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 Tepary bean (Phaseolus acutifolis A.

3 Tepary bean (Phaseolus acutifolius A.

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

5 e mothbean (Vigna acontifolia), tepary bean (Phaseolus acutifolius), and guar (Cyamopsis tetragonolob

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

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

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

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

10 us lunatus L.), one of the five domesticated Phaseolus bean crops, shows a wide range of ecological a

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

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

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

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

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

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

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

18 coordinately regulated during maturation of Phaseolus embryos.

19 Sequencing data analysis from 87 non-admixed Phaseolus genotypes, comprising different Phaseolus spec

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

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

22 nce throughout a diversity of undomesticated Phaseolus lines.

23 Lima bean (Phaseolus lunatus L.), one of the five domesticated Phas

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

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

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

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

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

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

30 ed Phaseolus genotypes, comprising different Phaseolus species and P. vulgaris populations, revealed

31 inearity and shared gene content among these Phaseolus species will facilitate engineering climate ad

32 the genomes of 29 accessions representing 12 Phaseolus species.

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

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

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

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

37 the divergence of the Glycine genus from the Phaseolus-Vigna lineage and exhibit strong structure-fun

38 3'-) sequences from the arcelin 5-I gene of Phaseolus vulgaris (cgl-IDUA-SEKDEL and Col-IDUA-SEKDEL,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 07A1 and PvCYP707A2 were isolated from bean (Phaseolus vulgaris L.) axes treated with (+)-ABA and tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

150 sport from small extracellular injections of Phaseolus vulgaris leucoagglutinin.

151 tracing of the nigrostriatal projection with Phaseolus vulgaris leucoagglutinin.

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

153 with injections of anterogradely transported Phaseolus vulgaris leucoagglutinin.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

240 66 gave rise to pseudonodules on legume host Phaseolus vulgaris, whereas the mutant suppressed by DNA

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 Phaseolus vulgaris-leucoagglutinin and cholera toxin B w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

293 R1-R5, in Phaseolus vulgaris.

294 fferentially expressed during development in Phaseolus vulgaris.

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

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

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

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

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

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