ライフサイエンスコーパス: leaves

1 No [(14) C]tartaric acid was found in tomato leaves.

2 olite profiling were performed on stalks and leaves.

3 sulting in lower levels of available iron in leaves.

4 ent and common to plants without sporophytic leaves.

5 plant tissues, especially in roots and older leaves.

6 ATP synthase (cATPase) purified from spinach leaves.

7 ts (using UPLC-PDA) were determined in dried leaves.

8 are less prone to photoinhibition than older leaves.

9 splays high JA pathway activity in undamaged leaves.

10 n granule initiation in Arabidopsis thaliana leaves.

11 cp3 tcp4 tcp10 mutant with strongly crinkled leaves.

12 te loss in variously washed and stored salad leaves.

13 echanisms in control and AHO-treated tobacco leaves.

14 that is prominently expressed in Arabidopsis leaves.

15 ations in the metabolite profiles of spinach leaves.

16 omposition and bioactive potential of stevia leaves.

17 er phase and the consumption of contaminated leaves.

18 d-heat than those from untreated and steamed leaves.

19 higher from spinach puree compared to whole leaves.

20 superhydrophobic surfaces inspired by plant leaves.

21 the nutraceutical effects ascribed to their leaves.

22 itu stilbenes on the same stressed grapevine leaves.

23 veins and enter the apoplastic space in the leaves.

24 he high content of steviol glycosides in its leaves.

25 subdivision of planar plant organs, such as leaves.

26 ielectric materials like hair, clothing, and leaves.

27 rough tree trunks as well as soft, flexible leaves.

28 flowers and fruits and red colors of autumn leaves.

29 gastric and intestinal phases than in fresh leaves.

30 increased photosynthetic performance of its leaves.

31 nd lysophosphatidylcholine (LPC) contents in leaves.

32 s PpeS6PDH in buds and represses the gene in leaves.

33 or pretreated leaves and 2.20g for in natura leaves.

34 loping C4 leaves compared with developing C3 leaves.

35 ent plant lineage with diversified evergreen leaves.

36 xin biosynthesis and transport in developing leaves.

37 through their tissues to roots, shoots, and leaves.

38 trikingly higher Klason lignin levels in the leaves.

39 F) mini sponge cakes fortified with broccoli leaves.

40 , P was quickly solubilized from decomposing leaves.

41 ip cells of glandular trichomes on stems and leaves.

42 ight, and [(15)N2]DNAN yielded (15)NO2(-) in leaves.

43 for the variation of anthocyanins in lettuce leaves.

44 ), which are also found in herbivore-induced leaves.

45 f 25% in the amount of ozone that enters the leaves.

46 respectively when compared with their fresh leaves.

47 iverse bacterial community washed from plant leaves.

48 to CBZ was highest in fruits (up to 2.5) and leaves (0.5), suggesting an intensive transformation of

49 reased under nutrient-enriched conditions on leaves (1.32x) and wood (1.38x), but not FBOM.

50 nscripts were found to be highly abundant in leaves (16-fold) as compared to flower tissues.

51 Additive gene expression was observed in leaves (3605 genes) and tubers (6156 genes) that contras

52 nt increases glucose plus sucrose content in leaves 80-fold relative to the wild type, total fatty ac

53 Upon excision, it leaves a short DNA footprint that can create in-frame an

54 This leaves a single variable-the transmittance spectrum of t

55 1 has cyclic phosphodiesterase activity that leaves a terminal 3' phosphate which prevents overproces

56 the United States, we find that seasonal flu leaves a transient wake of heterosubtypic immunity that

57 Leaves account for a large part of above-ground biomass

58 catechin and PAs in the rust-infected poplar leaves accumulated significantly at the site of fungal i

59 monitoring of H2O2 produced in A. tequilana leaves after inoculation of their endophytic bacteria (E

60 ared from Arabidopsis (Arabidopsis thaliana) leaves against lipid peroxidation.

61 Thicker leaves allow plants to grow in water-limited conditions.

62 on (photoacclimation) is the process whereby leaves alter their morphology and/or biochemistry to opt

63 es, but dramatically less so in mature adult leaves, an observation consistent with PP TC development

64 steviol glycosides was 4.02g for pretreated leaves and 2.20g for in natura leaves.

65 pruce in combination with regular harvest of leaves and birch sap and an understory of ground elder,

66 Specifically, we highlight newly added leaves and branches in the genomic tree of bacterial and

67 rminations were performed with extracts from leaves and branches of peach tree.

68 expressed in tobacco (Nicotiana benthamiana) leaves and does so in a manner that requires its RING do

69 ion of the aqueous extract from O. odorifera leaves and evaluate the correlation of their phytochemic

70 ition of polar extracts obtained from stems, leaves and flowers of R. eriocalyx by HPLC, and determin

71 nce was evaluated and validated to artichoke leaves and fruits according to DG-SANTE Guidelines.

72 al ion source for analysis, both surfaces of leaves and fruits of Macaranga vedeliana, an endemic New

73 natural and artificial surfaces (i.e. plant leaves and glass).

74 asmonate (MeJA) was applied in a vineyard on leaves and grape clusters of cv Sangiovese to test its a

75 s subjected to square wave light had thicker leaves and greater photosynthetic capacity compared with

76 (lfs) mutants fail to produce cotyledons and leaves and grow a naked pin while maintaining an active

77 soluble amino acids and carbohydrates in the leaves and high activity of enzymes involved in the C4 p

78 creased Mn concentrations in the apoplast of leaves and induced the toxicity symptoms.

79 hypothesized that the inhibitor expressed in leaves and inflorescence might be transported to the see

80 through both the consumption of contaminated leaves and neonicotinoids leaching from leaves into wate

81 plication caused stomatal closure in excised leaves and peeled epidermis.

82 stantial trait coordination occurred between leaves and roots, but the strength varied between growth

83 ansgenic lines emitted dimethyl sulfide from leaves and roots, no sulfur-containing volatiles were de

84 f an ultrasensitive biosensor in Arabidopsis leaves and roots.

85 d cellular neutral lipid homeostasis in both leaves and seeds.

86 PM was isolated from the intact leaves and size fractionated, and EPFRs on PM quantified

87 requently in nature as flowers, snow-flakes, leaves and so on.

88 wet weight (ww) and 94 ng g(-1) ww in birch leaves and spruce needles, respectively.

89 controlled by stomata, small pores on plant leaves and stems formed by guard cells.

90 s of sunlit leaves than light limited, shade leaves and sunlit foliage are more abundant in the upper

91 han those of extracts from untreated/steamed leaves and synthetic colorant.

92 d-heat was compared with that from untreated leaves and synthetic colorant.

93 ronments by fine-tuning energy production in leaves and the availability of water and nutrients from

94 e preceded the appearance of embolism in the leaves and the stem by several days.

95 From its leaves and thin stems different kinds of beverages are p

96 cent protein (GFP)-UVR8 fusions in Nicotiana leaves and transgenic Arabidopsis.

97 We performed circRNA-Seq on B73 seedling leaves and uncovered 2804 high-confidence maize circRNAs

98 ity such as the development of heteromorphic leaves and well-developed roots system.

99 ants of the over-expressing lines have curly leaves and were generally smaller in stature.

100 om what is typically observed in terrestrial leaves, and based on this finding, we discuss strategies

101 A trained panel was used to evaluate leaves, and chemical data were obtained for polyatomic i

102 promoting pectin degradation in Arabidopsis leaves, and Pst DC3000 might enhance its infection by ma

103 extract obtained by homogenization of rocket leaves, and stabilized by addition of CaCl2.

104 r also accumulates to higher levels in these leaves, and the rate of FA synthesis increases by 58%.

105 the tcp2 tcp4 mutant that has enlarged flat leaves, and the tcp2 tcp3 tcp4 tcp10 mutant with strongl

106 nd elevated (550 [ppm]) [CO2 ] overinvest in leaves, and this is predicted to decrease productivity a

107 environments only in arid conditions; small leaves are also found in high latitudes and elevations.

108 cclimate to high light and show that younger leaves are less prone to photoinhibition than older leav

109 he phytochemical constituents of B. oleracea leaves are polar and possess strong antioxidant potentia

110 e fitness value of leaves varies greatly and leaves are protected by jasmonate (JA)-inducible defense

111 All grass leaves are strap-shaped with a series of parallel veins

112 hern Brazil whose fruit (known as butia) and leaves are used to make many food products and crafts.

113 forests tended to allocate more nutrients to leaves as compared with angiosperm forests, whereas the

114 ts; oxalate and threonate are accumulated in leaves, as is oxalyl threonate.

115 auxin homeostasis and activity in developing leaves, as well as reduced leaf vein density and aberran

116 Leaves become yellow or disintegrate, and an off-odor ma

117 n and longitudinal phonons whose fast escape leaves behind a 2D-projected mass density increase endow

118 ry for the kinetics of the growth front that leaves behind thin-walled complex structures.

119 the level of succulence in roots, stems, and leaves being subject to a certain degree of evolutionary

120 They consist on stalks, inflorescences, and leaves, blanched and non-blanched, sharing the nutrition

121 the production of Pip in pathogen-inoculated leaves but is not the exclusive reducing enzyme involved

122 ubiquitous in mature cotyledons and juvenile leaves, but dramatically less so in mature adult leaves,

123 ts have longer hypocotyls and larger rosette leaves, but they also uniquely display early flowering,

124 ansverse sections of M x giganteus stems and leaves by atomic force microscopy indicates that phloem

125 Proteins from leaves can contribute to a more complete use of resource

126 rule, and that the phloem network in poplar leaves can generate the pressure gradient envisioned in

127 e how the optical method, used previously in leaves, can be adapted to measure the xylem vulnerabilit

128 hich the uORF was mutated exhibited serrated leaves, compact rosettes, and, most significantly, short

129 er auxin content were found in developing C4 leaves compared with developing C3 leaves.

130 igate the topology of developing Arabidopsis leaves composed solely of pavement cells.

131 The developmental changes in leaves conferred by this gene are associated with a phot

132 pment across juvenile, transition, and adult leaves correlated positively with levels of miR156, a ma

133 t thermal response of respiratory enzymes in leaves could be conserved.

134 argets important winter sources such as tree leaves could be highly effective for reducing P loading

135 n roots and the mercury content of vegetable leaves decreased significantly after water rinses.

136 In plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of

137 line in Rubisco constrained Vcmax and An for leaves developed at higher Tgrowth and resulted in poor

138 Although stomata in true leaves display normal density and morphology when PGX3 e

139 show greatly reduced accumulation of Pip in leaves distal to P. syringae inoculation, they display a

140 luding African savannas, many trees grow new leaves during the dry season - weeks or months before th

141 ion of volatile attractants from flowers and leaves, enabling attraction of the predators of pests du

142 The volatile profile of crushed rocket leaves (Eruca sativa and Diplotaxis tenuifolia) was inve

143 ained release and can be detected on sprayed leaves even 30 days after application.

144 experiments have confirmed that these young leaves express not only HSS but the whole PA biosyntheti

145 itions were combined with assays on detached leaves fed with ABA.

146 ssed in young seedlings and in roots, stems, leaves, flowers, and siliques of adult plants.

147 ration was observed in wild-type Arabidopsis leaves following 5-hour exposure to NaCl, no proliferati

148 f wall ingrowths was observed in rejuvenated leaves following prolonged defoliation.

149 uman population also use a poultice of these leaves for the relief of body pains.

150 the relevance of dietary exposure (e.g., via leaves) for systemic insecticides.

151 rts over mineral deposition, we investigated leaves from 10 Ficus species from vastly different envir

152 using data from a phenological study of 1099 leaves from 12 lowland Amazonian canopy trees in souther

153 -labeling of type VI glandular trichomes and leaves from a cultivated (Solanum lycopersicum LA4024) a

154 ate, target, and obtain edible fruits and/or leaves from a green foliage background instead of relyin

155 lected from 144 observations of upper canopy leaves from at least 65 species at two forest sites in P

156 nthase gene (PotriKCS1) was downregulated in leaves from non-alkene-producing accessions.

157 Leaves from plants fertilized with 25 and 50kgN ha(-1) a

158 s had up to 15% more polyphenols than larger leaves from similar elevation.

159 However, for individual sun-grown leaves from three species, photosynthesis is actually le

160 Small tea leaves had up to 15% more polyphenols than larger leaves

161 areas bolted sooner, grew larger, had fewer leaves, had an extended time between bolting and floweri

162 r (PM) deposited on Platanus acerifolia tree leaves has been sampled in the urban areas of 28 Europea

163 l scaling of phloem with respect to xylem in leaves has not been adequately studied to test alternati

164 Leaves have been collected close to streets characterize

165 We show here that wild-type leaves have distinct transcriptomic profiles in center a

166 nod mutant leaves have reduced size due to fewer and smaller cells

167 Ls show additive phenotypes, including thick leaves, higher ploidy levels, and larger palisade mesoph

168 g trait variation within and among stems and leaves, identification of trait syndromes within fine-ro

169 obtained by an extract of Calotropis procera leaves in comparison with those obtained by chymosin.

170 nderstory leaves (R(2) = 0.27-0.29), because leaves in different environments have distinct traits an

171 s of carnosic acid were detected in rosemary leaves in low light, indicating chronic oxidation of thi

172 mutant had delayed development and chlorotic leaves in mature plants.

173 l glycoconjugates were observed in fruit and leaves in particular, demonstrating glycosylation occurr

174 thesis in Arabidopsis (Arabidopsis thaliana) leaves in the light.

175 Stepwise conversion of floral organs into leaves in the most severe RNA interference lines suggest

176 e evidence that the integration of roots and leaves in the PES requires better accounting of the vari

177 ave measured the kinetics of PSI directly on leaves in unquenched and NPQ states; again, no differenc

178 Lateral plant organs, particularly leaves, initiate at the flanks of the shoot apical meris

179 t to convert extreme virus resistance in the leaves into mild nematode resistance in the roots, and v

180 ated leaves and neonicotinoids leaching from leaves into water.

181 the hypothesis that high vein density in C4 leaves is due to elevated auxin biosynthesis and transpo

182 hat, although the photosynthetic capacity of leaves is high enough to exploit brief periods of high l

183 High vein density, a distinctive trait of C4 leaves, is central to both C3-to-C4 evolution and conver

184 genes operating in the SMM cycle of rosette leaves, leading to elevated transport of SMM toward the

185 The unexpected nature of disasters leaves little time or resources for organized health sur

186 ts grown under fluctuating light had thinner leaves, lower leaf light absorption, but maintained simi

187 Therefore, photolysis inside leaves may be an important, yet under-explored, phytorem

188 n shelf life of minimally processed cilantro leaves (MPCL) was appraised through analysis of their se

189 ndard in chemotherapy, its 21% response rate leaves much room for further improvement.

190 nd tissues (i.e., roots, trunk/cores, twigs, leaves/needles) of the local plant community were taken,

191 with a certified reference material of apple leaves (NIST 1515).

192 t of cell cycle activity and growth of young leaves non-cellautonomously to available photosynthates

193 cosides, carotenoids and chlorophylls in the leaves of 14 genotypes from six different amaranth speci

194 y function rapidly declines) in upper canopy leaves of 218 plant species spanning seven biomes.

195 Leaves of a new variety of Stevia rebaudiana with a high

196 Hydathodes are water pores found on leaves of a wide range of vascular plants and are the si

197 riptional and metabolic changes occurring in leaves of AM plants differ from those induced by Pi fert

198 Leaves of Arabidopsis rbcs mutants expressing 'pyrenoid-

199 Tea prepared by infusion of dried leaves of Camellia sinensis (L.) Kuntze, is the second w

200 Using proteomic analyses of expanding leaves of corn (Zea mays L.), we show that this transiti

201 und that during early stages of development, leaves of da1-1 and bb/eod1-2 mutants were already large

202 to continuously monitor xylem cavitation in leaves of dehydrating grapevine (Vitis vinifera) in conc

203 nt than transcripts from the CA2 gene in the leaves of each species examined, constituting approximat

204 -ray microcomputed tomography of dehydrating leaves of four diverse angiosperm species showed that, a

205 clearly proved the formation of H2O2 in the leaves of plants 3h after the E. cloacae inoculation, ac

206 lorophyll fluorescence measurements from the leaves of polyprenol-deficient plants revealed impaired

207 Use of leaves of some species with prunasin, tyramine and beta-

208 take by the roots and biodistribution to the leaves of soybean plants was measured.

209 ent doses of nitrogen applied to soil and/or leaves of Syrah and Chardonnay grapevines in the Langued

210 ght tolerance and photosynthetic activity in leaves of the Arabidopsis (Arabidopsis thaliana) rosette

211 ned the hydraulic architecture of the mature leaves of the model species Populus tremula x alba acros

212 (KJT) is a health beverage prepared from the leaves of the plant Acer tataricum subsp. ginnala that h

213 Microsomal preparations from leaves of these mutants showed around 70% decrease in ac

214 Phenolic compounds of berries and leaves of thirteen various plant species were extracted

215 ncentrations (2%, 5%, 10%, and 15%) of olive leaves (OL) extract were immobilized in an adhesive form

216 We further investigated how different leaves on a rosette acclimate to high light and show tha

217 Because our study design leaves open the possibility of unmeasured confounding, w

218 This leaves open the question of a molecular control of phyll

219 hredders to avoid neonicotinoid-contaminated leaves, our results emphasize the relevance of dietary e

220 en the defensin was ectopically expressed in leaves, performance of Manduca sexta larvae, a folivore,

221 erform as well for mid-canopy and understory leaves (R(2) = 0.27-0.29), because leaves in different e

222 genes involved in salt response in roots and leaves, respectively.

223 31 also was expressed in vegetative tissues (leaves, roots, and stems).

224 (LAAPPI) and LDTD-APPI mass spectra of sage leaves (Salvia officinalis) using a field-deployable qua

225 peat1 lpeat2 showed impaired growth, smaller leaves, shorter roots, less seed setting, and reduced li

226 ater during development, da1-1 and bb/eod1-2 leaves showed a prolonged longevity, which was enhanced

227 n accumulation, and extracts from transgenic leaves showed higher activity on classic peroxidase subs

228 equate for the culinary process of grapevine leaves, since the product is considered edible and the p

229 ients suffered symptoms when peach trees had leaves, specifically during thinning and harvesting frui

230 analyzed compounds were detected in fruits, leaves, stems and roots of three L. barbarum varieties (

231 identified in different plant organs such as leaves, stems, (broccoli) heads, and roots.

232 In monocot leaves, stomatal cell files are positioned at the flanks

233 However, leaves stored at 12 degrees C did not loss a significant

234 Detached leaves stored at chilling temperature showed visual symp

235 For tea leaves, strong matrix effects are observed, thus, matrix

236 ene seems more dialysable than lutein in all leaves studied.

237 n gradual changes upon drought, Brachypodium leaves subjected to drought for 4, 8 and 12 days were co

238 tected in the hydroponically exposed plant's leaves, suggesting that either small amounts of particle

239 icant amount of metabolites respect to fresh leaves, suggesting the possibility to extend the storabi

240 dams converts mountaintops into islands and leaves surviving populations in a new environment.

241 g the first and second systemically infected leaves (termed 1 SL and 2 SL, respectively).

242 most of the pesticides which were higher for leaves than fruits.

243 a greater effect on photosynthesis of sunlit leaves than light limited, shade leaves and sunlit folia

244 lines developed brown necrotic spots on the leaves that did not appear on nulls.

245 ace expression of all class I molecules, but leaves the cells vulnerable to lysis by natural killer (

246 ay an additional excitation after the object leaves the field of view.

247 hout hematopoietic stem cell transplantation leaves the new liver at risk for similar EPP-related dam

248 tions, and to phenotypes observed in eudicot leaves, the increase in stomatal density did not enhance

249 opics harbor plants with exceptionally large leaves, the latitudinal gradient of leaf size has not be

250 otion causes a change in cortical state that leaves their selectivity unchanged but strengthens their

251 he desiccation tolerance of biocrusts, which leaves them frequently photosynthetically inactive and d

252 owest thermal safety margins in upper canopy leaves; these regions are at the greatest risk of damage

253 trients extracted by B. graminis from barley leaves through a process involving unique effectors.

254 lows residence times in the roots, stems and leaves to be estimated, calculated to be 8.3 min (combin

255 acity of both the whole plant and individual leaves to cope with excess excitation energy by followin

256 and its plant metabolites within Arabidopsis leaves to determine the potential impact of photolysis o

257 branes inside chloroplasts is conserved from leaves to developing embryos.

258 The flattening of leaves to form broad blades is an important adaptation t

259 control both the enhanced resistance of jazQ leaves to insect herbivory and restricted leaf growth of

260 asymmetric Kranz anatomy of Zea mays (maize) leaves to study the differential localization of two maj

261 on (R) - the flux of plant respired CO2 from leaves to the atmosphere.

262 t mechanism to move carbohydrates from their leaves to their roots.

263 ort sugars from regions of synthesis (mature leaves) to sugar sinks (roots, fruits).

264 bility of extracts from Centella asiatica L. leaves treated by steaming and metal-chlorophylls comple

265 g the purification of phytaspase from tomato leaves, two tomato phytaspase genes were identified, the

266 ocesses in chloroplast electron transport in leaves under canopy solar radiation was shown to be a ma

267 seq data from cassava shoot apices and young leaves under cold, drought stress and control conditions

268 teome analysis was conducted on Brachypodium leaves under drought stress.

269 Producing and retaining leaves underlie the performance and survivorship of seed

270 acts from Stevia (Stevia rebaudiana Bertoni) leaves using LC-MS in high resolution mode with a quadru

271 The fitness value of leaves varies greatly and leaves are protected by jasmon

272 Grapevine leaves (Vitis vinifera L. var. Malvasia Fina and Touriga

273 leaves was conducted.

274 atment day and relative water content of the leaves was measured for each time point.

275 Evapotranspiration of TCE from transgenic leaves was reduced by 80% and diffusion of TCE from tran

276 Sensitization to peach leaves was the cause of occupational respiratory symptom

277 Leaves were analyzed by LC-HRMS and a comprehensive stat

278 Odor-active compounds of leaves were characterized by GC-Olfactometry (GC-O) and

279 Sugar beet leaves were extracted with two proteomic protocols: solv

280 Total fresh weight and number of leaves were higher at 4th growth stage; however, at this

281 Total fresh weight and number of leaves were higher for successive harvests in both growi

282 lso, the mercury concentrations in vegetable leaves were much higher than those in roots and the merc

283 etardation, distorted branches and up-curled leaves were observed in miR156-impervious 35S::SPL13m ov

284 Spinach leaves were particularly prone to losing ascorbate durin

285 Sea buckthorn leaves were richest in phenolic compounds (7856mg/100g f

286 s of eighty commercial teas (sold in bags or leaves) were obtained at different time-temperature rati

287 avity in the upper epidermis of A. tequilana leaves, where the fabricated electrochemical sensor was

288 up-regulated by low temperature in buds and leaves, whereas desiccation treatment induces PpeS6PDH i

289 2% and 21% oxygen, in developing and mature leaves, which differed greatly in R in darkness.

290 G2, and increases PG activity in Arabidopsis leaves, which in turn reduces leaf pectin content and le

291 ommercial and laboratory extracts from olive leaves, which may have a pharmacological use as deduced

292 reen hue to those from untreated and steamed leaves, while zinc-chlorophylls extracts exhibited yello

293 We bombarded ACC2-defective Arabidopsis leaves with a vector carrying a selectable spectinomycin

294 interaction system by challenging C. roseus leaves with Manduca sexta larvae.

295 duction per panicle and dark green and thick leaves with prolonged source activity are among the desi

296 Chloroplasts in leaves with reduced ISE2 expression have previously been

297 However, leaves with reticulate vein networks required more secti

298 and an increase in variability of LD size in leaves, with concomitant increases in total neutral lipi

299 The leaves, young shoots or aerial parts of bistort are one

300 The main volatiles in fresh leaves [(Z)-3-hexenal, (Z)-3-hexen-1-ol, and (Z)-3-hexen