ライフサイエンスコーパス: plant cell

1 bedded in the fluctuating environment of the plant cell.

2 lling ion balance and ion homeostasis in the plant cell.

3 ptides from the cytoplasm to the apoplast of plant cells.

4 membrane-lined channels connecting adjacent plant cells.

5 lasmodesmata are small channels that connect plant cells.

6 to specific changes in gene transcription in plant cells.

7 ntrol of cytoskeletal organization in living plant cells.

8 into the roles of K63 polyubiquitination in plant cells.

9 hat can function in conditions like those in plant cells.

10 behavior of mitochondria and chloroplasts in plant cells.

11 o dynamically report MAPK activity in living plant cells.

12 the capacity of A. tumefaciens to transform plant cells.

13 e second most abundant forms of ubiquitin in plant cells.

14 A silencing stability against degradation by plant cells.

15 cal excitability to the central organelle of plant cells.

16 aging effects on the molecular components of plant cells.

17 her limited in turgid and cell wall-shielded plant cells.

18 om a marine plant endophyte can replicate in plant cells.

19 nvolved in nearly all regulatory pathways in plant cells.

20 the SA-dependent transcriptional response in plant cells.

21 uences blocked TBSV replication in yeast and plant cells.

22 el, two essential elements in K(+) uptake in plant cells.

23 enable fungi to sense the presence of living plant cells.

24 DNA (T-DNA) and virulence proteins into host plant cells.

25 hionylation as a means of redox signaling in plant cells.

26 and to support TBSV replication in yeast and plant cells.

27 rice leaf, enabling the fungus entry to host plant cells.

28 trafficking and cytoplasmic streaming in the plant cells.

29 nveying specificity of signaling pathways in plant cells.

30 tosol, vacuole, plasma membrane, and wall of plant cells.

31 nteracted with COP1 in yeast, mammalian, and plant cells.

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

33 dependent molecular flux between neighboring plant cells.

34 externally with the endoplasmic reticulum of plant cells.

35 ly interacts with SOS1 and SOS2 in yeast and plant cells.

36 ends on the delivery of part of their DNA to plant cells.

37 iting using CRISPR-Cas9 works efficiently in plant cells(1), but delivery of genome-editing machinery

38 id biosynthetic pathway that is expressed in plant cells accommodating fungal arbuscules.

39 associated with plant-specific MTOCs and how plant cells activate or inactivate MT nucleation activit

40 ctivity of isoprenoid-generating pathways in plant cells; additionally, it suggests an exchange of is

41 t the colonization site of a foreign entity, plant cells alter their trajectory of growth and develop

42 be rationally designed to efficiently enter plant cells and deliver cargoes to mature plants, and pr

43 Movement between plant cells and horizontal transmission have not been ob

44 cyanide (HCN) is coproduced with ethylene in plant cells and is primarily enzymatically detoxified by

45 ntitative detection by elemental analysis in plant cells and organelles.

46 ved, stable protein assemblies shared across plant cells and provides a mechanistic, biochemical fram

47 required for heterochromatin condensation in plant cells and show that H1 overexpression creates hete

48 nostructure affect both internalization into plant cells and subsequent gene silencing efficiency.

49 Interactions between plant cells and the environment rely on modulation of pr

50 tion of human/animal therapeutic proteins in plant cells and the specific study of plant biochemical

51 e (PM) provides a critical interface between plant cells and their environment to control cellular re

52 e cell wall is the primary interface between plant cells and their immediate environment and must bal

53 Osp24 is translocated into plant cells and two of its 8 cysteine-residues are requi

54 ium, and V. parahaemolyticus was produced in plants cells and triggered systemic and intestinal humor

55 ase backtracking/arrest frequently occurs in plant cells, and RNAPII-reactivation is essential for co

56 based method for delivering CRISPR/Cas9 into plant cells, and this should further expand the applicat

57 Plant cells are at high turgor pressure and are surround

58 Plant cells are embedded within cell walls, which provid

59 In some specialized cases, though, plant cells are programmed to detach, and root cap-deriv

60 Plant cells are uniquely endowed with ClpB proteins in t

61 asts, and respiration in mitochondria of the plant cells, as well as motility, chemotaxis, nutrient c

62 c piece of DNA (transferred DNA, T-DNA) into plant cells at the infection site.

63 MT nucleation is particularly noticeable in plant cells because it accounts for the primary source o

64 topic LTBentero was functionally produced in plant cells, being capable to trigger systemic and intes

65 In yeast and plant cells, both proteins interact directly with the mR

66 t only facilitate biomolecule transport into plant cells but also protect polynucleotides from nuclea

67 Mitochondrial fission occurs frequently in plant cells, but its biological significance is poorly u

68 c transformation delivers nucleic acids into plant cells by bombarding the cells with microprojectile

69 and disrupted organization of F-actin in Li1 plant cells by confocal microscopy.

70 ment of Agrobacterium-delivered VirE2 inside plant cells by using a split-GFP approach in real time.

71 Our results also illustrate that plant cells can respond flexibly to serious challenges o

72 reassessment of the mechanisms that control plant cell-cell communication.

73 e pollen an ideal system with which to study plant cell-cell interactions, tip growth, cell migration

74 Such model is useful for plant cell characterization allowing a single set of par

75 rt- and long-distance signaling molecules in plant cell communication has been undertaken.

76 Cell walls define the shape of plant cells, controlling the extent and orientation of c

77 Microtubules at the plant cell cortex influence cell shape by patterning the

78 that the ER membrane tethering machinery in plant cells could play a role with select SEIPIN isoform

79 It has been proposed that plant cells could sense and respond to cell swelling thr

80 e isolated directly from medicinal plants or plant cell culture(1).

81 ar-based medium modified from an established plant cell-culture medium to nourish detached leaves lai

82 ts that spontaneous epialleles that arise in plant cell cultures are stably maintained by siRNA and H

83 ion, the number of identified targets in the plant cell cycle is limited.

84 ide cytosine methylation dynamics during the plant cell cycle.

85 hat Me10 interaction with TFT7 occurs in the plant cell cytoplasm.

86 therefore a conserved feature of animal and plant cell death signaling pathways.

87 FSA-treated ECSs showed that FSA may induce plant cell death through regulating the expression of ge

88 (SERK4) redundantly and negatively regulate plant cell death.

89 the timing and extent of glyphosate-induced plant cell death.

90 ein with a signal peptide to secrete it from plant cells, did not passively re-enter the cells upon s

91 Cell fate maintenance is an integral part of plant cell differentiation and the production of functio

92 however, the nuclear envelope in animal and plant cells disassembles, allowing cytoplasmic and nucle

93 Plant cells divide their cytoplasmic content by forming

94 These signaling molecules control plant cell division and differentiation, organ growth, a

95 ave addressed this problem in the context of plant cell division in which a large number of TGN-deriv

96 ial infection of plant cells, the control of plant cell division leading to nodule development, autor

97 Investigations of plant cell division would greatly benefit from a fast, i

98 In plants, cells do not migrate.

99 The Plant Cell doi/ 10.1105/tpc.119.tt0819.

100 e is the delivery of pathogen effectors into plant cells during infection.

101 gy expenditure and mitochondrial activity in plant cells during the night.

102 evealed a diverse set of mechanisms by which plant cells dynamically monitor and regulate the composi

103 tion of secondary cell wall synthesis during plant cell elongation.

104 phenolic polymer in secondary cell walls of plant cells, enables strength in fibers and water transp

105 eterious effects of high and excess light on plant cells, especially within the chloroplast.

106 al and plant kingdoms; nevertheless, because plant cells exhibit major structural differences to anim

107 The process by which plant cells expand and gain shape has presented a challe

108 aterial, without transgene integration, into plant cells for diverse biotechnology applications.

109 However, isolating mitochondria from plant cells for physiological and biochemical analyses i

110 calmodulin (CaM)-binding TFs or proteins in plant cells form a buffering system such that the concen

111 c genome editing in regenerable protoplasts, plant cells free of their cell wall, could revolutionize

112 labelled probes across the walls of isolated plant cells from potato tuber, red kidney bean and banan

113 Auxin plays a central role in controlling plant cell growth and morphogenesis.

114 Plant cell growth involves a complex interplay among cel

115 Plant cell growth is constrained by the rate of water up

116 l wall and cellulose synthesis is pivotal to plant cell growth, and its regulation is poorly understo

117 ytoskeleton network has an important role in plant cell growth, division, and stress response.

118 In plant cells, H(2)O(2) triggers an influx of Ca(2+) ions,

119 Individual plant cells have a genetic circuit, the circadian clock,

120 Our findings suggest that plant cells have an intrinsic ability to polarize and th

121 he early 19(th) century from both animal and plant cells, human nucleoli and particularly the five hu

122 Thus, secretory trafficking in plant cells in general, and secretion of extracellular m

123 n thread-like structures and sparsely-packed plant cells in nodules suggest that bacteroid developmen

124 QD with chemical cargoes to chloroplasts in plant cells in vivo (74.6 +/- 10.8%) and more specific t

125 Single plant cells infected by bacteria were selected and sampl

126 ough still in infancy, can take advantage of plant cells' inherent capacity to synthesize and store v

127 The plant cell internal environment is a dynamic, intricate

128 rganizes polarity determinants necessary for plant cell invasion.

129 r events controlling fungal responses to the plant cell is not clear.

130 bunits, allow us to conclude that the TPC in plant cells is not recruited to the PM sequentially but

131 Bacterial accommodation inside living plant cells is restricted to the nitrogen-fixing root no

132 One method for RNP delivery into plant cells is the use of a biolistic gun.

133 The adhesion of plant cells is vital for support and protection of the p

134 Plant cells maintain remarkable developmental plasticity

135 g to phosphoinositides and liposomes and for plant cell membrane association.

136 d cells are widely recognized as the premier plant cell model for membrane transport, signaling, and

137 uranium (in the U(VI) oxidation state) in a plant cell model of Brassica napus.

138 Simple plant cell morphologies, such as cylindrical shoot cells

139 ack specialized immune cells, therefore each plant cell must defend itself against invading pathogens

140 nd to repair tissues following wounding; yet plant cells normally stably maintain consistent identiti

141 In the plant cell nucleus, the RRS1-R/RPS4 complex binds to and

142 tFTs for studying protein turnover in living plant cells of Arabidopsis (Arabidopsis thaliana) and Ni

143 tion of actin and MT cytoskeletons in single plant cells of Arabidopsis thaliana We show that the cyt

144 Plant cells often undergo endoreduplication, confounding

145 The Plant Cell (online), doi/ /10.1105/tpc.tt1219.

146 The Plant Cell (online), doi/10.1105/tpc.120.tt0720.

147 macronutrient, which helps understanding how plant cells orchestrate root morphogenesis to gene expre

148 ne (PM) has important implications for how a plant cell perceives and responds to invading microbial

149 BSK5 localized to the plant cell periphery, interacted in yeast and in planta

150 usion protein was tested on mammalian, whole plant cells, plant leaf protoplast and fungal cell cultu

151 e roles of actin organization in determining plant cell polarity, shape and plant growth.

152 organism with characteristics of animal and plant cells provide novel explanations regarding how pH

153 Upon exposure to light, plant cells quickly acquire photosynthetic competence by

154 Owing to their inability to migrate, plant cells rely on targeted cell division and expansion

155 One mechanism by which plant cells reprogram their cell surface is vesicular tr

156 Cell division in plant cells requires the deposition of a new cell wall b

157 the determination of superoxide anion in the plant cell samples.

158 nematode CLE effectors that is recognized by plant cell secretory machinery to redirect these peptide

159 e design of electronic systems of integrated plant cell sensors.

160 Plant cell separation and expansion require pectin degra

161 rocesses for the coordination and control of plant cell shape and cell growth.

162 cal forces are known to play a major role in plant cell shape by controlling the orientation of corti

163 ining such structures to show that a complex plant cell shape can derive from chemically induced loca

164 initial feeding cell could have an effect on plant cells so distant from where the nematode is feedin

165 the general picture of the advanced stage of plant cell specialization and to reveal novel participan

166 In plants, cell-surface immune receptors sense molecular no

167 wide frequency range, equivalent circuit for plant cell suspensions is presented.

168 ethylene-dependent and -independent roles in plant cells that affect responses to ABA.

169 robes, the control of microbial infection of plant cells, the control of plant cell division leading

170 In plant cells, the vacuole is a vital organelle that plays

171 esponse, differentiation, and development of plant cell, tissue, and organs.

172 to (Pst) delivers effector proteins into the plant cell to promote host susceptibility.

173 actome employs the structural framework of a plant cell to show metabolic, transport, genetic, develo

174 This nonlinear amplification allows plant cells to effectively distinguish the kinetics of d

175 appears well suited to noninvasively expose plant cells to signal specific depolarization signatures

176 sm, sending sRNAs as effector molecules into plant cells to silence plant immunity genes, whereas pla

177 ic fungi, secrete hundreds of effectors into plant cells to subvert host immunity and promote pathoge

178 in the cytosol, plastids and mitochondria of plant cells to support fundamental processes, including

179 Pathogens deliver effectors into plant cells to suppress immunity-related signaling.

180 i by small RNAs (sRNAs) that can move within plants cell to cell and long distance.

181 genomic analysis at the level of one single plant cell type, the root hair cell, and between two mod

182 and multiple plant species, operative across plant cell types, and can traffic other unrelated small

183 eneration of somatic mutations in particular plant cell types, tissues, and organs.

184 tes that DNA damage responses differ between plant cell types.

185 Plastids, the defining organelles of plant cells, undergo physiological and morphological cha

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

187 MT nucleation sites or flexible MTOCs in plant cells V.

188 nerate specific gene expression responses in plant cells via transcription.

189 s and xylans are important components of the plant cell wall and they are acetylated to be protected

190 ding of the molecular mechanisms involved in plant cell wall assembly.

191 aride acceptors will dramatically accelerate plant cell wall biosynthesis research.

192 ghput identification and characterization of plant cell wall biosynthetic glycosyltransferases (GTs).

193 s an additional layer of signaling following plant cell wall breakdown during cell wall remodeling or

194 Cellulose is an essential plant cell wall component and represents the most abunda

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

196 gineering is a promising strategy to improve plant cell wall composition for biofuel and bioproducts

197 Plant cell wall degrading enzymes (PCWDEs) are the prima

198 ng several virulence determinants, including plant cell wall degrading enzymes (PCWDEs), type III sec

199 assemble and provide the molecular basis for plant cell wall engineering.

200 grate nutritional information encoded in the plant cell wall into a regulatory hierarchy for optimal

201 The plant cell wall is a barrier that limits the ease and th

202 The plant cell wall is a hierarchical matrix of mainly cellu

203 The plant cell wall is a particularly challenging barrier fo

204 Dynamic changes and rearrangement of the plant cell wall is an important response to salt stress,

205 ion of structural feature of whole lignin in plant cell wall is of great importance for understanding

206 Expansins comprise a superfamily of plant cell wall loosening proteins that can be divided i

207 ed polyphenols to be in the range of 30-150% plant cell wall mass.

208 ted a high specificity toward the ubiquitous plant cell wall matrix glycan xyloglucan.

209 Candidate genes related to plant cell wall modification and various plant hormone s

210 ugar nucleotide donors to selected synthetic plant cell wall oligosaccharides on the array and that t

211 The plant cell wall plays an important role in communication

212 The plant cell wall plays an important role in damage-associ

213 atures that likely influence the assembly of plant cell wall polymers which is critical to the overal

214 genes with a predicted role in the decay of plant cell wall polymers, in the utilization of latex co

215 Plant cell wall polysaccharide analysis encompasses the

216 construction of cellulose, the most abundant plant cell wall polysaccharide, requires the cooperative

217 nic acid (UDP-GlcA) is the precursor of many plant cell wall polysaccharides and is required for prod

218 eir hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to t

219 hydrate active enzymes (CAZymes) that modify plant cell wall polysaccharides and other complex glycan

220 d by pectins, a network of covalently linked plant cell wall polysaccharides containing galacturonic

221 ities that improve digestion of recalcitrant plant cell wall polysaccharides may offer solutions for

222 beta-Mannans are plant cell wall polysaccharides that are commonly found

223 cilitate NMR structure analysis of insoluble plant cell wall polysaccharides, more so of minor cell w

224 acterized genes affecting the acetylation of plant cell wall polysaccharides, RWA2 and TBR.

225 elivery into plants is difficult because the plant cell wall poses a dominant transport barrier, ther

226 The plant cell wall presents a plant-specific route for poss

227 s of XyG biosynthesis and the role of XyG in plant cell wall structure and function.

228 extension (creep) relate to one another, to plant cell wall structure and to cell growth remain unse

229 ed to be incorporated into refined models of plant cell wall structure, growth and morphogenesis.

230 ver across the lignin-rich and multi-layered plant cell wall that poses the dominant physical barrier

231 ir preferential positioning in the secondary plant cell wall ultrastructure.

232 lfur cycle, metal resistance, degradation of plant cell wall was significantly increased in the degra

233 rldwide, infects its host by penetrating the plant cell wall without activating the plant's innate im

234 ndeed interact with polysaccharides from the plant cell wall, and an additional structure with the di

235 ctin, one of the main polysaccharides in the plant cell wall, and are of critical importance in plant

236 ranscriptional networks and/or modifying the plant cell wall, AvrHah1 may promote water uptake to enh

237 The plant cell wall, often the site of initial encounters be

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

239 nt types of copolymeric substructures in the plant cell wall, possibly because these LPMOs are functi

240 Plant cell wall-associated polygalacturonase-inhibiting

241 The plant cell wall-degrading enzyme repertoires of Schizoph

242 or VIB-1 in the regulation of genes encoding plant cell wall-degrading enzymes and nutrient scavengin

243 nt biomass by the secretion of an arsenal of plant cell wall-degrading enzymes, by remodeling metabol

244 actors involved in regulating genes encoding plant cell wall-degrading enzymes.

245 ulose and cello-oligosaccharides, as well as plant cell wall-derived hemicellulosic polysaccharides,

246 zymes that degrade various components of the plant cell wall.

247 lose, a major, recalcitrant component of the plant cell wall; however, expression of clr-1 in the abs

248 The structural complexity of plant cell-wall components also provides substrates for

249 We performed comparative analysis on plant-cell-wall-degrading enzymes (PCWDEs) and small sec

250 rils are the major load-bearing component in plant cell walls and are assembled from individual beta-

251 A galactan epitope is present in two woody plant cell walls and can be used for immmunological anal

252 Expansins are small proteins that loosen plant cell walls and cellulosic materials without lytic

253 callose deposition and the strengthening of plant cell walls and probably the degradation of oxalic

254 his review, we describe the architectures of plant cell walls and recent progress in overcoming recal

255 ort the interactions between polyphenols and plant cell walls and show that although polyphenols are

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

257 we explored the CXE action of HTG in native plant cell walls and tested whether expansin exposes cel

258 Plant cell walls are complex structures that are modifie

259 Plant cell walls are dynamic structures that are synthes

260 in provides essential mechanical support for plant cell walls but decreases the digestibility of fora

261 le and insoluble polysaccharide fractions of plant cell walls in organic solvents such as chloroform

262 ctinases predicted to mediate degradation of plant cell walls in the insect diet.

263 The main load-bearing component of plant cell walls is cellulose, and how plants regulate i

264 ls, such as inorganic ions, within secondary plant cell walls is central to many biomass applications

265 f intra-cell-wall diffusion within secondary plant cell walls is hindering the advancement of many li

266 The composition of plant cell walls is important in determining cereal end

267 late to those found in primary and secondary plant cell walls is uncertain, but their presence enable

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

269 pe to the mechanical properties of secondary plant cell walls remains elusive.

270 of such large, organized lipid aggregates in plant cell walls represents a new mechanism for structur

271 The complex structure of plant cell walls resists chemical or biological degradat

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

273 tocks has been hampered by the resistance of plant cell walls to enzymatic conversion, primarily owin

274 hat although polyphenols are associated with plant cell walls under hydrated conditions, they are not

275 new gene-editing approaches, the redesign of plant cell walls, and deciphering herbicide resistance e

276 Cellulose, the major component of plant cell walls, can be converted to bioethanol and is

277 lose fibers, one of the main constituents of plant cell walls, has been nanoengineered and broken dow

278 e fibers, one of the main building blocks of plant cell walls, has yielded unique families of cellulo

279 is an abundant and recalcitrant component of plant cell walls.

280 ctures that exist in the complex matrices of plant cell walls.

281 p as determined by nutrients obtainable from plant cell walls.

282 onan (HG) is one of the main constituents of plant cell walls.

283 roduction of biofuels is the modification of plant cell walls.

284 ces on the structural integrity of secondary plant cell walls.

285 sugars to the complex carbohydrates found in plant cell walls.

286 ss-bearing cellulose microfibrils in growing plant cell walls.

287 s is critical for the strength and growth of plant cell walls.

288 to interrogate the informational content of plant cell walls.

289 Xylans are a major component of plant cell walls.

290 hemicellulosic polysaccharides that comprise plant cell walls.

291 nizing fungi fine-tune the deconstruction of plant-cell walls (PCW) using different sets of enzymes a

292 o evidence for replication in two species of plant cells was detected, subcellular localization studi

293 lulose that comprise major components of the plant cell well-is a sustainable resource that could be

294 s rhizobia, are able to transfer DNA to host plant cells when they are provided with Agrobacterium DN

295 bilization operates in vivo, most notably in plant cells where turgor-driven tensile stresses exceed

296 riety of important cellular functions in the plant cell, which can, for example, regulate plant respo

297 t system is active in vitro and in human and plant cells with expanded target recognition capabilitie

298 nts, and into the primed state that provides plant cells with high regenerative competency.

299 e ability to monitor MAPK activity in living plant cells would be valuable.

300 Photosynthesis in plant cells would not be possible without the supportive