戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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  stress-modified flavonoid production in tea plant leaves.
2 f air quality by optimising PM deposition on plant leaves.
3 ing ROS production and leaf damage in tomato plant leaves.
4 , the dynamic ensemble of compounds covering plant leaves.
5 e to those of photocatalytic suspensions and plant leaves.
6 ce of endophytic lactic acid bacteria within plant leaves.
7 the opening and closure of stomatal pores on plant leaves.
8 livery and inducing gene silencing in mature plant leaves.
9 diterpenoids together with lipid droplets in plant leaves.
10 eria to survive the seemingly dry surface of plant leaves.
11 zed, diverse bacterial community washed from plant leaves.
12 ly the superhydrophobic surfaces inspired by plant leaves.
13 chanism controlling its diurnal breakdown in plant leaves.
14 ion and evaluate the effect of herbicides on plant leaves.
15 thesized and degraded in a diurnal manner in plant leaves.
16 ly related to an increase in SOD activity in plant leaves.
17 r salicylate accumulation in the apoplast of plant leaves.
18 t AvrPto is phosphorylated when expressed in plant leaves.
19 e activity, and attenuated virulence in host plant leaves.
20 uantify the effects of UVA radiation on live plant leaves.
21 ABA) that lead to stomatal closure in higher-plant leaves.
22 yunsaturated fatty acid (PUFA) substrates in plant leaves.
23 ty among the healthy and affected portion of plant leaves.
24 atmosphere and are likely to be deposited on plant leaves.
25 up to half of the soluble protein content in plant leaves.
26 A-LFT detected at least 4 ng of PVY per g of plant leaves, 0.04 ng/g for PVS, and 0.04 ng/g for PLRV.
27  understanding of morphogenetic processes in plant leaves and animal epithelia and perhaps even the f
28               SM6 efficiently accumulates in plant leaves and assembles correctly into heterooligomer
29 or synthetic sheets, such as rapidly growing plant leaves and crushed foils.
30 ther and with MIF in vitro, in yeast, and in plant leaves and formed hetero-oligomeric complexes with
31 applied PULSE to control immune responses in plant leaves and generated Arabidopsis transgenic plants
32 ion on natural and artificial surfaces (i.e. plant leaves and glass).
33 usly viewed as a static material property of plant leaves and insect cuticles, we here demonstrate a
34 atrices such as fruits, vegetables, cereals, plant leaves and other green parts were analysed, of whi
35 s(12) is conserved in the ADP-GlcPPases from plant leaves and other tissues except for the monocot en
36  and dimethylsulfoniopropionate, in detached plant leaves and rhizomes.
37 emical functional groups) and environmental (plant leaves and sand) surfaces can be described by clas
38  the coexistence of the two species on melon plant leaves and seeds.
39 hat is controlled by stomata, small pores on plant leaves and stems formed by guard cells.
40 athogens and pests present on the surface of plant leaves and the grain but also inside the seeds.
41 icity, such as the self-cleaning surfaces on plant leaves and trapped air on immersed insect surfaces
42 al understanding of the interactions between plant leaves and water.
43 mata control the gas exchange of terrestrial plant leaves, and are therefore essential to plant growt
44 misia tabaci (the TYLCV vector) feeding on R plant leaves, and even more strongly upregulated followi
45 d polystyrene (PS) polymers and oligomers in plant leaves, and identify that their levels increase wi
46  Guard cells are located in the epidermis of plant leaves, and in pairs surround stomatal pores.
47                                              Plant leaves are a major potential source of novel food
48                                              Plant leaves are diverse in their morphology, reflecting
49  make this complex chemistry more efficient, plant leaves are intricately constructed in 3 dimensions
50                                      In seed plants, leaves are born on radial shoots, but unlike sho
51                               Here, by using plant leaves as an example, we show that the causes of d
52  In the stomatal lineages on the surfaces of plant leaves, asymmetric and oriented divisions create d
53 d greenhouse experiment, we enriched pitcher-plant leaves at different rates with bovine serum albumi
54  Inspired by the stomatal closure feature of plant leaves at relatively high temperature, here we rep
55 alent steviol glycoside in Stevia rebaudiana plant leaves, but it has found limited applications in f
56 ght both influence physiological function in plant leaves, but their relative contributions to change
57 rains are then co-inoculated into 3-week-old plant leaves by one of three methods: a needleless syrin
58 orescence (DF) from Photosystem II (PSII) of plant leaves can be potentially used to sense herbicide
59                                              Plant leaves constitute a huge microbial habitat of glob
60 ard cells surround pores in the epidermis of plant leaves, controlling the aperture of the pore to ba
61             Carbon isotope discrimination in plant leaves (Deltaleaf ) is an established indicator of
62                          The water status of plant leaves depends on the efficiency of the water supp
63                                              Plants leaves develop proximodistal, dorsoventral (adaxi
64                                              Plant leaves display considerable variation in shape.
65 The process of nutrient retranslocation from plant leaves during senescence subsequently affects both
66   Electrolyte-release analysis of transgenic plant leaves established a correlation between the level
67 d plants (e.g., bird feathers, insect wings, plant leaves, etc.) are superhydrophobic with rough surf
68 of an ancestral shoot system from which seed plant leaves evolved.
69                                       Across plants, leaves exhibit profound diversity in shape.
70 te, and nonphotochemical quenching on intact plant leaves exhibiting distinct light responses.
71                                              Plant leaves feature epidermal stomata that are organize
72 from the furrows on our foreheads to crinkly plant leaves, from ripples on plastic-wrapped objects to
73                                         Many plant leaves have two layers of photosynthetic tissue: t
74 e fragments that activate defensive genes in plant leaves heretofore have been thought to be generate
75 mental inoculations with fungal pathogens of plant leaves in a tropical rain forest show that most fu
76 ed with the vast array of shape formation of plant leaves in nature.
77  one hand, a decrease in reflectance of host plant leaves in the near-infrared portion of the radiome
78                      The tracheary system of plant leaves is composed of a cellulose skeleton with di
79 cies that can function as a stress signal in plant leaves leading to programmed cell death.
80 xpression of CypA and its mutant in yeast or plant leaves led to inhibition of tombusvirus replicatio
81        The CO(2) transfer conductance within plant leaves (mesophyll conductance, g(m) ) is currently
82  natural and artificial materials, including plant leaves, metal sheets, and construction materials.
83 ption and accumulation of atmospheric MPs by plant leaves occur widely in the environment, and this s
84 stabilities occurring in animal epithelia or plant leaves, often emerge from mechanical instabilities
85 microbes have the ability to stably colonize plant leaves, overcoming the fluctuating environmental c
86                   In terrestrial ecosystems, plant leaves provide the largest biological habitat for
87 of tomato BI-1 by agroinfiltration of intact plant leaves provided protection from damage induced by
88                Antibody yields in transgenic plant leaves reached a maximum of 64 microg/g leaf fresh
89 f largely non-pathogenic fungi that colonize plant leaves remains an open question.
90 reased PE levels in yeast surrogate host and plant leaves replicating TBSV.
91 opment of the flattened laminar structure in plant leaves requires highly regulated cell division and
92                     The delta(13)C values of plant leaves, roots and soils in non-grazed (NG) and ove
93                                              Plant leaves sense various organic pollutants to generat
94                                              Plant leaves, simple or compound, initiate as peg-like s
95                        The stomatal pores of plant leaves, situated in the epidermis and surrounded b
96    Most PAH concentration data from vascular plant leaves suggest that contamination occurs by both d
97 ication of dsRNA-containing bacterial EVs to plant leaves suppressed B. cinerea infection.
98 anner with the aim of metabolic profiling of plant leaves that have been collected at different time
99 ta are the pores in the epidermal surface of plant leaves that regulate the exchange of water and CO(
100 rs from MMRT can serve as thermal traits for plant leaves that represent the collective temperature r
101 age of cAMP elevation in pathogen-inoculated plant leaves to Ca(2+) channels and immune signaling dow
102 THz radiation at multiple frequencies within plant leaves to determine absolute water content in real
103  microbial decomposer communities in pitcher plant leaves to investigate BEF.
104 rmore, the framework can locate the affected plant leaves under the occurrence of blurring, noise, ch
105 nor, sodium nitroprusside, on injection into plant leaves, was demonstrated by its abolition with O(3
106 spheric CO(2) and the stomatal index of land plant leaves, we reconstruct Late Cretaceous-Early Terti
107                                  Inspired by plant leaves, we used microfluidic devices consisting of
108                                              Plant leaves were extracted in methanol (80%), then the
109 duct from photolysis of HNO3/nitrate on most plant leaves, whereas NOx was the major product on most
110                                              Plant leaves, whose remarkable ability for morphogenesis

 
Page Top