コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 re difference (VPD) and on water feed to the leaf.
2 ines the pattern and volume of airspace in a leaf.
3 NOD plays a cell-autonomous function in the leaf.
4 ALIZATION1 (HvVRN1), HvBM3, and HvBM8 in the leaf.
5 F) mini sponge cakes fortified with broccoli leaves.
6 , P was quickly solubilized from decomposing leaves.
7 ip cells of glandular trichomes on stems and leaves.
8 ight, and [(15)N2]DNAN yielded (15)NO2(-) in leaves.
9 for the variation of anthocyanins in lettuce leaves.
10 f 25% in the amount of ozone that enters the leaves.
11 respectively when compared with their fresh leaves.
12 iverse bacterial community washed from plant leaves.
13 No [(14) C]tartaric acid was found in tomato leaves.
14 ), which are also found in herbivore-induced leaves.
15 olite profiling were performed on stalks and leaves.
16 ent and common to plants without sporophytic leaves.
17 through their tissues to roots, shoots, and leaves.
18 trikingly higher Klason lignin levels in the leaves.
19 to CBZ was highest in fruits (up to 2.5) and leaves (0.5), suggesting an intensive transformation of
22 Additive gene expression was observed in leaves (3605 genes) and tubers (6156 genes) that contras
28 ing variations in chlorophyll a:b ratio with leaf age and physiological stress, a further separation
30 on (photoacclimation) is the process whereby leaves alter their morphology and/or biochemistry to opt
32 boost crop yield, candidate regulators of C4 leaf anatomy were previously identified through an analy
34 hed and analyzed transcriptome datasets from leaf and fruit and identified members of gene families i
35 nalysis of different developmental stages of leaf and fruit suggests tissue-specific accumulation of
37 AGE: Comprehensive transcriptome analysis of leaf and root tissues of Nothapodytes nimmoniana unravel
40 expressed in tobacco (Nicotiana benthamiana) leaves and does so in a manner that requires its RING do
41 ion of the aqueous extract from O. odorifera leaves and evaluate the correlation of their phytochemic
42 (lfs) mutants fail to produce cotyledons and leaves and grow a naked pin while maintaining an active
49 ronments by fine-tuning energy production in leaves and the availability of water and nutrients from
51 We performed circRNA-Seq on B73 seedling leaves and uncovered 2804 high-confidence maize circRNAs
53 m for assessments of covariation among root, leaf, and wood traits, the role of fine roots in ecosyst
54 om what is typically observed in terrestrial leaves, and based on this finding, we discuss strategies
56 promoting pectin degradation in Arabidopsis leaves, and Pst DC3000 might enhance its infection by ma
57 nd elevated (550 [ppm]) [CO2 ] overinvest in leaves, and this is predicted to decrease productivity a
62 hern Brazil whose fruit (known as butia) and leaves are used to make many food products and crafts.
64 area exposed to intercellular air space per leaf area (Sm ) is closely associated with CO2 diffusion
68 ariation, CV = 36%) than when expressed on a leaf area basis (CV = 66%), and relationships for broadl
69 ieback to whole-tree mortality reduce canopy leaf area during the stress period and for a lagged reco
71 ht intensities were shown to produce greater leaf area over time, estimated by noninvasive imaging.
73 forests tended to allocate more nutrients to leaves as compared with angiosperm forests, whereas the
77 n and longitudinal phonons whose fast escape leaves behind a 2D-projected mass density increase endow
79 They consist on stalks, inflorescences, and leaves, blanched and non-blanched, sharing the nutrition
80 ansverse sections of M x giganteus stems and leaves by atomic force microscopy indicates that phloem
82 rule, and that the phloem network in poplar leaves can generate the pressure gradient envisioned in
83 e how the optical method, used previously in leaves, can be adapted to measure the xylem vulnerabilit
85 d into chloroplasts of Nicotiana benthamiana leaf cells, whereas N. munroi CA1a localized to the cyto
87 bolomics approach was implemented to examine leaf chemical composition of 9 Coffea species grown in t
89 linear relationships between camera-NDVI and leaf chlorophyll concentration, and between camera-NDVI
92 d include vein cutting, trenching, girdling, leaf clipping, and application of fluids from exocrine g
94 pment across juvenile, transition, and adult leaves correlated positively with levels of miR156, a ma
96 s, Cotton leaf curl Kokhran virus and Cotton leaf curl Alabad virus, several distinct species of alph
97 demic; Cotton leaf curl Multan virus, Cotton leaf curl Kokhran virus and Cotton leaf curl Alabad viru
98 stinct species of alphasatellites and cotton leaf curl Multan betasatellite were found associated wit
99 haracterized from the first epidemic; Cotton leaf curl Multan virus, Cotton leaf curl Kokhran virus a
100 lts suggest dual roles for ABA in regulating leaf cuticle formation: one that is fundamentally associ
102 that palaeo-LMA can be inferred from fossil leaf cuticles based on a tight relationship between LMA
103 ar (Populus trichocarpa), revealing that the leaf cuticular waxes are predominantly composed of alkan
107 , over 20 countries, with the aim of testing leaf deposited particles as indicator of atmospheric PM
108 rphological and elemental characteristics of leaf deposited particles, joined with the leaf magnetic
109 cell division, growth and separation during leaf development determines the pattern and volume of ai
110 hat LFY has more obvious roles in floral and leaf development in C. hirsuta than in A. thaliana.
112 show greatly reduced accumulation of Pip in leaves distal to P. syringae inoculation, they display a
115 luding African savannas, many trees grow new leaves during the dry season - weeks or months before th
118 strates that PLA1 stimulates the duration of leaf elongation by maintaining dividing cells in a proli
120 ion of volatile attractants from flowers and leaves, enabling attraction of the predators of pests du
122 ons with microbes that do not directly enter leaf epidermal cells were seemingly unaltered or showed
124 In another planar tissue, the Arabidopsis leaf epidermis [5], polarized, asymmetric divisions of s
126 n: one that is fundamentally associated with leaf expansion, independent of abiotic stress, and anoth
127 dental caries, was detected for the aqueous leaf extract and its bio-guided separation resulted in t
131 Foliar residues measured at the time of leaf fall were used as input parameters for a model pred
132 plitude modulation fluorometer, was the best leaf fluorescence parameter to correlate with canopy SIF
137 ate, target, and obtain edible fruits and/or leaves from a green foliage background instead of relyin
141 stimated using several techniques, including leaf gas exchange, stable isotope discrimination, and ed
142 nce research because of their importance for leaf growth and hence for plant fitness and crop yield.
144 r (PM) deposited on Platanus acerifolia tree leaves has been sampled in the urban areas of 28 Europea
145 l scaling of phloem with respect to xylem in leaves has not been adequately studied to test alternati
149 far-reaching implications for inferences in leaf hydraulics, gas exchange, water use, and isotope ph
150 obtained by an extract of Calotropis procera leaves in comparison with those obtained by chymosin.
151 l glycoconjugates were observed in fruit and leaves in particular, demonstrating glycosylation occurr
153 Stepwise conversion of floral organs into leaves in the most severe RNA interference lines suggest
154 ed further promote the consumption of jujube leaf infusion as a healthy antioxidant bedtime beverage,
156 l proliferation, the development of a normal leaf lamina requires photomorphogenesis-like hormonal re
157 18) OV effect was highest for delta(18) O of leaf lamina water, but 40% lower on delta(18) O of main
159 genes operating in the SMM cycle of rosette leaves, leading to elevated transport of SMM toward the
162 nts much more than the sum of its individual leaf-level components, and they should take into conside
165 Those bands could be two isoforms of peach leaf lipid transfer proteins( LTP), so the recognition f
166 ted the responses of AM fungi in a long-term leaf litter addition and removal experiment in a tropica
167 y patch, reward contagion produced by higher leaf litter levels resulted in greater abundance of beet
168 , which includes deposition of nutrient-rich leaf litter onto streets connected to storm drains.
170 uality) of within-patch resource abundances (leaf litter) using an experimental landscape of mesocosm
174 n performance of a nature-inspired synthetic leaf made of graphene oxide (GO) thin film material, whi
175 of leaf deposited particles, joined with the leaf magnetic content, may successfully allow urban PM s
176 s was considerably lower when expressed on a leaf mass basis (coefficient of variation, CV = 36%) tha
177 large differences were observed in terms of leaf metabolic fluxes, these variations were not tightly
178 EY MESSAGE: Exploration with high throughput leaf metabolomics along with functional genomics in wild
181 l regulation of rosette expansion growth and leaf movement in Arabidopsis (Arabidopsis thaliana).
182 petiole, because it optimizes the timing of leaf movement in response to neighbors and prevents hypo
183 n shelf life of minimally processed cilantro leaves (MPCL) was appraised through analysis of their se
185 riation in Rdark was examined in relation to leaf N and P content, leaf structure and maximum photosy
186 CO2 exchange and 3) functional diversity of leaf N concentration as estimated by Rao's Q quadratic d
189 l concentration, and between camera-NDVI and leaf nitrogen content, though weaker relationships betwe
191 ith increasing elevation did not affect tree leaf nutrient concentrations, but did reduce ground-laye
195 to continuously monitor xylem cavitation in leaves of dehydrating grapevine (Vitis vinifera) in conc
196 nt than transcripts from the CA2 gene in the leaves of each species examined, constituting approximat
197 -ray microcomputed tomography of dehydrating leaves of four diverse angiosperm species showed that, a
198 clearly proved the formation of H2O2 in the leaves of plants 3h after the E. cloacae inoculation, ac
199 lorophyll fluorescence measurements from the leaves of polyprenol-deficient plants revealed impaired
202 ent doses of nitrogen applied to soil and/or leaves of Syrah and Chardonnay grapevines in the Langued
203 ned the hydraulic architecture of the mature leaves of the model species Populus tremula x alba acros
205 ian networks of gene expression across early leaf ontogeny in these lines to compare the molecular ne
206 ng and perturbation experiments we show that leaf orientation, morphology and position are pre-patter
207 hredders to avoid neonicotinoid-contaminated leaves, our results emphasize the relevance of dietary e
208 pulations demonstrated substantially delayed leaf-out and senescence relative to northern populations
210 esults highlight the importance of soil- and leaf-P in defining the photosynthetic capacity of TMFs,
214 igh spatial and interspecific variability in leaf phenology has precluded regional generalizations.
215 ength Rhizobiales genomes were identified in leaf-pocket-enriched samples from ditch grown A. filicul
216 quenced DNA of natural ferns, their enriched leaf pockets and water filtrate from the surrounding dit
222 was driven by the prescribed seasonality of leaf quantity and quality derived from ground-based meas
224 rimarily from the connection between Chl and leaf reflectance and secondarily from the mismatch betwe
226 segregation, lowers the sugar content in the leaf required to achieve a given export rate and acceler
238 ironmental interactive mechanisms regulating leaf shape variation have not yet been investigated in d
239 ater during development, da1-1 and bb/eod1-2 leaves showed a prolonged longevity, which was enhanced
240 n accumulation, and extracts from transgenic leaves showed higher activity on classic peroxidase subs
241 a dominant-negative version of DA1 enhances leaf size in a broad range of natural accessions of this
242 , and relationships for broadleaf and needle-leaf species converged when using the mass-based index.
243 ients suffered symptoms when peach trees had leaves, specifically during thinning and harvesting frui
244 cookei (=Bipolaris sorghicola) causes target leaf spot, one of the most prevalent foliar diseases of
248 rated transcriptome sequences from the root, leaf, stem, and flower tissues, and performed de novo se
250 analyzed compounds were detected in fruits, leaves, stems and roots of three L. barbarum varieties (
251 ate soil nitrogen availability, the dominant leaf strategy may be either deciduous or evergreen depen
254 xamined in relation to leaf N and P content, leaf structure and maximum photosynthetic rates at ambie
256 tected in the hydroponically exposed plant's leaves, suggesting that either small amounts of particle
257 rning, development and cell proliferation of leaf support tissues, and for restricting auricle expans
260 lyze the antioxidant benefits from persimmon leaf tea, fruit and fibres taking into account their cha
261 ace expression of all class I molecules, but leaves the cells vulnerable to lysis by natural killer (
262 tions, and to phenotypes observed in eudicot leaves, the increase in stomatal density did not enhance
263 otion causes a change in cortical state that leaves their selectivity unchanged but strengthens their
267 tabolite were subsequently photolyzed within leaf tissue under simulated sunlight, and [(15)N2]DNAN y
268 NF may play a role in both by supplying N to leaf tissues for acclimation and by facilitating compens
270 lows residence times in the roots, stems and leaves to be estimated, calculated to be 8.3 min (combin
271 acity of both the whole plant and individual leaves to cope with excess excitation energy by followin
273 odern maize, TRU1 is highly expressed in the leaf trace vasculature of axillary internodes, while in
274 .e., founder controlled) due to feedbacks of leaf traits on soil nitrogen mineralization through litt
277 bility of extracts from Centella asiatica L. leaves treated by steaming and metal-chlorophylls comple
278 ocesses in chloroplast electron transport in leaves under canopy solar radiation was shown to be a ma
279 seq data from cassava shoot apices and young leaves under cold, drought stress and control conditions
282 e turgor loss point, only small fractions of leaf vein xylem conduits were embolized, and substantial
285 eggbeater heads inspired by Salvinia molesta leaf was fabricated by the Immersed surface accumulation
288 Severe drought caused major declines in leaf water potential, elevated foliar ABA concentrations
290 variation in two traits, leaf drip tips and leaf water repellency, in a series of nine tropical fore
291 ole in determining the susceptibility of the leaf water transport system during strong leaf dehydrati
295 lso, the mercury concentrations in vegetable leaves were much higher than those in roots and the merc
296 etardation, distorted branches and up-curled leaves were observed in miR156-impervious 35S::SPL13m ov
298 G2, and increases PG activity in Arabidopsis leaves, which in turn reduces leaf pectin content and le
299 reen hue to those from untreated and steamed leaves, while zinc-chlorophylls extracts exhibited yello
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。