ライフサイエンスコーパス: Manduca

1 could be played by central olfactory glia in Manduca.

2 primarily expressed in the nervous system of Manduca.

3 similar to the six postembryonic lineages in Manduca.

4 tacean that has many similarities to MHR3 in Manduca and DHR3 in Drosophila melanogaster.

5 In both Manduca and Drosophila, the broad (br) gene is expressed

6 nd defense mechanisms in model hosts such as Manduca and Drosophila.

7 -I cDNA are present in the nervous system of Manduca and that MsGC-I is expressed in a small populati

8 eation of the late-forming imaginal discs in Manduca appears to be controlled by unidentified endocri

9 the enteric nervous system (ENS) in the moth Manduca, approximately 300 neurons [enteric plexus (EP)

10 sitive filaments in the transverse nerves of Manduca are most likely to be intrinsic cells that subse

11 g dorsal longitudinal flight muscle (DLM) of Manduca arises from an anlage containing both remnants o

12 imilar role at the onset of metamorphosis in Manduca as it does in Drosophila, whereas MsE74A is regu

13 expressed in the embryonic labial segment of Manduca as two circular monolayers of epithelial cells i

14 Thus, the Manduca bombyxin acts as a metamorphosis-initiating fact

15 y feeding on sucrose or by bovine insulin or Manduca bombyxin in starved final instar larvae.

16 at recognize the core, Z2, and Z4 domains of Manduca BR-C proteins showed that BR-C appearance not on

17 Expression of Manduca Broad-Complex (BR-C) mRNA in the larval epidermi

18 d the formation of a second pupal cuticle in Manduca, but only in the abdomen of DROSOPHILA: Expressi

19 rmonal regulation of mE75 gene expression in Manduca CH1 cultured cells.

20 Using this assay, we have now identified Manduca Contactin (MsContactin) as an endogenous ligand

21 cribe the anisotropic material properties of Manduca cuticle.

22 In Manduca dorsal abdominal epidermis, BRC RNAs were not ob

23 A possible structural relationship of Manduca E3 to other pyridine-binding proteins, such as t

24 in substrate binding are highly conserved in Manduca E3.

25 at deviated only slightly from the predicted Manduca EH structure were generated in silico for the Bo

26 eptides were rationalized with the predicted Manduca EH structure, and we found that, on the basis of

27 During formation of the Manduca ENS, an identified set of approximately 300 neur

28 as a model system, we have explored whether Manduca ephrin (MsEphrin; a GPI-linked ligand) and its E

29 Previously, we identified two isoforms of Manduca fasciclin II (MFas II), a glycosyl phosphatidyli

30 xpression patterns for different isoforms of Manduca fasciclin II in the developing olfactory system.

31 Probes specific for Manduca fasciclin II show that while the EP cells expres

32 In the moth Manduca, fasciclin II (MFas II) is expressed both as a t

33 The sequences of the Manduca genes are highly similar to their mammalian homo

34 sion in both Manduca sexta epidermis and the Manduca GV1 cell line is induced by 20-hydroxyecdysone (

35 T) reporter by 2 micrograms of 20E per ml in Manduca GV1 cells was similar to that of endogenous MHR3

36 n the current study, we demonstrate that the Manduca H-cell is immunoreactive to antibodies raised ag

37 The Manduca high affinity Na+/Cl- dependent transporter shar

38 The Manduca homologs of the Eph receptor (MsEph) and ephrin

39 ue amino acid substitutions, detected in the Manduca homologue.

40 ld experiments demonstrated that ovipositing Manduca moths preferred (Z)-3-perfumed D. wrightii over

41 steroidogenesis, S6 cDNA was isolated from a Manduca prothoracic gland cDNA library and sequenced.

42 nalysis revealed that the phosphorylation of Manduca prothoracic gland S6 is limited exclusively to s

43 This Manduca S6 possesses a consensus recognition sequence fo

44 d a number of chimeras between the human and Manduca serotonin transporters (hSERT and MasSERT, respe

45 ared to the human (IC50 = 0.431 micro m) and Manduca serotonin transporters.

46 nin transport affinity compared to human and Manduca serotonin transporters.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 5 resulted in the total loss of toxicity for Manduca sexta and Heliothis virescens, another caused a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 71, affect insertion of the whole toxin into Manduca sexta brush border membrane vesicles (BBMVs).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 For Manduca sexta hawkmoths, how learning modifies foraging

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

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

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

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

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

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

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

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

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

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

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

115 Manduca sexta juvenile hormone diol kinase (JHDK) cataly

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

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

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

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

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

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

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

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

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

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

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

127 epithelium during growth and development of Manduca sexta larvae.

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

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

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

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

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

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

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

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

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

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

138 Manduca sexta PPO is a heterodimer consisting of 2 homol

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

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

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

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

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

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

145 ybridization and immunocytochemistry for the Manduca sexta sGCalpha1 subunit.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

250 ws a corresponding reduction of virulence to Manduca sexta.

251 ephila elpenor and the crepuscular-nocturnal Manduca sexta.

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

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

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

255 mmunoreactivity in the brain of the hawkmoth Manduca sexta.

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

257 Cry1A receptors from Heliothis virescens and Manduca sexta.

258 r for Bacillus thuringiensis Cry1A toxins in Manduca sexta.

259 ervate the terminal cardiac chamber of adult Manduca sexta.

260 responsive serpin from the tobacco hornworm, Manduca sexta.

261 l fractions of several alimentary tissues in Manduca sexta.

262 primary olfactory nerve pathway in the moth Manduca sexta.

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

264 ithelial membrane of Heliothis virescens and Manduca sexta.

265 gated the biological functions of hemolin in Manduca sexta.

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

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

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

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

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

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

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

273 uring development of the olfactory system in Manduca sexta.

274 cognition protein from the tobacco hornworm, Manduca sexta.

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

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

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

278 cdysteroids during metamorphosis of the moth Manduca sexta.

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

280 prothoracic glands of the tobacco hornworm, Manduca sexta.

281 sional reconstruction of deactivated V1 from Manduca sexta.

282 rgic neuromodulation in the antennal lobe of Manduca sexta.

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

284 ory serpins from Drosophila melanogaster and Manduca sexta.

285 reviously reported for the tobacco hornworm, Manduca sexta.

286 he midgut epithelium of the tobacco hornworm Manduca sexta.

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

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

289 Manduca sGC behaves much like its mammalian counterparts

290 als, we have used antisera generated against Manduca-specific isoforms of the homophilic adhesion mol

291 E74A is regulated differently at pupation in Manduca than at pupariation in Drosophila.

292 ed only one spook homolog in both Bombyx and Manduca that is expressed in both embryos and larva.

293 r known insect serotonin receptor types from Manduca (the Ms5HTRs).

294 In the developing larval leg of Manduca, the early patterning genes Distal-less and Extr

295 assay of neuronal migration in the hawkmoth Manduca to show that perturbations affecting APPL and Go

296 nsporters from these two latter species, the Manduca transporter is inhibited poorly by fluoxetine (I

297 n the central nervous system (CNS) of larval Manduca, we have mapped potential NO-producing neurons u

298 t immunohistochemical study of DA neurons in Manduca, we have provided the distribution pattern and m

299 tify three distinct classes of da neurons in Manduca, which we term the alpha, beta, and gamma classe

300 The identification of NSF ortholog from Manduca, whose neuroendocrine system is well studied, sh