ライフサイエンスコーパス: seminal plasma

1 albumin, another protein purified from human seminal plasma.

2 emoved inhibitory factors sometimes found in seminal plasma.

3 translational modifications (PTMs) in bovine seminal plasma.

4 ar to the inhibition previously described in seminal plasma.

5 immunodeficiency virus type 1 (HIV-1) RNA in seminal plasma.

6 as by a partially purified protease(s) from seminal plasma.

7 P94), another major protein component in the seminal plasma.

8 ctive role of spermine, a major component of seminal plasma.

9 utathione peroxidase [GPx]) were measured in seminal plasma.

10 talization, and viral diversity in blood and seminal plasma.

11 s for the quantitation of HIV RNA in CSF and seminal plasma.

12 in part, enhancement of bacterial growth by seminal plasma.

13 ivation status did not change in response to seminal plasma.

14 is acquired as the result of exposure to the seminal plasma.

15 ction persisted when HSV-2 was introduced in seminal plasma.

16 had at least 1 herpesvirus detected in their seminal plasma.

17 ed by real-time polymerase chain reaction in seminal plasma.

18 entage can be significantly suppressed under seminal plasma.

19 ng principal aspects of the Ect1 response to seminal plasma.

20 s simplex virus type 2 (HSV-2) introduced in seminal plasma.

21 plasma lipid levels, and HIV-1 RNA levels in seminal plasma.

22 in blood plasma (4.24 log(10) copies/mL) or seminal plasma (3.55 log(10) copies/mL; P<.05, each comp

23 idespread detection of organic pollutants in seminal plasma across all exposure classes.

24 IV-1 infection and inhibition in whole human seminal plasma and a synthetic simulant that we formulat

25 Median seminal plasma and blood plasma HIV-1 RNA concentrations

26 und DOR concentrations were observed in both seminal plasma and cervicovaginal fluid.

27 in these assays are typically purified from seminal plasma and contain many molecular forms (intact

28 quenced such a nuclease isolated from bovine seminal plasma and identified human, rat and mouse homol

29 CRISP3 is an abundant protein of the human seminal plasma and interacts with alpha-1-B glycoprotein

30 CRISP3 is an abundant protein of the human seminal plasma and interacts with prostate secretory pro

31 However, the unstable nature of human seminal plasma and its toxic effects on cells in culture

32 histopathological variables, sperm quality, seminal plasma and plasma oxidative stress, seminal plas

33 Elevated levels of cytokines in the seminal plasma and prostatic secretions have been detect

34 nd lamivudine achieve high concentrations in seminal plasma and significantly reduce HIV-1 RNA.

35 Understanding of the impacts of seminal plasma and sperm proteins on both animal and hum

36 udy, we characterized for the first time the seminal plasma and sperm proteomes of the critically end

37 e to the immunosuppressive activity of human seminal plasma and to the low immunogenicity of sperm.

38 od plasma were compared to those detected in seminal plasma and/or cerebral spinal fluid of six indiv

39 pathways including blood clotting cascades (seminal plasma) and both actin dynamics and immune pathw

40 a1, TGF-beta2, and TGF-beta3 are abundant in seminal plasma, and Affymetrix microarray revealed that

41 ebrospinal fluid (CSF), saliva, breast milk, seminal plasma, and cervical-vaginal lavage fluid (CVL).

42 ample to remove white blood cells, wash away seminal plasma, and reduce sample volume.

43 le removing white blood cells, replacing the seminal plasma, and reducing the volume of the sample to

44 LOC609402 and LOC100685620 (AGP) proteins in seminal plasma, and significantly reduced expression of

45 We detected VEGF-C in seminal plasma, and sperm liquefaction occurred concurre

46 253 (5%) cervicovaginal lavages, 20/322 (6%) seminal plasmas, and 6/85 (7%) rectal secretions.

47 ociated with higher HIV-1 loads in blood and seminal plasma; and (5) CMV seminal reactivation increas

48 Infection and inhibition in whole human seminal plasma are accurately mimicked by a stable synth

49 that they retain activity in the presence of seminal plasma are indicated.

50 synthases and secreted by the prostate into seminal plasma are thought to support reproduction, but

51 of differentially expressed proteins in the seminal plasma as diagnostic biomarker for primary and s

52 BPSA purified from prostate tissue and seminal plasma, as well as BPSA generated in vitro by mi

53 ecimens can be used as external controls for seminal plasma assays.

54 However, 8 men (27%) had measurable HIV-1 in seminal plasma at their last study visit, 4 with increas

55 Most men (77%) had HIV-1 RNA levels in seminal plasma below the limit of quantification during

56 ived from either NPD or LPD sperm (devoid of seminal plasma) but in the presence of NPD or LPD semina

57 A fraction isolated from llama seminal plasma by column chromatography was identified a

58 Quantitation of HIV-1 RNA in seminal plasma can be reliably accomplished using two co

59 In multivariate analysis, the presence of seminal plasma CMV (P = 0.04), detectable 2-long termina

60 The seminal plasma compartment was more dynamic than the blo

61 h an eightfold increase in virus load in the seminal plasma compartment.

62 ee viral populations in the blood plasma and seminal plasma compartments of men infected with subtype

63 Seminal plasma competitively inhibited binding of the mi

64 Median lamivudine blood and seminal plasma concentrations were 391.3 (range, 175.3-7

65 (25th-75th percentiles) zidovudine blood and seminal plasma concentrations were 64.2 (range, 48.4-206

66 Western blot analysis of llama and bull seminal plasma confirmed immunorecognition of OIF using

67 the possibility that endometrial exposure to seminal plasma could contribute to endometriotic disease

68 Standardization of seminal plasma derived PSA calibrant molecular form mass

69 al plasma) but in the presence of NPD or LPD seminal plasma (devoid of sperm).

70 Several other cytokines present in seminal plasma did not elicit Ect1 cell responses.

71 nocytes in the presence of high dilutions of seminal plasma did not express CD1a but showed high leve

72 uspension matrices that used blood plasma or seminal plasma did not make a difference in recovery of

73 h urethritis had HIV-1 RNA concentrations in seminal plasma eight times higher than those in seroposi

74 Pooled human seminal plasma enhanced E. coli growth in vitro in a dos

75 These data suggest that seminal plasma enhances the formation of endometriosis-l

76 Seminal plasma EVs (SP-EVs) were isolated and characteri

77 The non-sperm part of ejaculated semen, or seminal plasma, facilitates the delivery of sperm to the

78 lipid levels; and no detectable HIV-1 RNA in seminal plasma from all 8 participants tested.

79 Exposure to seminal plasma from HIV-1-infected and uninfected men wi

80 Seminal plasma from llamas and bulls was used as represe

81 nducted to characterize proteomic profile of seminal plasma from men with primary, or secondary infer

82 tion fluid derived from epididymal flush and seminal plasma from the prostate and seminal vesicle was

83 ion fluid generated from epididymal flush or seminal plasma from ZIKV infected males at 14 and 35 DPI

84 This is a human seminal plasma glycoprotein that is immunologically indi

85 efore therapy, 4 men had HIV-1 RNA levels in seminal plasma >6.0 log10 (1 million) copies/mL, markedl

86 nce of an ovulation-inducing factor (OIF) in seminal plasma has broad implications and evokes questio

87 There was no significant change in seminal plasma HIV-1 RNA concentrations during the 2-wee

88 CD4 cell counts and blood plasma and seminal plasma human immunodeficiency virus type 1 (HIV-

89 Seminal plasma immunocaptures yielded amplifiable virion

90 ressed HIV-1 RNA levels to <400 copies/mL in seminal plasma in the majority of patients, the first di

91 lored the relationship of HIV-1 in blood and seminal plasma in the presence and absence of urethritis

92 ed to examine organic chemical pollutants in seminal plasma, including both known priority environmen

93 ntagonists, and signaling inhibitors ablated seminal plasma induction of GM-CSF and IL-6, but did not

94 We found that seminal plasma interfered with the activity of PRO 2000

95 Seminal plasma is a critical and complex fluid that carr

96 Given that seminal plasma is an abundant source of transforming gro

97 We conclude that OIF in seminal plasma is beta-NGF and that it is highly conserv

98 Seminal plasma is not just a carrier for spermatozoa.

99 is unknown which compounds in spermatozoa or seminal plasma may be involved in the regulation of sper

100 By promoting a tolerogenic profile in DCs, seminal plasma might favor fertility, but might also com

101 ral blood mononuclear cells (PBMCs; n = 72), seminal plasma (n = 20), cerebrospinal fluid (CSF; n = 3

102 detectable (<400 copies/mL) in the blood and seminal plasma of 8/9 subjects after initiation of thera

103 autoantibody responses were detected in the seminal plasma of infertile patients, suggesting conserv

104 The seminal plasma of some species with internal fertilizati

105 beta, we evaluated the effect of exposure to seminal plasma on the growth of endometrial lesions.

106 prevented the tolerogenic effect induced by seminal plasma on the phenotype and function of DCs, sug

107 nsmitted viruses were evident in the donor's seminal plasma (one of five cases) and even more so in t

108 Human endometrial explants were exposed to seminal plasma or to control medium before transfer to P

109 HIV-1 RNA from blood plasma, seminal plasma, or cervical wicks was quantified at base

110 = 0.09) and more frequent shedding of CMV in seminal plasma (p = 0.002).

111 ce were protected if virus was introduced in seminal plasma (P=.0007, log rank test).

112 ed that %ViableSperm of bulls was related to seminal plasma peroxiredoxin-5, spermadhesin-1 and the s

113 Our results elucidate a mechanism whereby a seminal plasma pheromone attracts ready-to-mate females

114 83% were blood plasma positive and 63% were seminal plasma positive.

115 However, other forms of inactive seminal plasma prostate-specific antigen, either intact

116 have a role in the physiologic processing of seminal plasma proteins such as pro-PSA, as well as in t

117 This report is the largest dataset of bovine seminal plasma proteins.

118 The present study investigated the seminal plasma proteome of Holstein bulls with low (LF;

119 Proteome of seminal plasma provides profound information related to

120 To this end, seminal plasma purified PSA standards from different com

121 measured in log(10) RNA copies/milliliter of seminal plasma) ranging from 0.11 to 0.32; those of the

122 In this study, we show that seminal plasma redirects the differentiation of human de

123 iologically relevant events, the addition of seminal plasma resulted in enhanced virion binding to ep

124 In addition, HIV-1 virions in seminal plasma samples harbored dramatically higher leve

125 with paired blood plasma and CVL, saliva, or seminal plasma samples revealed 91% were blood plasma po

126 When HIV-1 virions were incubated with seminal plasma samples, infectivity in initially nondivi

127 .05) elevation in high grade prostate cancer seminal plasma samples.

128 Sperm characteristics, oxidative stress of seminal plasma, serum and sperm membrane fatty acids, di

129 Xenografts exposed to seminal plasma showed an eightfold increase in volume an

130 HIV-1 RNA was measured in seminal plasma (SP) and blood plasma (BP) at baseline, o

131 hieving first undetectable HIV-1 RNA (VL) in seminal plasma (SP) and blood plasma (BP) in 19 men star

132 weeks post-switch, we measured HIV-1 RNA in seminal plasma (SP) and blood plasma (BP), tenofovir (TF

133 Decay of HIV in seminal plasma (SP) and rectal fluid (RF) has not yet be

134 Antiretroviral pharmacology in seminal plasma (SP) and rectal tissue (RT) may provide i

135 accelerated dramatically in the presence of seminal plasma (SP) and that agitation is not required f

136 Therefore, seminal plasma (SP) collected from healthy individuals w

137 triple therapy donated blood plasma (BP) and seminal plasma (SP) during therapy.

138 and SF162 after incubation with centrifuged seminal plasma (SP) from HIV-negative donors and assesse

139 c concentrations of antiretroviral agents in seminal plasma (SP) may reduce virus burden and influenc

140 etroviral drug families on viral kinetics in seminal plasma (SP) of treatment-naive HIV-infected pati

141 f the intrinsic anti-HIV-1 activity of human seminal plasma (SP) was determined to reside in the cati

142 red (LOQ 40 copies/mL) in blood plasma (BP), seminal plasma (SP), rectal fluid (RF), and cervicovagin

143 ication, 40 copies/mL) in blood plasma (BP), seminal plasma (SP), rectal fluid (RF), and cervicovagin

144 oncentrations were measured in blood plasma, seminal plasma (SP), rectal tissue (RT), and cervicovagi

145 Seminal plasma (SP), the liquid portion of semen, harbor

146 h may facilitate HIV transmission.IMPORTANCE Seminal plasma (SP), the major vehicle for HIV, can modu

147 and of the transmembrane C regulator CD46 in seminal plasma (SP).

148 nd cardiovascular function in a sperm and/or seminal plasma specific manner.

149 paternal low protein diet in a sperm and/or seminal plasma specific manner.

150 rdiovascular function through both sperm and seminal plasma specific mechanisms over successive gener

151 ascular homeostasis and define the sperm and seminal plasma specific programming effects on cardiovas

152 HIV-RNA was quantified in seminal plasma (spVL) and in blood plasma (bpVL) from 2

153 Seminal plasma stimulated the production of a variety of

154 = .002), despite a more sensitive assay for seminal plasma than for cervical wicks.

155 lls were used to investigate agents in human seminal plasma that induce a proinflammatory response.

156 all three TGF-beta isoforms as key agents in seminal plasma that signal induction of proinflammatory

157 ganic pollutant exposures were measured from seminal plasma using gas chromatography, which showed wi

158 mplified from cell-free HIV RNA in blood and seminal plasma using the MiSeq Illumina platform.

159 he HIV-1 RNA viral loads was observed in the seminal plasma values than in the blood plasma values wh

160 All macaques were systemically infected, and seminal plasma virion-associated RNA (vRNA) levels were

161 seminal plasma and plasma oxidative stress, seminal plasma vitamin E, and plasma testosterone levels

162 Absence of seminal plasma was accompanied by down-regulation of the

163 Seminal plasma was assayed for HIV-1 RNA and semen was c

164 The concentration of HIV-1 RNA in seminal plasma was monitored as a potential surrogate ma

165 os developed in female tracts not exposed to seminal plasma were abnormal from the early cleavage sta

166 dine, lamivudine, and HIV-1 RNA in blood and seminal plasma were measured in 9 HIV-positive men over

167 Viral loads in whole semen and seminal plasma were strongly correlated with blood plasm

168 ml (range, <400 to 2.8 x 10(5) copies/ml) in seminal plasma, which is 10- to 1,000-fold higher than p