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 anin and PA biosynthesis in the model legume Medicago truncatula.

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

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

6 KNOXI genes in compound leaf development in Medicago truncatula.

7 taset with a nodule transcriptome dataset in Medicago truncatula.

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

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

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

11 odF mutations additively reduce infection of Medicago truncatula.

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

13 to investigate the male fertility control in Medicago truncatula.

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

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

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

17 ding the auxin biosynthetic enzyme YUCCA1 in Medicago truncatula.

18 the triterpene skeleton in the model legume Medicago truncatula.

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

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

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

22 zobium meliloti infection of its host legume Medicago truncatula.

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

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

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

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

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

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

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

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

31 m is sequencing the euchromatic genespace of Medicago truncatula.

32 taset with a nodule transcriptome dataset in Medicago truncatula.

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

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

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

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

37 2-NOA, which we found reduced nodulation of Medicago truncatula.

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

39 lycosylated flavonoids from the model legume Medicago truncatula.

40 ch direct triterpene saponin biosynthesis in Medicago truncatula.

41 induction of the infection marker ENOD11 in Medicago truncatula.

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

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

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

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

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

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

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

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

50 Toxicogenomic responses in Medicago truncatula A17 were monitored following exposur

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

52 Two Medicago truncatula accessions with contrasting response

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

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

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

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

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

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

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

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

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

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

63 We used Medicago truncatula and its oomycete pathogen Aphanomyce

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

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

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

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

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

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

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

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

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

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

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

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

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

77 1 (MOT1) were identified in the model legume Medicago truncatula and their expression in nodules was

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

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

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

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

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

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

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

85 Here Medicago truncatula bHLH MtTT8 was characterized as a ce

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

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

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

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

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

91 ,000 expressed sequence tags from a range of Medicago truncatula cDNA libraries resulted in the ident

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 Medicago truncatula encodes a family of >700 NCR peptide

107 The leguminous plant Medicago truncatula exhibits dissected leaves with three

108 Medicago truncatula exo70i mutants are unable to support

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 Medicago truncatula hairy roots expressing LaPT1 accumul

129 Medicago truncatula has become a model system to study l

130 Medicago truncatula has been developed into a model legu

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

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

133 The legume Medicago truncatula has two predicted NF receptors that

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

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

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

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

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

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

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

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

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 In Medicago truncatula, LCOs stimulate lateral root formati

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

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

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

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

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

163 Medicago truncatula LIN (MtLIN) was reported to interact

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

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

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

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

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

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

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

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

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

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

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

184 Using Medicago truncatula mutants in the recently described no

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

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

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

194 In Medicago truncatula nodules, the Sinorhizobium microsymb

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

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

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

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

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

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

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

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

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

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

205 Medicago truncatula plants defective in ERN1 are unable

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

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

208 Medicago truncatula plants inoculated with the double mu

209 Medicago truncatula plants were cocultured with the AM f

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

211 ly transformed Lotus japonicus and composite Medicago truncatula plants.

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

213 50 plant genomes resulted in 138 genes from Medicago truncatula predicted to function in AMS.

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

215 MtPAR (Medicago truncatula proanthocyanidin regulator) is an MY

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 2+) spiking and symbiotic gene expression in Medicago truncatula roots in response to rhizobial and a

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

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

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

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

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

243 4,000 M2 plants from fast neutron-irradiated Medicago truncatula seeds and isolated eight independent

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

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

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

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

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

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

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 two types of saponins, h

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

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

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

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

264 In Medicago truncatula, the symbiosome consists of the symb

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

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

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

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

271 Two Medicago truncatula Tnt1-insertion mutants were identifi

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

273 In Medicago truncatula, transcript levels of key regulatory

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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,