ライフサイエンスコーパス: Trichoplusia ni

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.

7 weight-gain assays with the cabbage looper (Trichoplusia ni), a generalist-chewing lepidopteran.

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

15 like aos, is susceptible to cabbage loopers (Trichoplusia ni) but, relative to aos, opr3 has enhanced

16 a cell line derived from the cabbage looper Trichoplusia ni, but not in IPLB-SF-21 (SF-21) cells, a

17 A Trichoplusia ni (cabbage looper) and a Helicoverpa zea (

18 wth of the generalist lepidopteran herbivore Trichoplusia ni (cabbage looper) and increased salt tole

19 The generalist insect herbivore Trichoplusia ni (cabbage looper) readily consumes Arabid

20 syringae, and herbivorous larvae of the moth Trichoplusia ni (cabbage looper) to characterize mechani

21 ic susceptibility to herbivory by an insect (Trichoplusia ni, cabbage looper), but this susceptibilit

22 rHuMig was purified from Trichoplusia ni cells after infection with a recombinant

23 Productive infection of Trichoplusia ni cells by the baculovirus Autographa cali

24 ranscription over the course of infection in Trichoplusia ni cells, by a combination of strand-specif

25 domain as a secreted glycosylated protein in Trichoplusia ni cells.

26 We found that cabbage loopers (Trichoplusia ni) display rhythmic feeding behavior that

27 o the Bt toxin Cry1Ac in the cabbage looper, Trichoplusia ni, evolved in greenhouses, is associated w

28 Substitution of granulin from the Trichoplusia ni granulosis virus (TnGV) for polyhedrin o

29 NPV E1 protein as well as the enhancins from Trichoplusia ni GV, Pseudaletia unipuncta GV, Helicoverp

30 c from the genome of the cabbage looper moth Trichoplusia ni has been observed in the laboratory to j

31 Both mutants were viable in Trichoplusia ni High 5 and Spodoptera frugiperda Sf9 cel

32 is study, (His)6-tagged Pgp was expressed in Trichoplusia ni (High Five) cells using the recombinant

33 of cultured Spodoptera frugiperda (Sf9) and Trichoplusia ni (High Five, BTN-TN-5B1-4) insect cells,

34 e, high levels of expression of each cDNA in Trichoplusia ni insect cells demonstrate that both CKbet

35 Trichoplusia ni insect cells were coinfected with a bacu

36 bit reticulocyte lysate, Escherichia coli or Trichoplusia ni insect cells.

37 y specialist (Manduca sexta) and generalist (Trichoplusia ni) insect herbivores triggered proteolytic

38 apsid AC141 associates with the lepidopteran Trichoplusia ni KLC and kinesin-1 heavy chain (KHC) by c

39 (AcMNPV), is critical for oral infection of Trichoplusia ni larvae.

40 al mucin (IIM), was recently identified from Trichoplusia ni larvae.

41 ere infectious to midgut epithelial cells of Trichoplusia ni larvae.

42 induced defense responses on cabbage looper (Trichoplusia ni) larval feeding.

43 mon pharmaceuticals on an agricultural pest, Trichoplusia ni (Lepidoptera: Noctuidae).

44 cid identity to the enhancin proteins of the Trichoplusia ni, Pseudaletia unipuncta, and Helicoverpa

45 Trichoplusia ni showed increased developmental time and

46 In this study, the fitness costs in Trichoplusia ni strains associated with two genetically

47 nd subsequent transfer to primary consumers, Trichoplusia ni (T. ni).

48 No signs of apoptosis were observed in Trichoplusia ni TN-368 cells transfected with ie-1, a re

49 These studies indicate that Trichoplusia ni TN-5B1-4 cells are capable of terminal g

50 of cells derived from other insect species, Trichoplusia ni (TN-368 and BTI-TN-5B1-4) and Helicoverp

51 of a heterologous murine IgG2a produced from Trichoplusia ni (TN-5B1-4, High Five) insect cells were

52 cadherin-like receptor from the insect pest Trichoplusia ni (TnCAD) that is not natively bound by wi

53 transposable element from the cabbage looper Trichoplusia ni was tested for gene transfer vector func

54 periments wherein newly molted fourth-instar Trichoplusia ni were challenged with doses of ODV-S or O

55 structure of a secreted insect ferritin from Trichoplusia ni, which reveals equal numbers of H and L