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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

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