ライフサイエンスコーパス: plant

1 tions from a biological wastewater treatment plant.

2 on of functional Tyr motifs also operates in plants.

3 nt players in cell-to-cell communications in plants.

4 ucing nutrient loads to wastewater treatment plants.

5 sing of progenitor sgRNAs occurs natively in plants.

6 her downstream factors regulate SAR in jmj14 plants.

7 on and inactivation of PVCV occurred in aged plants.

8 control a variety of biological processes in plants.

9 and internal hormonal functions in flowering plants.

10 ed to distinguish between non-TEs and TEs in plants.

11 best studied mRNA modification in flowering plants.

12 cterized CIF peptides conserved among higher plants.

13 iver from demographic studies of terrestrial plants.

14 oorganisms long before the evolution of land plants.

15 on of sequence-divergent peptide hormones in plants.

16 leaves and generated Arabidopsis transgenic plants.

17 ressed mainly in the siliques of Arabidopsis plants.

18 become the most complete database of SSPs in plants.

19 gulator of the nitrogen signaling pathway in plants.

20 t Britain Database of Insects and their Food Plants.

21 despread reproductive strategy in long-lived plants.

22 eak selective pressures, such as animals and plants.

23 ypothesized to contribute to hybrid vigor in plants.

24 ther studied by phenotyping knock-out mutant plants.

25 eased PEPc activity compared with warm-grown plants.

26 sh fruits, processed foods and as functional plants.

27 alent conjugation of recombinant proteins in plants.

28 used by the Fukushima Dai-ichi Nuclear Power Plant accident has aroused great concern regarding a pos

29 d offer potential explanations for how green plants adapt to extreme environments.

30 ost impactful environmental factors to which plants adjust their growth and development.

31 We also observed plant analogs of animal complexes with distinct molecula

32 a population of 19 independent R1 regenerant plants analyzed.

33 We show that local plant and animal diversity dropped markedly during Young

34 e of morphological (growth, mass allocation, plant and leaf morphology) and leaf ionomic traits.

35 ingly, we find that for all ten predictions, plants and animals show similar patterns.

36 ight scattering and what can be learned from plants and animals to produce photonic materials from bi

37 verify the authenticity of organically grown plants and derived organic food products.

38 , emphasizing conserved UPR elements between plants and metazoans and highlighting unique plant-speci

39 Interactions between plants and soil fungi and bacteria are ubiquitous and ha

40 link of delta(13) C with WUE(i) in this C(4) plant, and can potentially be used as a screening tool f

41 s, confirmed complexes predicted to occur in plants, and identified previously unknown interactions c

42 Grasses are among the most resilient plants, and some can survive prolonged desiccation in se

43 urred independently multiple times in algae, plants, animals, and fungi.

44 fully discovered and published for the model plant Arabidopsis thaliana.

45 In plants, as in other organisms, sHSPs are upregulated by

46 ften exhibit relatively weaker NDD than rare plants at local scales is difficult to reconcile with th

47 efflux and greater nutrient availability to plants at thaw.

48 the associations between different types of plant-based diets and incident metabolic syndrome (MetS)

49 raction technique, was used to fortify three plant-based food models: carbohydrates/acidic pH/sweet -

50 565 plant-based food samples were analyzed using UHPLC-HRMS

51 Wines fined with egg albumin and plant-based proteins from potato, pea, and grape seed as

52 nivores, relying on a mix of animal prey and plant-based resources.

53 We report a plant-beneficial interaction between Arabidopsis thalian

54 if there is a genetic relationship in a C(4) plant between delta(13) C(leaf) and WUE(plant) under wel

55 y as cradles and museums of tropical African plant biodiversity.

56 In seed plants, branching is achieved by stem-cell-containing ax

57 Plant breeding would benefit from borrowing approaches f

58 Here, we show a molecular mechanism of how plants can sense parasitic Cuscuta.

59 ce and distribution of organisms, especially plants, can alter resource landscapes for mobile consume

60 Consistently, plants carrying the BRI1(Y898F) mutation were hypersensi

61 here is considerable interest in engineering plant cell wall components, particularly lignin, to impr

62 Thus, the plant cell wall, outside of the cell itself, is an activ

63 Plant cell wall-associated polygalacturonase-inhibiting

64 ted covalent cellulose-xyloglucan bonding in plant cell walls and showed that CXE and MXE action was

65 therefore envisioned as models of secondary plant cell walls prior to lignification.

66 alysis of minor polysaccharide components of plant cell walls that are particularly difficult to assi

67 Single plant cells infected by bacteria were selected and sampl

68 xchange of metabolites and signal molecules, plant cells use the extracellular matrix as an alternati

69 itself, is an active participant in shaping plant cells.

70 Plant cellulose is synthesized by rosette-structured cel

71 dress these issues by constructing the first plant clock models based on the S-System formalism origi

72 wfall will affect ecosystem productivity and plant community structure during the growing season.

73 ighted that (i) the fate of Zn in water-soil-plant compartments was similar, regardless of the type o

74 esentation of water and nutrient limitation, plant compositional shifts and tree mortality.

75 rolonged drought and reduced photosynthesis, plants consume stored nonstructural carbohydrates (NSCs)

76 istry with implications for the geography of plant-consumer interactions.

77 Emerging infectious diseases (EIDs) of plants continue to devastate ecosystems and livelihoods

78 However, it is not fully understood how plants control light-dependent FAS regulation to meet th

79 Whether and how plants control phyllosphere microbiota to ensure plant h

80 The mechanisms by which plants coordinately respond to distinct levels of water

81 to the Galapagos Islands and considered the plant counterpart to Darwin's finches [1, 7-9].

82 of control, applied from 27 to 77 days after planting (DAP).

83 rning approaches to a comprehensive vascular plant database for the United States and generate predic

84 ion of callose deposition, and targeting the plant defense regulator NPR1 and analyses receptor FLS2.

85 n addition, C(18)-SMe(2)(+) activates innate plant defense.

86 in aphid saliva that elicits effective host plant defenses and warranted the theory of host speciali

87 ning metabolic homeostasis while suppressing plant defenses, but the metabolic connections and requir

88 can be attributed to tolerance of increased planting density(2-4).

89 ded in gustatory receptor neurons to sense a plant-derived bitter compound, aristolochic acid (ARI).

90 vation that is dependent on the secretion of plant-derived coumarins.

91 ication plays important roles in both normal plant development and in stress responses.

92 fferentially expressed in root system during plant development.

93 al networks, hormone signaling pathways, and plant developmental processes.

94 ions in cold acclimation ability structuring plant distributions across biomes.

95 pothesis is that pollinators affect rates of plant diversification through their effects on pollen di

96 edly during Younger Dryas cooling, but while plant diversity recovered in the early Holocene, animal

97 pt, we show significant losses in functional plant diversity when converting natural forests to agric

98 lopment was fundamental in generating extant plant diversity.

99 to reconcile with the maintenance of overall plant diversity.

100 The plant Dwarf14-Like (D14L) receptor conditions pre-symbio

101 Many biological surfaces of animals and plants (e.g., bird feathers, insect wings, plant leaves,

102 limate and land use change are causing woody plant encroachment in arctic, alpine, and arid/semi-arid

103 etative propagation through cuttings in some plants, especially woody species.

104 ns conserved over 1.1 billion years of green plant evolution.

105 Plants evolved lysine motif (LysM) receptors to recogniz

106 analysis, we also showed that qPCR-negative plants exhibited HLB-specific spectral characteristics t

107 both greenhouse and field environments, with plants exposed to different levels of water stress or to

108 We developed transgenic B. distachyon plants expressing Tnt1 (R0) and in the subsequent regene

109 e sampled from 10 plots hosting 10 different plant families across three forest environments (Terra F

110 synthesis in a broad range of flowering land plant families and in both monocots and dicots.

111 ation of water and carbon fluxes in vascular plants, finally examining specific evidence for evolutio

112 n about the impact of microbial diversity on plant fitness trade-offs, intraspecific-interactions, an

113 ncealed nectar and that their visits enhance plant fitness.

114 quitous and have large effects on individual plant fitness.

115 offee) and lower consumption of less-healthy plant foods (refined grains, potatoes, sugar-sweetened b

116 e represented greater consumption of healthy plant foods (whole grains, fruits, vegetables, nuts, leg

117 dietary intake, inability to classify a few plant foods as healthy and less-healthy, lack of data on

118 yan communities cultivate a great variety of plant foods that could be of interest due to their nutri

119 e diterpenoids are natural products found in plants from a subset of genera within the figwort family

120 lls provide a physical barrier that protects plants from pathogens, promotes tolerance to abiotic str

121 terfering RNA has potential applications for plant functional genomics, crop improvement and crop pro

122 s to be used within predictive frameworks of plant-fungal relationships.

123 gressing to a more mechanistic prediction of plant gas exchange is challenging because of the diversi

124 s (CNVs) are pervasive in several animal and plant genomes and contribute to shaping genetic diversit

125 Our results indicate that plant genomes are remarkably plastic, and that dynamic G

126 In higher plants, germline differentiation occurs during a relativ

127 t a model for UVR8 action in UV-B-acclimated plants growing in photoperiodic conditions that incorpor

128 depleted compost retained its structure, but plants grown in this medium were severely stunted in gro

129 significant environmental threat that limits plant growth and agricultural productivity.

130 a1 was the highly abundant transcript during plant growth and developmental stages.

131 verexpression of DWF1 significantly improves plant growth and overall N accumulation.

132 nter of 2015/2016 led to a February onset of plant growth and the ecosystem became a sustained carbon

133 role of microbes in sustaining agricultural plant growth has great potential consequences for human

134 ophosphate (Pi) is an essential nutrient for plant growth, and its availability strongly impacts crop

135 ng due to a warming-induced earlier onset of plant growth, but decreased in autumn due mainly to incr

136 pted during evolution into the regulation of plant growth, development and differentiation.

137 kinases (RLKs) play key roles in regulating plant growth, development and stress adaptations.

138 Although microbes influence plant growth, little is known about the impact of microb

139 -type, fails to form spores, does not confer plant growth-promoting effect, and displays altered colo

140 , thus confirming the role of these genes in plant growth.

141 We conclude that, in early plants, H3K27me3 played an essential role in heterochrom

142 o varying rainfall can provide insights into plant habitat distribution and drought adaptation.

143 c resources, terrestrial mammalian game, and plants had in supporting population growth, geographic d

144 jective was to determine if the asymptomatic plants harbored the latent blueberry red ringspot virus

145 example, previous authors have proposed that plants have broader environmental tolerances than animal

146 Plants have to interpret temperature fluctuations, over

147 ts control phyllosphere microbiota to ensure plant health is not well understood.

148 letted phenotype with pleiotropic effects on plant height and fertility.

149 For annual plants, higher temperatures, CO(2) and drought stress in

150 l closure upon perception of abscisic acid-a plant hormone associated with abiotic stresses.

151 Land plants host a vast and diverse virome that is dominated

152 ely on insect vectors for transmission among plant hosts, but many of the specifics of virus-vector i

153 location and the role of root growth on soil-plant hydraulics.

154 the diversity of organic matter derived from plants (i.e. litter) affect rates of decomposition.

155 plains the prevalence of certain patterns in plants, i.e. Fibonacci phyllotaxis.

156 Plant identities critical for retaining interaction dive

157 Their role in plant immunity against hemibiotrophic fungal infection r

158 verexpression of CsACD2 in citrus suppresses plant immunity and promotes Las multiplication, phenocop

159 into the cell death or survival decisions in plant immunity by modulating multiple stress-responsive

160 on transporter activity in the regulation of plant immunity is corroborated by experiments using the

161 SDE15 suppression of plant immunity is dependent on CsACD2, and overexpressio

162 2 and PLDgamma3, is specifically involved in plant immunity.

163 gnalling and their potential for engineering plant immunity.

164 ate that was installed at a coal-fired power plant in Germany.

165 ression (and their binary combinations) were planted in a diseased field plot in the Great Basin Dese

166 colonization of continents by vascular land plants in late Paleozoic, would certainly affect terrest

167 phenotyping facility was used to measure WUE(plant) in a recombinant inbred line (RIL) population cre

168 entially be used as a screening tool for WUE(plant) in sorghum.

169 Cold-grown Miscanthus plants increased in vitro activities of RuBisCO and PPDK

170 DCL3 in a natural setting was revealed when plants individually silenced in their expression (and th

171 es, barley, cow milk, vegetable drinks, tea, plant infusions and plant mixtures.

172 Here we propose that nonnative plants introduced to Great Britain may function as analo

173 Moreover, plant iron stress triggers immune activation, suggesting

174 The plant is a useful source of essential bioactive compound

175 tween the two bryophyte genomes and vascular plants is limited, suggesting extensive rearrangements s

176 essing GFP-CENH3 and CENH3-YFP in callus and plants is not and can be partly deposited normally.

177 However, its mechanism of transport into plants is poorly understood.

178 ne factor limiting HFA accumulation in these plants is the inefficient removal of HFA from the site o

179 In plants, it is not clear if palindromic repeats play a ro

180 oteins (PGIPs) are widely distributed in the plant kingdom.

181 e for a ubiquitous class of receptors in the plant kingdom.

182 applied PULSE to control immune responses in plant leaves and generated Arabidopsis transgenic plants

183 d plants (e.g., bird feathers, insect wings, plant leaves, etc.) are superhydrophobic with rough surf

184 In the zmnlp5 mutant plants, loss of the ZmNLP5 function led to changes in ex

185 tic process, and it is not known whether the plant lysin-motif receptor-like kinase MtLYK10 intervene

186 Despite intensive study, plant lysine catabolism beyond the 2-oxoadipate (2OA) in

187 s resulted in significant variation in total plant mass, diaspore mass, mass allocation to stem and r

188 rodent coprolites found in association with plant material, and tentatively assign them to the woodr

189 microbes that ferment otherwise indigestible plant matter, resist colonization by pathogens, and trai

190 ycorrhizal-acquired nutrient assimilation by plants may be symmetrically linked to carbon (C) transfe

191 response to photosynthesis occurring within plant mesophyll.

192 The scaling exponents of whole-plant metabolic rate vs body size numerically converge o

193 water content, body size and temperature on plant metabolic rates.

194 Although the central role of NAD in plant metabolism and its regulatory role have been inves

195 s is proposed, based on molecular docking of plant metabolites within the ATP and D-cycloserine bindi

196 Plant-microbial interactions in the rhizosphere are an e

197 As members of the plant microbiota, arbuscular mycorrhizal fungi (AMF, Glo

198 Cure on a set of manually curated animal and plant miRNAs and demonstrated great accuracy.

199 sheath cells, for the chilling-tolerant C(4) plant Miscanthus x giganteus grown at 14 and 25 degrees

200 , vegetable drinks, tea, plant infusions and plant mixtures.

201 Plants must manage cell swelling during flooding, rehydr

202 is suggests that in animals, as in yeast and plants, myosin/actin can drive long-range transport.

203 ential link in soil nitrogen (N) cycling and plant N supply.

204 itions in which indirect defence generates a plant-natural enemy mutualism.

205 In plants, NO is generated in pollen tubes (PTs) and affect

206 also establish symbiotic relationships with plants, notably the arbuscular and ecto mycorrhizal fung

207 er systems after the Chernobyl Nuclear Power Plant (NPP) accident in 1986 and in freshwater and marin

208 Applying synthetic signaling approaches to plants offers the promise of mitigating the worst effect

209 However, the observation that common plants often exhibit relatively weaker NDD than rare pla

210 strategy to meet our demands for specialized plant oils with industrial applications.

211 e current energy-lossy buildings into energy plants on Earth and possibly even enable extraterrestria

212 Research on eukaryotes such as animals, plants, oomycetes and fungi has shown that P450s profile

213 ubstantially in their expression profiles in plant organs and in response to environmental stresses,

214 A plant-origin deconjugase enzyme (Arabidopsis thaliana) f

215 R4 is not only reduced in ago4-1 but also in plants overexpressing a constitutively stable version of

216 Plant-parasitic nematodes pose a significant threat to a

217 tructure and specificity among a sampling of plant pathogen Cdc14 homologs.

218 Among them, several are involved in plant-pathogen response, which could explain why the 20r

219 The method is applicable to plant pathogens in general, to supply epidemiological pa

220 This is exemplified by the plant-peptide hormone mimics, the CLAVATA3/EMBRYO SURROU

221 Simulation results demonstrated how plant physiological stress can depend on the interaction

222 cts of future climate and land-use change on plants, pollinators, and herbivores.

223 oaches to quantify intrinsic growth rates of plant populations, including experiments beyond range bo

224 variable and synchronous seed production by plant populations, or masting, is a widespread reproduct

225 The donor plants prepared for regeneration purposes had 5.75% and

226 ovides chemical evidence for milk, meat, and plant processing by ancient herding societies in eastern

227 the maintenance of Fe homeostasis will alter plant productivity and the quality of their derived prod

228 effects of multisite phosphorylation on the plant protein kinase brassinosteroid insensitive 1-assoc

229 ll-studied experimental systems-encompassing plants, protists, and algae with grazers-we show that th

230 s giant daisies), an iconic and understudied plant radiation endemic to the Galapagos Islands and con

231 ng of iron depletion is a mechanism by which plants recognize a pathogen threat.

232 light and temperature signaling pathways in plants remain poorly understood.

233 Nacreous walls in land plants resemble the reversibly swellable walls found in

234 eline to constrain model-based hypotheses of plant responses to eCO(2) under P limitation, thereby im

235 We conclude that SDG8 is involved in plant responses to environmental nitrogen supply, affect

236 Induced plant responses to herbivores promote resistance and oft

237 Gene expression analyses of these plants reveal a trade-off between VTE and natural variat

238 Our results showcase the key role of plant root traits, especially root diameter, root nitrog

239 zosphere, the thin layer of soil surrounding plant roots, plays a critical role in plant's adaptation

240 AMF, Glomeromycotina) symbiotically colonize plant roots.

241 unding plant roots, plays a critical role in plant's adaptation to the environment.

242 iption factors BPC1/BPC2 positively regulate plant salt tolerance by repressing GALS1 expression and

243 djustments to the skillsets and mind sets of plant scientists.

244 However, the mechanisms by which plants sense temperature are not well understood.

245 ich to better dissect the genetic control of plant shoot morphogenesis at the cellular level.

246 Strigolactones are an important class of plant signalling molecule with both external rhizospheri

247 s study provides a proof-of-concept that the plant-soil feedback concept can be applied to steer soil

248 Pollinators influence patterns of plant speciation, and one intuitive hypothesis is that p

249 itical for the long-term persistence of many plant species and communities.

250 ses during foraging, but the consequences of plant species composition for infection is unknown.

251 Distantly related plant species show more divergent responses to each othe

252 tion in soil microbial communities modulates plant species' distributions remains largely untested.

253 of MADS-box genes have been reported in many plant species, but its identification and characterizati

254 eletion-only MMEJ-mediated mutations in many plant species.

255 oil microbiota compared with closely related plant species.

256 plants and metazoans and highlighting unique plant-specific features.

257 h water transport and the physical weight of plant structures.

258 of phenotypic variation have been a focus of plant studies aimed at improving agricultural yield and

259 xogenous Pip partially restored SAR in jmj14 plants, suggesting that JMJ14 regulated Pip biosynthesis

260 association between the delta(13) C and WUE(plant) suggests an intrinsic link of delta(13) C with WU

261 The plant supplies carbon substrates and other nutrients to

262 Lso was also detected in several weed plants surrounding carrot and parsnip fields.

263 Although beneficial for plant survival, active growth inhibition is often undesi

264 In plants, synthetic riboswitches were used to regulate gen

265 s and generate predictive models of regional plant taxonomic and phylogenetic diversity in response t

266 ly, and spatially distinct subdomains of the plant TGN and suggest that functional redundancy can be

267 evolution of stomata-pores on the surface of plants that regulate gas exchange.

268 ly been paid to the above ground portions of plants (the phyllosphere).

269 mity of the organogenesis process across all plants then explains the prevalence of certain patterns

270 the vegetative heat tolerance of adult rice plants through visual (stay-green) and chlorophyll fluor

271 subcellular redox dynamics of NAD in living plant tissues has been challenging.

272 In seed-derived progeny of R1 plants, Tnt1 segregated in a Mendelian ratio of 3:1 and

273 etrically linked to carbon (C) transfer from plant to fungus or governed by sink-source dynamics.

274 ough this capacity partly allows animals and plants to acutely adapt to oxygen deprivation, its funct

275 The natural ability of plants to exchange small RNAs with invading eukaryotic o

276 expression of SLG1 enhances the tolerance of plants to high temperature.

277 We demonstrate that plant traits can predict mean annual tree growth rates w

278 th additional analysis of 305 non-angiosperm plant transcriptomes.

279 first year of growth, overwintering biennial plants transport Suc through the phloem from photosynthe

280 SOC) must be considered to determine whether planting trees for climate change mitigation results in

281 s of the flavin mononucleotide (FMN) and the plant-type [2Fe-2S] cluster of CntB and also of the Ries

282 We grew plants under current ambient (440 ppm) and projected fut

283 C(4) plant between delta(13) C(leaf) and WUE(plant) under well watered and water-limited growth condi

284 Plant viruses rely on insect vectors for transmission am

285 The origin of land plants was accompanied by new adaptations to life on lan

286 triphasic nature of the relationship between plant water potential (Psi) at predawn and midday and de

287 how fruits regulate flowering in polycarpic plants, we focused on alternate bearing in Citrus trees

288 ble soils include high nitrate, moisture and plants; we investigate how differences in the soil micro

289 brates, surface water, sediments, soils, and plants were analyzed for 24 PFASs including branched iso

290 d treatment and a drought treatment in which plants were subjected to three cycles of drought.

291 Stems were the richest tissue in woody plants, whereas roots were the richest tissue in gramino

292 pha-2 and impalpha-3 resulted in Arabidopsis plants with a rapid flowering phenotype similar to that

293 NAE 18:3 being a lipid signaling molecule in plants with a requirement for G-proteins to mediate sign

294 Opening of stomata in plants with crassulacean acid metabolism (CAM) is mainly

295 rapid flowering phenotype similar to that of plants with mutations in lhp1 due to the upregulation of

296 n distinct subcellular compartments provides plants with the metabolic flexibility to maintain physio

297 Dysfunction of SLG1 results in plants with thermosensitive phenotype, while overexpress

298 gene targets with zero surviving background plants within 8 d.

299 atures were obtained of wastewater treatment plant (WWTP) influent samples.

300 wall sequential extraction performed on dry plant yielded 1.1, 2.4, 0.3 and 0.9% of pectin fractions