ライフサイエンスコーパス: shoot

1 and technological objects in a single laser shot.

2 rise to lasing or no lasing depending on the shot.

3 d in roots instead of being allocated to the shoot.

4 optimally arrange and support the flowering shoot.

5 a in the root and pathogenic microbes in the shoot.

6 ancestral to extant seed plant reproductive shoots.

7 OsCADT1 gene was expressed in both roots and shoots.

8 than soil P concentrations in both roots and shoots.

9 expression of AM-inducible genes even in the shoots.

10 sponses, ABA levels were unchanged in the OX shoots.

11 lowing allantoin translocation from roots to shoots.

12 reezing predicted faster subsequent accurate shooting.

13 (reference areas), both before and after the shooting.

14 temporal characteristics that change shot-to-shot(14-16).

15 y (IPET) is an approach for obtaining a snap-shot 3D structure of an individual macromolecule particl

16 TRUFI), and three-dimensional fast low angle shot (3D FLASH) using breath-hold and respiratory trigge

17 ila wing disc respond to loss of Short stop (Shot), a cytoskeletal crosslinking spectraplakin protein

18 vidence during a criminal investigation of a shooting accident.

19 s to be linked with the away team's impaired shooting accuracy (i.e., movement precision) and rebound

20 home-court advantage on winning percentage, shooting accuracy, and rebounding.

21 time zones reduces winning percentage, team shooting accuracy, and turnover percentage, whereas trav

22 r require event repetition or provide single-shot acquisition with no more than 10(13) frames per sec

23 T1 functions in both root uptake and root to shoot allocation of a broad spectrum of amino acids in r

24 Standard FAIMS single-shot analyses identified around 15-20% additional phosph

25 reduction in cell division activity in both shoot and root apical meristems observed in fbl17 loss-o

26 g to gravity, which ultimately controls both shoot and root architecture.(1) Gravitropism is a dynami

27 during longitudinal and radial expansion of shoot and root axes differs fundamentally with respect t

28 Taken together, our findings show that shoot and root developmental responses to temperature ar

29 Here, we found that shoot and root growth responses to high ambient temperat

30 105 have only a limited impact on regulating shoot and root growth.

31 results showed that at the community level, shoot and root mass decreased with drought but increased

32 that control seed weight, root architecture, shoot and root traits, and shoot traits alone.

33 sed K(+) and lowered Na(+) concentrations in shoot and root under stress.

34 e and mixture treatments improved per plant (shoot and root) growth and nutrient assimilation as well

35 Uniform growth of the main shoot and tillers significantly influences rice plant ar

36 xillary meristems (AMs) give rise to lateral shoots and are critical to plant architecture.

37 her sulphur and selenium accumulation in the shoots and grains.

38 tant accumulated more Cd in roots but not in shoots and grains.

39 tabolites were more abundant in the flowers, shoots and leaves compared to smaller molecular weight o

40 fferentially expressed in plants with heated shoots and low yield that had been previously associated

41 r (p < 0.005) BPA accumulation in roots than shoots and nonsignificant variances in biomass, chloroph

42 ant growth patterns, including stunted bushy shoots and poor seed set.

43 -rich repeat receptor-like kinases acting in shoots and proposed to perceive signaling peptides produ

44 Transcriptomic analysis of the shoots and roots of one representative OX line indicated

45 particles displayed different effects in the shoots and roots of plants at different concentrations,

46 AA in their embryo, produced longer seedling shoots and roots, than the null segregant (NS) controls.

47 butions to total Cho kinase activity in both shoots and roots.

48 lation of barley APL transcripts in both the shoots and roots.

49 s showed increased Fe accumulation in roots, shoots and seeds when grown in Fe-sufficient condition,

50 Finally, co-depletion of Shot and GADD45 induced significantly higher rates of ch

51 l regulation, shoot hydraulic conductance (K(shoot) ) and stem xylem embolism resistance in Selaginel

52 silencing signal from cell to cell, root to shoot, and even between host and pathogen.

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

54 the genes are down-regulated by ethylene in shoots, and a DNA binding motif was identified that is i

55 through greater branching and enlargement of shoots, and possibly faster root branching.

56 e single-cell transcriptomic analyses of the shoot apex yield insight into the processes of stem-cell

57 n regulates rhythmic organ production at the shoot apex, but the spatio-temporal dynamics of auxin gr

58 In the shoot apex, VRN2 differentially modulates flowering time

59 ene expression atlas of the vegetative maize shoot apex, we show here that distinct sets of genes gov

60 nd the MADS-Box gene APETALA1(AP1)/MC at the shoot apex.

61 ively kills epidermal and niche cells in the shoot apex.

62 The AP2 genes maintain shoot apical meristem (SAM) activity in part by keeping

63 In flowering plants, the shoot apical meristem (SAM) contains a pluripotent stem

64 rstanding how the distinct cell types of the shoot apical meristem (SAM) withstand ultraviolet radiat

65 KANADI and HD-ZIPIII genes within the plant shoot apical meristem (SAM).

66 in the rate of leaf initiation, an enlarged shoot apical meristem and an increase in the number of j

67 ow the primary wall CESA complex acts during shoot apical meristem development.

68 te of mutation accumulation per unit time in shoot apical meristem is lower than that in root apical

69 ATA3 pathway genes play an essential role in shoot apical meristem maintenance and floral organ devel

70 Leaves are derived from the shoot apical meristem with three distinct axes: dorsoven

71 ely reduced root and shoot growth, a smaller shoot apical meristem, and an enlarged root cap.

72 omponent of a FAC promoting flowering at the shoot apical meristem, downstream of OsFD1.

73 guard cells in leaves, root vasculature, and shoot apical meristem, implicating it in both local and

74 cell population originally detached from the shoot apical meristem.

75 Along the vertical axis of plant shoot apical meristems (SAMs), stem cells are located at

76 ain populations of pluripotent stem cells in shoot apical meristems (SAMs), which continuously produc

77 Thorns arise from axillary shoot apical meristems that proliferate for a time and t

78 Global transcriptome profiling in developing shoot apices and inflorescences of mutant and wild-type

79 oadband transmitter, we demonstrate a single-shot approach for link discovery which can be accomplish

80 Shoot architecture is critical for optimizing plant adap

81 future study of TAC1 and LAZY1 regulation of shoot architecture.

82 o understand optimization trade-offs made by shoot architectures and provides evidence that these tra

83 nding the optimization objectives that shape shoot architectures remains a critical problem in plant

84 -theoretic analysis to show that Arabidopsis shoot architectures strike a Pareto optimal that can be

85 we performed 3D scanning of 152 Arabidopsis shoot architectures, including wildtype and 10 mutant st

86 , in which a high proportion of mutations in shoots are themselves transmissible, but not in annuals,

87 stable transformation system using axillary shoots as the initial explant.

88 ticipant must rapidly decide to shoot or not shoot at White and Black men who either are or are not h

89 After the shooting at a synagogue in Pittsburgh, Pennsylvania, dis

90 The formation of any lateral shoots at the grafted sites were studied in two of four

91 y can get their hands on to have a realistic shot at it.

92 is and Medicago control overall RSA, LR GSA, shoot auxin levels and rootward auxin transport.

93 ase in rootward auxin transport and elevated shoot auxin levels.

94 iofrequency energy or single-application one-shot balloons is either technically challenging or have

95 vel task without any direct experience (zero shot), based on its relationship to previous tasks.

96 Maize shoot biomass and P uptake were greater in the heterogen

97 asite infection significantly decreased host shoot biomass and shoot : root ratio more severely in hi

98 d showing that aspects of plant performance (shoot biomass, relative water content, sugar and proline

99 elayed maturity and greater non-reproductive shoot biomass, whereas plants with both heated roots and

100 of basil with 500 mg/L of ChL increased the shoot biomass.

101 As a key integrator of shoot branching, BRANCHED 1 (BRC1) coordinates and is or

102 ion to regulate M. truncatula organ size and shoot branching, providing a new genetic tool for increa

103 arious developmental processes, particularly shoot branching, root development, and leaf senescence.

104 itiation is slower and there is no change in shoot branching.

105 PHLOEM PROTEIN2 genes was upregulated in the shoots, but downregulated in root tissues.

106 nded roots was sufficient to trigger root-to-shoot Ca(2+) waves and slow wave potentials (SWPs).

107 The promotive effect of auxin on shoot cell expansion provided the bioassay used to isola

108 We show by functional expression in shoot cells that the different RNA isoforms of CCT101 en

109 le and could potentially be used for shot-to-shot CEP tagging applications requiring orders-of-magnit

110 Single-shot cIEF-MS/MS identified 711 proteoforms from an Esche

111 belowground competition, unlike aboveground shoot competition, is hampered by our inability to obser

112 rs, which is mirrored by a decline in bamboo shoot consumption by primates; but an increase in propor

113 Grafting showed that CEPR1 in the shoot controls GSA.

114 e lack of TAC1 did not influence gravitropic shoot curvature responses.

115 uits (N = 54), revealed that preparation for shooting decisions under threat is associated with postu

116 port theanine and participate in its root-to-shoot delivery in the tea plant.

117 Shoot density diminishes non-linearly with depth, while

118 DL single-shot detector (SSD) algorithms were constructed and trai

119 Conclusion Deep-learning single-shot detector models detected nearly all brain metastase

120 we show that UV-B induces genes involved in shoot development and organ patterning.

121 es a community resource for further study of shoot development and response to internal and environme

122 nt to harmonize internode morphogenesis with shoot development.

123 By contrast, newly emerging shoots display an opposite epigenetic scenario associate

124 it, disruption of which causes enhanced main shoot dominance and tiller dwarfism by an unknown mechan

125 dwarf dwt1 phenotype but abolishes the main shoot dominance.

126 0 muM and accumulated up to 1300 mg of Se/kg shoot dry weight.

127 r lesion visibility for MUSE DWI over single-shot DWI (kappa = 0.70).Conclusion: MUSE DWI is a promis

128 diffusion-weighted imaging (DWI) and single-shot DWI for lesion visibility and differentiation of ma

129 improved image quality compared with single-shot DWI in phantoms (SNR, P = .001) and participants (l

130 ences were found between MUSE DWI and single-shot DWI in the mean, maximum, and minimum ADC values (P

131 ard-approved study, both MUSE DWI and single-shot DWI sequences were first optimized in breast phanto

132 tive differences between MUSE DWI and single-shot DWI were assessed using the Mann-Whitney U test; si

133 e yields only a mild reduction of the single-shot efficiency, therefore the number of accumulated ele

134 stly synthesized in roots and transported to shoots either for organic nitrogen translocation in legu

135 tam/z = 0.036) in the ICR cell, using single-shot ejections after broadband ejections and MS/MS based

136 rome, inducing responses such as accelerated shoot elongation and early flowering.

137 ed, and the accumulation mode, where shot-to-shot energy jitter is reduced.

138 efficiency degradation caused by the shot-to-shot energy jitter, an optimized gun phase yields only a

139 cision criterion, increasing the tendency to shoot, even when controlling for psychomotor vigilance,

140 the spatial resolution obtained from single shot experiments lags averaging static experiments.

141 -grafting experiments revealed dependence on shoot-expressed MPK4 for N. attenuata to vary its yield

142 on recovery method for labeling and a single-shot fast spin echo sequence for image readout.

143 steady-state free precession (SSFP), single-shot fast spin-echo, 2D and 3D T1-weighted spoiled gradi

144 Interestingly, in plants with heated shoots, flowers stayed closed during the day while the c

145 large energy spread, divergence and shot-to-shot fluctuations require a specific transport line, to

146 ealing in seedling grafts along with lateral shoot formation occurring in two of four grafting approa

147 Growth rate and lateral shoot formation, on the other hand, were different among

148 In this study, tea shoots from two cultivars (cvs.

149 ol II initiation in yeast, which we term the shooting gallery.

150 for auxin-mediated PIN3 re-polarization and shoot gravitropic bending termination.

151 A/I94A) had the profound effect of switching shoot gravity responses from negative (upward bending) t

152 tic cells from the quiescent state, root and shoot growth and architecture, to flowering and seed pro

153 We propose that the photoperiodic control of shoot growth in poplar involves a balance between FT2 ac

154 al repression that leads to an inhibition of shoot growth in response to ethylene.

155 s during plant life cycle and in relation to shoot growth phenology remains understudied.

156 Pi content and was associated with improved shoot growth under low external Pi supply and no deleter

157 pressor TREE1 interacts with EIN3 to inhibit shoot growth via transcriptional repression in response

158 defects, including severely reduced root and shoot growth, a smaller shoot apical meristem, and an en

159 that can act as a potent signal to modulate shoot growth, yet the molecular mechanisms involved are

160 decreased, which was accompanied by reduced shoot growth.

161 EE1-targeted genes leads to an inhibition of shoot growth.

162 t signaling pathways that integrate root and shoot growth.

163 ortage results in the inhibition of root and shoots growth, but the underlying mechanism of this resp

164 Furthermore, plants with heated shoots had delayed maturity and greater non-reproductive

165 ated, quinoa yield losses were attributed to shoot heating.

166 -related traits such as stomatal regulation, shoot hydraulic conductance (K(shoot) ) and stem xylem e

167 ional profile of roots is highly affected by shoot illumination.

168 Finally, after the Walmart shooting in El Paso, Texas, hate crime perceptions were

169 0,000 American students experienced a school shooting in the last two decades, little is known about

170 Conversely, after the tram shooting in Utrecht, Netherlands (which was perpetrated

171 tase (SOD) and peroxidase (POD) in roots and shoots indicate a general increase of activities after e

172 g the QAOA output with high-fidelity, single-shot, individual qubit measurements.

173 ently, the application of auxin to wild-type shoots induced a steeper GSA and auxin transport inhibit

174 transcriptionally upregulated as part of the shot-induced apoptotic response.

175 tion errors in cultured cells and suppressed shot-induced mitotic arrest.

176 An excess of Shot induces ectopic acentrosomal luminal branching poin

177 flowers but also upon developing appropriate shoot internodes that optimally arrange and support the

178 seedlings from shaded environments optimize shoot investment, and seedlings experiencing frequent de

179 avanna and forest species, with low and high shoot investment, respectively.

180 Shot is enriched in cells undergoing the initial steps o

181 ast to other known spindle-regulating genes, Shot knockdown induces apoptosis in the absence of Jun k

182 the subsequent recollection accuracy of one-shot learned episodic memory associations.

183 We present DeepKinZero, the first zero-shot learning approach to predict the kinase acting on a

184 lerance to scale and position changes in one-shot learning by measuring recognition accuracy of Korea

185 on networks serve as the scaffolding for one-shot learning by replaying, reversing, refining, and reg

186 e kinases with no known sites through a zero-shot learning model.

187 for subtomogram classification based on few-shot learning.

188 value-based social choices following single-shot learning.

189 bility and language-based approaches to zero-shot learning.

190 egument and nucellus together developed in a shoot-like fashion, potentially ancestral to extant seed

191 WL2 to coordinate the uniform growth of rice shoots, likely to be through nuclear phosphoinositide si

192 rhizodeposits) vs litter inputs (i.e. root + shoot litter) are poorly understood.

193 Shot loss leads to double-strand break (DSB) DNA damage,

194 Plants with heated shoots lost 60-85% yield as compared with control plants

195 1;1 results in less Mo being translocated to shoots, lower Mo concentration in grains and higher sens

196 In shoots, many differentially expressed genes, either up-

197 d intensity contouring (TRIC) enables single-shot measurement of laser-plasma dynamics.

198 However, through a one-shot measurement within a few seconds, phase-shifting in

199 We show that hypoxia localized to the shoot meristem inhibits the proteolysis of an N-degron-p

200 E1 (ATH1) maintains the meristem marker gene SHOOT MERISTEMLESS (STM) expression in the leaf axil to

201 idly translocated out of the treated leaf to shoot meristems and roots than in plants grown under con

202 and in vivo oxygen measurements, that plant shoot meristems develop embedded in a low-oxygen niche,

203 s(6-8)-and thereby regulates the activity of shoot meristems.

204 surized liquid extraction followed by double-shot microfurnace pyrolysis coupled to gas chromatograph

205 Although many signals from shoots might be important for triggering root growth, th

206 In the single-shot mode, we numerically optimized the monochromator ef

207 gy spread is advantageous in both the single shot mode, where the momentum resolution in diffraction

208 In addition to the HY5/PIF-dependent shoot module, a regulatory axis composed of auxin biosyn

209 (3) species through a greater enlargement of shoot modules and quicker secondary branching of roots.

210 better dissect the genetic control of plant shoot morphogenesis at the cellular level.

211 Furthermore, while widespread shoot mortality is commonly observed with browning event

212 GRIN cascades form the basis of a new single-shot Muller matrix polarimeter with potential for endosc

213 which attains several new records in single-shot multi-dimensional imaging speeds.

214 2 human cell line protein digests via single-shot nanoLC-MS/MS analysis on a Q Exactive HF system.

215 outside the superconducting gap region, the shot noise agrees quantitatively with independent tunnel

216 Shot noise reference doses in the range from 820 to 1,70

217 lication of a century-old result describing "shot noise" in an electronic system repairs the deficien

218 egmentation of spiking cells compared to the shot-noise-limited performance of single pixels.

219 ages of stems revealed that the decline in K(shoot) occurred with the formation of an air-filled lacu

220 declines in K(shoot) , with a 50% loss of K(shoot) occurring at -1.7 and -2.5 MPa in S. haematodes a

221 nt racial biases, including more and quicker shooting of Black targets compared to White targets.

222 ical methodology to the bending movements of shoots of common beans (Phaseolus vulgaris L.) in two co

223 asitic plants of the genus Cuscuta penetrate shoots of host plants with haustoria and build a connect

224 spin manipulation, and high-fidelity single-shot optical readout of the hyperfine spin state of sing

225 task, the participant must rapidly decide to shoot or not shoot at White and Black men who either are

226 bers of a gene family that regulates lateral shoot orientation in plants.

227 s revealed that TAC1- and LAZY1 influence on shoot orientation is more complex than a simple direct n

228 sponse to light, while LAZY1 promotes upward shoot orientations in response to gravity via altered au

229 negatively regulate LAZY1 to promote outward shoot orientations.

230 Here, using a dramatic one-shot perceptual learning paradigm, we observed that prio

231 that prior knowledge acquired from fast, one-shot perceptual learning sharpens neural representation

232 One-shot PFA catheters have been developed for pulmonary vei

233 One-shot PFA catheters have been shown capable of performing

234 type, indicating it is epistatic to the tac1 shoot phenotype.

235 estingly, deletion of the uORF led to higher shoot Pi content and was associated with improved shoot

236 Increased shoot Pi content was linked to the absence of the PHO1 u

237 uORF exhibit higher PHO1 protein levels and shoot Pi content.

238 In shoots, pmt1 pmt2 pmt3 enhanced the phenotype of pmt1 pm

239 They then played a one-shot Prisoner's Dilemma Game with their chosen partner.

240 using a dilute/precipitate, centrifuge, and shoot process coupled with on-line sample clean-up using

241 eas plants with both heated roots and heated shoots produced higher yields from the panicles that had

242 Within this framework, feedforward (or one-shot) production is responsible for feedforward audience

243 dentified that the spectraplakin Short-stop (Shot) promotes the crosstalk between MTs and actin, whic

244 with programs like TCGA and the Cancer Moon Shot, provides an instructive example as we see differen

245 several orders of magnitude, enabling single-shot quantum nondemolition readout of the ion's spin wit

246 strategy to combine mutations for condensed shoots, rapid flowering (SP5G) and precocious growth ter

247 After 12 h of ENS treatment, the root/shoot rate of both cultivars were lower than that of CLN

248 tly glycine betaine and an increased root-to-shoot ratio to explore more soil volume for water.

249 as plant height, leaf mass ratio, and root : shoot ratio.

250 are realizing long spin coherence and single-shot readout in photonic resonators.

251 High-fidelity single-shot readout of spin qubits requires distinguishing stat

252 ortest coherence time and demonstrate single-shot readout of the protected qubit under stabilization.

253 tes efficient spin initialization and single-shot readout with conditional fidelity greater than 95 p

254 gnificantly decreased host shoot biomass and shoot : root ratio more severely in high water than low

255 nce the resistance in distal organs via root-shoot-root communication.

256 We describe a root-shoot-root signaling mechanism which simultaneously enab

257 compared with DDG for conventional step-and-shoot scans.

258 eadout with conventional platforms in single-shot screening and multipoint profiling modes.

259 early seedling development in Arabidopsis A shoot signaling module that includes HY5, the phytochrom

260 Shoot silicon concentrations also increased significantl

261 index (LAI), which is governed by changes in shoot size and density.

262 ty diminishes non-linearly with depth, while shoot size increases to a maximum followed by a decline.

263 steep Suc concentration gradient between the shoot (source) and the taproot (sink).

264 recently used to enable a successive single-shot spectral measurement over a couple of milliseconds

265 0.5 x 10(12) fps, allowing the first single-shot spectrally resolved fluorescence lifetime imaging m

266 wing high-fidelity initialization and single-shot spin measurement of six rare-earth (Er(3+)) ions, w

267 Here, we demonstrate single-shot spin readout of a single rare earth ion qubit, Er(3

268 Expression of WUSCHEL (WUS) defines the shoot stem cell niche in the apical meristems of many an

269 f the transcriptional landscape of the maize shoot stem-cell niche and its differentiating cellular d

270 owning events, recent observations show that shoot stress responses are also common, and manifest as

271 vascular maturation and thereby adapting the shoot system to the developmental needs of the ensuing r

272 ek to bridge this divide by using a "penalty shot" task in which pairs of monkeys competed against ea

273 lectionist logic can predict a lower rate in shoot than in root and in longer-lived terminal tissues

274 Leaf removal (LR), shoot thinning (ST) and their combination (LRST) are kno

275 duced growth and enhanced production of side shoots (tiller).

276 Shoot tip hormone levels were similar between tac1, lazy

277 rite in the root tissues and ammonium in the shoot tissues.

278 it functions to increase O(2) diffusion from shoot to root.

279 -Seq based transcriptomic analysis in apical shoots to check regulation of gene expression.

280 s scalable and could potentially be used for shot-to-shot CEP tagging applications requiring orders-o

281 s improved, and the accumulation mode, where shot-to-shot energy jitter is reduced.

282 ate the efficiency degradation caused by the shot-to-shot energy jitter, an optimized gun phase yield

283 t by the large energy spread, divergence and shot-to-shot fluctuations require a specific transport l

284 ut with temporal characteristics that change shot-to-shot(14-16).

285 oot architecture, shoot and root traits, and shoot traits alone.

286 to 5 miles from a school that experienced a shooting (treatment areas) to the number of prescription

287 d coronal T2 half-Fourier acquisition single-shot turbo spin-echo (HASTE), spectrally attenuated inve

288 ing ants, frame-by-frame, from video footage shot under the natural conditions of a tropical forest f

289 bodies are the basis of several current "one-shot" universal influenza vaccine efforts because they p

290 These data demonstrate robust single-shot vaccine protection against SARS-CoV-2 in non-human

291 PHOSPHATE1 (PHO1) transfers Pi from root to shoot via Pi export into root xylem vessels.

292 The increased tendency to shoot was also observed in participants who reported bel

293 ry of root-synthesized amino acids to Oslht1 shoots were also significantly decreased, which was acco

294 tial heating system where only roots or only shoots were heated, quinoa yield losses were attributed

295 ots and is subsequently transported to young shoots, which are harvested for tea production.

296 st, what is the problem: How many people get shot, who are they, where does it happen, what is the re

297 This induces meristems that produce shoots with targeted DNA modifications, and gene edits a

298 ies were found to close before declines in K(shoot) , with a 50% loss of K(shoot) occurring at -1.7 a

299 ples, FAIMS enables the collection of single-shot XL-MS data with a comparable depth to the correspon

300 estingly, both Col-0 and CSHL-5 have similar shoot Zn concentrations.