ライフサイエンスコーパス: tobacco hornworm

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 The tobacco hornworm Manduca sexta, like many holometabolous

17 In the tobacco hornworm Manduca sexta, recombinant hemolymph pr

18 or localized in the midgut epithelium of the tobacco hornworm Manduca sexta.

19 isolated and sequenced from the brain of the tobacco hornworm Manduca sexta.

20 ring hormone, Mas-ETH, is described from the tobacco hornworm Manduca sexta.

21 utant was compromised in its defense against tobacco hornworm (Manduca sexta) attack.

22 Botrytis cinerea and to feeding by larvae of tobacco hornworm (Manduca sexta) but not to the bacteria

23 lation of engineered nanomaterials (ENMs) by tobacco hornworm (Manduca sexta) caterpillars resulting

24 Using cryo-electron microscopy of the tobacco hornworm (Manduca sexta) enzyme, we have calcula

25 ccompanied by an increased resistance toward tobacco hornworm (Manduca sexta) larvae.

26 SP component (SPC) acquisition, we used the tobacco hornworm (Manduca sexta), which uses a blend of

27 n for Bt Cry1A toxins in midgut epithelia of tobacco hornworm (Manduca sexta).

28 of extractable protein were highly toxic to tobacco hornworm (Manduca sexta).

29 ding proteins in the larval epidermis of the tobacco hornworm (Manduca sexta).

30 ato DC3000, and larvae of the chewing insect tobacco hornworm (Manduca sexta).

31 unolocalization of a GABA transporter in the tobacco hornworm, Manduca sexta (MasGAT), using an affin

32 ning and hormonal regulation of E74 from the tobacco hornworm, Manduca sexta (MsE74).

33 The larger of two diuretic hormones of the tobacco hornworm, Manduca sexta, (Mas-DH) is a peptide o

34 We have isolated from the tobacco hornworm, Manduca sexta, a cDNA encoding a modul

35 We have purified from hemolymph of the tobacco hornworm, Manduca sexta, a new serine proteinase

36 We have isolated from the tobacco hornworm, Manduca sexta, a serine proteinase tha

37 ed for activation of moricin promoter in the tobacco hornworm, Manduca sexta, and a 140-bp region in

38 Drosophila melanogaster was cloned from the tobacco hornworm, Manduca sexta, and its developmental e

39 (this paper) and B1, were isolated from the tobacco hornworm, Manduca sexta, and shown to be similar

40 , diamondback moth, Plutella xylostella, and tobacco hornworm, Manduca sexta, as well as the spotted

41 an 20 serine proteinases in hemolymph of the tobacco hornworm, Manduca sexta, but functions are known

42 Serpin gene-1 from the tobacco hornworm, Manduca sexta, encodes, through altern

43 s beginning with endocrine influences of the tobacco hornworm, Manduca sexta, host and its parasitoid

44 ted the cDNA that encodes three FaRPs in the tobacco hornworm, Manduca sexta, including the amidated

45 In the tobacco hornworm, Manduca sexta, pupal diapause can be i

46 We have cloned a cDNA and gene from the tobacco hornworm, Manduca sexta, which is related to the

47 oad Complex (BRC) gene was isolated from the tobacco hornworm, Manduca sexta, which shows a predicted

48 imilar manner as previously reported for the tobacco hornworm, Manduca sexta.

49 hort isoforms (MsRel2A and MsRel2B) from the tobacco hornworm, Manduca sexta.

50 new serpins (serpin-4 and serpin-5) from the tobacco hornworm, Manduca sexta.

51 solated an immune-responsive serpin from the tobacco hornworm, Manduca sexta.

52 mmulectin-2, was isolated from plasma of the tobacco hornworm, Manduca sexta.

53 beta1,3-glucan-recognition protein from the tobacco hornworm, Manduca sexta.

54 ydroxyecdysone (20E) in the epidermis of the tobacco hornworm, Manduca sexta.

55 oidogenesis in the prothoracic glands of the tobacco hornworm, Manduca sexta.

56 cDNA phage display library derived from the tobacco hornworm moth Manduca sexta L. was constructed a

57 In starved larvae of the tobacco hornworm moth Manduca sexta, larval and imaginal

58 egmental muscles after adult eclosion in the tobacco hornworm moth, Manduca sexta.

59 ned from acid hydrolysates of Manduca sexta (tobacco hornworm) pupal cuticle exuviae and products obt

60 d truncated sGC proteins from Manduca sexta (tobacco hornworm) that bind NO, CO, and stimulatory comp

61 ssion system for sGC from Manduca sexta (the tobacco hornworm) that retains the N-terminal two-thirds