ライフサイエンスコーパス: Pisum

1 tolerance of pea aphid hosts (Acyrthosiphon pisum).

2 ent speciation, the pea aphid (Acyrthosiphon pisum).

3 a polymorphic state for millions of years in Pisum.

4 trol the proliferation of PDR1 insertions in Pisum.

5 .5 MYA) are mostly found in small subsets of Pisum.

6 tterns, were isolated and characterized from Pisum.

7 r morphs of clonal pea aphids, Acyrthosiphon pisum.

8 ctor protein in the pea aphid, Acyrthosiphon pisum.

9 s carried by 1,104 pea aphids, Acyrthosiphon pisum.

10 onary responses of pea aphids (Acyrthosiphon pisum), a common agricultural pest, to increased frequen

11 YA) tend to be found in small subsets of the Pisum accessions set, "middle-aged" insertions (between

12 ertions has been assessed across 47 selected Pisum accessions, representing the diversity of the genu

13 apoptotic pathway in the aphid Acyrthosiphon pisum, an insect pest belonging to the Hemiptera, an ear

14 tion to annotate the apoptotic pathway in A. pisum and found low caspase diversity and a large expans

15 d to discover putative novel sequences of A. pisum and its symbionts.

16 to parasitism is a general phenomenon in A. pisum and that, at least for the isolates and genotypes

17 s of 50 Spanish wild taxa of Lathyrus, Lens, Pisum and Vicia have been compared.

18 biosis, between the pea aphid (Acyrthosiphon pisum) and its maternally transmitted symbiont, Buchnera

19 ualism involving the pea aphid Acyrthosiphon pisum, and its heritable symbiont, Hamiltonella defensa,

20 vior of an herbivorous insect, Acyrthosiphon pisum, and its predator beetle, Hippodamia convergens.

21 ty against both the pea aphid, Acyrthosiphon pisum, and the green peach aphid, Myzus persicae.

22 l-DOPA, released from roots of Acyrtosiphon pisum aphid-infested Vicia faba plants, as an active com

23 ed populations, derived from wide crosses in Pisum are described.

24 sly documented for pea aphids (Acyrthosiphon pisum) attacked by the parasitoid wasp Aphidius ervi.

25 In another aphid host, Acyrthosiphon pisum, B. aphidicola has no functional metR and shows no

26 ssed and/or highly enriched in Acyrthosiphon pisum bacteriocyte tissues.

27 enty-nine parthenogenetic clones of three A. pisum biotypes, defined by their capacity to use the leg

28 Genomic resources are becoming available for Pisum but to link these to phenotypic diversity requires

29 mbiont isolates underlies variation among A. pisum clones in resistance to A. ervi.

30 idis, Schizaphis graminum, and Acyrthosiphon pisum contain the genes for anthranilate synthase (trpEG

31 rental genotypes of pea aphid (Acyrthosiphon pisum) differing in virulence on a Medicago truncatula h

32 During Pisum evolution, translocation and transposition differe

33 in immunity to the pea aphid (Acyrthosiphon pisum), for which Arabidopsis is normally a nonhost.

34 lla defensa protects the aphid Acyrthosiphon pisum from attack by the parasitoid Aphidius ervi by kil

35 brane separating the pea aphid Acyrthosiphon pisum from its intracellular symbiont Buchnera aphidicol

36 A mutant line of Pisum fulvum was identified that lacked seed lipoxygenas

37 shed five H. defensa isolates in a common A. pisum genetic background.

38 he corresponding retrotransposons within the Pisum genus.

39 one side alone, from a diverse collection of Pisum germ plasm.

40 osis, the transporter ApGLNT1 (Acyrthosiphon pisum glutamine transporter 1) supplies glutamine, an am

41 8, LOC100159667 (named here as Acyrthosiphon pisum glutamine transporter 1, ApGLNT1) functioning as t

42 e performance of the pea aphid Acyrthosiphon pisum Harris, a sap-feeding insect with piercing-sucking

43 Experiments on pea aphids (Acyrthosiphon pisum) have demonstrated that facultative symbionts prot

44 polymorphism in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae).

45 n of the essential amino acid arginine in A. pisum hemolymph reduces the transport of the precursor g

46 tent with the transport of glutamine from A. pisum hemolymph to the bacteriocyte cytoplasm.

47 The pea aphid, Acyrthosiphon pisum, maintains extreme variation in resistance to its

48 enetic cause of the pea aphid (Acyrthosiphon pisum) male wing dimorphism, wherein males exhibit one o

49 roposed that the crop-feeding biotypes of A. pisum may have diversified within the last 100 000 years

50 ogaster and four aphid species Acyrthosiphon pisum, Myzus persicae, Toxoptera citricida, and Aphis go

51 iont Buchnera aphidicola The transporter, A. pisum nonessential amino acid transporter 1, or ApNEAAT1

52 stimate of the effective population size for Pisum of approximately 7.5 x 10(5).

53 the survival of the pea aphid (Acyrthosiphon pisum) on fava bean, a host plant.

54 d host races of the pea aphid (Acyrthosiphon pisum pisum; Hemiptera : Aphididae).

55 ant species with behavioural tests on two A. pisum races, to identify metabolites that explain variat

56 e differential acceptability of plants to A. pisum races.

57 ieved following mapping to the Acyrthosiphon pisum reference genome and its mitochondrial and symbion

58 We show that when four aphid pest species-A. pisum, Rhopalosiphum padi, Aphis glycines and Myzus pers

59 r oligosaccharide distribution, highlighting Pisum sativum (9.22 g/100 g) as the richest source of th

60 ther t-loops exist in the higher order plant Pisum sativum (garden pea).

61 ave isolated a DESD-box containing cDNA from Pisum sativum (Pea) and named it as PDH45.

62 The complex was purified from Pisum sativum (pea) chloroplast envelopes by native gel

63 The Pisum sativum (pea) mutants degenerate leaves (dgl) and

64 us analysis of the MAP kinase homologue from Pisum sativum (PsMAPK) revealed a potential MAP kinase m

65 and characterization of recombinant p68 from Pisum sativum (Psp68) is presented.

66 e required for plant life in that a UGT from Pisum sativum (PsUGT1) controls plant development by opp

67 lectins Galanthus nivalis agglutinin (GNA), Pisum sativum agglutinin (PSA), and Lens culinaris agglu

68 ously selected for resistance to pea lectin (Pisum sativum agglutinin) and shown to behave dominantly

69 phage galactose-type lectin, a plant lectin, Pisum sativum agglutinin, and the bacterial Gal-/Glc-bin

70 ectin, Griffonia simplicifolia lectin I, and Pisum sativum agglutinin.

71 against equine plasma amine oxidase (EPAO), Pisum sativum amine oxidase (PSAO), Pichia pastoris lysy

72 n of leaf complexity to different degrees in Pisum sativum and Lotus japonicus.

73 ein fusions, and import assays with purified Pisum sativum chloroplasts, indicated chloroplastic loca

74 of aggregated proteins from tobacco and pea (Pisum sativum cv "Little Marvel") chloroplasts showed th

75 is localized to developing vacuoles in pea (Pisum sativum cv Extra Early Alaska).

76 romoter fragment of the Blec4 gene from pea (Pisum sativum cv. Alaska) and demonstrate that it is cap

77 t phenotype was introgressed into a standard Pisum sativum cv. Birte to provide near-isogenic lines w

78 full-length CPCT cDNA (designated PCT2) from Pisum sativum cv. Feltham First using an Arabidopsis pro

79 olymorphic PDR1 retrotransposon insertion in Pisum sativum have been developed.

80 Pisum sativum is of great economic and nutritional inter

81 solated a class 1 knox cDNA from pea, Pskn1 (Pisum sativum knotted1) and examined its expression patt

82 ndisturbed grassland (GP), winter wheat-pea (Pisum sativum L) rotations under conventional tillage (W

83 of tendrils in the compound leaves of pea - Pisum sativum L.

84 ravitropic curvature response of intact pea (Pisum sativum L. cv Alaska) epicotyls was examined by ge

85 were extracted from 7 day old etiolated pea (Pisum sativum L. cv Alaska) epicotyls with 3 molar LiCl.

86 Pea (Pisum sativum L. cv Alcan) endocarp tissue challenged wi

87 cDNA has been cloned and sequenced from pea (Pisum sativum L. cv. Birte).

88 was imported and processed by isolated pea (Pisum sativum L. Laxton's Progress No. 9) chloroplasts a

89 was investigated in etiolated pea seedlings (Pisum sativum L. var Alaska) by excising the cotyledons.

90 ation zone of the epicotyl of etiolated pea (Pisum sativum L. var Alaska) seedlings, there is little

91 When pea (Pisum sativum L. var Onward) seedlings are treated with

92 GalAT activity in homogenates from pea (Pisum sativum L. var. Alaska) stem internodes co-localiz

93 at (Triticum aestivum L.) (WW) - spring pea (Pisum sativum L.) (SP) rotation (WW-SP) under both CT an

94 , WF with different tillage (WT), wheat-pea (Pisum sativum L.) (WP), WF under different crop residue

95 5% of the SMM was extrachloroplastic in pea (Pisum sativum L.) and spinach (Spinacia oleracea L.), wh

96 A cDNA fragment coding for the pea (Pisum sativum L.) chloroplastic glyceraldehyde-3-P dehyd

97 phatase was purified from the stroma of Pea (Pisum sativum L.) chloroplasts that is capable of dephos

98 t across the inner-envelope membrane of pea (Pisum sativum L.) chloroplasts was directly measured by

99 We show for pea (Pisum sativum L.) epicotyl sections that this hypothesis

100 The lip1 mutant of pea (Pisum sativum L.) exhibits a de-etiolated phenotype.

101 tely 80% identical with Arabidopsis and pea (Pisum sativum L.) homologs.

102 lin (GA) controlling stem elongation in pea (Pisum sativum L.) is GA1, which is formed from GA20 by 3

103 Stem elongation in peas (Pisum sativum L.) is under partial control by gibberelli

104 P21 complex purified from heat-stressed pea (Pisum sativum L.) leaves contained no proteins other tha

105 ase (ACCase) have been characterized in pea (Pisum sativum L.) leaves; a heteromeric chloroplast enzy

106 Field pea (Pisum sativum L.) needs improvement to increase producti

107 A pea (Pisum sativum L.) nuclear enzyme with protein tyrosine p

108 op genetics and processing in two pea lines (Pisum sativum L.) on starch digestion kinetics.

109 Pea (Pisum sativum L.) ornithine transcarbamylase (OTC) antis

110 A cDNA of pea (Pisum sativum L.) RbcS 3A, encoding a small subunit prot

111 e), T(o) (optimal), T(m) (maximum)] for pea (Pisum sativum L.) seed germination and seedling growth t

112 lene biosynthesis in stems of etiolated pea (Pisum sativum L.) seedlings by rapidly increasing the ex

113 Treatment of 5- to 6-day-old etiolated pea (Pisum sativum L.) seedlings with indole-3-acetic acid (I

114 In pea (Pisum sativum L.) seeds, GA 2-oxidation is controlled by

115 on on pods of specific genetic lines of pea (Pisum sativum L.) stimulates cell division at the sites

116 zation and N fertilizer supply in maize/pea (Pisum sativum L.) strip intercropping was evaluated in a

117 Among a set of genes in pea (Pisum sativum L.) that were induced under drought-stress

118 ed how mixed-cropping between two field pea (Pisum sativum L.) varieties (Winfreda and Ambassador) in

119 An artificial gene encoding PBGS of pea (Pisum sativum L.) was designed to overcome previous prob

120 ntil (Lens culinaris Merr.), and yellow pea (Pisum sativum L.) were investigated over a 6-day germina

121 tivum L.), barley (Hordeum vulgare L.), pea (Pisum sativum L.), and fallow with or without N fertiliz

122 In this study, we used vegetable peas (Pisum sativum L.), harvested for human consumption as im

123 In pea (Pisum sativum L.), source to sink partitioning of amino

124 ox and GA 3beta-hy transcript levels in pea (Pisum sativum L.).

125 them to the introduced cash crop, green pea (Pisum sativum L.).

126 Yellow pea (Pisum sativum L., YP) grain is generally milled into flo

127 Herein, we show that Pisum sativum LecRLK (PsLecRLK) localized in plasma memb

128 rmation of individual transcription units in Pisum sativum plant nucleoli using a novel labelling tec

129 Thermal profiles of viable, aged, and dead Pisum sativum seeds were recorded, and image analysis of

130 dopsis thaliana, Lycopersicon esculentum and Pisum sativum tissues.

131 opersicon lycopersicum), and sugar snap pea (Pisum sativum var. macrocarpon) from an industrially imp

132 um meliloti, required for nodulation of pea (Pisum sativum) and alfalfa (Medicago sativum), respectiv

133 ng of endogenous Toc75 POTRA domains in pea (Pisum sativum) and Arabidopsis (Arabidopsis thaliana) co

134 Pea (Pisum sativum) and Arabidopsis contain similar, if not i

135 l proteins OEP21, OEP24, and OEP37 from pea (Pisum sativum) and Arabidopsis thaliana contain informat

136 We characterized the class II smHSPs of pea (Pisum sativum) and compared them with class I smHSPs.

137 originally studied by Gregor Mendel in pea (Pisum sativum) and involved in the degradation of photos

138 ologs from other legume species, namely pea (Pisum sativum) and Lotus japonicus, we show that this mo

139 rminal in some legume species, such as peas (Pisum sativum) and peanuts (Arachis hypogaea), likely du

140 enhancer sequences from a plant virus, pea (Pisum sativum) and wheat (Triticum aestivum), was just u

141 ke cells." Whereas root border cells of pea (Pisum sativum) are clearly involved in defense against f

142 The Tic20 protein was identified in pea (Pisum sativum) as a component of the chloroplast protein

143 hese complexes by the embryo, using the pea (Pisum sativum) as a model species.

144 Here we use in vitro pea (Pisum sativum) chloroplast import assays and transient e

145 nd alpha-CT were imported into isolated pea (Pisum sativum) chloroplasts and became integrated into A

146 Dual import assays with purified pea (Pisum sativum) chloroplasts and mitochondria, and subcel

147 d AtBCCP2 was competent for import into pea (Pisum sativum) chloroplasts and processed to a 25-kD pol

148 Import assays with pea (Pisum sativum) chloroplasts showed that PyrR and PyrD ar

149 An in vitro assay with pea (Pisum sativum) chloroplasts was developed to conduct mut

150 vement across the thylakoid membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

151 t across the inner envelope membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

152 Upon incubation of the precursor with pea (Pisum sativum) chloroplasts, it was imported and process

153 been studied extensively using isolated pea (Pisum sativum) chloroplasts.

154 I integral membrane protein abundant in pea (Pisum sativum) clathrin-coated vesicles (CCVs) that bind

155 uncatula nodule root (noot) mutants and pea (Pisum sativum) cochleata (coch) mutants, which are chara

156 An apyrase from pea (Pisum sativum) complements a yeast (Saccharomyces cerevi

157 A protein of 80 kD from developing pea (Pisum sativum) cotyledons has previously been shown to e

158 r chaperones, Escherichia coli DnaK and pea (Pisum sativum) CSS1, was investigated in detail.

159 ansport chain, we overexpressed a minor pea (Pisum sativum) Fd isoform (PsFd1) in tobacco (Nicotiana

160 sgenic tobacco (Nicotiana tabacum), the pea (Pisum sativum) Ferredoxin 1 (Fed-1) mRNA dissociates fro

161 -1,4-D-glucanase (EGase, EC 3.2.1.4) of pea (Pisum sativum) has been cloned and characterized.

162 The inheritance of flower color in pea (Pisum sativum) has been studied for more than a century,

163 Pea (Pisum sativum) has served as a model for development of

164 eral ramosus (rms) branching mutants in pea (Pisum sativum) have SL defects, perturbed xylem CK level

165 The function of PsBRC1, the pea (Pisum sativum) homolog of the maize (Zea mays) TEOSINTE

166 tured firefly luciferase (Luc) bound to pea (Pisum sativum) Hsp18.1 as a model to define the minimum

167 t Aux/IAA proteins from Arabidopsis and pea (Pisum sativum) interact in vitro with recombinant phytoc

168 Here, we show that this dwarfism in pea (Pisum sativum) is not attributable to the strong branchi

169 eversibly glycosylated polypeptide from pea (Pisum sativum) is thought to have a role in the biosynth

170 quantified protein import into isolated pea (Pisum sativum) leaf chloroplasts and root leucoplasts an

171 Subcellular fractionation of pea (Pisum sativum) leaf protoplasts indicated that 30% of ly

172 The vacuoles of pea (Pisum sativum) leaves and red beet (Beta vulgaris) stora

173 Three pea (Pisum sativum) loci controlling photoperiod sensitivity,

174 Dual-import assays with purified pea (Pisum sativum) mitochondria and chloroplasts, and subcel

175 hread formation, as a null SL-deficient pea (Pisum sativum) mutant forms significantly fewer infectio

176 ula ortholog of the Lotus japonicus and pea (Pisum sativum) NIN gene.

177 rries a nonsense mutation in the single pea (Pisum sativum) ortholog of the ethylene signaling gene E

178 Two pea (Pisum sativum) P450 cDNAs (CYP73A9v1, encoding trans-cin

179 ify the role of GA3ox expression during pea (Pisum sativum) plant growth and development, we generate

180 In this study, pea (Pisum sativum) plants overexpressing AMINO ACID PERMEASE

181 ortant for the metabolism and growth of pea (Pisum sativum) plants.

182 Our data indicate that moss and pea (Pisum sativum) plastid transport systems are functionall

183 a nucleolar protein was selected from a pea (Pisum sativum) plumule library, cloned, and sequenced.

184 t) DC3000 hrcC(-) and to the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC

185 r a pea seed nuclear DNA-binding protein (of Pisum sativum) present at the cell expansion phase.

186 d IV of the AUX/IAA protein PsIAA4 from pea (Pisum sativum) revealed a globular ubiquitin-like beta-g

187 iptomic and metabolomic analyses of the pea (Pisum sativum) rhizosphere, a suite of bioreporters has

188 took a systematic, detailed analysis of pea (Pisum sativum) root tip cell walls.

189 Pea (Pisum sativum) root tips incubated with [(32)P]dCTP duri

190 the production of root border cells by pea (Pisum sativum) root tips.

191 Yet, when pea (Pisum sativum) roots are inoculated with the pea pathoge

192 rrying genes encoding soybean lectin or pea (Pisum sativum) seed lectin (PSL) were inoculated with Br

193 c activity found within the germinating pea (Pisum sativum) seed, 4 days from the initiation of imbib

194 eolin mRNA using plumules of dark-grown pea (Pisum sativum) seedlings.

195 complex (mt-PDC) by using intact green pea (Pisum sativum) seedlings.

196 Here, we show that in pea (Pisum sativum) seeds, 4-chloroindole-3-acetic acid is sy

197 However, in maturing pea (Pisum sativum) seeds, the level of the chlorinated auxin

198 from endoplasmic reticula of developing pea (Pisum sativum) seeds.

199 ids, Percoll-isolated chloroplasts from pea (Pisum sativum) synthesized FAD from imported riboflavin.

200 n nodulation in Medicago truncatula and pea (Pisum sativum) that form indeterminate nodules.

201 t at the LATE BLOOMER2 (LATE2) locus in pea (Pisum sativum) that is late-flowering with a reduced res

202 m of 45Ca2+ transport into the lumen of pea (Pisum sativum) thylakoid membranes using silicone-oil ce

203 We purified from pea (Pisum sativum) tissue an approximately 40 kDa reversibly

204 s trend is found in the Fabaceae, where pea (Pisum sativum) uses UNIFOLIATA, an ortholog of the flora

205 n the Toc159 GTPase domain (Toc159G) of pea (Pisum sativum) using cleavage by bound preproteins conju

206 profile from the oil of harvested field pea (Pisum sativum) varieties as part of a research project t

207 The STERILE NODES (SN) locus in pea (Pisum sativum) was one of the first photoperiod response

208 Nectria haematococca infection of pea (Pisum sativum) was used as a model to explore possible m

209 nt steps of ABA biosynthesis as well as pea (Pisum sativum) wilty and tomato (Solanum lycopersicum) f

210 istatic isoflavonoid produced by garden pea (Pisum sativum), a host for this fungus.

211 al phenolic compounds (TPC) from green peas (Pisum sativum), a matrix not previously explored with th

212 In leguminous plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic

213 fected region of soybean (Glycine max), pea (Pisum sativum), clover (Trifolium pratense), and common

214 bi5 mutants in a second legume species, pea (Pisum sativum), confirmed a role for ABI5 in the regulat

215 sponds to a native protein of 159 kD in pea (Pisum sativum), designated Toc159.

216 il seven pairs of contrasting traits in pea (Pisum sativum), establishing the foundational principles

217 ha and beta subunits of the ch-cpn60 of pea (Pisum sativum), expressed them individually in Escherich

218 ariations were then cross-compared with pea (Pisum sativum), leading to the identification of candida

219 to Arabidopsis (Arabidopsis thaliana), pea (Pisum sativum), or tomato (Lycopersicon esculentum) tiss

220 phenylpropanoid biosynthetic pathway of pea (Pisum sativum), partial cDNAs representing four distinct

221 eat (Triticum aestivum); but the dicots pea (Pisum sativum), soybean (Glycine max Merr.), and spinach

222 In pea (Pisum sativum), the protein-lysine methyltransferase (Ps

223 In pea (Pisum sativum), the reverse reaction, phenylpyruvate to

224 In contrast to peas (Pisum sativum), where mitochondrial lipoamide dehydrogen

225 We describe here the FRO1 gene from pea (Pisum sativum), which encodes an Fe(III)-chelate reducta

226 mutants at the Crispoid (Crd) locus in pea (Pisum sativum), which have altered auxin homeostasis and

227 ll wall of the root cap in two species: pea (Pisum sativum), which makes border cells, and Brassica n

228 coordinately regulate bud outgrowth in pea (Pisum sativum).

229 Arabidopsis (Arabidopsis thaliana) and pea (Pisum sativum).

230 d in the supernodulating nod3 mutant of pea (Pisum sativum).

231 shoot tip removal (decapitation) in the pea (Pisum sativum).

232 ontrol pathways in the long-day legume, pea (Pisum sativum).

233 the patterns he observed in the garden pea (Pisum sativum).

234 ed or regulated during bud outgrowth in pea (Pisum sativum).

235 nd Tha4 and disulfide bond formation in pea (Pisum sativum).

236 s for their hormonal activity in garden pea (Pisum sativum).

237 tematic cells exist within root tips of pea (Pisum sativum): the root apical meristem, which gives ri

238 cotyledon phenotypes, has been identified in Pisum sativum, Arabidopsis thaliana, and Festuca pratens

239 ivity in nuclei purified from etiolated pea (Pisum sativum, L.) plumules is present in a single enzym

240 bacteriophages were isolated from leaves of Pisum sativum, Phaseolus vulgaris, Lycopersicon esculent

241 Rhizobium leguminosarum 3841, a symbiont of Pisum sativum, using chemical methods, mass spectrometry

242 ith legumes belonging to the galegoid clade (Pisum sativum, Vicia faba and Vicia hirsuta).

243 part of the chloroplast import machinery in Pisum sativum.

244 lar, is phytotoxic to etiolated seedlings of Pisum sativum.

245 syltransferase, was cloned from root tips of Pisum sativum.

246 -hydroxymaackiain 3-O-methyltransferase from Pisum sativum.

247 s type of learning occurs in the garden pea, Pisum sativum.

248 curonosyltransferase-encoding gene from pea (Pisum sativum; PsUGT1).

249 een used to precipitate PCNA from crude pea (Pisum savitum) extracts.

250 In pea aphids (Acyrthosiphon pisum), several inherited endosymbiont species protect t

251 ia and Lens, respectively, whereas the genus Pisum showed the lowest protein-digestibility corrected

252 ucts coming from other Lathyrus or Vicia and Pisum species.

253 In pea aphids (Acyrthosiphon pisum), strain-level variation in the type of toxin-enco

254 differences between the genomes of these two Pisum subspecies.

255 these facultative symbioses in Acyrthosiphon pisum (the pea aphid) for vulnerability of the aphid hos

256 tative symbionts of pea aphid (Acyrthosiphon pisum), the bacterium Regiella insecticola, has a major

257 We use the pea aphid (Acyrthosiphon pisum) to address this problem.

258 red populations derived from wide crosses in Pisum, together with the associated marker data, are mad

259 of their host, the pea aphid (Acyrthosiphon pisum), under natural conditions.

260 ) in the gut of the pea aphid, Acyrthosiphon pisum, using a far-Western blot method.

261 tic diversity in the pea aphid Acyrthosiphon pisum was investigated by a restriction fragment length

262 and non-ant-attended Pea aphid Acyrthosiphon pisum were monitored over two years.

263 on dodder vines by pea aphids (Acyrthosiphon pisum) were reduced significantly when dodder parasitize

264 to the hemocoel of pea aphids, Acyrthosiphon pisum, without virion assembly.