ライフサイエンスコーパス: root

1 g the developmental zones of the Arabidopsis root.

2 d to observe their expression domains in the root.

3 esponses and maintaining auxin levels in the root.

4 olic Ca(2+) increase in Arabidopsis seedling roots.

5 t modules and quicker secondary branching of roots.

6 ly similar between grafts and control aortic roots.

7 nce and high carbohydrate-containing storage roots.

8 ulates arbuscule formation/degradation in AM roots.

9 lomeromycotina) symbiotically colonize plant roots.

10 arley APL transcripts in both the shoots and roots.

11 blueberry red ringspot virus (BRRV) in their roots.

12 cal transcriptional component, MED16, in the root adaptive responses to a scarce plant macronutrient,

13 ux parameters of photosynthesis and leaf and root anatomy, up-regulation of Si channel and transporte

14 on about a library of synthetic peptides and root and nodule phenotyping data from synthetic peptide

15 es the biosynthesis of ethylene to fine-tune root and root hair development, which are important for

16 meristematic cells from the quiescent state, root and shoot growth and architecture, to flowering and

17 Root and stomatal functions rapidly recover from water l

18 ort formation of the highly functional tooth root and the periodontal attachment apparatus, while fac

19 in the primary sensory neurons of the dorsal root and trigeminal ganglia.

20 reeding and genetic studies in yam and other root and tuber crops.

21 e I. echinospora rootlets, S. moellendorffii roots and A. thaliana roots compared to the leaves of ea

22 osite direction to that of O(2) , across the roots and diffusive boundary layer.

23 and (3) mature lianas had shallowest coarse roots and evergreen trees had the deepest.

24 and that their mRNAs are also detectable in roots and pods, which clearly suggests that these heme p

25 Models were developed from images of pits in roots and stems of Picea mariana (Mill.) BSP.

26 The occurrence of particular RAF in both roots and thaw front soil was positively correlated with

27 osing velocities were similar between native roots and the SG group, and were significantly lower tha

28 synthesis, formed reduced numbers of lateral roots and tt7-2 had elevated levels of kaempferol.

29 Here plant stems, roots and various other structures available in nature t

30 r such 'catastrophe compassion', discuss its roots, and consider how it might be cultivated in more m

31 of AAK6 reduces cell production in the aak6 root apex, but this is partially compensated for by long

32 in cell division activity in both shoot and root apical meristems observed in fbl17 loss-of-function

33 Adventitious root (AR) formation is critically important in vegetativ

34 And when it comes to calculations, square roots are the gravest challenges to overcome.

35 Mean change in square root area of MA from baseline to month 24 was +0.36 mm (

36 keleton for development of "short-but-heavy" roots as an adaptive response to water deficit in rice.

37 sponse), our results show that 1) individual roots as well as the root system as a whole adapt to the

38 ion events were also observed in rrb3 mutant roots associated with a reduced Nod factor induction of

39 Root-associated microbes can improve plant growth, and t

40 Root-associated microbial communities are important for

41 cyte infiltrates, was observed in the dorsal root, autonomic, and enteric ganglia.

42 Here, we report that in Arabidopsis thaliana roots, auxin controls the spatiotemporal expression of t

43 Maize demonstrated root avoidance in maize/maize, with reduced root growth

44 ent outbreak of COVID-19 pandemic traces its roots back many decades and is worsened by a number of i

45 nalysis revealed loud signals due to a plume root beneath Hawaii and a previously unrecognized ultral

46 ic impact of such neosinuses on valvular and root biomechanics and the potential influence on long-te

47 ft most closely recapitulating native aortic root biomechanics.

48 The mutant accumulated more Cd in roots but not in shoots and grains.

49 s exhibited distinct spatial profiles in the root, but only vacuolar Pi sequestration corresponded wi

50 ied IRT1-interacting proteins in Arabidopsis roots by mass spectrometry and established an interactom

51 Plant tissues, particularly roots, can be subjected to periods of hypoxia due to env

52 microbiome and the "common denominators" of root canal infections and identified taxa whose virulenc

53 ent study demonstrated the complexity of the root canal microbiome and the "common denominators" of r

54 nd newly mineralized tissue deposited in the root canal system, while FM group presented inflammatory

55 i(+)) and Na ions (Na(+)) is the fundamental root cause for the poor stability, reversibility, and en

56 -drug and precision therapies addressing the root cause of CF disease.

57 le point defect population explains a common root cause of performance losses.

58 The root cause of the observed antiinflammatory phenotype in

59 isms and neural circuits and targeted to the root cause of the pathophysiology.

60 ng quality improvement program incorporating root-cause analysis of hospital-associated VTE (HA-VTE).

61 o develop mechanistic treatments directed at root causes of AF.

62 t intrinsic molecular features are potential root causes.

63 linkages that do not directly reflect cereal root cell wall polysaccharide structures.

64 gels that can play distinct roles in legume root cell walls.

65 s partially compensated for by longer mature root cells.

66 rified pectin states is essential for proper root clock function and the subsequent initiation of lat

67 (hours of post infestation) in both stem and roots compared to non-silicon treated plants against pin

68 ets, S. moellendorffii roots and A. thaliana roots compared to the leaves of each respective species.

69 y reallocating internal resources to greater root construction (increased aerenchyma content, larger

70 and the initiation of cell divisions in the root cortex.

71 sequent bidirectional nutrient exchange, the root cortical cells undergo substantial transcriptional

72 CTG showed significantly better relative root coverage percentage than GTR after 3 (P = 0.026) an

73 on having performed a root coverage, or non-root coverage procedure.

74 ture pertaining to the outcomes of validated root coverage procedures in specific scenarios, which ca

75 ation (GTR) using bioabsorbable barriers for root coverage therapy.

76 type of approach based on having performed a root coverage, or non-root coverage procedure.

77 keratinized tissue (KT) width, percentage of root coverage, patient-centered outcomes were compared b

78 The root crop is one of the outstanding examples of the camb

79 After a dorsal root crush injury, centrally-projecting sensory axons fa

80 Recent work has shown that fibrous root decline occurs in HLB-affected trees before symptom

81 sponses to severe drought; and how potential rooting depths varied across gradients in soil texture a

82 of cellular and molecular mechanism driving root development is mainly based on studies of the dicot

83 The PC and GM groups showed favorable root development without inflammation and newly minerali

84 S is dispensable for its function in lateral root development.

85 nflammatory changes with the continuation of root development.

86 er and length and fewer correlations between root diameter and architectural traits.

87 e availability were correlated to aspects of root diameter and branching.

88 he key role of plant root traits, especially root diameter, root nitrogen and specific root length, i

89 Here, we show that IAA33 maintains root distal stem cell identity and negatively regulates

90 ys that following a combined cervical dorsal root/dorsal column lesion (DRL/DCL), both motor and S1 C

91 Glycine max (soybean) Sec4 functions in the root during its defense against the parasitic nematode H

92 he transcriptomic response occurring in rice roots during NLS formation, 7 days post-treatment (dpt)

93 t on fungal community assembly in leaves and roots early in host development and when sorghum is drou

94 would provide better understanding of plant root effects on soil carbon sequestration and the sensit

95 Moreover, we show that low N-induced root elongation is associated with aboveground N content

96 vel that contributes to natural variation of root elongation under low N.

97 n accumulation and callose deposition in the root elongation zone under Pi deficiency increased with

98 ide concentration and ROS-stimulated lateral root emergence.

99 opposite effects of these mutants on lateral root emergence.

100 Root-enriched CLE ligands bind the BAM1 extracellular do

101 y axons fail to regenerate across the dorsal root entry zone (DREZ) to extend into the spinal cord.

102 eveloping, and germinated seeds, leaves, and roots exposed to different abiotic stresses.

103 idify our comprehension of the importance of root exudates in ecosystem response to drought.

104 Analysis of the high-molecular-weight (HMW) root exudates of both wheat and maize plants indicate th

105 hrough a process termed systemically induced root exudation of metabolites (SIREM), different microbi

106 es affecting DOM in the rhizosphere, such as root exudation, microbial processes, and soil organic ma

107 s induce specific systemic changes in tomato root exudation.

108 have altered visual cues used by the cabbage root flies in their host plant selection.

109 orld, and it occurs concomitantly with tooth root formation.

110 ch, employing combinatorial concatenation of roots from Latin and Greek to create linguistically corr

111 rphism in molecular signatures of the dorsal root ganglia (DRG) and spinal cord response, not observe

112 egulation of VIP in the corresponding dorsal root ganglia (DRG) and the dorsal horn of the spinal cor

113 in was assessed by von Frey assay and dorsal root ganglia (DRG) expression of Calca and Tac1 genes.

114 increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a c

115 In dorsal root ganglia (DRG), there is an increase in CGRP(+), TH(

116 es lie predominantly in thoracolumbar dorsal root ganglia (DRG).

117 afferent neurons, with cell bodies in dorsal root ganglia (DRG).

118 Dorsal root ganglia nociceptors protect against STm colonizatio

119 ociated inflammatory processes in the dorsal root ganglia, likely by activating stress-response prote

120 line, 50-100 nl) were made into L3-L5 dorsal root ganglia.

121 n-hindbrain boundary, spinal cord and dorsal root ganglia.

122 lar distribution of mammalian PATs in dorsal root ganglion (DRG) neurons and, strikingly, found that

123 ore proximately to promote latency in dorsal root ganglion (DRG) neurons.

124 s (TCA), we focused on large-diameter dorsal-root ganglion (L-DRG) neurons with myelinated axons.

125 apparatus, we demonstrate that chick dorsal root ganglion axons exhibit a tension buffering or strai

126 oform Na(V)1.7 is highly expressed in dorsal root ganglion neurons and is obligatory for nociceptive

127 lishment and reactivation using human dorsal root ganglion-derived neuronal HD10.6 cells as an in vit

128 Our findings suggest that the timing of the root gravitropic response is orchestrated by the reversi

129 CYCD6;1) to drive formative divisions during root ground tissue development.

130 hen required to advance our understanding of root growth and development.

131 ated poplar mutant nf-yb21 exhibited reduced root growth and drought resistance.

132 ene expression changes during cambium-driven root growth and have implications with regard to future

133 g grapevine rootstocks are coupled with fine root growth dynamics during drought and return of soil m

134 root avoidance in maize/maize, with reduced root growth in 'shared' soil, and increased growth away

135 reveals mechanisms for the understanding of root growth in mechanically impeding soil conditions and

136 k, hypocotyl elongation is promoted, whereas root growth is greatly reduced as a result of changes in

137 trols over carbon allocation and the role of root growth on soil-plant hydraulics.

138 Here, we found that shoot and root growth responses to high ambient temperature are co

139 Limitation to root growth results from forces required to overcome soi

140 moisture was negatively correlated with fine-root growth, highlighting that drying of these typically

141 and freeze/thaw) and biological (e.g. plant root growth, soil microbial and faunal activity) mechani

142 nsight into gene regulation that accompanies root growth, we generated comprehensive transcript profi

143 d elongation zones is critical for efficient root growth; new work from Salvi et al.

144 ROOT HAIR DEFECTIVE3 (RHD3) is an atlastin GTPase involv

145 osynthesis of ethylene to fine-tune root and root hair development, which are important for seedling

146 Furthermore, in Arabidopsis, KAR-induced root hair elongation depends on ACS7 Thus, we reveal a c

147 pirodela, which both lack root hairs and the root hair expansin clade EXPA-X.

148 OS in trichoblasts and elevated frequency of root hair formation compared with the wild type.

149 Auxin-induced root hair initiation and ROS accumulation were reduced i

150 ithin distinct motile puncta in L. japonicus root hairs and in Nicotiana benthamiana leaves.

151 r Utricularia and Spirodela, which both lack root hairs and the root hair expansin clade EXPA-X.

152 imiting conditions requires infection of the root hairs by soil symbiotic bacteria, collectively refe

153 dicago truncatula requires repolarization of root hairs, including the rearrangement of cytoskeletal

154 micro-CT), fluorescence microscopy, and fine root hydraulic conductivity measurements (Lp(r) ), we ex

155 hanistic insights on this unknown, a dynamic root-hydraulic modeling framework was developed that set

156 effect emerges from fairness considerations rooted in a psychological incompatibility between the al

157 rodegenerative and neurological diseases are rooted in dysfunction of the neuroimmune system; therefo

158 The strength of this approach is rooted in its simplicity and accuracy.

159 argely observational field of ecology to one rooted in mechanistic understanding.

160 m may therefore use audiovisual correlations rooted in oral acoustics to extract detailed spectrotemp

161 propose an improvement of a search algorithm rooted in the ergodic theory of dynamical systems which

162 CMP is rooted in the principled physics of driving forces and r

163 t is today, an illuminating field of science rooted in the rational design of photochromic molecules

164 n deprivation, its functional and historical roots in hypoxia emphasize a broader evolutionary role.

165 cleotides as second messengers and finds its roots in the old RNA world hypothesis.

166 improved aeration, and better penetration of roots in the soil.

167 y to compute models of other agents has deep roots in the strategic social behavior of primates and t

168 her AGPase activity and lower sucrose in the roots, indicating that feedforward loops enhanced sink c

169 hyllotaxis, flower morphogenesis, or lateral root initiation, have been extensively studied, and gene

170 ological features had higher rates of aortic root injury (p < 0.001), moderate-to-severe paravalvular

171 aining snack bars, comprising mainly chicory root inulin-type fructans (ITF), on gut microbiota in he

172 R397b activity increased LAC2 expression and root length, and decreased lignin content in root vascul

173 ly root diameter, root nitrogen and specific root length, in driving rhizosphere fungal community com

174 OsNLA1 promoter activity was observed in roots, ligules, leaves, sheaths, pollen grains, and surr

175 spontaneous age-induced periodontal bone and root loss are observed in this mouse model.

176 cing of VuPOB1 expression in transgenic B301 roots lowers the frequency of HR and increases the level

177 gravitropic set-point angle (GSA) of lateral roots (LRs), auxin levels and auxin transport.

178 howed that at the community level, shoot and root mass decreased with drought but increased with micr

179 Total, spherical and coma root mean square (RMS) postoperative ocular higher-order

180 The mean +/- standard deviation of the root mean square deviation was 4.39 +/- 2.55 dB.

181 h a mean unsigned error of 0.86 kcal/mol and root mean square error of 1.11 kcal/mol, comparable with

182 yield variations well with average relative root mean square error of 26%, although uncertainty in m

183 ardized uptake value (SUV) of the normalized root mean square error, the peak signal-to-noise ratio,

184 It had lower root mean square prediction error (RMSPE) than when usin

185 equation tested, however, they showed a high root mean squared error.

186 The C-CNN also achieved an average root-mean-square deviation (RMSD) of 1.24 angstrom on a

187 this simple method predicts the T(g) with a root-mean-square error of 13 degrees C for conjugated po

188 C) of the Arabidopsis (Arabidopsis thaliana) root meristem acts as an organizer that promotes stem ce

189 ng how RGF1 regulates the development of the root meristem is essential for understanding stem cell f

190 on in the Arabidopsis (Arabidopsis thaliana) root meristem.

191 e to moderate high temperature and protected root meristematic cells from heat-induced cell death.

192 raction between Arabidopsis thaliana and the root microbiota under iron deprivation that is dependent

193 ps understanding how plant cells orchestrate root morphogenesis to gene expression with the STOP1-ALM

194 in signaling as well as in the regulation of root morphogenesis under both normal and stress conditio

195 l day 0 (PN0), just before the initiation of root morphogenesis.

196 f histone acetylation in auxin signaling and root morphogenesis.

197 A comprehensive time-dependent root morphological analysis integrated with molecular si

198 suggesting substantial modifications in fine-root morphology during transitions from woody to nonwood

199 However, the modifications in root morphology may also coincide with new modifications

200 We addressed this gap by evaluating the root morphology, anatomy and transcriptome of bmr12 muta

201 Work is just beginning towards understanding root mucilage and the proposed adhesive polymers involve

202 d a genome-wide association study (GWAS) for root Na(+) /K(+) ratio in a population consisting of 369

203 the functional and phylogenetic structure of root neighborhoods remains unclear, hindering the unders

204 Markov chain Monte Carlo algorithm to sample rooted networks and the embedding of phylogenetic trees

205 plant root traits, especially root diameter, root nitrogen and specific root length, in driving rhizo

206 Nitrogen-fixing root nodulation in legumes challenged with nitrogen-limi

207 ip between legumes and rhizobium bacteria in root nodules has a high demand for iron, and questions r

208 Sites of GA biosynthesis in the roots of 7-d-old Arabidopsis thaliana seedlings were inv

209 isplayed different effects in the shoots and roots of plants at different concentrations, which may b

210 s of the maxillary first molars and in the M roots of the mandibular first molars, respectively.

211 m from the apex was 89.3% and 100% in the MB roots of the maxillary first molars and in the M roots o

212 ll reveal information about the evolutionary roots of this major signaling pathway, will shed light o

213 Fine roots of trees exhibit varying degree of plasticity to a

214 l substrate explained variation, with deeper roots on sandy, nutrient-poor soils relative to clayey,

215 orders, where the distal (first and second) root orders had lower lignin compared to higher orders.

216 the total quantity of lignins varied only by root orders, where the distal (first and second) root or

217 diazotrophic rhizobia or Frankia bacteria in root organs known as nodules.

218 er supported by analysis of transgenic hairy roots overexpressing soybean GmWRI1b-OE and GmLEC2a-OE.

219 We studied tree rooting patterns in Southern African savannas to ask: ho

220 During the root phase of the tree of life, before the last common a

221 We found substantial variation in all 23 root phenes measured.

222 and MPK6, MKK4 and MKK5, or YDA show a short-root phenotype, which is associated with reduced mitotic

223 ustering revealed several clusters of unique root phenotypes related to plant performance under water

224 uth, multicenter study evaluated scaling and root planing (SRP) with and without EMD in 51 patients p

225 periodontitis were treated with scaling and root planing (SRP).

226 evere periodontitis treated with scaling and root planing and systemic metronidazole and amoxicillin.

227 mal weight patients submitted to scaling and root planing.

228 G-AgP patients received scaling and root planning (SRP), per quadrant at a 1-week-interval,

229 re, the thin layer of soil surrounding plant roots, plays a critical role in plant's adaptation to th

230 As a control, non-treated forced roots powder (FRP-BE) was tested.

231 IAA redistribution occurred in maize roots, preceding hydrotropic bending.

232 derivative (EMD) added to papilla reflection/root preparation (PR/RP) could enhance clinical and infl

233 increased level of kaempferol in the lateral root primordia of tt7-2 reduces superoxide concentration

234 ion and the subsequent initiation of lateral root primordia.

235 recipitation change may critically influence root productivity and soil carbon dynamics under future

236 ing the leucoplast motif usually has greater root protein abundance.

237 ia GLUTAMATE RECEPTOR-LIKE (GLR) channels in root protoplasts.

238 system, clinically used valve-sparing aortic root replacement conduit configurations have comparable

239 Root resection therapy remains a treatment solution for

240 We then calculated the root resorption volume and examined periodontal tissue c

241 thesis and auxin perception factors controls root responses to high ambient temperature.

242 These findings suggest that root responses to precipitation change may critically in

243 h precipitation alteration, the magnitude of root responses was greater in dry areas than in wet area

244 White root rot disease is threatening rubber tree (Hevea brasi

245 Leonian, the causal agent of foliar blight, root rot, fruit rot and crown rot syndromes in squash (C

246 Moreover, root samples revealed activity against all tested cell l

247 d actin organization and dynamics in control roots; short-term IAA treatments stimulated denser and m

248 atdro1 primary and lateral roots showed impairment in establishing an auxin gradien

249 In Arabidopsis, the SHORT-ROOT (SHR)/SCARECROW (SCR) transcription factor dimer ac

250 We use a multi-layer canopy-root-soil model to calculate the energy and entropy flux

251 These genes include, root-specific auxin transport, strigolactone and gibbere

252 Here, a root-specific nuclear factor Y (NF-Y) transcription fact

253 two different specialized cell types in the root stem cell niche.

254 hese MADS-box genes were analyzed in leaves, roots, stem sections and after hormones treatment.

255 n Southern African savannas to ask: how tree rooting strategies affected species responses to severe

256 involved in the formation of rhizosheaths at root surfaces and for the secretions involved in host pl

257 he clinical assessment of lesion activity on root surfaces.

258 Calculus remained on the roots surfaces after they were judged to be clean using

259 show that 1) individual roots as well as the root system as a whole adapt to the pattern of water ava

260 ve transcript profiles of Brachypodium whole-root system at four developmental stages.

261 ctors (TFs) were differentially expressed in root system during plant development.

262 visible soil) to avoid restricting vertical root system growth for most if not all of the life cycle

263 Root systems are dynamic and adaptable organs that play

264 Singular morphological measurements of the root systems cannot entirely explain variations in citra

265 orrelated with morphological measures of the root systems to determine which had the most benefit.

266 eum vulgare, barley), exhibiting contrasting root systems, were analysed.

267 ess, as expected; (2) lianas were not deeper-rooted than trees as had been previously proposed; and (

268 antly higher (p < 0.005) BPA accumulation in roots than shoots and nonsignificant variances in biomas

269 embryo, produced longer seedling shoots and roots, than the null segregant (NS) controls.

270 ped a multicellular model of the Arabidopsis root tip.

271 s auxin and AtDRO1 gene expression levels in root tips were unaffected by the addition of auxin.

272 icantly increased the nitrate content in the root tissues compared with that of the zmnlp5 mutants.

273 the phenylpropanoid biosynthesis in leaf and root tissues respectively.

274 the leaf, male and female flowers, stem, and root tissues.

275 em, which indicated their transport from the roots to the upper parts of the plant.

276 orm was the only factor associated with fine-root traits in statistical models including mycorrhizal

277 examining other anatomical and physiological root traits should be a priority for understanding savan

278 composition, demonstrating the potential for root traits to be used within predictive frameworks of p

279 Our results showcase the key role of plant root traits, especially root diameter, root nitrogen and

280 t and field phenotyping for seed, shoot, and root traits.

281 Using Arabidopsis root transcriptome data and coexpression clustering, we

282 Their root transcriptome reveals elevated ethylene responses a

283 uction in the mean rate of GA growth (square root transformation) over 12 months was 27.4% (P = 0.007

284 rate of new atrophy area (P = 0.479, square-root transformed) or time to detection of new MA (P = 0.

285 nally regulated by microRNA397b (miR397b) in roots under normal and water-deficit conditions.

286 nd ethylene on the metabolome of Arabidopsis roots using a high-resolution 24 h time course, conducte

287 root length, and decreased lignin content in root vasculature.

288 The distance penetrated by O(2) into the roots was shorter at lower O(2) .

289 logical basis behind the restoration of fine root water uptake capacity during water recovery remains

290 d the point of contact around the trigeminal root were respectively proximal in 82.7% (67/81) and sup

291 atdro1 lateral roots were able to respond to exogenous auxin and AtDRO1

292 positively regulate cell differentiation in roots were either exclusively or preferentially expresse

293 the richest tissue in woody plants, whereas roots were the richest tissue in graminoids.

294 losing forces approaching that of the native root, whereas relative forces were >5-fold higher in the

295 sed; and (3) evergreen trees had the deepest roots, which is necessary to maintain canopy during simu

296 ctive tissue disorder that results in aortic root widening and aneurysm if unmanaged.

297 rove penetrability of hard, dry soils (thick roots with a larger proportion of stele, and smaller dis

298 ological traits related to leaves, stems and roots with high heritability.

299 Most absorbed indium accumulated at the roots, with only a tiny portion reaching the grains.

300 y matches intracellular cytokinin content in roots, yet we also find cytokinins in extracellular flui