ライフサイエンスコーパス: sexual behavior

1 HPV types even after complete adjustment for sexual behavior.

2 ld misunderstand it, causing increased risky sexual behavior.

3 dicating the importance of these neurons for sexual behavior.

4 ecent years and is associated with high-risk sexual behavior.

5 cessory olfactory system controls social and sexual behavior.

6 ssues, such as drug use, firearm safety, and sexual behavior.

7 ot required for initiation or performance of sexual behavior.

8 different species, including aggression and sexual behavior.

9 y studied for its effects on food intake and sexual behavior.

10 rents about the early onset of nonconsensual sexual behavior.

11 cers and novel downstream regulators of male sexual behavior.

12 ssion of experience-induced reinforcement of sexual behavior.

13 fic females and contact a neural circuit for sexual behavior.

14 well known for its role in the modulation of sexual behavior.

15 the ancestral function of this gene in male sexual behavior.

16 e locomotion in association with feeding and sexual behavior.

17 showed no effect on either component of male sexual behavior.

18 ruitless controls sexual differentiation and sexual behavior.

19 egion and were predominately associated with sexual behavior.

20 of STI, and had a higher frequency of risky sexual behavior.

21 ess fruitless, a tra gene target controlling sexual behavior.

22 reoptic area (MPOA), which is vital for male sexual behavior.

23 d during copulation and facilitates male rat sexual behavior.

24 use similar belief systems to set limits on sexual behavior.

25 ale aggression, maternal behavior, or female sexual behavior.

26 tic area (MPOA) is an integral site for male sexual behavior.

27 lular mechanism for the regulation of female sexual behavior.

28 ions in this behavioral measure could affect sexual behavior.

29 esponsible for the long-term effects on male sexual behavior.

30 essants produces lasting impairments in male sexual behavior.

31 uts to control gonad maturation, puberty and sexual behavior.

32 ngle continuum from opposite-sex to same-sex sexual behavior.

33 ploration in the elevated plus maze test and sexual behavior.

34 e effects of neonatal citalopram exposure on sexual behavior.

35 riod is sufficient to produce impairments in sexual behavior.

36 rm the neuronal framework necessary for male sexual behavior.

37 creased release of serotonin (5-HT) inhibits sexual behavior.

38 ecific estrogen-dependent, aroused behavior, sexual behavior.

39 low meaningful prediction of an individual's sexual behavior.

40 unexpected relationship between APP and male sexual behavior.

41 crine control of reproductive physiology and sexual behavior.

42 uronal function had profound effects on male sexual behavior.

43 pressed fruitless (fru), a regulator of male sexual behavior.

44 reveal genes involved in maintenance of male sexual behavior.

45 al preoptic area (MPOA) is critical for male sexual behavior.

46 ite for the dopaminergic enhancement of male sexual behavior.

47 mples for analysis of glutamate and measured sexual behavior.

48 IR52a is also required in females for normal sexual behavior.

49 a fundamental aspect of social, parental and sexual behavior.

50 ng of IR52a+ neurons decrease levels of male sexual behavior.

51 rs and are activated by oxytocin during male sexual behavior.

52 loci significantly associated with same-sex sexual behavior.

53 ther by psychological characteristics beyond sexual behavior.

54 fru (M) and dsx, but does not affect female sexual behavior.

55 use (IVDU), imprisonment and increased risk sexual behavior.

56 ly accounted for cohort-dependent changes in sexual behavior.

57 r to circuits in the brain that drive female sexual behavior.

58 ovide access to neural circuits that control sexual behaviors.

59 juvenile tail tips, and displaying defective sexual behaviors.

60 fied by sociodemographic characteristics and sexual behaviors.

61 or unreported sexual debut or nonpenetrative sexual behaviors.

62 rly and standard ART groups reported similar sexual behaviors.

63 obtain information on sociodemographics and sexual behaviors.

64 n first reported HPV detection and noncoital sexual behaviors.

65 ith HIV seroconversion, after adjustment for sexual behaviors.

66 a that used cash awards to incentivize safer sexual behaviors.

67 ole in mediating pheromone-evoked social and sexual behaviors.

68 al circuit that governs most aspects of male sexual behaviors.

69 urons to balance arousal levels and modulate sexual behaviors.

70 elihood of further consummatory, social, and sexual behaviors.

71 le circumcision, viral-load suppression, and sexual behaviors.

72 ize of various subgroups defined by specific sexual behaviors across different locations and over tim

73 Age- and sexual behavior-adjusted overall, total, and indirect (h

74 We estimated the effect of sexual behavior, age, and immunodeficiency on the number

75 12 months by year and stratified by sex and sexual behavior, age, and race/ethnicity.

76 to brain areas involved in the regulation of sexual behavior, aggression, circadian rhythm, drug abus

77 Low PrEP adherence was associated with sexual behavior, alcohol use, younger age, and length of

78 the importance of continuing surveillance of sexual behaviors, alongside vaccine status, to predict f

79 he imprinted gene PEG3 confers parenting and sexual behaviors, alters growth and development, and reg

80 Risky sexual behavior among Ethiopian university students, esp

81 We assessed changes in sexual behavior among men who have sex with men (MSM), b

82 xual partners and stronger associations with sexual behaviors among men.

83 nown neurotransmitter system responsible for sexual behavior and a component of olfactory learning.

84 ce of HR-HPV types is associated with recent sexual behavior and age.

85 ing development on the organization of adult sexual behavior and androgen receptor (AR) expression in

86 days 1-7 (0=day of birth) and examined adult sexual behavior and AR-immunoreactivity (AR-ir) in the a

87 onatal RU-486 treatment increased adult male sexual behavior and AR-ir in several brain areas in male

88 ium-to-high risk (hr) based on self-reported sexual behavior and as qualified or unqualified using Du

89 trate an interdependent relationship between sexual behavior and church attendance on timing of human

90 ve to HIV-negative women after adjusting for sexual behavior and concurrent genital tract infections.

91 examined the relationship between high-risk sexual behavior and condom use.

92 t animals show deficits in maternal care and sexual behavior and fail to exhibit increases in these b

93 Testing guidelines should incorporate sexual behavior and gender identity.

94 of HSV-2 acquisition, after controlling for sexual behavior and HIV-1 acquisition.

95 r year between 2016 and 2025, with high-risk sexual behavior and injecting drug use remaining at curr

96 Reductions in transmission attributable to sexual behavior and injection drug use are feasible, but

97 A face-to-face interview on sexual behavior and intravaginal practices, and a nurse-

98 ns in the hypothalamus that are required for sexual behavior and male aggression.

99 lifetime prevalence of consensual male-male sexual behavior and male-on-male sexual violence (victim

100 Sexual behavior and motivation were examined and compare

101 ession of experience-induced facilitation of sexual behavior and neural activation in mesolimbic area

102 incident HPV detection is driven by current sexual behavior and new viral acquisition in older women

103 ecifically related to the occurrence of male sexual behavior and not simply involved in general arous

104 ty, from overeating and obesity to impulsive sexual behavior and STDs.

105 eta(ST)(L-/L-) males display mildly impaired sexual behavior and that ERbeta(ST)(L-/L-) females are s

106 delay (>/=2.08 y) between the onset of male sexual behavior and the age at which males first sire yo

107 sights into the genetics underlying same-sex sexual behavior and underscore the complexity of sexuali

108 ction of a high-grade lesion, and changes in sexual behaviors and Chlamydia trachomatis, an infection

109 c involvement in appetitive and consummatory sexual behaviors and consummatory aggressive behaviors i

110 and prevalence ratios (PRs) with respect to sexual behaviors and demographic characteristics.

111 at CD4(+) T-cell counts >350 cells/mm(3)) on sexual behaviors and human immunodeficiency virus type 1

112 models were used to assess the influence of sexual behaviors and STIs on the redetection of oncogeni

113 ects chemical signals that affect social and sexual behaviors and that elicit responses to predator o

114 After accounting for sexual behaviors and viral load, we estimated that the p

115 mission rates were estimated on the basis of sexual behaviors and viral load-specific per-act HIV tra

116 dds of sexually transmitted illness or risky sexual behavior, and a 32% increased odds of obesity.

117 ctions such as the control of maternal care, sexual behavior, and emotions.

118 ion, gender identity, stigma, mental health, sexual behavior, and HIV testing.

119 school/peer problems, family relationships, sexual behavior, and mental health in adolescence (ages

120 bstance use, education/socioeconomic status, sexual behavior, and mental health in young adulthood (a

121 porates state-specific demographic dynamics, sexual behavior, and migratory patterns.

122 ction compared with nonusers, independent of sexual behavior, and Papanicolaou test diagnosis (AHR: 0

123 stance use problems, social isolation, early sexual behavior, and psychiatric problems.

124 ed cervicovaginal specimens and demographic, sexual behavior, and self-reported vaccination data from

125 relationships between serial HPV prevalence, sexual behavior, and suspected bacterial vaginosis (BV)

126 g were collected, together with demographic, sexual behavior, and vaccine status data.

127 del of HPV epidemiology, which includes host sexual behavior, and we find evolutionarily stable strat

128 e progesterone receptor (PR) controls female sexual behavior, and we find many sex differences in num

129 1 neurons, part of a command center for male sexual behaviors, and function oppositely to regulate mu

130 vel ART and MMC coverage, sociodemographics, sexual behaviors, and HIV prevalence and incidence were

131 e associations between age, PrEP acceptance, sexual behaviors, and incident STIs.

132 rily reflects cohort-specific differences in sexual behaviors, and is only marginally attributable to

133 Sexual behavior appears to be an important factor affect

134 ompared using prevalence ratios adjusted for sexual behavior (aPRs).

135 strating that these two components of female sexual behavior are functionally separable.

136 reporting a history of consensual male-male sexual behavior are more likely to have been a victim of

137 s suggest that HPV types 6 and 11 and recent sexual behavior are strongly associated with incident co

138 tivated behaviors such as hunger, thirst and sexual behaviors arise.

139 users have identified the effects of drug on sexual behavior as a reason for further use.

140 d to evaluate significant changes in student sexual behavior, as well as condom procurement and assoc

141 nts has become largely associated with risky sexual behaviors, as the rate of transmission from verti

142 ction was attributable to past, not current, sexual behavior at older ages supports a natural history

143 ptor, but not D2 receptor, in the NAc during sexual behavior attenuated DeltaFosB induction and preve

144 precursor protein (APP), displayed enhanced sexual behavior before castration and maintained sexual

145 els of dynamic variation in individual-level sexual behavior brought the theoretical predictions of H

146 IRKOGFAP mice show normal sexual behavior but hypothalamic-pituitary-gonadotropin

147 that showed that E2 can rapidly affect male sexual behaviors but fail to support a role for the spec

148 stent with the muriqui's observed social and sexual behavior, but the long delay (>/=2.08 y) between

149 nstead that Sxl controls an aspect of female sexual behavior by acting on a target other than or in a

150 tive transcription factors that promote male sexual behavior by controlling the development of sexual

151 at an increased need for sleep inhibits male sexual behavior by decreasing the activity of the male-s

152 Intense feeding, drinking, aggressive, and sexual behaviors can be produced by a simple neuronal st

153 tributions of infection into four gender and sexual behavior categories: (i) cisgender men who have s

154 Experience with sexual behavior causes cross-sensitization of amphetamin

155 ior, followed by a period of abstinence from sexual behavior, causes increased reward for amphetamine

156 hical distributions, and (3) demographic and sexual behavior characteristics are different among segm

157 and females, overall and by demographic and sexual behavior characteristics.

158 osure produced persistent reductions in male sexual behavior characterized by significant dose-depend

159 was either concurrent or non-concurrent with sexual behavior: concurrent animals were mated with a re

160 We collected self-reported sexual behavior data every 3 months from HIV-positive MS

161 hich is generated on the basis of real world sexual behavior data.

162 Balfour and Shuker introduce animal sexual behaviors directed to members of the same sex.

163 ss, disruption of encampments, and trends in sexual behaviors, drug use and syringe availability amon

164 ity of many intervention strategies, such as sexual behavior education, barrier methods, and the cost

165 ere was no association between correlates of sexual behavior (eg, number of lifetime sex partners and

166 When both sexual behaviors exist as subcultures in a population, d

167 , but sexual cognition/fantasy (P = .01) and sexual behavior/experience (P = .01) improved in women.

168 association with appetitive and consummatory sexual behavior expression, while a small number of regi

169 Specifically, experience with sexual behavior, followed by a period of abstinence from

170 he initiation of sexual behavior, uncoupling sexual behavior from reproductive status.

171 hic information, hormonal contraceptive use, sexual behavior, genital tract coinfection, and Papanico

172 Many studies of sexual behavior have shown that individuals vary greatly

173 High-risk sexual behaviors have been suggested as drivers of the r

174 a computer-assisted self-interview regarding sexual behavior, human immunodeficiency virus (HIV) stat

175 analysis was applied to standard measures of sexual behavior in 73 male hamsters (Mesocricetus auratu

176 avior results in impairment of inhibition of sexual behavior in a conditioned sex aversion (CSA) para

177 r is highly dependent upon gonadal steroids, sexual behavior in a large proportion of these hybrid ma

178 he preoptic area and leading to male-typical sexual behavior in adulthood.

179 at single-neuron resolution to suppress male sexual behavior in Drosophila.

180 njection activates a naturalistic pattern of sexual behavior in female A. burtoni.

181 in preoptic neurons significantly decreased sexual behavior in female mice and increased aggression

182 novo Dnmt isoform, Dnmt3a, also masculinized sexual behavior in female mice.

183 ng in masculinized neuronal markers and male sexual behavior in female rats.

184 f the mediobasal hypothalamus that regulates sexual behavior in female rodents, estrogens induce the

185 s mesoaccumbens dopaminergic activity during sexual behavior in freely behaving mice.

186 These results suggest that male sexual behavior in hamsters is organized differently fro

187 the mPOA is linked to the production of male sexual behavior in Japanese quail (Coturnix japonica), a

188 ural pathways activated during inhibition of sexual behavior in male rats and the effects of concurre

189 in the control of erectile function and male sexual behavior in mammals.

190 and symptomatic infection and heterogeneous sexual behavior in men who have sex with men (MSM).

191 ical for reproductive endocrine function and sexual behavior in mice, indicating KNDy cells may provi

192 ting these neurons, however, does not elicit sexual behavior in non-estrus females.

193 nces on the male brain and may increase male sexual behavior in part by increasing AR expression, and

194 OA in experience-induced enhancement of male sexual behavior in rats.

195 how that these connections are essential for sexual behavior in receptive females.

196 ith lower educational attainment and riskier sexual behavior in rural females 15-24 years old.

197 lation and increase song rate, an appetitive sexual behavior in songbirds, but T action in other area

198 In addition, sexual behavior in the absence of Meth triggered reinsta

199 aversive stimuli in males trained to inhibit sexual behavior in the CSA paradigm increased pERK expre

200 ys a critical role in the regulation of male sexual behavior in the hamster.

201 locations, suggesting a need to incorporate sexual behavior in the investigation of clusters of food

202 locations, suggesting a need to incorporate sexual behavior in the investigation of clusters of food

203 ic area (mPOA) is for the activation of male sexual behavior in vertebrates, we recently developed an

204 Sexual behaviors in a host population determine the succ

205 Testosterone regulates dimorphic sexual behaviors in all vertebrates.

206 Sexual behaviors in animals are governed by inputs from

207 e sex-specific interaction between sleep and sexual behaviors in Drosophila, and provide insights int

208 through its receptor CCKLR-17D3 to suppress sexual behaviors in flies.

209 roles of responses to environmental cues and sexual behaviors in longevity regulation, we examined Ca

210 involved in the activation and expression of sexual behavior, including in quail the medial preoptic

211 V infection was 3.2% and was associated with sexual behavior, independent of demographic characterist

212 ng that the chlamydial organisms may use the sexual behavior-independent circulation pathway to infec

213 le effect of FVA adjustment on biological or sexual behavior indicators (primary outcomes); however,

214 self-interviews (ACASI) were used to collect sexual behavior information.

215 rkers in Mombasa, Kenya, completed a monthly sexual behavior interview and clinical examination.

216 n of whether dynamic variation in individual sexual behavior is a real phenomenon that can be observe

217 Although the initiation of sexual behavior is common among adolescents and young ad

218 most laboratory rodent species in which male sexual behavior is highly dependent upon gonadal steroid

219 and family studies have shown that same-sex sexual behavior is partly genetically influenced, but pr

220 Sexual behavior is variable between individuals, ranging

221 us (HR-HPV) infection associated with recent sexual behaviors is undefined in mid-adult women (define

222 Concerns about the vaccine's effect on sexual behavior, low perceived risk of HPV infection, so

223 es controlling the pattern or extent of male sexual behavior, male aggression, maternal behavior, or

224 er controlling for sociodemographic factors, sexual behavior, male circumcision, sexually transmitted

225 CP safety, cost, and the potential impact on sexual behavior--many of the same concerns being voiced

226 re were neither effects of the supplement on sexual behavior, mass of reproductive tissues, nor plasm

227 ved in many behaviors, including locomotion, sexual behavior, maternal care, and aggression.

228 Sexual behavior may partly explain the observed associat

229 Individuals were stratified according to sexual behavior (men who have sex with men [MSM] vs non-

230 her lineage into the picture by reporting on sexual behavior of Darwin's bark spider, Caerostris darw

231 We report here an assessment of the sexual behavior of ERbeta(ST)(L-/L-) null mice.

232 National Survey for STD Prevalence Rate and Sexual Behavior of the High-Risk Sexual Community.

233 cs of sex work, the accumulating data on the sexual behaviors of the general population suggest a shi

234 rats and the effects of concurrent Meth and sexual behavior on neural activity, using ERK phosphoryl

235 ounted for 8 to 25% of variation in same-sex sexual behavior, only partially overlapped between males

236 However, the role of mesolimbic dopamine for sexual behavior or cross-sensitization between natural a

237 produced 100% infertility without effects on sexual behavior or function.

238 d on sociodemographic characteristics, risky sexual behavior, or history of an STI.

239 show that sensory exploitation changes male sexual behavior over evolutionary time.

240 e initial experience-induced facilitation of sexual behavior over repeated mating sessions, or condit

241 Inferred trends in sexual behavior over the past decades paralleled the inc

242 nsmission models that include variability in sexual behavior over time have shown increased incidence

243 und evidence for individual heterogeneity in sexual behavior over time.

244 l rats were infertile because of deficits in sexual behavior, ovulation, and uterine endometrial diff

245 olates clustered on the phylogeny by patient sexual behavior (p&0.001) and race/ethnicity (p&0.001).

246 te to experience-induced enhancement of male sexual behavior, perhaps through a PKA regulated mechani

247 ity, anxiety, and depressive symptoms; risky sexual behavior; poor coping strategies; and negative pr

248 o natural variations in both male and female sexual behavior, potentially via underlying effects on b

249 y nucleus, a region of the brain involved in sexual behavior, prevented puberty and fertility.

250 al population in some countries suggest that sexual behavior profiles of high and low sexual activity

251 ug self-administration concurrent with socio-sexual behavior provides a useful model for studying the

252 Uganda; 26 couples, 3 individuals) completed sexual behavior questionnaires every 3 months over a 9 m

253 ens for HPV testing and completed health and sexual behavior questionnaires.

254 results show that ERbeta plays a key role in sexual behavior regulation and the recently uncovered co

255 ctivity in the medial preoptic area, whereas sexual behavior remains normal.

256 of the diaphragm would result in more risky sexual behaviors, reported condom use increased and numb

257 s (VMH) mediating control of male and female sexual behavior, respectively.

258 (Meth), when administered concurrently with sexual behavior results in impairment of inhibition of s

259 echanisms involved in the interplay of risky sexual behaviors (RSBs) and alcohol dependence (AD), we

260 With changing sexual behaviors, SCCA incidence and patient demographic

261 Each participant's sexual behavior score (SBS) was estimated based on the n

262 =-0.43) crime conviction scores, lower risky sexual behavior scores (standardized estimate=-0.24), an

263 analysis adjusting for household wealth and sexual behavior showed that experiencing drought increas

264 nt) only for dramatic increases in different sexual behaviors simulated simultaneously.

265 TD clinic provided sociodemographic data and sexual behavior; STI, obstetric, and gynecologic history

266 These findings indicate commonalities in sexual behavior stigma affecting MSM across sub-Saharan

267 The 3-factor model of sexual behavior stigma cut across social contexts among

268 structure and psychometric properties of 13 sexual behavior stigma items among 10,396 MSM across 8 s

269 es evolved giant sizes are known for extreme sexual behaviors such as sexual cannibalism, opportunist

270 th and mating experience causes maladapative sexual behavior that is associated with alterations in n

271 lications of these results for impairment of sexual behavior that results from administration of SSRI

272 nce of specific motivated behaviors, such as sexual behaviors that depend on sexual arousal?

273 ide a framework for quantifying variation in sexual behaviors that helps in understanding the HIV epi

274 osing of a master regulator of male-specific sexual behavior to control one module of female-specific

275 connections in the adult female brain links sexual behavior to the estrus phase of the estrous cycle

276 tem required for reproduction and associated sexual behaviors to occur.

277 are, including interventions targeting risky sexual behaviors to prevent STIs (alone or in combinatio

278 rride the circuitry that normally suppresses sexual behavior toward unproductive targets.

279 hat Ptgfr is necessary for the initiation of sexual behavior, uncoupling sexual behavior from reprodu

280 hip between time since diagnosis and several sexual behavior variables: numbers of (a) total partners

281 t, executive function, emotional processing, sexual behavior, violence, and self-awareness.

282 appetitive and consummatory aspects of male sexual behavior was investigated.

283 Sexual behavior was significantly reduced in female mice

284 ), cognitive (water-maze), and reproductive (sexual) behavior was examined.

285 contribute to individual differences in male sexual behavior, we used hybrid B6D2F1 male mice, which

286 To establish population level trends in sexual behavior, we used negative binomial regression to

287 On the basis of reported values of sexual behaviors, we estimated that early ART had an 89%

288 Age group, education, marital status, and sexual behavior were associated with detection.

289 romissions, ejaculations) components of male sexual behavior were measured in a bilevel testing appar

290 Pain-induced reductions in female sexual behavior were observed in the absence of sex diff

291 population-level viral-load suppression and sexual behaviors were also examined.

292 Specific sexual behaviors were associated with persistence, sugge

293 Demographics and sexual behaviors were collected through interviews and H

294 raphic, parental-and-peer communication, and sexual behaviors were collected.

295 Modeled trends in sexual behaviors were compared to incidence data for cer

296 ions (including gonadotropin suppression and sexual behavior) were assessed.

297 xperience, the potential for a more flexible sexual behavior, which could be evolutionarily conserved

298 ng and are necessary and sufficient for male sexual behaviors, while VMHvl-projecting PA(Esr1+) cells

299 ntified a neural mechanism that links female sexual behavior with the estrus, the ovulatory phase of

300 most by images showing conspecifics such as sexual behavior, yawning, or grooming, and not as much-a