ライフサイエンスコーパス: Arabidopsis thaliana

1 era cyst nematode parasitism of Arabidopsis (Arabidopsis thaliana).

2 TIR1/AFB-mediated processes in Arabidopsis (Arabidopsis thaliana).

3 duction in accD-C794 editing in Arabidopsis (Arabidopsis thaliana).

4 has been studied intensively in Arabidopsis (Arabidopsis thaliana).

5 the literature, with a focus on Arabidopsis (Arabidopsis thaliana).

6 al to vernalization response in Arabidopsis (Arabidopsis thaliana).

7 tial PME genes are contained in Arabidopsis (Arabidopsis thaliana).

8 matode Heterodera schachtii and Arabidopsis (Arabidopsis thaliana).

9 marker genes in the model plant Arabidopsis (Arabidopsis thaliana).

10 ing early anther development in Arabidopsis (Arabidopsis thaliana).

11 nalyses in the pap7-1 mutant of Arabidopsis (Arabidopsis thaliana).

12 tories of PP2A gene families in Arabidopsis (Arabidopsis thaliana).

13 nthetic processes and growth of Arabidopsis (Arabidopsis thaliana).

14 has been extensively studied in Arabidopsis (Arabidopsis thaliana).

15 ion growth and leaf movement in Arabidopsis (Arabidopsis thaliana).

16 a core set of mRNA m(6) A writer proteins in Arabidopsis thaliana.

17 a PORB-deficient knock-out mutant (porB) of Arabidopsis thaliana.

18 opmental trajectories of shoot stem cells in Arabidopsis thaliana.

19 20), one of the 73 members of this family in Arabidopsis thaliana.

20 evelopmental genes regulated by silencing in Arabidopsis thaliana.

21 n non-coding RNA-directed DNA methylation in Arabidopsis thaliana.

22 involved in male reproductive development in Arabidopsis thaliana.

23 controlling As accumulation and tolerance in Arabidopsis thaliana.

24 genes for 7 flowering time-related traits in Arabidopsis thaliana.

25 e contribution of MYC TFs to JA responses in Arabidopsis thaliana.

26 ey identify a ferroptosis-like cell death in Arabidopsis thaliana.

27 nse machinery against microbial pathogens in Arabidopsis thaliana.

28 of GBF3 in drought tolerance was studied in Arabidopsis thaliana.

29 nomous key regulators of phloem formation in Arabidopsis thaliana.

30 lesterases (PMEs; 66 members in Arabidopsis [Arabidopsis thaliana]).

31 imilar number of genes to that for the plant Arabidopsis thaliana (25,000), the CMR is close to its k

32 In Arabidopsis thaliana, 45S rRNA genes are found in two la

33 on HY5 has been carried out in Arabidopsis (Arabidopsis thaliana), a dicot.

34 In Arabidopsis thaliana, a glycosyl transferase family 37 (

35 of variation in ABA levels among nearly 300 Arabidopsis thaliana accessions exposed to the same low

36 ta from seedling, floral bud, and root of 19 Arabidopsis thaliana accessions to examine the age and s

37 erance after salt stress is widespread among Arabidopsis thaliana accessions(2).

38 Using natural Arabidopsis thaliana accessions, we identified two major

39 by characterizing and comparing MITEs in 19 Arabidopsis thaliana accessions.

40 soil WD was investigated in 18 Arabidopsis (Arabidopsis thaliana) accessions using PHENOPSIS, an aut

41 Here, we show that the Arabidopsis (Arabidopsis thaliana) ADF3 is required in the phloem for

42 alyzed how hydroponically grown Arabidopsis (Arabidopsis thaliana) adjusts its physiology and Fe prot

43 gated the effects of SV on the resistance of Arabidopsis thaliana against Botrytis cinerea infection.

44 MESSAGE: Cytokinin membrane receptors of the Arabidopsis thaliana AHK2 and AHK3 play opposite roles i

45 In this study, we characterize the Arabidopsis thaliana Alpha Thalassemia-mental Retardatio

46 l regulators of phosphate stress response in Arabidopsis thaliana also directly repress defence, cons

47 The hypocotyls of Arabidopsis (Arabidopsis thaliana) also elongate in response to sucro

48 genes (DEGs) in the pistil transcriptomes of Arabidopsis thaliana and Arabidopsis halleri during self

49 tion requirement in the Brassicaceae species Arabidopsis thaliana and Arabis alpina, respectively.

50 enomes of three relatives of the model plant Arabidopsis thaliana and assembled all three genomes int

51 We show in Arabidopsis thaliana and Brassica nigra that localized F

52 ic study between the closely related species Arabidopsis thaliana and Cardamine hirsuta.

53 ified and analyzed GET pathway components in Arabidopsis thaliana and found reduced root hair elongat

54 challenge, we introduced the LxL cycle into Arabidopsis thaliana and functionally isolated it from t

55 transcriptomic and genomic analysis between Arabidopsis thaliana and Glycine max root hair genes rev

56 ant pathogens that infect the model organism Arabidopsis thaliana and important crops such as Brassic

57 uces the kinetics of stomatal conductance in Arabidopsis thaliana and its dependence on vapor pressur

58 ation toward inter-nucleosomal linker DNA in Arabidopsis thaliana and mouse.

59 We engineered an H3.3 knockdown in Arabidopsis thaliana and observed transcription reductio

60 Using Arabidopsis (Arabidopsis thaliana) and barley (Hordeum vulgare), we s

61 role in lignin biosynthesis in Arabidopsis (Arabidopsis thaliana) and later in Medicago truncatula H

62 , and between two model plants: Arabidopsis (Arabidopsis thaliana) and soybean (Glycine max).

63 We used mutants of Arabidopsis (Arabidopsis thaliana) and the expression of oleogenic fa

64 Using Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum)

65 rom those of its close relative Arabidopsis (Arabidopsis thaliana), and allelic variation at many loc

66 alyzed four flowering time related traits in Arabidopsis thaliana, and detected some previously repor

67 are conspicuously absent in the model plant Arabidopsis thaliana, and little is known about the enzy

68 m ) than previously characterized TNT-active Arabidopsis thaliana (Arabidopsis) GSTs.

69 lysis of apple bHLH (MdbHLH) genes and their Arabidopsis thaliana (Arabidopsis) orthologs indicated t

70 igh-affinity ammonium transporters (AMTs) in Arabidopsis thaliana are efficiently inactivated by phos

71 usly suggested that blunt-ended telomeres in Arabidopsis thaliana are protected by Ku, a DNA repair f

72 Using Arabidopsis thaliana as a model, we present evidence for

73 -oxoglutarate/Fe(II)-dependent oxygenases in Arabidopsis thaliana as JA hydroxylases and show that th

74 S on 18 FAAs from a 313-ecotype Arabidopsis (Arabidopsis thaliana) association panel.

75 ion RNA-seq time series of methyl JA-treated Arabidopsis thaliana at 15 time points over a 16-h perio

76 atments that both change root development in Arabidopsis thaliana at an unprecedented level of tempor

77 nds inhibited Plasmodium falciparum (Pf) and Arabidopsis thaliana (At) SHMT in target assays and PfNF

78 tiated by the ER-localized co-chaperone from Arabidopsis thaliana, AtBAG7.

79 rization of the ion selectivity of TPC1 from Arabidopsis thaliana (AtTPC1) and compared its selectivi

80 consisting of primarily interphase cells in Arabidopsis thaliana, AUG8 is an integral component [2].

81 entified MtLAX2, a paralogue of Arabidopsis (Arabidopsis thaliana) AUX1, as being induced at early st

82 Finally, both Arabidopsis thaliana auxin efflux transporter pin1 and i

83 re confirmed to regulate stomatal closure in Arabidopsis thaliana, B. napus or both species.

84 Arabidopsis thaliana backgrounds with altered activities

85 The LIL3 protein of Arabidopsis (Arabidopsis thaliana) belongs to the light-harvesting co

86 an be attacked by two different Arabidopsis (Arabidopsis thaliana) beta-glucosidases from glycoside h

87 th mutations in a homolog of an Arabidopsis (Arabidopsis thaliana) boron efflux transporter displayed

88 by reverse genetics analyses in Arabidopsis (Arabidopsis thaliana), but corresponding information is

89 both structure and activity to Arabidopsis (Arabidopsis thaliana) CAD5 and Populus tremuloides sinap

90 CBL10 is a true ortholog of the Arabidopsis (Arabidopsis thaliana) CBL10 gene, supporting that the es

91 m and metaxylem vessel cells of Arabidopsis (Arabidopsis thaliana) ccr1 mutants.

92 -used human drugs from the Profen family, in Arabidopsis thaliana cells and the Arabidopsis plant.

93 lling plant development, on two Arabidopsis (Arabidopsis thaliana) CI mutants: a new insertion mutant

94 n to correspond to orthologs of Arabidopsis (Arabidopsis thaliana) circadian clock genes EARLY FLOWER

95 hways for input of sugar to the Arabidopsis (Arabidopsis thaliana) circadian network.

96 internal subunit arrangement of Arabidopsis (Arabidopsis thaliana) complex II.

97 In Arabidopsis thaliana, CONSTANS (CO) plays an essential r

98 ER bodies in Arabidopsis thaliana contain large amounts of beta-gluco

99 Arabidopsis (Arabidopsis thaliana) contains two enzymes (encoded by t

100 pressor of light signaling, the Arabidopsis (Arabidopsis thaliana) COP1/SPA E3 ubiquitin ligase cause

101 The Arabidopsis (Arabidopsis thaliana) COP1/SPA ubiquitin ligase is a cen

102 Arabidopsis (Arabidopsis thaliana) CPK4 and soybean (Glycine max) CDP

103 we report that mutation in the Arabidopsis (Arabidopsis thaliana) CPO-coding gene At5g63290 (AtHEMN1

104 The prototype, Arabidopsis thaliana cry1, regulates several light respo

105 alytic tool for exploring multiple levels of Arabidopsis thaliana data through a zoomable user interf

106 mutants for the three annotated Arabidopsis (Arabidopsis thaliana) DHARs.

107 In Arabidopsis thaliana, disruption of two subunits of the

108 Here, we characterize an Arabidopsis (Arabidopsis thaliana) double mutant, yellow stripe1-like

109 as functional PMEIs induced in Arabidopsis (Arabidopsis thaliana) during B. cinerea infection.

110 Here, we report that, in Arabidopsis thaliana, during the onset of the HR, the ba

111 owering3 (Efl3), an ortholog of Arabidopsis (Arabidopsis thaliana) EARLY FLOWERING3 (ELF3) that confe

112 Arabidopsis (Arabidopsis thaliana) ecotype Columbia-0 is nonhost to t

113 Landsberg erecta (Ler) and a number of other Arabidopsis thaliana ecotypes.

114 tivity were explored within the Arabidopsis (Arabidopsis thaliana) embryo by putting seeds under GA-l

115 rom maternal tissues in nearly all published Arabidopsis thaliana endosperm and early embryo transcri

116 n of innate immune signaling in Arabidopsis (Arabidopsis thaliana) epidermal cells; however, the immu

117 alyze a large panel of over 500 Arabidopsis (Arabidopsis thaliana) epigenetic hybrid plants (epiHybri

118 Out of 23 Arabidopsis thaliana EXO70 isoforms, we analyzed seven i

119 arrested meristematic region of Arabidopsis (Arabidopsis thaliana) experiences a local energy depriva

120 ng a fully functional fluorescent version of Arabidopsis thaliana FLA4 we show that this protein is l

121 At early stages of Arabidopsis (Arabidopsis thaliana) flowering, the inflorescence stem

122 IPTION FACTOR1), was strongly upregulated in Arabidopsis thaliana flowers subjected to Cu deficiency.

123 ional regulation of selected target genes of Arabidopsis Thaliana from microarray time series data ob

124 ssociating with mitochondrial DNA (mtDNA) in Arabidopsis thaliana Gain- and loss-of-function mutants

125 The Arabidopsis thaliana gene XYLEM NAC DOMAIN1 (XND1) is up

126 Here, we identified a single Arabidopsis thaliana gene, At3g57630, in clade E of the

127 A systematic search for Arabidopsis (Arabidopsis thaliana) genes encoding proteins resembling

128 The Arabidopsis (Arabidopsis thaliana) genome contains nine beta-amylase

129 The Arabidopsis (Arabidopsis thaliana) genome encodes homologs of the Gui

130 on sequence data from 488 recombinant inbred Arabidopsis thaliana genomes, we identified 6502 segrega

131 ine was evaluated using the Oryza sativa and Arabidopsis thaliana genomes.

132 oxy-d-xylulose-5-phosphate synthase (SlDXS), Arabidopsis thaliana geranyl diphosphate synthase 1 (AtG

133 sive study of the age-related changes in the Arabidopsis thaliana glycated proteome, including the pr

134 The Arabidopsis (Arabidopsis thaliana) gynoecium consists of two congenit

135 In this study, we show that Arabidopsis thaliana HAP2/GCS1 is sufficient to promote

136 their biogenesis and action in Arabidopsis (Arabidopsis thaliana) has been described, these processe

137 Studies with model plants such as Arabidopsis thaliana have revealed that phytohormones ar

138 enes involved in the process in Arabidopsis (Arabidopsis thaliana) have been identified and analyzed.

139 Recent findings in Arabidopsis (Arabidopsis thaliana) have demonstrated that auxin-induc

140 gulates glycolysis and lipid biosynthesis in Arabidopsis thaliana Here, we identify mechanistic links

141 In this study, Lipaphis erysimi induced Arabidopsis thaliana HIPVs were collected using headspac

142 AtHB1 is an Arabidopsis (Arabidopsis thaliana) homeodomain-leucine zipper transcr

143 liflower (Brassicaoleracea) and Arabidopsis (Arabidopsis thaliana) hydathodes.

144 Using periodic diurnal variation in Arabidopsis thaliana hypocotyl growth, we found that cel

145 nscriptional regulation of photosynthesis in Arabidopsis thaliana in an evolutionary context, to prov

146 The flowering plant Arabidopsis thaliana is a dicot model organism for resea

147 previously that the full-length IP5 2-K from Arabidopsis thaliana is a zinc metallo-enzyme, including

148 Polycomb Group regulation in Arabidopsis (Arabidopsis thaliana) is required to maintain cell diffe

149 sing from the genomes of fungi and the plant Arabidopsis thaliana, it remains unclear how UPF1 is act

150 , a Kelch domain-containing F-box protein in Arabidopsis thaliana KFB(CHS) physically interacts with

151 lutathionylation induced deactivation of the Arabidopsis thaliana kinase BRASSINOSTEROID INSENSITIVE

152 e binding CENPC-k motif at the C terminus of Arabidopsis thaliana KNL2, which is conserved among a wi

153 e of GH1-containing proteins of Arabidopsis (Arabidopsis thaliana [L.] Heynh) that will be useful for

154 on of normal starch granules in Arabidopsis (Arabidopsis thaliana) leaf chloroplasts requires STARCH

155 l proteins involved in granule initiation in Arabidopsis thaliana leaves.

156 ylakoid membranes prepared from Arabidopsis (Arabidopsis thaliana) leaves against lipid peroxidation.

157 ame time as starch synthesis in Arabidopsis (Arabidopsis thaliana) leaves in the light.

158 In Arabidopsis (Arabidopsis thaliana) leaves, ATP pretreatment induced r

159 center and marginal regions of Arabidopsis (Arabidopsis thaliana) leaves.

160 s from the apoplastic fluids of Arabidopsis (Arabidopsis thaliana) leaves.

161 ation tag screen, we identified a transgenic Arabidopsis thaliana line with longer etiolated hypocoty

162 types exhibited by the roots of Arabidopsis (Arabidopsis thaliana) lines carrying insertions in the U

163 Here, we show that Arabidopsis (Arabidopsis thaliana) lines carrying mutations in differ

164 By screening an Arabidopsis thaliana lncRNA custom-made array we identif

165 We have identified a role for Arabidopsis (Arabidopsis thaliana) MAP KINASE17 (MPK17) in affecting

166 ion of 16 members in the entire Arabidopsis (Arabidopsis thaliana) MCTP family.

167 The Arabidopsis (Arabidopsis thaliana) member ROOT HAIR DEFECTIVE3 (RHD3)

168 exploration and analysis of the Arabidopsis (Arabidopsis thaliana) metabolic network in the chloropla

169 loem sieve elements in stems of Arabidopsis (Arabidopsis thaliana), Miscanthus x giganteus, and notab

170 se phosphatases (MKPs), such as Arabidopsis (Arabidopsis thaliana) MKP1, are important negative regul

171 Arabidopsis thaliana mlo2 mlo6 mlo12 triple mutant plant

172 Although all four members of the Arabidopsis thaliana Mn-CDF family can transport Mn, her

173 l., analyzing PSI particles isolated from an Arabidopsis thaliana mutant that accumulates zeaxanthin

174 Arabidopsis thaliana mutants deficient in flavonoid bios

175 derived from analysis of feedback-resistant Arabidopsis thaliana mutants for the three allosteric co

176 actolipids that accumulate in the respective Arabidopsis thaliana mutants.

177 type, we isolated E-2-hexenal response (her) Arabidopsis thaliana mutants.

178 nt and under extended darkness, Arabidopsis (Arabidopsis thaliana) mutants with disruption of autopha

179 We used two Arabidopsis thaliana mutation accumulation (MA) lines an

180 In Arabidopsis (Arabidopsis thaliana), mutations in either CCS52A1 or CC

181 In Arabidopsis thaliana, mutations in the MAP65-3 gene lead

182 We found that Arabidopsis thaliana MYB36, which have been previously s

183 ification of N-terminal peptides in prt6, an Arabidopsis thaliana N-end rule mutant lacking the E3 li

184 ter flowering regulator, forms a trimer with Arabidopsis thaliana NF-YB2/NF-YC3 to efficiently bind t

185 In Arabidopsis (Arabidopsis thaliana), NORTIA, a member of the MILDEW RE

186 In Arabidopsis (Arabidopsis thaliana), OR increases carotenoid levels by

187 equencing data from distinct species such as Arabidopsis thaliana, Oryza sativa, and Physcomitrella p

188 nisms, Mus musculus, Drosophila melanogaste, Arabidopsis thaliana, Oryza sativa, Physcomitrella paten

189 lecular basis of PME3 inhibition by PMEI7 in Arabidopsis thaliana Our complementary approach uncovere

190 of, to our knowledge, the first Arabidopsis (Arabidopsis thaliana) pex1 missense alleles: pex1-2 and

191 Arabidopsis (Arabidopsis thaliana) PGK1 was localized exclusively in

192 es regulating the expression of Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comp

193 The Arabidopsis (Arabidopsis thaliana) PI-PLC gene family is composed of

194 we have generated a transgenic Arabidopsis (Arabidopsis thaliana) plant expressing H(+)-ATPase isofo

195 In this work, Arabidopsis thaliana plants containing a T-DNA disruptio

196 a promoter-GUS fusion study with transgenic Arabidopsis thaliana plants found that SbCAD2 promoter i

197 We exposed Arabidopsis thaliana plants to herbivory and investigate

198 02530) is required for growth acclimation of Arabidopsis thaliana plants under controlled photoinhibi

199 onmental cues, focusing on vernalization, in Arabidopsis thaliana plants.

200 d SGC (specifically guard cell) Arabidopsis (Arabidopsis thaliana) plants in which the oscillator gen

201 study, we generated transgenic Arabidopsis (Arabidopsis thaliana) plants overexpressing the Rieske F

202 Here, we show that Arabidopsis (Arabidopsis thaliana) plants require starch for survivin

203 xogenous treatment of flowering Arabidopsis (Arabidopsis thaliana) plants with GA specifically affect

204 acids, have been synthesized in Arabidopsis (Arabidopsis thaliana) plants.

205 examined the biochemical properties of three Arabidopsis thaliana PMTs (AtPMT1-3) and determined the

206 etic analyses we identified a novel class of Arabidopsis thaliana pollen-borne CRPs, the PCP-Bs (for

207 Arabidopsis (Arabidopsis thaliana) possesses six LAZY genes having sp

208 ) but 100-fold less frequent in Arabidopsis (Arabidopsis thaliana), preventing its use in plastid bio

209 and its importance was investigated using an Arabidopsis thaliana protoplast system.

210 gated the conformational dynamics of two key Arabidopsis thaliana receptor-like kinases, brassinoster

211 ew high-depth Structure-seq data analysis in Arabidopsis thaliana, released with this work.

212 Their function in Arabidopsis (Arabidopsis thaliana) remained unclear because neither t

213 er cells (TCs) in leaf veins of Arabidopsis (Arabidopsis thaliana) represents a novel trait of hetero

214 In vegetative tissues of Arabidopsis (Arabidopsis thaliana), repressive methylation marks are

215 -specific patterns of gene expression during Arabidopsis thaliana reproduction using single nucleotid

216 ns in the pericentromeric heterochromatin of Arabidopsis thaliana requires SMC4, a core subunit of co

217 lear gene expression in various Arabidopsis (Arabidopsis thaliana) retrograde signalling mutants.

218 es AOX1A, AOX1C, and AOX1D from Arabidopsis (Arabidopsis thaliana) revealed that cysteine residues, C

219 e of the N-terminal IMS domain of Toc75 from Arabidopsis thaliana, revealing three tandem polypeptide

220 previously produced transgenic Arabidopsis (Arabidopsis thaliana) RNA interference (RNAi) seeds with

221 The Arabidopsis thaliana root epidermis is comprised of two

222 erial genes required for colonization of the Arabidopsis thaliana root system.

223 future root hair cells (trichoblasts) of the Arabidopsis thaliana root where they positively regulate

224 epeat dsRNA specifically in the Arabidopsis (Arabidopsis thaliana) root tip, allowing a genetic scree

225 hetic activity in leaves of the Arabidopsis (Arabidopsis thaliana) rosette throughout the vegetative

226 In the model organism Arabidopsis thaliana, SA glucose conjugates are formed b

227 binding domains of starch synthase III from Arabidopsis thaliana (SBD123) binds preferentially to ce

228 Arabidopsis thaliana seed development requires the conco

229 ion of proteins integral to the Arabidopsis (Arabidopsis thaliana) seed coat mucilage, a specialized

230 proliferating endosperm of the Arabidopsis (Arabidopsis thaliana) seed.

231 ylene in roots from light-grown Arabidopsis (Arabidopsis thaliana) seedlings, which were overlaid on

232 protein synthesis in vegetative Arabidopsis (Arabidopsis thaliana) seedlings.

233 Unlike maize, Arabidopsis thaliana seeds contain several RFOs (raffino

234 Arabidopsis (Arabidopsis thaliana) seeds of exoribonuclease4 (xrn4) a

235 e analyses and modeling, we show that during Arabidopsis thaliana sepal development, fluctuations in

236 sin propeptide-like inhibitor 1 (SPI-1) from Arabidopsis thaliana Sequence similarity and the shared

237 Here, we demonstrate the Arabidopsis thaliana SG2-type R2R3-MYB transcription fac

238 Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) Shewanella-like protein phosphatas

239 ion of coding and noncoding RNAs in roots of Arabidopsis thaliana shifted from replete to deficient p

240 Experiments using the model system Arabidopsis thaliana showed that monothioarsenate is les

241 subunits KIN10 and KIN11 of the Arabidopsis (Arabidopsis thaliana) SnRK1 complex interact with the ST

242 Arabidopsis (Arabidopsis thaliana) spongy (spg) and uneven pattern of

243 IDIC ACID PHOSPHOHYDROLASE (PAH) activity in Arabidopsis thaliana stimulates biosynthesis of the majo

244 s (ROS) in guard cells to close Arabidopsis (Arabidopsis thaliana) stomata.

245 The Arabidopsis thaliana strain Cvi has depleted gene body m

246 One mechanism in the model plant Arabidopsis thaliana studied here comprises irreversible

247 The Arabidopsis thaliana suppressor of quenching1 (soq1) mut

248 sp hordei) in Arabidopsis thaliana Surprisingly, VPS9a acts in additio

249 A new mutant in Arabidopsis thaliana that displays twisting in petals an

250 The SNARE SYP121 of Arabidopsis thaliana that facilitates vesicle fusion at

251 ds and other irregularities in cell walls of Arabidopsis thaliana that increase enzyme accessibility

252 hree pathways limiting meiotic crossovers in Arabidopsis thaliana that rely on the activity of FANCM,

253 a protein of 99 amino acids in Arabidopsis (Arabidopsis thaliana) that has similarities to the cyste

254 tart site (TSS) of a reporter gene fusion in Arabidopsis thaliana The intron increased expression fro

255 of cell proliferation during organ growth in Arabidopsis thaliana The peptidase is activated by two R

256 o NPQ in biologically relevant conditions in Arabidopsis thaliana The possible role of zeaxanthin in

257 lethal pathway in response to heat stress in Arabidopsis thaliana The similarity of ferroptosis in an

258 lent to 4.5x genome coverage in Arabidopsis (Arabidopsis thaliana), the constructed LTR library showe

259 In Arabidopsis (Arabidopsis thaliana), the cytokinin signal is perceived

260 In Arabidopsis (Arabidopsis thaliana), the lysine (Lys) aminotransferase

261 In Arabidopsis (Arabidopsis thaliana), the stress and ABA-induced Delta1

262 In the rosid species Arabidopsis thaliana, the AP2-type AP2 transcription fac

263 In Arabidopsis thaliana, the GLX system is encoded by three

264 In plants such as Arabidopsis thaliana, the most prominent corepressor is

265 In Arabidopsis thaliana, these include marked stem elongati

266 In Arabidopsis (Arabidopsis thaliana), three regions on the pollen surfa

267 re investigated after 10 days of exposure of Arabidopsis thaliana to 10 mg.L(-1) of negatively or pos

268 Headspace exposure of Arabidopsis thaliana to a mixture of the bicyclic monote

269 nting (TCSPC) measurements were performed on Arabidopsis thaliana to quantify the dependence of the r

270 CrY2H-seq to investigate sparsely annotated Arabidopsis thaliana transcription factors interactions.

271 Here, we show that two Arabidopsis thaliana transcription factors, FAR1 RELATED

272 In the reference plant Arabidopsis thaliana, tRFs are processed by Dicer-like 1

273 erceived as signal molecules in Arabidopsis (Arabidopsis thaliana), triggering a signaling cascade th

274 his gene, At1g45231, encodes an Arabidopsis (Arabidopsis thaliana) trimethylguanosine synthase (TGS1)

275 cal genomics studies have been published for Arabidopsis thaliana, uncovering many expression quantit

276 four different rare RNA species from plant, Arabidopsis thaliana, using surface-enhanced Raman spect

277 ier protein and two channels in Arabidopsis (Arabidopsis thaliana) vacuoles.

278 elp, but unlike the model plant Arabidopsis (Arabidopsis thaliana), very little is known about floral

279 sms, natural variation of metal tolerance in Arabidopsis thaliana was investigated.

280 CID28 (IAA28, DII) protein from Arabidopsis (Arabidopsis thaliana) was modified for use in maize (Zea

281 f this histone variant on gene expression in Arabidopsis thaliana We demonstrate that the arp6 mutant

282 titative mapping of m(5)C in the model plant Arabidopsis thaliana We discovered more than a thousand

283 gene expression divergence following WGDs in Arabidopsis thaliana We identified a set of 92 homoeolog

284 kinase CYTOKININ-INDEPENDENT 1 (CKI1RD) from Arabidopsis thaliana We observed that the crystal struct

285 ght into the organellar peptidase network in Arabidopsis thaliana We present a compendium of known an

286 ded DNA pararetrovirus, with the model plant Arabidopsis thaliana We show that the autophagy cargo re

287 ation (MA) lines of the model plant species, Arabidopsis thaliana We then show that MMR deficiency gr

288 water deprivation treatment in Arabidopsis (Arabidopsis thaliana), we investigated the malleability

289 By transforming exogenous TEs into Arabidopsis thaliana, we circumvented identity-based sil

290 d molecular impacts of Ga in the model plant Arabidopsis thaliana were investigated in medium culture

291 leaf senescence Loss-of-function mutants of Arabidopsis thaliana were used to study the role of cyto

292 sica napus) and the model plant Arabidopsis (Arabidopsis thaliana), were unique in showing NLR expres

293 al histone acetylation marks in Arabidopsis (Arabidopsis thaliana), which was strongly diminished in

294 biosynthesis has been dissected in the dicot Arabidopsis thaliana, which has green, photosynthetic se

295 Here, mutants of Arabidopsis thaliana with altered root hair phenotypes w

296 of CH3Cl was investigated using variants of Arabidopsis thaliana with low, wild-type and high expres

297 ms of sugar uptake during the interaction of Arabidopsis thaliana with the necrotrophic fungus Botryt

298 -based experimental system from Arabidopsis (Arabidopsis thaliana) with high temporal resolution allo

299 uorescence measurements on PSI isolated from Arabidopsis thaliana WT in dark-adapted and high-light-s

300 ge (DTU) have been observed for thousands of Arabidopsis thaliana, Zea mays and Vitis vinifera genes,