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1 ard the lepidopteran predator Manduca sexta (tobacco hornworm).
2 ximately 72 and 49% identity to subunit F of tobacco hornworm and yeast, respectively.
3 ously identified in vacuolar proton pumps of tobacco hornworm and yeast, was present in mammalian pum
4 greenhouse experiments, we document that the tobacco hornworm caterpillar, Manduca sexta, reduced fee
5 was compromised in defense against attack by tobacco hornworm larvae.
6           The growth rates of Manduca sexta (tobacco hornworm) larvae feeding on tomato plants consti
7       A cDNA clone encoding a subunit of the tobacco hornworm Manduca sexta (Ms) hemolymph (serum) fe
8 re a 2.7 A crystal structure of JHE from the tobacco hornworm Manduca sexta (MsJHE) in complex with t
9 al structure of the JH esterase (JHE) of the tobacco hornworm Manduca sexta (MsJHE).
10  studied the pattern of cell division in the tobacco hornworm Manduca sexta and found that both the r
11 sing the enteric nervous system (ENS) of the tobacco hornworm Manduca sexta as a model system, we hav
12 -regulated in the abdominal epidermis of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20
13 a their isomeric composition: feeding of the tobacco hornworm Manduca sexta converts (Z)-3- to (E)-2-
14 NH2 (FLP15-2B), and to a lesser extent, by a tobacco hornworm Manduca sexta FaRP, GNSFLRFNH2 (F7G) (p
15  to appear in the abdominal epidermis of the tobacco hornworm Manduca sexta in a pattern-specific man
16 gh-throughput screening, using larvae of the tobacco hornworm Manduca sexta, combining diagnostic ima
17                                          The tobacco hornworm Manduca sexta, like many holometabolous
18                                       In the tobacco hornworm Manduca sexta, recombinant hemolymph pr
19  feeding preference assay was performed with tobacco hornworm Manduca sexta.
20 or localized in the midgut epithelium of the tobacco hornworm Manduca sexta.
21 isolated and sequenced from the brain of the tobacco hornworm Manduca sexta.
22 ring hormone, Mas-ETH, is described from the tobacco hornworm Manduca sexta.
23 utant was compromised in its defense against tobacco hornworm (Manduca sexta) attack.
24 Botrytis cinerea and to feeding by larvae of tobacco hornworm (Manduca sexta) but not to the bacteria
25 lation of engineered nanomaterials (ENMs) by tobacco hornworm (Manduca sexta) caterpillars resulting
26  When three herbivores were allowed to feed, tobacco hornworm (Manduca sexta) caterpillars, gained mo
27                     Cells were isolated from Tobacco hornworm (Manduca sexta) embryos and subsequentl
28        Using cryo-electron microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calcula
29                          Feeding assays with tobacco hornworm (Manduca sexta) larvae revealed the def
30 ccompanied by an increased resistance toward tobacco hornworm (Manduca sexta) larvae.
31  SP component (SPC) acquisition, we used the tobacco hornworm (Manduca sexta), which uses a blend of
32 ato DC3000, and larvae of the chewing insect tobacco hornworm (Manduca sexta).
33 n for Bt Cry1A toxins in midgut epithelia of tobacco hornworm (Manduca sexta).
34  of extractable protein were highly toxic to tobacco hornworm (Manduca sexta).
35 ding proteins in the larval epidermis of the tobacco hornworm (Manduca sexta).
36 unolocalization of a GABA transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affin
37 ning and hormonal regulation of E74 from the tobacco hornworm, Manduca sexta (MsE74).
38   The larger of two diuretic hormones of the tobacco hornworm, Manduca sexta, (Mas-DH) is a peptide o
39                    We have isolated from the tobacco hornworm, Manduca sexta, a cDNA encoding a modul
40       We have purified from hemolymph of the tobacco hornworm, Manduca sexta, a new serine proteinase
41                    We have isolated from the tobacco hornworm, Manduca sexta, a serine proteinase tha
42 ed for activation of moricin promoter in the tobacco hornworm, Manduca sexta, and a 140-bp region in
43  Drosophila melanogaster was cloned from the tobacco hornworm, Manduca sexta, and its developmental e
44  (this paper) and B1, were isolated from the tobacco hornworm, Manduca sexta, and shown to be similar
45 , diamondback moth, Plutella xylostella, and tobacco hornworm, Manduca sexta, as well as the spotted
46 an 20 serine proteinases in hemolymph of the tobacco hornworm, Manduca sexta, but functions are known
47                       Serpin gene-1 from the tobacco hornworm, Manduca sexta, encodes, through altern
48 s beginning with endocrine influences of the tobacco hornworm, Manduca sexta, host and its parasitoid
49 ted the cDNA that encodes three FaRPs in the tobacco hornworm, Manduca sexta, including the amidated
50                                       In the tobacco hornworm, Manduca sexta, pupal diapause can be i
51 eat, but in larger caterpillars, such as the tobacco hornworm, Manduca sexta, the movement is a defen
52 c and monophenic strains of the black mutant tobacco hornworm, Manduca sexta, were evolved via geneti
53      We have cloned a cDNA and gene from the tobacco hornworm, Manduca sexta, which is related to the
54 oad Complex (BRC) gene was isolated from the tobacco hornworm, Manduca sexta, which shows a predicted
55 imilar manner as previously reported for the tobacco hornworm, Manduca sexta.
56 new serpins (serpin-4 and serpin-5) from the tobacco hornworm, Manduca sexta.
57 solated an immune-responsive serpin from the tobacco hornworm, Manduca sexta.
58 hort isoforms (MsRel2A and MsRel2B) from the tobacco hornworm, Manduca sexta.
59 mmulectin-2, was isolated from plasma of the tobacco hornworm, Manduca sexta.
60  beta1,3-glucan-recognition protein from the tobacco hornworm, Manduca sexta.
61 ydroxyecdysone (20E) in the epidermis of the tobacco hornworm, Manduca sexta.
62 oidogenesis in the prothoracic glands of the tobacco hornworm, Manduca sexta.
63  cDNA phage display library derived from the tobacco hornworm moth Manduca sexta L. was constructed a
64                     In starved larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal
65 egmental muscles after adult eclosion in the tobacco hornworm moth, Manduca sexta.
66 ned from acid hydrolysates of Manduca sexta (tobacco hornworm) pupal cuticle exuviae and products obt
67 d truncated sGC proteins from Manduca sexta (tobacco hornworm) that bind NO, CO, and stimulatory comp
68 ssion system for sGC from Manduca sexta (the tobacco hornworm) that retains the N-terminal two-thirds