ライフサイエンスコーパス: Manduca

1 on that has not previously been described in Manduca.

2 could be played by central olfactory glia in Manduca.

3 primarily expressed in the nervous system of Manduca.

4 similar to the six postembryonic lineages in Manduca.

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

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

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

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

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

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

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

20 cribe the anisotropic material properties of Manduca cuticle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 5 resulted in the total loss of toxicity for Manduca sexta and Heliothis virescens, another caused a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 71, affect insertion of the whole toxin into Manduca sexta brush border membrane vesicles (BBMVs).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 For Manduca sexta hawkmoths, how learning modifies foraging

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

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

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

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

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

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

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

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

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

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

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

113 Manduca sexta juvenile hormone diol kinase (JHDK) cataly

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

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

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

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

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

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

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

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

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

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

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

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

126 epithelium during growth and development of Manduca sexta larvae.

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

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

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

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

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

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

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

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

135 Manduca sexta PPO is a heterodimer consisting of 2 homol

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

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

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

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

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

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

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

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

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

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

146 ybridization and immunocytochemistry for the Manduca sexta sGCalpha1 subunit.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

183 During metamorphosis 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 In the moth Manduca sexta, glial reduction experiments have directly

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 he midgut epithelium of the tobacco hornworm Manduca sexta.

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

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

251 ws a corresponding reduction of virulence to 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 mmunoreactivity in the brain of the hawkmoth Manduca sexta.

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

256 Cry1A receptors from Heliothis virescens and Manduca sexta.

257 r for Bacillus thuringiensis Cry1A toxins in Manduca sexta.

258 ervate the terminal cardiac chamber of adult Manduca sexta.

259 responsive serpin from the tobacco hornworm, Manduca sexta.

260 l fractions of several alimentary tissues in Manduca sexta.

261 primary olfactory nerve pathway in the moth Manduca sexta.

262 ithelial membrane of Heliothis virescens and Manduca sexta.

263 gated the biological functions of hemolin in Manduca sexta.

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

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

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

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

268 ephila elpenor and the crepuscular-nocturnal Manduca sexta.

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

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

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

272 uring development of the olfactory system in Manduca sexta.

273 el2A and MsRel2B) from the tobacco hornworm, 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 (DA), in the antennal lobe (AL) of the moth Manduca sexta.

279 cdysteroids during metamorphosis of the moth Manduca sexta.

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

281 sional reconstruction of deactivated V1 from Manduca sexta.

282 rgic neuromodulation in the antennal lobe of Manduca sexta.

283 ce assay was performed with tobacco hornworm Manduca sexta.

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

285 ory serpins from Drosophila melanogaster and Manduca sexta.

286 reviously reported for 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