ライフサイエンスコーパス: prothoracic

1 us marmoratus, ejects a milky fluid from its prothoracic defensive glands when disturbed.

2 Surprisingly, the dorsal prothoracic expression of Scr is also present in the pri

3 nterneuron PTG-DC, with the cell body in the prothoracic ganglion (PTG) and a contralaterally descend

4 d two axons that ascend bilaterally into the prothoracic ganglion.

5 ons: one in the mesothoracic and four in the prothoracic ganglion.

6 t from the brain, subesophageal ganglion, or prothoracic ganglion.

7 from the brain, subesophageal ganglion, and prothoracic ganglion.

8 We establish that the prothoracic gland (PG), a tissue required for fly develo

9 rvae, torso is expressed specifically in the prothoracic gland (PG), and its loss phenocopies the rem

10 osophila, a component of the ring gland, the prothoracic gland (PG), assesses growth to determine whe

11 of steroid molting hormone ecdysone from the prothoracic gland (PG).

12 t of insects, ecdysone is synthesized in the prothoracic gland (PG).

13 has multiple target tissues as follows: the prothoracic gland and aorta in the larva and the crop an

14 t tissues, dib expression is observed in the prothoracic gland and follicle cells of the ovaries resp

15 or in this tissue, Tsl also localizes to the prothoracic gland and influences developmental timing.

16 Tor has a second function in the prothoracic gland as the receptor for prothoracicotropic

17 Instead, we find that innervation of the prothoracic gland by the PG neurons is absent in gt hypo

18 genesis, S6 cDNA was isolated from a Manduca prothoracic gland cDNA library and sequenced.

19 idogenesis (downregulation); and (c) how the prothoracic gland cells convert cholesterol to the precu

20 ression of both genes is concentrated in the prothoracic gland cells of the developing ring gland.

21 ed primarily during larval stages within the prothoracic gland cells of the ring gland.

22 ved rhythms of period gene expression in the prothoracic gland for 4-7 days.

23 vity of the insulin-signaling pathway in the prothoracic gland of Drosophila modulates ecdysone relea

24 ircadian culture system from Drosophila, the prothoracic gland provides unique advantages for investi

25 on of calcium signaling in the steroidogenic prothoracic gland results in the accumulation of unrelea

26 revealed that the phosphorylation of Manduca prothoracic gland S6 is limited exclusively to serine re

27 ons of 20E in the hemolymph feed back on the prothoracic gland to decrease rates of ecdysteroidogenes

28 ctivin signaling regulates competence of the prothoracic gland to receive PTTH and insulin signals, a

29 In the differentiated prothoracic gland, expression of 3B11 is restricted to s

30 in signaling, specifically in the Drosophila prothoracic gland, results in developmental arrest prior

31 steroid hormone 20-hydroxyecdysone from the prothoracic gland, the primary endocrine organ of juveni

32 iates a transductory cascade in cells of the prothoracic gland, which results in an increased rate of

33 activity of target of rapamycin (TOR) in the prothoracic gland.

34 least in part, via ecdysone synthesis in the prothoracic gland.

35 pends on the insulin-dependent growth of the prothoracic glands (PGs) in Drosophila larvae.

36 )/Target of Rapamycin (TOR) signaling in the prothoracic glands (PGs) regulates ecdysone biosynthesis

37 The prothoracic glands are the predominate source of ecdyste

38 in vitro secretion of ecdysteroids from the prothoracic glands of last instar larvae of Spodoptera l

39 is and subsequent ecdysteroidogenesis in the prothoracic glands of the tobacco hornworm, Manduca sext

40 version of ecdysone and 3-dehydroecdysone by prothoracic glands was not detectable.

41 ially express 3B11 represent the presumptive prothoracic glands.

42 hat a portion of the timing may occur in the prothoracic glands.

43 hich Tsh, in concert with Scr, specifies the prothoracic identity.

44 In the absence of hedgehog activity, prothoracic leg disc fragments fail to undergo anterior/

45 Prothoracic leg disc fragments possess exceptional regul

46 were used to describe the remodeling of the prothoracic leg sensory system.

47 ir morphology, only the fate map for the T1 (prothoracic) leg disc has been generated.

48 f the femoral chordotonal organ (FCO) in the prothoracic legs.

49 er, Scr expression at the dorsal base of the prothoracic limb in two other winged insects, crickets (

50 europteran exocrine gland systems, including prothoracic, metathoracic, abdominal, dermal, and anal g

51 e larva is differentially localized at adult prothoracic NMJs; and 4) while all type I terminals cont

52 ly gives way to restricted expression in the prothoracic portion of the ring gland.

53 ion of the steroid hormone ecdysone from the prothoracic ring gland coordinates and triggers events s

54 originates from the posterior region of the prothoracic segment.

55 localized in contact chemosensory neurons in prothoracic tarsi and in sensory neurons and accessory c

56 ed, results in an ectopic T1 flap similar to prothoracic winglets present in fossil hemipteroids and

57 onsistent with Scr acting as a suppressor of prothoracic wings in these insects.