ライフサイエンスコーパス: prothoracic gland

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

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

3 ially express 3B11 represent the presumptive prothoracic glands.

4 hat a portion of the timing may occur in the 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 Instead, we find that innervation of the prothoracic gland by the PG neurons is absent in gt hypo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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