ライフサイエンスコーパス: Medicago

1 tion for early flowering in LD conditions in Medicago.

2 ed ectopically in transformed hairy roots of Medicago.

3 erases in triterpene saponin biosynthesis in Medicago.

4 les in the response of ER and salt stress in Medicago.

5 meostasis at root hair tips of Trifolium and Medicago.

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

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

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

9 In Medicago and related legume species, the bacteria underg

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

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

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

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

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

15 fication to demonstrate that Arabidopsis and Medicago CEP (C-TERMINALLY ENCODED PEPTIDE)-CEP RECEPTOR

16 We showed that soil-grown Arabidopsis and Medicago CEP receptor mutants have a narrower RSA, which

17 endent signalling outputs in Arabidopsis and Medicago control overall RSA, LR GSA, shoot auxin levels

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

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

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

21 In the Medicago lineage, nodule-specific Polycystin-1, Lipoxyge

22 s, each unique to either Glycine, Arachis or Medicago lineages.

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

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

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

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

27 Medicago NCR antimicrobial peptides (AMPs) mediate the d

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

29 rhiza nor increased bacterial sensitivity to Medicago NCRs.

30 tCBS1 expression occurred exclusively during Medicago-rhizobium symbiosis.

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

32 y for proper nuclear shaping and movement in Medicago root hairs, and are important for infection thr

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

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

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

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

37 g vegetative and reproductive development in Medicago sativa L.

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

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

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

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

42 w within physiological gradients produced by Medicago sativa roots.

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

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

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

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

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

48 natural diploid and autotetraploid alfalfa (Medicago sativa) lineages with a diverse panel of Sinorh

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

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

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

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

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

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

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

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

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

58 tile system using cell suspension culture of Medicago sativa, which ensures control over the reaction

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

60 ps, at capturing the pollinators of alfalfa, Medicago sativa.

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

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

63 a successful nitrogen-fixing symbiosis with Medicago species.

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

65 21 is needed for an effective symbiosis with Medicago spp., and the succinyl modification to this pol

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

67 In Medicago, such discrepancies were partly reconciled by t

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

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

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

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

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

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

74 Toxicogenomic responses in Medicago truncatula A17 were monitored following exposur

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

76 Two Medicago truncatula accessions with contrasting response

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

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

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

80 ion of this bacterial derived signal in both Medicago truncatula and barley and show its perception b

81 molecular and phenotypic data in the legume Medicago truncatula and determined that genes controllin

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

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

84 We used Medicago truncatula and its oomycete pathogen Aphanomyce

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

86 equired for SNF in two model legume species, Medicago truncatula and Lotus japonicus, and two crop sp

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

88 thologs required for leaf blade outgrowth in Medicago truncatula and Nicotiana sylvestris, respective

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

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

91 itrogen-fixing symbiosis established between Medicago truncatula and Sinorhizobium meliloti Our analy

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

93 1 (MOT1) were identified in the model legume Medicago truncatula and their expression in nodules was

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

95 Here Medicago truncatula bHLH MtTT8 was characterized as a ce

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

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

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

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

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

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

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

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

104 Medicago truncatula encodes a family of >700 NCR peptide

105 The leguminous plant Medicago truncatula exhibits dissected leaves with three

106 Medicago truncatula exo70i mutants are unable to support

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

108 directly upstream of the NIN start codon in Medicago truncatula Furthermore, we identify a remote up

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

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

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

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

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

114 bacterium Ensifer meliloti with one of five Medicago truncatula genotypes that vary in how strongly

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

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

117 k-down constructs reducing PRP expression in Medicago truncatula hairy root tumors disrupted cortical

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

119 Medicago truncatula hairy roots expressing LaPT1 accumul

120 Medicago truncatula has been developed into a model legu

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

122 The legume Medicago truncatula has two predicted NF receptors that

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

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

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

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

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

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

129 ly signalling events in the Ensifer meliloti-Medicago truncatula interaction.

130 Medicago truncatula is a legume species belonging to the

131 Medicago truncatula is a long-established model for the

132 Medicago truncatula is a model for investigating legume

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

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

135 Medicago truncatula is one of the model species for legu

136 Medicago truncatula is one of the most studied model pla

137 Medicago truncatula is widely used for analyses of arbus

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

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

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

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

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

143 Here, using Medicago truncatula leaf marking as a model, we show tha

144 Medicago truncatula LIN (MtLIN) was reported to interact

145 systemic pathways have been reported in the Medicago truncatula model to regulate root nitrogen-fixi

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

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

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

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

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

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

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

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

154 We tested Medicago truncatula mutants in the LysM-RLK MtLYK9 for t

155 Using Medicago truncatula mutants in the recently described no

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

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

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

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

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

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

162 he nodule-specific M. truncatula ferroportin Medicago truncatula nodule-specific gene Ferroportin2 (M

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

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

165 In Medicago truncatula nodules, the Sinorhizobium microsymb

166 ISPR/Cas9 multiplex genome editing to create Medicago truncatula NPD knockout lines, targeting one to

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

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

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

170 oducing modified succinoglycan, in wild-type Medicago truncatula plants and in Mtlyk10 mutant plants.

171 Medicago truncatula plants defective in ERN1 are unable

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

173 Medicago truncatula plants were cocultured with the AM f

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

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

176 50 plant genomes resulted in 138 genes from Medicago truncatula predicted to function in AMS.

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

178 MtPAR (Medicago truncatula proanthocyanidin regulator) is an MY

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

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

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

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

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

184 t cell colonization by symbiotic rhizobia in Medicago truncatula requires repolarization of root hair

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

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

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

188 RRB-encoding gene most strongly expressed in Medicago truncatula roots and nodules, significantly dec

189 2+) spiking and symbiotic gene expression in Medicago truncatula roots in response to rhizobial and a

190 dules that initiate from the inner layers of Medicago truncatula roots in response to rhizobial perce

191 Moreover, SlDLK2 overexpression in Medicago truncatula roots showed the same altered phenot

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

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

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

195 ies in the model legumes Lotus japonicus and Medicago truncatula showed that rhizobium LCOs are perce

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

197 cell program in cortical cells of the legume Medicago truncatula specifies their distinct fate.

198 esent the functional characterization of the Medicago truncatula SUPERMAN (MtSUP) gene based on gene

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

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

201 The model legume Medicago truncatula synthesizes two types of saponins, h

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

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

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

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

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

207 ll as one double mutant, in the model legume Medicago truncatula These plants exhibit growth phenotyp

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

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

210 Two Medicago truncatula Tnt1-insertion mutants were identifi

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

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

213 racterize LINC complexes in the model legume Medicago truncatula We show that LINC complex characteri

214 Ferroportin family members in model legume Medicago truncatula were identified and their expression

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

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

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

218 mes and the model legumes for indeterminate (Medicago truncatula) and determinate (Lotus japonicus) n

219 dicate that the growth benefit to the plant (Medicago truncatula) has greater weight in determining t

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

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

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

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

224 We also show that in Medicago truncatula, a homeotic mutation in the co-trans

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

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

227 mutant population of the model legume plant Medicago truncatula, a mutant line with altered leaflet

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

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

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

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

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

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

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

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

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

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

238 In Medicago truncatula, LCOs stimulate lateral root formati

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

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

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

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

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

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

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

250 In Medicago truncatula, the symbiosome consists of the symb

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

252 In the legume Medicago truncatula, these nuclear Ca(2+) signals are ge

253 In Medicago truncatula, this process is orchestrated by nod

254 onal traits in the wild model plant species, Medicago truncatula, using geographical locations as cov

255 In Medicago truncatula, VAPYRIN (VPY) and a putative E3 lig

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

257 eum vulgare), wheat (Triticum aestivum), and Medicago truncatula, we demonstrate a role for MLO in co

258 ertion mutant population of the model legume Medicago truncatula, we identified SMALL LEAF AND BUSHY1

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

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

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

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

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

264 the indeterminate nodules of a model legume Medicago truncatula, ~700 nodule-specific cysteine-rich

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

266 The Medicago truncatula-Sinorhizobium meliloti association i

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

268 ch direct triterpene saponin biosynthesis in Medicago truncatula.

269 induction of the infection marker ENOD11 in Medicago truncatula.

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

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

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

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

274 taset with a nodule transcriptome dataset in Medicago truncatula.

275 KNOXI genes in compound leaf development in Medicago truncatula.

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

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

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

279 odF mutations additively reduce infection of Medicago truncatula.

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

281 to investigate the male fertility control in Medicago truncatula.

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

283 ding the auxin biosynthetic enzyme YUCCA1 in Medicago truncatula.

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

285 olar iron Transporter-Like (VTL) proteins in Medicago truncatula.

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

287 the triterpene skeleton in the model legume Medicago truncatula.

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

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

290 ET family sugar exporters in AM symbiosis in Medicago truncatula.

291 ection of 174 accessions of the model legume Medicago truncatula.

292 m CO4-CO8 can induce symbiosis signalling in Medicago truncatula.

293 ted a near-saturated insertion population in Medicago truncatula.

294 taset with a nodule transcriptome dataset in Medicago truncatula.

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

296 2-NOA, which we found reduced nodulation of Medicago truncatula.

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

298 lycosylated flavonoids from the model legume Medicago truncatula.

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

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