ライフサイエンスコーパス: Manduca sexta

1 ique 1 (DEO1) muscle during metamorphosis in Manduca sexta ().

2 otein were highly toxic to tobacco hornworm (Manduca sexta).

3 he larval epidermis of the tobacco hornworm (Manduca sexta).

4 rvae of the chewing insect tobacco hornworm (Manduca sexta).

5 ins in midgut epithelia of tobacco hornworm (Manduca sexta).

6 s of salient odor perception using the moth (Manduca sexta).

7 D76 binds to a hemocyte-specific integrin of Manduca sexta.

8 subunits (Masburs and Maspburs) in the moth Manduca sexta.

9 ws a corresponding reduction of virulence to Manduca sexta.

10 development time of eggs of a sphingid moth, Manduca sexta.

11 n-4 and serpin-5) from the tobacco hornworm, Manduca sexta.

12 mmunoreactivity in the brain of the hawkmoth Manduca sexta.

13 ed this critical issue in the AL of the moth Manduca sexta.

14 Cry1A receptors from Heliothis virescens and Manduca sexta.

15 r for Bacillus thuringiensis Cry1A toxins in Manduca sexta.

16 ervate the terminal cardiac chamber of adult Manduca sexta.

17 responsive serpin from the tobacco hornworm, Manduca sexta.

18 l fractions of several alimentary tissues in Manduca sexta.

19 primary olfactory nerve pathway in the moth Manduca sexta.

20 ithelial membrane of Heliothis virescens and Manduca sexta.

21 gated the biological functions of hemolin in Manduca sexta.

22 mmodus and Gryllus bimaculatus, and the moth Manduca sexta.

23 al (olfactory) lobe of the brain of the moth Manduca sexta.

24 rly heavily in the antennal lobe of the moth Manduca sexta.

25 preference exhibited by larvae of the moth, Manduca sexta.

26 olfactory system (antennal lobe) of the moth Manduca sexta.

27 solated from plasma of the tobacco hornworm, Manduca sexta.

28 ach antennal lobe of the female sphinx moth, Manduca sexta.

29 uring development of the olfactory system in Manduca sexta.

30 cognition protein from the tobacco hornworm, Manduca sexta.

31 E) in the epidermis of the tobacco hornworm, Manduca sexta.

32 , that is expressed in the nervous system of Manduca sexta.

33 ochic acid) all inhibited feeding rapidly in Manduca sexta.

34 ephila elpenor and the crepuscular-nocturnal Manduca sexta.

35 el2A and MsRel2B) from the tobacco hornworm, Manduca sexta.

36 cdysteroids during metamorphosis of the moth Manduca sexta.

37 zed insect olfactory system of the hawkmoth, Manduca sexta.

38 prothoracic glands of the tobacco hornworm, Manduca sexta.

39 enced from the brain of the tobacco hornworm Manduca sexta.

40 retina and the outer optic lobes in the moth Manduca sexta.

41 (DA), in the antennal lobe (AL) of the moth Manduca sexta.

42 of the adult outer optic ganglia in the moth Manduca sexta.

43 -ETH, is described from the tobacco hornworm Manduca sexta.

44 adult eclosion in the tobacco hornworm moth, Manduca sexta.

45 uscles control flight in an agile hawk moth, Manduca sexta.

46 sional reconstruction of deactivated V1 from Manduca sexta.

47 rgic neuromodulation in the antennal lobe of Manduca sexta.

48 ce assay was performed with tobacco hornworm Manduca sexta.

49 adult olfactory (antennal) lobe of the moth Manduca sexta.

50 ory serpins from Drosophila melanogaster and Manduca sexta.

51 reviously reported for the tobacco hornworm, Manduca sexta.

52 he midgut epithelium of the tobacco hornworm Manduca sexta.

53 Sacred Datura (Datura wrightii) and the moth Manduca sexta[11, 12] to determine how olfactory network

54 ntly challenged with (1) chewing herbivores (Manduca sexta), (2) piercing-sucking insects (Empoasca s

55 We have isolated from the tobacco hornworm, Manduca sexta, a cDNA encoding a modular protein designa

56 fied from hemolymph of the tobacco hornworm, Manduca sexta, a new serine proteinase that cleaves prop

57 During the last larval molt in Manduca sexta, a number of transcription factors are seq

58 an orthologue of APP (msAPPL) from the moth, Manduca sexta, a preparation that permits in vivo manipu

59 We have isolated from the tobacco hornworm, Manduca sexta, a serine proteinase that activates proPO,

60 During metamorphosis of the hawkmoth, Manduca sexta, accessory planta retractor (APR) motoneur

61 In larvae of the hawkmoth, Manduca sexta, accessory planta retractor (APR) motoneur

62 stitutively overproduced in the hemolymph of Manduca sexta, activating the prophenoloxidase system.

63 Manduca Sexta adults insects have two defined lipophorin

64 Manduca sexta allatotropin (Mas-AT) was isolated and fir

65 Diploptera punctata allatostatin (Dip-AST), Manduca sexta allatotropin (Mas-AT), and serotonin (5HT)

66 eveloping enteric nervous system of the moth Manduca sexta, an identified set of neurons (the EP cell

67 es a homolog of proteins associated with the Manduca sexta and bovine chromaffin granule V-ATPase.

68 ern of cell division in the tobacco hornworm Manduca sexta and found that both the rate of cell divis

69 eme domain of sGC proteins from the hawkmoth Manduca sexta and from human.

70 8RRP370, called B4, abolished potency toward Manduca sexta and Heliothis virescens, and the loss of t

71 5 resulted in the total loss of toxicity for Manduca sexta and Heliothis virescens, another caused a

72 residues in receptor binding and toxicity to Manduca sexta and Heliothis virescens.

73 O)-sensitive guanylyl cyclase were cloned in Manduca sexta and implicated in several cellular, develo

74 stembryonic neurons in the tobacco hawkmoth, Manduca sexta and is restricted to six identifiable post

75 ecticidal activities of the mutant toxins on Manduca sexta and Lymantria dispar larvae were examined.

76 The hawkmoth Manduca sexta and one of its preferred hosts in the Nort

77 secondary form isolates are virulent towards Manduca sexta and several other insects.

78 nce homologous to a binding epitope found in Manduca sexta and Tenebrio molitor Bt cadherin functiona

79 d after attack by the leaf-chewing herbivore Manduca sexta and the stem borer Trichobaris mucorea.

80 encode complexes with high oral toxicity to Manduca sexta and therefore they represent potential alt

81 We wanted to know if these peptides occur in Manduca sexta and what functions they might have.

82 Ingestion of tomato foliage by specialist (Manduca sexta) and generalist (Trichoplusia ni) insect h

83 ly (Danaus plexippus), Carolina sphinx moth (Manduca sexta), and Death's head sphinx moth (Acherontia

84 of moricin promoter in the tobacco hornworm, Manduca sexta, and a 140-bp region in the moricin promot

85 llatostatin C (AstC) was first isolated from Manduca sexta, and it has an important conserved feature

86 gaster was cloned from the tobacco hornworm, Manduca sexta, and its developmental expression and horm

87 physiological studies in the AL of the moth, Manduca sexta, and recorded odor-evoked calcium changes

88 B1, were isolated from the tobacco hornworm, Manduca sexta, and shown to be similar to the correspond

89 ystem including tomato plants, the herbivore Manduca sexta, and the parasitoid Cotesia congregata.

90 -collected caterpillars of the model species Manduca sexta Antibiotic suppression of gut bacterial ac

91 Manduca sexta apolipophorin-III, apoLp-III, is an exchan

92 Finally, we compare the NMR structures of Manduca sexta apoLp-III and L. migratoria apoLp-III and

93 e wing imaginal discs, the imaginal discs of Manduca sexta are not formed until early in the final la

94 , the primary olfactory centers, of the moth Manduca sexta are sexually dimorphic.

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

96 With Manduca sexta as a model system, we analyzed how natural

97 nervous system (ENS) of the tobacco hornworm Manduca sexta as a model system, we have explored whethe

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

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

100 , Plutella xylostella, and tobacco hornworm, Manduca sexta, as well as the spotted wing drosophila, D

101 rnaria sp. U10, and the specialist herbivore Manduca sexta At least 15 different O-AS structures belo

102 sed in its defense against tobacco hornworm (Manduca sexta) attack.

103 he intersegmental muscles (ISMs) of the moth Manduca sexta become committed to die at the end of meta

104 he interaction of the N-terminal domain from Manduca sexta betaGRP2 (N-betaGRP2) with laminarin, a so

105 ding two peptides by alternative splicing in Manduca sexta, Bombyx mori, and Aedes aegypti: A C-termi

106 f subunit c homologues from Homo sapiens and Manduca sexta, both species sensitive to benzolactone en

107 71, affect insertion of the whole toxin into Manduca sexta brush border membrane vesicles (BBMVs).

108 nd to feeding by larvae of tobacco hornworm (Manduca sexta) but not to the bacterial pathogen Pseudom

109 inases in hemolymph of the tobacco hornworm, Manduca sexta, but functions are known for only a few of

110 abdominal epidermis of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20E) during larval

111 ignificantly with predation of the herbivore Manduca sexta by native predators.

112 tion of NO in the antennal lobe of the moth, Manduca sexta, by using immunocytochemistry and real-tim

113 , obtained by incubating Cry1Ac toxin with a Manduca sexta cadherin fragment, with BBMV from both str

114 subunit and examples from the invertebrates Manduca sexta, Caenorhabditis elegans, and Drosophila me

115 maginal disks of non-feeding wandering stage Manduca sexta can be stopped by removal of the brain, in

116 Their main hawkmoth pollinator, Manduca sexta, can perceive minute variation (0.5 ppm) i

117 We tested a potential invertebrate host (Manduca sexta caterpillars) but found they were not susc

118 ation of different "bitter" taste stimuli in Manduca sexta caterpillars.

119 adaptation to specific "bitter" compounds in Manduca sexta caterpillars.

120 om the peripheral taste system of an insect (Manduca sexta caterpillars; Sphingidae) contribute to th

121 ed nanomaterials (ENMs) by tobacco hornworm (Manduca sexta) caterpillars resulting from the ingestion

122 ores were allowed to feed, tobacco hornworm (Manduca sexta) caterpillars, gained more mass on seedlin

123 s protein from a larval lepidopteran midgut (Manduca sexta) cDNA library.

124 In the nervous system of the hawkmoth, Manduca sexta, cells expressing the period (per)gene wer

125 eening, using larvae of the tobacco hornworm Manduca sexta, combining diagnostic imaging modalities f

126 abdominal body wall muscles in the hawkmoth, Manduca sexta, consist of large, elongated fibers that a

127 composition: feeding of the tobacco hornworm Manduca sexta converts (Z)-3- to (E)-2-GLVs thereby attr

128 if the olfactory system of female hawkmoths, Manduca sexta, could differentiate between crucial and b

129 This discovery of a Manduca sexta CRABP (msCRABP) demonstrates the presence

130 ctural immunocytochemistry of infected host (Manduca sexta) cuticle demonstrated that MeCPA participa

131 ponse gene RNA levels and protection against Manduca sexta damage were influenced by LapA RNA and pro

132 Caterpillars (e.g., Manduca sexta) detect these compounds with a few bitter-

133 In the moth Manduca sexta, developing olfactory receptor axons encou

134 In the moth Manduca sexta, development of glomeruli in the antennal

135 In the moth Manduca sexta, development of the adult olfactory system

136 and is expressed in the midgut epithelium of Manduca sexta during larval development.

137 In Manduca sexta, E. faecalis is an infrequent member of th

138 In the sphinx moth Manduca sexta, each of the paired antennal lobes (ALs; t

139 ach to generate a hypothetical structure for Manduca sexta EH.

140 Cells were isolated from Tobacco hornworm (Manduca sexta) embryos and subsequently adapted to singl

141 rom the central nervous system of the insect Manduca sexta enabled us to define domains that affect a

142 n the juvenile hormone-regulatory pathway in Manduca sexta enables heat stress to reveal a hidden rea

143 ke flight muscles of an insect, the hawkmoth Manduca sexta, encode torque during yaw turns.

144 Serpin gene-1 from the tobacco hornworm, Manduca sexta, encodes, through alternative exon usage,

145 electron microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calculated the first 3D r

146 ranscription factor whose expression in both Manduca sexta epidermis and the Manduca GV1 cell line is

147 nd to a lesser extent, by a tobacco hornworm Manduca sexta FaRP, GNSFLRFNH2 (F7G) (potency ranking FL

148 Additionally, early instar Manduca sexta fed on mowed flower-based artificial diets

149 In the moth Manduca sexta, glial reduction experiments have directly

150 Larvae of Manduca sexta grew faster when consuming inverted-repeat

151 e of apolipophorin III from the sphinx moth, Manduca sexta, has been determined in the lipid-free sta

152 Studies in Manduca sexta have indicated that just before they enter

153 he N-linked glycans of aminopeptidase 1 from Manduca sexta have revealed unusual structures not previ

154 For Manduca sexta hawkmoths, how learning modifies foraging

155 e been purified from the larval hemolymph of Manduca sexta: hemolymph proteinase 14 (HP14), which aut

156 ct the regulation of direct defenses against Manduca sexta herbivory or P. syringae pv tomato DC3000

157 line to annotate leaf metabolic responses to Manduca sexta herbivory.

158 ndocrine influences of the tobacco hornworm, Manduca sexta, host and its parasitoid wasp Apanteles co

159 the enteric nervous system (ENS) of the moth Manduca sexta, identified populations of neurons and gli

160 inning of the final larval (fifth) instar of Manduca sexta, imaginal precursors including wing discs

161 abdominal epidermis of the tobacco hornworm Manduca sexta in a pattern-specific manner as the 20-hyd

162 own to suppress melanization of hemolymph in Manduca sexta in part by inhibiting the enzymatic activi

163 ring flower-feeding behavior in the hawkmoth Manduca sexta In the laboratory, moths feed from a robot

164 ontrolling floral preference in the hawkmoth Manduca sexta in the semiarid grassland of Arizona.

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

166 Larvae of Manduca sexta increase up to ten-fold in mass between mo

167 In the hawkmoth, Manduca sexta, individual accessory planta retractor (AP

168 on, resulted in attenuated virulence against Manduca sexta insects.

169 ired by X. nematophila for full virulence in Manduca sexta insects.

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

171 on of neural precursors in the optic lobe of Manduca sexta is controlled by circulating steroids and

172 Based on studies in the moth, Manduca sexta, it has been postulated that the neuropept

173 Manduca sexta juvenile hormone diol kinase (JHDK) cataly

174 The gene sequence of Manduca sexta juvenile hormone diol kinase (JHDK) codes

175 brary derived from the tobacco hornworm moth Manduca sexta L. was constructed and screened for protei

176 uron, MN5, which during the metamorphosis of Manduca sexta (L.) changes from a slow motoneuron that i

177 Each hemisegment of the Manduca sexta larva is supplied with a subepidermal plex

178 Manduca sexta larvae are a model for growth control in i

179 Hemolymph of fifth instar Manduca sexta larvae collected under non-sterile conditi

180 it for the proleg withdrawal reflex (PWR) of Manduca sexta larvae exhibits activity-dependent plastic

181 Spodoptera frugiperda, S. exigua and Manduca sexta larvae fed BvSTI leaves had significant re

182 Attack from Manduca sexta larvae on IRcdpk4/5 plants induced high le

183 st proteins that accumulate in the midgut of Manduca sexta larvae reared on tomato (Solanum lycopersi

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

185 n response to mechanical wounding, attack by Manduca sexta larvae, and Prosystemin over-expression.

186 novel visceral-locomotory piston in crawling Manduca sexta larvae, in which the gut slides forward in

187 conjugates (FACs) in oral secretions (OS) of Manduca sexta larvae, which are introduced into wounds d

188 epithelium during growth and development of Manduca sexta larvae.

189 system by challenging C. roseus leaves with Manduca sexta larvae.

190 pathway is highly susceptible to attacks by Manduca sexta larvae.

191 ability to form ion channels and toxicity in Manduca sexta larvae.

192 Feeding assays with tobacco hornworm (Manduca sexta) larvae revealed the defensive functions o

193 ncreased resistance toward tobacco hornworm (Manduca sexta) larvae.

194 starved larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal tissues stop growing,

195 In the month, Manduca sexta, larval ecdysis is accompanied by increase

196 During metamorphosis in the hawkmoth Manduca sexta, larval leg motoneurons survive the degene

197 mpromised prosystemin-mediated resistance to Manduca sexta (Lepidoptera) herbivory, demonstrating tha

198 isoforms, mE75A and mE75B, were reported in Manduca sexta (Lepidoptera).

199 The tobacco hornworm Manduca sexta, like many holometabolous insects, makes t

200 vidual retrocerebral complexes from the moth Manduca sexta maintained in tissue culture and to identi

201 o diuretic hormones of the tobacco hornworm, Manduca sexta, (Mas-DH) is a peptide of 41 residues.

202 a GABA transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affinity-purified antib

203 e in the main flight muscles of the hawkmoth Manduca sexta, mechanical function (net work) does depen

204 dysteroid responsive gene, HHR3, a potential Manduca sexta MHR3 homologue in the American lobster, Ho

205 were sensitive to degradation by trypsin or Manduca sexta midgut juice.

206 nding and a slower rate of pore formation in Manduca sexta midgut membrane vesicles compared to the w

207 nic enteric nervous system (ENS) of the moth Manduca sexta, migratory neurons forming the enteric ple

208 tura wrightii flowers, a nectar resource for Manduca sexta moths, and show that the scent was dynamic

209 n cloned via homology with the corresponding Manduca sexta (Ms) gene.

210 e encoding a subunit of the tobacco hornworm Manduca sexta (Ms) hemolymph (serum) ferritin (Fer) has

211 Manduca sexta (Ms) larvae are known to efficiently excre

212 regulation of E74 from the tobacco hornworm, Manduca sexta (MsE74).

213 l structure of JHE from the tobacco hornworm Manduca sexta (MsJHE) in complex with the transition sta

214 he JH esterase (JHE) of the tobacco hornworm Manduca sexta (MsJHE).

215 have cloned the NSF ortholog from the moth, Manduca sexta (MsNSF).

216 ergence and divergence ratios of a hawkmoth (Manduca sexta) nervous system can reproduce the relative

217 We have cloned Manduca sexta nitric oxide synthase (MsNOS) and two sGCs

218 nt of the adult olfactory system of the moth Manduca sexta, olfactory receptor neurons extend axons f

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

220 y and isolated overlapping lambda clones for Manduca sexta PAP-2, hemolymph proteinase 12 (HP12), and

221 ental muscles (ISMs) of the tobacco hawkmoth Manduca sexta participate in the emergence behavior of t

222 Manduca sexta PPO is a heterodimer consisting of 2 homol

223 Here, we report that tobacco hawkmoths (Manduca sexta) preferentially oviposit on Jimson weed (D

224 d via hemolymph (serine) protease 5 (HP5) in Manduca sexta Previous studies have demonstrated a prote

225 atLFG) in the antennal lobe (AL) of the moth Manduca sexta previously were shown to respond preferent

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

227 In the tobacco hornworm, Manduca sexta, pupal diapause can be induced by exposure

228 In the tobacco hornworm Manduca sexta, recombinant hemolymph proteinase 14 precu

229 ument that the tobacco hornworm caterpillar, Manduca sexta, reduced feeding by 30-40% owing to the ri

230 Studies in the hawkmoth Manduca sexta revealed that pulses of the steroid hormon

231 atura wrightii, and its hawkmoth pollinator, Manduca sexta, reveals that floral relative humidity act

232 Manduca sexta serpin gene-1 encodes a family of serpins

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

234 Manduca sexta serpin-4 and serpin-5 suppress pro-PO acti

235 HP5 is inhibited by Manduca sexta serpin-4, serpin-1A, and serpin-1J to regu

236 We recently isolated Manduca sexta serpin-6 from hemolymph of the bacteria-ch

237 uggest that the multicatalytic proteinase of Manduca sexta serves multiple functions and is associate

238 In the brain of the sphinx moth Manduca sexta, sex-pheromonal information is processed i

239 We determined structures of full-length Manduca sexta sGC in both inactive and active states usi

240 eric full-length and N-terminal fragments of Manduca sexta sGC in Escherichia coli, the first time th

241 ybridization and immunocytochemistry for the Manduca sexta sGCalpha1 subunit.

242 ur studies on the isolated nervous system of Manduca sexta show that the peptides ecdysis-triggering

243 The eye primordium of the moth, Manduca sexta, shows two different developmental respons

244 The hawkmoth, Manduca sexta (Sphingidae), oviposits on solanaceous pla

245 earning, we developed an in vivo protocol in Manduca sexta that allows continuous monitoring of neura

246 gs from visual neurons in the optic lobes of Manduca sexta that are selectively activated by certain

247 uces transcripts for 12 serpin-1 isoforms in Manduca sexta that differ only in the region encoding th

248 indings in Drosophila with those in the moth Manduca sexta that indicate a critical role for glia in

249 soform from the nervous system of the insect Manduca sexta that we have named M. sexta guanylyl cycla

250 ect larva feeding (Spodoptera littoralis and Manduca sexta) that triggers distant APs, variation pote

251 e cloned a 2.4-kb E3 cDNA from an arthropod, Manduca sexta, that codes for 497 amino acids and transl

252 loped a novel expression system for sGC from Manduca sexta (the tobacco hornworm) that retains the N-

253 Under normal growth conditions in Manduca sexta, the endocrine cascade that causes the bra

254 During metamorphosis of the moth, Manduca sexta, the larval legs degenerate and are replac

255 the enteric nervous system (ENS) in the moth Manduca sexta, the migration of an identified set of neu

256 caterpillars, such as the tobacco hornworm, Manduca sexta, the movement is a defensive strike target

257 During metamorphosis of the hawkmoth, Manduca sexta, the muscles, cuticular structures, and mo

258 During metamorphosis of the moth Manduca sexta, the neuromuscular system of the thoracic

259 In larvae of the moth Manduca sexta, the tip of each abdominal proleg (locomot

260 [HRGP] from Phaseolus vulgaris; Serpin from Manduca sexta) to direct a modified beta-glucuronidase (

261 its innervation is investigated in the moth, Manduca sexta, to address the specificity of neuromuscul

262 C-PNs) in the antennal lobe of the male moth Manduca sexta, to encode naturally intermittent sex pher

263 assay of neuronal migration in the hawkmoth, Manduca sexta, to show that APPL-Goalpha signaling restr

264 The growth rates of Manduca sexta (tobacco hornworm) larvae feeding on tomat

265 d adducts obtained from acid hydrolysates of Manduca sexta (tobacco hornworm) pupal cuticle exuviae a

266 ion, we examined truncated sGC proteins from Manduca sexta (tobacco hornworm) that bind NO, CO, and s

267 resistance toward the lepidopteran predator Manduca sexta (tobacco hornworm).

268 etractor (APR) motoneurons of the hawk moth, Manduca sexta, undergo a segment-specific pattern of pro

269 sis the leg neuromuscular system of the moth Manduca sexta undergoes an extensive remodeling as the l

270 isolated abdominal central nervous system of Manduca sexta undergoes an increase in cyclic GMP (cGMP)

271 P14), an initiating protease in hemolymph of Manduca sexta, upon the binding of beta-1,3-glucan by it

272 Innervation of the heart and aorta of Manduca sexta was studied by using anatomic, neuronal tr

273 tle larvae and to the solanaceous specialist Manduca sexta was verified in no-choice bioassays.

274 ni and the facultative Solanaceae-specialist Manduca sexta, was significantly increased on tgg1tgg2 d

275 units controlling the wings of a hawk moth, Manduca sexta We simultaneously recorded nearly every ac

276 Using larvae of Manduca sexta, we discovered that clot nucleation is a t

277 In the insect, Manduca sexta, we examined the developmental plasticity

278 he enteric nervous system (ENS) of the moth, Manduca sexta, we examined the role of NO and NO-sensiti

279 m the tractable gustatory system of the moth Manduca sexta, we found chemical-specific information is

280 In the moth Manduca sexta, we found that odor presentations that sup

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

282 hanical energy exchange in flight muscles of Manduca sexta, we produced high-speed movies of x-ray eq

283 In the moth Manduca sexta, we showed previously that fasciclin II, a

284 In the olfactory pathway of the moth Manduca sexta,we find that different odorants evoke gamm

285 center of the olfactory pathway, of the moth Manduca sexta were studied with laser scanning confocal

286 trains of the black mutant tobacco hornworm, Manduca sexta, were evolved via genetic accommodation of

287 ically silenced and its hawkmoth pollinator, Manduca sexta, were used in semi-natural tent and wind-t

288 Wild-type Egf1.0 inhibited PAP-3 from Manduca sexta, whereas Egf1.0(R51A), whose reactive-site

289 ) acquisition, we used the tobacco hornworm (Manduca sexta), which uses a blend of mono-, di-, and un

290 ify the ETH receptor (ETHR) gene in the moth Manduca sexta, which encodes two subtypes of GPCR (ETHR-

291 d a cDNA and gene from the tobacco hornworm, Manduca sexta, which is related to the vertebrate cellul

292 gene was isolated from the tobacco hornworm, Manduca sexta, which shows a predicted 88% amino acid id

293 more attractive to the specialist herbivore Manduca sexta with respect to feeding and oviposition.