ライフサイエンスコーパス: seedling

1 buted to the different organs of the growing seedling.

2 dlings resulted in rapid death of the entire seedling.

3 lipid mobilization, thus impairing the rice seedling.

4 ly pure mitochondria from 1 g of Arabidopsis seedlings.

5 ) in regulating Buta (4 uM) toxicity in rice seedlings.

6 cena species were inoculated onto B. pendula seedlings.

7 ndance of pathogenic fungi than roots of ECM seedlings.

8 ledons in Arabidopsis (Arabidopsis thaliana) seedlings.

9 NSCs decreased from L to LD to D seedlings.

10 sed ability to cause disease lesions on rice seedlings.

11 ults, while plant pathogens were dominant in seedlings.

12 rapidly enhance phototropism in Arabidopsis seedlings.

13 root number components for Euphrates poplar seedlings.

14 eed weight affects many root traits of young seedlings.

15 ark-to-light transition in Arabidopsis young seedlings.

16 ersity was two-fold greater in DT than in DI seedlings.

17 pread translational repression in dark-grown seedlings.

18 erstand the molecular responses of date palm seedlings.

19 rphogenesis and timely photomorphogenesis in seedlings.

20 orthologue, and activity against Arabidopsis seedlings.

21 rom adult trees while Diaporthe prevailed in seedlings.

22 y associated with drought tolerance of maize seedlings.

23 seedling specific leaf area (SLA), and tall seedlings.

24 chlorophyll content in 5113-treated stressed seedlings.

25 or conventional transplanting of susceptible seedlings.

26 he cryptochrome receptor cry1 in Arabidopsis seedlings.

27 found significantly upregulated in infected seedlings.

28 raulic properties in 2.5-year-old Scots pine seedlings.

29 pmental processes in Arabidopsis embryos and seedlings.

30 opsis thaliana) plants relative to wild-type seedlings.

31 half-life of several miRNAs in de-etiolated seedlings.

32 howing significant transfer of (32) P to the seedlings.

33 orylated at Ser-448 and Ser-452 in etiolated seedlings.

34 TRANSCRIPT PROCESSING 84 (OTP84), and YELLOW SEEDLINGS 1 (YS1).

35 wild-type (WT) seedlings, the zmnlp5 mutant seedlings accumulated less nitrate and nitrite in the ro

36 sed model to estimate the probability that a seedling achieves reproductive maturity after several ye

37 s essential for the survival of de-etiolated seedlings after long-term skotomorphogenesis and their o

38 ion in leaves of tobacco (Nicotiana tabacum) seedlings after transfer from moderate light to physiolo

39 e consistent across screening conditions and seedling age while qAG1-2 and qAG7-4 were specific to sc

40 These seedlings also showed upregulated expression of genes fo

41 ction and cell-fate acquisition in the maize seedling and provide a valuable scaffold on which to bet

42 ce plants to high-temperature stress at both seedling and reproductive stages.

43 Relationships of seedling and root traits to more commonly measured trait

44 ent (metagenomic) approaches, a total of 381 seedlings and 144 adults distributed across three remote

45 g parent-offspring relationships between 604 seedlings and 518 adult trees sampled within five popula

46 seedling mortality was higher and growth of seedlings and adults were lower in unwatered than watere

47 Results suggested that grafting seedlings and allowing time to heal graft wounds prior t

48 wild-type Arabidopsis (Arabidopsis thaliana) seedlings and mutant seedlings defective in essential co

49 licit defense (or other) responses in tomato seedlings and plants was assessed upon the expression of

50 s for metabolic reprograming in 5113-treated seedlings and showed that several common stress metaboli

51 alysis of Arabidopsis (Arabidopsis thaliana) seedlings and studied their response to interference wit

52 xpression of GAPC enhances heat tolerance of seedlings and the expression of heat-inducible genes whe

53 cts of cell swelling on Arabidopsis thaliana seedlings and to test the contributions of the mechanose

54 ffered at the phylum level between DT and DI seedlings, and diversity was two-fold greater in DT than

55 cankers in trees of all ages, damping-off in seedlings, and mortality in cuttings and mother plants f

56 ysaccharide release along root axes of young seedlings, and their presence at root hair surfaces and

57 s showed that several genetic differences in seedling architectures could persist throughout developm

58 by N-dose and W interactions (N/W or NxW) in seedlings are associated with crop outcomes in replicate

59 dwestern United States, and as a result, the seedlings are exposed to a wide range of temperature reg

60 When Arabidopsis (Arabidopsis thaliana) seedlings are grown in the dark, hypocotyl elongation is

61 The present results indicate that date palm seedlings are tolerant towards seawater exposure to some

62 al skoto- and photomorphogenesis in juvenile seedlings as well as long-term adult plant development.

63 rtant role in growth and development of rice seedlings at low temperatures.

64 e modeled hydraulic stress in ponderosa pine seedlings at multiple scales to examine its influence on

65 biosynthesis and deposition in fdl1-1 mutant seedlings at the coleoptile stage.

66 photosynthetic rates declined in warm-grown seedlings, but the strength of these changes varied betw

67 ativa) conferred increased NaCl tolerance to seedlings by enhancing root suberin deposition.

68 mproving alkaline stress tolerance in tomato seedlings, by modifying the endogenous Na(+) and K(+) co

69 ancial costs of enrollment (e.g., purchasing seedlings) can affect who participates in a PES program.

70 etic and phenotypic data from European beech seedlings collected along an elevation gradient, and gro

71 ransport, J(max) ) was reduced in warm-grown seedlings, correlating with reductions in leaf N and chl

72 atic, chemical, and genetic perturbations in seedling cotyledons, we found that augmenting HG modific

73 ve- and below-ground traits of tropical tree seedlings could explain observed occurrence along gradie

74 (Arabidopsis thaliana) seedlings and mutant seedlings defective in essential components in the signa

75 vel modeling approach, we combined long-term seedling demographic data from a subtropical forest plot

76 al warming on density-dependent feedbacks on seedling demography in a wet tropical forest in Puerto R

77 Postfire tree seedling density was reduced sixfold relative to the pre

78 rade-offs in the allocation of tropical tree seedlings depend on different stressors remains poorly u

79 hey become photoautotrophic juvenile plants, seedlings depend upon the reserves stored in seed tissue

80 nes, which are involved in the transition to seedling development are examined and reveal complex int

81 global analysis of photosynthesis and early seedling development in an emerging C(4) model.

82 ent temperature are coordinated during early seedling development in Arabidopsis A shoot signaling mo

83 xygen species and inhibited plant growth and seedling development more strongly than negatively charg

84 in smoke that can influence germination and seedling development of many plants.

85 sponse to extracellular ATP manifests during seedling development under chronic Pi deprivation but ca

86 h of grain imbibition, germination and early seedling development, as well as the spatial distributio

87 tosynthetically competent state during early seedling development.

88 olism and IBA responses leading to disrupted seedling development.

89 energy and metabolic building blocks during seedling development.

90 ay during Arabidopsis (Arabidopsis thaliana) seedling development.

91 ing salt tolerance versus sensitivity at the seedling developmental stage.

92 EMF communities of DT seedlings did not shift with water treatment and were do

93 AHL4-OE seedlings displayed decreased expression of genes involv

94 nspecific plants, while survival of ECM tree seedlings displays positive density dependence over this

95 immune sensor XA21 promotes survival of rice seedlings during dehydration stress.

96 he beneficial impacts of Si and SA on tomato seedlings during high-pH (9.0) stress.

97 penoid biosynthesis, transcriptome data from seedlings elicited with methyl jasmonate were also obtai

98 Application of auxin to light-grown seedlings elicits both axial growth and transverse patte

99 Hypocotyl growth during seedling emergence is a crucial developmental transition

100 Flooding reduced seedling emergence of all genotypes, though emergence of

101 The seedling emergence rate at 14 days after sowing was sign

102 re identified for depth of seed dormancy and seedling emergence timing (SET).

103 Seedling emergence timing is crucial in competitive plan

104 rstand the mechanistic basis of variation in seedling emergence timing, we exploited the contrasting

105 d light regulate hypocotyl growth, including seedling emergence, during the dark-to-light transition

106 of experiments conducted in the greenhouse, seedling emergence, growth, and carbohydrate mobilizatio

107 1 in generating altered seasonal patterns of seedling emergence.

108 sition with mortality could limit successful seedling establishment and growth in high-mortality site

109 tion growth, driven especially by changes in seedling establishment and seed production.

110 eate in the seed oil had significantly lower seedling establishment and vigor, delayed flowering and

111 Seed germination and seedling establishment are important for the reproductiv

112 ot hair development, which are important for seedling establishment at the beginning of the plant lif

113 plants regulate hypocotyl elongation during seedling establishment by coordinating light-induced eth

114 ue (seed) development, seed germination, and seedling establishment in Arabidopsis (Arabidopsis thali

115 on that is critical for seed germination and seedling establishment in Arabidopsis.

116 -mediated inhibition of seed germination and seedling establishment is thwarted.

117 nd the potential for mutualism limitation of seedling establishment via altered EMF communities.

118 rations in the LD proteome were those during seedling establishment, indicating a switch in the physi

119 ng plants have low seed oil content and poor seedling establishment, indicating that Arabidopsis lack

120 d beta-oxidation during seed germination and seedling establishment.

121 essary energy for seed germination and early seedling establishment.

122 ing and is critical for seed germination and seedling establishment.

123 phenotype, demonstrating a role for BADCs in seedling establishment.

124 owing tree mortality could negatively affect seedling establishment.

125 ipid degradation during seed germination and seedling establishment.

126 environments optimize shoot investment, and seedlings experiencing frequent defoliation store resour

127 cuticle-dependent leaf permeability in maize seedlings exposed to drought as well as abscisic acid tr

128 Proteasomes from seedlings exposed to the proteasome inhibitor MG132 accu

129 Seedlings expressing PIF3(K13R) show an elongated hypoco

130 The early seedling foliar application of nanoscale Cu to modulate

131 Simulated mortality in seedlings from 2001 to 2015 correlated with the current

132 We genotyped 472 seedlings from a natural hybrid zone of Populus alba and

133 long gradients of resources and defoliation: seedlings from dry areas invest in deep roots, seedlings

134 edlings from dry areas invest in deep roots, seedlings from shaded environments optimize shoot invest

135 We confirmed that removing seedlings from the light led to a discernible shift in m

136 g growth making them similar to the zmdreb2a seedlings from unaged seeds.

137 Seedling grafting could provide additional crop improvem

138 e, the rapid and consistent wound healing in seedling grafts along with lateral shoot formation occur

139 ression of ABT promotes seed germination and seedling greening in the presence of ABA, whereas knocko

140 DT seedlings grew larger than DI seedlings in high (28%) an

141 lso significantly reduced bacterial loads in seedlings grown from contaminated seeds, without affecti

142 This response is common in eudicot seedlings grown in the dark and is characterized by redu

143 Seedlings grown in the greenhouse were transplanted at f

144 In controlled greenhouse experiments, hemp seedlings grown in Turface supplied with 40-320 muM sele

145 A detailed analysis of seedling growth and alterations in biomass composition w

146 Seed aging tolerance and rapid seedling growth are important agronomic traits for crop

147 ABA-mediated inhibition of post-germination seedling growth by acting downstream to COP1.

148 f soybean (Glycine max) seed reserves during seedling growth by initially constructing a genome-scale

149 ng or presoaking can enhance germination and seedling growth in anaerobic soils.

150 , together leading to higher germination and seedling growth in flooded soils.

151 pposite pattern to that of ABI5 during early seedling growth in response to abscisic acid (ABA).

152 d, germinating NS seeds increased subsequent seedling growth making them similar to the zmdreb2a seed

153 Accordingly, the seedling growth of multiple Arabidopsis gcn2 mutants was

154 Normal seedling growth of the OE lines was restored by sucrose

155 am of seed formation, germination, and early seedling growth requires not only tight regulation of ce

156 cid (ABA) prevents premature germination and seedling growth under unfavorable conditions.

157 itive phenotypes during seed germination and seedling growth, and decreased drought stress resistance

158 s provides energy and substrates for initial seedling growth, but how this process is regulated is no

159 witch from heterotrophic to photoautotrophic seedling growth, for which cytoplasmic lipid droplets (L

160 vector-transformed controls, in germination, seedling growth, grain size and grain weight.

161 During mung bean post-germination seedling growth, various metabolic and physiological cha

162 Mycena pura and Mycena galopus both enhanced seedling growth, with M. pura showing significant transf

163 nections between lipid mobilization and rice seedling growth.

164 mary metabolites during the post-germination seedling growth.

165 ulation in mung bean during post-germination seedling growth.

166 uated, triacylglycerol (TAG) degradation and seedling growth.

167 d dormancy during seed germination and early seedling growth.

168 cy and enable the subsequent germination and seedling growth.

169 (IBA) to indole-3-acetic acid, because ech2 seedlings have altered IBA responses.

170 dent root growth promotion, since dark-grown seedlings have reduced root apical meristem activity, as

171 Here, we show that ech2 seedlings have reduced root length, smaller cotyledons,

172 t DNA sequence and non-DNA sequence QTLs for seedling height and diameter growth in different years.

173 the germination percentage, root length, and seedling height measurements of the most sensitive rice

174 to measure profiles across roots of chickpea seedlings in aerated or hypoxic conditions.

175 DT seedlings grew larger than DI seedlings in high (28%) and low (50%) watering treatment

176 Seedlings in moist tropical forests must cope with deep

177 latome of Arabidopsis (Arabidopsis thaliana) seedlings in response to hypoxia and reoxygenation.

178 erential hypocotyl growth of red light-grown seedlings in response to these phytohormones.

179 We grew wheat seedlings in sealed petri dishes without obstacle and in

180 However, community composition of seedlings in the interspecific interaction treatment was

181 e screened for the segregation of pale-green seedlings in the M(3) generation, and a subset of these

182 In conclusion, tree seedlings in this study show root trait syndromes, which

183 s longer root hairs compared with tZ-treated seedlings, increasing the total absorbing surface.

184 network that is implicated in MBI600-tomato seedling interactions was mapped.

185 The shift of dark-grown seedlings into light causes enormous transcriptome chang

186 cold tolerance by OsCAF1B in transgenic rice seedlings involved OsCAF1B deadenylase gene expression,

187 Although GGCT2;1 is induced throughout seedlings, its expression is concentrated in the primary

188 We measured seedling leaf, architectural and biomass distribution tr

189 responses to incipient biotin deficiency in seedling leaves.

190 The cpsfl1 mutants are seedling lethal, show a defect in thylakoid structure, a

191 enhanced the phenotype of pmt1 pmt3, showing seedling lethality and further reduced PC content withou

192 fluorescent (flu) mutant, its release causes seedling lethality and inhibits mature plant growth.

193 ts may therefore reflect a trade-off between seedling light interception efficiency and susceptibilit

194 ive species of warm climates an advantage in seedling light interception efficiency over small-leaved

195 Etiolated seedlings maintain low levels of primary miRNAs (pri-miR

196 unselected, whole WCR neonates which fed on seedling maize with and without eCry3.1Ab for 12 and 24

197 g climates, root traits may be critical, and seedlings may be the vulnerable stage.

198 d tested it using in situ monitoring data on seedling mortality from reforestation efforts.

199 nnual grassland where winter drought-induced seedling mortality is driving a long-term decline in nat

200 structural damage to chloroplasts and a high seedling mortality rate.

201 nally dry winter of 2017-2018, we found that seedling mortality was higher and growth of seedlings an

202 y weakly correlated with seedling traits and seedling mortality.

203 one is also rapidly depleted in ggct2;1 null seedlings, much higher glutathione is maintained in the

204 Studies with purified UVR8 and seedlings not previously exposed to UV-B have generated

205 We implemented an experiment in which seedlings of 12 European/North African oaks were grown u

206 In this study, potted seedlings of B. asiatica Lour.

207 s on establishment by transplanting soil and seedlings of meadow and tree species across climate grad

208 e of seeds and through parentage analyses of seedlings of the legume Parkia panurensis from the distu

209 evelopment and may lead to pigment-deficient seedlings or seedlings with variegated leaves.

210 eover, survival of naturally-regenerating AM seedlings over ten years is negatively related to the de

211 Of these, four transgenic seedlings overexpressing previously uncharacterized TF g

212 t illuminated (LD) and compared responses to seedling pairs in full light (L).

213 We connected well-watered Pinus ponderosa seedling pairs via ectomycorrhizal (EM) networks where o

214 alized pathogens were the mechanism reducing seedling performance in maternal soils.

215 ever, the interspecific relationship between seedling performance in shade and drought remains unsett

216 ize within wild plant populations, affecting seedling performance near conspecific adults and influen

217 A screen of 190 insertion lines for seed and seedling phenotypes identified mutations in biotin, pyri

218 All BonnMu insertions and phenotypic seedling photographs of Mu-tagged F(2)-families can be a

219 t PIFs accumulated in darkness and repressed seedling photomorphogenesis, and that PIFs linked differ

220 tified as regulators of Arabidopsis thaliana seedling photomorphogenesis.

221 izal fungal (EMF) communities of pinyon pine seedlings (Pinus edulis) planted in a wildland ecosystem

222 When the seedlings protrude from soil, light perception by photor

223 (5-EU) in Arabidopsis (Arabidopsis thaliana) seedlings provides insight into plant transcriptome dyna

224 ting from surviving tissues (resprouters) or seedling recruitment (seeders).

225 to a lesser extent insect herbivores, reduce seedling recruitment and survival at high adult conspeci

226 ggests host-specific natural enemies inhibit seedling recruitment at high conspecific density (negati

227 fungi are primarily responsible for reducing seedling recruitment near conspecific adults in ectomyco

228 between ant species, and seed dispersal and seedling recruitment of four myrmecochore species among

229 Insects, in contrast, primarily inhibit seedling recruitment of shade-intolerant species near co

230 While many have asked how seedling recruitment varies between restoration treatmen

231 d no effect of interspecific interactions on seedling recruitment.

232 le transgenic Lr67res barley lines exhibited seedling resistance to the barley-specific pathogens Puc

233 thickness whereas application of PA to dgk1 seedlings restored the LR density and SR thickness to th

234 plementation of DAG to OsDGK1-overexpressing seedlings restored the LR density and SR thickness where

235 ucible expression of PrsS in PrpS-expressing seedlings resulted in rapid death of the entire seedling

236 Defective photosynthesis in ven4 seedlings results from reduced accumulation of photosynt

237 translatome analyses of wild-type and dcp5-1 seedlings revealed that p-bodies can attenuate the prema

238 ese two metabolites, was important for maize seedling root defense against F. graminearum.

239 ong these species, constitutive variation in seedling root length explained most of the variation in

240 rsenic (in As-addition treatments) and Cu in seedling roots (SRs) were 1.45 and 1.58 times those in s

241 Seedling roots can sense and respond to temperature in a

242 ensity dependence over this interval, and AM seedling roots contain greater abundance of pathogenic f

243 The addition of recombinant PrsS to seedling roots expressing the cognate PrpS resulted in h

244 seedlings was higher in species with shorter seedling roots, and also in species with the correlated

245 usly unknown antifungal metabolites in maize seedling roots, and investigated the genetic and physiol

246 hate limitation and robustly colonizes maize seedling roots.

247 ted cytosolic Ca(2+) increase in Arabidopsis seedling roots.

248 s resistance against F. graminearum in maize seedling roots.

249 d here is expected to aid in marker-assisted seedling selection (MASS) targeted towards widening peac

250 By contrast, DI seedlings shifted to basidiomycete dominance with increa

251 Arsenic and Cu concentrations in seedling shoots (SSs) were 79% and 54% lower than those

252 creased IAA in their embryo, produced longer seedling shoots and roots, than the null segregant (NS)

253 In fact, cZ-treated seedlings show longer root system as well as longer root

254 h the correlated traits of small seeds, high seedling specific leaf area (SLA), and tall seedlings.

255 egulate the ABA signaling pathway during the seedling stage specifically in darkness.

256 elded plants that did not advance beyond the seedling stage, hyperaccumulated ceramides, and showed a

257 At the seedling stage, positive phototropism is mainly regulate

258 owing it to phenocopy cultivated rice at the seedling stage.

259 iole elongation and hyponastic growth at the seedling stage.

260 isoforms at both the vegetative (14-day old seedlings, stage 1.04) and reproductive stages (stage 6.

261 l brassinosteroid-induced cell elongation in seedling stems, which depends upon a distinct, permissiv

262 bfamily B19 (ABCB19) by phot1 in phototropic seedlings suggests that phot1 may directly regulate ABCB

263 s and root, and the auxin response of mutant seedlings supported the hypothesis that mutants lacking

264 4 degrees C warming treatment, we found that seedling survival increased with increasing density of t

265 lower number of barren siliques and a higher seedling survival rate under heat.

266 s grow faster and have greater survival than seedlings that are isolated from external fungal mycelia

267 Here, we show that tree seedlings that interact via root-associated fungal hypha

268 x atlas of the cytosol of living Arabidopsis seedlings that revealed pronounced differences in NAD re

269 supply, compared with that of wild-type (WT) seedlings, the zmnlp5 mutant seedlings accumulated less

270 e also promotes phototropism of de-etiolated seedlings through repression of phytochrome B, presumabl

271 -metabolism of several stages of growth from seedling to senescence at hourly intervals.

272 ding to increasingly fewer opportunities for seedlings to establish after wildfires and may lead to e

273 ) genetic markers and transcript levels from seedlings to predict mature plant traits, we found that

274 The response of wild-type seedlings to S-starvation was compared to ggct2;1 null m

275 values, and were only weakly correlated with seedling traits and seedling mortality.

276 osperm cell expansion to control the seed-to-seedling transition.

277 Young seedlings transitioning from dark to light undergo photo

278 enhanced callose deposition in hydathodes of seedlings treated with a bacterial pathogen-associated m

279 Seedlings treated with Bacillus were exposed to heat, co

280 eproductive success of plants, but seeds and seedlings typically encounter constantly changing enviro

281 sub-tissue level across Arabidopsis thaliana seedlings under multiple environmental conditions and ge

282 prenylated pterocarpans produced in soybean seedlings upon fungus elicitation.

283 back, by imparting a negative effect on rice seedling vigor.

284 via ectomycorrhizal (EM) networks where one seedling was shaded (D) and the other kept illuminated (

285 Mortality of unwatered seedlings was higher in species with shorter seedling ro

286 induced callose deposition in leaves of pen3 seedlings was partially reverted by the addition of 4-me

287 Finally, by applying heat stress to whole seedlings, we address the longstanding question of possi

288 te abundances in leaves and roots, date palm seedlings were exposed to flooding with seawater and its

289 Wheat seedlings were grown to maturity and the spikes infected

290 Seedlings were grown under controlled conditions, and ir

291 in the roots of 7-d-old Arabidopsis thaliana seedlings were investigated using tissue-specific GA ina

292 ess Na(+) In contrast, 4- to 11-d-old camta6 seedlings were more sensitive to NaCl.

293 eatly reduced in the root tips of dark-grown seedlings, which could be reversed by exposing plants to

294 Transcriptome analysis of seedlings, which do not have striking phenotypic abnorma

295 A complete tobacco seedling with an image size of 9.2 x 15.0 mm(2) was anal

296 Two POST rates of HM were applied to seedlings with 1-2 leaves (Zadoks stages 11-12), and the

297 We inoculated seedlings with a 185-member bacterial synthetic communit

298 d may lead to pigment-deficient seedlings or seedlings with variegated leaves.

299 Studies on proteasomes enriched from whole seedlings, with or without ATP needed to maintain the ho

300 simulated hydraulic stress and mortality in seedlings within the Bitterroot River watershed of Monta