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1 omposition that is expressed from the female accessory gland.
2 produced in the Drosophila melanogaster male accessory gland.
3 ne sets along with those associated with the accessory glands.
4  projection neurons (PNs) that innervate the accessory glands.
5 s, and larvae, as well as in male and female accessory glands.
6 novel genes are expressed in Heliconius male accessory glands.
7 ounds did not parallel stimulation of sexual accessory glands.
8 tors--usually peptides--secreted by the male accessory glands.
9 ty in other tissues such as the reproductive accessory glands.
10                     Males selected for large accessory glands (a major site of Sfp synthesis) produce
11 nd is controlled by the products of the male accessory glands, a family of approximately 80 small pep
12  the seminal fluid proteins derived from the accessory gland (Acps) to investigate the role of these
13 es of proteins normally produced by the male accessory gland (Acps).
14          It is secreted from the paired male accessory glands (AGs), which, like the mammalian prosta
15 ty of seminal peptides, many produced by the accessory glands (AGs).
16                             Males with large accessory glands also had significantly increased compet
17 velopmental stages and derived from both the accessory gland and other female organs.
18 he mosquito midgut, female ovaries, and male accessory glands and spreads rapidly throughout mosquito
19                      We found that both male accessory glands and testes contribute to its formation.
20 steroid hormone that is produced by the male accessory glands and transferred during copulation, and
21          Morphological changes of gonads and accessory glands attributed to androgen effects, such as
22 duces production of storage proteins and key accessory gland components, a feature that impacts adult
23 tringent criteria for encoding putative male accessory gland extracellular proteins, thus bringing th
24 in the size of mating plugs and reproductive accessory glands from which major plug proteins originat
25 that of the D-protein gene, three Drosophila accessory gland genes and two Drosophila 20-OH ecdysone-
26 e predict that approximately 90% of the male accessory gland genes have been identified.
27                              With the 57 new accessory gland genes reported here, we predict that app
28 s (Accessory gland proteins) from the male's accessory gland induce behavioral, physiological, and li
29 , permitting more rapid replenishment of the accessory gland luminal contents.
30 n regulate growth and maturation of the male accessory gland (MAG) in the red flour beetle, Tribolium
31 in the squamous epithelium of the adult male accessory gland (MAG) up-regulates PI3K/Akt/TOR signalin
32  mating or treatment with extracts from male accessory glands (MAG), which make seminal fluid molecul
33 ighest Dopa levels present in mfp-1 from the accessory gland near the tip of the foot decreasing grad
34 ant cell type of the seminal fluid-producing accessory gland of Drosophila melanogaster, we detected
35  compare the sequences of ESTs from the male accessory gland of Drosophila simulans to their ortholog
36 expressed sequence tags (ESTs) from the male accessory gland of H. erato and H. melpomene, species re
37 nvolved in 13 lesions; 2 lesions arose in an accessory gland of Krause.
38                 Among the genes expressed in accessory glands of D. mayaguana almost half are likely
39                              The paired male accessory glands of Drosophila melanogaster enhance sper
40 those of the D-protein gene expressed in the accessory glands of Tenebrio reveals similar sequences p
41 ntharidin is stored by the male in the large accessory glands of the reproductive system.
42                                     The male accessory glands produce a small number of abundant nove
43 n nature and the sterilizing effects of male accessory gland products asymmetrically favoring A. albo
44 expression of NlSPATA5 led to decreased male accessory gland protein content and reproductive system
45 NAi led to decreases in body weight, soluble accessory gland protein content, arginine content, and r
46                    We previously showed that accessory gland protein genes (Acp's) of Drosophila moja
47 s focused primarily on melanogaster subgroup accessory gland protein genes (Acp's).
48          We also report the transfer of male accessory-gland protein (Acp) transcripts from males to
49        In Drosophila melanogaster, sperm and accessory gland proteins ("Acps," a major component of s
50 genes encoding seminal proteins, also called accessory gland proteins (Acp's), we conducted a sequenc
51 ositive selection in the genes encoding five accessory gland proteins (Acps) (Acp26Aa, Acp32CD, Acp53
52  , a cost that is mediated by male ejaculate accessory gland proteins (Acps) .
53 ed by seminal fluid proteins from the male's accessory gland proteins (Acps) and by sperm.
54                                          The accessory gland proteins (Acps) of Drosophila have becom
55 s of known protein structures with predicted accessory gland proteins (Acps) revealed similarities un
56                                          The accessory gland proteins (Acps) that male Drosophila mel
57  approximately 90% of the predicted secreted accessory gland proteins (Acps).
58 rate and lower remating propensity, but that accessory gland proteins also increase female death rate
59 val males and adult testes, but they are not accessory gland proteins and their loss does not affect
60                                              Accessory gland proteins are a major component of Drosop
61 in the transfer and subsequent processing of accessory gland proteins by females nor to the presence
62       The extreme rates of evolution seen in accessory gland proteins may be driven by sperm competit
63                                 Male-derived accessory gland proteins that are transferred to females
64                  Among these proteins, ACPs (Accessory gland proteins) from the male's accessory glan
65 , and (3) the transfer and processing of two accessory gland proteins, Acp26Aa or Acp36De.
66 molecules transferred from the male (Acps or accessory gland proteins; reviewed in [1] [2] [3]).
67  have associated it with allelic variants of accessory-gland proteins.
68             We previously showed that in fly accessory glands, secondary cells (SCs) and their nuclei
69 state and the paired Drosophila melanogaster accessory glands secrete seminal fluid components that e
70                         Conversely, a set of accessory gland-specific genes and mitochondrial genes w
71                   Genes that encode putative accessory gland-specific seminal fluid proteins had a si
72 ogaster, seminal proteins made in the male's accessory gland stimulate females' egg production and ov
73 l of these processes and is required for the accessory gland to produce its normal effects on female
74  have shown that seminal fluid from the male accessory gland triggers a series of postmating response
75              In both species only a third of accessory gland unigenes were also found among genes exp
76 clusively in the secondary cells of the male accessory gland, where it seems to accumulate in nuclei.
77  melanogaster, most SFPs are produced in the accessory glands, which are composed of ~1,000 fertility