ライフサイエンスコーパス: seminal fluid

1 hat functions to produce a major fraction of seminal fluid.

2 r to those of native PSA isolated from human seminal fluid.

3 ing that spermatids can be activated by male seminal fluid.

4 in the mother's breast milk and the father's seminal fluid.

5 matozoa, presumably due to contact with male seminal fluid.

6 d rate of remating and increased toxicity of seminal fluid.

7 extracellular TRY-5 protease present in male seminal fluid.

8 d into prostatic fluid, a major component of seminal fluid.

9 ycoproteins from a secretory epithelium into seminal fluid.

10 man cervix in response to the male partner's seminal fluid.

11 ld not activate without the addition of male seminal fluid.

12 ly 80 small peptides transferred in the male seminal fluid.

13 f mice were challenged with HSV delivered in seminal fluid.

14 ced sperm mortality and/or the redundancy of seminal fluid.

15 proteins are a major component of Drosophila seminal fluid.

16 hat this requires neither incoming sperm nor seminal fluids.

17 ase (EVD) survivor who showed Ebola virus in seminal fluid 531 days after onset of disease.

18 Seminal fluid a2NTD levels were significantly correlated

19 Drosophila seminal fluid also contains a "sex peptide" (SP, Acp70A)

20 Seventy-six of 86 males requiring seminal fluid analysis as part of a separate study were

21 d the hypothesis that NlSPATA5 occurs in BPH seminal fluid and it operates in fecundity via mating.

22 , the successful oral transmission of HIV by seminal fluid and milk is unexplained.

23 Whether seminal fluid and milk successfully transmit HIV orally

24 osal surfaces [1], despite their presence in seminal fluid and mucosal secretions from infected indiv

25 id changes in sperm velocity are mediated by seminal fluid and the effect of seminal fluid on sperm v

26 eting males; both are usually transferred in seminal fluids and represent forms of chemical mate guar

27 ng sperm, (ii) direct displacement mainly by seminal fluid, and (iii) direct displacement mainly by s

28 and normal donor samples of milk, colostrum, seminal fluid, and blood were studied for their ability

29 body responses in the rectum, vagina, urine, seminal fluid, and blood.

30 scribe the diverse features and functions of seminal fluid, and its role in evolution and medicine.

31 detect hK2 protein in human prostate tissue, seminal fluid, and sera.

32 ytokine environment induced in the cervix by seminal fluid appears competent to initiate adaptations

33 The constituents of seminal fluid are a complex mixture of proteins and othe

34 , when spe-27 mutant male spermatids without seminal fluid are artificially inseminated into hermaphr

35 ynovium and synovial fluid, breast milk, and seminal fluid are universally CCR9(-).

36 processing; consistent with this hypothesis, seminal fluids are rich in proteolysis regulators.

37 of male survivors clear Ebola virus RNA from seminal fluid at 115 days (90% prediction interval 72-16

38 Participants provided samples of seminal fluid at follow-up every 3-6 weeks, which we tes

39 offspring of ablating the plasma fraction of seminal fluid by surgical excision of the seminal vesicl

40 capacitate females physically from receiving seminal fluids by a second male.

41 Across a diversity of animals, male seminal fluid coagulates upon ejaculation to form a hard

42 les during and after mating are triggered by seminal fluid components in conjunction with female-deri

43 To determine the role of seminal fluid components in mediating changes in attract

44 Functional redundancy between seminal fluid components may occur.

45 ses, the magnitude of responses due to other seminal fluid components, and whether SP accounts for th

46 r that sperm act as carriers for SP or other seminal fluid components.

47 These findings show that paternal seminal fluid composition affects the growth and health

48 rus are rendered temporarily unattractive by seminal fluids containing myristyl acetate and geranylge

49 In addition, the seminal fluid contains antibacterial peptides and protea

50 The seminal fluid conveyed with the sperm inhibits the procl

51 e to sperm damage and partly to an effect of seminal fluid deficiency on the female tract, because in

52 ted from five diverse sources (i.e., plasma, seminal fluid, dendritic cells, mast cells, and ovarian

53 Here we show that seminal fluids do not kill rival sperm and that any 'inc

54 Seminal fluid does more than transport sperm.

55 ide (SP), which is transferred with the male seminal fluid during insemination.

56 In mice, seminal fluid elicits an inflammation-like response in t

57 A component in seminal fluid elicits an ovulatory response and has been

58 Some seminal fluid-encoding genes also show high rates of evo

59 firmed reports of Zika virus (ZIKV) in human seminal fluid for months after the clearance of viremia

60 F-beta1 (P<0.01) levels when compared to the seminal fluid from fertile men.

61 with Drosophila melanogaster have shown that seminal fluid from the male accessory gland triggers a s

62 Infertile men's seminal fluid had significantly lower G-CSF (P<0.01), GM

63 lastic adjustment of ejaculate quality, that seminal fluid harbours the mechanism for the rapid adjus

64 In contrast to these benefits to males, seminal fluid has substantial toxic side effects in fema

65 Human seminal fluid (HSF) is a complex mixture of reacting gla

66 esponse, and related pathways are induced by seminal fluid in cervical tissues.

67 the physiological response of the cervix to seminal fluid in vivo.

68 Drosophila seminal fluid includes proteins that fall into biochemic

69 ribe the dynamics of Ebola virus RNA load in seminal fluid, including clearance parameters.

70 eins and peptides in Drosophila melanogaster seminal fluid induce mated females to increase their rat

71 , and subsequent life-span decrease, whereas seminal fluid induces DAF-16-dependent life-span decreas

72 We conclude that seminal fluid introduced at intercourse elicits expressi

73 of free prostate specific antigen from human seminal fluid is demonstrated in less than 5 min.

74 a predicted astacin-type metalloprotease in seminal fluid, is necessary to process two other seminal

75 suggest that TGF-beta in the male partner's seminal fluid may influence cervical immune function aft

76 sification, and maintenance of variation in, seminal fluid-mediated traits.

77 an ideal habitat for microbes or a potential seminal fluid microbiome (SFM).

78 that successful oral transmission of HIV by seminal fluid, milk, and colostrum may be due to their i

79 ster this stimulation is initially caused by seminal fluid molecules transferred from the male (Acps

80 mean clearance rate of Ebola virus RNA from seminal fluid of -0.58 log units per month, although the

81 swabs of 1 patient and up to 101 days in the seminal fluid of 4 patients.

82 n by mosquitoes, ZIKV can be detected in the seminal fluid of affected males for extended periods of

83 e 1 (HIV-1) virions in peripheral plasma and seminal fluid of infected men.

84 The seminal fluid of male Drosophila contains a cocktail of

85 e potential impacts of male PHF7, existed in seminal fluid of Nilaparvata lugens (NlPHF7), on fecundi

86 eriments using spermless males show that the seminal fluid of the conspecific male is largely respons

87 t a multi-functional peptide provided in the seminal fluid of their mates induces this behavior.

88 mediated by seminal fluid and the effect of seminal fluid on sperm velocity directly impacts paterni

89 analyse the dynamics of virus persistence in seminal fluid over time.

90 ickly lead to a change in the quality of the seminal fluid produced by a male Chinook salmon as he re

91 Seminal fluid profoundly influences cervical immune func

92 NAi to knock down individually 11 Drosophila seminal fluid proteases and protease inhibitors.

93 The Drosophila seminal fluid protein (SFP) sex peptide (SP) elicits num

94 Seminal fluid protein genes are expressed only in males,

95 as immunosuppressive [12, 13], and the male seminal fluid protein Sex Peptide (SP) activates JH bios

96 a melanogaster Acp29AB gene, which encodes a seminal fluid protein that is transferred from males to

97 Acp36DE is a male seminal fluid protein whose localization in mated female

98 One seminal-fluid protein, ovulin (Acp26Aa), stimulates an e

99 We report here that of eight Drosophila seminal fluid proteins (Acps) and one non-Acp tested, on

100 Several seminal fluid proteins (Acps) made in the Drosophila mal

101 anges are the direct result of the sperm and seminal fluid proteins (Acps) that females receive from

102 y of these changes are elicited by sperm and seminal fluid proteins (Acps) that males transfer to fem

103 Seminal fluid proteins (SFPs) are emerging as fundamenta

104 Seminal fluid proteins (SFPs) produced in reproductive t

105 of 19 previously unannotated genes encoding seminal fluid proteins (Sfps) that are transferred from

106 Male Seminal Fluid Proteins (SFPs) transferred during copulat

107 For example, in many insect species, male seminal fluid proteins (Sfps) transferred in a female's

108 components of the ejaculate [3, 4], such as seminal fluid proteins (Sfps).

109 In D. melanogaster, seminal fluid proteins affect female receptivity, ovulat

110 Drosophila melanogaster males transfer seminal fluid proteins along with sperm during mating.

111 nctional classes of mammalian and Drosophila seminal fluid proteins are conserved, despite difference

112 osophila melanogaster males deficient in the seminal fluid proteins derived from the accessory gland

113 g changes in female insects are triggered by seminal fluid proteins from the male's accessory gland p

114 hat encode putative accessory gland-specific seminal fluid proteins had a significantly elevated leve

115 ection results in more adaptive evolution of seminal fluid proteins in the repleta group flies.

116 Cross-species transfer of sperm and active seminal fluid proteins including HP-I may contribute to

117 Research on seminal fluid proteins is providing fundamental insights

118 Some seminal fluid proteins may provide protective functions

119 We found that specific seminal fluid proteins or female secretions mediate some

120 melanogaster, mating and the receipt of male seminal fluid proteins results in reduced resistance to

121 semen by virtue of its ability to cleave the seminal fluid proteins semenogelins I and II.

122 Drosophila melanogaster seminal fluid proteins stimulate sperm storage and egg l

123 during and after mating, including sperm and seminal fluid proteins.

124 and transferred normal amounts of sperm and seminal fluid proteins.

125 are novel associations with uncharacterized seminal fluid proteins.

126 petitive proteins considered to be candidate seminal fluid proteins; proteins encoded by one of these

127 with Drosophila melanogaster indicating that seminal fluid reduces the competitive ability of sperm f

128 In Drosophila melanogaster, seminal fluid regulates the reproductive and immune resp

129 Infectious virus was detected in 1 seminal fluid sample obtained 82 days after disease onse

130 rs formed from a peptide ubiquitous in human seminal fluid (semen-derived enhancer of viral infection

131 Injection of the seminal fluid sex peptide (SP) induces both responses in

132 resenting a new genotype was isolated from a seminal fluid specimen.

133 We enrolled 26 participants and tested 130 seminal fluid specimens; median follow up was 197 days (

134 ating behavior and the transfer of sperm and seminal fluid (SSFT) provide a model for understanding h

135 le, and sperm incapacitation, where incoming seminal fluids supposedly interfere with resident sperm,

136 agment (PAP(248-286)) has been isolated from seminal fluid that dramatically enhances HIV infectivity

137 The seminal fluid that is transferred along with sperm durin

138 During mating, males provide females with seminal fluids that include proteins affecting female ph

139 ale reproductive glands secrete signals into seminal fluid to facilitate reproductive success.

140 gland proteins ("Acps," a major component of seminal fluid) transferred by males during mating trigge

141 10 d, viral RNA was detectable in saliva and seminal fluids until the end of the study, 3 weeks after

142 IgG, has been detected in the genital tract, seminal fluid, urethral swabs, urine, and vaginal wash s

143 cles (prostasomes) that can be isolated from seminal fluid, urine, and blood.

144 N: Time to clearance of Ebola virus RNA from seminal fluid varies greatly between individuals and cou

145 Male Anopheles mosquitoes coagulate their seminal fluids via cross-linking of a substrate, called

146 and secreted chemokine-cytokine profiles in seminal fluid were measured.

147 Seminal fluid, which affects female reproductive tract g

148 Such effects could be due to the seminal fluid, which is slightly basic and enriched with

149 his obstacle, while another study reports on seminal fluid with very specific spermicidal activity, s