ライフサイエンスコーパス: Phaseolus vulgaris

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

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

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

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

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

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

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

8 R1-R5, in Phaseolus vulgaris.

9 fferentially expressed during development in Phaseolus vulgaris.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 3'-) sequences from the arcelin 5-I gene of Phaseolus vulgaris (cgl-IDUA-SEKDEL and Col-IDUA-SEKDEL,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 07A1 and PvCYP707A2 were isolated from bean (Phaseolus vulgaris L.) axes treated with (+)-ABA and tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 sport from small extracellular injections of Phaseolus vulgaris leucoagglutinin.

136 tracing of the nigrostriatal projection with Phaseolus vulgaris leucoagglutinin.

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

138 with injections of anterogradely transported Phaseolus vulgaris leucoagglutinin.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Phaseolus vulgaris-leucoagglutinin and cholera toxin B w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 66 gave rise to pseudonodules on legume host Phaseolus vulgaris, whereas the mutant suppressed by DNA

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

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