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1 sicicola as well as the generalist herbivore Trichoplusia ni.
2 tructure of a full-length p97 homologue from Trichoplusia ni.
3 iated with the ability to deter herbivory by Trichoplusia ni.
4 creased resistance to the leaf-eating insect Trichoplusia ni.
5 ugiperda but not in a cell line derived from Trichoplusia ni.
6 was identified from a lepidopterous insect, Trichoplusia ni.
8 and desaturase from the cabbage looper moth, Trichoplusia ni, a species in which all unsaturated pher
9 velopmental disruption in the cabbage looper Trichoplusia ni, an important agricultural pest, at low
10 amely, High Five cells from the lepidopteran Trichoplusia ni and S2 cells from the dipteran Drosophil
11 ight gain of two Lepidoptera, the generalist Trichoplusia ni and the facultative Solanaceae-specialis
12 assembled a cell transcriptome from the host Trichoplusia ni and used that transcriptome to analyze c
13 e expressed human ST8Sia IV in insect cells, Trichoplusia ni, and found that the enzyme produced in t
14 erin-encoding genes (Hex) were isolated from Trichoplusia ni, and sequences necessary for, or affecti
16 iggyBac transposon, originally discovered in Trichoplusia ni as a 2472 bp functional element, that wa
17 f Spodoptera frugiperda ascovirus (SfAV) and Trichoplusia ni ascovirus (TnAV) at 7, 14, and 21 days p
18 like aos, is susceptible to cabbage loopers (Trichoplusia ni) but, relative to aos, opr3 has enhanced
19 a cell line derived from the cabbage looper Trichoplusia ni, but not in IPLB-SF-21 (SF-21) cells, a
21 wth of the generalist lepidopteran herbivore Trichoplusia ni (cabbage looper) and increased salt tole
23 syringae, and herbivorous larvae of the moth Trichoplusia ni (cabbage looper) to characterize mechani
24 ic susceptibility to herbivory by an insect (Trichoplusia ni, cabbage looper), but this susceptibilit
27 ranscription over the course of infection in Trichoplusia ni cells, by a combination of strand-specif
29 of ligands captured by MR1 produced in Hi5 (Trichoplusia ni) cells from Mycobacterium smegmatis via
32 o the Bt toxin Cry1Ac in the cabbage looper, Trichoplusia ni, evolved in greenhouses, is associated w
35 NPV E1 protein as well as the enhancins from Trichoplusia ni GV, Pseudaletia unipuncta GV, Helicoverp
36 c from the genome of the cabbage looper moth Trichoplusia ni has been observed in the laboratory to j
38 is study, (His)6-tagged Pgp was expressed in Trichoplusia ni (High Five) cells using the recombinant
39 of cultured Spodoptera frugiperda (Sf9) and Trichoplusia ni (High Five, BTN-TN-5B1-4) insect cells,
40 ) confers host resistance to the caterpillar Trichoplusia ni However, it is unclear whether CCA1 play
43 e, high levels of expression of each cDNA in Trichoplusia ni insect cells demonstrate that both CKbet
46 y specialist (Manduca sexta) and generalist (Trichoplusia ni) insect herbivores triggered proteolytic
47 apsid AC141 associates with the lepidopteran Trichoplusia ni KLC and kinesin-1 heavy chain (KHC) by c
51 rences between the enantiomers, we performed Trichoplusia ni larval choice assays and tested resistan
54 r larvae that were either highly permissive (Trichoplusia ni) or less susceptible (Spodoptera frugipe
55 cid identity to the enhancin proteins of the Trichoplusia ni, Pseudaletia unipuncta, and Helicoverpa
57 lants known to be hosts for the lepidopteran Trichoplusia ni (soybean, green bean, cotton, and cabbag
62 of cells derived from other insect species, Trichoplusia ni (TN-368 and BTI-TN-5B1-4) and Helicoverp
63 of a heterologous murine IgG2a produced from Trichoplusia ni (TN-5B1-4, High Five) insect cells were
64 cadherin-like receptor from the insect pest Trichoplusia ni (TnCAD) that is not natively bound by wi
66 transposable element from the cabbage looper Trichoplusia ni was tested for gene transfer vector func
67 periments wherein newly molted fourth-instar Trichoplusia ni were challenged with doses of ODV-S or O
68 structure of a secreted insect ferritin from Trichoplusia ni, which reveals equal numbers of H and L