.

15 Greater intake of green leafy and cruciferous vegetables was associated with low

16 er vegetable consumption, particularly green leafy and cruciferous vegetables, was associated with be

17 n varieties of samples classified as fruits, leafy and fruity vegetables, tubers, legumes and cereals

18 t whether the known regulatory links between LEAFY and its MADS-box gene targets, central to flower d

19 (p>0.1) in xanthophyll content between fresh leafy and non-leafy samples.

20 Thirteen vegetables were grouped into green-leafy and non-leafy.

21 PRESSOR OF OVEREXPRESSION OF CONSTANS1-1 and LEAFY and the timely development of the wheat spike.

22 e SAM, leading to activation of APETALA1 and LEAFY and thereby promoting floral meristem identity.

23 and surprisingly, some of these factors are LEAFY and UNUSUAL FLORAL ORGANS.

24 domain is, in part, specified redundantly by LEAFY and UNUSUAL FLORAL ORGANS.

25 carpel development by STM is independent of LEAFY and WUSCHEL, but requires the function of AGAMOUS.

26 QUAMOSA PROMOTER-BINDING PROTEIN LIKE genes, LEAFY, and APETALA1.

27 s SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1, LEAFY, and FRUITFUL.

28 directly bind to the promoters of APETALA1, LEAFY, and FRUITFULL, thus mediating their activation by

29 be involved in the GA-promoted activation of LEAFY, and in the regulation of anther development.

30 am target genes, including TERMINAL FLOWER1, LEAFY, and MADS box homologs, and to facilitate cross-re

31 Meristem identity genes, such as LEAFY, APETALA 1 and CAULIFLOWER, prevent TERMINAL FLOWE

32 g mutations also suppress bract formation in leafy, apetala1 and apetala2 mutant backgrounds.

33 tion factors without gene duplication, using LEAFY as an archetype.

34 s) in tobacco and edible plants (spinach and leafy beets) at costs that will allow commercialization.

35 thin floral tissues, but that changes in the leafy bracts and nonbolt leaves as the plant shifts from

36 tiation, as further supported by the loss of leafy carpelloid features in stm leafy double mutants.

37 embryos share many characteristics with the leafy cotyledon (lec) class of mutants in that they accu

38 gulators of seed development and include the LEAFY COTYLEDON (LEC) genes LEC1, LEC1-LIKE, LEC2, and F

39 transcription factor that is a member of the LEAFY COTYLEDON (LEC) group of genes.

40 etwork of transcription factors that include LEAFY COTYLEDON 1 (LEC1), LEC1-LIKE (L1L), and B3 domain

41 of the embryo development master regulators LEAFY COTYLEDON 1 and 2, FUSCA 3, and ABSCICIC ACID INSE

42 Knockout of GLABRA2 did not affect LEAFY COTYLEDON 1 and PICKLE expression in developing em

43 the expression of key seed maturation genes LEAFY COTYLEDON 1/2 (LEC1/2), ABSCISIC ACID INSENSITIVE

44 C1), LEC1-LIKE (L1L), and B3 domain factors, LEAFY COTYLEDON 2 (LEC2), FUSCA3 (FUS3), and ABSCISIC AC

45 arrying a lesion in the transcription factor LEAFY COTYLEDON 2 (LEC2; At1g28300).

46 e that PKL acts as a master regulator of the LEAFY COTYLEDON genes, and that joint derepression of th

47 Transcripts for all three LEAFY COTYLEDON genes, LEC1, LEC2, and FUS3, exhibit PKL

48 sed on genome scale searches for homologs of LEAFY COTYLEDON-LIKE (L1L; AtNF-YB6), NF-YB transcriptio

49 The BABY BOOM (BBM) and LEAFY COTYLEDON1 (LEC1) and LEC2 transcription factors a

50 genes encoding auxin response factor (ARF ), Leafy cotyledon1 (LEC1) and somatic embryogenesis recept

51 LEAFY COTYLEDON1 (LEC1) is a central regulator that is r

52 Arabidopsis LEAFY COTYLEDON1 (LEC1) is a critical regulator required

53 The LEAFY COTYLEDON1 (LEC1) transcription factor is a centra

54 ecessary for the repression of expression of LEAFY COTYLEDON1 (LEC1), a central regulator of embryoge

55 LEAFY COTYLEDON1 (LEC1), an atypical subunit of the nucl

56 oil content, which involve WRINKLED1 (WRI1), LEAFY COTYLEDON1 (LEC1), and LEC2 in Arabidopsis, have b

57 t it represents a gain-of-function mutant of LEAFY COTYLEDON1 (LEC1), due to a promoter mutation.

58 By screening mutants in leafy cotyledon1 (LEC1)-inducible transcription factors

59 is are initiated by the transcription factor LEAFY COTYLEDON1 (LEC1).

60 port that overexpression of maize (Zea mays) LEAFY COTYLEDON1 (ZmLEC1) increases seed oil by as much

61 n particular, we find that PKL is present at LEAFY COTYLEDON1 and LEAFY COTYLEDON2 during germination

62 uding those encoded by the Arabidopsis LEC1 (LEAFY COTYLEDON1), FUS3 (FUSCA3), and abscisic acid-inse

63 f the central regulator of seed development, LEAFY COTYLEDON1, to transactivate DOG1 during maturatio

64 , along with B3 domain transcription factors LEAFY COTYLEDON2 (LEC2) and FUSCA3 (FUS3), and LEC1, a s

65 The Arabidopsis LEAFY COTYLEDON2 (LEC2) gene is a central embryonic regu

66 WOUND INDUCED DEDIFFERENTIATION3 (WIND3) and LEAFY COTYLEDON2 (LEC2) genes are among the PRC2 targets

67 LEAFY COTYLEDON2 (LEC2) is a central regulator of embryo

68 LEAFY COTYLEDON2 (LEC2) is among a small number of key t

69 The B3 domain protein LEAFY COTYLEDON2 (LEC2) is required for several aspects

70 related regulators with a B3 domain, namely LEAFY COTYLEDON2 (LEC2), ABSCISIC ACID INSENSITIVE3 (ABI

71 ACID-INSENSITIVE3 (ABI3), FUSCA3 (FUS3), and LEAFY COTYLEDON2 (LEC2; AFL) and VIVIPAROUS1/ABI3-LIKE (

72 in part by repressing the master regulators LEAFY COTYLEDON2 and FUSCA3 and identify the trihelix tr

73 that PKL is present at LEAFY COTYLEDON1 and LEAFY COTYLEDON2 during germination, which is when PKL a

74 LEAFY COTYLEDON2, FUSCA3, and ABA INSENSITIVE3, which en

75 the loss of leafy carpelloid features in stm leafy double mutants.

76 which contests their model and supports that LEAFY evolves through duplications.

77 history of plants and ignores evidence that LEAFY evolves through gene duplications.

78 kers, the rbcL barcoding marker (cpDNA), the LEAFY exon 3 (nrDNA), and the trnL((UAA)) P6 loop (cpDNA

79 TMERISTEMLESS (STM), PHANTASTICA (PHAN), and LEAFY/FLORICAULA (LFY/FLO) during leaf development was a

80 MADS box transcription factors, resulting in leafy flower formation.

81 HYL1 gene of PnWB (PHYL1 plants), which show leafy flower phenotypes, up-regulate SVP of Arabidopsis

82 Leafy flowers are the major symptoms of peanut witches'

83 aric acids were isolated and quantified in a leafy food matrix.

84 In the moss, Physcomitrella patens, a 3D leafy gametophore originates from filamentous cells that

85 (LG3) domain had a milder effect, perturbing leafy gametophore patterning and archegonia development.

86 change from young filamentous protonemata to leafy gametophores in the moss Physcomitrella patens, op

87 and results in filamentous colonies lacking leafy gametophores.

88 The leafy gametophyte inhabits the intertidal zone that unde

89 ory loop involving the WUSCHEL, AGAMOUS, and LEAFY genes controls the switch from continuous meristem

90 t, suppressor of overexpression of CO1, and leafy, genes regulating anther and pistil development, a

91 Leafy green produce has been associated with numerous ou

92 ions is most relevant for E. coli O157:H7 on leafy green produce, we developed and applied a propidiu

93 affected the survival of E. coli O157:H7 in leafy green producing soils and the development of good

94 to stone fruit, caramel apples, and packaged leafy green salad contaminated with Listeria monocytogen

95 nitrate group, and -0.5 +/- 6.6 mm Hg in the leafy green vegetable group.

96 African nightshade leaves as a nutrient rich leafy green vegetable is safe and can contribute to food

97 Kale is a leafy green vegetable regularly grown using non-organic

98 ore, the cultivation and consumption of this leafy green vegetable should be promoted.

99 Africa, was investigated and compared to the leafy green vegetable Spinacia oleracea (Spinach).

100 lic compounds and bioactivity of the African leafy green vegetable, Bidens pilosa, known as Blackjack

101 tection against methylation was observed for leafy green vegetables [odds ratio (OR) = 0.83 per 12 mo

102 Inorganic nitrate, abundant in leafy green vegetables and beetroot, is thought to have

103 The quality of leafy green vegetables changes during storage.

104 etables + nitrate pills (300 mg nitrate), or leafy green vegetables containing 300 mg nitrate + place

105 Both leafy green vegetables had beneficial effects, but all B

106 h suggests that inorganic nitrate present in leafy green vegetables is converted into NO in vivo to i

107 In this study, we evaluated the effect of leafy green vegetables on BP in subjects with elevated B

108 A 5-wk dietary supplementation with leafy green vegetables or pills containing the same amou

109 usly unreported metabolite associations with leafy green vegetables, sugar-sweetened beverages, citru

110 present in especially high concentrations in leafy green vegetables.

111 , mean that so far only lettuce and related 'leafy green' vegetables are cultivated in urban farms(5)

112 We report on the largest multistate leafy green-linked STEC O157 outbreak in several decades

113 n play a role in bacterial infiltration into leafy greens by keeping stomata open and providing photo

114 We report on the largest multistate leafy greens-linked STEC O157 outbreak in several decade

115 on of polyphenols and carotenoids present in leafy greens.

116 dopsis thaliana, the floral identity protein LEAFY has strong non-autonomous effects when expressed i

117 inductive signals are integrated upstream of LEAFY Here we show that gibberellins activate the LEAFY

118 Previous experiments with leafy heterozygous plants and agamous mutants grown in c

119 mutants suggests that these maize FLORICAULA/LEAFY homologs act as upstream regulators of the ABC flo

120 While roles for FLORICAULA/LEAFY homologs in flower development have been demonstra

121 stigate the role of two duplicate FLORICAULA/LEAFY homologs in maize (Zea mays L. ssp. mays) - a mono

122 , we examine expression of the SEP-like gene LEAFY HULL STERILE1 (LHS1) in phylogenetically disparate

123 leafy hull sterile1/OsMADS1, from a grass-specific subgr

124 on of floral meristem-identity genes such as LEAFY, indicating that floral inductive signals are inte

125 ercome this effect, the transcription factor LEAFY induces expression of a gibberellin catabolism gen

126 Thus, LEAFY is a direct upstream regulator of floral homeotic

127 othesis that the transcriptional activity of LEAFY is dependent on specific co-regulators.

128 tly of AGAMOUS, and that the primary role of LEAFY is either direct repression of shoot identity gene

129 We identified leafy (lfy) and apetala1 (ap1) alleles in a mutant scree

130 LEAFY (LFY) and APETALA1 (AP1) are pivotal for the switc

131 show that the floral meristem identity genes LEAFY (LFY) and APETALA1 (AP1) are required for the acti

132 LEAFY (LFY) and APETALA1 (AP1) encode unrelated transcri

133 y in young flowers whereas the expression of LEAFY (LFY) and APETALA1 (AP1) is not substantially affe

134 Floral meristem identity genes LEAFY (LFY) and APETALA1 (AP1) promote establishment and

135 The transcription factors LEAFY (LFY) and APETALA1 (AP1), together with the AP1 pa

136 PTLF, the Populus trichocarpa homolog of LEAFY (LFY) and FLORICAULA, was cloned to assess its fun

137 tors of class B and class C gene expression, LEAFY (LFY) and SEPALLATA3 (SEP3).

138 ession of the floral meristem-identity genes LEAFY (LFY) and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS

139 ERMINAL FLOWER 1 (TFL1), APETALA 1 (AP1) and LEAFY (LFY) and the floral repression gene EMBRYONIC FLO

140 I expression are positively regulated by the LEAFY (LFY) and UNUSUAL FLORAL ORGANS (UFO) genes.

141 hologs of the flower meristem identity genes LEAFY (LFY) and UNUSUAL FLORAL ORGANS (UFO) in Gerbera h

142 nding sites for two direct activators of AG, LEAFY (LFY) and WUSCHEL (WUS), along with other putative

143 dentify the master regulator of floral fate, LEAFY (LFY) as a target under dual opposite regulation b

144 ption factor and meristem identity regulator LEAFY (LFY) controls this developmental transition by in

145 ption factor and meristem identity regulator LEAFY (LFY) controls this switch in Arabidopsis, in part

146 The major floral meristem identity gene LEAFY (LFY) directly activates FD, creating a positive f

147 The plant-specific transcription factor LEAFY (LFY) has central, evolutionarily conserved roles

148 c overexpression of the transcription factor LEAFY (LFY) in callus.

149 The plant-specific transcriptional activator LEAFY (LFY) is a central regulator of the transition to

150 Current models for Arabidopsis state that LEAFY (LFY) is central to the integration of floral sign

151 The plant-specific transcription factor LEAFY (LFY) is necessary and sufficient for this transit

152 enotype that is similar to that seen for the leafy (lfy) mutant.

153 The floral meristem identity gene LEAFY (LFY) of Arabidopsis thaliana is essential for the

154 enetic studies suggest that FLORICAULA (FLO)/LEAFY (LFY) orthologs function to control compound leaf

155 The floral meristem identity gene LEAFY (LFY) plays a role in the initiation phase through

156 in parallel with the meristem-identity gene LEAFY (LFY) to induce flowering of Arabidopsis, was isol

157 The Arabidopsis LEAFY (LFY) transcription factor is crucial in integrati

158 We show that a binding site for the LEAFY (LFY) transcription factor, present in the AG intr

159 We show that the floral identity protein LEAFY (LFY), a transcription factor expressed throughout

160 LEAFY (LFY), a transcription factor involved in the regu

161 on of CONSTANS (CO), FLOWERING LOCUS T (FT), LEAFY (LFY), and SUPPRESSOR OF OVEREXPRESSION OF CONSTAN

162 ies of at least three genes: APETALA1 (AP1), LEAFY (LFY), and UNUSUAL FLORAL ORGANS (UFO).

163 AGO1 is required for full expression of LEAFY (LFY), APETALA1 (AP1) and AGAMOUS (AG).

164 1 (TFL1), the floral meristem identity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER (CAL), and

165 tivity of the flower meristem identity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER.

166 equent activity of the transcription factors LEAFY (LFY), FRUITFULL (FUL), and APETALA1 (AP1).

167 f the floral regulators FLORICAULA (FLO) and LEAFY (LFY), in place of KNOX1 genes to regulate compoun

168 code known regulators of flower development: LEAFY (LFY), which specifies floral fate, and two AINTEG

169 of the key regulators of this transition is LEAFY (LFY), whose threshold levels of activity are prop

170 ontrolled by the meristem identity regulator LEAFY (LFY).

171 ncluding FRUITFULL (FUL), APETALA1 (AP1) and LEAFY (LFY).

172 mplex and the flower meristem identity gene, LEAFY (LFY).

173 We found that WelLFY, one of two LEAFY-like genes in Welwitschia, could be an upstream re

174 The seed plants and simple leafy liverworts each independently derived a low level

175 Here, we present evidence that LEAFY maintains floral meristem identity independently o

176 scribed as the strong green-grassy and green-leafy odour, respectively.

177 iption factors FLORICAULA of Antirrhinum and LEAFY of Arabidopsis share conserved roles in flower mer

178 y preventing the meristem from responding to LEAFY or APETALA 1.

179 e regulatory genes, the duplicate FLORICAULA/LEAFY orthologs zfl1 and zfl2.

180 data set, we identified a moss with multiple LEAFY orthologs, which contests their model and supports

181 nts that overexpress a closely related gene, LEAFY PETIOLE (LEP).

182 nducted to quantify N leaching in a tropical leafy production system (Ipomoea aquatica Forsk) and to

183 e daylength response, demonstrating that the LEAFY promoter integrates environmental and endogenous s

184 Here we show that gibberellins activate the LEAFY promoter through cis elements that are different f

185 The LEAFY protein, which is expressed throughout the flower,

186 Analysis of a LEAFY-responsive enhancer in the homeotic gene AGAMOUS i

187 thophyll content between fresh leafy and non-leafy samples.

188 Using a low-copy nuclear gene region (LEAFY second intron) we show multiple instances of allop

189 al. propose that the identification of novel LEAFY sequences contradicts our model of evolution throu

190 ion of PpRSL1 and PpRSL2 converts developing leafy shoot axes (gametophores) into rhizoids.

191 r rooting (stigmarian) systems were modified leafy shoot systems, distinct from the roots of all othe

192 A simple model co-ordinating the activity of leafy shoot tips can account for branching patterns, and

193 Leafy shoots formed on DeltaTEL1 mutants exhibit shorter

194 otype in which plants continuously elaborate leafy shoots in place of flowers.

195 brk1 phenotypes in protonema are severe, the leafy shoots or gametophores are normally shaped but stu

196 brane-targeted PIN proteins are expressed in leafy shoots, and pin mutants resemble plants treated wi

197 a complete homeotic conversion of flowers to leafy shoots, mimicking lfy ap1 double mutants in A. tha

198 h approximately one-third those measured for leafy shoots.

199 Leafy spurge (Euphorbia esula L.) is a deep-rooted peren

200 Leafy spurge (Euphorbia esula L.) is an herbaceous peren

201 Leafy spurge (Euphorbia esula) is an herbaceous perennia

202 Underground adventitious buds of leafy spurge (Euphorbia esula) undergo three well-define

203 e genes as markers to follow this process in leafy spurge (Euphorbia esula).

204 Leafy spurge DAM genes are preferentially expressed in s

205 global transcriptome data-sets obtained from leafy spurge exposed to a ramp down in both temperature

206 ed germination and vegetative propagation, a leafy spurge gene (Accession No.

207 ee different sources: (1) 3 stably expressed leafy spurge genes (60S, bZIP21, and MD-100) identified

208 , while ORE9 and ARF2 were selected from 171 leafy spurge genes, it was more efficient to identify go

209 Nevertheless, the two newly identified leafy spurge genes, ORE9 and ARF2, can serve as ortholog

210 nsus, cis-acting elements in the promoter of leafy spurge genomic clones similar to Arabidopsis RVE1

211 of the DAM gene promoters between poplar and leafy spurge have identified several conserved sequences

212 Leafy spurge is a model for studying well-defined phases

213 growth from underground adventitious buds of leafy spurge is critical for survival of this invasive p

214 and MD-100) identified from the analyses of leafy spurge microarray data; (2) 3 orthologs of Arabido

215 Leafy spurge seeds do not germinate when incubated for 2

216 buds of the model herbaceous perennial weed leafy spurge were investigated using a 23 K element cDNA

217 ed transcriptome changes in Euphorbia esula (leafy spurge) seeds with a focus on the effect of consta

218 s associated with vegetative reproduction of leafy spurge, greenhouse plants were exposed to mild- (3

219 or the transition to endodormancy in UABs of leafy spurge, which strengthened the roles of circadian

220 ar markers for endodormancy in crown buds of leafy spurge.

221 ition from para- to endo-dormancy in UABs of leafy spurge.

222 titious underground bud, and other organs of leafy spurge.

223 MADS box genes from the model perennial weed leafy spurge.

224 tiation of shoot growth (forward library) in leafy spurge.

225 rabidopsis, but were most abundant in green, leafy tissues.

226 reased levels of miR159 cause a reduction in LEAFY transcript levels, delay flowering in short-day ph

227 r further uptake is varying depending on the leafy type.

228 ing leaf morphogenesis and together with the LEAFY/UNIFOLIATA orthologue plays an important role in o

229 egulates the expression of the M. truncatula LEAFY/UNIFOLIATA orthologue SINGLE LEAFLET1 (SGL1), enco

230 moter regions of APETALA1 and 3, SEPALLATA3, LEAFY, UNUSUAL FLORAL ORGANS, TERMINAL FLOWER1, AGAMOUS-

231 For both countries leafy vegetable and vegetable food groups consistently c

232 racea L.) is an economically important green leafy vegetable crop.

233 Spinach is an important leafy vegetable enriched with multiple necessary nutrien

234 Higher dietary nitrate and green leafy vegetable intake was associated with a lower POAG

235 Green leafy vegetable intake was more strongly associated with

236 Po activity concentration follows the trend: leafy vegetable>flour>rice>fruits>pasta>other vegetables

237 ettuce (Lactuca sativa L.), the most popular leafy vegetable, are susceptible to downy mildew disease

238 Lettuce is an important leafy vegetable, consumed across the world, containing b

239 The nutritional composition of ten leafy vegetables (chicory, green lettuce, lamb's lettuce

240 commonly consumed cereals, pulses and green leafy vegetables (GLV) was determined.

241 aflatoxin (AF) in agricultural soils, green leafy vegetables (GLVs) and persistence in processed foo

242 gestion method in 20 commonly consumed green leafy vegetables (GLVs) from the typical Indian diet, pr

243 % CI: 0.35, 0.95; P for trend = 0.04), green leafy vegetables (OR: 0.59; 95% CI: 0.36, 0.96; P for tr

244 For current smokers, green leafy vegetables (ptrend = 0.05) and beta-carotene-rich

245 Green leafy vegetables (relative risk with 1-serving/d increas

246 1 serving per day; 95% CI, 0.49-0.94), green leafy vegetables (RR, 0.79; 95% CI, 0.62-0.99), citrus f

247 (mainly beta-carotene) from yellow and green leafy vegetables [carrots, pechay (bok choy), squash, an

248 Green leafy vegetables accounted for 56.7% of nitrate intake v

249 Women consuming the most green leafy vegetables also experienced slower decline than wo

250 Dietary nitrate, abundant in green leafy vegetables and beetroot, can increase NO bioactivi

251 Dietary nitrate, which is in green leafy vegetables and beetroot, decreases blood pressure

252 egetables-particularly cruciferous and green leafy vegetables and citrus fruit and juice-and ischemic

253 trations of nitrates were registered in some leafy vegetables and mussels samples, while high nitrite

254 all women consumed >=4 servings/wk of green leafy vegetables and refined grains.

255 of fruits and vegetables, particularly green leafy vegetables and vitamin C-rich fruits and vegetable

256 Dark green leafy vegetables are primary food sources for lutein and

257 85 samples of meat, dairy, fish products and leafy vegetables are reported.

258 Green-leafy vegetables are rich in nutritionally important con

259 d tatsoi) and quality traits of the selected leafy vegetables in relation to the light intensity (low

260 potent source of macular pigments than green leafy vegetables like spinach.

261 findings suggest that higher intake of green leafy vegetables may reduce the risk of cardiovascular d

262 Daily consumption of cooked, pureed green leafy vegetables or sweet potatoes has a positive effect

263 Lutein is a bioactive found in dark leafy vegetables that may be used as a nutraceutical age

264 g for potential confounders, intake of green leafy vegetables was positively associated with normaliz

265 ruit and vegetables, citrus fruit, and green leafy vegetables were 0.61 (0.43, 0.86), 0.64 (0.46, 0.8

266 Among subgroups of vegetables, green leafy vegetables were associated with a lower risk of co

267 When leafy vegetables were harvested at low as opposed to hig

268 nd zeaxanthin are carotenoids found in green leafy vegetables with interesting antioxidant properties

269 tochemicals and antioxidant activities in 25 leafy vegetables with two common boiling practices viz.,

270 attern (whole grains, fruit, nuts, and green leafy vegetables) was inversely associated with CRP, IL-

271 No associations were observed for green leafy vegetables, 8 botanical groups, and 17 specific fr

272 l practice of eating staples with dark-green leafy vegetables, and 2 study groups, who were given eit

273 A higher consumption of citrus fruit, green leafy vegetables, and beta-carotene- and vitamin C-rich

274 getables, total fruits and vegetables, green leafy vegetables, and several botanically and phytochemi

275 t types of food (fish, chicken, canned tuna, leafy vegetables, bread and butter).

276 itrate, found in high concentration in green leafy vegetables, can be converted to NO in vivo and dem

277 meat, and margarine, and low intake of green leafy vegetables, cruciferous vegetables, and coffee may

278 The method was tested in different green leafy vegetables, evidencing diverse tocochromanol profi

279 tervention was a daily snack made from green leafy vegetables, fruit, and milk (treatment group) or l

280 A daily snack providing additional green leafy vegetables, fruit, and milk before conception and

281 Lutein, abundant in dark leafy vegetables, has been associated with several healt

282 Amongst green leafy vegetables, new varieties of lettuce enriched in l

283 rate, which is found in high levels in green leafy vegetables, on liver steatosis associated with met

284 in lutein and zeaxanthin, such as dark-green leafy vegetables, or by supplementation with lutein or z

285 Carotene-rich yellow and green leafy vegetables, when ingested with minimal fat, enhanc

286 hod for quantification of vitamin E in green leafy vegetables.

287 h consisted largely of squashes and root and leafy vegetables.

288 use if similar effects were found for other leafy vegetables.

289 ed lettuce were higher compared to the other leafy vegetables.

290 in roots and tubers, but 0.155 mg kg(-1) in leafy vegetables.

291 gumes, soy-based foods, rice, and dark-green leafy vegetables; and a salad and wine diet, high in let

292 e inverse association was stronger for green leafy vegetables; in multivariate analysis, persons cons

293 was characterized by high intakes of green, leafy vegetables; salad dressings; tomatoes; other veget

294 Green leafy volatiles (GLV), six-carbon aldehydes, alcohols, a

295 le production of jasmonates (JAs), and green leafy volatiles (GLVs) respectively.

296 s conferred by a gain-of-function transgene, LEAFY:VP16, that appears to act as a dominant negative,

297 PRESSOR OF OVEREXPRESSION OF CONSTANS1-1 and LEAFY, whereas inhibition of GA biosynthesis with paclob

298 uch as Matricaria inodora RAY2 and M inodora LEAFY, which determine floret and phyllary identity.

299 er action of meristem-identity genes such as LEAFY, which encodes a transcription factor that determi

300 AGAMOUS indicates that direct interaction of LEAFY with this enhancer is required for its activity in