ライフサイエンスコーパス: Arabidopsis thaliana

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

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

3 CLP protease subunit, CLPP2, in Arabidopsis (Arabidopsis thaliana).

4 ect reproductive development in Arabidopsis (Arabidopsis thaliana).

5 nkage, to the pollen surface of Arabidopsis (Arabidopsis thaliana).

6 and SAA during light stress in Arabidopsis (Arabidopsis thaliana).

7 in seeds of the model organism Arabidopsis (Arabidopsis thaliana).

8 ase families in the model plant Arabidopsis (Arabidopsis thaliana).

9 e largely been characterized in Arabidopsis (Arabidopsis thaliana).

10 f K63 polyubiquitin networks in Arabidopsis (Arabidopsis thaliana).

11 tor promoting miRNA activity in Arabidopsis (Arabidopsis thaliana).

12 rop species and the model plant Arabidopsis (Arabidopsis thaliana).

13 ecombineering approaches beyond Arabidopsis (Arabidopsis thaliana).

14 sistance and leaf senescence in Arabidopsis (Arabidopsis thaliana).

15 tation sequencing (ChIP-seq) in Arabidopsis (Arabidopsis thaliana).

16 ions during secondary growth of Arabidopsis (Arabidopsis thaliana).

17 ve oxygen species (ROS) wave in Arabidopsis (Arabidopsis thaliana).

18 oxia-induced gene regulation in Arabidopsis (Arabidopsis thaliana).

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

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

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

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

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

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

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

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

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

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

29 discovered and published for the model plant Arabidopsis thaliana.

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

31 of the JA, ET and SA signalling pathways in Arabidopsis thaliana.

32 ber in the third and fourth floral whorls of Arabidopsis thaliana.

33 six MATH-BTB genes (BPM1-6) is described in Arabidopsis thaliana.

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

35 e of alternative splicing in plants, such as Arabidopsis thaliana.

36 wth architecture among natural accessions of Arabidopsis thaliana.

37 yperpolarization-activated K(v) channel from Arabidopsis thaliana.

38 dynamics during the vernalization process in Arabidopsis thaliana.

39 ic regions associated with open chromatin in Arabidopsis thaliana.

40 true roots of Selaginella moellendorffii and Arabidopsis thaliana.

41 ntitative determination of these analytes in Arabidopsis thaliana.

42 , bZIP28, BAG7, NAC089 and NAC103 factors in Arabidopsis thaliana.

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

44 use experiment with 35 natural accessions of Arabidopsis thaliana.

45 ated loci in the predominantly selfing plant Arabidopsis thaliana.

46 ively charged nanoplastics can accumulate in Arabidopsis thaliana.

47 opment is limited mostly to the model dicot, Arabidopsis thaliana.

48 ered Ca(2+) influx and freezing tolerance in Arabidopsis thaliana.

49 -GALS1 module aggravates salt sensitivity in Arabidopsis thaliana.

50 via the ubiquitin-26S proteasome pathway in Arabidopsis thaliana.

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

52 ir regulatory relationship resembles that in Arabidopsis thaliana.

53 cerevisiae and dodecameric AHAS complexes of Arabidopsis thaliana.

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

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

56 were addressed using simple case studies in Arabidopsis thaliana.

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

58 We determined that, in Arabidopsis thaliana, 16:1t biosynthesis requires both F

59 m (67.5%) that were much higher than that of Arabidopsis thaliana (3.9%).

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

61 Arabidopsis thaliana ABSCISIC ACID INSENSITIVE3 (ABI3) i

62 us protein CsACD2, a homolog of Arabidopsis (Arabidopsis thaliana) ACCELERATED CELL DEATH 2 (ACD2).

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

64 es of sequencing data for >1000 Arabidopsis (Arabidopsis thaliana) accessions focused on small variat

65 On a panel of 210 natural Arabidopsis (Arabidopsis thaliana) accessions, we were able to not on

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

67 cumented minimal role of SA in resistance of Arabidopsis thaliana against necrotrophic pathogens.

68 Arabidopsis thaliana AKR2A plays an important role in pl

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

70 ous expression of OsWAKL21.2 in Arabidopsis (Arabidopsis thaliana) also activates plant immune respon

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

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

73 tors of the genes encoding class A ARFs from Arabidopsis thaliana and demonstrate that each gene is c

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

75 Most co-occurrences regarded Arabidopsis thaliana and Zea mays.

76 ll as in widely used model species in plant (Arabidopsis thaliana) and animal (Drosophila melanogaste

77 egulates anthocyanin content in Arabidopsis (Arabidopsis thaliana) and influences the survivability o

78 n regulating shade avoidance in Arabidopsis (Arabidopsis thaliana) and investigated how KDR regulates

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

80 ging behind, but recent work in Arabidopsis (Arabidopsis thaliana) and other plant species is startin

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

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

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

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

85 Allium cepa), the model eudicot Arabidopsis (Arabidopsis thaliana), and moss (Physcomitrella patens)

86 lti-domain FK506-binding proteins present in Arabidopsis thaliana, and it is known to get targeted to

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

88 own that genome-wide methylation patterns in Arabidopsis thaliana are highly stable over generations,

89 Many genes in the model plant Arabidopsis thaliana are regulated by diel cycles via pa

90 ed ERF102 to ERF105 transcription factors of Arabidopsis thaliana are regulated by different stresses

91 ession and protein abundance in Arabidopsis (Arabidopsis thaliana) are predominantly confined to meri

92 dinated activation by dimers of Arabidopsis (Arabidopsis thaliana) ARF-GEF GNOM, which is involved in

93 In Arabidopsis thaliana, ARR1 is one of the most abundantly

94 is of nitrogen deficiency of the model plant Arabidopsis thaliana as well as two important vegetable

95 THE GREEN LINEAGE20 (CGL20) in Arabidopsis (Arabidopsis thaliana; AtCGL20), which is a Pro-rich, ~10

96 1, and its putative ortholog in Arabidopsis (Arabidopsis thaliana), AtCYP94B1, which are involved in

97 se regions in the LAZY1 gene of Arabidopsis (Arabidopsis thaliana; AtLAZY1) was tested by mutating ea

98 the crystal structures of Metacaspase 4 from Arabidopsis thaliana (AtMC4) that modulates Ca(2+)-depen

99 Arabidopsis (Arabidopsis thaliana) atnfs and atfh mutants, with reduc

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

101 ction of two SEIPIN isoforms in Arabidopsis (Arabidopsis thaliana), AtSEIPIN2 and AtSEIPIN3, may depe

102 In Arabidopsis thaliana, AUXIN RESISTANT1 (AXR1) functions

103 The model plant Arabidopsis thaliana avoids these practical problems and

104 , AT4G00650) has been extensively studied in Arabidopsis thaliana because of its role creating flower

105 -limiting for vascular cell proliferation in Arabidopsis thaliana Both regulators have origins predat

106 y the changes in physiology and phenology in Arabidopsis thaliana (Brassicaceae) due to contemporary

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

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

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

110 The Arabidopsis thaliana Calmodulin-binding Transcription Ac

111 The Arabidopsis (Arabidopsis thaliana) calmodulin-binding transcription a

112 owth and meristem phenotypes of Arabidopsis (Arabidopsis thaliana) CCS52A2-deficient plants in a supp

113 Arabidopsis (Arabidopsis thaliana) cells were briefly labeled with 5-

114 Independent Arabidopsis (Arabidopsis thaliana) cepr1 null mutants showed dispropo

115 AtCLCa (Arabidopsis thaliana Chloride Channel a) is a vacuolar N

116 w that in the background of the Arabidopsis (Arabidopsis thaliana) chloroplast (cp)ATP synthase assem

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

118 The Arabidopsis (Arabidopsis thaliana) clathrin adaptor EPSIN1 (EPS1) is

119 Arabidopsis (Arabidopsis thaliana) contains 12 ALAs in five phylogene

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

121 lopment.(1) During reproduction, plants like Arabidopsis thaliana continuously generate flowers on gr

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

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

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

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

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

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

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

129 Here, we showed that Arabidopsis (Arabidopsis thaliana) DGK2 and DGK4 are crucial for game

130 l biosynthesis, we utilized the Arabidopsis (Arabidopsis thaliana) diacylglycerol acyltransferase mut

131 hade-avoiding plants, including Arabidopsis (Arabidopsis thaliana), display a number of growth respon

132 sured from the dry seeds of the Arabidopsis (Arabidopsis thaliana) diversity panel using all potentia

133 In Arabidopsis (Arabidopsis thaliana), DNA-dependent RNA polymerase IV (

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

135 The Arabidopsis thaliana E3 ubiquitin ligase COP1 functions

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

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

138 uingly, before seed maturation, Arabidopsis (Arabidopsis thaliana) embryos are also photosyntheticall

139 The SIAMESE (SIM) gene of Arabidopsis (Arabidopsis thaliana) encodes a cyclin-dependent kinase

140 Here, we study the family of Arabidopsis thaliana Epsin-like proteins, which are acce

141 ein fused to a GFP:Strep tag in Arabidopsis (Arabidopsis thaliana) exclusively decorates mitochondria

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

143 The Arabidopsis (Arabidopsis thaliana) fatty acid biosynthesis1 (fab1) mu

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

145 At Arabidopsis thaliana FLC, antisense transcription quanti

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

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

148 The ETHYLENE RESPONSE FACTOR (ERF) genes of Arabidopsis thaliana form a large family encoding plant-

149 how that the tail region of the Arabidopsis (Arabidopsis thaliana) FRA1 kinesin physically interacts

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

151 tability of a GA-insensitive DELLA allele in Arabidopsis thaliana Furthermore, the degradation of DEL

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

153 AtGA2ox9 and AtGA2ox10, in the Arabidopsis (Arabidopsis thaliana) genome.

154 m the glycosyl hydrolase 43 (GH43) family in Arabidopsis thaliana GH43 loss-of-function mutants exhib

155 VHH-Fc) antibody against the highly abundant Arabidopsis thaliana globulin seed storage protein cruci

156 we analyzed the transcriptomes of a suite of Arabidopsis thaliana glucosinolate-deficient mutants usi

157 Arabidopsis thaliana glutamate receptor-like (GLR) chann

158 GPT2 reported the viability of Arabidopsis (Arabidopsis thaliana) gpt2 mutants, whereas heterozygous

159 lus vulgaris, Ricinus communis, Arabidopsis [Arabidopsis thaliana], Helianthus annuus, Solanum lycope

160 An Arabidopsis thaliana HglS homolog coexpresses with known

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

162 The Arabidopsis thaliana histone acetyltransferase GCN5 regu

163 Here, we show that the Arabidopsis (Arabidopsis thaliana) histone methyltransferase SET DOMA

164 In Arabidopsis thaliana, HPAT1 and HPAT3 are redundantly re

165 35A), and wild-type recombinant Arabidopsis (Arabidopsis thaliana) HPR1, it was found that HPR1-T335D

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

167 idate molecular networks that control QDR in Arabidopsis thaliana in response to the bacterial pathog

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

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

170 Expression of HopO1-1 in Arabidopsis (Arabidopsis thaliana) increases the distance of PD-depen

171 lipid fractions of the seed of Arabidopsis (Arabidopsis thaliana) indicates that omega-9 monoenes ar

172 At the leaf margin of Arabidopsis thaliana, interplay between auxin transport

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

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

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

176 holder of the image (the herbarium sheet of Arabidopsis thaliana) is the first author, Derek Denney.

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

178 ion of light stress by a single Arabidopsis (Arabidopsis thaliana) leaf was recently shown to activat

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

180 s in the methylome of senescent Arabidopsis (Arabidopsis thaliana) leaves induced by darkness and mon

181 -LOXs) produce JA precursors in Arabidopsis (Arabidopsis thaliana) leaves, but the 13-LOXs responsibl

182 Here, we present the crystal structure of Arabidopsis thaliana legumain isoform beta (AtLEGbeta) i

183 Arabidopsis (Arabidopsis thaliana), like most dicotyledonous plants,

184 Arabidopsis thaliana lines with altered lignin through d

185 We wanted to expand this knowledge by using Arabidopsis thaliana lines with constitutive ectopic ove

186 g-read sequencing of cDNAs from Arabidopsis (Arabidopsis thaliana) lines deficient in multiple layers

187 3 physically interacts with two Arabidopsis (Arabidopsis thaliana) LUNAPARK proteins, LNP1 and LNP2,

188 at epidermis specific transcription factors, ARABIDOPSIS THALIANA MERISTEM LAYER 1 (ATML1) and its cl

189 Arabidopsis (Arabidopsis thaliana) mitochondria contain four OXA homo

190 CP (mtACP) isoforms support the Arabidopsis (Arabidopsis thaliana) mitochondrially localized Type II

191 In the model plant Arabidopsis thaliana, most components of the pathway wer

192 microscopy structures of a MscS homolog from Arabidopsis thaliana, MSL1, presumably in both the close

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

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

195 ignaling from chloroplasts, we have used the Arabidopsis thaliana mutant plastid ferrochelatase two (

196 Here, we show that PTs of Arabidopsis thaliana mutants impaired in the pollen-spec

197 Here we analyzed clock function in Arabidopsis thaliana mutants with defective immune respo

198 al roles for flavonols in this process using Arabidopsis thaliana mutants with defects in genes encod

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

200 series of fertile, hypomorphic Arabidopsis (Arabidopsis thaliana) mutants for the essential glucosin

201 ed mutagenomics to a screen for Arabidopsis (Arabidopsis thaliana) mutants involved in the response t

202 n-depth comparative analysis of Arabidopsis (Arabidopsis thaliana) mutants lacking the NMD-related pr

203 e show the impact of temperature increase on Arabidopsis thaliana mutation, studying whole genome pro

204 Here, we show that the Arabidopsis (Arabidopsis thaliana) Na(+):K(+):2Cl(-) (NKCC) cotranspo

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

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

207 report the mapping of the SA-binding core of Arabidopsis thaliana NPR4 and its ligand-bound crystal s

208 sful in vitro reconstitution of Arabidopsis (Arabidopsis thaliana) OHPs with chlorophylls and caroten

209 echanisms involved are largely unexplored in Arabidopsis thaliana or other plant species.

210 We identified Arabidopsis (Arabidopsis thaliana) ORESARA1 (ORE1), the developmental

211 y of clustered biosynthetic pathway genes in Arabidopsis thaliana Our analyses reveal that biosynthet

212 Arabidopsis (Arabidopsis thaliana) OXIDATION RESISTANCE2 (AtOXR2) is

213 tissue (leaf, root, seed, and stem) model of Arabidopsis thaliana, p-ath773, uniquely capturing the c

214 irst plant purinergic receptor, Arabidopsis (Arabidopsis thaliana) P2K1 (L-type lectin receptor kinas

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

216 e 5' untranslated region of the Arabidopsis (Arabidopsis thaliana) PHO1 inhibits its translation and

217 We previously reported that Arabidopsis (Arabidopsis thaliana) phosphoinositide-specific phosphol

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

219 s with a genetic complementation assay using Arabidopsis thaliana plants, we provide evidence that in

220 output of the stress and metabolic status of Arabidopsis thaliana plants.

221 y-fatty acids (HFA) onto TAG in Arabidopsis (Arabidopsis thaliana) plants expressing the castor (Rici

222 MEcPP-accumulating ceh1 mutant Arabidopsis (Arabidopsis thaliana) plants relative to wild-type seedl

223 screening of PIN2:PIN1-HA;pin2 Arabidopsis (Arabidopsis thaliana) plants, which ectopically express

224 The Arabidopsis (Arabidopsis thaliana) PLD family consists of 12 members,

225 resistance protein (R) with homology to the Arabidopsis thaliana PM resistance protein, RPW8.

226 ic transfer of PrpS and PrsS to Arabidopsis (Arabidopsis thaliana) pollen and pistil.

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

228 Our previous study showed that the Arabidopsis thaliana protein arginine methyltransferase

229 ein localizes to the nucleus in Arabidopsis (Arabidopsis thaliana) protoplasts, and VEN4 homologs are

230 se-like proteins or MDLs) of the model plant Arabidopsis thaliana Recombinant Arabidopsis MDLs (AtMDL

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

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

233 study, we found that mutation of FERONIA in Arabidopsis thaliana resulted in plants showing low susc

234 e crystal structure of the FN3K homolog from Arabidopsis thaliana revealed that it forms an unexpecte

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

236 We show that Arabidopsis (Arabidopsis thaliana) RING Finger ABA-Related1 (RFA1) an

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

238 The Arabidopsis (Arabidopsis thaliana) root epidermis consists of a posit

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

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

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

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

243 s of two signaling compounds in Arabidopsis (Arabidopsis thaliana) roots revealed that ABA treatment

244 phloem unloading interfaces of Arabidopsis (Arabidopsis thaliana) roots.

245 to cytosolic Pi homeostasis in Arabidopsis (Arabidopsis thaliana) roots.

246 In Arabidopsis thaliana, ROS produced by RBOHC was previous

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

248 teins (BBX) were identified as regulators of Arabidopsis thaliana seedling photomorphogenesis.

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

250 say to study the effects of cell swelling on Arabidopsis thaliana seedlings and to test the contribut

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

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

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

254 ced degreening of cotyledons in Arabidopsis (Arabidopsis thaliana) seedlings.

255 The eudicot model plant Arabidopsis (Arabidopsis thaliana) served as a reference organism for

256 Arabidopsis thaliana serves as a model plant for genetic

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

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

259 show that DRT111 interacts with Arabidopsis (Arabidopsis thaliana) Splicing Factor1, involved in 3' s

260 In autogamous plants like Arabidopsis (Arabidopsis thaliana), stamen filament elongation must b

261 1 encodes an F-box protein, an orthologue of Arabidopsis thaliana STERILE APETALA (SAP), that forms p

262 eptor, corresponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2-1 (AtSMAX1) that

263 ng single-cell RNA sequencing (scRNA-seq) in Arabidopsis thaliana tetraploid lines and isogenic diplo

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

265 In Arabidopsis (Arabidopsis thaliana), the brassinosteroid (BR) receptor

266 In Arabidopsis (Arabidopsis thaliana), the F-box protein F-BOX-LIKE17 (F

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

268 ant protection during stress in Arabidopsis (Arabidopsis thaliana), the mechanism and molecular compo

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

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

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

272 In Arabidopsis thaliana, the cold-induced epigenetic regula

273 In Arabidopsis thaliana, the METTL3 homolog, mRNA adenosine

274 In Arabidopsis (Arabidopsis thaliana), these processes are primarily mod

275 constitutively expressed PCO4 and PCO5 from Arabidopsis thaliana to 1.24 and 1.91 angstrom resolutio

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

277 netic variation of 252 natural accessions of Arabidopsis thaliana to conduct genome-wide association

278 VPC in Populus tremula x alba, Zea mays, and Arabidopsis thaliana to determine its role in trait vari

279 rowth, here we used the natural variation in Arabidopsis thaliana to perform a genome-wide associatio

280 nucleosome positioning (MNase-Seq) data for Arabidopsis thaliana to understand how nucleosome positi

281 rse plant species, ranging from Arabidopsis (Arabidopsis thaliana) to wheat (Triticum spp.), includin

282 Arabidopsis thaliana transcriptomes have been extensivel

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

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

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

286 In Arabidopsis thaliana, two E3 ligases, BIG BROTHER (BB) a

287 regulation in long-term WUE in Arabidopsis (Arabidopsis thaliana) under light and dark conditions.

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

289 nalyzed this membrane system in Arabidopsis (Arabidopsis thaliana) using mass spectrometry-based prot

290 uring systemic responses to root wounding in Arabidopsis thaliana We found that root wounding or the

291 nd MT cytoskeletons in single plant cells of Arabidopsis thaliana We show that the cytoskeleton align

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

293 ent D-type cyclins, CYCD3;1 and CYCD4;2 from Arabidopsis thaliana, were expressed by agrobacterial in

294 in stark contrast with the angiosperm model Arabidopsis thaliana, where DNA methylation is strongly

295 Unlike Arabidopsis thaliana whose members of the CBF/DREB1 fami

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

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

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

299 mechanistic characterization of Arabidopsis (Arabidopsis thaliana) xylan O-acetyltransferase 1 (XOAT1

300 The Arabidopsis thaliana zinc finger transcription factor (Z