ライフサイエンスコーパス: prothoracic gland

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

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

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

4 ially express 3B11 represent the presumptive prothoracic glands.

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

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

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

8 The prothoracic glands are the predominate source of ecdyste

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

10 ary source of pupal ecdysone is not from the prothoracic gland but from dorsal internal oblique muscl

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

12 et Lgr3, which is expressed in the brain and prothoracic gland, by the disc epithelial barrier.

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

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

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

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

17 unctions by promoting the endoreplication of prothoracic gland cells, a process that increases ploidy

18 tioning revealed subcuticular, male-specific prothoracic glands connected to pits in the cuticle, whi

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

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

21 signals and cellular pathways that regulate prothoracic gland function are relatively well studied,

22 lysine demethylase 5 (KDM5) is essential for prothoracic gland function.

23 ndeed, restoring kdm5 expression only in the prothoracic gland in an otherwise kdm5 null mutant anima

24 In Drosophila, the larval prothoracic gland integrates nutritional status with dev

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

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

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

28 s due to impaired ecdysone production in the prothoracic gland, our data show that dre4 is required f

29 The prothoracic gland (PG) is a major insect endocrine organ

30 In insects, the prothoracic gland (PG) requires entry of extracellular i

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

32 brain and a peripheral clock located in the prothoracic gland (PG), an endocrine gland whose only kn

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

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

35 lock and the peripheral clock located in the prothoracic gland (PG), which together control the circa

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

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

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

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

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

41 ucial functions in the larval neuroendocrine prothoracic gland, providing a model to study its role i

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

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

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

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

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

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

48 This study demonstrated the utility of the prothoracic gland trait for predicting pheromone use in

49 e sterol biosynthesis Halloween genes in the prothoracic gland via its receptor Pvr.

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

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

52 Using fed and starved larvae that lack prothoracic glands, which synthesize ecdysone, we show t