ライフサイエンスコーパス: Arabidopsis

1 CESA3 and one of four CESA6-like proteins in Arabidopsis.

2 odified H3K4 histone marks, respectively, in Arabidopsis.

3 ale gametophytes by multiple pollen tubes in Arabidopsis.

4 ating the pathogenic response was studied in Arabidopsis.

5 on with KCS1 to affect VLCFA biosynthesis in Arabidopsis.

6 pocotyl growth under ambient temperatures in Arabidopsis.

7 ion of HpasRNA-induced target suppression in Arabidopsis.

8 s defence gene expressions and Pip levels in Arabidopsis.

9 s mainly based on studies of the dicot model Arabidopsis.

10 er normal and cold temperature conditions in Arabidopsis.

11 ilencing pathways in low-oxygen signaling in Arabidopsis.

12 HISTONE (CENH3) gene induces paternal HI in Arabidopsis(4-6).

13 dinated during early seedling development in Arabidopsis A shoot signaling module that includes HY5,

14 variation influences flowering responses of Arabidopsis accessions resulting in an interplay between

15 non-coding cis variation at FLC has enabled Arabidopsis accessions to adapt to different climatic co

16 SK1) Ds insertion allele, ask1, in different Arabidopsis accessions.

17 factor contributing to root growth control: Arabidopsis Adenylate Kinase 6 (AAK6).

18 (AIL6)/PLETHORA 3 (PLT3), two members of the Arabidopsis AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) transcr

19 n, defense gene expression and cell death in Arabidopsis, all of which constitute a hallmark of PTI.

20 ts for all leucine-rich repeat (LRR)-RLKs in Arabidopsis and analyzed their expression patterns durin

21 e assess the use of alternative promoters in Arabidopsis and compare the accuracy of existing TSS ann

22 d hormone quantification to demonstrate that Arabidopsis and Medicago CEP (C-TERMINALLY ENCODED PEPTI

23 CEP receptor-dependent signalling outputs in Arabidopsis and Medicago control overall RSA, LR GSA, sh

24 ch, to capitalise on the discoveries made in Arabidopsis and other plants.

25 In contrast to the model plants Arabidopsis and rice, many of the pathways associated wi

26 uplex structures are strongly folded in both Arabidopsis and rice, providing direct evidence of RNA G

27 between the cell-type transcript profiles of Arabidopsis and rice.

28 e that ASK1 is a predominant Skp1 protein in Arabidopsis and that the fertile ask1 mutant allowed us

29 Here, we exploit the MSH1 system in Arabidopsis and tomato to introduce rootstock epigenetic

30 we have identified a plant-specific GET2 in Arabidopsis, and its sequence allows the analysis of cro

31 We assembled a list of all Arabidopsis (Arabid opsis thaliana) plastid preproteins

32 copersicum) neoxanthin-deficient1 (nxd1) and Arabidopsis (Arabidopsis thaliana) ABA-deficient4 (aba4)

33 but not DOAG2, rescues floral defects in the Arabidopsis (Arabidopsis thaliana) ag-4 mutant, includin

34 Our comprehensive RNA sequencing analysis in Arabidopsis (Arabidopsis thaliana) allowed us to obtain

35 Gene expression analyses in Arabidopsis (Arabidopsis thaliana) and Oryza sativa reve

36 of two synthetic autopolyploid accessions of Arabidopsis (Arabidopsis thaliana) and their diploid pro

37 ate significant phenotypic diversity in both Arabidopsis (Arabidopsis thaliana) and tomato (Solanum l

38 We established Peredox-mCherry lines of Arabidopsis (Arabidopsis thaliana) and validated the bio

39 performed a genome-wide association study in Arabidopsis (Arabidopsis thaliana) and we show here that

40 transcription start sites located within the Arabidopsis (Arabidopsis thaliana) AtSCS gene results in

41 As a part of this network, we show that Arabidopsis (Arabidopsis thaliana) chloroplast glutamyl

42 TPC in Arabidopsis (Arabidopsis thaliana) contains six evolutio

43 modeling and simulation, to demonstrate that Arabidopsis (Arabidopsis thaliana) CSLD3 is a UDP-glucos

44 The Arabidopsis (Arabidopsis thaliana) cyclin-dependent kina

45 6 CBL-Interacting Protein Kinases (CIPKs) of Arabidopsis (Arabidopsis thaliana) decode the calcium si

46 sed on nascent RNA approaches concluded that Arabidopsis (Arabidopsis thaliana) does not produce PROM

47 Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) EXO70A2 (At5g52340) i

48 Genetic approaches using mutants of Arabidopsis (Arabidopsis thaliana) in combination with b

49 isms among the 1,135 sequenced accessions of Arabidopsis (Arabidopsis thaliana) in GRANULE-BOUND STAR

50 JA-triggered depletion of JAZ proteins in Arabidopsis (Arabidopsis thaliana) is also associated wi

51 We evaluated these claims using Arabidopsis (Arabidopsis thaliana) knock-out mutants lac

52 here that RHD3 physically interacts with two Arabidopsis (Arabidopsis thaliana) LUNAPARK proteins, LN

53 e analyses during dark-induced senescence of Arabidopsis (Arabidopsis thaliana) mutants deficient in

54 and physiological assays to characterize the Arabidopsis (Arabidopsis thaliana) NatB complex.

55 om ecotypes Columbia and Landsberg erecta of Arabidopsis (Arabidopsis thaliana) respond differently t

56 characterized four canola homologues of the Arabidopsis (Arabidopsis thaliana) ROD1 gene.

57 The quiescent center (QC) of the Arabidopsis (Arabidopsis thaliana) root meristem acts as

58 egulator of stem cell differentiation in the Arabidopsis (Arabidopsis thaliana) root meristem.

59 in epidermis, cortex, and pericycle cells of Arabidopsis (Arabidopsis thaliana) roots challenged with

60 ndscape of cotranslational mRNA decay during Arabidopsis (Arabidopsis thaliana) seedling development.

61 When Arabidopsis (Arabidopsis thaliana) seedlings are grown i

62 c uridine analog 5-ethynyl uridine (5-EU) in Arabidopsis (Arabidopsis thaliana) seedlings provides in

63 Here, we have determined that Arabidopsis (Arabidopsis thaliana) SINE1 and SINE2 play

64 The Arabidopsis (Arabidopsis thaliana) SnRK2 family comprise

65 We could not recover viable Arabidopsis (Arabidopsis thaliana) tfIIs plants constitu

66 An Arabidopsis (Arabidopsis thaliana) transfer DNA insertio

67 In Arabidopsis (Arabidopsis thaliana), although GAMYB-like

68 lis, AoCYP94B1, and its putative ortholog in Arabidopsis (Arabidopsis thaliana), AtCYP94B1, which are

69 In Arabidopsis (Arabidopsis thaliana), FER-LIKE FE DEFICIEN

70 In particular, in Arabidopsis (Arabidopsis thaliana), high temperature rev

71 In Arabidopsis (Arabidopsis thaliana), hydrogen sulfide neg

72 Here, we show that the RNA degradomes of Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa),

73 In Arabidopsis (Arabidopsis thaliana), the MADS-box transcr

74 In Arabidopsis (Arabidopsis thaliana), the transcription fa

75 In Arabidopsis (Arabidopsis thaliana), TREHALOSE-6-PHOSPHAT

76 In this study we demonstrate that in Arabidopsis (Arabidopsis thaliana), two distinctly local

77 t control wound-triggered JA accumulation in Arabidopsis (Arabidopsis thaliana), unlike its orthologs

78 rexpression lines during leaf development in Arabidopsis (Arabidopsis thaliana), we show that E2FB in

79 licated in the granule initiation process in Arabidopsis (Arabidopsis thaliana), with each protein ex

80 for control of nuclear-encoded transgenes in Arabidopsis (Arabidopsis thaliana).

81 nal regulation of SMAX1 from the model plant Arabidopsis (Arabidopsis thaliana).

82 n the Brassicales, including the model plant Arabidopsis (Arabidopsis thaliana).

83 ) type class II histone deacetylase HDA15 in Arabidopsis (Arabidopsis thaliana).

84 2 are essential for life cycle completion in Arabidopsis (Arabidopsis thaliana).

85 consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).

86 s is BRASSINOSTEROID INSENSITIVE 1 (BRI1) in Arabidopsis (Arabidopsis thaliana).

87 d germination, and seedling establishment in Arabidopsis (Arabidopsis thaliana).

88 state transition kinases (STN7 and STN8) in Arabidopsis (Arabidopsis thaliana).

89 of plant development and stress responses in Arabidopsis (Arabidopsis thaliana).

90 despread auxin-related phenotypic defects in Arabidopsis (Arabidopsis thaliana).

91 ES20) targets the catalytic site of CESA6 in Arabidopsis (Arabidopsis thaliana).

92 ation patterns in C. reinhardtii compared to Arabidopsis are discussed in the context of the stronger

93 Using Arabidopsis as a model system, we tested our approach to

94 We generated site-specific mutations in Arabidopsis At2OGO by CRISPR/Cas9 gene editing.

95 FAH12 with PfLCAT-PLA or RcLCAT-PLA, but not Arabidopsis AtLCAT-PLA, resulted in increased occupation

96 Arabidopsis AtNFS1 and AtFH overexpressor lines displaye

97 Consistent with this hypothesis, Arabidopsis badc1 badc3 mutant lines grown in a light-da

98 In contrast, in Arabidopsis both GAs and BRs regulate ovule number indep

99 d protein-coding gene families compared with Arabidopsis, but an additional 20% of proteins matched a

100 owards the heterozygous regions in wild type Arabidopsis, but not in msh2 mutants.

101 Here, we report that the Arabidopsis calcium-dependent protein kinase CPK3 is a k

102 hat it also constrains chromoplast number in Arabidopsis calli.

103 duction in the Brassicaceae seed oil species Arabidopsis, Camelina and oilseed rape.

104 Here, we used immortalized Arabidopsis cell suspensions to sort replicating nuclei

105 reverse genetics to investigate the role of Arabidopsis cellulose synthase like-C (CSLC) proteins in

106 NASP(SIM3) is co-expressed with Arabidopsis CenH3 in dividing cells and binds directly t

107 Arabidopsis CGEP null mutant alleles (cgep) had no visib

108 In Arabidopsis, CGL20 is encoded by segmentally duplicated

109 of NFU1 in Fe-S client protein maturation in Arabidopsis chloroplasts among other SUF components.

110 SEC, specifically modulates the pace of the Arabidopsis circadian clock.

111 The Arabidopsis circadian oscillator is a gene network which

112 han plant-derived JA molecules in regulating Arabidopsis clock.

113 Arabidopsis CME appears to follow the constant curvature

114 ECTIVE (EMB) genes identified throughout the Arabidopsis community; include important details on 2200

115 that overexpress either EPF1 or Stomagen in Arabidopsis cotyledons, we reveal a range within the epi

116 v2OGO gene is functionally equivalent to its Arabidopsis counterpart and, hence, may have a similar r

117 40), which acts through the receptor kinases ARABIDOPSIS CRINKLY4 (ACR4) and CLAVATA1 (CLV1) to contr

118 reverse reactions of photooligomerization of Arabidopsis CRY1 and CRY2 provide a previously unrecogni

119 tants containing a T-DNA in each of the five Arabidopsis CSLC genes had normal levels of XyG.

120 The Arabidopsis DMR6 gene encodes a putative 2-oxoglutarate

121 Recent evidence suggests that in Arabidopsis, DNA polymerase theta (PolQ) may be a crucia

122 ast estimates of 500-1000 total EMB genes in Arabidopsis; document 83 double mutant combinations repo

123 An Arabidopsis DXO1 variant is active toward 5'-OH RNA but

124 The Arabidopsis E3 ubiquitin ligases RING-H2 FINGER A3A (RHA

125 Some of the salicylic acid-deficient Arabidopsis eds5 mutants have an unnoticed fah1-2 backgr

126 the function of two types of proton pumps in Arabidopsis embryo development and pattern formation.

127 Accordingly, the seedling growth of multiple Arabidopsis gcn2 mutants was retarded under excess light

128 The Arabidopsis genome encodes six TIR1/AFB proteins represe

129 ay an important role in this restriction and Arabidopsis growth and survival.

130 ears, mostly from studies of the model dicot Arabidopsis Here, we employed a CRISPR/Cas9-based approa

131 ncluding 13 alleles of the gene encoding the ARABIDOPSIS HIS KINASE4 cytokinin receptor.

132 ged phyB (phyB-FP) in the epidermal cells of Arabidopsis hypocotyl and cotyledon.

133 dress this problem through identification of Arabidopsis INCURVATA11 (ICU11) as a Polycomb Repressive

134 BABA perception in Arabidopsis is mediated by the aspartyl tRNA synthetase

135 fedtschenkoi compared with that observed in Arabidopsis is reported and tissue-specific localization

136 in plants-with a focus on the model organism Arabidopsis-is presented.

137 Furthermore, in Arabidopsis, KAR-induced root hair elongation depends on

138 We investigated this paradigm during Arabidopsis lateral root formation, when the lateral roo

139 complexities: Results from experiments with Arabidopsis leaves in conventional controlled environmen

140 pregulated in the metabolome of MeJA-treated Arabidopsis leaves, on the breast cancer cell cycle, is

141 d cell expansion underlie the dwarfism of an Arabidopsis lignin mutant ref8, and report the identific

142 Without this LNP-mediated stabilization, in Arabidopsis lnp1-1 lnp2-1 mutant cells, the ER becomes a

143 rated the presence of several ubiquinones in Arabidopsis mitochondria.

144 ed HI has not been successful outside of the Arabidopsis model system(7).

145 An Arabidopsis mutant defective in two peroxisomal acyl-CoA

146 We investigated Arabidopsis NMCPs (called CRWNs) to study the interrelat

147 Hundreds of Arabidopsis NMD targets possess evident EJC footprints,

148 CWC15 associates with core components of the Arabidopsis NTC and its loss leads to inefficient splici

149 y, the haploid male gametophyte or pollen in Arabidopsis, on the other hand, can cope without functio

150 study, we investigated an OR(His) variant of Arabidopsis OR, genetically mimicking the melon OR(His)

151 pression and developmental importance of the Arabidopsis ortholog of yeast CWC15.

152 gic receptor, P2K2, by complementation of an Arabidopsis p2k1 mutant.

153 ch closer to genes in Capsella compared with Arabidopsis, perhaps explaining the essential role of Po

154 Glutamate, ATP, Arabidopsis PLANT ELICITOR PEPTIDE, and glutathione disu

155 pha-1, impalpha-2 and impalpha-3 resulted in Arabidopsis plants with a rapid flowering phenotype simi

156 2ox10 is expressed mainly in the siliques of Arabidopsis plants.

157 We demonstrate here that Arabidopsis PLDgamma1, but not its close homologs PLDgam

158 g different colors of fluorescent protein in Arabidopsis pollen tetrads.

159 nal 20% of proteins matched against the full Arabidopsis proteome, indicating a unique evolution of p

160 Here we show that the Arabidopsis quadruple mutant (min7 fls2 efr cerk1; herea

161 Iron absorption in Arabidopsis root epidermal cells requires the IRT1 trans

162 respond to local and systemic signals in the Arabidopsis root tip, including those directly activated

163 g, we developed a multicellular model of the Arabidopsis root tip.

164 Using Arabidopsis root transcriptome data and coexpression clu

165 s (ROS) along the developmental zones of the Arabidopsis root.

166 ound responses after laser-based wounding in Arabidopsis root.

167 , we identified IRT1-interacting proteins in Arabidopsis roots by mass spectrometry and established a

168 ated auxin and ethylene on the metabolome of Arabidopsis roots using a high-resolution 24 h time cour

169 o acid-elicited cytosolic Ca(2+) increase in Arabidopsis seedling roots.

170 required to rapidly enhance phototropism in Arabidopsis seedlings.

171 e light of the cryptochrome receptor cry1 in Arabidopsis seedlings.

172 but insignificant increases in HFA levels in Arabidopsis seeds compared with RcFAH12 expression alone

173 functional influence of a well-characterized Arabidopsis Skp1-Like1 (ASK1) Ds insertion allele, ask1,

174 Arabidopsis stomatal development requires asymmetric cel

175 we show that TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOPSIS (TAA1), a key enzyme in the auxin biosynthes

176 In this work, we studied the roles of Arabidopsis TEOSINTE BRANCHED1, CYCLOIDEA, PCF15 (TCP15)

177 ured phenotypes on a 216-year time series of Arabidopsis thaliana accessions from across its native r

178 Arabidopsis thaliana AKR2A plays an important role in pl

179 rom a wild-type accession of the model plant Arabidopsis thaliana and a mutant defective in mRNA meth

180 eport a plant-beneficial interaction between Arabidopsis thaliana and the root microbiota under iron

181 The model plant Arabidopsis thaliana avoids these practical problems and

182 Here we report that the Arabidopsis thaliana Ca(2+)-permeable channel OSCA1.3 co

183 The Arabidopsis thaliana Calmodulin-binding Transcription Ac

184 lling endodermal function in the model plant Arabidopsis thaliana contribute to the plant microbiome

185 Utilizing the photosensitive protein Arabidopsis thaliana cryptochrome 2, the light-inducible

186 e and stress specific nat-siRNAs in multiple Arabidopsis thaliana datasets.

187 the combined loss of AHA6, AHA8, and AHA9 in Arabidopsis thaliana delays pollen germination and cause

188 Here we use Arabidopsis thaliana ecotypes, mutants and transgenic li

189 e exploited the contrasting behaviour of two Arabidopsis thaliana ecotypes: Cape Verde Islands (Cvi)

190 enced accessions of the model annual species Arabidopsis thaliana from across a wide climate range an

191 iations between functional annotations in an Arabidopsis thaliana gene network.

192 Arabidopsis thaliana glutamate receptor-like (GLR) chann

193 Protein-only RNase P 1 (PRORP1) in Arabidopsis thaliana is an endoribonuclease that uses it

194 enzyme in the auxin biosynthesis pathway in Arabidopsis thaliana is phosphorylated at Threonine 101

195 ouse embryonic fibroblast cell cultures, and Arabidopsis thaliana leaves.

196 We isolate a strong hypomorphic Arabidopsis thaliana mutant of the POL2A catalytic subun

197 Transcriptome analysis of Arabidopsis thaliana mutant plants in PAP-SAL1 pathway r

198 na FT1 or FT3 genes under the control of the Arabidopsis thaliana phloem specific SUCROSE SYNTHASE 2

199 [Ca(2+) ](stroma) in the aerial part of the Arabidopsis thaliana plant.

200 he biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing eve

201 Here, we report that in Arabidopsis thaliana roots, auxin controls the spatiotem

202 s of GA biosynthesis in the roots of 7-d-old Arabidopsis thaliana seedlings were investigated using t

203 We found that exposure of Arabidopsis thaliana to a known plant growth-promoting r

204 Arabidopsis thaliana transcriptomes have been extensivel

205 f leaf explants from the non-medicinal plant Arabidopsis thaliana with human breast cancer cells, sel

206 The Arabidopsis thaliana zinc finger transcription factor (Z

207 eoxanthin-deficient1 (nxd1) and Arabidopsis (Arabidopsis thaliana) ABA-deficient4 (aba4), were identi

208 , rescues floral defects in the Arabidopsis (Arabidopsis thaliana) ag-4 mutant, including reiteration

209 sive RNA sequencing analysis in Arabidopsis (Arabidopsis thaliana) allowed us to obtain a complete pi

210 Gene expression analyses in Arabidopsis (Arabidopsis thaliana) and Oryza sativa revealed that sev

211 tic autopolyploid accessions of Arabidopsis (Arabidopsis thaliana) and their diploid progenitors, as

212 nt phenotypic diversity in both Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum).

213 lished Peredox-mCherry lines of Arabidopsis (Arabidopsis thaliana) and validated the biophysical and

214 enome-wide association study in Arabidopsis (Arabidopsis thaliana) and we show here that noncoding va

215 start sites located within the Arabidopsis (Arabidopsis thaliana) AtSCS gene results in two in-frame

216 t of this network, we show that Arabidopsis (Arabidopsis thaliana) chloroplast glutamyl peptidase (CG

217 TPC in Arabidopsis (Arabidopsis thaliana) contains six evolutionarily conser

218 simulation, to demonstrate that Arabidopsis (Arabidopsis thaliana) CSLD3 is a UDP-glucose-dependent b

219 The Arabidopsis (Arabidopsis thaliana) cyclin-dependent kinase G1 (CDKG1)

220 ting Protein Kinases (CIPKs) of Arabidopsis (Arabidopsis thaliana) decode the calcium signals elicite

221 t RNA approaches concluded that Arabidopsis (Arabidopsis thaliana) does not produce PROMPTs.

222 Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) EXO70A2 (At5g52340) is the main ex

223 A plant-origin deconjugase enzyme (Arabidopsis thaliana) for deconjugation of folates (PE-L

224 tic approaches using mutants of Arabidopsis (Arabidopsis thaliana) in combination with biochemical an

225 e 1,135 sequenced accessions of Arabidopsis (Arabidopsis thaliana) in GRANULE-BOUND STARCH SYNTHASE (

226 ed depletion of JAZ proteins in Arabidopsis (Arabidopsis thaliana) is also associated with reduced gr

227 We evaluated these claims using Arabidopsis (Arabidopsis thaliana) knock-out mutants lacking either p

228 3 physically interacts with two Arabidopsis (Arabidopsis thaliana) LUNAPARK proteins, LNP1 and LNP2,

229 ring dark-induced senescence of Arabidopsis (Arabidopsis thaliana) mutants deficient in key steps of

230 ical assays to characterize the Arabidopsis (Arabidopsis thaliana) NatB complex.

231 olumbia and Landsberg erecta of Arabidopsis (Arabidopsis thaliana) respond differently to phosphate s

232 d four canola homologues of the Arabidopsis (Arabidopsis thaliana) ROD1 gene.

233 he quiescent center (QC) of the Arabidopsis (Arabidopsis thaliana) root meristem acts as an organizer

234 tem cell differentiation in the Arabidopsis (Arabidopsis thaliana) root meristem.

235 cortex, and pericycle cells of Arabidopsis (Arabidopsis thaliana) roots challenged with two immunity

236 translational mRNA decay during Arabidopsis (Arabidopsis thaliana) seedling development.

237 When Arabidopsis (Arabidopsis thaliana) seedlings are grown in the dark, h

238 log 5-ethynyl uridine (5-EU) in Arabidopsis (Arabidopsis thaliana) seedlings provides insight into pl

239 Here, we have determined that Arabidopsis (Arabidopsis thaliana) SINE1 and SINE2 play an important

240 The Arabidopsis (Arabidopsis thaliana) SnRK2 family comprises the abscisi

241 We could not recover viable Arabidopsis (Arabidopsis thaliana) tfIIs plants constitutively expres

242 An Arabidopsis (Arabidopsis thaliana) transfer DNA insertion mutant of L

243 In Arabidopsis (Arabidopsis thaliana), although GAMYB-like genes are con

244 1, and its putative ortholog in Arabidopsis (Arabidopsis thaliana), AtCYP94B1, which are involved in

245 In Arabidopsis (Arabidopsis thaliana), FER-LIKE FE DEFICIENCY-INDUCED TR

246 In particular, in Arabidopsis (Arabidopsis thaliana), high temperature reversibly inact

247 In Arabidopsis (Arabidopsis thaliana), hydrogen sulfide negatively regul

248 show that the RNA degradomes of Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), worm (Caenor

249 In Arabidopsis (Arabidopsis thaliana), the MADS-box transcription factor

250 In Arabidopsis (Arabidopsis thaliana), the transcription factor ILR3 pla

251 In Arabidopsis (Arabidopsis thaliana), TREHALOSE-6-PHOSPHATE SYNTHASE1 (

252 is study we demonstrate that in Arabidopsis (Arabidopsis thaliana), two distinctly localized acetate-

253 nd-triggered JA accumulation in Arabidopsis (Arabidopsis thaliana), unlike its orthologs in tobacco.

254 ines during leaf development in Arabidopsis (Arabidopsis thaliana), we show that E2FB in association

255 e granule initiation process in Arabidopsis (Arabidopsis thaliana), with each protein exerting a vary

256 f nuclear-encoded transgenes in Arabidopsis (Arabidopsis thaliana).

257 n of SMAX1 from the model plant Arabidopsis (Arabidopsis thaliana).

258 ales, including the model plant Arabidopsis (Arabidopsis thaliana).

259 II histone deacetylase HDA15 in Arabidopsis (Arabidopsis thaliana).

260 al for life cycle completion in Arabidopsis (Arabidopsis thaliana).

261 STEROID INSENSITIVE 1 (BRI1) in Arabidopsis (Arabidopsis thaliana).

262 rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).

263 , and seedling establishment in Arabidopsis (Arabidopsis thaliana).

264 tion kinases (STN7 and STN8) in Arabidopsis (Arabidopsis thaliana).

265 lopment and stress responses in Arabidopsis (Arabidopsis thaliana).

266 n-related phenotypic defects in Arabidopsis (Arabidopsis thaliana).

267 the catalytic site of CESA6 in Arabidopsis (Arabidopsis thaliana).

268 base-resolution methylation data in humans, Arabidopsis thaliana, and rice (Oryza sativa), we presen

269 have been characterized in the model species Arabidopsis thaliana, but little is known about how tran

270 e, and across different organisms, including Arabidopsis thaliana, Caenorhabditis elegans, and Danio

271 In the model plant Arabidopsis thaliana, floral organogenesis requires AINT

272 te-acting Fe-S cluster-carrier proteins from Arabidopsis thaliana, NFU4 and NFU5.

273 For TuMV in Arabidopsis thaliana, profiles were obtained for mechani

274 how OOPS can be applied in human cell lines, Arabidopsis thaliana, Schizosaccharomyces pombe and Esch

275 We demonstrate that, in Arabidopsis thaliana, the 2 RNL families contribute spec

276 In Arabidopsis thaliana, the AT-hook motif nuclear-localize

277 a patens as the second plant system, besides Arabidopsis thaliana, with viable mutants with an essent

278 s in cortical cells of M. truncatula but not Arabidopsis thaliana.

279 ir regulatory relationship resembles that in Arabidopsis thaliana.

280 cerevisiae and dodecameric AHAS complexes of Arabidopsis thaliana.

281 er Solanaceae crops is distinct from that in Arabidopsis thaliana.

282 ression of one-third of the 207 NLR genes in Arabidopsis thaliana.

283 were addressed using simple case studies in Arabidopsis thaliana.

284 y osmotic stress as well as ABA signaling in Arabidopsis thaliana.

285 s, and microarray and metabolomics data from Arabidopsis thaliana.

286 ic regions associated with open chromatin in Arabidopsis thaliana.

287 tubulin-like GTPase protein gene FtsZ1 from Arabidopsis thaliana.

288 discovered and published for the model plant Arabidopsis thaliana.

289 od to capture the intact mRNA structurome in Arabidopsis thaliana.

290 In Arabidopsis, the SHORT-ROOT (SHR)/SCARECROW (SCR) transc

291 In Arabidopsis they were expressed in similar tissues and d

292 In Arabidopsis this process is controlled by a gene network

293 varied upon long-term (weeks) acclimation of Arabidopsis to low (LL), moderate (ML) and high (HL) gro

294 Screening of Arabidopsis transcription factors identifies nuclear fac

295 mune responses in plant leaves and generated Arabidopsis transgenic plants.

296 thus promoting endoreplication in developing Arabidopsis trichomes.

297 The Arabidopsis type-A response regulators (type-A ARR) are

298 Our results indicate that Arabidopsis uL18-Like proteins are targeted to either mi

299 decrease of H2A.Z-containing nucleosomes in Arabidopsis under standard growing conditions.

300 he germ cell lineage within floral organs of Arabidopsis using light sheet fluorescence microscopy.