ライフサイエンスコーパス: Glycine max

1 ines, the most damaging pathogen of soybean (Glycine max).

2 a divergent (CaM4) CaM isoform from soybean (Glycine max).

3 sposon as a mutagenesis strategy in soybean (Glycine max).

4 thylene on somatic embryogenesis in soybean (Glycine max).

5 es for many crop species, including soybean (Glycine max).

6 ssociated with the domestication in soybean (Glycine max).

7 ntial for proper trichome growth in soybean (Glycine max).

8 he most damaging chronic disease of soybean (Glycine max).

9 an analysis of retrotransposons in soybean (Glycine max).

10 of FLO/LFY orthologs in transgenic soybean (Glycine max).

11 rtant temperate food crops, such as soybean (Glycine max).

12 lencing of genes for this enzyme in soybean (Glycine max).

13 cture of a group 1 LEA protein from soybean (Glycine max).

14 lizing enzyme, has been cloned from soybean (Glycine max).

15 mechanism for chitin perception in soybean (Glycine max).

16 bidopsis (Arabidopsis thaliana) and soybean (Glycine max).

17 ic interaction with the legume host soybean (Glycine max).

18 virguliforme that are pathogenic to soybean (Glycine max).

19 wild-type roots of the crop legume soybean (Glycine max).

20 thaliana, rice (Oryza sativa), and soybean (Glycine max).

21 defense-related SA accumulation in soybean (Glycine max).

22 ago truncatula and the grain legume soybean (Glycine max).

23 alance during nodule development in soybean (Glycine max).

24 dule development in the crop legume soybean (Glycine max).

25 ne integration, and gene editing in soybean (Glycine max).

26 of transgenic plants, including for soybean (Glycine max).

27 ) closely related to the cultivated soybean (Glycine max).

28 synthetic apatite nanoparticles on soybean (Glycine max).

29 ne expression in two developmental stages of Glycine max.

30 nes in Danio rerio, Arabidopsis thaliana and Glycine max.

31 he diploid Lotus japonicus and the polyploid Glycine max.

32 ions of 18 Vigna species and protein sets of Glycine max.

33 g pathways in disease resistance in soybean (Glycine max), 13, nine, and 10 genes encoding distinct M

34 and temperature (+3.5 degrees C) on soybean (Glycine max) A, biomass, and yield were tested over two

35 To test this idea in soybean (Glycine max), a full-length cDNA encoding a putative ort

36 hemical capacity was measured in 67 soybean (Glycine max) accessions showing large variation in leaf

37 a from Medicago truncatula, Lotus japonicus, Glycine max and Arabidopsis thaliana.

38 T) control pigmentation of the seed coats in Glycine max and are genetically distinct from those cont

39 use transcriptome data from various soybean (Glycine max and Glycine soja) tissues treated under diff

40 go truncatula, Lotus japonicus, and soybean (Glycine max and Glycine soja) to nonlegume unigene sets,

41 of three model legumes, Medicago truncatula, Glycine max and Lotus japonicus plus two reference plant

42 rrangement than two other sequenced legumes, Glycine max and Lotus japonicus.

43 gene families with those of fellow legumes, Glycine max and Phaseolus vulgaris, in addition to the m

44 ST) sequences we have identified 25 soybean (Glycine max) and 42 maize (Zea mays) clones and obtained

45 opsis lineage diverged from that of soybean (Glycine max) and before it diverged from its sister genu

46 gh-antioxidant black legumes, black soybean (Glycine max) and black turtle bean (Phaseolus vulgaris),

47 g TTM2 orthologs in the crop plants soybean (Glycine max) and canola (Brassica napus), suggesting tha

48 Soybean (Glycine max) and common bean (Phaseolus vulgaris) share

49 repeat (LRR) gene cluster found in soybean (Glycine max) and common bean (Phaseolus vulgaris) that i

50 h higher diversity and less LD than soybean (Glycine max) and exhibits patterns of LD and recombinati

51 d annotations for two accessions of soybean (Glycine max) and for one accession of Glycine soja, the

52 e and portal integrate Arabidopsis, soybean (Glycine max) and grapevine (Vitis vinifera) data.

53 a genetic map to reference legumes, soybean (Glycine max) and Medicago truncatula, revealed extensive

54 studies of photosynthetic oilseeds, soybean (Glycine max) and rapeseed (Brassica napus).

55 of an elaborate G-protein family in soybean (Glycine max) and the availability of appropriate molecul

56 y Pseudomonas syringae pv tomato in soybean (Glycine max) and tobacco (Nicotiana tabacum), as monitor

57 , as well as the DGAT2 enzymes from soybean (Glycine max), and castor (Ricinus communis), followed by

58 oded by a small multigene family in soybean (Glycine max), and cDNA clones for the different members

59 ty, which spanned maize (Zea mays), soybean (Glycine max), and eggplant (Solanum melongena).

60 by the mouse BAX protein in yeast, soybean (Glycine max), and Nicotiana benthamiana cells.

61 s and symbiotic soil bacteria (e.g. soybean [Glycine max] and Bradyrhizobium japonicum) initiated by

62 ified genes HAR1 (Lotus japonicus) and NARK (Glycine max) are orthologs based on gene sequence and sy

63 We developed a soybean (Glycine max) assay, BARCSoySNP6K, containing 6000 marker

64 e of ATP sulfurylase isoform 1 from soybean (Glycine max ATP sulfurylase) in complex with APS was det

65 eologous regions were identified in soybean (Glycine max) based on microsynteny and fluorescence in s

66 ted PLMT cDNAs from Arabidopsis and soybean (Glycine max) based upon primary amino acid sequence homo

67 gnificant agricultural losses, with soybean (Glycine max) being highly sensitive to this oxidant.

68 DNA-binding transcription factor now renamed Glycine max bHLH membrane 1 (GmbHLHm1).

69 0 microm Mn decreased the growth of soybean (Glycine max), but white lupin (Lupinus albus), narrow-le

70 m is a nurse cell formed within the roots of Glycine max by the plant parasitic nematode Heterodera g

71 set of genes in the paleopolyploid soybean (Glycine max) by comparing the orthologs between soybean

72 oja, the wild relative of cultivated soybean Glycine max, by sequencing and de novo assembly of seven

73 rhizobium fredii HH103 in three host plants: Glycine max, Cajanus cajan and the IRLC legume Glycyrrhi

74 By contrast, soybean (Glycine max) can distinguish between these effectors, wi

75 Here we show that soybean (Glycine max) CAS and OASS form alpha-aminoacrylate react

76 e-hybrid screen was used to isolate soybean (Glycine max) cDNA encoding a GAGA-binding protein (GBP)

77 We used soybean (Glycine max) cDNA microarrays to identify candidate gene

78 proteins encoded by Arabidopsis thaliana and Glycine max cDNAs revealed a unique family of proteins c

79 sis (Arabidopsis thaliana) CPK4 and soybean (Glycine max) CDPKbeta are RcCDPK1 orthologs that effecti

80 pproximately 1 million-bp region in soybean (Glycine max) centered on the Rpg1-b disease resistance g

81 chitinase involved in pathogen defense, and Glycine max chalcone synthase1 (Gmachs1), chalcone synth

82 and functionally characterized five soybean (Glycine max) chalcone isomerases (CHIs), key enzymes in

83 The pericentromeric regions of soybean (Glycine max) chromosomes contain >3,200 intact copies of

84 this work, we identified the entire soybean (Glycine max) CIPK gene family, which comprised 52 genes

85 In soybean (Glycine max) commercial plantings, the identification an

86 The overexpression of AraEXLB8 in soybean (Glycine max) composite plants remarkably decreased the n

87 ns at within-membrane residues in the legume Glycine max Cox2 could enable yeast COX2 allotopic expre

88 onsible for the damage it causes in soybean (Glycine max) crop.

89 eat flux (lambdaET) of a commercial soybean (Glycine max) cultivar (Pioneer 93B15), exposed to a grad

90 okinin-inducible beta-expansin from soybean (Glycine max cv Mandarin) called Cim1.

91 Roots of soybean, Glycine max cv. Kent L. Merr., plants susceptible to the

92 or symbiotic nitrogen fixation with soybean (Glycine max cv. Williams 82).

93 of proteins during seed filling in soybean (Glycine max) cv Maverick.

94 embrane electron flow mediated by a soybean (Glycine max) cytochrome b561 associated with a dopamine

95 h significant identity (74%) to the soybean (Glycine max) early nodulin (ENOD) gene GmENOD93.

96 suggested an important role for the soybean (Glycine max) ecto-apyrase GS52 in rhizobial root hair in

97 l-CoA desaturase homolog in somatic soybean (Glycine max) embryos behind a strong seed-specific promo

98 icotiana tabacum) callus or somatic soybean (Glycine max) embryos resulted in the accumulation of ver

99 uxes, we rapidly labeled developing soybean (Glycine max) embryos with [(14)C]acetate and [(14)C]glyc

100 abundant Suc, and Gln to developing soybean (Glycine max) embryos.

101 tic embryogenesis, we characterized soybean (Glycine max) epigenomes sampled from embryos at 10 diffe

102 ys in mung bean (Vigna radiata) and soybean (Glycine max) following growth at low temperature.

103 sulfonate mutagenized population of soybean (Glycine max) 'Forrest' was screened to identify mutants

104 ns consist of elite cultivars and landraces (Glycine max, fully domesticated (FD)), annual wild type

105 of the tomato FW2.2 gene, here named GmFWL1 (Glycine max FW2.2-like 1), was found to respond strongly

106 A Glycine max gene encoding a putative protein similar to

107 designed to simultaneously silence soybean (Glycine max) genes fatty acid omega-6 desaturase 2 (FAD2

108 of a transgene and nine endogenous soybean (Glycine max) genes using zinc-finger nucleases (ZFNs).

109 f polyploidy that contributed to the current Glycine max genome: a genome triplication before the ori

110 in cowpea using a readily available soybean (Glycine max) genome array.

111 The soybean (Glycine max) genome contains 18 members of the 14-3-3 pr

112 The soybean (Glycine max) genome has been shown to be composed of app

113 nt studies have documented that the soybean (Glycine max) genome has undergone two rounds of large-sc

114 rgeting of transgenes to predefined soybean (Glycine max) genome sites using the yeast FLP-FRT recomb

115 to induce deletion mutations in the soybean (Glycine max) genome.

116 31 resequenced wild and cultivated soybean (Glycine max) genomes and detected 34,154 unique nonrefer

117 and define a research strategy for soybean (Glycine max) genomics began with the establishment of a

118 complished by isolating syncytial cells from Glycine max genotype Peking (PI 548402) by laser capture

119 variations were assessed among four soybean (Glycine max) genotypes using array hybridization and tar

120 rst and gene expression across four soybean (Glycine max) genotypes.

121 at are related to the auxin-induced soybean (Glycine max) GH3 gene product synthesize IAA-amino acid

122 RNA interference, the synthesis of soybean (Glycine max) glycinin and conglycinin storage proteins h

123 AGL15) and a putative ortholog from soybean (Glycine max), GmAGL15, are able to promote somatic embry

124 t cells, we have cloned a cDNA from soybean (Glycine max), GmMan1, encoding the resident Golgi protei

125 Studies on the soybean (Glycine max) GmPTP have shown that, compared with its ma

126 operties of a recombinant form of a soybean (Glycine max) group 2 LEA (rGmDHN1).

127 nd among-cultivar components across soybean (Glycine max) grown under both controlled and field condi

128 terize the AM fungal communities of soybean (Glycine max) grown under elevated and ambient atmospheri

129 elopment at elevated [CO(2)] using soybeans (Glycine max) grown under fully open air conditions at th

130 Soybean (Glycine max) has undergone at least two rounds of polypl

131 subgenomes in maize (Zea mays) and soybean (Glycine max) have followed different trajectories.

132 ), cotton (Gossypium hirsutum), and soybean (Glycine max), have contributed to important agronomic tr

133 ific Gbeta and Ggamma proteins of a soybean (Glycine max) heterotrimeric G-protein complex are involv

134 S), we determined the structures of soybean (Glycine max) hGS in three states: apoenzyme, bound to ga

135 tic organisms (rice [Oryza sativa], soybean [Glycine max], human [Homo sapiens], yeast [Saccharomyces

136 n to address this question, we grew soybean (Glycine max) in a Temperature by Free-Air CO(2) Enrichme

137 t waves were applied to field-grown soybean (Glycine max) in central Illinois, three in 2010 and two

138 hamnus spp.) and the secondary host soybean (Glycine max) in North America where it is invasive.

139 between corn (Zea mays) and nonhost soybean (Glycine max) in the United States.

140 adversely affects the production of soybean, Glycine max, in many areas of the world, particularly in

141 leaf size in both M. truncatula and soybean (Glycine max), indicating functional conservation.

142 CR and proteomics to study putative soybean (Glycine max) iron transporters GmVTL1a and GmVTL1b and h

143 Soybean (Glycine max) is a major legume crop plant providing over

144 Soybean (Glycine max) is a major plant source of protein and oil

145 Soybean (Glycine max) is a self-pollinating species that has rela

146 Soybean (Glycine max) is considered a major allergenic food.

147 Soybean (Glycine max) is one of the most important crop plants fo

148 Globally, soybean (Glycine max) is one of the most important oilseed crops

149 Soybean (Glycine max) is particularly sensitive to O(3); therefor

150 Soybean (Glycine max) is the most widely grown oilseed in the wor

151 ell characterized symbiosis between soybean (Glycine max L.

152 e (p,p'-DDE; DDT metabolite) accumulation by Glycine max L. (soybean) and Cucurbita pepo L. (zucchini

153 metabolite) by Cucurbita pepo L. (zucchini), Glycine max L. (soybean), and Solanum lycopersicum L. (t

154 In prior work, we observed that soybean (Glycine max L. cv Merr.) seeds inoculated with a mutant

155 ochondria of 14-d-old cotyledons of soybean (Glycine max L. cv Stevens).

156 thesis, thereby limiting growth and yield of Glycine max L. Merr.

157 Glycine max L. Merr. (soybean) resistance to Heterodera

158 induced from immature cotyledons of soybean (Glycine max L. Merr. cv Jack) placed on high levels of t

159 Soybean (Glycine max L. Merr.) contains two related and abundant

160 Soybean (Glycine max L. Merr.) cv Young (Al-sensitive) and PI 416

161 P frequency in coding and noncoding soybean (Glycine max L. Merr.) DNA sequence amplified from genomi

162 al makeup of heterochromatin in the soybean (Glycine max L. Merr.) genome.

163 Sudden death syndrome (SDS) of soybean (Glycine max L. Merr.) is an economically important disea

164 study used mutagenesis to identify soybean (Glycine max L. Merr.) lines with reduced sensitivity to

165 mplementing association analysis in soybean (Glycine max L. Merr.), we analyzed the structure of LD i

166 A single, recessive mutation in soybean (Glycine max L. Merr.), which confers a seed phenotype of

167 eity from cotyledons of germinated soybeans (Glycine max L. Merr.).

168 ned for peptides that interact with soybean (Glycine max L.) CDPKalpha, an isoform of calcium-depende

169 Soybean (Glycine max L.) has undergone two separate polyploidy ev

170 Soybean (Glycine max L.) is a major crop providing an important s

171 paraveinal mesophyll cell layer of soybean (Glycine max L.) leaves where individual isoforms are pro

172 tosol of a single cell layer in the soybean (Glycine max L.) pod wall.

173 A consistent risk for soybean (Glycine max L.) production is the impact of drought on g

174 esting (H) under corn (Zea mays L.)-soybean (Glycine max L.) rotation.

175 es were detected in Arabidopsis and soybean (Glycine max L.), but not in corn (Zea mays L.).

176 ), the most damaging insect pest of soybean (Glycine max (L.) Merr.) in North America.

177 Soybean (Glycine max (L.) Merr.) is an important crop that provid

178 Soybean (Glycine max (L.) Merr.) is an O3 -sensitive crop species

179 The pigmented seed coats of several soybean (Glycine max (L.) Merr.) plant introductions and isolines

180 Two types of resistant soybean (Glycine max (L.) Merr.) sources are widely used against

181 rophyll a during germination of the soybean (Glycine max (L.) Merr.) sprout varieties, 'Pungsannamulk

182 milies comprising 32370 elements in soybean (Glycine max (L.) Merr.).

183 o officinalis L.; 37% LA and 23% GLA) or SO [Glycine max (L.) Merr.; 50% LA and 0% GLA] for 4 wk, fol

184 h the intensity of greenness of the soybean [Glycine max (L.) Merr.] canopy as determined by the Dark

185 We collected soybean [Glycine max (L.) Merr.] data were collected from field e

186 Cultivated soybean [Glycine max (L.) Merr.] is a primary source of vegetable

187 Soybean [Glycine max (L.) Merr.] is an economically important cro

188 Soybean [Glycine max (L.) Merr.] is the most important oilseed cr

189 es along with expression studies in soybean [Glycine max (L.) Merr.] were leveraged to dissect the ge

190 d to amplify related sequences from soybean [Glycine max (L.) Merr.].

191 Soybean (Glycine max (L.) Merrill) is one of the most important f

192 uctural variants observed among 264 soybean [Glycine max (L.) Merrill] plants sampled from a large fa

193 ize with another crop, principally soybeans, Glycine max (L.), was the primary management strategy ut

194 Nodulated soybean plants (Glycine max [L.] Merr. cv Ransom) in a growth-chamber st

195 NH4+ by roots, nonnodulated soybean plants (Glycine max [L.] Merr. cv Ransom) were grown for 24 days

196 nflower (Helianthus annuus L.), and soybean (Glycine max [L.] Merr.) caused bending away from that si

197 The development of a universal soybean (Glycine max [L.] Merr.) cytogenetic map that associates

198 57 forms nitrogen-fixing nodules on soybean (Glycine max [L.] Merr.) in a cultivar-specific manner.

199 Soybean (Glycine max [L.] Merr.) is one of the most important oil

200 ecreased dry weight accumulation by soybean (Glycine max [L.] Merrill cv Wells II).

201 Soybean (Glycine max [L.] Merrill) mutant aj6 carries a single re

202 Decreased N2 fixation in soybean (Glycine max) L. Merr. during water deficits has been ass

203 have isolated a 12-aa peptide from soybean (Glycine max) leaves that causes a pH increase of soybean

204 ein, we report a novel peptide from soybean (Glycine max) leaves that is capable of alkalinizing the

205 We labeled soybean (Glycine max) leaves with 200 and 600 ppm (13) CO(2) spik

206 jimson weed (Datura metel), but not soybean (Glycine max), like that of tobacco, possess ProteinaseK-

207 rization of a giant retrovirus-like soybean (Glycine max) LTR retrotransposon family, SNARE.

208 ductance (gs )) for legumes Cicer arietinum, Glycine max, Lupinus alba and Vicia faba, nonlegume dico

209 Soybean (Glycine max Merr.) is a widely grown oilseed crop and sh

210 We have identified a novel soybean (Glycine max) metalloproteinase gene, GmMMP2, that is tra

211 A soybean (Glycine max) MIPS cDNA (GmMIPS1) was isolated by reverse

212 French bean (Phaseolus vulgaris) or soybean (Glycine max), most of the fixed nitrogen is used for syn

213 pression cassette consisting of the soybean (Glycine max) native promoter modified for enhanced expre

214 tal SS (nodulin-100) pool in mature soybean (Glycine max) nodules is apparently associated with the p

215 A cDNA was isolated from soybean (Glycine max) nodules that encodes a putative transporter

216 kinase and PEPC phosphorylation in soybean (Glycine max) nodules, we now report the molecular clonin

217 e that is similar to the archetype, soybean (Glycine max) nodulin 26, and another that is characteris

218 Inoculation of soybean (Glycine max) plants with Phakopsora pachyrhizi, the caus

219 Soybean (Glycine max) possesses three CDA genes, but only two enc

220 degrees C, Rubisco from Hordeum vulgare and Glycine max presented, respectively, the highest and low

221 bean rust is a formidable threat to soybean (Glycine max) production in many areas of the world, incl

222 The increasing use of soybean (Glycine max) products in processed foods poses a potenti

223 Nonuniformly labeled Glycine max protein was used to demonstrate the technolo

224 or AvrB interacts with four related soybean (Glycine max) proteins (GmRIN4a-d), three (GmRIN4b, c, d)

225 was developed for a large number of soybean (Glycine max) putative regulatory genes available in the

226 sequential stages of development in soybean (Glycine max), rapeseed (Brassica napus), and Arabidopsis

227 ommon bean (Phaseolus vulgaris) and soybean (Glycine max) reference genomes.

228 hought to play an important role in soybean (Glycine max) resistance to Phytophthora sojae.

229 new insights into the mechanism of soybean (Glycine max) resistance to the soybean cyst nematode (He

230 olonization of maize (Zea mays) and soybean (Glycine max), respectively.

231 storage protein beta-conglycinin of soybean (Glycine max) resulted in good AAMD and flux estimates if

232 ic analysis between Arabidopsis thaliana and Glycine max root hair genes reveals the evolution of the

233 By incubating soybean (Glycine max) root extract enriched in GS in a metal-cata

234 e analyzed the proteome of isolated soybean (Glycine max) root hair cells using two-dimensional polya

235 Nodulation of soybean (Glycine max) root hairs by the nitrogen-fixing symbiotic

236 We report here that soybean (Glycine max) root nodules contain at least 14 forms of G

237 which DNA methylation is altered in soybean (Glycine max) roots during the susceptible interaction wi

238 anced imaging techniques to examine soybean (Glycine max) roots exposed to Al.

239 rence to silence GS52 expression in soybean (Glycine max) roots using Agrobacterium rhizogenes-mediat

240 Soybean (Glycine max) RPG1-B (for resistance to Pseudomonas syrin

241 or portion of the phosphorus in the soybean (Glycine max) seed and chelates divalent cations.

242 The soybean (Glycine max) seed coat has distinctive, genetically prog

243 that accumulate specifically within soybean (Glycine max) seed regions, subregions, and tissues durin

244 we investigated the mobilization of soybean (Glycine max) seed reserves during seedling growth by ini

245 , beta-conglycinin and glycinin, in soybean (Glycine max) seeds hinder the isolation and characteriza

246 Soybean (Glycine max) seeds store significant amounts of their bi

247 seeds in planta, Brassica napus and soybean (Glycine max) seeds were rapidly dissected from plants gr

248 orably alter carbon partitioning in soybean (Glycine max) seeds.

249 Glycine max serine acetyltransferase 2;1 (GmSerat2;1) is

250 the use of horse (Equus caballus), soybean (Glycine max), sheep (Ovis aries), poultry (Meleagris mel

251 tagenesis of legume genomes such as soybean (Glycine max) should aid in identifying genes responsible

252 Two dominant alleles of the I locus in Glycine max silence nine chalcone synthase (CHS) genes t

253 th the Gag extension encoded by the soybean (Glycine max) SIRE1 element, and an interaction was found

254 and analyzed an expression atlas of soybean (Glycine max) small RNAs, identifying over 500 loci gener

255 to screen PS-SGCL against two plant lectins, Glycine max soybean agglutinin and Vicia villosa.

256 a and Lotus japonicus, and two crop species, Glycine max (soybean) and Phaseolus vulgaris (common bea

257 We chose Glycine max (soybean) as a model to investigate SEO prot

258 l dynamics of lighting for a rendered mature Glycine max (soybean) canopy to review the relative impo

259 We reinvestigated Glycine max (soybean) for its indoles and found indole-3

260 Recent examination of the Glycine max (soybean) genome reveals a larger set of G-p

261 Using a Glycine max (soybean) GS1 transgene, with and without it

262 96 and a homologous gene, PsAvh163, from the Glycine max (soybean) pathogen Phytophthora sojae.

263 loidy (by duplication or hybridization) like Glycine max (soybean) present challenges during genome a

264 Glycine max (soybean) Sec4 functions in the root during

265 s (corn), Solanum lycopersicum (tomato), and Glycine max (soybean) was investigated.

266 plied to three plants, Arabidopsis thaliana, Glycine max (soybean), and Zea mays (maize) to discover

267 for six legume species: Medicago truncatula, Glycine max (soybean), Lotus japonicus, Phaseolus vulgar

268 this question, we have compared R genes from Glycine max (soybean), Rpg1-b, and Arabidopsis thaliana,

269 or candidate genes stimulating cell death in Glycine max (soybean), we transiently overexpressed full

270 information concerning the relevant genes in Glycine max (soybean).

271 , constitutes an eight-member gene family in Glycine max (soybean).

272 nel of wild (Glycine soja) and domesticated (Glycine max) soybeans.

273 We have named this peptide signal Glycine max Subtilase Peptide (GmSubPep).

274 PS2 and 3 are present in Lotus japonicus and Glycine max, suggesting the existence of a specific cons

275 Zea mays) floury-2 (fl2) mutant and soybean (Glycine max) suspension cultures treated with tunicamyci

276 We show that Glycine max symbiotic ammonium transporter 1 is actually

277 Glycine max symbiotic ammonium transporter 1 was first d

278 A Glycine max syntaxin 31 homolog (Gm-SYP38) was identifie

279 specially useful for plants such as soybean (Glycine max) that are recalcitrant to transformation.

280 Rj4 is a dominant gene in soybeans (Glycine max) that restricts nodulation by many strains o

281 metabolites (i.e. phytoalexins) of soybean (Glycine max) that, collectively with other 5-deoxyisofla

282 In tolerant plants like soybean (Glycine max), the chemical nonetheless causes necrotic p

283 Weeds reduce yield in soybeans (Glycine max) through incompletely defined mechanisms.

284 ore innate developmental process in soybean (Glycine max) to establish its feeding structure, syncyti

285 abolic processes of seed filling in soybean (Glycine max), two complementary proteomic approaches, tw

286 work reports a detailed characterization of Glycine max UreG (GmUreG), a urease accessory protein.

287 In some legumes like soybean (Glycine max), ureides are used for nodule-to-shoot trans

288 We addressed this in soybean (Glycine max) using a combination of physiological and ge

289 e A (CoA) carboxylase (ACCase) from soybean (Glycine max) was characterized.

290 n g(s) at the leaf to ecosystem ET, soybean (Glycine max) was grown in field conditions under control

291 hora sojae, an oomycete pathogen of soybean (Glycine max), we show that a pair of sequence motifs, RX

292 ic auxin-responsive DR5 promoter in soybean (Glycine max), we show that there is relatively low auxin

293 PC phosphorylation in N(2)-fixing nodules of Glycine max, we now present a detailed molecular analysi

294 ehydrogenase (NADP-IDH) isozymes of soybean (Glycine max) were characterized.

295 ce in the Peking-type resistance of soybean (Glycine max), which also requires the rhg1 gene.

296 the Calvin cycle) in the cultivated soybean (Glycine max), which has experienced two rounds of whole-

297 e and easily dissected seedlings of soybean (Glycine max 'Williams 82'), we show that genes involved

298 onstrate that the transformation of soybean (Glycine max) with sense suppression constructs using int

299 proteins from both Arabidopsis and soybean (Glycine max) within two highly conserved nitrate-induced

300 Soybean (Glycine max) yields high levels of both protein and oil,