ライフサイエンスコーパス: Arabidopsis

1 ein is a major regulator of seed dormancy in Arabidopsis.

2 tigate MYBS1 and MYBS2 in sugar signaling in Arabidopsis.

3 cible RNA interference to knock down SCY2 in Arabidopsis.

4 stomata that are more complex than those of Arabidopsis.

5 r extended darkness and control condition in Arabidopsis.

6 equired for long-term epigenetic fidelity in Arabidopsis.

7 IKE (COL) genes regulate photoperiodicity in Arabidopsis.

8 , members of which control flowering time in Arabidopsis.

9 mediating a proper vernalization response in Arabidopsis.

10 seed germination and seedling development in Arabidopsis.

11 ccumulation triggers cell differentiation in Arabidopsis.

12 ng hydrogen peroxide (H2 O2 ) homeostasis in Arabidopsis.

13 entary way, involved in growth regulation in Arabidopsis.

14 e involved in numerous signaling pathways in Arabidopsis.

15 containment of stress-induced cell death in Arabidopsis.

16 ellular ATP impacts the stability of JAZ1 in Arabidopsis.

17 mon gate-latch-lock mechanism resembling the Arabidopsis ABA receptors, but the ABA binding pocket in

18 Here, we identified novel cofactors of Arabidopsis AGOs, named RICE1 and RICE2.

19 emented the low-K(+) -sensitive phenotype of Arabidopsis akt1 mutant, indicating that ZxAKT1 function

20 ble overexpression of select IQD proteins in Arabidopsis altered cellular MT orientation, cell shape,

21 Gretchen Hagen 3 (GH3) family of proteins in Arabidopsis and belongs to the adenylate-forming family

22 x and dynamic nature of interactions between Arabidopsis and its bacterial pathogen, Pseudomonas syri

23 ar regions of the stomata complexes, both in Arabidopsis and other plants, suggesting a widespread oc

24 l role in root development, DRO1 homologs in Arabidopsis and peach showed root-specific expression.

25 Transactivation activity assays performed in Arabidopsis and rice protoplasts showed that OsPCF2 and

26 Root length was measured in Arabidopsis and rice treated with synthetic RaxX peptide

27 LEN-triggered DSBs to characterize diRNAs in Arabidopsis and rice.

28 and the catalog of ubiquitylation targets in Arabidopsis and show that this post-translational modifi

29 essential function of CBL10 is conserved in Arabidopsis and tomato.

30 for efficient transcriptional repression in Arabidopsis, and demonstrated a more than tenfold reduct

31 Shoot-/root-specific expression of PS-GFP in Arabidopsis, and grafting experiments, revealed that the

32 Here, we show that the Arabidopsis (Arabidopsis thaliana) ADF3 is required in t

33 oot hair cell, and between two model plants: Arabidopsis (Arabidopsis thaliana) and soybean (Glycine

34 The LIL3 protein of Arabidopsis (Arabidopsis thaliana) belongs to the light-

35 Plants with mutations in a homolog of an Arabidopsis (Arabidopsis thaliana) boron efflux transpor

36 ealed that SlCBL10 is a true ortholog of the Arabidopsis (Arabidopsis thaliana) CBL10 gene, supportin

37 factor controlling plant development, on two Arabidopsis (Arabidopsis thaliana) CI mutants: a new ins

38 estigate the internal subunit arrangement of Arabidopsis (Arabidopsis thaliana) complex II.

39 ause a key repressor of light signaling, the Arabidopsis (Arabidopsis thaliana) COP1/SPA E3 ubiquitin

40 The Arabidopsis (Arabidopsis thaliana) COP1/SPA ubiquitin li

41 ized Early flowering3 (Efl3), an ortholog of Arabidopsis (Arabidopsis thaliana) EARLY FLOWERING3 (ELF

42 he first 5 min of innate immune signaling in Arabidopsis (Arabidopsis thaliana) epidermal cells; howe

43 At early stages of Arabidopsis (Arabidopsis thaliana) flowering, the inflor

44 The Arabidopsis (Arabidopsis thaliana) genome contains nine

45 s involved in their biogenesis and action in Arabidopsis (Arabidopsis thaliana) has been described, t

46 Recent findings in Arabidopsis (Arabidopsis thaliana) have demonstrated tha

47 to protect thylakoid membranes prepared from Arabidopsis (Arabidopsis thaliana) leaves against lipid

48 curs at the same time as starch synthesis in Arabidopsis (Arabidopsis thaliana) leaves in the light.

49 n for visual exploration and analysis of the Arabidopsis (Arabidopsis thaliana) metabolic network in

50 ovel TF modules regulating the expression of Arabidopsis (Arabidopsis thaliana) phosphate transporter

51 The Arabidopsis (Arabidopsis thaliana) PI-PLC gene family is

52 have generated SGC (specifically guard cell) Arabidopsis (Arabidopsis thaliana) plants in which the o

53 Arabidopsis (Arabidopsis thaliana) possesses six LAZY ge

54 a (PP) transfer cells (TCs) in leaf veins of Arabidopsis (Arabidopsis thaliana) represents a novel tr

55 tments on nuclear gene expression in various Arabidopsis (Arabidopsis thaliana) retrograde signalling

56 roles, we had previously produced transgenic Arabidopsis (Arabidopsis thaliana) RNA interference (RNA

57 he zygote and proliferating endosperm of the Arabidopsis (Arabidopsis thaliana) seed.

58 interrogate protein synthesis in vegetative Arabidopsis (Arabidopsis thaliana) seedlings.

59 Arabidopsis (Arabidopsis thaliana) seeds of exoribonucle

60 Here, we demonstrate that Arabidopsis (Arabidopsis thaliana) Shewanella-like prote

61 CF222 encodes a protein of 99 amino acids in Arabidopsis (Arabidopsis thaliana) that has similarities

62 This gene, At1g45231, encodes an Arabidopsis (Arabidopsis thaliana) trimethylguanosine sy

63 east one carrier protein and two channels in Arabidopsis (Arabidopsis thaliana) vacuoles.

64 a single cell-based experimental system from Arabidopsis (Arabidopsis thaliana) with high temporal re

65 ine hirsuta from those of its close relative Arabidopsis (Arabidopsis thaliana), and allelic variatio

66 In Arabidopsis (Arabidopsis thaliana), OR increases caroten

67 tiana tabacum) but 100-fold less frequent in Arabidopsis (Arabidopsis thaliana), preventing its use i

68 reads equivalent to 4.5x genome coverage in Arabidopsis (Arabidopsis thaliana), the constructed LTR

69 llulose are perceived as signal molecules in Arabidopsis (Arabidopsis thaliana), triggering a signali

70 would be of help, but unlike the model plant Arabidopsis (Arabidopsis thaliana), very little is known

71 ed rape (Brassica napus) and the model plant Arabidopsis (Arabidopsis thaliana), were unique in showi

72 ance of several histone acetylation marks in Arabidopsis (Arabidopsis thaliana), which was strongly d

73 n the photosynthetic processes and growth of Arabidopsis (Arabidopsis thaliana).

74 rnalization, has been extensively studied in Arabidopsis (Arabidopsis thaliana).

75 osette expansion growth and leaf movement in Arabidopsis (Arabidopsis thaliana).

76 uring Heterodera cyst nematode parasitism of Arabidopsis (Arabidopsis thaliana).

77 east 66 potential PME genes are contained in Arabidopsis (Arabidopsis thaliana).

78 77 and the reduction in accD-C794 editing in Arabidopsis (Arabidopsis thaliana).

79 entiation during early anther development in Arabidopsis (Arabidopsis thaliana).

80 pectin methylesterases (PMEs; 66 members in Arabidopsis [Arabidopsis thaliana]).

81 raploids formed between A. thaliana (At) and Arabidopsis arenosa (Aa), AtCCA1 is expressed at lower l

82 Using Arabidopsis as a host plant species, we conducted a comp

83 In this study, we identified MPK1 and MPK6 (Arabidopsis AtMPK6 and AtMPK4 orthologs, respectively) a

84 dicate that MtLAX2 is a functional analog of Arabidopsis AUX1 and is required for the accumulation of

85 a detailed molecular characterization of the Arabidopsis B-box domain gene BBX32 We showed that the c

86 MtBRI1 is able to complement an Arabidopsis BRI1 mutant, bri1-5.

87 ave improved salt tolerance, was observed in Arabidopsis, but is not well understood.

88 revealed that DELLAs limit meristem size in Arabidopsis by directly upregulating the cell-cycle inhi

89 of DNA methylation at CpG sites, mediated in Arabidopsis by MET1, plays a central role in epigenetic

90 it has been shown that liquid-culture-grown Arabidopsis can take up and store palladium as nanoparti

91 ith stomatal opening experiments in selected Arabidopsis cell wall mutants.

92 essing those primitive bona fide CHIs in the Arabidopsis chi mutant restores the seed coat transparen

93 Arabidopsis contains two OsMYBS1 homologs.

94 viously characterized L407F mutant allele of Arabidopsis cry1 is biologically hyperactive and seems t

95 Arabidopsis cryptochrome 2 (CRY2) can simultaneously und

96 d small molecules in preformed and inducible Arabidopsis defense, a role previously dominated by tryp

97 s in regulating glucose and ABA signaling in Arabidopsis during seed germination and early seedling d

98 ndicating that ET signaling was activated in Arabidopsis early by SCN infection.

99 sperm, in contrast to WOX2 expression in the Arabidopsis embryo.

100 is increased in aox1a knockout mutants from Arabidopsis (especially after restriction of the cytochr

101 part by enhancing the enzymatic activity of Arabidopsis FAAH (AtFAAH).

102 Here we focus on an Arabidopsis gene OXT6 (Oxidative Tolerant-6) that has be

103 This updated Arabidopsis genome annotation with a substantially incre

104 Synteny analysis between the grape and Arabidopsis genomes provided a potential functional rele

105 aracterized TNT-active Arabidopsis thaliana (Arabidopsis) GSTs.

106 Arabidopsis has been used as a source for virus-resistan

107 tained 12 genes whose predicted orthologs in Arabidopsis have been reported as key during pollen deve

108 In species such as Arabidopsis having a single canonical Galpha, this rate

109 directly or indirectly trigger heterosis in Arabidopsis hybrids independent of genetic changes.

110 The behavior of SoPIN1 and PIN1b in Arabidopsis illustrates how membrane and tissue-level ac

111 downstream physical interacting proteins in Arabidopsis interactome.

112 he recognition that the duplicated ACCase in Arabidopsis is an impediment to plastid transformation p

113 o the LATE MERISTEM IDENTITY1 (LMI1) gene of Arabidopsis is the causal gene underlying the l-D1 locus

114 t species, including model organisms such as Arabidopsis, is a major constraint in accurate quantific

115 In another planar tissue, the Arabidopsis leaf epidermis [5], polarized, asymmetric di

116 st DC3000 by promoting pectin degradation in Arabidopsis leaves, and Pst DC3000 might enhance its inf

117 G) gene, ADPG2, and increases PG activity in Arabidopsis leaves, which in turn reduces leaf pectin co

118 sis of transgenic 5' upstream deletion::gusA Arabidopsis lines showed that this region is important f

119 the subcellular localization of the DHARs in Arabidopsis lines stably transformed with GFP fusion pro

120 to the highly-expressed MzASMT9 resulted in Arabidopsis lines with enhanced salt tolerance than wild

121 Analyses of Arabidopsis loss-of-function lines revealed that the eli

122 Previously, we demonstrated that Arabidopsis mitogen-activated protein kinase 6 (MPK6) an

123 In Arabidopsis, MODIFIER OF snc1-1 (MOS1) modulates a numbe

124 can rescue the Mn-sensitive phenotype of the Arabidopsis mtp11-3 knockout mutant.

125 Arabidopsis mucilage has both nonadherent and adherent l

126 In this study, we established another Arabidopsis mutant line harbouring a different allele of

127 genetic mapping and characterization of the Arabidopsis nonhost resistance Phytophthora sojae-suscep

128 DSBs within the examined endogenous genes in Arabidopsis or rice.

129 s or plants (in our laboratory we use either Arabidopsis or tobacco plant seedlings): a Petri dish co

130 roduces a transcript coding for AtCPSF30, an Arabidopsis ortholog of 30 kDa subunit of the Cleavage a

131 conserved, as heterologous (human, mouse and Arabidopsis) Oxs1 and Pap1-homologues can bind interchan

132 The Arabidopsis PENETRATION 3 (PEN3) ATP binding cassette (A

133 e present a compendium of known and putative Arabidopsis peptidases and inhibitors, and compare the d

134 We identified Arabidopsis pex6 and pex26 mutants by screening for inef

135 In this study, two Arabidopsis phospholipase Dzeta genes (AtPLDzeta1 and At

136 Here we show that the C-terminal module of Arabidopsis phytochrome B (PHYB) is sufficient to mediat

137 n-regulated in both OsbHLH068-overexpressing Arabidopsis plants and Atbhlh112 mutant plants, whereas

138 ssion and protein localization in developing Arabidopsis plants and Nicotiana benthamiana leaf epider

139 We grew Arabidopsis plants in very short photoperiods and used a

140 Arabidopsis plants store part of the carbon fixed by pho

141 highly expressed in AtbHLH112-overexpressing Arabidopsis plants.

142 rectly with the regulative N terminus of the Arabidopsis plasma membrane Ca(2+)-ATPase isoform 8 (ACA

143 eal-time dynamics of HG during elongation of Arabidopsis pollen tubes and root hairs.

144 e opposite functions to control flowering in Arabidopsis, presumably due to the evolutionary function

145 Ruthenium Red and Gd(3+), as well as to the Arabidopsis protein MICU, a regulatory MCUC component.

146 Among them, the plasma membrane-associated Arabidopsis proteins OCTOPUS (OPS) and BREVIS RADIX (BRX

147 Transient co-transfections in Arabidopsis protoplasts showed that A-ZIP53 inhibited th

148 In Arabidopsis, PS protein can be processed and SYS is secr

149 hylesterase inhibitors (PMEIs; 76 members in Arabidopsis) questions the specificity of the PME-PMEI i

150 ccessfully enhanced the drought tolerance in Arabidopsis, rapeseed, maize, rice and wheat plants.

151 , which is reminiscent of sex differences in Arabidopsis recombination.

152 The Arabidopsis reductase ornithine cyclodeaminase/mu-crysta

153 BBX32 We showed that the circadian clock in Arabidopsis regulates BBX32 and expressed in the early m

154 Thus PRC2 recruitment in Arabidopsis relies in large part on binding of trans-act

155 lines respectively decrease and increase the Arabidopsis resistance to Pst DC3000, indicating that th

156 found that ectopic expression of PS improves Arabidopsis resistance to the necrotrophic fungus Botryt

157 nscriptional network initiated by the type-B ARABIDOPSIS RESPONSE REGULATORs (ARRs) that mediate the

158 eas overexpression of LecRK-I.8 enhances the Arabidopsis response to NAD(+).

159 ionally, heterologous functional analyses in Arabidopsis resulted in flowering time phenotypes in lin

160 the crosstalk between the three hormones in Arabidopsis root development.

161 g of the transcriptional networks underlying Arabidopsis root endodermal differentiation.

162 BS: beta-glucuronidase (GUS) was detected in Arabidopsis root tips as early as 6 h post infection, in

163 sess the dynamic changes in the methylome of Arabidopsis roots in response to H. schachtii infection.

164 to show that phloem unloading of solutes in Arabidopsis roots occurs through plasmodesmata by a comb

165 ogical function, and chemical composition of Arabidopsis roots.

166 koc1 Arabidopsis seedlings had reduced survival rates after t

167 Here, we report that the Arabidopsis SITE-1 PROTEASE (S1P) cleaves endogenous RAP

168 S analysis of closely-related plant species (Arabidopsis spp.) has many advantages over laboratory-ba

169 n the N-terminal region of SS4 and GS in the Arabidopsis ss4 mutant.

170 C3000, indicating that the gene promotes the Arabidopsis susceptibility to Pst DC3000.

171 eubacteria, and oomycete) converge onto the Arabidopsis TCP14 transcription factor to manipulate hos

172 rived from chloroplast-derived precursors in Arabidopsis tgd1-1 is converted into oligogalactolipids,

173 We confirmed that Arabidopsis TGS1 is a functional ortholog of other trime

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

189 Arabidopsis thaliana backgrounds with altered activities

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

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

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

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

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

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

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

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

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

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

200 lutathionylation induced deactivation of the Arabidopsis thaliana kinase BRASSINOSTEROID INSENSITIVE

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

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

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

204 actolipids that accumulate in the respective Arabidopsis thaliana mutants.

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

206 We exposed Arabidopsis thaliana plants to herbivory and investigate

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

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

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

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

211 Arabidopsis thaliana seed development requires the conco

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 In Arabidopsis thaliana, disruption of two subunits of the

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

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

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

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

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

283 In Arabidopsis thaliana, these include marked stem elongati

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

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

286 nomous key regulators of phloem formation in Arabidopsis thaliana.

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

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

289 nse machinery against microbial pathogens in Arabidopsis thaliana.

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

291 sm affecting the reproductive development in Arabidopsis that could be translated to crops for increa

292 r AtMUTE, which defines GC precursor fate in Arabidopsis The novel role of BdMUTE in specifying later

293 ge in hypocotyl length when overexpressed in Arabidopsis, the overexpression of full-length OsbZIP48

294 We have recently established that in Arabidopsis, the regulator of G-protein signaling (RGS1)

295 In many plants, including Arabidopsis, the sepals and petals form distinctive nano

296 that associate with the THO core complex of Arabidopsis TREX.

297 nucleus following UV-B exposure, similar to Arabidopsis UVR8, but M. polymorpha UVR8 has weaker dime

298 The role of the GET system in Arabidopsis was investigated by monitoring the membrane

299 Here, using co-purification with TOC159 from Arabidopsis, we discovered a novel component of the chlo

300 lates in coriander, a study was conducted in Arabidopsis, where twofold increase in folates occurred

301 orthologs, by genetic complementation of the Arabidopsis wri1 mutant.