ライフサイエンスコーパス: sexta

1 idgut epithelia of tobacco hornworm (Manduca sexta).

2 ient odor perception using the moth (Manduca sexta).

3 re highly toxic to tobacco hornworm (Manduca sexta).

4 l epidermis of the tobacco hornworm (Manduca sexta).

5 the chewing insect tobacco hornworm (Manduca sexta).

6 ins from Drosophila melanogaster and Manduca sexta.

7 y reported for the tobacco hornworm, Manduca sexta.

8 t epithelium of the tobacco hornworm Manduca sexta.

9 s to a hemocyte-specific integrin of Manduca sexta.

10 s (Masburs and Maspburs) in the moth Manduca sexta.

11 responding reduction of virulence to Manduca sexta.

12 ent time of eggs of a sphingid moth, Manduca sexta.

13 serpin-5) from the tobacco hornworm, Manduca sexta.

14 he dual clip-domain serine proteinases in M. sexta.

15 ctivity in the brain of the hawkmoth Manduca sexta.

16 critical issue in the AL of the moth Manduca sexta.

17 ceptors from Heliothis virescens and Manduca sexta.

18 ensitization of the defensive behavior in M. sexta.

19 integrity of larval midgut epithelium in M. sexta.

20 mino acids 1363-1464 recently reported in M. sexta.

21 cillus thuringiensis Cry1A toxins in Manduca sexta.

22 he terminal cardiac chamber of adult Manduca sexta.

23 ase activation system in the hemolymph of M. sexta.

24 ve serpin from the tobacco hornworm, Manduca sexta.

25 osynthesis of N-linolenoyl-l-glutamine in M. sexta.

26 ons of several alimentary tissues in Manduca sexta.

27 olfactory nerve pathway in the moth Manduca sexta.

28 pro-PO-activating proteinases (PAPs) from M. sexta.

29 membrane of Heliothis virescens and Manduca sexta.

30 e biological functions of hemolin in Manduca sexta.

31 nd Gryllus bimaculatus, and the moth Manduca sexta.

32 e PER/corazonin-expressing Ia(1) cells of M. sexta.

33 ctory) lobe of the brain of the moth Manduca sexta.

34 ily in the antennal lobe of the moth Manduca sexta.

35 nce exhibited by larvae of the moth, Manduca sexta.

36 s of volatiles released by host plants of M. sexta.

37 inst Gram-negative bacterial infection in M. sexta.

38 y system (antennal lobe) of the moth Manduca sexta.

39 from plasma of the tobacco hornworm, Manduca sexta.

40 nnal lobe of the female sphinx moth, Manduca sexta.

41 lpenor and the crepuscular-nocturnal Manduca sexta.

42 MsRel2B) from the tobacco hornworm, Manduca sexta.

43 n the antennal lobe (AL) of the moth Manduca sexta.

44 ommensal and pathogenic interactions with M. sexta.

45 econstruction of deactivated V1 from Manduca sexta.

46 romodulation in the antennal lobe of Manduca sexta.

47 was performed with tobacco hornworm Manduca sexta.

48 inst rapidly feeding specialist herbivore M. sexta.

49 secondary metabolites, and resistance to M. sexta.

50 lfactory (antennal) lobe of the moth Manduca sexta.

51 atura (Datura wrightii) and the moth Manduca sexta[11, 12] to determine how olfactory networks in thi

52 llenged with (1) chewing herbivores (Manduca sexta), (2) piercing-sucking insects (Empoasca spp.), an

53 isolated from the tobacco hornworm, Manduca sexta, a cDNA encoding a modular protein designated hemo

54 m hemolymph of the tobacco hornworm, Manduca sexta, a new serine proteinase that cleaves prophenoloxi

55 During the last larval molt in Manduca sexta, a number of transcription factors are sequentiall

56 logue of APP (msAPPL) from the moth, Manduca sexta, a preparation that permits in vivo manipulations

57 uring metamorphosis of the hawkmoth, Manduca sexta, accessory planta retractor (APR) motoneurons unde

58 era punctata allatostatin (Dip-AST), Manduca sexta allatotropin (Mas-AT), and serotonin (5HT) raised

59 Rel2-RHD suppressed activation of several M. sexta AMP gene promoters.

60 o examined stimulator binding to sGC from M. sexta and bacterial H-NOX homologs.

61 olog of proteins associated with the Manduca sexta and bovine chromaffin granule V-ATPase.

62 ells can activate AMP gene promoters from M. sexta and D. melanogaster.

63 to peptide antigens translated from both M. sexta and Drosophila melanogaster per cDNAs.

64 ell division in the tobacco hornworm Manduca sexta and found that both the rate of cell division and

65 in of sGC proteins from the hawkmoth Manduca sexta and from human.

66 tive guanylyl cyclase were cloned in Manduca sexta and implicated in several cellular, developmental,

67 The hawkmoth Manduca sexta and one of its preferred hosts in the North Americ

68 both pathogenesis and gut persistence in M. sexta and produced enhanced biofilms compared with the w

69 y form isolates are virulent towards Manduca sexta and several other insects.

70 logous to a binding epitope found in Manduca sexta and Tenebrio molitor Bt cadherin functional recept

71 Using M. sexta and the floral traits of two important nectar reso

72 odies labeled known synaptic neuropils in M. sexta and yielded similar labeling patterns in the devel

73 ion of tomato foliage by specialist (Manduca sexta) and generalist (Trichoplusia ni) insect herbivore

74 us plexippus), Carolina sphinx moth (Manduca sexta), and Death's head sphinx moth (Acherontia atropos

75 in promoter in the tobacco hornworm, Manduca sexta, and a 140-bp region in the moricin promoter conta

76 gical studies in the AL of the moth, Manduca sexta, and recorded odor-evoked calcium changes in respo

77 ed caterpillars of the model species Manduca sexta Antibiotic suppression of gut bacterial activity d

78 ly, we compare the NMR structures of Manduca sexta apoLp-III and L. migratoria apoLp-III and present

79 maginal discs, the imaginal discs of Manduca sexta are not formed until early in the final larval ins

80 The adult legs of the hawkmoth Manduca sexta are supplied by a diverse array of sensory organs

81 With Manduca sexta as a model system, we analyzed how natural odor mi

82 system (ENS) of the tobacco hornworm Manduca sexta as a model system, we have explored whether Manduc

83 This is noted in the hornworm, Manduca sexta, as a defensive strike response.

84 identified its ortholog in the moth, Manduca sexta, as a prelude to physiological studies.

85 la xylostella, and tobacco hornworm, Manduca sexta, as well as the spotted wing drosophila, Drosophil

86 p. U10, and the specialist herbivore Manduca sexta At least 15 different O-AS structures belonging to

87 ts defense against tobacco hornworm (Manduca sexta) attack.

88 idase N (APN) purified from L. dispar and M. sexta BBMVs using surface plasmon resonance (BIAcore).

89 To M. sexta BBMVs, (c)RR-AA and (c)RR-EE showed great reductio

90 action of the N-terminal domain from Manduca sexta betaGRP2 (N-betaGRP2) with laminarin, a soluble fo

91 an inhibit hemocyte proteinase 1, another M. sexta blood proteinase.

92 peptides by alternative splicing in Manduca sexta, Bombyx mori, and Aedes aegypti: A C-terminally am

93 t c homologues from Homo sapiens and Manduca sexta, both species sensitive to benzolactone enamides,

94 ct insertion of the whole toxin into Manduca sexta brush border membrane vesicles (BBMVs).

95 toxin or by surface plasmon resonance to M. sexta brush border membrane vesicles.

96 eding by larvae of tobacco hornworm (Manduca sexta) but not to the bacterial pathogen Pseudomonas syr

97 n hemolymph of the tobacco hornworm, Manduca sexta, but functions are known for only a few of them.

98 al epidermis of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20E) during larval and pupa

99 ntly with predation of the herbivore Manduca sexta by native predators.

100 t of synapses within the antennal lobe of M. sexta by reporting on the localization of synaptotagmin,

101 NO in the antennal lobe of the moth, Manduca sexta, by using immunocytochemistry and real-time optica

102 ed by incubating Cry1Ac toxin with a Manduca sexta cadherin fragment, with BBMV from both strains.

103 and examples from the invertebrates Manduca sexta, Caenorhabditis elegans, and Drosophila melanogast

104 disks of non-feeding wandering stage Manduca sexta can be stopped by removal of the brain, indicating

105 Their main hawkmoth pollinator, Manduca sexta, can perceive minute variation (0.5 ppm) in CO(2)

106 different "bitter" taste stimuli in Manduca sexta caterpillars.

107 on to specific "bitter" compounds in Manduca sexta caterpillars.

108 eripheral taste system of an insect (Manduca sexta caterpillars; Sphingidae) contribute to the discri

109 aterials (ENMs) by tobacco hornworm (Manduca sexta) caterpillars resulting from the ingestion of plan

110 ity and disrupts the midgut epithelium of M. sexta, caused a 50% decrease in calcium-induced vesicle

111 the nervous system of the hawkmoth, Manduca sexta, cells expressing the period (per)gene were mapped

112 uring development of the antennal lobe of M. sexta confirmed and extended previous electron microscop

113 ion: feeding of the tobacco hornworm Manduca sexta converts (Z)-3- to (E)-2-GLVs thereby attracting p

114 We found that M. sexta could discriminate between salicin and those bitte

115 M. sexta could not discriminate between salicin and a bitte

116 ne RNA levels and protection against Manduca sexta damage were influenced by LapA RNA and protein lev

117 In the moth Manduca sexta, developing olfactory receptor axons encounter sev

118 In the moth Manduca sexta, development of glomeruli in the antennal (olfacto

119 In the moth Manduca sexta, development of the adult olfactory system depends

120 xpressed in the midgut epithelium of Manduca sexta during larval development.

121 In Manduca sexta, E. faecalis is an infrequent member of the commen

122 In the sphinx moth Manduca sexta, each of the paired antennal lobes (ALs; the prima

123 rket against H. halys, P. xylostella, and M. sexta, eggs.

124 enerate a hypothetical structure for Manduca sexta EH.

125 central nervous system of the insect Manduca sexta enabled us to define domains that affect antagonis

126 venile hormone-regulatory pathway in Manduca sexta enables heat stress to reveal a hidden reaction no

127 t muscles of an insect, the hawkmoth Manduca sexta, encode torque during yaw turns.

128 The corazonin receptor cDNA in M. sexta encodes a protein of 436 amino acids with seven pu

129 microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calculated the first 3D reconstru

130 tion factor whose expression in both Manduca sexta epidermis and the Manduca GV1 cell line is induced

131 M. sexta exhibits an aversive behavioral response to many p

132 read distribution of per gene products in M. sexta eyes, optic lobes, brains, and retrocerebral compl

133 lesser extent, by a tobacco hornworm Manduca sexta FaRP, GNSFLRFNH2 (F7G) (potency ranking FLP15-2A >

134 5, and MsexD6 abundantly expressed in the M. sexta female pheromone gland.

135 maging in the primary olfactory center of M. sexta females with GLV structural isomers.

136 coded message is monitored by ovipositing M. sexta females.

137 undetectable in Drosophila S2 cells, and M. sexta Fkh (MsFkh) interacted with Relish-Rel-homology do

138 rpillars are sufficient to deter a female M. sexta from ovipositing on a plant and that this deterren

139 sed against a characterized high-affinity M. sexta GABA transporter with high sequence homology to kn

140 In the moth Manduca sexta, glial reduction experiments have directly implica

141 Larvae of Manduca sexta grew faster when consuming inverted-repeat stable

142 cial diets and germination medium reduced M. sexta growth and fungal spore germination, respectively.

143 ving O-AS from the leaf surface increased M. sexta growth rate and plant fungal susceptibility.

144 levels of defense metabolites that slowed M. sexta growth.

145 lipophorin III from the sphinx moth, Manduca sexta, has been determined in the lipid-free state.

146 ked glycans of aminopeptidase 1 from Manduca sexta have revealed unusual structures not previously ob

147 For Manduca sexta hawkmoths, how learning modifies foraging decision

148 The binding properties of M. sexta hemolin suggest that it functions as a pattern-rec

149 sociate with a bacteria-binding lectin in M. sexta hemolymph, indicating that they may be important f

150 urified from the larval hemolymph of Manduca sexta: hemolymph proteinase 14 (HP14), which autoactivat

151 ed nectar source and oviposition host for M. sexta Hence, the hawkmoth is an important pollinator whi

152 egulation of direct defenses against Manduca sexta herbivory or P. syringae pv tomato DC3000 infectio

153 annotate leaf metabolic responses to Manduca sexta herbivory.

154 influences of the tobacco hornworm, Manduca sexta, host and its parasitoid wasp Apanteles congregatu

155 omic analysis of frass from tomato-reared M. sexta identified pTD2 as one of the most abundant protei

156 ric nervous system (ENS) of the moth Manduca sexta, identified populations of neurons and glial cells

157 f the final larval (fifth) instar of Manduca sexta, imaginal precursors including wing discs and eye

158 , which is similar to the organization of M. sexta immulectin-1.

159 uppress melanization of hemolymph in Manduca sexta in part by inhibiting the enzymatic activity of pr

160 wer-feeding behavior in the hawkmoth Manduca sexta In the laboratory, moths feed from a robotically a

161 ng floral preference in the hawkmoth Manduca sexta in the semiarid grassland of Arizona.

162 three FaRPs in the tobacco hornworm, Manduca sexta, including the amidated decapeptide F10.

163 Larvae of Manduca sexta increase up to ten-fold in mass between molts, lea

164 In the hawkmoth, Manduca sexta, individual accessory planta retractor (APR) moton

165 lted in attenuated virulence against Manduca sexta insects.

166 X. nematophila for full virulence in Manduca sexta insects.

167 ow that the induced feeding preference of M. sexta involves the formation of a template to a steroida

168 The hawkmoth Manduca sexta is an important pollinator for many night-blooming

169 ural precursors in the optic lobe of Manduca sexta is controlled by circulating steroids and by local

170 Based on studies in the moth, Manduca sexta, it has been postulated that the neuropeptide Crus

171 ication of the D. melanogaster homolog of M. sexta JHDK from adult D. melanogaster gave material with

172 D. melanogaster dSCP2 is a homolog of M. sexta JHDK, and these proteins constitute a novel kinase

173 retention in three systems compared with M. sexta JHDK.

174 Manduca sexta juvenile hormone diol kinase (JHDK) catalyzes the

175 The gene sequence of Manduca sexta juvenile hormone diol kinase (JHDK) codes for an e

176 taken up by pericardial cells and native M. sexta juvenile hormone esterase in fat body tissue, wher

177 rived from the tobacco hornworm moth Manduca sexta L. was constructed and screened for proteins that

178 5, which during the metamorphosis of Manduca sexta (L.) changes from a slow motoneuron that is involv

179 ed reduced resistance against herbivorous M. sexta larvae and the necrotrophic fungal pathogen Botryt

180 Manduca sexta larvae are a model for growth control in insects,

181 moth is an important pollinator while the M. sexta larvae are specialized herbivores of the plant.

182 M. sexta larvae damaged less foliage and displayed delays i

183 Spodoptera frugiperda, S. exigua and Manduca sexta larvae fed BvSTI leaves had significant reductions

184 hexenal acting as a feeding stimulant for M. sexta larvae in OPR3-RNAi plants.

185 Attack from Manduca sexta larvae on IRcdpk4/5 plants induced high levels of

186 M. sexta larvae performed 2-fold better when reared on irHE

187 ins that accumulate in the midgut of Manduca sexta larvae reared on tomato (Solanum lycopersicum) pla

188 expressed in leaves, performance of Manduca sexta larvae, a folivore, decreased.

189 se to mechanical wounding, attack by Manduca sexta larvae, and Prosystemin over-expression.

190 erexpress arginase were more resistant to M. sexta larvae, and this effect was correlated with reduce

191 s not bind to BT-R(1) and is not toxic to M. sexta larvae, did not affect BBMV aggregation.

192 sceral-locomotory piston in crawling Manduca sexta larvae, in which the gut slides forward in advance

193 .5-55.6% to first instar H. virescens and M. sexta larvae, suggesting a critical function for this ca

194 es (FACs) in oral secretions (OS) of Manduca sexta larvae, which are introduced into wounds during fe

195 to form ion channels and toxicity in Manduca sexta larvae.

196 4 from the hemolymph of bacteria-injected M. sexta larvae.

197 ium during growth and development of Manduca sexta larvae.

198 by challenging C. roseus leaves with Manduca sexta larvae.

199 mproving the performance and viability of M. sexta larvae.

200 resistance toward tobacco hornworm (Manduca sexta) larvae.

201 isolated from an Escherichia coli-induced M. sexta larval fat body cDNA library.

202 larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal tissues stop growing, the for

203 d prosystemin-mediated resistance to Manduca sexta (Lepidoptera) herbivory, demonstrating that MPK1 a

204 s, mE75A and mE75B, were reported in Manduca sexta (Lepidoptera).

205 The tobacco hornworm Manduca sexta, like many holometabolous insects, makes two versi

206 ecruited for biosynthesis of 3UFA SPCs in M. sexta lineage via gene duplication and neofunctionalizat

207 mammalian counterparts, H. virescens and M. sexta lipid rafts are enriched in cholesterol, sphingoli

208 etrocerebral complexes from the moth Manduca sexta maintained in tissue culture and to identify JH II

209 transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affinity-purified antibody deve

210 served molecular actions, we suggest that M. sexta may be a valuable model for studying the electroph

211 a complex of serpin-1K in a complex with M. sexta midgut chymotrypsin was identified, suggesting ser

212 r membrane vesicles (BBMVs) prepared from M. sexta midgut epithelium.

213 during differentiation and development of M. sexta midgut epithelium.

214 nsitive to degradation by trypsin or Manduca sexta midgut juice.

215 and threonine deaminase (TD), act in the M. sexta midgut to catabolize the essential amino acids Arg

216 ons, when analyzed by voltage clamping of M. sexta midguts.

217 ric nervous system (ENS) of the moth Manduca sexta, migratory neurons forming the enteric plexus (EP

218 ghtii flowers, a nectar resource for Manduca sexta moths, and show that the scent was dynamic and rap

219 Manduca sexta (Ms) larvae are known to efficiently excrete inges

220 on of E74 from the tobacco hornworm, Manduca sexta (MsE74).

221 ure of JHE from the tobacco hornworm Manduca sexta (MsJHE) in complex with the transition state analo

222 terase (JHE) of the tobacco hornworm Manduca sexta (MsJHE).

223 e adult olfactory system of the moth Manduca sexta, olfactory receptor neurons extend axons from the

224 Six are highly similar to their Manduca sexta orthologs that regulate innate immunity.

225 )-linalool, reported to oppositely affect M. sexta oviposition, in the Arizona and Utah accessions.

226 olated overlapping lambda clones for Manduca sexta PAP-2, hemolymph proteinase 12 (HP12), and HP24.

227 uch as widespread nuclear localization of M. sexta PER and rhythmic expression in glial cells, are re

228 d riboprobes were transcribed from a 1-kb M. sexta per cDNA.

229 ty purification of serpin-1 isoforms from M. sexta plasma, followed by two-dimensional PAGE and ident

230 Manduca sexta PPO is a heterodimer consisting of 2 homologous po

231 In H. virescens and M. sexta, pretreatment of membranes with the cholesterol-de

232 molymph (serine) protease 5 (HP5) in Manduca sexta Previous studies have demonstrated a protease casc

233 n the antennal lobe (AL) of the moth Manduca sexta previously were shown to respond preferentially to

234 structure of dual clip domains from Manduca sexta prophenoloxidase activating proteinase-2.

235 se complexes, identified three endogenous M. sexta proteinase targets of serpin-1.

236 e report here functions of two additional M. sexta proteinases, hemolymph proteinases 6 and 8 (HP6 an

237 In the tobacco hornworm, Manduca sexta, pupal diapause can be induced by exposure of fift

238 In the tobacco hornworm Manduca sexta, recombinant hemolymph proteinase 14 precursor (pr

239 at the tobacco hornworm caterpillar, Manduca sexta, reduced feeding by 30-40% owing to the risk of pr

240 amine by membrane-associated enzyme(s) in M. sexta represents direct evidence of fatty acid amide syn

241 ut were 8, 30, and 12 times less toxic to M. sexta, respectively, than the wild-type Cry1Ab.

242 Studies in the hawkmoth Manduca sexta revealed that pulses of the steroid hormone 20-hyd

243 Our findings suggest that M. sexta's sensitization occurs through central signal ampl

244 Our results suggest that M. sexta serpin-1 isoforms A, E, and J can inhibit hemolymp

245 Recombinant M. sexta serpin-1I reduced prophenoloxidase activation by i

246 from the hinge region in the RCL of Manduca sexta serpin-3 and found they were able to block serpin-

247 M. sexta serpin-3 is constitutively present in hemolymph at

248 This inhibitor, M. sexta serpin-3, contains a reactive site loop strikingly

249 Manduca sexta serpin-4 and serpin-5 suppress pro-PO activation i

250 HP5 is inhibited by Manduca sexta serpin-4, serpin-1A, and serpin-1J to regulate its

251 We recently isolated Manduca sexta serpin-6 from hemolymph of the bacteria-challenged

252 M. sexta serpin-6 is 55% similar in amino acid sequence to

253 determined structures of full-length Manduca sexta sGC in both inactive and active states using cryo-

254 l-length and N-terminal fragments of Manduca sexta sGC in Escherichia coli, the first time this has b

255 determined the overall shape of truncated M. sexta sGC using analytical ultracentrifugation and small

256 tion and immunocytochemistry for the Manduca sexta sGCalpha1 subunit.

257 The hawkmoth, Manduca sexta (Sphingidae), oviposits on solanaceous plants.

258 A cDNA clone coding for M. sexta synaptotagmin was characterized and found to encod

259 s raised against the unique N-terminus of M. sexta synaptotagmin, and a monoclonal antibody (DSYT) wa

260 we developed an in vivo protocol in Manduca sexta that allows continuous monitoring of neural ensemb

261 visual neurons in the optic lobes of Manduca sexta that are selectively activated by certain of these

262 nscripts for 12 serpin-1 isoforms in Manduca sexta that differ only in the region encoding the carbox

263 in Drosophila with those in the moth Manduca sexta that indicate a critical role for glia in antennal

264 a feeding (Spodoptera littoralis and Manduca sexta) that triggers distant APs, variation potentials,

265 novel expression system for sGC from Manduca sexta (the tobacco hornworm) that retains the N-terminal

266 Under normal growth conditions in Manduca sexta, the endocrine cascade that causes the brain to in

267 During metamorphosis of the moth, Manduca sexta, the larval legs degenerate and are replaced by ad

268 llars, such as the tobacco hornworm, Manduca sexta, the movement is a defensive strike targeted to a

269 During metamorphosis of the moth Manduca sexta, the neuromuscular system of the thoracic legs is

270 In larvae of the moth Manduca sexta, the tip of each abdominal proleg (locomotory appe

271 In the moth M. sexta, these peptides are expressed in two, regionally d

272 We explored the behavioral responses of M. sexta to artificial flowers with different combinations

273 rvation is investigated in the moth, Manduca sexta, to address the specificity of neuromuscular inter

274 neuronal migration in the hawkmoth, Manduca sexta, to show that APPL-Goalpha signaling restricts ect

275 The growth rates of Manduca sexta (tobacco hornworm) larvae feeding on tomato plants

276 examined truncated sGC proteins from Manduca sexta (tobacco hornworm) that bind NO, CO, and stimulato

277 (APR) motoneurons of the hawk moth, Manduca sexta, undergo a segment-specific pattern of programmed

278 abdominal central nervous system of Manduca sexta undergoes an increase in cyclic GMP (cGMP) when ex

279 initiating protease in hemolymph of Manduca sexta, upon the binding of beta-1,3-glucan by its recogn

280 two types of looming-sensitive neurons in M. sexta use different mechanisms to detect the approach or

281 genes that are upregulated in the gut of M. sexta using recombinase-based in vivo expression technol

282 nnervation of the heart and aorta of Manduca sexta was studied by using anatomic, neuronal tracing an

283 ae and to the solanaceous specialist Manduca sexta was verified in no-choice bioassays.

284 he facultative Solanaceae-specialist Manduca sexta, was significantly increased on tgg1tgg2 double mu

285 ontrolling the wings of a hawk moth, Manduca sexta We simultaneously recorded nearly every action pot

286 Using larvae of Manduca sexta, we discovered that clot nucleation is a two-step

287 In the insect, Manduca sexta, we examined the developmental plasticity of OA sy

288 actable gustatory system of the moth Manduca sexta, we found chemical-specific information is as foll

289 In the moth Manduca sexta, we found that odor presentations that support ass

290 In a well-established insect model, Manduca sexta, we identified the putative homologue of the embry

291 energy exchange in flight muscles of Manduca sexta, we produced high-speed movies of x-ray equatorial

292 In the moth Manduca sexta, we showed previously that fasciclin II, a cell ad

293 In the olfactory pathway of the moth Manduca sexta,we find that different odorants evoke gamma-band o

294 , responses to A. solani, P. syringae, or M. sexta were similar to the wild-type plants.

295 scens and the 120-kDa aminopeptidase from M. sexta, were preferentially partitioned into lipid rafts.

296 ilenced and its hawkmoth pollinator, Manduca sexta, were used in semi-natural tent and wind-tunnel as

297 ild-type Egf1.0 inhibited PAP-3 from Manduca sexta, whereas Egf1.0(R51A), whose reactive-site arginin

298 ition, we used the tobacco hornworm (Manduca sexta), which uses a blend of mono-, di-, and uncommon t

299 ETH receptor (ETHR) gene in the moth Manduca sexta, which encodes two subtypes of GPCR (ETHR-A and ET

300 tractive to the specialist herbivore Manduca sexta with respect to feeding and oviposition.