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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.
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
16 at recognize the core, Z2, and Z4 domains of Manduca BR-C proteins showed that BR-C appearance not on
18 d the formation of a second pupal cuticle in Manduca, but only in the abdomen of DROSOPHILA: Expressi
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
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.
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
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
44 d a number of chimeras between the human and Manduca serotonin transporters (hSERT and MasSERT, respe
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
51 a GABA transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affinity-purified antib
54 l structure of JHE from the tobacco hornworm Manduca sexta (MsJHE) in complex with the transition sta
57 loped a novel expression system for sGC from Manduca sexta (the tobacco hornworm) that retains the N-
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
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
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.
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
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
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
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
93 ponse gene RNA levels and protection against Manduca sexta damage were influenced by LapA RNA and pro
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
102 he N-linked glycans of aminopeptidase 1 from Manduca sexta have revealed unusual structures not previ
104 ct the regulation of direct defenses against Manduca sexta herbivory or P. syringae pv tomato DC3000
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.
114 on of neural precursors in the optic lobe of Manduca sexta is controlled by circulating steroids and
117 brary derived from the tobacco hornworm moth Manduca sexta L. was constructed and screened for protei
122 st proteins that accumulate in the midgut of Manduca sexta larvae reared on tomato (Solanum lycopersi
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
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
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
137 y and isolated overlapping lambda clones for Manduca sexta PAP-2, hemolymph proteinase 12 (HP12), and
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.
144 eric full-length and N-terminal fragments of Manduca sexta sGC in Escherichia coli, the first time th
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)
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
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
162 ctural immunocytochemistry of infected host (Manduca sexta) cuticle demonstrated that MeCPA participa
164 electron microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calculated the first 3D r
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
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
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,
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
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
198 abdominal body wall muscles in the hawkmoth, Manduca sexta, consist of large, elongated fibers that a
205 Serpin gene-1 from the tobacco hornworm, Manduca sexta, encodes, through alternative exon usage,
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.
214 starved larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal tissues stop growing,
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
220 ument that the tobacco hornworm caterpillar, Manduca sexta, reduced feeding by 30-40% owing to the ri
223 e cloned a 2.4-kb E3 cDNA from an arthropod, Manduca sexta, that codes for 497 amino acids and transl
226 the enteric nervous system (ENS) in the moth Manduca sexta, the migration of an identified set of neu
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
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
240 hanical energy exchange in flight muscles of Manduca sexta, we produced high-speed movies of x-ray eq
242 ically silenced and its hawkmoth pollinator, Manduca sexta, were used in semi-natural tent and wind-t
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
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
290 als, we have used antisera generated against Manduca-specific isoforms of the homophilic adhesion mol
292 ed only one spook homolog in both Bombyx and Manduca that is expressed in both embryos and larva.
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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