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1 lepidopteran predator Manduca sexta (tobacco hornworm).
2  72 and 49% identity to subunit F of tobacco hornworm and yeast, respectively.
3 entified in vacuolar proton pumps of tobacco hornworm and yeast, was present in mammalian pumps.
4 n results in movement similar to that of the hornworm by patterned cell culture method.
5 se experiments, we document that the tobacco hornworm caterpillar, Manduca sexta, reduced feeding by
6                   Our findings indicate that hornworm caterpillars use temporally dynamic compensator
7 F = 0.16) compared to a previous study where hornworm caterpillars were fed plants that had previousl
8 urface chemistry and regional differences in hornworm gut chemistry.
9 n of accumulated Au ENMs not associated with hornworm gut contents; and (4) regional differences in t
10 tion of Au ENMs into tissues surrounding the hornworm gut, possibly the result of the interaction bet
11                                              Hornworm larvae raised on IE plants exhibited stunted gr
12 romised in defense against attack by tobacco hornworm larvae.
13   The growth rates of Manduca sexta (tobacco hornworm) larvae feeding on tomato plants constitutively
14 cDNA clone encoding a subunit of the tobacco hornworm Manduca sexta (Ms) hemolymph (serum) ferritin (
15  A crystal structure of JHE from the tobacco hornworm Manduca sexta (MsJHE) in complex with the trans
16 ture of the JH esterase (JHE) of the tobacco hornworm Manduca sexta (MsJHE).
17  the pattern of cell division in the tobacco hornworm Manduca sexta and found that both the rate of c
18  enteric nervous system (ENS) of the tobacco hornworm Manduca sexta as a model system, we have explor
19 ed in the abdominal epidermis of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20E) durin
20 isomeric composition: feeding of the tobacco hornworm Manduca sexta converts (Z)-3- to (E)-2-GLVs the
21 15-2B), and to a lesser extent, by a tobacco hornworm Manduca sexta FaRP, GNSFLRFNH2 (F7G) (potency r
22 ar in the abdominal epidermis of the tobacco hornworm Manduca sexta in a pattern-specific manner as t
23 ghput screening, using larvae of the tobacco hornworm Manduca sexta, combining diagnostic imaging mod
24                                  The tobacco hornworm Manduca sexta, like many holometabolous insects
25                               In the tobacco hornworm Manduca sexta, recombinant hemolymph proteinase
26  preference assay was performed with tobacco hornworm Manduca sexta.
27 ized in the midgut epithelium of the tobacco hornworm Manduca sexta.
28  and sequenced from the brain of the tobacco hornworm Manduca sexta.
29 mone, Mas-ETH, is described from the tobacco hornworm Manduca sexta.
30 s compromised in its defense against tobacco hornworm (Manduca sexta) attack.
31  cinerea and to feeding by larvae of tobacco hornworm (Manduca sexta) but not to the bacterial pathog
32 f engineered nanomaterials (ENMs) by tobacco hornworm (Manduca sexta) caterpillars resulting from the
33 ree herbivores were allowed to feed, tobacco hornworm (Manduca sexta) caterpillars, gained more mass
34             Cells were isolated from Tobacco hornworm (Manduca sexta) embryos and subsequently adapte
35 sing cryo-electron microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calculated the
36                  Feeding assays with tobacco hornworm (Manduca sexta) larvae revealed the defensive f
37 ed by an increased resistance toward tobacco hornworm (Manduca sexta) larvae.
38 onent (SPC) acquisition, we used the tobacco hornworm (Manduca sexta), which uses a blend of mono-, d
39 00, and larvae of the chewing insect tobacco hornworm (Manduca sexta).
40  Cry1A toxins in midgut epithelia of tobacco hornworm (Manduca sexta).
41 actable protein were highly toxic to tobacco hornworm (Manduca sexta).
42 teins in the larval epidermis of the tobacco hornworm (Manduca sexta).
43 ization of a GABA transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affinity-puri
44  hormonal regulation of E74 from the tobacco hornworm, Manduca sexta (MsE74).
45 rger of two diuretic hormones of the tobacco hornworm, Manduca sexta, (Mas-DH) is a peptide of 41 res
46            We have isolated from the tobacco hornworm, Manduca sexta, a cDNA encoding a modular prote
47  have purified from hemolymph of the tobacco hornworm, Manduca sexta, a new serine proteinase that cl
48            We have isolated from the tobacco hornworm, Manduca sexta, a serine proteinase that activa
49 ctivation of moricin promoter in the tobacco hornworm, Manduca sexta, and a 140-bp region in the mori
50 ila melanogaster was cloned from the tobacco hornworm, Manduca sexta, and its developmental expressio
51 aper) and B1, were isolated from the tobacco hornworm, Manduca sexta, and shown to be similar to the
52                         This is noted in the hornworm, Manduca sexta, as a defensive strike response.
53 dback moth, Plutella xylostella, and tobacco hornworm, Manduca sexta, as well as the spotted wing dro
54 rine proteinases in hemolymph of the tobacco hornworm, Manduca sexta, but functions are known for onl
55               Serpin gene-1 from the tobacco hornworm, Manduca sexta, encodes, through alternative ex
56 ing with endocrine influences of the tobacco hornworm, Manduca sexta, host and its parasitoid wasp Ap
57 cDNA that encodes three FaRPs in the tobacco hornworm, Manduca sexta, including the amidated decapept
58                               In the tobacco hornworm, Manduca sexta, pupal diapause can be induced b
59  in larger caterpillars, such as the tobacco hornworm, Manduca sexta, the movement is a defensive str
60 nophenic strains of the black mutant tobacco hornworm, Manduca sexta, were evolved via genetic accomm
61 have cloned a cDNA and gene from the tobacco hornworm, Manduca sexta, which is related to the vertebr
62 lex (BRC) gene was isolated from the tobacco hornworm, Manduca sexta, which shows a predicted 88% ami
63 anner as previously reported for the tobacco hornworm, Manduca sexta.
64 ins (serpin-4 and serpin-5) from the tobacco hornworm, Manduca sexta.
65 an immune-responsive serpin from the tobacco hornworm, Manduca sexta.
66 forms (MsRel2A and MsRel2B) from the tobacco hornworm, Manduca sexta.
67 n-2, was isolated from plasma of the tobacco hornworm, Manduca sexta.
68 -glucan-recognition protein from the tobacco hornworm, Manduca sexta.
69 dysone (20E) in the epidermis of the tobacco hornworm, Manduca sexta.
70 sis in the prothoracic glands of the tobacco hornworm, Manduca sexta.
71 age display library derived from the tobacco hornworm moth Manduca sexta L. was constructed and scree
72             In starved larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal tissues
73  muscles after adult eclosion in the tobacco hornworm moth, Manduca sexta.
74  acid hydrolysates of Manduca sexta (tobacco hornworm) pupal cuticle exuviae and products obtained fr
75 ted sGC proteins from Manduca sexta (tobacco hornworm) that bind NO, CO, and stimulatory compound YC-
76 stem for sGC from Manduca sexta (the tobacco hornworm) that retains the N-terminal two-thirds of both