ライフサイエンスコーパス: accessory gland

1 produced in the Drosophila melanogaster male accessory gland.

2 projection neurons (PNs) that innervate the accessory glands.

3 novel genes are expressed in Heliconius male accessory glands.

4 ounds did not parallel stimulation of sexual accessory glands.

5 tors--usually peptides--secreted by the male accessory glands.

6 Males selected for large accessory glands (a major site of Sfp synthesis) produce

7 nd is controlled by the products of the male accessory glands, a family of approximately 80 small pep

8 the seminal fluid proteins derived from the accessory gland (Acps) to investigate the role of these

9 es of proteins normally produced by the male accessory gland (Acps).

10 ty of seminal peptides, many produced by the accessory glands (AGs).

11 Males with large accessory glands also had significantly increased compet

12 he mosquito midgut, female ovaries, and male accessory glands and spreads rapidly throughout mosquito

13 We found that both male accessory glands and testes contribute to its formation.

14 steroid hormone that is produced by the male accessory glands and transferred during copulation, and

15 Morphological changes of gonads and accessory glands attributed to androgen effects, such as

16 tringent criteria for encoding putative male accessory gland extracellular proteins, thus bringing th

17 that of the D-protein gene, three Drosophila accessory gland genes and two Drosophila 20-OH ecdysone-

18 e predict that approximately 90% of the male accessory gland genes have been identified.

19 With the 57 new accessory gland genes reported here, we predict that app

20 s (Accessory gland proteins) from the male's accessory gland induce behavioral, physiological, and li

21 n regulate growth and maturation of the male accessory gland (MAG) in the red flour beetle, Tribolium

22 ighest Dopa levels present in mfp-1 from the accessory gland near the tip of the foot decreasing grad

23 compare the sequences of ESTs from the male accessory gland of Drosophila simulans to their ortholog

24 expressed sequence tags (ESTs) from the male accessory gland of H. erato and H. melpomene, species re

25 nvolved in 13 lesions; 2 lesions arose in an accessory gland of Krause.

26 Among the genes expressed in accessory glands of D. mayaguana almost half are likely

27 The paired male accessory glands of Drosophila melanogaster enhance sper

28 those of the D-protein gene expressed in the accessory glands of Tenebrio reveals similar sequences p

29 ntharidin is stored by the male in the large accessory glands of the reproductive system.

30 The male accessory glands produce a small number of abundant nove

31 n nature and the sterilizing effects of male accessory gland products asymmetrically favoring A. albo

32 expression of NlSPATA5 led to decreased male accessory gland protein content and reproductive system

33 NAi led to decreases in body weight, soluble accessory gland protein content, arginine content, and r

34 We previously showed that accessory gland protein genes (Acp's) of Drosophila moja

35 s focused primarily on melanogaster subgroup accessory gland protein genes (Acp's).

36 We also report the transfer of male accessory-gland protein (Acp) transcripts from males to

37 In Drosophila melanogaster, sperm and accessory gland proteins ("Acps," a major component of s

38 genes encoding seminal proteins, also called accessory gland proteins (Acp's), we conducted a sequenc

39 ositive selection in the genes encoding five accessory gland proteins (Acps) (Acp26Aa, Acp32CD, Acp53

40 , a cost that is mediated by male ejaculate accessory gland proteins (Acps) .

41 ed by seminal fluid proteins from the male's accessory gland proteins (Acps) and by sperm.

42 The accessory gland proteins (Acps) of Drosophila have becom

43 s of known protein structures with predicted accessory gland proteins (Acps) revealed similarities un

44 The accessory gland proteins (Acps) that male Drosophila mel

45 approximately 90% of the predicted secreted accessory gland proteins (Acps).

46 rate and lower remating propensity, but that accessory gland proteins also increase female death rate

47 val males and adult testes, but they are not accessory gland proteins and their loss does not affect

48 Accessory gland proteins are a major component of Drosop

49 in the transfer and subsequent processing of accessory gland proteins by females nor to the presence

50 The extreme rates of evolution seen in accessory gland proteins may be driven by sperm competit

51 Male-derived accessory gland proteins that are transferred to females

52 Among these proteins, ACPs (Accessory gland proteins) from the male's accessory glan

53 , and (3) the transfer and processing of two accessory gland proteins, Acp26Aa or Acp36De.

54 molecules transferred from the male (Acps or accessory gland proteins; reviewed in [1] [2] [3]).

55 have associated it with allelic variants of accessory-gland proteins.

56 Conversely, a set of accessory gland-specific genes and mitochondrial genes w

57 Genes that encode putative accessory gland-specific seminal fluid proteins had a si

58 ogaster, seminal proteins made in the male's accessory gland stimulate females' egg production and ov

59 l of these processes and is required for the accessory gland to produce its normal effects on female

60 have shown that seminal fluid from the male accessory gland triggers a series of postmating response

61 In both species only a third of accessory gland unigenes were also found among genes exp