ライフサイエンスコーパス: Phaseolus vulgaris

1 yproline-rich glycoproteins (HRGPs) in bean (Phaseolus vulgaris).

2 romosomes based on synteny with common bean (Phaseolus vulgaris).

3 d systemically infect leaves of common bean (Phaseolus vulgaris).

4 sis thaliana) and other plants such as bean (Phaseolus vulgaris).

5 e development of halo blight in common bean (Phaseolus vulgaris).

6 tudies in soybean as well as in common bean (Phaseolus vulgaris).

7 of PvD(1), the defensin from the common bean Phaseolus vulgaris.

8 ALANINE AMMONIA-LYASE 2 (PAL2) promoter from Phaseolus vulgaris.

9 ll phases of vegetative development in bean, Phaseolus vulgaris.

10 s-zeatin and UDP-xylose in immature seeds of Phaseolus vulgaris.

11 R1-R5, in Phaseolus vulgaris.

12 fferentially expressed during development in Phaseolus vulgaris.

13 he integration of leaf and xylem function in Phaseolus vulgaris.

14 ted in establishing symbiosis with its host, Phaseolus vulgaris.

15 of the inheritance of PD in the common bean (Phaseolus vulgaris), a major domesticated grain legume.

16 The common-bean (Phaseolus vulgaris), a widely consumed legume, originate

17 eoli strain 8002, which forms symbiosis with Phaseolus vulgaris, a determinate nodulating legume.

18 topic expression of the transcription factor Phaseolus vulgaris ABI3-like factor (ALF) and applicatio

19 aris), is activated in two sequential steps: Phaseolus vulgaris ABI3-like factor (Pv-ALF)-dependent p

20 nsitive3 (ABI3), maize viviparous1 (VP1) and Phaseolus vulgaris ABI3-like factor (PvALF) in the spati

21 is when it is potentiated by the presence of Phaseolus vulgaris ABI3-like factor (PvALF), a plant-spe

22 abscission-specific expression of the bean (Phaseolus vulgaris) abscission cellulase (BAC) promoter.

23 alpha AI) protects seeds of the common bean (Phaseolus vulgaris) against predation by certain species

24 Phytohemagglutinin (Phaseolus vulgaris agglutinin; PHA; E- and L-forms) and

25 Common beans (Phaseolus vulgaris), an ozone-sensitive crop, are widely

26 syringae-triggered stomatal closure in both Phaseolus vulgaris and Arabidopsis (Arabidopsis thaliana

27 did not prevent normal nodule development on Phaseolus vulgaris and had very little effect on the occ

28 atches were applied to leaves of heterobaric Phaseolus vulgaris and homobaric Commelina communis, chl

29 during symbiotic infection of the host plant Phaseolus vulgaris and produced abnormal symbiosome stru

30 ng serial passage through N. benthamiana and Phaseolus vulgaris and, after three to five passages, be

31 rates and metabolites were measured in bean (Phaseolus vulgaris) and Arabidopsis (Arabidopsis thalian

32 s leading to the cloning of KAP-2 from bean (Phaseolus vulgaris) and barrel medic (Medicago truncatul

33 In other legume species, such as beans (Phaseolus vulgaris) and cowpeas (Vigna unguiculata), dif

34 new study reports the genome of common bean (Phaseolus vulgaris) and genome-wide resequencing data fr

35 imary monofoliate leaves of the common bean (Phaseolus vulgaris) and in early Arabidopsis rosette lea

36 g symbiosis established between common bean (Phaseolus vulgaris) and Rhizobium etli.

37 n this study in closely related common bean (Phaseolus vulgaris) and soybean (Glycine max) reference

38 s), peppers (Capsicum annuum), common beans (Phaseolus vulgaris), and cotton (Gossypium hirsutum).

39 mato (Solanum lycopersicum L.), green beans (Phaseolus vulgaris), and cowpeas (Vigna unguiculata), wi

40 several species including Arabidopsis, bean (Phaseolus vulgaris), and potato (Solanum tuberosum).

41 germinating seeds and seedlings of the bean Phaseolus vulgaris, and a smaller but consistently detec

42 second soybean genotype, Glycine tomentella, Phaseolus vulgaris, and Medicago truncatula), which enab

43 cis-epoxicarotenoid dioxygenase GB:AAF26356 [Phaseolus vulgaris] and to NCED3 GB:AB020817 [Arabidopsi

44 unflower [Helianthus annuus] and dwarf bean [Phaseolus vulgaris]; and three species without bundle sh

45 Using Rhizobium tropici CIAT 899 and Phaseolus vulgaris as working models, we demonstrated th

46 after injury was calculated for green bean (Phaseolus vulgaris), bamboo (Phyllostachys nuda), squash

47 soybean (Glycine max) and black turtle bean (Phaseolus vulgaris), belonging to two different genera w

48 ate 4-hydroxylase sequence from French bean (Phaseolus vulgaris), but codes for a unique N-terminus.

49 eous sizes are formed during colonization of Phaseolus vulgaris by Pseudomonas syringae.

50 purified from seed meal of the common bean (Phaseolus vulgaris) by membrane fractionation, solubiliz

51 ted a comprehensive analysis of common bean (Phaseolus vulgaris) centromeric satellite DNA using geno

52 3'-) sequences from the arcelin 5-I gene of Phaseolus vulgaris (cgl-IDUA-SEKDEL and Col-IDUA-SEKDEL,

53 Andean beans (Phaseolus vulgaris) chemical compositions and cooking ch

54 cess to extrafloral nectar (EFN) produced by Phaseolus vulgaris (common bean) can protect companion Z

55 ula, Glycine max (soybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer arietinum (chick

56 two crop species, Glycine max (soybean) and Phaseolus vulgaris (common bean).

57 attern was found in 0.94 Mb of sequence from Phaseolus vulgaris (common bean).

58 vy and etiolated hypocotyls of kidney beans (Phaseolus vulgaris), contained differentiating tracheary

59 The I locus of the common bean, Phaseolus vulgaris, controls the development of four dif

60 city by comparing responses of two snapbean (Phaseolus vulgaris) cultivars (cv Dade and cv Romano) kn

61 ologous to plant defensins was purified from Phaseolus vulgaris cv. 'King Pole Bean' by anion-exchang

62 a viral resistance response in common bean (Phaseolus vulgaris cv. Othello) were identified by inocu

63 related to two legume cysteine proteinases (Phaseolus vulgaris EP-C1 and Vigna mungo SHEP) which are

64 On the contrary, Phaseolus vulgaris erythroagglutinating lectin (E-PHA),

65 lli lectin (ECL), Sambucus nigra lectin, and Phaseolus vulgaris Erythroagglutinin (PHA-E) are used to

66 y galactosylated N-glycans recognized by the Phaseolus Vulgaris erythroagglutinin lectin.

67 and domesticated accessions of common bean (Phaseolus vulgaris) from Mesoamerica.

68 and in the apoplast of the susceptible plant Phaseolus vulgaris Genes within the functional categorie

69 Transcripts mapped to the Phaseolus vulgaris genome-another phaseoloid legume with

70 leaf area and leaf mass in the common bean (Phaseolus vulgaris) grown in two contrasting environment

71 ong recombinant inbred lines of common bean (Phaseolus vulgaris) having four distinct root phenotypes

72 ion of genetic variation of the common bean (Phaseolus vulgaris) in its centres of domestication.

73 leaf area vs. leaf mass for the common bean (Phaseolus vulgaris) in two different environments.

74 ith those of fellow legumes, Glycine max and Phaseolus vulgaris, in addition to the model plant Arabi

75 etic activities of Fagioli di Sarconi beans (Phaseolus vulgaris), including 21 ecotypes protected by

76 eam of the G564 ortholog in the Common Bean (Phaseolus vulgaris), indicating that the regulation of G

77 ding the major seed storage protein of bean (Phaseolus vulgaris) is confined to the cotyledons of dev

78 odes the major seed storage protein in bean (Phaseolus vulgaris), is activated in two sequential step

79 onging to the species Lens culinaris Medik., Phaseolus vulgaris L. and Cicer arietinum L. after soaki

80 ) on the phenolic composition of dark beans (Phaseolus vulgaris L. c.v. Tolosana) and their effect on

81 the non-destructive discrimination of three Phaseolus vulgaris L. cultivars (Agro ANfc9, IPR-Andorin

82 toplasts isolated from the primary leaves of Phaseolus vulgaris L. were used in transient expression

83 of a group 6 LEA protein from a common bean (Phaseolus vulgaris L.) (PvLEA6) by circular dichroism an

84 insect community on smallholder bean farms (Phaseolus vulgaris L.) and its relationship with the pla

85 ack bean (BB) and pinto bean (PB) varieties (Phaseolus vulgaris L.) and pure phenolic compounds (ruti

86 Common beans (Phaseolus vulgaris L.) are widely consumed legumes in La

87 07A1 and PvCYP707A2 were isolated from bean (Phaseolus vulgaris L.) axes treated with (+)-ABA and tha

88 We have constructed a common bean (Phaseolus vulgaris L.) bacterial artificial chromosome (

89 ersal via pod shattering during common bean (Phaseolus vulgaris L.) domestication.

90 rostructural characteristics of common bean (Phaseolus vulgaris L.) during 270 days of post-harvest s

91 orophyll content was studied in common bean (Phaseolus vulgaris L.) exposed to excess Mn.

92 White kidney bean (Phaseolus vulgaris L.) extracts can aid weight managemen

93 nt process in the preparation of navy beans (Phaseolus vulgaris L.) for canning.

94 Twenty-four different beans' genotypes (Phaseolus vulgaris L.) grown onto two different sites ha

95 r-managed experimental plots of common bean (Phaseolus vulgaris L.) in Nicaragua, durum wheat (Tritic

96 The cultivation of common beans (Phaseolus vulgaris L.) in semi-arid regions is affected

97 bending movements of shoots of common beans (Phaseolus vulgaris L.) in two conditions: with and witho

98 The common bean (Phaseolus vulgaris L.) is a crucial legume crop and an i

99 Wild common bean (Phaseolus vulgaris L.) is distributed throughout the Ame

100 The utilization of beans (Phaseolus vulgaris L.) is hindered by unpleasant flavors

101 Among cultivated plants, common bean (Phaseolus vulgaris L.) is the most important grain legum

102 Common bean (Phaseolus vulgaris L.) is the most important grain legum

103 es the effects of three Chilean boiled bean (Phaseolus vulgaris L.) landraces 'Negro', 'Peumo', and '

104 Proton excretion from bean (Phaseolus vulgaris L.) leaf cells is increased by bright

105 cDNA, PvNCED1, was cloned from wilted bean (Phaseolus vulgaris L.) leaves.

106 ed the effect of germination of black beans (Phaseolus vulgaris L.) on the antioxidant capacity and a

107 ypeptides of glutamine synthetase from bean (Phaseolus vulgaris L.) root nodules are very similar.

108 Treatment of bean (Phaseolus vulgaris L.) seedlings with low levels of sali

109 s, cotyledons and seed coats of black beans (Phaseolus vulgaris L.) subjected to germination over fiv

110 e baking performances of 25 edible dry bean (Phaseolus vulgaris L.) varieties and to investigate corr

111 Common bean (Phaseolus vulgaris L.) was introduced in Europe after 14

112 Common beans (Phaseolus vulgaris L.), represent the most consumed legu

113 It is a sister species of common bean (Phaseolus vulgaris L.), the most important legume protei

114 Common bean (Phaseolus vulgaris L.), the staple crop of Nicaragua, pr

115 op and characterize an extruded common bean (Phaseolus vulgaris L.)-based milk-type beverage added wi

116 e major seed storage protein of common bean, Phaseolus vulgaris L., accounting for up to 50 % of the

117 s of a Mesoamerican genotype of common bean (Phaseolus vulgaris L., BAT93).

118 larly species such as Macrotyloma uniflorum, Phaseolus vulgaris L., Glycine max L. and Vigna umbellat

119 Photosynthesis of Phaseolus vulgaris leaves, which do not make isoprene, e

120 on chickpea (Cicer arietinum), common bean (Phaseolus vulgaris), lentil (Lens culinaris) and lupin (

121 With the anterograde anatomical tracer Phaseolus vulgaris leuccoagglutinin, we examined the eff

122 First, the anterograde axonal marker Phaseolus vulgaris leuco-agglutinin (PHA-L) was injected

123 e studied with the anterograde axonal marker Phaseolus vulgaris leuco-agglutinin (PHA-L) with a parti

124 in beta fragment, or the anterograde tracer, Phaseolus vulgaris-leucoagglutin, into nuclei of the pre

125 using cholera toxin subunit-B (retrograde), Phaseolus vulgaris leucoagglutinin (anterograde), and ps

126 cral lamina I neurons were investigated with Phaseolus vulgaris leucoagglutinin (PHA-L) and labeled d

127 kittens with the anterograde neuronal tracer Phaseolus vulgaris leucoagglutinin (PHA-L) and performed

128 d small injections of the anterograde tracer Phaseolus vulgaris leucoagglutinin (PHA-L) and the retro

129 on of fibers and terminals in PAG labeled by Phaseolus vulgaris leucoagglutinin (PHA-L) injected into

130 RCx axons were labeled by Phaseolus vulgaris leucoagglutinin (PHA-L) injections, w

131 sident VTA neurons by intra-VTA injection of Phaseolus vulgaris leucoagglutinin (PHA-L) or an adeno-a

132 Injections of the anterograde tracer Phaseolus vulgaris leucoagglutinin (PHA-L) or the retrog

133 The anterograde tracer Phaseolus vulgaris leucoagglutinin (PHA-L) was injected

134 axonal tracing method using the plant lectin Phaseolus vulgaris leucoagglutinin (PHA-L) was used to d

135 The anterograde tracer, Phaseolus vulgaris leucoagglutinin (PHA-L), was iontophr

136 IL and the neighboring cortical areas using Phaseolus vulgaris leucoagglutinin (PHA-L).

137 of the amygdala (BMA) was examined with the Phaseolus vulgaris leucoagglutinin (PHAL) method in adul

138 Iontophoretic injections of Phaseolus vulgaris leucoagglutinin (PHAL) were placed in

139 e rat PVH with an anterograde axonal tracer, Phaseolus vulgaris leucoagglutinin (PHAL), and studied t

140 d in vivo with the anterograde lectin tracer Phaseolus vulgaris leucoagglutinin (PHAL).

141 nvestigated by using the anterograde tracers Phaseolus vulgaris leucoagglutinin and biotinylated dext

142 he rat by using the anterograde transport of Phaseolus vulgaris leucoagglutinin and Fluororuby.

143 By using the anterograde tracer Phaseolus vulgaris leucoagglutinin and the retrograde tr

144 e projection was labelled anterogradely with Phaseolus vulgaris leucoagglutinin and the second with b

145 the stria terminalis) was analyzed with the Phaseolus vulgaris leucoagglutinin anterograde tract tra

146 s that project to crus IIA was studied using Phaseolus vulgaris leucoagglutinin as an anterograde tra

147 ar nucleus of rats using the neuronal tracer Phaseolus vulgaris leucoagglutinin in combination with u

148 d by iontophoresis of the anterograde tracer Phaseolus vulgaris leucoagglutinin into its anterior, do

149 beled by injection of the anterograde tracer Phaseolus vulgaris leucoagglutinin into lamina A of the

150 were labeled by iontophoretic injections of Phaseolus vulgaris leucoagglutinin into layer IV.

151 abeled anterogradely following injections of Phaseolus vulgaris leucoagglutinin into the basolateral

152 Injections of the anterograde tracer Phaseolus vulgaris leucoagglutinin into the BSTp of adul

153 placed injections of the anterograde tracer Phaseolus vulgaris leucoagglutinin into the LHb or the R

154 Also, injections of either CTb or Phaseolus vulgaris leucoagglutinin into the medial subdi

155 sits of either biotinylated dextran amine or Phaseolus vulgaris leucoagglutinin into the rat ventrola

156 A single small iontophoretic injection of Phaseolus vulgaris leucoagglutinin labels projections fr

157 To confirm these results, injections of Phaseolus vulgaris leucoagglutinin or biotinylated dextr

158 transport of biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to demonstrate direct

159 We used biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to examine the intrac

160 olfactory structures, the anterograde tracer Phaseolus vulgaris leucoagglutinin was injected into orb

161 First, the anterograde tracer Phaseolus vulgaris leucoagglutinin was used to label axo

162 l focal injections of the anterograde tracer Phaseolus vulgaris leucoagglutinin were aimed at differe

163 amino acids, biotinylated dextran amine, and Phaseolus vulgaris leucoagglutinin were injected into th

164 Here, using transport of Phaseolus vulgaris leucoagglutinin(PHA-L) or carbocyanin

165 In this study we used both an anterograde (Phaseolus vulgaris leucoagglutinin) and a retrograde (ch

166 By using the anterograde anatomical tracer, Phaseolus vulgaris leucoagglutinin, and the retrograde t

167 ic injections of biotinylated dextran amine, Phaseolus vulgaris leucoagglutinin, Fluoro-Gold or tetra

168 Injection of an anterograde tracer, Phaseolus vulgaris leucoagglutinin, into the RVM resulte

169 r, profiles did vary with peanut agglutinin, Phaseolus vulgaris leucoagglutinin, Sophora japonica agg

170 are identified with the anterograde tracer, Phaseolus vulgaris leucoagglutinin, with projections to

171 In the AVPV, Phaseolus vulgaris leucoagglutinin-labeled fibers were s

172 Within the hypothalamus, Phaseolus vulgaris leucoagglutinin-labeled, lateral geni

173 sport from small extracellular injections of Phaseolus vulgaris leucoagglutinin.

174 tracing of the nigrostriatal projection with Phaseolus vulgaris leucoagglutinin.

175 by using the anterograde anatomical tracer, Phaseolus vulgaris leucoagglutinin.

176 with injections of anterogradely transported Phaseolus vulgaris leucoagglutinin.

177 nal (ECIC) cortices, the anterograde tracers Phaseolus vulgaris-leucoagglutinin (PHA-L) and biotinyla

178 With the anterograde tracers Phaseolus vulgaris-leucoagglutinin (PHA-L) and biotinyla

179 eling of biotinylated dextran amine (BDA) or Phaseolus vulgaris-leucoagglutinin (PHA-L) from the NTS

180 Following large bilateral injections of Phaseolus vulgaris-leucoagglutinin (PHA-L) in the SN, th

181 ectron microscopic double immunostaining for Phaseolus vulgaris-leucoagglutinin (PHA-L) injected into

182 Injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) into discrete

183 ex with injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) into lamina A

184 oinjections of the anterograde axonal tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) into restrict

185 llowing injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) into the pars

186 By means of anterograde tracing of Phaseolus vulgaris-leucoagglutinin (PHA-L) it was determ

187 First, Phaseolus vulgaris-leucoagglutinin (PHA-L) was injected

188 Phaseolus vulgaris-leucoagglutinin (PHA-L) was injected

189 iscrete injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHA-L) were made in

190 racers, biotinylated dextran amine (BDA) and Phaseolus vulgaris-leucoagglutinin (PHA-L), into four su

191 anterogradely transported marker substance, Phaseolus vulgaris-leucoagglutinin (PHA-L).

192 re characterized with the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHA-L).

193 als were labeled by anterograde transport of Phaseolus vulgaris-leucoagglutinin (PHA-L); and gamma-am

194 ng iontophoretic co-injection of the tracers Phaseolus vulgaris-leucoagglutinin (PHA-L; for outputs)

195 Thus, the present study used Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tr

196 and from the BSTsc were determined with the Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tr

197 terminalis (BST) was characterized with the Phaseolus vulgaris-leucoagglutinin (PHAL) anterograde tr

198 eceived injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) in the perirhi

199 mbining injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) into the neoco

200 ia terminalis (BSTju) were examined with the Phaseolus vulgaris-leucoagglutinin (PHAL) method in the

201 ain (diencephalon) is analyzed here with the Phaseolus vulgaris-leucoagglutinin (PHAL) method.

202 horetic injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin (PHAL) were performed

203 Phaseolus vulgaris-leucoagglutinin and cholera toxin B w

204 e compared by using anterograde transport of Phaseolus vulgaris-leucoagglutinin and retrograde transp

205 edial nucleus (BSTdm), was analyzed with the Phaseolus vulgaris-leucoagglutinin anterograde pathway t

206 ons from the rat BSTam was analyzed with the Phaseolus vulgaris-leucoagglutinin anterograde pathway t

207 a toxin B subunit as a retrograde tracer and Phaseolus vulgaris-leucoagglutinin as an anterograde tra

208 traced anterogradely following injections of Phaseolus vulgaris-leucoagglutinin in the central amygda

209 We then injected Phaseolus vulgaris-leucoagglutinin in the optic tract an

210 pulvinar axons were anterogradely labeled by Phaseolus vulgaris-leucoagglutinin injections in the occ

211 Injection of the orthograde tracer Phaseolus vulgaris-leucoagglutinin into the area of the

212 Following an injection of Phaseolus vulgaris-leucoagglutinin into the ventral coch

213 nucleus was determined in male rats with the Phaseolus vulgaris-leucoagglutinin method.

214 Injections of the anterograde tracers Phaseolus vulgaris-leucoagglutinin or biotinylated dextr

215 oretic injections of the anterograde tracers Phaseolus vulgaris-leucoagglutinin or biotinylated dextr

216 inals labeled anterogradely with the tracers Phaseolus vulgaris-leucoagglutinin or biotinylated dextr

217 The anterograde tracer Phaseolus vulgaris-leucoagglutinin was used to identify

218 Injections of Phaseolus vulgaris-leucoagglutinin, biocytin, or dextran

219 Anterograde tracers ((3)H-amino acids, Phaseolus vulgaris-leucoagglutinin, biotinylated dextran

220 rat by using the anterograde anatomic tracer Phaseolus vulgaris-leucoagglutinin.

221 by use of the anterograde anatomical tracer Phaseolus vulgaris-leucoagglutinin.

222 Pathways were traced with the axonal marker phaseolus vulgaris-leucoagglutinin.

223 )-bearing N-glycans, which are recognized by Phaseolus vulgaris leukoagglutinating lectin (L-PHA).

224 ad been injected with the anterograde tracer Phaseolus vulgaris leukoagglutinin (PHA-L).

225 ns of this region in primates, injections of Phaseolus vulgaris leukoagglutinin, biotinylated dextran

226 s performed by using the anterograde tracers Phaseolus vulgaris-leuocoagglutinin (PHA-L) and biotinyl

227 were isolated from leaves of Pisum sativum, Phaseolus vulgaris, Lycopersicon esculentum, Daucus caro

228 unds of three varieties of red kidney beans (Phaseolus vulgaris) namely Kashmiri red, Sharmili and Ch

229 imer is formed in planta by the common bean (Phaseolus vulgaris) NF-Y subunits, revealing the existen

230 lover (Trifolium pratense), and common bean (Phaseolus vulgaris) nodules.

231 In tropical legumes like French bean (Phaseolus vulgaris) or soybean (Glycine max), most of th

232 are grown in the presence of the host plant, Phaseolus vulgaris, or its seed exudates.

233 se expression of a heterologous French bean (Phaseolus vulgaris) peroxidase (FBP1) cDNA in Arabidopsi

234 se expression of a heterologous French bean (Phaseolus vulgaris) peroxidase cDNA construct.

235 I-oligosaccharide complex in the presence of Phaseolus vulgaris PGIP indicate that the inhibitor cont

236 NAi-mediated down-regulation of common bean (Phaseolus vulgaris) PI3K severely impaired symbiosis in

237 ia exposure (62.5-500 mg/kg) on kidney bean (Phaseolus vulgaris) productivity and seed quality as a f

238 and the orthologous region from common bean (Phaseolus vulgaris), Pv5.

239 glutinin, peanut lectin, concanavalin A, and Phaseolus vulgaris (red kidney bean) lectins, were copre

240 g in SimRoot indicates that, in common bean (Phaseolus vulgaris), reduced root secondary growth reduc

241 s of lima bean (Phaseolus lunatus) and bean (Phaseolus vulgaris), respectively.

242 P2) transcription factor in the common bean (Phaseolus vulgaris)-Rhizobium etli symbiosis.

243 e uncovered the role of TOR during the bean (Phaseolus vulgaris)-Rhizobium tropici (Rhizobium) symbio

244 es of six species spanning the Pentapetalae (Phaseolus vulgaris, Ricinus communis, Arabidopsis [Arabi

245 Soybean (Glycine max) and snap bean (Phaseolus vulgaris) RIN4 homologs without glutamate at t

246 obium etli CE3 bacteroids were isolated from Phaseolus vulgaris root nodules.

247 vacuolar targeting, which we generated from Phaseolus vulgaris roots, a Rhizobium-responsive sucrose

248 stication-associated changes in common bean (Phaseolus vulgaris) roots were due to direct selection f

249 is rapidly metabolized to O-xylosylzeatin in Phaseolus vulgaris seeds.

250 no.) was isolated and cloned from bush bean (Phaseolus vulgaris) seeds.

251 hydroxyproline-rich glycoprotein [HRGP] from Phaseolus vulgaris; Serpin from Manduca sexta) to direct

252 Soybean (Glycine max) and common bean (Phaseolus vulgaris) share a paleopolyploidy (whole-genom

253 The increasing volume of genomic data on the Phaseolus vulgaris species have contributed to its impor

254 cowpea (Vigna unguiculata) and common bean (Phaseolus vulgaris), specifically respond to OS via reco

255 ndrial mutation designated pvs-or f 239 (for Phaseolus vulgaris sterility sequence open reading frame

256 Common bean (Phaseolus vulgaris) symbiotically associates with its pa

257 we identified 2,606 genes from common bean (Phaseolus vulgaris) that are differentially regulated at

258 nd in soybean (Glycine max) and common bean (Phaseolus vulgaris) that is associated with several dise

259 It has been shown in bean (Phaseolus vulgaris) that the gene encoding the cleavage

260 In French bean (Phaseolus vulgaris), the ABI3-like factor, PvALF, activa

261 In common bean (Phaseolus vulgaris), the principal global grain legume s

262 e (MIPS; EC 5.5.1.4) in developing organs of Phaseolus vulgaris to define genetic controls that spati

263 roagglutinating phytohemagglutin lectin from Phaseolus vulgaris to the bisecting structures on the EG

264 made using a stress induced CHS17 cDNA from Phaseolus vulgaris under the control of the constitutive

265 Kidney bean plants (Phaseolus vulgaris var. red hawk) grown in soil contamin

266 cose were not altered in symbiosis with host Phaseolus vulgaris, whereas mutants lacking only 2-O-met

267 66 gave rise to pseudonodules on legume host Phaseolus vulgaris, whereas the mutant suppressed by DNA

268 uring transitory starch degradation in bean (Phaseolus vulgaris), wild-type Arabidopsis (Arabidopsis

269 ium meliloti did not nodulate the plant host Phaseolus vulgaris without rosR.