ライフサイエンスコーパス: Medicago

1 ed ectopically in transformed hairy roots of Medicago.

2 erases in triterpene saponin biosynthesis in Medicago.

3 tion for early flowering in LD conditions in Medicago.

4 n seed dispersal strategies that occurred in Medicago, a genus belonging to the large legume family.

5 at SpWRKY functions in a manner analogous to Medicago and Arabidopsis homologs that regulate cell wal

6 to characterize conserved AS events between Medicago and Arabidopsis.

7 pathogen that causes anthracnose disease in Medicago and other closely related legumes.

8 In Medicago and related legume species, the bacteria underg

9 upinus angustifolius, was investigated using Medicago and Trifolium as test plants.

10 nother is likely key to regulatory output in Medicago, and they may be located kilobases distal to th

11 Genes encoding the single Medicago anthocyanidin synthase (ANS; EC 1.14.11.19) and

12 sely related nonhost species, spotted medic (Medicago arabica), unique profiles were released.

13 of the in silico-predicted AS events within Medicago, as well as to characterize conserved AS events

14 teraction between Sinorhizobium meliloti and Medicago, bacteroid differentiation is driven by an endo

15 MtNST1 is the only family member in Medicago, but has three homologs (AtNST1-AtNST3) in Arab

16 RN2 represses the transition to flowering in Medicago by regulating the onset of expression of the po

17 egrees C but did not cold acclimate, whereas Medicago falcata cold acclimated and survived -14 degree

18 the tobacco retrotransposon Tnt1 to tag the Medicago genome and generated over 7600 independent line

19 Conversely, Medicago has a VERNALISATION2-LIKE VEFS-box gene (MtVRN2

20 ng in the model legume, Medicago truncatula (Medicago) is accelerated by winter cold (vernalisation)

21 However, Medicago, like some other plants, lacks the activator CO

22 phased siRNAs (phasiRNAs) found at least 114 Medicago loci, the majority of which were defense-relate

23 ursor for proanthocyanidin biosynthesis, and Medicago MATE1 complements the seed proanthocyanidin phe

24 Here, we show that Arabidopsis TT12, like Medicago MATE1, functions to transport epicatechin 3'-O-

25 toxic compound extrusion (MATE) transporter, Medicago MATE1, was identified at the molecular level an

26 with legume plant host species of the genera Medicago, Melilotus, and Trigonella.

27 ndicate that, in contrast to the S. meliloti-Medicago model symbiosis, bacteroids in the S. fredii HH

28 Ectopic expression of Medicago NB-LRR-targeting miRNAs in Arabidopsis showed t

29 hed to >60% of all approximately 540 encoded Medicago NB-LRRs; in the potato, a model for mycorrhizal

30 Medicago NCR antimicrobial peptides (AMPs) mediate the d

31 dii HH103 showed little or no sensitivity to Medicago NCR247 and NCR335 peptides.

32 rhiza nor increased bacterial sensitivity to Medicago NCRs.

33 For Medicago, poplar and Arabidopsis, but not in rice, alter

34 ree dicotyledon species Medicago truncatula (Medicago), Populus trichocarpa (poplar) and Arabidopsis

35 tCBS1 expression occurred exclusively during Medicago-rhizobium symbiosis.

36 quencing libraries from Arabidopsis, tomato, Medicago, rice, maize and Physcomitrella Elevated rates

37 nt host plant systems: Ncotiana benthamiana, Medicago sativa (alfalfa) and Nicotiana tabacum NT1 cell

38 We previously showed that transgenic Medicago sativa (alfalfa) plants overexpressing microRNA

39 soil in search of its leguminous plant host, Medicago sativa (alfalfa).

40 mmunication between the roots of two plants (Medicago sativa and Arabidopsis thaliana) and the bacter

41 bles the bacterium to invade root nodules on Medicago sativa and establish a nitrogen-fixing symbiosi

42 ly 56-60% identities with C. microcarpa ACS, Medicago sativa chalcone synthase (CHS), and the previou

43 abidopsis IRT1 (AtIRT1) under control of the Medicago sativa EARLY NODULIN 12B promoter in our previo

44 g vegetative and reproductive development in Medicago sativa L.

45 Lucerne (Medicago sativa L.) has been widely used in the region t

46 Tolerance of alfalfa (Medicago sativa L.) to animal grazing varies widely with

47 In this study effect of Glomus mosseae/Medicago sativa mycorrhiza on atrazine degradation was i

48 long A17 small GTPase MtROP9, orthologous to Medicago sativa Rac1, via an RNA interference silencing

49 s analysis of two alfalfa varieties, Wisfal (Medicago sativa ssp. falcata var. sativa var. Chilean),

50 parative analyses of Medicago truncatula and Medicago sativa subsp. falcata.

51 eliloti Rm1021 contributes to symbiosis with Medicago sativa under some conditions.

52 ese findings for the development of alfalfa (Medicago sativa) as a dedicated bioenergy crop.

53 lignin levels in the forage legume alfalfa (Medicago sativa) by down-regulation of the monolignol bi

54 ryegrass (Lolium perenne) and dicot alfalfa (Medicago sativa) COMTs.

55 Its close relative alfalfa (Medicago sativa) is the most widely grown forage legume

56 Forage crops like alfalfa (Medicago sativa) lack both polyphenol oxidase and o-diph

57 le cress (Arabidopsis thaliana) and alfalfa (Medicago sativa) leads to strongly reduced lignin levels

58 ositional changes in two low-lignin alfalfa (Medicago sativa) lines with antisense down-regulation of

59 The behavior of Hg in alfalfa (Medicago sativa) plants grown under controlled condition

60 In contrast, alfalfa (Medicago sativa) plants, which have limited numbers of p

61 ssion of MtPAR in the forage legume alfalfa (Medicago sativa) resulted in detectable levels of PA in

62 ptake and distribution of silver in alfalfa (Medicago sativa) were quantified and visualized upon hyd

63 . truncatula is a close relative of alfalfa (Medicago sativa), a widely cultivated crop with limited

64 el legume Medicago truncatula or in alfalfa (Medicago sativa).

65 ngineering PAs in the forage legume alfalfa (Medicago sativa).

66 to seed exudates of its host plant alfalfa (Medicago sativa).

67 these systems, such as Trifolium repens and Medicago sativa, do not contain any substantial amounts

68 One eudicotyledon was found to have tricin (Medicago sativa, Fabaceae).

69 umol N2 (g dry weight nodule)(-1) h(-1) of a Medicago sativa-Rhizobium consortium by continuously ana

70 e symbiosis between S. meliloti and its host Medicago sativa.

71 tablishment of symbiosis with its host plant Medicago sativa.

72 ogen fixation when they were inoculated onto Medicago sativa.

73 red to establish a successful symbiosis with Medicago sativa.

74 ter for proanthocyanidin biosynthesis in the Medicago seed coat.

75 ix newly-sequenced genomes (Carica, Glycine, Medicago, Sorghum, Vitis and Zea) to identify a set of s

76 nt diversifying selection in NCRs within the Medicago species indicates rapid and recent evolution, a

77 a successful nitrogen-fixing symbiosis with Medicago species.

78 ly curated to remove non-plant pathways, and Medicago-specific pathways including isoflavonoid, ligni

79 MsDef1 and MtDef4 from Medicago spp. are small cysteine-rich defensins with pot

80 Repeat-Lacking Clade (IRLC) legumes such as Medicago spp., the bacteroids are kept under control by

81 In Medicago, such discrepancies were partly reconciled by t

82 e we identify in Sinorhizobium meliloti, the Medicago symbiont, a cAMP-signaling regulatory cascade c

83 ilt of this rigid barrier is varied, we find Medicago transitions between randomly directed root coil

84 CLE peptide-encoding genes was identified in Medicago truncatula (52) and Lotus japonicus (53), inclu

85 Flowering in the model legume, Medicago truncatula (Medicago) is accelerated by winter

86 ngiosperm genomes: three dicotyledon species Medicago truncatula (Medicago), Populus trichocarpa (pop

87 the HDH enzyme from the model legume plant, Medicago truncatula (MtHDH).

88 cation of an HPP enzyme from a model legume, Medicago truncatula (MtHPP) was based on the highest seq

89 haracterized a WD40 repeat protein gene from Medicago truncatula (MtWD40-1) via a retrotransposon-tag

90 Toxicogenomic responses in Medicago truncatula A17 were monitored following exposur

91 um meliloti NRG247 has a Fix(+) phenotype on Medicago truncatula A20 and is Fix(-) on M. truncatula A

92 Two Medicago truncatula accessions with contrasting response

93 vacuoles, and symbiosomes in root nodules of Medicago truncatula and analyzed the expression and loca

94 We isolated mutants of Medicago truncatula and Arabidopsis thaliana with second

95 In both Medicago truncatula and Arabidopsis thaliana, loss of NG

96 erved large blocks of conserved synteny with Medicago truncatula and estimated that the two species d

97 d RopGEF gene families from the model legume Medicago truncatula and from the crop legume soybean.

98 titative proteomic atlas of the model legume Medicago truncatula and its rhizobial symbiont Sinorhizo

99 documented in the two model legume species, Medicago truncatula and Lotus japonicus, as well as data

100 cium oscillations in root epidermal cells of Medicago truncatula and Lotus japonicus.

101 se questions through comparative analyses of Medicago truncatula and Medicago sativa subsp. falcata.

102 WOX5 transcription factor upon nodulation in Medicago truncatula and pea (Pisum sativum) that form in

103 ctional and structural analyses of CCRs from Medicago truncatula and Petunia hybrida and of an atypic

104 of seed size and weight in the model legume Medicago truncatula and the grain legume soybean (Glycin

105 1 (MOT1) were identified in the model legume Medicago truncatula and their expression in nodules was

106 at three cyclic nucleotide-gated channels in Medicago truncatula are required for nuclear Ca(2+) osci

107 Here Medicago truncatula bHLH MtTT8 was characterized as a ce

108 tes the establishment of the AM symbiosis in Medicago truncatula by promoting fungal colonization at

109 The glycosyltransferase UGT78G1 from Medicago truncatula catalyzes the glycosylation of vario

110 Here, we report a regulatory mechanism of Medicago truncatula CCaMK (MtCCaMK) through autophosphor

111 comprising either the visinin-like domain of Medicago truncatula CCaMK, which contains EF-hand motifs

112 fragment mapping to analyze the structure of Medicago truncatula chloroplast DNA (cpDNA).

113 vity of S. meliloti 1021 with the host plant Medicago truncatula cv. Jemalong A17.

114 ether the failure to initiate nodules in the Medicago truncatula cytokinin perception mutant cre1 (cy

115 We show that ROD1 from the legume Medicago truncatula directs male germline-specific expre

116 odulation, but not rhizobial infection, to a Medicago truncatula dmi1 mutant.

117 s characterized in roots of the model legume Medicago truncatula during the symbiotic interaction wit

118 A Tnt1-insertion mutant population of Medicago truncatula ecotype R108 was screened for defect

119 analysis on EST database of the model legume Medicago truncatula enabled us to identify nine cDNA seq

120 Medicago truncatula encodes a family of >700 NCR peptide

121 The leguminous plant Medicago truncatula exhibits dissected leaves with three

122 Medicago truncatula exo70i mutants are unable to support

123 perception), is a key protein in the legume Medicago truncatula for the perception of lipochitooligo

124 NAi, we demonstrate that the expression of a Medicago truncatula gene named Vapyrin is essential for

125 sesquiterpene synthase MtTPS5 isolated from Medicago truncatula generates 27 optically pure products

126 The model legume Medicago truncatula generates phasiRNAs from many PHAS l

127 ions in the current Arabidopsis thaliana and Medicago truncatula genome databases using SPADA, most o

128 Systematic reannotation of the Medicago truncatula genome identified 1,970 homologs of

129 ansporter family comprises 70 members in the Medicago truncatula genome, and they play seemingly impo

130 longevity in plant seeds, we first used two Medicago truncatula genotypes with contrasting seed qual

131 nction of genes that an earlier GWA study in Medicago truncatula had identified as candidates contrib

132 els of PA precursors and their conjugates in Medicago truncatula hairy roots and anthocyanin-overprod

133 Medicago truncatula hairy roots expressing LaPT1 accumul

134 Medicago truncatula has been developed into a model legu

135 calcium oxalate deficient 5 (cod5) mutant of Medicago truncatula has been previously shown to contain

136 Over the last decade, Medicago truncatula has emerged as a major model plant f

137 The legume Medicago truncatula has two predicted NF receptors that

138 Our work in Medicago truncatula highlights the complexity of NIN act

139 thosiphon pisum) differing in virulence on a Medicago truncatula host carrying the RAP1 and RAP2 resi

140 bidopsis (Arabidopsis thaliana) and later in Medicago truncatula However, the general function of thi

141 ystemic changes in the leaves of mycorrhized Medicago truncatula in conditions with no improved Pi st

142 the nitrogen-fixing root nodule symbiosis in Medicago truncatula In this study, we show that PUB1 als

143 gests a model for the systemic regulation in Medicago truncatula in which root signaling peptides are

144 Medicago truncatula is a fast-emerging model for the stu

145 Medicago truncatula is a legume species belonging to the

146 Medicago truncatula is a long-established model for the

147 Medicago truncatula is a model for investigating legume

148 The formation of symbiotic nodule cells in Medicago truncatula is driven by successive endoreduplic

149 utcomes, the perception of symbiotic LCOs in Medicago truncatula is mediated by the LysM receptor kin

150 Medicago truncatula is one of the model species for legu

151 Medicago truncatula is one of the most studied model pla

152 Medicago truncatula is widely used for analyses of arbus

153 We investigated the role of Medicago truncatula Jemalong A17 small GTPase MtROP9, or

154 The Medicago truncatula LATD/NIP gene plays an essential rol

155 nd can rescue the root growth defects of the Medicago truncatula lateral root-organ defective (latd)

156 A partial suppression of this gene in Medicago truncatula leads to a decrease in number of lat

157 Deletion of NST1 expression in Medicago truncatula leads to a loss of S lignin associat

158 loss of function of LAR in the model legume Medicago truncatula leads unexpectedly to loss of solubl

159 in cytokinin signaling, the nodule-enhanced Medicago truncatula Mt RR1 response regulator (RR).

160 rbuscule formation is severely impaired in a Medicago truncatula Mtdella1/Mtdella2 double mutant; GA

161 ins including phosphate transporters such as Medicago truncatula MtPT4, which are essential for symbi

162 ule-specific Suc transporter, MtSWEET11 from Medicago truncatula MtSWEET11 belongs to a clade of plan

163 Accordingly, expression of CYP716A75 in a Medicago truncatula mutant lacking C-28 oxidase activity

164 Using a new allele of the Medicago truncatula mutant Lumpy Infections, lin-4, whic

165 Here, we report a Medicago truncatula mutant, stunted arbuscule (str), in

166 A screen for supernodulating Medicago truncatula mutants defective in this regulatory

167 ical meristem)-like protein (here designated Medicago truncatula NAC SECONDARY WALL THICKENING PROMOT

168 We herein report the cloning of the Medicago truncatula NFS1 gene that regulates the fixatio

169 The Medicago truncatula NIP/LATD (for Numerous Infections an

170 ent of the nitrate transporter MtNPF6.8 (for Medicago truncatula NITRATE TRANSPORTER1/PEPTIDE TRANSPO

171 The objective of the study was to follow Medicago truncatula nodule activity after nitrate provis

172 Using Medicago truncatula nodule root (noot) mutants and pea (

173 Here, a Medicago truncatula nodules with activated defense 1 (na

174 It was found that inside Medicago truncatula nodules, NFP and LYK3 localize at th

175 In Medicago truncatula nodules, the Sinorhizobium microsymb

176 plants and carefully examined the ability of Medicago truncatula nsp1 mutants to respond to Myc-LCOs

177 We recently identified Medicago truncatula nuclear factor-YA1 (MtNF-YA1) and Mt

178 obium meliloti and its leguminous host plant Medicago truncatula occurs in a specialized root organ c

179 anthocyanin biosynthesis in the model legume Medicago truncatula or in alfalfa (Medicago sativa).

180 We show that this locus encodes the Medicago truncatula ortholog of the Arabidopsis ethylene

181 Previously we identified MtPT4, a Medicago truncatula phosphate transporter located in the

182 Medicago truncatula plants defective in ERN1 are unable

183 A population of 156,000 Medicago truncatula plants has been structured as 13 tow

184 e study the primary root growth of wild-type Medicago truncatula plants in heterogeneous environments

185 Medicago truncatula plants were cocultured with the AM f

186 materials with soil that had been sown with Medicago truncatula plants.

187 Here we show that Lotus japonicus and Medicago truncatula possess very similar LysM pattern-re

188 50 plant genomes resulted in 138 genes from Medicago truncatula predicted to function in AMS.

189 scanner to directly image the morphology of Medicago truncatula primary roots.

190 MtPAR (Medicago truncatula proanthocyanidin regulator) is an MY

191 he root nodules of certain legumes including Medicago truncatula produce >300 different nodule-specif

192 latory module by overexpression of miR390 in Medicago truncatula promotes lateral root growth but pre

193 Here, by using a Medicago truncatula pt4 mutant in which arbuscules degen

194 d characterization of an insertion allele of Medicago truncatula Reduced Arbuscular Mycorrhiza1 (RAM1

195 Here, we characterize RAM2, a gene of Medicago truncatula required for colonization of the roo

196 investigate early stages of IT formation in Medicago truncatula root hairs (RHs) expressing fluoresc

197 Therefore, we transcriptionally profiled Medicago truncatula root hairs prior to and during the i

198 Fs) activate a specific signaling pathway in Medicago truncatula root hairs that involves the complex

199 2+) spiking and symbiotic gene expression in Medicago truncatula roots in response to rhizobial and a

200 -biosynthesis enzymes to generate transgenic Medicago truncatula roots with different flavonoid profi

201 tion of the inducible promoters, transformed Medicago truncatula roots, and quantified YFP fluorescen

202 tegrated metabolomics and transcriptomics of Medicago truncatula seedling border cells and root tips

203 f the primary root during postgermination of Medicago truncatula seedlings is a multigenic trait that

204 ctor transcription factors and is related to Medicago truncatula somatic embryo-related factor1 (MtSE

205 Using the Sinorhizobium meliloti and Medicago truncatula symbiotic system, we previously desc

206 We show that the Medicago truncatula SYNTAXIN 132 (SYP132) gene undergoes

207 is a TIR-NBS-LRR-type resistance (R) gene in Medicago truncatula that confers resistance to multiple

208 designated elongated petiolule1 (elp1) from Medicago truncatula that fails to fold its leaflets in t

209 Here, we show in Medicago truncatula that GA signaling mediated by DELLA1

210 we show by grafting and genetic analysis in Medicago truncatula that, in the AON pathway, RDN1, func

211 toxic compound extrusion family, MtMATE67 of Medicago truncatula The MtMATE67 gene was induced early

212 t) in the root epidermis of the model legume Medicago truncatula Tissue-specific transcriptome analys

213 gens, we did a forward-genetics screen using Medicago truncatula Tnt1 retrotransposon insertion lines

214 Two Medicago truncatula Tnt1-insertion mutants were identifi

215 ivation of the nodule organogenic program in Medicago truncatula TR25 (symrk knockout mutant) in the

216 es and one partial sequence were obtained in Medicago truncatula via inverse PCR.

217 The Medicago truncatula WOX gene, STENOFOLIA (STF), and its

218 enetic tool, we examined the function of the Medicago truncatula WOX gene, STENOFOLIA (STF), in contr

219 The Medicago truncatula WUSCHEL-related homeobox (WOX) gene,

220 etabolic profiling of elicited barrel medic (Medicago truncatula) cell cultures using high-performanc

221 ransposon insertion mutants of barrel medic (Medicago truncatula) that show reduced lignin autofluore

222 gume species (chickpea [Cicer arietinum] and Medicago truncatula), but almost 200 homeologous lincRNA

223 Glycine tomentella, Phaseolus vulgaris, and Medicago truncatula), which enabled us to determine how

224 e observed similar patterns in barrel medic (Medicago truncatula), which shared the older genome dupl

225 irement for tissue culture activation (Tnt1: Medicago truncatula).

226 e of the model legume species, barrel medic (Medicago truncatula).

227 lator of symbiosome differentiation (RSD) of Medicago truncatula, a member of the Cysteine-2/Histidin

228 s at the SMOOTH LEAF MARGIN1 (SLM1) locus in Medicago truncatula, a model legume species with trifoli

229 In Medicago truncatula, a Pi transporter, PT4, is required

230 cells, which are a layer in the seed coat of Medicago truncatula, accumulate large amounts of phytoch

231 fferent plant species: Solanum lycopersicum, Medicago truncatula, and Oryza sativa.

232 dopsis thaliana, potato (Solanum tuberosum), Medicago truncatula, and poplar (Populus trichocarpa) re

233 associated enzyme activity in barrel medic (Medicago truncatula, dicot, Leguminosae), poplar (Populu

234 retrotransposon-tagged mutant population of Medicago truncatula, four petiolule-like pulvinus (plp)

235 d phylogenetic trees for six legume species: Medicago truncatula, Glycine max (soybean), Lotus japoni

236 he genomic sequences of three model legumes, Medicago truncatula, Glycine max and Lotus japonicus plu

237 In the model legume Medicago truncatula, iron is delivered by the vasculatur

238 neered nanomaterials (ENMs) on the growth of Medicago truncatula, its symbiosis with Sinorhizobium me

239 fication of a mutant in nodule regulation in Medicago truncatula, like sunn supernodulator (lss), whi

240 edge, that 4-Cl-IAA is found in the seeds of Medicago truncatula, Melilotus indicus, and three specie

241 thologue of BRI1 in the model legume species Medicago truncatula, MtBRI1, was identified and characte

242 In Medicago truncatula, MtCEP1 affects root development by

243 alfa is congeneric with the reference legume Medicago truncatula, providing an opportunity to use M.

244 One of them is the closest homolog of Medicago truncatula, REDUCED ARBUSCULAR MYCORRHIZATION1

245 LUX putative ortholog in the closely related Medicago truncatula, rendered the channel solo sufficien

246 og of Required For Arbuscular Mycorrhiza1 in Medicago truncatula, renders the interaction completely

247 reference legumes, soybean (Glycine max) and Medicago truncatula, revealed extensive macrosynteny enc

248 of endogenous metabolites from legume plant, Medicago truncatula, root nodules.

249 in four plant species (Arabidopsis thaliana, Medicago truncatula, Solanum lycopersicum, and Oryza sat

250 d whether a gene regulating nodule number in Medicago truncatula, Super Numeric Nodules (SUNN ), is i

251 In the model legume Medicago truncatula, the genomic set of AMT-type ammoniu

252 In Medicago truncatula, the symbiosome consists of the symb

253 Recently, it has been discovered that in Medicago truncatula, the Vapyrin (VPY) gene is essential

254 In Medicago truncatula, this process is orchestrated by nod

255 ins genes encoding forisome subunits in e.g. Medicago truncatula, Vicia faba, Dipteryx panamensis and

256 rization of transporters in the model legume Medicago truncatula, we identified 3,830 transporters an

257 ve trait locus analysis on seed longevity in Medicago truncatula, we identified the bZIP transcriptio

258 rotransposon1 (Tnt1) insertion population in Medicago truncatula, we isolated a weak allele of the no

259 tate association studies in the model legume Medicago truncatula, we present a genome-scale polymorph

260 y cell wall biosynthesis in the model legume Medicago truncatula, we screened a Tnt1 retrotransposon

261 lycopersicum), tobacco (Nicotiana tabacum), Medicago truncatula, wheat (Triticum aestivum), and barl

262 Therefore, Medicago truncatula, which has a relatively small diploi

263 -like homeobox transcriptional regulator, in Medicago truncatula, which is required for blade outgrow

264 We characterized a Medicago truncatula-ASR pathosystem to study molecular m

265 The Medicago truncatula-Sinorhizobium meliloti association i

266 However, in the Medicago truncatula-Sinorhizobium meliloti symbiosis, in

267 ically in arbuscule-containing root cells of Medicago truncatula.

268 nd MYB14 (a TT2 homolog) in the model legume Medicago truncatula.

269 KNOXI genes in compound leaf development in Medicago truncatula.

270 obulins in seeds of the model legume species Medicago truncatula.

271 of legumes, which includes the model legume Medicago truncatula.

272 ring the last 3 weeks of seed development in Medicago truncatula.

273 cies, Arabidopsis (Arabidopsis thaliana) and Medicago truncatula.

274 odF mutations additively reduce infection of Medicago truncatula.

275 yzing a recessive mutant in the model legume Medicago truncatula.

276 anidin (PA) biosynthesis in the model legume Medicago truncatula.

277 nd toxin extrusion transporter (MATE2), from Medicago truncatula.

278 -function point mutation in the NST1 gene of Medicago truncatula.

279 the triterpene skeleton in the model legume Medicago truncatula.

280 ArgF) were characterized in the model legume Medicago truncatula.

281 identified two CCR genes in the model legume Medicago truncatula.

282 zobium meliloti infection of its host legume Medicago truncatula.

283 tic, nitrogen-fixing nodules on the roots of Medicago truncatula.

284 of proanthocyanidins (PAs) in hairy roots of Medicago truncatula.

285 sis thaliana and in the roots and nodules of Medicago truncatula.

286 2-NOA, which we found reduced nodulation of Medicago truncatula.

287 elated Pi transporters of the PHT1 family of Medicago truncatula.

288 ingle leaflet1 (sgl1), from the model legume Medicago truncatula.

289 MtDef5 has been identified in a model legume Medicago truncatula.

290 lycosylated flavonoids from the model legume Medicago truncatula.

291 ch direct triterpene saponin biosynthesis in Medicago truncatula.

292 induction of the infection marker ENOD11 in Medicago truncatula.

293 are present on the host-microbe interface in Medicago truncatula.

294 anin and PA biosynthesis in the model legume Medicago truncatula.

295 cription factor TRANSPARENT TESTA 2 (TT2) in Medicago trunculata hairy roots induces both proanthocya

296 wth when this construct was transformed into Medicago until dexamethasone was applied.

297 Silencing of these Medicago VAMP72 genes has a minor effect on nonsymbiotic

298 Comparative transcriptome analysis of Medicago versus Arabidopsis revealed significant diverge

299 CR2 is involved in a route to monolignols in Medicago whereby coniferaldehyde is formed via caffeyl a

300 ositively correlated between Arabidopsis and Medicago, with no correlation between dicots and rice.