ライフサイエンスコーパス: Medicago truncatula

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

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

3 bean (Phaseolus vulgaris) and barrel medic (Medicago truncatula).

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

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

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

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

8 odF mutations additively reduce infection of Medicago truncatula.

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

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

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

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

13 the triterpene skeleton in the model legume Medicago truncatula.

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

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

16 zobium meliloti infection of its host legume Medicago truncatula.

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

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

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

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

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

22 2-NOA, which we found reduced nodulation of Medicago truncatula.

23 factor genes WXP1 and its paralog WXP2 from Medicago truncatula.

24 cell culture exudates from the model legume, Medicago truncatula.

25 m is sequencing the euchromatic genespace of Medicago truncatula.

26 nscription factor gene from the model legume Medicago truncatula.

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

28 ve cysteine-rich defensins was discovered in Medicago truncatula.

29 cterization of one such gene from the legume Medicago truncatula.

30 mately 10,000 probe sets for the plant host, Medicago truncatula.

31 e proteins function as metal transporters in Medicago truncatula.

32 x new metal transporters in the model legume Medicago truncatula.

33 different tissues of the model legume plant, Medicago truncatula.

34 lycosylated flavonoids from the model legume Medicago truncatula.

35 ch direct triterpene saponin biosynthesis in Medicago truncatula.

36 induction of the infection marker ENOD11 in Medicago truncatula.

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

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

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

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

41 KNOXI genes in compound leaf development in Medicago truncatula.

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

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

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

45 In Medicago truncatula, a model legume used widely for stud

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

47 Toxicogenomic responses in Medicago truncatula A17 were monitored following exposur

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

49 Two Medicago truncatula accessions with contrasting response

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

51 Cell suspensions of the model legume Medicago truncatula accumulated the isoflavonoid phytoal

52 alcium partitioning in the model forage crop Medicago truncatula affects calcium bioavailability.

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

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

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

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

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

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

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

60 and AM symbioses from the two model legumes, Medicago truncatula and Lotus japonicus, provide a uniqu

61 Genome sequencing of the model legumes, Medicago truncatula and Lotus japonicus, provides an opp

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

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

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

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

66 that GRIK1, GRIK2, and related kinases from Medicago truncatula and rice (Oryza sativa) are most sim

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

68 1 (MOT1) were identified in the model legume Medicago truncatula and their expression in nodules was

69 sed to predict the metabolic composition for Medicago truncatula and these pathways were engineered t

70 m), alfalfa (Medicago sativa), barrel medic (Medicago truncatula), and chickpea (Cicer arietinum), 4'

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

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

73 The saponins of the model legume Medicago truncatula are glycosides of at least five diff

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

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

76 Here Medicago truncatula bHLH MtTT8 was characterized as a ce

77 the UDP flavonoid/triterpene GT UGT71G1 from Medicago truncatula bound to UDP or UDP-glucose.

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

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

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

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

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

83 ,000 expressed sequence tags from a range of Medicago truncatula cDNA libraries resulted in the ident

84 xtracellular secondary product metabolome of Medicago truncatula cell suspension cultures responding

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

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

87 related to these OMTs from the model legume Medicago truncatula cluster as separate branches of the

88 MtDFR2) were isolated from the model legume Medicago truncatula cv Jemalong.

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

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

91 rough computational screens (e.g., against a Medicago truncatula database) and direct hybridization o

92 a novel symbiotic mutant of the model legume Medicago truncatula, designated nip (numerous infections

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

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

95 ed genes in this signaling pathway including Medicago truncatula DMI1 (Doesn't Make Infections 1) tha

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

97 The Medicago truncatula DMI3 (DOESN'T MAKE INFECTIONS3) gene

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

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

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

101 LS (BAN) genes from Arabidopsis thaliana and Medicago truncatula encode anthocyanidin reductase, whic

102 Medicago truncatula encodes a family of >700 NCR peptide

103 Here, we show that NSP2 from Medicago truncatula encodes a GRAS protein essential for

104 Mining of Medicago truncatula EST databases and screening of a roo

105 The leguminous plant Medicago truncatula exhibits dissected leaves with three

106 Medicago truncatula exo70i mutants are unable to support

107 The Medicago truncatula expressed sequence tag (EST) databas

108 ligonucleotide microarray representing 9,935 Medicago truncatula expressed sequences.

109 We used transgenic Medicago truncatula expressing a "cameleon" Ca(2+) senso

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

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

112 In the barrel medic Medicago truncatula Gaertn., these crystals accumulate p

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

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

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

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

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

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

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

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

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

122 UGT71G1 from the model legume barrel medic (Medicago truncatula) glycosylates flavonoids, isoflavono

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

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

125 Medicago truncatula hairy roots expressing LaPT1 accumul

126 Medicago truncatula has become a model system to study l

127 Medicago truncatula has been developed into a model legu

128 A core genetic map of the legume Medicago truncatula has been established by analyzing th

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

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

131 anesulfonate mutagenesis of the model legume Medicago truncatula has previously identified several ge

132 The legume Medicago truncatula has two predicted NF receptors that

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

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

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

136 the isolation and characterization of a new Medicago truncatula hyper-nodulation mutant, designated

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

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

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

140 dules on the primary root of the host plant, Medicago truncatula, indicating that sinI-dependent QS r

141 We show that, in the Sinorhizobium meliloti-Medicago truncatula interaction, bacteria elicit a calci

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

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

144 Medicago truncatula is a legume species belonging to the

145 Medicago truncatula is a long-established model for the

146 Medicago truncatula is a model for investigating legume

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

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

149 Medicago truncatula is one of the model species for legu

150 Medicago truncatula is one of the most studied model pla

151 Medicago truncatula is widely used for analyses of arbus

152 The LATD gene of the model legume, Medicago truncatula, is required for the normal function

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

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

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

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

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

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

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

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

161 LAST algorithms to compare unigene sets from Medicago truncatula, Lotus japonicus, and soybean (Glyci

162 intuitive navigation of transcript data from Medicago truncatula, Lotus japonicus, Glycine max and Ar

163 545% in roots of alfalfa (Medicago sativa), Medicago truncatula, maize (Zea mays), and wheat (Tritic

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

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

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

167 Here, we show that MtPT4, a Medicago truncatula member of subfamily I, is essential

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

169 archers have selected the cool season legume Medicago truncatula (Mt) as a model system for legume re

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

171 In Medicago truncatula, MtCEP1 affects root development by

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

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

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

175 utive expression of isoflavone synthase from Medicago truncatula (MtIFS1).

176 n of the first AGC kinase gene identified in Medicago truncatula, MtIRE.

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

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

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

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

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

182 One such Medicago truncatula mutant, dmi3, exhibits calcium spiki

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

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

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

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

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

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

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

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

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

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

193 In Medicago truncatula nodules, the Sinorhizobium microsymb

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

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

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

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

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

199 haracterization of two mutant alleles of the Medicago truncatula ortholog of the Lotus japonicus and

200 pecies: Arabidopsis thaliana, Carica papaya, Medicago truncatula, Oryza sativa and Populus trichocarp

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

202 Medicago truncatula plants defective in ERN1 are unable

203 substantial 14N to pheophytin isolated from Medicago truncatula plants grown in symbiosis with Sinor

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

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

206 Medicago truncatula plants inoculated with the double mu

207 ly calcium responses of wild-type and mutant Medicago truncatula plants to nodulation factors produce

208 Medicago truncatula plants were cocultured with the AM f

209 ly transformed Lotus japonicus and composite Medicago truncatula plants.

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

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

212 50 plant genomes resulted in 138 genes from Medicago truncatula predicted to function in AMS.

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

214 MtPAR (Medicago truncatula proanthocyanidin regulator) is an MY

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

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

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

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

219 mulate in the seed coats of the model legume Medicago truncatula, reaching maximal levels at around 2

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

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

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

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

224 Arabidopsis and Medicago truncatula represent sister clades within the d

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

226 yanin-containing leaves of the forage legume Medicago truncatula resulted in production of a specific

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

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

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

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

231 In Medicago truncatula root hairs, wall expansion exhibits

232 peroxide (H(2)O(2)) efflux was measured from Medicago truncatula root segments exposed to purified No

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

234 explore transcriptional changes triggered in Medicago truncatula roots and shoots as a result of AM s

235 ing of early stages of the symbiosis between Medicago truncatula roots and Sinorhizobium meliloti wou

236 DNA arrays to examine transcript profiles in Medicago truncatula roots during the development of an A

237 2+) spiking and symbiotic gene expression in Medicago truncatula roots in response to rhizobial and a

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

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

240 hate transporter genes, MtPT1 and MtPT2 from Medicago truncatula roots.

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

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

243 elops along the root axis in A. thaliana and Medicago truncatula seedlings.

244 4,000 M2 plants from fast neutron-irradiated Medicago truncatula seeds and isolated eight independent

245 The Medicago truncatula-Sinorhizobium meliloti association i

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

247 ishment of nitrogen-fixing nodules (Fix+) in Medicago truncatula-Sinorhizobium meliloti symbiosis.

248 In the Medicago truncatula/Sinorhizobium meliloti symbiosis, th

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

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

251 Four Medicago truncatula sunn mutants displayed shortened roo

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

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

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

255 The model legume Medicago truncatula synthesizes more than 30 different s

256 Here, we show in the model legume Medicago truncatula that a novel family of six calmoduli

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

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

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

260 s, nodulation-signaling pathway 2 (NSP2), of Medicago truncatula that is involved in Nod factor signa

261 we isolated a cDNA from mycorrhizal roots of Medicago truncatula that is predicted to encode an XTH.

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

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

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

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

266 In Medicago truncatula, the symbiosome consists of the symb

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

268 In Medicago truncatula, this process is orchestrated by nod

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

270 in microsomes isolated from Arabidopsis and Medicago truncatula tissues, indicating the general prev

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

272 Two Medicago truncatula Tnt1-insertion mutants were identifi

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

274 In Medicago truncatula, transcript levels of key regulatory

275 by Sinorhizobium meliloti on the model plant Medicago truncatula, tubules called infection threads ar

276 We cloned two FNS II genes from Medicago truncatula using known FNS II sequences from ot

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

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

279 The presence of eATP in plants (Medicago truncatula) was detected by constructing a nove

280 proteomes of the model legume barrel medic (Medicago truncatula) was performed.

281 like sequences (DEFLs) from the model legume Medicago truncatula, we built motif models to search the

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

283 terference-based screen for gene function in Medicago truncatula, we identified a gene that is involv

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

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

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

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

288 o integrate the physical and genetic maps of Medicago truncatula, we surveyed the frequency and distr

289 nsformed with an SA-inducible RdRP gene from Medicago truncatula were more resistant to infection by

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

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

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

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

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

295 By contrast, MtDef2 from Medicago truncatula, which shares 65% amino acid sequenc

296 ltransferase, UGT85H2, from the model legume Medicago truncatula with activity towards a number of ph

297 mpared sequenced regions of the model legume Medicago truncatula with those of the diploid Lotus japo

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

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

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