ライフサイエンスコーパス: thaliana

1 (STN7 and STN8) in Arabidopsis (Arabidopsis thaliana).

2 in mature leaves of Arabidopsis (Arabidopsis thaliana).

3 stress responses in Arabidopsis (Arabidopsis thaliana).

4 subunit, CLPP2, in Arabidopsis (Arabidopsis thaliana).

5 tive development in Arabidopsis (Arabidopsis thaliana).

6 e pollen surface of Arabidopsis (Arabidopsis thaliana).

7 ing light stress in Arabidopsis (Arabidopsis thaliana).

8 the model organism Arabidopsis (Arabidopsis thaliana).

9 in the model plant Arabidopsis (Arabidopsis thaliana).

10 en characterized in Arabidopsis (Arabidopsis thaliana).

11 iquitin networks in Arabidopsis (Arabidopsis thaliana).

12 g miRNA activity in Arabidopsis (Arabidopsis thaliana).

13 and the model plant Arabidopsis (Arabidopsis thaliana).

14 g approaches beyond Arabidopsis (Arabidopsis thaliana).

15 leaf senescence in Arabidopsis (Arabidopsis thaliana).

16 ncing (ChIP-seq) in Arabidopsis (Arabidopsis thaliana).

17 secondary growth of Arabidopsis (Arabidopsis thaliana).

18 ecies (ROS) wave in Arabidopsis (Arabidopsis thaliana).

19 enotypic defects in Arabidopsis (Arabidopsis thaliana).

20 ic site of CESA6 in Arabidopsis (Arabidopsis thaliana).

21 coded transgenes in Arabidopsis (Arabidopsis thaliana).

22 rom the model plant Arabidopsis (Arabidopsis thaliana).

23 ing the model plant Arabidopsis (Arabidopsis thaliana).

24 eacetylase HDA15 in Arabidopsis (Arabidopsis thaliana).

25 cycle completion in Arabidopsis (Arabidopsis thaliana).

26 NSITIVE 1 (BRI1) in Arabidopsis (Arabidopsis thaliana).

27 ng establishment in Arabidopsis (Arabidopsis thaliana).

28 nd published for the model plant Arabidopsis thaliana.

29 e GTPase protein gene FtsZ1 from Arabidopsis thaliana.

30 ET and SA signalling pathways in Arabidopsis thaliana.

31 hird and fourth floral whorls of Arabidopsis thaliana.

32 array and metabolomics data from Arabidopsis thaliana.

33 B genes (BPM1-6) is described in Arabidopsis thaliana.

34 tive splicing in plants, such as Arabidopsis thaliana.

35 ture among natural accessions of Arabidopsis thaliana.

36 tion-activated K(v) channel from Arabidopsis thaliana.

37 ssociated with open chromatin in Arabidopsis thaliana.

38 ing the vernalization process in Arabidopsis thaliana.

39 f Selaginella moellendorffii and Arabidopsis thaliana.

40 termination of these analytes in Arabidopsis thaliana.

41 G7, NAC089 and NAC103 factors in Arabidopsis thaliana.

42 nt with 35 natural accessions of Arabidopsis thaliana.

43 the predominantly selfing plant Arabidopsis thaliana.

44 I that is conserved between P. patens and A. thaliana.

45 d nanoplastics can accumulate in Arabidopsis thaliana.

46 mited mostly to the model dicot, Arabidopsis thaliana.

47 influx and freezing tolerance in Arabidopsis thaliana.

48 e the intact mRNA structurome in Arabidopsis thaliana.

49 l cells of M. truncatula but not Arabidopsis thaliana.

50 n regions of higher sequence diversity in A. thaliana.

51 y relationship resembles that in Arabidopsis thaliana.

52 nd dodecameric AHAS complexes of Arabidopsis thaliana.

53 ne-third of the 207 NLR genes in Arabidopsis thaliana.

54 e crops is distinct from that in Arabidopsis thaliana.

55 sed using simple case studies in Arabidopsis thaliana.

56 B disaggregase, in particular, ClpB3 from A. thaliana.

57 ress as well as ABA signaling in Arabidopsis thaliana.

58 We determined that, in Arabidopsis thaliana, 16:1t biosynthesis requires both FATTY ACID DE

59 ficient1 (nxd1) and Arabidopsis (Arabidopsis thaliana) ABA-deficient4 (aba4), were identified previou

60 Arabidopsis thaliana ABSCISIC ACID INSENSITIVE3 (ABI3) is a transcri

61 sACD2, a homolog of Arabidopsis (Arabidopsis thaliana) ACCELERATED CELL DEATH 2 (ACD2).

62 pes on a 216-year time series of Arabidopsis thaliana accessions from across its native range and app

63 om genome-wide association studies of 199 A. thaliana accessions.

64 methylation are highly variable among 725 A. thaliana accessions.

65 anel of 210 natural Arabidopsis (Arabidopsis thaliana) accessions, we were able to not only accuratel

66 oral defects in the Arabidopsis (Arabidopsis thaliana) ag-4 mutant, including reiteration of stamenoi

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

68 Arabidopsis thaliana AKR2A plays an important role in plant response

69 uencing analysis in Arabidopsis (Arabidopsis thaliana) allowed us to obtain a complete picture of the

70 In Arabidopsis (Arabidopsis thaliana), although GAMYB-like genes are constitutively

71 ype accession of the model plant Arabidopsis thaliana and a mutant defective in mRNA methylation (m(6

72 genes encoding class A ARFs from Arabidopsis thaliana and demonstrate that each gene is controlled by

73 rowth rate and metabolite accumulation in A. thaliana and P. trichocarpa accessions as the outcome of

74 h increased neighborhood mutation risk in A. thaliana and rice.

75 t-beneficial interaction between Arabidopsis thaliana and the root microbiota under iron deprivation

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

77 ely used model species in plant (Arabidopsis thaliana) and animal (Drosophila melanogaster) research.

78 hocyanin content in Arabidopsis (Arabidopsis thaliana) and influences the survivability of plants und

79 ression analyses in Arabidopsis (Arabidopsis thaliana) and Oryza sativa revealed that several homolog

80 but recent work in Arabidopsis (Arabidopsis thaliana) and other plant species is starting to give in

81 ploid accessions of Arabidopsis (Arabidopsis thaliana) and their diploid progenitors, as well as one

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

83 ox-mCherry lines of Arabidopsis (Arabidopsis thaliana) and validated the biophysical and biochemical

84 ssociation study in Arabidopsis (Arabidopsis thaliana) and we show here that noncoding variations of

85 , the model eudicot Arabidopsis (Arabidopsis thaliana), and moss (Physcomitrella patens) were examine

86 K506-binding proteins present in Arabidopsis thaliana, and it is known to get targeted to the nucleus

87 tion methylation data in humans, Arabidopsis thaliana, and rice (Oryza sativa), we present evidence t

88 ome-wide methylation patterns in Arabidopsis thaliana are highly stable over generations, with the ex

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

90 ERF105 transcription factors of Arabidopsis thaliana are regulated by different stresses and are inv

91 rotein abundance in Arabidopsis (Arabidopsis thaliana) are predominantly confined to meristematic cel

92 vation by dimers of Arabidopsis (Arabidopsis thaliana) ARF-GEF GNOM, which is involved in polar recyc

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

94 en deficiency of the model plant Arabidopsis thaliana as well as two important vegetable crops, Pak C

95 Whereas growth of A. thaliana at standard temperature (ST; 23 degrees C) is a

96 INEAGE20 (CGL20) in Arabidopsis (Arabidopsis thaliana; AtCGL20), which is a Pro-rich, ~10-kD protein

97 utative ortholog in Arabidopsis (Arabidopsis thaliana), AtCYP94B1, which are involved in apoplastic b

98 n the LAZY1 gene of Arabidopsis (Arabidopsis thaliana; AtLAZY1) was tested by mutating each region an

99 structures of Metacaspase 4 from Arabidopsis thaliana (AtMC4) that modulates Ca(2+)-dependent, damage

100 Arabidopsis (Arabidopsis thaliana) atnfs and atfh mutants, with reduced AtNFS1 or

101 located within the Arabidopsis (Arabidopsis thaliana) AtSCS gene results in two in-frame transcripts

102 In Arabidopsis thaliana, AUXIN RESISTANT1 (AXR1) functions as the E1-li

103 The model plant Arabidopsis thaliana avoids these practical problems and has provide

104 has been extensively studied in Arabidopsis thaliana because of its role creating flowering time div

105 r vascular cell proliferation in Arabidopsis thaliana Both regulators have origins predating vascular

106 s in physiology and phenology in Arabidopsis thaliana (Brassicaceae) due to contemporary climate chan

107 aracterized in the model species Arabidopsis thaliana, but little is known about how transcriptional

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

109 s different organisms, including Arabidopsis thaliana, Caenorhabditis elegans, and Danio rerio.

110 The Arabidopsis thaliana Calmodulin-binding Transcription Activator (CAM

111 The Arabidopsis (Arabidopsis thaliana) calmodulin-binding transcription activator3 (C

112 istem phenotypes of Arabidopsis (Arabidopsis thaliana) CCS52A2-deficient plants in a suppressor mutag

113 Arabidopsis (Arabidopsis thaliana) cells were briefly labeled with 5-ethynyl-2'-d

114 Independent Arabidopsis (Arabidopsis thaliana) cepr1 null mutants showed disproportionately l

115 AtCLCa (Arabidopsis thaliana Chloride Channel a) is a vacuolar NO(3) (-)/H(+

116 e background of the Arabidopsis (Arabidopsis thaliana) chloroplast (cp)ATP synthase assembly mutant c

117 twork, we show that Arabidopsis (Arabidopsis thaliana) chloroplast glutamyl peptidase (CGEP) is a hom

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

119 Arabidopsis (Arabidopsis thaliana) contains 12 ALAs in five phylogenetic clusters

120 TPC in Arabidopsis (Arabidopsis thaliana) contains six evolutionarily conserved subunits

121 rmal function in the model plant Arabidopsis thaliana contribute to the plant microbiome assembly.

122 izing the photosensitive protein Arabidopsis thaliana cryptochrome 2, the light-inducible homo-intera

123 to demonstrate that Arabidopsis (Arabidopsis thaliana) CSLD3 is a UDP-glucose-dependent beta-1,4-gluc

124 The Arabidopsis (Arabidopsis thaliana) cyclin-dependent kinase G1 (CDKG1) is necessar

125 ntally validated interactions in multiple A. thaliana datasets.

126 specific nat-siRNAs in multiple Arabidopsis thaliana datasets.

127 Kinases (CIPKs) of Arabidopsis (Arabidopsis thaliana) decode the calcium signals elicited by environ

128 loss of AHA6, AHA8, and AHA9 in Arabidopsis thaliana delays pollen germination and causes pollen tub

129 ere, we showed that Arabidopsis (Arabidopsis thaliana) DGK2 and DGK4 are crucial for gametogenesis an

130 is, we utilized the Arabidopsis (Arabidopsis thaliana) diacylglycerol acyltransferase mutant dgat1-1

131 g plants, including Arabidopsis (Arabidopsis thaliana), display a number of growth responses, such as

132 he dry seeds of the Arabidopsis (Arabidopsis thaliana) diversity panel using all potential ratios bet

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

134 ches concluded that Arabidopsis (Arabidopsis thaliana) does not produce PROMPTs.

135 The Arabidopsis thaliana E3 ubiquitin ligase COP1 functions in ABA-media

136 Here we use Arabidopsis thaliana ecotypes, mutants and transgenic lines to deter

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

138 re seed maturation, Arabidopsis (Arabidopsis thaliana) embryos are also photosynthetically active, th

139 AMESE (SIM) gene of Arabidopsis (Arabidopsis thaliana) encodes a cyclin-dependent kinase (CDK) inhibi

140 we demonstrate that Arabidopsis (Arabidopsis thaliana) EXO70A2 (At5g52340) is the main exocyst EXO70

141 The Arabidopsis (Arabidopsis thaliana) fatty acid biosynthesis1 (fab1) mutant has inc

142 In Arabidopsis (Arabidopsis thaliana), FER-LIKE FE DEFICIENCY-INDUCED TRANSCRIPTION

143 At Arabidopsis thaliana FLC, antisense transcription quantitatively inf

144 In the model plant Arabidopsis thaliana, floral organogenesis requires AINTEGUMENTA (AN

145 Choosing A. thaliana for further analysis, the defensin pathway was

146 plant-origin deconjugase enzyme (Arabidopsis thaliana) for deconjugation of folates (PE-LC-MS/MS), or

147 E RESPONSE FACTOR (ERF) genes of Arabidopsis thaliana form a large family encoding plant-specific tra

148 tail region of the Arabidopsis (Arabidopsis thaliana) FRA1 kinesin physically interacts with cellulo

149 ions of the model annual species Arabidopsis thaliana from across a wide climate range and scored eac

150 een functional annotations in an Arabidopsis thaliana gene network.

151 d AtGA2ox10, in the Arabidopsis (Arabidopsis thaliana) genome.

152 yl hydrolase 43 (GH43) family in Arabidopsis thaliana GH43 loss-of-function mutants exhibited root ce

153 body against the highly abundant Arabidopsis thaliana globulin seed storage protein cruciferin with t

154 the transcriptomes of a suite of Arabidopsis thaliana glucosinolate-deficient mutants using RNAseq an

155 Arabidopsis thaliana glutamate receptor-like (GLR) channels are amin

156 ed the viability of Arabidopsis (Arabidopsis thaliana) gpt2 mutants, whereas heterozygous gpt1 mutant

157 idate the implication of these genes into A. thaliana growth, six of them were further studied by phe

158 , Ricinus communis, Arabidopsis [Arabidopsis thaliana], Helianthus annuus, Solanum lycopersicum, and

159 ) exchanger regulating stomata aperture in A thaliana Here, we used a genetically encoded biosensor,

160 An Arabidopsis thaliana HglS homolog coexpresses with known lysine cata

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

162 The Arabidopsis thaliana histone acetyltransferase GCN5 regulates histon

163 e, we show that the Arabidopsis (Arabidopsis thaliana) histone methyltransferase SET DOMAIN GROUP8 (S

164 In Arabidopsis thaliana, HPAT1 and HPAT3 are redundantly required for f

165 ld-type recombinant Arabidopsis (Arabidopsis thaliana) HPR1, it was found that HPR1-T335D exhibits re

166 In Arabidopsis (Arabidopsis thaliana), hydrogen sulfide negatively regulates autopha

167 lar networks that control QDR in Arabidopsis thaliana in response to the bacterial pathogen Xanthomon

168 es using mutants of Arabidopsis (Arabidopsis thaliana) in combination with biochemical and physiologi

169 enced accessions of Arabidopsis (Arabidopsis thaliana) in GRANULE-BOUND STARCH SYNTHASE (GBSS), encod

170 ssion of HopO1-1 in Arabidopsis (Arabidopsis thaliana) increases the distance of PD-dependent molecul

171 ions of the seed of Arabidopsis (Arabidopsis thaliana) indicates that omega-9 monoenes are synthesize

172 imited number of experimentally validated A. thaliana interactions and were adapted to fit these spec

173 otein-only RNase P 1 (PRORP1) in Arabidopsis thaliana is an endoribonuclease that uses its PPR domain

174 he auxin biosynthesis pathway in Arabidopsis thaliana is phosphorylated at Threonine 101 (T101).

175 of JAZ proteins in Arabidopsis (Arabidopsis thaliana) is also associated with reduced growth and see

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

177 these claims using Arabidopsis (Arabidopsis thaliana) knock-out mutants lacking either phot2 or chup

178 ic fibroblast cell cultures, and Arabidopsis thaliana leaves.

179 ce JA precursors in Arabidopsis (Arabidopsis thaliana) leaves, but the 13-LOXs responsible for growth

180 present the crystal structure of Arabidopsis thaliana legumain isoform beta (AtLEGbeta) in its zymoge

181 Arabidopsis thaliana lines with altered lignin through down-regulati

182 o expand this knowledge by using Arabidopsis thaliana lines with constitutive ectopic overexpression

183 ncing of cDNAs from Arabidopsis (Arabidopsis thaliana) lines deficient in multiple layers of TE repre

184 interacts with two Arabidopsis (Arabidopsis thaliana) LUNAPARK proteins, LNP1 and LNP2, at three-way

185 specific transcription factors, ARABIDOPSIS THALIANA MERISTEM LAYER 1 (ATML1) and its close homolog,

186 Arabidopsis (Arabidopsis thaliana) mitochondria contain four OXA homologs: OXA1a,

187 soforms support the Arabidopsis (Arabidopsis thaliana) mitochondrially localized Type II FAS.

188 In the model plant Arabidopsis thaliana, most components of the pathway were identified

189 tructures of a MscS homolog from Arabidopsis thaliana, MSL1, presumably in both the closed and open s

190 We isolate a strong hypomorphic Arabidopsis thaliana mutant of the POL2A catalytic subunit of DNA po

191 Transcriptome analysis of Arabidopsis thaliana mutant plants in PAP-SAL1 pathway revealed that

192 m chloroplasts, we have used the Arabidopsis thaliana mutant plastid ferrochelatase two (fc2) that co

193 Here, we show that PTs of Arabidopsis thaliana mutants impaired in the pollen-specific DIACYLG

194 re we analyzed clock function in Arabidopsis thaliana mutants with defective immune responses and fou

195 flavonols in this process using Arabidopsis thaliana mutants with defects in genes encoding key enzy

196 duced senescence of Arabidopsis (Arabidopsis thaliana) mutants deficient in key steps of the PAO/phyl

197 ertile, hypomorphic Arabidopsis (Arabidopsis thaliana) mutants for the essential glucosinolate biosyn

198 ics to a screen for Arabidopsis (Arabidopsis thaliana) mutants involved in the response to the phytoh

199 arative analysis of Arabidopsis (Arabidopsis thaliana) mutants lacking the NMD-related proteins UPF3,

200 mpact of temperature increase on Arabidopsis thaliana mutation, studying whole genome profiles of mut

201 e, we show that the Arabidopsis (Arabidopsis thaliana) Na(+):K(+):2Cl(-) (NKCC) cotransporter CCC1 ha

202 to characterize the Arabidopsis (Arabidopsis thaliana) NatB complex.

203 -S cluster-carrier proteins from Arabidopsis thaliana, NFU4 and NFU5.

204 apping of the SA-binding core of Arabidopsis thaliana NPR4 and its ligand-bound crystal structure.

205 o reconstitution of Arabidopsis (Arabidopsis thaliana) OHPs with chlorophylls and carotenoids and sho

206 We identified Arabidopsis (Arabidopsis thaliana) ORESARA1 (ORE1), the developmental master regu

207 ed biosynthetic pathway genes in Arabidopsis thaliana Our analyses reveal that biosynthetic gene clus

208 Arabidopsis (Arabidopsis thaliana) OXIDATION RESISTANCE2 (AtOXR2) is a mitochondr

209 , root, seed, and stem) model of Arabidopsis thaliana, p-ath773, uniquely capturing the core-metaboli

210 In contrast to A. thaliana, P. patens has more robust CHH methylation, sim

211 urinergic receptor, Arabidopsis (Arabidopsis thaliana) P2K1 (L-type lectin receptor kinase-I.9), was

212 3 genes under the control of the Arabidopsis thaliana phloem specific SUCROSE SYNTHASE 2 (AtSUC2) pro

213 lated region of the Arabidopsis (Arabidopsis thaliana) PHO1 inhibits its translation and influences P

214 ously reported that Arabidopsis (Arabidopsis thaliana) phosphoinositide-specific phospholipase C2 fun

215 troma) in the aerial part of the Arabidopsis thaliana plant.

216 e stress and metabolic status of Arabidopsis thaliana plants.

217 s (HFA) onto TAG in Arabidopsis (Arabidopsis thaliana) plants expressing the castor (Ricinus communis

218 ulating ceh1 mutant Arabidopsis (Arabidopsis thaliana) plants relative to wild-type seedlings.

219 f PIN2:PIN1-HA;pin2 Arabidopsis (Arabidopsis thaliana) plants, which ectopically express predominantl

220 bled a list of all Arabidopsis (Arabid opsis thaliana) plastid preproteins encoded by recently duplic

221 The Arabidopsis (Arabidopsis thaliana) PLD family consists of 12 members, and for som

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

223 For TuMV in Arabidopsis thaliana, profiles were obtained for mechanically inocul

224 Overexpression of this gene in A. thaliana promotes androecium development.

225 r previous study showed that the Arabidopsis thaliana protein arginine methyltransferase AtPRMT3 regu

226 y (PTI) responses already characterized in A thaliana Protein-protein interaction network reconstitut

227 s to the nucleus in Arabidopsis (Arabidopsis thaliana) protoplasts, and VEN4 homologs are present in

228 eins or MDLs) of the model plant Arabidopsis thaliana Recombinant Arabidopsis MDLs (AtMDLs) share sim

229 s of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in conse

230 Landsberg erecta of Arabidopsis (Arabidopsis thaliana) respond differently to phosphate starvation.

231 ound that mutation of FERONIA in Arabidopsis thaliana resulted in plants showing low susceptibility t

232 ructure of the FN3K homolog from Arabidopsis thaliana revealed that it forms an unexpected strand-exc

233 e RNA degradomes of Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), worm (Caenorhabditis ele

234 We show that Arabidopsis (Arabidopsis thaliana) RING Finger ABA-Related1 (RFA1) and RFA4 E3 ub

235 a homologues of the Arabidopsis (Arabidopsis thaliana) ROD1 gene.

236 The Arabidopsis (Arabidopsis thaliana) root epidermis consists of a position-dependen

237 center (QC) of the Arabidopsis (Arabidopsis thaliana) root meristem acts as an organizer that promot

238 ferentiation in the Arabidopsis (Arabidopsis thaliana) root meristem.

239 ora rootlets, S. moellendorffii roots and A. thaliana roots compared to the leaves of each respective

240 Here, we report that in Arabidopsis thaliana roots, auxin controls the spatiotemporal expres

241 pericycle cells of Arabidopsis (Arabidopsis thaliana) roots challenged with two immunity elicitors,

242 naling compounds in Arabidopsis (Arabidopsis thaliana) roots revealed that ABA treatment and uptake d

243 ading interfaces of Arabidopsis (Arabidopsis thaliana) roots.

244 c Pi homeostasis in Arabidopsis (Arabidopsis thaliana) roots.

245 In Arabidopsis thaliana, ROS produced by RBOHC was previously reported

246 These results provide evidence that A. thaliana's germination niche and correlated life-history

247 E and myosin XI phenotypes are rescued by A. thaliana's Rab-E1c and myosin XI-K/E, respectively.

248 be applied in human cell lines, Arabidopsis thaliana, Schizosaccharomyces pombe and Escherichia coli

249 were identified as regulators of Arabidopsis thaliana seedling photomorphogenesis.

250 l mRNA decay during Arabidopsis (Arabidopsis thaliana) seedling development.

251 the effects of cell swelling on Arabidopsis thaliana seedlings and to test the contributions of the

252 ynthesis in the roots of 7-d-old Arabidopsis thaliana seedlings were investigated using tissue-specif

253 When Arabidopsis (Arabidopsis thaliana) seedlings are grown in the dark, hypocotyl elo

254 l uridine (5-EU) in Arabidopsis (Arabidopsis thaliana) seedlings provides insight into plant transcri

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

256 Arabidopsis thaliana serves as a model plant for genetic research, i

257 ave determined that Arabidopsis (Arabidopsis thaliana) SINE1 and SINE2 play an important role in stom

258 The Arabidopsis (Arabidopsis thaliana) SnRK2 family comprises the abscisic acid (ABA)

259 T111 interacts with Arabidopsis (Arabidopsis thaliana) Splicing Factor1, involved in 3' splicing site

260 F-box protein, an orthologue of Arabidopsis thaliana STERILE APETALA (SAP), that forms part of an SK

261 sponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2-1 (AtSMAX1) that functions i

262 ll RNA sequencing (scRNA-seq) in Arabidopsis thaliana tetraploid lines and isogenic diploids, we show

263 not recover viable Arabidopsis (Arabidopsis thaliana) tfIIs plants constitutively expressing TFIISmu

264 In Arabidopsis (Arabidopsis thaliana), the F-box protein F-BOX-LIKE17 (FBL17) was pr

265 In Arabidopsis (Arabidopsis thaliana), the MADS-box transcription factor FRUITFULL i

266 on during stress in Arabidopsis (Arabidopsis thaliana), the mechanism and molecular components of all

267 In Arabidopsis (Arabidopsis thaliana), the transcription factor ILR3 plays a central

268 We demonstrate that, in Arabidopsis thaliana, the 2 RNL families contribute specific functio

269 In Arabidopsis thaliana, the AT-hook motif nuclear-localized (AHL) tran

270 In Arabidopsis thaliana, the cold-induced epigenetic regulation of FLOW

271 In Arabidopsis thaliana, the METTL3 homolog, mRNA adenosine methylase (

272 In Arabidopsis (Arabidopsis thaliana), these processes are primarily modulated by th

273 ely expressed PCO4 and PCO5 from Arabidopsis thaliana to 1.24 and 1.91 angstrom resolution, respectiv

274 We found that exposure of Arabidopsis thaliana to a known plant growth-promoting rhizobacteriu

275 ion of 252 natural accessions of Arabidopsis thaliana to conduct genome-wide association studies (GWA

276 us tremula x alba, Zea mays, and Arabidopsis thaliana to determine its role in trait variation indepe

277 we used the natural variation in Arabidopsis thaliana to perform a genome-wide association study of E

278 positioning (MNase-Seq) data for Arabidopsis thaliana to understand how nucleosome positioning modula

279 ecies, ranging from Arabidopsis (Arabidopsis thaliana) to wheat (Triticum spp.), including many crop

280 We demonstrate that the complexity of the A. thaliana transcriptomes has been substantially under-est

281 Arabidopsis thaliana transcriptomes have been extensively studied an

282 An Arabidopsis (Arabidopsis thaliana) transfer DNA insertion mutant of LAC2 displaye

283 In Arabidopsis (Arabidopsis thaliana), TREHALOSE-6-PHOSPHATE SYNTHASE1 (TPS1) cataly

284 demonstrate that in Arabidopsis (Arabidopsis thaliana), two distinctly localized acetate-activating e

285 In Arabidopsis thaliana, two E3 ligases, BIG BROTHER (BB) and DA2, acti

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

287 JA accumulation in Arabidopsis (Arabidopsis thaliana), unlike its orthologs in tobacco.

288 membrane system in Arabidopsis (Arabidopsis thaliana) using mass spectrometry-based proteomics.

289 ic responses to root wounding in Arabidopsis thaliana We found that root wounding or the application

290 eletons in single plant cells of Arabidopsis thaliana We show that the cytoskeleton aligns with the l

291 leaf development in Arabidopsis (Arabidopsis thaliana), we show that E2FB in association with RBR pla

292 yclins, CYCD3;1 and CYCD4;2 from Arabidopsis thaliana, were expressed by agrobacterial infiltration i

293 Our results show increased sensitivity in A. thaliana when using the PAREameters inferred criteria an

294 ntrast with the angiosperm model Arabidopsis thaliana, where DNA methylation is strongly enriched at

295 Unlike Arabidopsis thaliana whose members of the CBF/DREB1 family respond o

296 nts from the non-medicinal plant Arabidopsis thaliana with human breast cancer cells, selectively sup

297 itiation process in Arabidopsis (Arabidopsis thaliana), with each protein exerting a varying degree o

298 the second plant system, besides Arabidopsis thaliana, with viable mutants with an essentially comple

299 characterization of Arabidopsis (Arabidopsis thaliana) xylan O-acetyltransferase 1 (XOAT1), a member

300 The Arabidopsis thaliana zinc finger transcription factor (ZF-TF), S-nit