ライフサイエンスコーパス: Glycine max

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

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

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

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

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

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

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

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

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

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

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

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

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

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

15 um), alfalfa (Medicago sativa), and soybean (Glycine max).

16 entity to a 1,3-beta-glucanase from soybean (Glycine max).

17 ired in symbiotic interactions with soybean (Glycine max).

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

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

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

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

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

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

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

25 synthetic apatite nanoparticles on soybean (Glycine max).

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

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

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

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

30 ne expression in two developmental stages of Glycine max.

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

32 he diploid Lotus japonicus and the polyploid Glycine max.

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

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

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

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

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

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

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

40 evels and pattern of variability detected in Glycine max and G. soja genotypes.

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

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

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

44 s could be identified in the genomes of both Glycine max and Medicago sativa.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 0 microm Mn decreased the growth of soybean (Glycine max), but white lupin (Lupinus albus), narrow-le

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 We previously cloned the soybean (Glycine max cv. Century) DapA gene in Escherichia coli t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 A Glycine max gene encoding a putative protein similar to

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

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

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

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

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

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

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

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

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

113 31 resequenced wild and cultivated soybean (Glycine max) genomes and detected 34,154 unique nonrefer

114 py of this element has been recovered from a Glycine max genomic library.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Soybean agglutinin (SBA) (Glycine max) is a tetrameric GalNAc/Gal-specific lectin

142 The nutritional quality of soybeans (Glycine max) is compromised by a relative deficiency of

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

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

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

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

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

148 In previous work with soybean (Glycine max), it was reported that the initial product o

149 ell characterized symbiosis between soybean (Glycine max L.

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

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

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

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

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

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

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

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

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

159 Diverse functions for three soybean (Glycine max L. Merr.) cysteine proteinase inhibitors (Cy

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

161 and pN2) have been isolated from a soybean (Glycine max L. Merr.) embryo library.

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 Soybean (Glycine max L. Merr.) mutants lacking the ability to pro

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

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

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

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

170 level and activity were measured in soybean (Glycine max L.) embryos from the reserve deposition stag

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

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

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

174 found in the bacteroid membranes of soybean (Glycine max L.) nodules; At-NLM1 is an active aquaporin

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

176 of the major acid phosphatase from soybean (Glycine max L.) root nodules.

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

178 late choline kinase-like cDNAs from soybean (Glycine max L.).

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

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

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

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

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

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

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

186 port a mariner element in the plant soybean (Glycine max (L.) Merr.).

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

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

189 Two soybean [Glycine max (L.) Merr.] lipoxygenase cDNA clones were is

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

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

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

193 Somatic embryos of jack, a Glycine max (L.) Merrill cultivar, were transformed usin

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

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

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

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

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

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

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

201 57 forms nitrogen-fixing nodules on soybean (Glycine max [L.] Merr.) in a cultivar-specific manner.

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

203 Previously, a protein of soybean (Glycine max [L.] Merr.) leaves was shown to possess prop

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

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

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

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

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

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

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

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

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

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

214 but the dicots pea (Pisum sativum), soybean (Glycine max Merr.), and spinach (Spinacia oleracea) cont

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

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

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

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

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

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

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

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

223 eripheral to the infected region of soybean (Glycine max), pea (Pisum sativum), clover (Trifolium pra

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 A soybean (Glycine max) root-nodule cDNA encoding GTR was isolated

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

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

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

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

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

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

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

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

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

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

253 n animal diets when engineered into soybean (Glycine max) seeds.

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

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

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

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

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

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

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

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

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

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

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

265 96 and a homologous gene, PsAvh163, from the Glycine max (soybean) pathogen Phytophthora sojae.

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

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

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

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

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

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

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

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

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

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

276 Glycine max symbiotic ammonium transporter 1 was first d

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

278 rsed copies of a very large DNA element from Glycine max that has features characteristic of retrovir

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

298 morphism mapping data from nine populations (Glycine max x G. soja and G. max x G. max) of the Glycin

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