ライフサイエンスコーパス: leaves

1 kg(-1) (berries) and 1.88-3.72 g GAE.kg(-1) (leaves).

2 0 mug of Se/g dry weight (DW) in flowers and leaves.

3 glucuronidase (GUS) reporter gene in tobacco leaves.

4 m various plant sources, including green tea leaves.

5 (-1) in berries and 71.54-153.99 g.kg(-1) in leaves.

6 y correlated with mahanine content in the MK-leaves.

7 type and transgenic oil-accumulating tobacco leaves.

8 last cell cultures, and Arabidopsis thaliana leaves.

9 ion of IVDV-treated as compared to untreated leaves.

10 g different tissues, including trichome-free leaves.

11 f drought-induced tissue death in individual leaves.

12 city and control of acyl lipid metabolism in leaves.

13 to 3.5 times, in extracts from IVDV-treated leaves.

14 to fungal and bacterial pathogens in tomato leaves.

15 em and an increase in the number of juvenile leaves.

16 ommon in species with high construction cost leaves.

17 red light induces stomatal opening in intact leaves.

18 ze of aerial plant organs, such as seeds and leaves.

19 tes rootlets are true roots and not modified leaves.

20 the cholesterol freely interchanges between leaves.

21 The other states that rootlets are modified leaves.

22 r driving M-cell-specific expression in rice leaves.

23 damaged leaves compared to undamaged control leaves.

24 hexoside, and rutin were identified blanched leaves.

25 he xylem in the leaf midrib embolized across leaves.

26 ected trees before symptom development among leaves.

27 was affected differently in floral buds and leaves.

28 hloroplast-to-chromoplast differentiation in leaves.

29 al carotenoid concentration in fresh lettuce leaves.

30 icus root hairs and in Nicotiana benthamiana leaves.

31 ntent and the antioxidant potential of olive leaves.

32 but is dispensable for midvein formation in leaves.

33 reaction in wild-type and engineered tobacco leaves.

34 ely, within 90 min after infection of pepper leaves.

35 aize (Zea mays) transcription factor ZmFUSED LEAVES 1 (FDL1)/MYB94.

36 omponents Dicer-like 1 (DCL1) and Hyponastic Leaves 1 (HYL1) with RNA Polymerase II.

37 uch as Dicer-like 1, SERRATE, and HYPONASTIC LEAVES 1, whereas during de-etiolation both pri-miRNAs a

38 derably lower (76.1-205.2 mg.kg(-1)) than in leaves (1477.7-8709.0 mg.kg(-1)).

39 The fast drying of solvent at liquid surface leaves 3D-like perovskites which surprisingly templates

40 otides from the 3' end of U6 and, in humans, leaves a 2',3' cyclic phosphate that is recognized by th

41 bubbles at a free surface, and their rupture leaves a collection of small drops and bubbles.

42 This leaves a lipid bilayer with a relatively high density of

43 show that implementation of current policies leaves a median emission gap of 22.4 to 28.2 GtCO(2)eq b

44 This decrease in TREK-1 levels leaves a subset of channels amendable to pharmacological

45 This ask1 mutant produces twisted rosette leaves, a reduced number of petals, fewer viable pollen

46 Wheat leaves also host epiphytic bacteria; these include ice-n

47 mical aglycones in edible African nightshade leaves, an underutilized food resource in the sub-Sahara

48 standing of morphogenetic processes in plant leaves and animal epithelia and perhaps even the formati

49 used to predict water and CO(2) fluxes from leaves and canopies.

50 vivo Cl(-) distribution in Spinacia oleracea leaves and chloroplasts shows that sufficient Cl(-) is p

51 onutrient (Fe, Zn, Mn, Cu) concentrations of leaves and edible parts of three East African staple cro

52 relations between nutrient concentrations of leaves and edible parts than annuals.

53 largest differences in correlations between leaves and edible parts.

54 there is a prompt accumulation of proline in leaves and effective protection of chlorophyll during pe

55 BIA metabolism, occurring primarily in young leaves and embryos of sacred lotus.

56 ure perception on plastid metabolism in both leaves and fruit, specifically on the accumulation of is

57 Their cladodes, leaves and fruits are notable for water-soluble compound

58 ids (GA) are alkylphenol constituents of the leaves and fruits of Ginkgo biloba.

59 Fungal challenge assays on leaves and fruits showed that the transgenic lines were

60 Actium(R), on Capsicum annuum L. cv Palermo leaves and fruits.

61 d compounds in tomato (Solanum lycopersicum) leaves and fruits.

62 d PULSE to control immune responses in plant leaves and generated Arabidopsis transgenic plants.

63 LAI, with the reverse found for short-lived leaves and higher maximum photosynthetic capacity.

64 tte leaves and systemically infected cauline leaves and inflorescence.

65 e bread with addition of the stinging nettle leaves and its extract, and bread's composition in pheno

66 larvae were more likely to move from damaged leaves and leaves that had been exposed to volatiles fro

67 locusts the choice between untreated millet leaves and leaves that received one of the two fertiliza

68 ance to drought such as small sclerophyllous leaves and lower percent loss of hydraulic conductivity.

69 A wave of green leaves and multi-colored flowers advances from low to hi

70 al activity at early stages gives radialized leaves and no traps.

71 ce is common in seeds and spores but rare in leaves and other vegetative green tissues.

72 metabolic profile of its edible parts (blade leaves and petioles) also related to quality, freshness

73 n thrips, chlorogenic acid concentrations in leaves and plant growth.

74 ence of 26and 29 common polyphenols in olive leaves and pulp extracts, respectively.

75 esis by investigating gene expression in the leaves and rootlets of Isoetes echinospora.

76 spersal) act on fungal community assembly in leaves and roots early in host development and when sorg

77 Using a plastid preprotein expressed in both leaves and roots of stable transgenic plants, we showed

78 ter exposure increased Na and Cl contents in leaves and roots, but did not affect sulfate contents si

79 o17 conferred less N accumulation in the ear leaves and seed kernels resembling that of the zmnlp5 mu

80 A reduction in caffeine in coffee leaves and seeds might result in decreased ability again

81 A, aba4 nxd1 exhibits reduced levels in both leaves and seeds.

82 udy, we mimicked natural injuries in growing leaves and stems to study the reunion between mechanical

83 obtained for mechanically inoculated rosette leaves and systemically infected cauline leaves and infl

84 able amounts of bioactive compounds in olive leaves and the effect of abiotic stresses on their synth

85 to controlling the movement of toxic ions to leaves and, therefore, can be seen as a mechanism to cop

86 angles increased from the top to the bottom leaves, and compared to cultivated grain sorghums, the a

87 is work has taken place and been assessed in leaves, and limited consideration has been given to the

88 ynthesis efficiency and growth rate, smaller leaves, and lower grain yields than wild-type (WT) plant

89 ll division and gene expression in expanding leaves, and reverse genetic analyses of homologous NS1 t

90 om mature, developing, and germinated seeds, leaves, and roots exposed to different abiotic stresses.

91 tive growth and expansion to form wide, flat leaves are unclear.

92 e that the consumption of African nightshade leaves as a nutrient rich leafy green vegetable is safe

93 o synthesize carbon dots (CDs) from Rosemary leaves, as a carbon source.

94 result in AM initiation only in the axils of leaves at a certain age.

95 nhouse experiment, we enriched pitcher-plant leaves at different rates with bovine serum albumin (BSA

96 e (WT) and demeter-like 3 (dml3) Arabidopsis leaves at three developmental stages revealed hypermethy

97 Oligodendrocyte loss in neurological disease leaves axons vulnerable to damage and degeneration, and

98 nthetic photon flux density (PPFD) until the leaves become light saturated.

99 find that sufficiently long-ranged dispersal leaves behind a mosaic of monoallelic patches, whose num

100 rcane (Saccharum officinarum L.) cultivation leaves behind around 20 t ha(-1) of biomass residue afte

101 f the colony and trigger an instability that leaves behind striking flower-like patterns.

102 This is despite the leaves being exposed to water twice during formation and

103 mart canopy" ideotype has been proposed with leaves being upright at the top and more horizontal towa

104 Of the four endogenous hormones measured in leaves, both indole-3-acetic acid and abscisic acid cont

105 In young leaves, both RBR and E2FB are abundant and form a repres

106 to 2% of the total Rca protein in unstressed leaves but increased three-fold in leaves exposed to ele

107 and capsianosides decreased with ripening in leaves, but organic acids, monosaccharides, and caroteno

108 th influence physiological function in plant leaves, but their relative contributions to changes in t

109 Direct measurements of leaves by attenuated total reflectance Fourier-transform

110 Blast resistance was determined in rice leaves by spray and punch inoculations.

111 In axils of young leaves, BZR1 and PIF4 repress AGO10 expression to preven

112 The evolved enzyme leaves C-H bonds present in the silane substrates untouc

113 ral envelopes and diminishes infectivity but leaves cellular membranes intact.

114 scriptomic and metabolomic data on the fresh leaves collected from 136 representative tea accessions

115 st levels of phenolic compounds and that the leaves collected in the summer presented a number of com

116 beetles were more likely to choose undamaged leaves compared to damaged leaves or those exposed to vo

117 een exposed to volatiles from nearby damaged leaves compared to undamaged control leaves.

118 ogenins in 20 differently sourced nightshade leaves, comprising two African species Solanum scabrum a

119 Nonetheless, olive leaves (containing thin branches), which are separated d

120 habitats, chemical information from mangrove leaves could provide a source of settlement cues for coa

121 In this work, six olive leaves cultivars, including three wild cultivars, and tw

122 l of bioactive phytochemical, mahanine in MK leaves depending upon geographical location, weather sui

123 llulosic biomasses, the composition of olive leaves depends on cultivar and to know it is essential f

124 The plant tissue (fruit or leaves) did not influence C. fioriniae repellency effect

125 the scarcity of model TKI material families leaves difficulties in disentangling key ingredients fro

126 Structure factors of components in both leaves display a peak at nonzero wavevector.

127 Natural selection leaves distinct signatures in the genome that can reveal

128 ti-nutritive compounds in African nightshade leaves during moist cooking.

129 tential, which may impede carbon export from leaves during the day because the xylem is the source of

130 Given a binary tree [Formula: see text] of n leaves, each leaf labeled by a string of length at most

131 of stem-like structures and repositioning of leaves, elicited by shade cues, including a reduction in

132 ession of Ma1 expression in 'McIntosh' apple leaves, 'Empire' apple fruit, and 'Orin' apple calli res

133 ts (e.g., bird feathers, insect wings, plant leaves, etc.) are superhydrophobic with rough surfaces a

134 A crude extract of Schinus terebinthifolia leaves exhibited 80% inhibition at 256 ug/mL and underwe

135 P deficiency after 7 d, while newly emerging leaves exhibited partial restoration compared with untre

136 k and Sesamum calycinum subsp. angustifolium leaves exhibited strong quorum sensing inhibition activi

137 hesis is built upon measurements made on dry leaves experiencing direct light.

138 nstressed leaves but increased three-fold in leaves exposed to elevated temperatures for 5 d and rema

139 Olive leaves extract (OLE) was spray-dried with maltodextrin (

140 Olive leaves farmed from trees are valuable for the production

141 In this study, the chemical composition of leaves, flowers and stems of jambu cultivated in hydropo

142 and accumulated up to 200 mg of Se/kg DW in leaves, flowers, and seeds.

143 Although long-dsRNA remained in the treated leaves for at least 10 days, its systemic movement was n

144 Remarkably, Welwitschiophyllum leaves from Early Cretaceous, Brazil provide the first c

145 exes and epidermal oil cells with angiosperm leaves from the lower Potomac Group.

146 Food choice experiments with leaves from wild-type and SOT1 knockdown trees suggest t

147 and antioxidant capacity associated with the leaves, fruit, and flowers.

148 The aerial parts of plants, including the leaves, fruits and non-lignified stems, are covered with

149 xperimental reefs supplemented with mangrove leaves grown away from humans attracted more fish recrui

150 sity of species than reefs supplemented with leaves grown near humans.

151 Conversely leaf shape, specifically rounder leaves, had a strong positive impact on both fruit sugar

152 such as Stupice and Glacier, with very round leaves, had the highest performance in both fruit sugar

153 factory cues, that nests containing wormwood leaves have lower ectoparasite loads, and that nests wit

154 ape to fruit quality in tomato, with rounder leaves having significantly improved fruit quality.

155 y the discontinuous frost pattern on natural leaves, here we report findings on the condensation fros

156 is, and reduction of carotenoid synthesis in leaves in a PHYB1B2-dependent manner.

157 Here, we find that juvenile and adult leaves in all three species photosynthesize at different

158 ticle concluded that the extract substitutes leaves in bread as a product of a high benefit.

159 s: Results from experiments with Arabidopsis leaves in conventional controlled environments are not n

160 aken under steady-state conditions; however, leaves in crop fields experience frequent fluctuations i

161 acteristics of oilseed rape (Brassica napus) leaves in different growth stages under different K leve

162 e of the transcriptional changes in cucumber leaves in response to spider-mite herbivory and that of

163 and, a decrease in reflectance of host plant leaves in the near-infrared portion of the radiometric s

164 ucting transcriptomic analysis of developing leaves in the WT and the three mutants we identified dif

165 temperature, including heat avoidance, where leaves increase water loss to evaporatively cool regardl

166 While thermal treatment of lettuce leaves increases carotenoid availability, resulting in h

167 pression of ShMYB78 in Nicotiana benthamiana leaves induced the ectopic deposition of suberin and its

168 we examined the global AS changes in tomato leaves infected with Phytophthora infestans, the infamou

169 Its activation leaves innate behavior unaffected, however.

170 ted that the incorporation of fresh wormwood leaves into nests may serve a similar function for sparr

171 incorporate wormwood (Artemisia verlotorum) leaves into their nests around the same time that local

172 These findings demonstrate that amylose in leaves is not essential for the viability of some natura

173 We show that delivery of N to host leaves is not increased by host nutrient deficiency but

174 ptake (FWU), the direct uptake of water into leaves, is a global phenomenon, having been observed in

175 to the lower-to-mid continental crust, which leaves little footprint behind by the time magmas reach

176 ht tolerance was greater among species whose leaves lost turgor (wilted) at more negative water poten

177 the dwarf mutant showed shorter stems, wider leaves, lower canopy height, and a darker green color th

178 cient cells where PS is low, LDL cholesterol leaves lysosomes but fails to reach the ER, instead accu

179 ria delavayi) varies among populations, with leaves matching their local backgrounds most closely.

180 species became more pronounced and unique as leaves matured.

181 Many plant water use models predict leaves maximize carbon assimilation while minimizing wat

182 Leaves may provide information on plant health, however

183 centrate (PC) from Moringa Oleifera defatted leaves (MODL) by enzymatic extraction using Viscozyme L

184 articularly in the roots, but showed that in leaves more than 50% of the response is independent of S

185 crease in absolute triacylglycerol levels in leaves, more than 4-fold higher than in wild-type plants

186 nder conditions of slow mass transport, this leaves no protons to support hydrogen evolution.

187 ess of carbon uptake; or heat failure, where leaves non-adaptively lose water also regardless of carb

188 We quantify vein networks for leaves of 260 southeast Asian tree species in samples of

189 ttime O(2) consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).

190 assess potential pathways for water entry in leaves of beech, a widely distributed tree species from

191 genes showed similar expression patterns in leaves of both desiccation-tolerant and -sensitive speci

192 At higher elevations, leaves of broadleaf species tend to become narrower, but

193 Microscopic examination of the Cg-challenged leaves of chilli-CgCOM1i lines revealed highly suppresse

194 the two points were measured in the top four leaves of each plant.

195 roots and A. thaliana roots compared to the leaves of each respective species.

196 es for differential expression of genes from leaves of ecologically well-characterized ecotypes of tu

197 which we quantified in both rhizosphere and leaves of field-grown plants using 16S-v4 and ITS1 ampli

198 ransiently expressed with these effectors in leaves of Nicotiana glutinosa.

199 xidant activity were analyzed in berries and leaves of nine cultivars of sea buckthorn (Hippophae rha

200 , which is 16.9 times higher than that of MK-leaves of north-eastern part of India (which measured as

201 his study evaluated the metabolic profile of leaves of olive cultivars (Arbequina, Manzanilla and Pic

202 ophosphorus herbicide that is applied to the leaves of plants and crops to kill broadleaf plants and

203 Whereas leaves of rice (Oryza sativa) cultivar Nipponbare predom

204 quantitative analysis data comprised that MK-leaves of southern part of India contains highest amount

205 results it was possible to observe that the leaves of the cultivar Manzanilla presented the highest

206 bial assemblage that inhabits the cup-shaped leaves of the pitcher plant Sarracenia purpurea.

207 Larvae damaged many leaves on a plant but removed relatively little tissue f

208 The characteristic shape that imprinting leaves on influenza susceptibility could foster importan

209 rafting without cotyledon node and cotyledon leaves on rootstocks, and with cotyledon node but withou

210 stocks, without cotyledon node and cotyledon leaves on scions and rootstocks or halved cotyledon node

211 nd with cotyledon node but without cotyledon leaves on scions were easy to perform and suitable for i

212 n the metabolome of MeJA-treated Arabidopsis leaves, on the breast cancer cell cycle, is associated w

213 Phyllotaxis, the regular arrangement of leaves or other lateral organs in plants including pinea

214 photosynthesis beside the other organs like leaves or the flag leaf.

215 choose undamaged leaves compared to damaged leaves or those exposed to volatile cues of damage.

216 gle has, to date, been studied on one or two leaves, or data have been merged from multiple leaves to

217 This leaves people living with HIV-1 burdened by a lifelong c

218 gh amounts in above-ground tissues including leaves, petioles, and stems, but were also found at lowe

219 In fab1 leaves, phosphatidylglycerol, the major chloroplast phos

220 ctance spectra of intact vs dried and ground leaves points to cuticular development - and not interna

221 ite loads, and that nests with more wormwood leaves produce heavier chicks.

222 Acute SARS-CoV-2 infection leaves protracted beneficial (ie, activation of T cells)

223 d traits correlated with metabolic traits in leaves rather than in the stem or storage roots.

224 ed flowering had lower SLA (thicker, tougher leaves) regardless of the competitive environment, a pat

225 velopmental stages and outgrowth of compound leaves remains largely unknown.

226 ually defined ground-truth regions from >700 leaves representing 50 southeast Asian plant families.

227 The US multi-payer system leaves residents uninsured or underinsured, despite over

228 g dry weight in cultivated and wild purslane leaves, respectively.

229 foliar nitrogen and water contents in shaded leaves resulted in feedback and necessity consumption pa

230 We also found that TARK1 OE in leaves resulted in increased susceptibility to bacterial

231 focused on the cotyledon node and cotyledon leaves retained on scions, rootstocks, without cotyledon

232 mparison between the dwarf mutant and the WT leaves revealed 360 differentially-expressed genes (DEGs

233 Treated leaves reverted to P deficiency after 7 d, while newly e

234 obtain a phytocomplex from Lippia citriodora leaves rich in bioactive compounds.

235 n the phloem-loading zone and guard cells in leaves, root vasculature, and shoot apical meristem, imp

236 les of these MADS-box genes were analyzed in leaves, roots, stem sections and after hormones treatmen

237 fermentation index (r = 0.670, p < 0.05) of leaves samples.

238 ter activity was observed in roots, ligules, leaves, sheaths, pollen grains, and surrounding the vasc

239 Wounded leaves show faster, more extensive STB, suggesting that

240 Source leaves, sink leaves, stems and storage roots were harves

241 n of RNA synthesis is fully retracted, which leaves space in the active-site cavity for RNA elongatio

242 several agro-morphological traits related to leaves, stems and roots with high heritability.

243 Source leaves, sink leaves, stems and storage roots were harvested during st

244 ) nanoparticles with diameters <50 nm in the leaves, stems, and roots.

245 The leaves studied here were nearly poikilothermic, with no

246 In young leaves subjected to biotic stress, we found up-regulatio

247 situ hybridization assays of maize embryonic leaves suggested that maize ANT1 (ZmANT1) regulates vasc

248 ILTPS genes were detected in infected poplar leaves, suggesting possible involvement of these recentl

249 ine stevioside standard solutions and stevia leaves suspensions in water and ethanol/water solvents b

250 nd UBP13 were downregulated produced smaller leaves that contained fewer and smaller cells.

251 tudies report pesticide residues on milkweed leaves that could act as a contributing factor when inge

252 more likely to move from damaged leaves and leaves that had been exposed to volatiles from nearby da

253 e choice between untreated millet leaves and leaves that received one of the two fertilization treatm

254 We show here that ISOW leaves the boundary and spreads into the interior toward

255 om linear orthogonal transformation key that leaves the likelihood of quantitative trait data unchang

256 al response of a single cell to stimuli that leaves the membrane intact.

257 has previously been shown that some cyclin C leaves the nucleus following cytotoxic stress to induce

258 enters embryonic diapause until the newborn leaves the pouch 9 mo later.

259 Despite considerable variation between leaves, the amount of embolized vessels in the xylem of

260 In species with compound leaves, the positions of leaflet primordium initiation a

261 interface with ATP-bound HSP70 dimers, which leaves them intact and thereby eliminates an inhibitory

262 Leaves themselves decreased the quality of the bread, wh

263 ent conditions were sprayed with Fe in their leaves, they were unable to deactivate root Fe uptake.

264 efects, standard Monte Carlo (MC) simulation leaves this ice model stuck in a state of disordered pro

265 r the formation of both planar and nonplanar leaves through adaxial-abaxial domains of gene activity

266 multiple evolutionary origins of cup-shaped leaves through simple shifts in gene expression.

267 ent post-harvest drying techniques for betel leaves through the quantitative analysis of unambiguousl

268 diation at multiple frequencies within plant leaves to determine absolute water content in real-time.

269 aves, or data have been merged from multiple leaves to generate average values.

270 ucrose from photosynthetically active source leaves to seed sinks.

271 ls in coordinating the response of different leaves to stress.

272 ion of miR399 and up-regulation of miR482 in leaves treated with dsDNA compared to the control.

273 nd palisade tissue thickness, in K-deficient leaves triggered significant enlargement of mesophyll ce

274 orted by the results obtained in Arabidopsis leaves under basal and autophagy-activating conditions.

275 supply established nests with fresh wormwood leaves using olfactory cues, that nests containing wormw

276 topic labeling were carried out on sunflower leaves, using glucose that was (13) C-enriched at specif

277 Leaves vary from planar sheets and needle-like structure

278 g(-1) in berries and 22.81-46.32 g.kg(-1) in leaves, vitamin E content was 6.98-29.91 g.kg(-1) in ber

279 The proportion of CLas-positive leaves was 2.5% for nymphs and 36.3% for adults.

280 VDV) on extraction of polyphenols from olive leaves was investigated.

281 mber of embolized vessels in the petioles of leaves was observed across the canopy of plants that had

282 m C(4) to C(4) -CAM hybrid photosynthesis in leaves was strictly under environmental control.

283 Extractions of TPC from leaves were achieved either using 100% water as a solven

284 Brassicaceae leaves were also moderate dietary sources of Se, Ni, Zn

285 rall, unfermented and fermented P. pellucida leaves were best dried with microwaving and freeze dryin

286 es regardless of fertilization rate, whereas leaves were effective only against HeLa cell line.

287 Recently, tobacco (Nicotiana tabacum) leaves were engineered to accumulate oil at 15% of dry w

288 e alkaloids and sapogenins in all nightshade leaves were evaluated and found to be safe for consumpti

289 Leaves were significantly richer source of total flavono

290 and adults into healthy (uninfected) citron leaves when both vector stages were reared from eggs on

291 21- and 22-nt) were detected in non-treated leaves, which indicates endogenous processing and transp

292 L. asiaticus titer within the infected leaves, which suggests that melatonin might play an anti

293 intensify, tall trees with drought-sensitive leaves will be most vulnerable to immediate and longer-t

294 auxin concentration; feeding the transgenic leaves with exogenous auxin partially restores leaf widt

295 Further, we found juvenile leaves with high SLA were associated with better photosy

296 lant shares the presence of gum ducts inside leaves with its presumed extant relative the gnetalean W

297 Long-lived leaves with lower maximum photosynthetic capacity maximi

298 ants, and some transcripts migrate to distal leaves within several plant species.

299 evalent, namely Sanguiin H-10, especially in leaves without fertilization (control).

300 Repeated pregnancy leaves young mothers nutritionally deprived which may in