ライフサイエンスコーパス: Phaseolus

1 o be both abundant and active in Glycine and Phaseolus.

2 a AI-Pa present in seeds of the tepary bean (Phaseolus acutifolius) and alpha AI-Pc in seeds of the s

3 Starch from the seeds of Phaseolus and Inga feuillei, the flesh of Cucurbita mosc

4 onset of seed maturation in embryos of both Phaseolus and tobacco.

5 In Phaseolus and wild-type Arabidopsis, beta-maltose levels

6 Mungbean (Phaseolus aureus Roxb.) seedlings were grown hypobarical

7 ta provide early archaeological evidence for Phaseolus beans and I. feuillei, an important tree crop,

8 upstream region of the Scarlet Runner Bean (Phaseolus coccineus) G564 gene in order to understand ho

9 upstream region of the scarlet runner bean (Phaseolus coccineus) G564 gene to understand how genes a

10 he giant embryos of the scarlet runner bean (Phaseolus coccineus) to gain understanding of the proces

11 a AI-Pc in seeds of the scarlet runner bean (Phaseolus coccineus), with the midgut extracts of severa

12 st-to-chloroplast transition in runner bean (Phaseolus coccineus).

13 ng a trans-zeatin O-glucosyltransferase from Phaseolus (EC ), a cis-zeatin-specific O-glucosyltransfe

14 coordinately regulated during maturation of Phaseolus embryos.

15 tative progenitor sequence was identified in Phaseolus glabelus in substoichiometric levels, suggesti

16 V of area 17 were filled by iontophoresis of Phaseolus lectin into lamina A of the lateral geniculate

17 nce throughout a diversity of undomesticated Phaseolus lines.

18 (EC 2.4.1.203) was previously isolated from Phaseolus lunatus seeds.

19 ic: the O-glucosyltransferase encoded by the Phaseolus lunatus ZOG1 gene has high affinity for trans-

20 ransferase, occurring in seeds of lima bean (Phaseolus lunatus) and bean (Phaseolus vulgaris), respec

21 sses in experimental systems of bean plants (Phaseolus lunatus), herbivorous mites (Tetranychus urtic

22 associated with this response in lima bean (Phaseolus lunatus), we have cloned an HSP100/ClpB homolo

23 a and shared 99% homology each with BBI from Phaseolus parvulus, Vigna trilobata and Vigna vexilata.

24 the genomes of 29 accessions representing 12 Phaseolus species.

25 ecause of the extensive plant collections of Phaseolus spp and the degree to which cytoplasmic male s

26 s homologous to Arl-3 and Arl-4 alleles from Phaseolus spp.

27 s were mainly found in elicited seedlings of Phaseolus, Vigna and Lablab, whereas pterocarpans were m

28 from seven species of tribe Phaseoleae, i.e. Phaseolus, Vigna, Lablab and Psophocarpus, were investig

29 3'-) sequences from the arcelin 5-I gene of Phaseolus vulgaris (cgl-IDUA-SEKDEL and Col-IDUA-SEKDEL,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 07A1 and PvCYP707A2 were isolated from bean (Phaseolus vulgaris L.) axes treated with (+)-ABA and tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

119 sport from small extracellular injections of Phaseolus vulgaris leucoagglutinin.

120 tracing of the nigrostriatal projection with Phaseolus vulgaris leucoagglutinin.

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

122 with injections of anterogradely transported Phaseolus vulgaris leucoagglutinin.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 66 gave rise to pseudonodules on legume host Phaseolus vulgaris, whereas the mutant suppressed by DNA

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 Phaseolus vulgaris-leucoagglutinin and cholera toxin B w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 R1-R5, in Phaseolus vulgaris.

248 fferentially expressed during development in Phaseolus vulgaris.

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

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

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

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

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

254 protein of 51.1 kDa with 41% identity to the Phaseolus ZOG1 protein.