ライフサイエンスコーパス: seed

1 tween cells are referred to as 'pathological seeds'.

2 t amounts of squalene (2.5 and 1.1 mg /100 g seeds).

3 food challenges to all other nuts and sesame seed.

4 ncreased emergence by 7-10% over that of dry seeds.

5 higher amounts in ATP sulfurylase transgenic seeds.

6 ed to improve the nutritive value of soybean seeds.

7 ined from spectroscopic signatures of peanut seeds.

8 of the structural properties of pathological seeds.

9 cycle synthesized more fatty acids in their seeds.

10 of longan wine produced by incorporating the seeds.

11 s, 57.9% meats, 4.7% eggs, and 0.5% nuts and seeds.

12 nt and antibacterial activities of fenugreek seeds.

13 ly accumulate large amounts of lipids in the seeds.

14 d by about 3% when compared to the wild-type seeds.

15 conformation and properties of pathological seeds.

16 portant in abscisic acid (ABA) signalling in seeds.

17 eCO(2) could improve the sprouting of plant seeds.

18 hen compared to the non-transgenic wild-type seeds.

19 the best results were achieved with unviable seeds.

20 I still occurred in the presence of UBA III seeds.

21 y efficient removal of HFA from PC in castor seeds.

22 of scrapie prions using ultrasensitive prion seeding.

23 Of the 800 treated seeds, 415 germinated and were advanced up to four (M4)

24 t to quantitatively detect such pathological seeding activities in patient biosamples, e.g. cerebrosp

25 This seeding activity can be ameliorated by targeting specifi

26 found that astrocytes are neuroprotective to seeded aggregation within motor neurons by reducing (mis

27 e more potent than those of idiopathic PD in seeding aggregation.

28 ears with at least 1 confirmed nut or sesame seed allergy underwent sequential diagnostic food challe

29 f coexistent peanut, tree nut, and/or sesame seed allergy.

30 therapeutically targetable pathogenic Abeta seeds already exist during the lag phase of protein aggr

31 tation of longan juice supplemented with 50% seed and 20% initial soluble solids at an optimal temper

32 lmost every aspect of plant development from seed and bud dormancy, liberation of meristematic cells

33 ectroscopy allow obtaining information about seed and grain chemical composition, which can be relate

34 lyphenol extracts from grape seed (G), grape seed and olive (O) or grape total (T), called ESG, ESO a

35 failure due to waterlogged conditions after seeding and allows water to be used as a means of weed c

36 d mixtures, application of manure soon after seeding and low-intensity grazing) allowed the ecosystem

37 ary body medulloepithelioma with concomitant seeding and neovascular glaucoma in the right eye was se

38 Seeding and ultrasound-assisted pre-crystallization can

39 n influence the quality attributes of sesame seeds and oil and should be considered during processing

40 that, the tannins content and composition of seeds and skins at three different maturity stages were

41 n plants, desiccation tolerance is common in seeds and spores but rare in leaves and other vegetative

42 that is particularly abundant in edible pine seeds and that exhibits an unusual polymethylene-interru

43 turnover to accumulate TAG production in oil seeds and that NPC6 has a great application potential fo

44 s to investigate how mRNAs are stored in dry seeds and whether they are indeed translated during seed

45 pression matrix, RecBic starts with a column seed, and grows it into a full-sized bicluster by simply

46 such as trunk (stem and bark), leaf, flower, seed, and root.

47 was associated with a lower intake of nuts, seeds, and legumes (beta = -0.05 per gram; 95% CI: -0.09

48 dairy products, lean protein sources, nuts, seeds, and liquid vegetable oils.

49 Allergies to peanuts, tree nuts, and sesame seeds are among the most important food-related causes o

50 t-based proteins from potato, pea, and grape seed as recent alternative, were compared to unfined con

51 Initially, these cells are seeded as a proliferative monolayer over the shaped scaf

52 ds, which are nominated as novel markers for seed authentication.

53 edial prefrontal cortex (mPFC) combined with seed-based connectivity analysis with the striatum recap

54 disease patient's location of atrophy using seed-based functional connectivity in a large (n = 1000)

55 iRNAs can base-pair with a target mimic in a seed-based manner, and that the target-bound AGO2 can be

56 bodies for their ability to neutralize Abeta seeds before Abeta deposition becomes detectable in Abet

57 drives systemic metastasis, where polyclonal seeding between sites is common.

58 ormation of an assembly-competent nucleation seed, but we find an unanticipated role for them in enha

59 f hard foods, such as mechanically-protected seeds, but dental microwear analyses are not.

60 gle-chain variable fragment (scFv) inhibited seeding by IL15-induced tau oligomers and pathological e

61 We observed that cross-seeding by sRPT fibrils accelerates the rate of lRPT agg

62 ghly variable and synchronised production of seeds by plant populations, known as masting, is implica

63 seed (FINOLA variety) cake and defatted hemp seed cake by SC-CO(2) was carried out using Flavorpro 75

64 The high level of injury to seeds caused by pentatomids is related to their feeding

65 limatic associations of natural variation in seed chilling responses and associated life-history synd

66 antigens select recurrent BCR clonotypes to seed chronic PP GC responses.

67 ts to offset nitrogen fertilizer inputs, (2) seed coatings to increase germination rates and (3) foli

68 In seed coats, no phloem occlusion was observed, and CLas a

69 cotyledonous taxa with the highest number of seeds collected were analyzed; we estimated propagule pr

70 icant increases in HFA levels in Arabidopsis seeds compared with RcFAH12 expression alone.

71 osphorylated species of soluble, oligomeric, seed-competent tau.

72 Only rabbits with cell-seeded constructs had normal pregnancies (four in ten) i

73 and were reconstructed with autologous cell-seeded constructs, with nonseeded scaffolds or by suturi

74 Viable seeds contained higher levels of alpha-tocopherol (6.7 m

75 s greater than the adjustment accounting for seed cost.

76 Interannual variability of seed crops (CVp) has profound consequences for plant pop

77 Addition of UBA I seed crystals modified this pathway such that only UBA I

78 The major dechlorinating species in the seed culture, Dehalococcoides, were not responsible for

79 r-ripening (DAR), and for SL measured by the seed decay rate and survivability in the soil of a rice

80 t the branching patterns are directed by the seed defects, with the emergence of branches from the se

81 Here, we demonstrate that the majority of seed-dehydration-related genes showed similar expression

82 The frequency- and seed-dependent functional organizations of LAI may enlig

83 In seed-derived progeny of R1 plants, Tnt1 segregated in a

84 gote showed defective pollen tube growth and seed development because of nonviable mutant gametes.

85 d that RBOH1-mediated ROS promote pollen and seed development by triggering PCD and tapetal cell degr

86 Seed development largely depends on the long-distance tr

87 anscription factor is a central regulator of seed development, because it controls diverse biological

88 controls diverse biological programs during seed development, such as embryo morphogenesis, photosyn

89 fferent developmental phases during silique (seed) development, seed germination, and seedling establ

90 nd MADS 79 are essential regulators of early seed developmental transition and impact both seed size

91 content: an insect diet (low content), or a seed diet (high content).

92 ls given the insect compared to those on the seed diet.

93 artitions into oligomeric forms that inhibit seeding differently, and crystal structures of the M204-

94 es are generally wider for species with high seed dispersal or persistence abilities.

95 aptive benefits of CVp (wind pollination and seed dispersal) and climatic variability (variability of

96 Because beech has long distance pollen and seed dispersal, these results illustrate a 'best case sc

97 lation plays critical roles in regulation of seed dormancy during seed germination and early seedling

98 ing RNA that regulates expression of the key seed dormancy regulator, DELAY OF GERMINATION1, is a typ

99 ased activation of sgACC was examined with a seed-driven analysis assessing group differences and cha

100 describe changes in concentration in cowpea seed during two germination phases: before 14 h and afte

101 synthesise, at the global level, the alpine seed ecological spectrum.

102 While seed emegence and stand establishments were enhanced by

103 ity could be one of the molecular mechanisms seeding evolutionary co-option.

104 f CNT in the BO-planner experiments over the seed experiments up to a factor 8; (2) rapidly improve i

105 rmance regardless of the number or origin of seed experiments; (4) exploit a high-dimensional, comple

106 n decades ago in Vonnegut's pioneering cloud seeding experiments, it remains unclear what makes a mat

107 and their precursor material, enriched grape seed extract (e-GSE; Vitis vinifera).

108 ed to characterize the nanoemulsion of anise seed extract and to compare its efficacy with the bulk e

109 cts, with the emergence of branches from the seed faces consistent with minimizing volumetric strain

110 r assigning specimens to race and found that seed features were particularly informative.

111 Enzymatic hydrolysis of the oil hemp seed (FINOLA variety) cake and defatted hemp seed cake b

112 ry seed PBAA composition plays a key role in seed fitness and therefore is rigorously maintained even

113 t have uncovered fluid dynamic mechanisms of seed flight, protective measures against fire, and relea

114 a translation repressor to an activator and "seed" for further translationally active aggregation.

115 Seed from populations at the CO(2) spring and an adjacen

116 isture, and linolenic acid content of sesame seeds from different countries.

117 this study, M. oleifera flowers, fruits and seeds from Guinea-Bissau were characterized for their nu

118 Our data are consistent with numerous seeds from multiple sources and a prolonged period of un

119 In this work, seeds from selected Mertensia species were analyzed for

120 The as-formed MoS(2) seeds function as a capping layer that reduces the nucle

121 fferent solid polyphenol extracts from grape seed (G), grape seed and olive (O) or grape total (T), c

122 Finally, starting from one or multiple seed genes, a shortest path algorithm is applied to dete

123 Rice seeds germinating in flooded soils encounter hypoxia or

124 oss a wide climate range and scored each for seed germination across a range of 13 cold stratificatio

125 e synthesized from carotenoids, functions in seed germination and abiotic stress responses.

126 unter hypoxia or even anoxia leading to poor seed germination and crop establishment.

127 the seed, to supply the necessary energy for seed germination and early seedling establishment.

128 roles in regulation of seed dormancy during seed germination and early seedling growth.

129 Efficient seed germination and establishment are important traits

130 own about how the ABA-mediated inhibition of seed germination and seedling establishment is thwarted.

131 A together regulate lipid degradation during seed germination and seedling establishment.

132 ization and fatty acid beta-oxidation during seed germination and seedling establishment.

133 Overexpression of ABT promotes seed germination and seedling greening in the presence o

134 Seed priming uses treatments to improve seed germination and thus potentially increase growth an

135 phytochrome B photoreceptor, such as delayed seed germination in the dark and long hypocotyl growth.

136 al phases during silique (seed) development, seed germination, and seedling establishment in Arabidop

137 anslation of these mRNAs occurs during early seed germination, even before the requirement of transcr

138 urther, down-regulation of AtPAM16L affected seed germination, even in the presence of its seemingly

139 nd whether they are indeed translated during seed germination.

140 ng the role of lipid homeostasis during rice seed germination.

141 regulation of the assembly pathways through seeded growth can accelerate the assembly kinetics and i

142 hybrid structures require complex sequential seeded growth, where each section requires its own set o

143 r. capitata L. (leaf), and Bixa orellana L. (seed) had the highest nutritional and functional value f

144 However, date fruit and seeds have not been fully considered as potential functi

145 Seed hydro-priming or pre-soaking increased emergence by

146 ormulation of Irinotecan-loaded Drug Eluting Seeds (iDES) for insertion into the margin of the GBM re

147 ry plexus, reenter systemic circulation, and seed in the brain.

148 When seeded in fibrous gels, pairs of cells or cell aggregate

149 es are defined by tissue and nerve type, are seeded in part prenatally, and self-maintain via prolife

150 minoglycans and inhibition of Tau uptake and seeding in cells.

151 ncer-related mortality, mechanisms governing seeding in distal tissues are poorly understood.

152 hen normalized to standard space and used as seeds in a high-resolution normative resting state funct

153 ontrivial adaption and application of spaced seeds in the context of optical mapping, which allows fo

154 The presence of seeds in the jam affected directly yield stress, apparen

155 llagitannin, quebracho, grape-skin and grape-seed) in comparison with ascorbic acid (AA), sulfur diox

156 epiphyte Pseudomonas protegens Pf-5, a maize seed inoculant.

157 Mango seed kernel is a by-product which is usually discarded.

158 he signal of the film from the signal of the seed layer and the data are carefully analysed and conte

159 RNA from mature, developing, and germinated seeds, leaves, and roots exposed to different abiotic st

160 ipulation of seed size, through selection of seed length versus seed width and height, was deemed pos

161 ven colocalized outlier SNPs associated with seed mass and precipitation that also carry signatures o

162 Our findings suggest that seed mass in sorghum was shaped by diversifying selectio

163 The climatic drivers and genomic basis of seed mass variation remain poorly understood.

164 Genetic studies of seed maturation regulators, combining transcriptomics an

165 egulated targets reflect the role of ABI3 in seed maturation, desiccation tolerance, entry into a qui

166 as embryo morphogenesis, photosynthesis, and seed maturation.

167 pathology from cell-to-cell by a prion like seeding mechanism.

168 h levels of the chemokine receptor CXCR6 and seed meninges shortly after birth.

169 e-use of topsoil, hydroseeding of commercial seed mixtures, application of manure soon after seeding

170 interplay between germination physiology and seed morphological traits further reflects pressures to

171 me and germination synchrony; accounting for seed morphology (mass, embryo : seed ratio) and phylogen

172 Seed movement and delayed germination have long been tho

173 Exposure of bioreactor-seeded MSCs to inflammatory stimuli reproducibly switche

174 Black seeds (Nigella sativa), is considered a traditional folk

175 p to coordinate ovule patterning and thereby seed number with gynoecium and fruit growth through a se

176 ble information in the literature, fruit and seed of date palm are rich in phytochemicals, such as ph

177 Finally, this segment also inhibits seeding of Abeta catalyzed by Abeta fibrils extracted fr

178 e are no inhibitors that specifically target seeding of Parkinson's disease (PD)-associated alpha-syn

179 wn what controls the formation and templated seeding of strain-specific structures associated with in

180 hanced chemokine and alarmin production, and seeding of the skin with antigen-presenting cells capabl

181 how that the combination of the SDO and self-seeding of X-rays increases the pulse energy and makes i

182 rus replication in neuronal cells can induce seeds of aggregated alpha-synuclein or DISC1 that may be

183 chinery that directs oil accumulation in the seeds of B. napus and other oil crops.

184 by ABI3 and PIF1, is upregulated in imbibed seeds of drt111-2 mutants.

185 , increasing the O(2) deficit and sowing the seeds of exercise intolerance.

186 polymeric procyanidins was determined in the seeds of fruit.

187 nt showed 101-153% higher emergence over dry seeds of intolerant genotypes in the field.

188 od was also effective in extracting RNA from seeds of other cereals including field-grown sorghum and

189 s for phenolic compound determination in the seeds of these mustard species.

190 The unaged seeds of two independent maize DEHYDRATION-RESPONSIVE EL

191 his study aimed at encapsulating pomegranate seed oil (PSO) by emulsification followed by spray dryin

192 rassicaceae present a great heterogeneity of seed oil and fatty acid composition, accumulating Very L

193 Most strategies to alter seed oil composition involve the overexpression of lipid

194 To better understand lipid metabolism and seed oil synthesis in canola (Brassica napus), we have c

195 Linden seed oil was characterised by very high contents of phyt

196 re thought to contribute to the formation of seed oil, and previous characterizations of various DGAT

197 MSCs were seeded on the extraluminal side of hollow fibers within

198 for adding 3% black quinoa (either as whole seeds or as a fiber-rich fraction of quinoa from its wet

199 ch may serve to minimize competition between seeds or facilitate equal resource allocation.

200 ot analyses revealed that transgenic soybean seeds overexpressing ATP sulfurylase accumulated very lo

201 Seeds overexpressing MADS78 and MADS 79 exhibited delaye

202 aining seeds (P1WS and P2WS) and two without seeds (P1WHS and P2WHS).

203 ild species of Physalis spp., two containing seeds (P1WS and P2WS) and two without seeds (P1WHS and P

204 s evident between tissue P concentration and seed PA concentration (8-61 ppm).

205 d 0.3 mm as precipitation generated by cloud seeding passed over the instruments.

206 Together, our data show that the dry seed PBAA composition plays a key role in seed fitness a

207 plasms harboring the qSw17-1 QTL for the big-seeded phenotype indicated that reduced expression of Gm

208 e taxonomic and phylogenetic data for >7,500 seed plant species from the flora of Java with >16,500 s

209 ublished concentrations in dust from treated seed planting activities.

210 In seed plants, branching is achieved by stem-cell-containi

211 e proteins EDS1, SAG101, and PAD4 evolved in seed plants, on top of existing phytohormone and nucleot

212 ion for maturation programs, particularly in seed plants.

213 likely relationship to subsequently dominant seed plants.

214 nology can affect plant reproduction of mast-seeding plants, with subsequent implications for communi

215 We sought to determine the impact of seeding point errors (SPEs) as a source of low test reli

216 As a potential bentonite alternative, grape seeds powder (GSP) was added to four wines and two grape

217 ction have increased selection pressure from seed predators but not from pollination efficiency.

218 sting has become less effective at satiating seed predators.

219 Introgression of AG2 and AG1 + AG2 QTLs with seed pretreatment showed 101-153% higher emergence over

220 Seed priming uses treatments to improve seed germination

221 ce and stand establishments were enhanced by seed priming, total phenolics radical-scavenging activit

222 ruit production, which lowered the number of seeds produced per plant.

223 Annually variable and synchronous seed production by plant populations, or masting, is a w

224 ore, recent climate-driven increases in mean seed production have increased selection pressure from s

225 ntially increase inter-annual variability of seed production of masting species.

226 Masting-temporally variable seed production with high spatial synchrony-is a pervasi

227 improvement and reduce the cost of goods in seed production(1-3).

228 ot growth and architecture, to flowering and seed production.

229 st commonly used form of CMS in maize hybrid seed production.

230 from a clonally propagated tetraploid into a seed-propagated, inbred-line-based hybrid, but this proc

231 multichain PrP assemblies that propagate by seeded protein misfolding.

232 Lipid catabolism in germinating seeds provides energy and substrates for initial seedlin

233 al novel non-linear criteria for the initial seed pulse that will finally open the door to efficient

234 ze and seed weight (7-25%), without altering seed quality traits like fatty acid composition, glucosi

235 counting for seed morphology (mass, embryo : seed ratio) and phylogeny.

236 It is thus conceivable that seeds recalled or renovated ancient programs of stress-i

237 The siRNA with ANA at position 7 in the seed region was active in a mouse model.

238 repression is the base pairing between the 'seed' region of the miRNA and its counterpart mRNA(1).

239 neurocircuitry using nucleus accumbens (NAc) seed regions of interest, and then characterized how cha

240 6 eyes), and 100% of vitreous and subretinal seeds regressed, with 100% globe salvage.

241 However, we identified a small set of seed-related orthologs with expression specific to desic

242 Mulberry seeds revealed the strongest inhibition (p < 0.05) again

243 Accordingly, mutations in the miR-125b seed sequence abrogated the regulatory effect of the miR

244 miR-217 isomiR) are endowed with alternative seed sequences and share less than half of the predicted

245 striking genetic cline of seven-fold greater seed set at higher latitudes in the introduced but not t

246 nd invest more in sepals to insure their own seed set.

247 rns, including stunted bushy shoots and poor seed set.

248 identified for three QTLs that enhance spike seed setting and grain size using gene expression data a

249 g1 (SvLes1) as a gene whose product controls seed shattering.

250 rolled-environment and field phenotyping for seed, shoot, and root traits.

251 m photosynthetically active source leaves to seed sinks.

252 Furthermore, using seed site randomized genomes and evolutionary selection

253 nocking down the microRNAs or deleting their seed sites on Drd1 mimicked the cilia-beating and ventri

254 eed developmental transition and impact both seed size and quality in rice.

255 Two genes associated with seed size and shattering showed signatures of selection.

256 maternal reproductive tissue in determining seed size and yield, likely via the control of nitrogen

257 attern implies that CEPR1 controls yield and seed size from the maternal tissue.

258 Seed size shapes plant evolution and ecosystems, and may

259 erentiation of the carpel and the control of seed size, acting downstream of floral homeotic factors.

260 Manipulation of seed size, through selection of seed length versus seed

261 ate or early chilling damage associated with seed sowing or conventional transplanting of susceptible

262 c composition of the three in natura mustard seeds species, and support future reliable phenolic comp

263 llows the early screening of candidate hiPSC seed stocks for clinical use by facilitating safety and

264 o clarify whether other similar proteopathic seeds, such as tau or alpha-synuclein, can also be trans

265 ted advantage at initial steps of metastatic seeding, suggesting that Rab27a may alter cell-autonomou

266 ine but also the impact of grape maturity on seed tannins extractability.

267 of this work is to describe and explain the seed tannins kinetics release in wine but also the impac

268 highly toxic due to their strong ability to seed tau misfolding and propagate the pathology seen acr

269 ine-linked frameworks and their (001) facets seed the C=C bond formation reaction to constitute 2D sp

270 s generates cells of the T cell lineage that seed the lymphatic and blood systems.

271 rotection, contributing to pathogenesis, and seeding the human placenta.

272 In eudicot seeds the endosperm surrounding the radicle confers coat

273 ted that after 10 and 100 infected hens were seeded, the likelihood of detecting an infected parent f

274 d mRNAs are associated with monosomes in dry seeds; therefore, we focus on monosomes in this study.

275 ature enables the as-formed high-index grain seed to expand throughout the entire Cu foil.

276 nal photosynthesis, via food reserves in the seed, to supply the necessary energy for seed germinatio

277 'Mandilaria' scored the highest value in seed total flavanols compared to all biotypes and cultiv

278 estigate the effects of germination of spelt seeds under different stress conditions on the antioxida

279 omic changes in rare metastatic cells during seeding using single-cell RNA sequencing and patient-der

280 nase (HrCHI4) was purified from seabuckthorn seeds using chitin-affinity chromatography that showed a

281 rate transporter TaNRT2.5 with a key role in seed vigour.

282 (ccIIV4) vaccine was produced using A(H3N2) seed virus propagated exclusively in cell culture, thus

283 Polyclonal seeding was common in untreated lymph node metastases (n

284 This cross-seeding was unidirectional, as RPT fibrils did not influ

285 he overall protein content of the transgenic seeds was lowered by about 3% when compared to the wild-

286 plants with increased height, organ size and seed weight (7-25%), without altering seed quality trait

287 e oil content and fatty acids profile of the seed were investigated.

288 etabolite profiling in skin + pulp/flesh and seeds were also determined.

289 and oleic (10.09%) acids from unroasted chia seeds were higher than those from roasted ones.

290 sessments regarding opium alkaloids in poppy seeds were mainly based on the morphine level, whereas o

291 For the treatments, quinoa seeds were washed, cooked, and/or germinated.

292 , some tools have been augmented with spaced seeds, which are capable of tolerating mismatches.

293 ize, through selection of seed length versus seed width and height, was deemed possible, providing a

294 Here we use biodegradable polymer scaffolds seeded with autologous cells to restore uterine structur

295 The wells are seeded with cell-laden collagen, which, in response to t

296 is considered among the most primitive known seeds, with highly lobed integument and exposed nucellus

297 providing a new genetic tool for increasing seed yield and biomass production in crop and forage leg

298 variations during the crop growing season on seed yield, nutrient uptake and stoichiometry from 2001

299 Climate and soil fertility influence seed yield, nutrient uptake, and nutrient stoichiometry

300 sport is a successful strategy for improving seed yields and nutritional quality in legumes.