ライフサイエンスコーパス: thaliana

1 atode parasitism of Arabidopsis (Arabidopsis thaliana).

2 diated processes in Arabidopsis (Arabidopsis thaliana).

3 es are contained in Arabidopsis (Arabidopsis thaliana).

4 died intensively in Arabidopsis (Arabidopsis thaliana).

5 re, with a focus on Arabidopsis (Arabidopsis thaliana).

6 ization response in Arabidopsis (Arabidopsis thaliana).

7 odera schachtii and Arabidopsis (Arabidopsis thaliana).

8 ccD-C794 editing in Arabidopsis (Arabidopsis thaliana).

9 in the model plant Arabidopsis (Arabidopsis thaliana).

10 he pap7-1 mutant of Arabidopsis (Arabidopsis thaliana).

11 ther development in Arabidopsis (Arabidopsis thaliana).

12 ensively studied in Arabidopsis (Arabidopsis thaliana).

13 nd leaf movement in Arabidopsis (Arabidopsis thaliana).

14 esses and growth of Arabidopsis (Arabidopsis thaliana).

15 egulators of phloem formation in Arabidopsis thaliana.

16 n chromatin modification in root cells of A. thaliana.

17 f mRNA m(6) A writer proteins in Arabidopsis thaliana.

18 ization or limited translocation of Ga in A. thaliana.

19 cient knock-out mutant (porB) of Arabidopsis thaliana.

20 jectories of shoot stem cells in Arabidopsis thaliana.

21 the 73 members of this family in Arabidopsis thaliana.

22 genes regulated by silencing in Arabidopsis thaliana.

23 RNA-directed DNA methylation in Arabidopsis thaliana.

24 esponsible for most of CH3Cl emissions by A. thaliana.

25 male reproductive development in Arabidopsis thaliana.

26 As accumulation and tolerance in Arabidopsis thaliana.

27 flowering time-related traits in Arabidopsis thaliana.

28 on of MYC TFs to JA responses in Arabidopsis thaliana.

29 mulation, translocation and speciation in A. thaliana.

30 nd leaf development in C. hirsuta than in A. thaliana.

31 y against microbial pathogens in Arabidopsis thaliana.

32 karyotes tested, including C. elegans and A. thaliana.

33 50% in B. distachyon and by about 35% in A. thaliana.

34 drought tolerance was studied in Arabidopsis thaliana.

35 PMEs; 66 members in Arabidopsis [Arabidopsis thaliana]).

36 xon, and 0.6695 nucleotide structure) and A. thaliana (0.5808 for CDS, 0.5955 for exon, and 0.8839 nu

37 r of genes to that for the plant Arabidopsis thaliana (25,000), the CMR is close to its known wild-ty

38 In Arabidopsis thaliana, 45S rRNA genes are found in two large ribosoma

39 been carried out in Arabidopsis (Arabidopsis thaliana), a dicot.

40 In Arabidopsis thaliana, a glycosyl transferase family 37 (GT37) fucosy

41 n in ABA levels among nearly 300 Arabidopsis thaliana accessions exposed to the same low water-potent

42 ling, floral bud, and root of 19 Arabidopsis thaliana accessions to examine the age and sequence dive

43 salt stress is widespread among Arabidopsis thaliana accessions(2).

44 Using natural Arabidopsis thaliana accessions, we identified two major recombinati

45 rizing and comparing MITEs in 19 Arabidopsis thaliana accessions.

46 of coding sequence and expression across A. thaliana accessions.

47 investigated in 18 Arabidopsis (Arabidopsis thaliana) accessions using PHENOPSIS, an automated pheno

48 e, we show that the Arabidopsis (Arabidopsis thaliana) ADF3 is required in the phloem for controlling

49 ydroponically grown Arabidopsis (Arabidopsis thaliana) adjusts its physiology and Fe protein composit

50 fects of SV on the resistance of Arabidopsis thaliana against Botrytis cinerea infection.

51 ted "S"-shaped conformation when bound to A. thaliana AHAS (AtAHAS) with the pyrimidinyl group insert

52 this study, we characterize the Arabidopsis thaliana Alpha Thalassemia-mental Retardation X-linked (

53 of phosphate stress response in Arabidopsis thaliana also directly repress defence, consistent with

54 The hypocotyls of Arabidopsis (Arabidopsis thaliana) also elongate in response to sucrose.

55 ment in the Brassicaceae species Arabidopsis thaliana and Arabis alpina, respectively.

56 ree relatives of the model plant Arabidopsis thaliana and assembled all three genomes into only a few

57 We show in Arabidopsis thaliana and Brassica nigra that localized FR enrichment

58 ween the closely related species Arabidopsis thaliana and Cardamine hirsuta.

59 s that infect the model organism Arabidopsis thaliana and important crops such as Brassica.

60 of GBF3 in imparting drought tolerance in A. thaliana and indicate the conserved role of this gene in

61 etics of stomatal conductance in Arabidopsis thaliana and its dependence on vapor pressure difference

62 In our performance tests on E. coli, A. thaliana and Maylandia zebra data sets, HALC was able to

63 inter-nucleosomal linker DNA in Arabidopsis thaliana and mouse.

64 engineered an H3.3 knockdown in Arabidopsis thaliana and observed transcription reduction that predo

65 Using Arabidopsis (Arabidopsis thaliana) and barley (Hordeum vulgare), we show that the

66 n two model plants: Arabidopsis (Arabidopsis thaliana) and soybean (Glycine max).

67 We used mutants of Arabidopsis (Arabidopsis thaliana) and the expression of oleogenic factors to inv

68 Using Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum) as models, w

69 its close relative Arabidopsis (Arabidopsis thaliana), and allelic variation at many loci contribute

70 flowering time related traits in Arabidopsis thaliana, and detected some previously reported genes th

71 uously absent in the model plant Arabidopsis thaliana, and little is known about the enzymatic steps

72 viously characterized TNT-active Arabidopsis thaliana (Arabidopsis) GSTs.

73 le bHLH (MdbHLH) genes and their Arabidopsis thaliana (Arabidopsis) orthologs indicated that they can

74 ammonium transporters (AMTs) in Arabidopsis thaliana are efficiently inactivated by phosphorylation

75 ed that blunt-ended telomeres in Arabidopsis thaliana are protected by Ku, a DNA repair factor with a

76 Using Arabidopsis thaliana as a model, we present evidence for the involve

77 e/Fe(II)-dependent oxygenases in Arabidopsis thaliana as JA hydroxylases and show that they down-regu

78 from a 313-ecotype Arabidopsis (Arabidopsis thaliana) association panel.

79 time series of methyl JA-treated Arabidopsis thaliana at 15 time points over a 16-h period.

80 both change root development in Arabidopsis thaliana at an unprecedented level of temporal detail.

81 In the allotetraploids formed between A. thaliana (At) and Arabidopsis arenosa (Aa), AtCCA1 is ex

82 d Plasmodium falciparum (Pf) and Arabidopsis thaliana (At) SHMT in target assays and PfNF54 strains i

83 e ER-localized co-chaperone from Arabidopsis thaliana, AtBAG7.

84 the ion selectivity of TPC1 from Arabidopsis thaliana (AtTPC1) and compared its selectivity with the

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

86 AX2, a paralogue of Arabidopsis (Arabidopsis thaliana) AUX1, as being induced at early stages of nodu

87 Finally, both Arabidopsis thaliana auxin efflux transporter pin1 and influx transp

88 to regulate stomatal closure in Arabidopsis thaliana, B. napus or both species.

89 Arabidopsis thaliana backgrounds with altered activities based on ta

90 The LIL3 protein of Arabidopsis (Arabidopsis thaliana) belongs to the light-harvesting complex (LHC)

91 ed by two different Arabidopsis (Arabidopsis thaliana) beta-glucosidases from glycoside hydrolase fam

92 in a homolog of an Arabidopsis (Arabidopsis thaliana) boron efflux transporter displayed boron defic

93 enetics analyses in Arabidopsis (Arabidopsis thaliana), but corresponding information is lacking outs

94 ic hyperaccumulation can be engineered in A. thaliana by knocking out the HAC1 gene and expressing Pv

95 this study, we modified the cell wall of A. thaliana by targeting the starch-binding domains of A. t

96 ure and activity to Arabidopsis (Arabidopsis thaliana) CAD5 and Populus tremuloides sinapyl alcohol d

97 Transient expression of seven TPSs from A. thaliana, Capsella rubella, and Brassica oleracea in Nic

98 rue ortholog of the Arabidopsis (Arabidopsis thaliana) CBL10 gene, supporting that the essential func

99 lem vessel cells of Arabidopsis (Arabidopsis thaliana) ccr1 mutants.

100 drugs from the Profen family, in Arabidopsis thaliana cells and the Arabidopsis plant.

101 glutamine, and further with peptides, in A. thaliana cells.

102 ction in a background in which the native A. thaliana CENH3 is replaced with CENH3s from distant spec

103 on outcrossing, show a binding pattern on A. thaliana centromere repeats that is indistinguishable fr

104 development, on two Arabidopsis (Arabidopsis thaliana) CI mutants: a new insertion mutant interrupted

105 ond to orthologs of Arabidopsis (Arabidopsis thaliana) circadian clock genes EARLY FLOWERING3 (ELF3),

106 put of sugar to the Arabidopsis (Arabidopsis thaliana) circadian network.

107 unit arrangement of Arabidopsis (Arabidopsis thaliana) complex II.

108 In Arabidopsis thaliana, CONSTANS (CO) plays an essential role in the r

109 ER bodies in Arabidopsis thaliana contain large amounts of beta-glucosidases, but

110 Arabidopsis (Arabidopsis thaliana) contains two enzymes (encoded by the At1g80950

111 ight signaling, the Arabidopsis (Arabidopsis thaliana) COP1/SPA E3 ubiquitin ligase causes the degrad

112 The Arabidopsis (Arabidopsis thaliana) COP1/SPA ubiquitin ligase is a central repress

113 Arabidopsis (Arabidopsis thaliana) CPK4 and soybean (Glycine max) CDPKbeta are Rc

114 hat mutation in the Arabidopsis (Arabidopsis thaliana) CPO-coding gene At5g63290 (AtHEMN1) adversely

115 The prototype, Arabidopsis thaliana cry1, regulates several light responses during

116 for exploring multiple levels of Arabidopsis thaliana data through a zoomable user interface.

117 the three annotated Arabidopsis (Arabidopsis thaliana) DHARs.

118 In Arabidopsis thaliana, disruption of two subunits of the transcriptio

119 al PMEIs induced in Arabidopsis (Arabidopsis thaliana) during B. cinerea infection.

120 Here, we report that, in Arabidopsis thaliana, during the onset of the HR, the bacterial effe

121 l3), an ortholog of Arabidopsis (Arabidopsis thaliana) EARLY FLOWERING3 (ELF3) that confers early flo

122 ecta (Ler) and a number of other Arabidopsis thaliana ecotypes.

123 explored within the Arabidopsis (Arabidopsis thaliana) embryo by putting seeds under GA-limiting cond

124 immune signaling in Arabidopsis (Arabidopsis thaliana) epidermal cells; however, the immune signals t

125 e panel of over 500 Arabidopsis (Arabidopsis thaliana) epigenetic hybrid plants (epiHybrids), which w

126 Out of 23 Arabidopsis thaliana EXO70 isoforms, we analyzed seven isoforms expr

127 istematic region of Arabidopsis (Arabidopsis thaliana) experiences a local energy deprivation state a

128 unctional fluorescent version of Arabidopsis thaliana FLA4 we show that this protein is localized at

129 At early stages of Arabidopsis (Arabidopsis thaliana) flowering, the inflorescence stem undergoes ra

130 R1), was strongly upregulated in Arabidopsis thaliana flowers subjected to Cu deficiency.

131 tion of selected target genes of Arabidopsis Thaliana from microarray time series data obtained under

132 ith mitochondrial DNA (mtDNA) in Arabidopsis thaliana Gain- and loss-of-function mutants provided evi

133 The Arabidopsis thaliana gene XYLEM NAC DOMAIN1 (XND1) is upregulated in

134 Here, we identified a single Arabidopsis thaliana gene, At3g57630, in clade E of the inverting Gl

135 stematic search for Arabidopsis (Arabidopsis thaliana) genes encoding proteins resembling enzymes inv

136 The Arabidopsis (Arabidopsis thaliana) genome contains nine beta-amylase (BAM) genes,

137 The Arabidopsis (Arabidopsis thaliana) genome encodes homologs of the Guided Entry of

138 data from 488 recombinant inbred Arabidopsis thaliana genomes, we identified 6502 segregating structu

139 uated using the Oryza sativa and Arabidopsis thaliana genomes.

140 se-5-phosphate synthase (SlDXS), Arabidopsis thaliana geranyl diphosphate synthase 1 (AtGPS) and Ment

141 f the age-related changes in the Arabidopsis thaliana glycated proteome, including the proteins affec

142 The Arabidopsis (Arabidopsis thaliana) gynoecium consists of two congenitally fused c

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

144 nesis and action in Arabidopsis (Arabidopsis thaliana) has been described, these processes and their

145 tudies with model plants such as Arabidopsis thaliana have revealed that phytohormones are central re

146 d in the process in Arabidopsis (Arabidopsis thaliana) have been identified and analyzed.

147 Recent findings in Arabidopsis (Arabidopsis thaliana) have demonstrated that auxin-induced SMALL AUX

148 olysis and lipid biosynthesis in Arabidopsis thaliana Here, we identify mechanistic links between KIN

149 study, Lipaphis erysimi induced Arabidopsis thaliana HIPVs were collected using headspace system and

150 AtHB1 is an Arabidopsis (Arabidopsis thaliana) homeodomain-leucine zipper transcription facto

151 assicaoleracea) and Arabidopsis (Arabidopsis thaliana) hydathodes.

152 For comparison, average speed in the A. thaliana hypocotyl expressing GFP-AtCESA6 was 184 +/- 86

153 ng periodic diurnal variation in Arabidopsis thaliana hypocotyl growth, we found that cellulose synth

154 regulation of photosynthesis in Arabidopsis thaliana in an evolutionary context, to provide new insi

155 The flowering plant Arabidopsis thaliana is a dicot model organism for research in many

156 e genomes of fungi and the plant Arabidopsis thaliana, it remains unclear how UPF1 is activated outsi

157 t sufficient for root hair development in A. thaliana, it suggests that there are differences in the

158 main-containing F-box protein in Arabidopsis thaliana KFB(CHS) physically interacts with CHS and spec

159 tion induced deactivation of the Arabidopsis thaliana kinase BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED

160 An analysis of all known sequences in the A. thaliana kinome found that alphaC helix disorder may be

161 NPC-k motif at the C terminus of Arabidopsis thaliana KNL2, which is conserved among a wide spectrum

162 taining proteins of Arabidopsis (Arabidopsis thaliana [L.] Heynh) that will be useful for both the id

163 starch granules in Arabidopsis (Arabidopsis thaliana) leaf chloroplasts requires STARCH SYNTHASE 4 (

164 nvolved in granule initiation in Arabidopsis thaliana leaves.

165 ranes prepared from Arabidopsis (Arabidopsis thaliana) leaves against lipid peroxidation.

166 starch synthesis in Arabidopsis (Arabidopsis thaliana) leaves in the light.

167 reen, we identified a transgenic Arabidopsis thaliana line with longer etiolated hypocotyls, which ov

168 ted by the roots of Arabidopsis (Arabidopsis thaliana) lines carrying insertions in the UDP-Glc:stero

169 Here, we show that Arabidopsis (Arabidopsis thaliana) lines carrying mutations in different steps of

170 By screening an Arabidopsis thaliana lncRNA custom-made array we identified CDF5 LON

171 entified a role for Arabidopsis (Arabidopsis thaliana) MAP KINASE17 (MPK17) in affecting peroxisome d

172 mbers in the entire Arabidopsis (Arabidopsis thaliana) MCTP family.

173 and analysis of the Arabidopsis (Arabidopsis thaliana) metabolic network in the chloroplast and relat

174 lements in stems of Arabidopsis (Arabidopsis thaliana), Miscanthus x giganteus, and notably sugar bee

175 ses (MKPs), such as Arabidopsis (Arabidopsis thaliana) MKP1, are important negative regulators of MAP

176 Arabidopsis thaliana mlo2 mlo6 mlo12 triple mutant plants exhibit co

177 g PSI particles isolated from an Arabidopsis thaliana mutant that accumulates zeaxanthin constitutive

178 m analysis of feedback-resistant Arabidopsis thaliana mutants for the three allosteric committed enzy

179 lated E-2-hexenal response (her) Arabidopsis thaliana mutants.

180 hat accumulate in the respective Arabidopsis thaliana mutants.

181 extended darkness, Arabidopsis (Arabidopsis thaliana) mutants with disruption of autophagy (atg muta

182 In Arabidopsis (Arabidopsis thaliana), mutations in either CCS52A1 or CCS52A2 activa

183 In Arabidopsis thaliana, mutations in the MAP65-3 gene lead to serious

184 We found that Arabidopsis thaliana MYB36, which have been previously shown to regu

185 N-terminal peptides in prt6, an Arabidopsis thaliana N-end rule mutant lacking the E3 ligase PROTEOL

186 In Arabidopsis (Arabidopsis thaliana), NORTIA, a member of the MILDEW RESISTANCE LOC

187 In Arabidopsis (Arabidopsis thaliana), OR increases carotenoid levels by posttranscr

188 ta from distinct species such as Arabidopsis thaliana, Oryza sativa, and Physcomitrella patens to exa

189 usculus, Drosophila melanogaste, Arabidopsis thaliana, Oryza sativa, Physcomitrella patens and Chlamy

190 Production of CH3Cl by A. thaliana paralleled HOL1 expression, as assessed by a fl

191 nowledge, the first Arabidopsis (Arabidopsis thaliana) pex1 missense alleles: pex1-2 and pex1-3pex1-2

192 Arabidopsis (Arabidopsis thaliana) PGK1 was localized exclusively in the chloropl

193 g the expression of Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comprising MYB15

194 loromethane dehalogenase cmuA gene in the A. thaliana phyllosphere correlated with HOL1 genotype, as

195 The Arabidopsis (Arabidopsis thaliana) PI-PLC gene family is composed of nine members

196 erated a transgenic Arabidopsis (Arabidopsis thaliana) plant expressing H(+)-ATPase isoform 2 (AHA2)

197 In this work, Arabidopsis thaliana plants containing a T-DNA disruption of the bil

198 GUS fusion study with transgenic Arabidopsis thaliana plants found that SbCAD2 promoter is functional

199 We exposed Arabidopsis thaliana plants to herbivory and investigated plasticity

200 quired for growth acclimation of Arabidopsis thaliana plants under controlled photoinhibitory light a

201 s, focusing on vernalization, in Arabidopsis thaliana plants.

202 fically guard cell) Arabidopsis (Arabidopsis thaliana) plants in which the oscillator gene CIRCADIAN

203 enerated transgenic Arabidopsis (Arabidopsis thaliana) plants overexpressing the Rieske FeS protein (

204 Here, we show that Arabidopsis (Arabidopsis thaliana) plants require starch for surviving submergenc

205 atment of flowering Arabidopsis (Arabidopsis thaliana) plants with GA specifically affects the proces

206 been synthesized in Arabidopsis (Arabidopsis thaliana) plants.

207 biochemical properties of three Arabidopsis thaliana PMTs (AtPMT1-3) and determined the X-ray crysta

208 s we identified a novel class of Arabidopsis thaliana pollen-borne CRPs, the PCP-Bs (for pollen coat

209 Arabidopsis (Arabidopsis thaliana) possesses six LAZY genes having spatially dist

210 ld less frequent in Arabidopsis (Arabidopsis thaliana), preventing its use in plastid biology.

211 rtance was investigated using an Arabidopsis thaliana protoplast system.

212 nformational dynamics of two key Arabidopsis thaliana receptor-like kinases, brassinosteroid-insensit

213 etabolite profiling utilizing a number of A. thaliana relatives within Brassicaceae identified a clea

214 h Structure-seq data analysis in Arabidopsis thaliana, released with this work.

215 Their function in Arabidopsis (Arabidopsis thaliana) remained unclear because neither tan1 nor air9

216 s) in leaf veins of Arabidopsis (Arabidopsis thaliana) represents a novel trait of heteroblasty.

217 getative tissues of Arabidopsis (Arabidopsis thaliana), repressive methylation marks are enriched in

218 tterns of gene expression during Arabidopsis thaliana reproduction using single nucleotide polymorphi

219 ricentromeric heterochromatin of Arabidopsis thaliana requires SMC4, a core subunit of condensins I a

220 erexpression of both EcGBF3 and AtGBF3 in A. thaliana resulted in improved tolerance to osmotic stres

221 pression in various Arabidopsis (Arabidopsis thaliana) retrograde signalling mutants.

222 X1C, and AOX1D from Arabidopsis (Arabidopsis thaliana) revealed that cysteine residues, CysI and CysI

223 erminal IMS domain of Toc75 from Arabidopsis thaliana, revealing three tandem polypeptide transport-a

224 Manipulation of A. thaliana RFO content by overexpressing ZmGOLS2, ZmRS, or

225 produced transgenic Arabidopsis (Arabidopsis thaliana) RNA interference (RNAi) seeds with lower trans

226 10, the most abundant beta-glucosidase in A. thaliana root ER bodies, hydrolyzes indole glucosinolate

227 required for colonization of the Arabidopsis thaliana root system.

228 hair cells (trichoblasts) of the Arabidopsis thaliana root where they positively regulate root hair c

229 specifically in the Arabidopsis (Arabidopsis thaliana) root tip, allowing a genetic screen to identif

230 ty in leaves of the Arabidopsis (Arabidopsis thaliana) rosette throughout the vegetative stage of gro

231 Arabidopsis thaliana seed development requires the concomitant devel

232 l RFO amounts, positively correlated with A. thaliana seed vigor, to which stachyose and verbascose c

233 ins integral to the Arabidopsis (Arabidopsis thaliana) seed coat mucilage, a specialized layer of the

234 ng endosperm of the Arabidopsis (Arabidopsis thaliana) seed.

235 ts from light-grown Arabidopsis (Arabidopsis thaliana) seedlings, which were overlaid on time-matched

236 hesis in vegetative Arabidopsis (Arabidopsis thaliana) seedlings.

237 Unlike maize, Arabidopsis thaliana seeds contain several RFOs (raffinose, stachyos

238 Arabidopsis (Arabidopsis thaliana) seeds of exoribonuclease4 (xrn4) and varicose

239 Here, we demonstrate the Arabidopsis thaliana SG2-type R2R3-MYB transcription factor MYB15 as

240 we demonstrate that Arabidopsis (Arabidopsis thaliana) Shewanella-like protein phosphatase 2 (AtSLP2)

241 g and noncoding RNAs in roots of Arabidopsis thaliana shifted from replete to deficient phosphorous (

242 periments using the model system Arabidopsis thaliana showed that monothioarsenate is less toxic than

243 Interspecific pollination of A.thaliana significantly up-regulated thionins and defensi

244 10 and KIN11 of the Arabidopsis (Arabidopsis thaliana) SnRK1 complex interact with the STOREKEEPER RE

245 that is inherently less stable within the A. thaliana species.

246 Arabidopsis (Arabidopsis thaliana) spongy (spg) and uneven pattern of exine (upex

247 y targeting the starch-binding domains of A. thaliana starch synthase III to this structure.

248 OSPHOHYDROLASE (PAH) activity in Arabidopsis thaliana stimulates biosynthesis of the major phospholip

249 The Arabidopsis thaliana strain Cvi has depleted gene body methylation r

250 high methylation variability across many A. thaliana strains at that site are the strongest predicto

251 the phylogenetic lineage from cassava to A. thaliana, suggests that alterations in the electrogenici

252 The Arabidopsis thaliana suppressor of quenching1 (soq1) mutant exhibits

253 sp hordei) in Arabidopsis thaliana Surprisingly, VPS9a acts in addition to two pre

254 A new mutant in Arabidopsis thaliana that displays twisting in petals and roots, at

255 The SNARE SYP121 of Arabidopsis thaliana that facilitates vesicle fusion at the plasma m

256 irregularities in cell walls of Arabidopsis thaliana that increase enzyme accessibility without nega

257 s limiting meiotic crossovers in Arabidopsis thaliana that rely on the activity of FANCM, RECQ4, and

258 f 99 amino acids in Arabidopsis (Arabidopsis thaliana) that has similarities to the cysteine-rich zin

259 SS) of a reporter gene fusion in Arabidopsis thaliana The intron increased expression from all transc

260 iferation during organ growth in Arabidopsis thaliana The peptidase is activated by two RING E3 ligas

261 logically relevant conditions in Arabidopsis thaliana The possible role of zeaxanthin in PSI photopro

262 ay in response to heat stress in Arabidopsis thaliana The similarity of ferroptosis in animal cells a

263 genome coverage in Arabidopsis (Arabidopsis thaliana), the constructed LTR library showed excellent

264 In Arabidopsis (Arabidopsis thaliana), the lysine (Lys) aminotransferase AGD2-LIKE D

265 In the rosid species Arabidopsis thaliana, the AP2-type AP2 transcription factor represen

266 In Arabidopsis thaliana, the GLX system is encoded by three homologs of

267 In plants such as Arabidopsis thaliana, the most prominent corepressor is TOPLESS (TPL

268 In Arabidopsis thaliana, these include marked stem elongation and leaf

269 In Arabidopsis (Arabidopsis thaliana), three regions on the pollen surface lack depo

270 ted after 10 days of exposure of Arabidopsis thaliana to 10 mg.L(-1) of negatively or positively char

271 The transcriptomic response of A. thaliana to 2,5-dichlorobiphenyl (2,5-DCB), and its OH m

272 ) measurements were performed on Arabidopsis thaliana to quantify the dependence of the response of N

273 o investigate sparsely annotated Arabidopsis thaliana transcription factors interactions.

274 Here, we show that two Arabidopsis thaliana transcription factors, FAR1 RELATED SEQUENCE 7

275 In the reference plant Arabidopsis thaliana, tRFs are processed by Dicer-like 1 and incorpo

276 signal molecules in Arabidopsis (Arabidopsis thaliana), triggering a signaling cascade that shares so

277 1g45231, encodes an Arabidopsis (Arabidopsis thaliana) trimethylguanosine synthase (TGS1), previously

278 studies have been published for Arabidopsis thaliana, uncovering many expression quantitative trait

279 ent rare RNA species from plant, Arabidopsis thaliana, using surface-enhanced Raman spectroscopy (SER

280 and two channels in Arabidopsis (Arabidopsis thaliana) vacuoles.

281 ike the model plant Arabidopsis (Arabidopsis thaliana), very little is known about floral induction i

282 variation of metal tolerance in Arabidopsis thaliana was investigated.

283 , DII) protein from Arabidopsis (Arabidopsis thaliana) was modified for use in maize (Zea mays).

284 ne variant on gene expression in Arabidopsis thaliana We demonstrate that the arp6 mutant exhibits an

285 ping of m(5)C in the model plant Arabidopsis thaliana We discovered more than a thousand m(5)C sites

286 ININ-INDEPENDENT 1 (CKI1RD) from Arabidopsis thaliana We observed that the crystal structures of free

287 organellar peptidase network in Arabidopsis thaliana We present a compendium of known and putative A

288 retrovirus, with the model plant Arabidopsis thaliana We show that the autophagy cargo receptor NEIGH

289 ines of the model plant species, Arabidopsis thaliana We then show that MMR deficiency greatly increa

290 vation treatment in Arabidopsis (Arabidopsis thaliana), we investigated the malleability of the DNA m

291 Using a reverse genetic strategy in A. thaliana, we identified PRR2 as a positive regulator of

292 impacts of Ga in the model plant Arabidopsis thaliana were investigated in medium culture.

293 and the model plant Arabidopsis (Arabidopsis thaliana), were unique in showing NLR expression skewed

294 cetylation marks in Arabidopsis (Arabidopsis thaliana), which was strongly diminished in the presence

295 has been dissected in the dicot Arabidopsis thaliana, which has green, photosynthetic seeds, but our

296 Here, mutants of Arabidopsis thaliana with altered root hair phenotypes were used to

297 s investigated using variants of Arabidopsis thaliana with low, wild-type and high expression of HOL1

298 uptake during the interaction of Arabidopsis thaliana with the necrotrophic fungus Botrytis cinerea u

299 imental system from Arabidopsis (Arabidopsis thaliana) with high temporal resolution allowing for inv

300 easurements on PSI isolated from Arabidopsis thaliana WT in dark-adapted and high-light-stressed (NPQ