ライフサイエンスコーパス: sexual behavior

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

2 ruitless controls sexual differentiation and sexual behavior.

3 egion and were predominately associated with sexual behavior.

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

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

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

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

8 d during copulation and facilitates male rat sexual behavior.

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

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

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

12 lular mechanism for the regulation of female sexual behavior.

13 ions in this behavioral measure could affect sexual behavior.

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

15 essants produces lasting impairments in male sexual behavior.

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

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

18 e effects of neonatal citalopram exposure on sexual behavior.

19 riod is sufficient to produce impairments in sexual behavior.

20 rm the neuronal framework necessary for male sexual behavior.

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

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

23 unexpected relationship between APP and male sexual behavior.

24 crine control of reproductive physiology and sexual behavior.

25 uronal function had profound effects on male sexual behavior.

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

27 reveal genes involved in maintenance of male sexual behavior.

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

29 ite for the dopaminergic enhancement of male sexual behavior.

30 mples for analysis of glutamate and measured sexual behavior.

31 ory role played by preoptic dopamine on male sexual behavior.

32 nfections requires the collection of data on sexual behavior.

33 appetitive and consummatory aspects of male sexual behavior.

34 eases sucrose intake and promotes aspects of sexual behavior.

35 including aggregation, mate recognition, and sexual behavior.

36 n studied extensively for its role in female sexual behavior.

37 tion is important for the expression of male sexual behavior.

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

39 ocortin (POMC) neurons, are activated during sexual behavior.

40 rylation of NMDA receptors and impaired male sexual behavior.

41 accumbens DA previously observed during male sexual behavior.

42 , it is important to consider the effects of sexual behavior.

43 an important site for the regulation of male sexual behavior.

44 nternalization, leading to diminished female sexual behavior.

45 for the expression and sensitization of male sexual behavior.

46 ransmission; of these, 11 reported high-risk sexual behavior.

47 he hypothalamus, a region involved in female sexual behavior.

48 rousal state essential for the expression of sexual behavior.

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

50 HPV types even after complete adjustment for sexual behavior.

51 ld misunderstand it, causing increased risky sexual behavior.

52 dicating the importance of these neurons for sexual behavior.

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

54 cessory olfactory system controls social and sexual behavior.

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

56 ot required for initiation or performance of sexual behavior.

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

58 rents about the early onset of nonconsensual sexual behavior.

59 cers and novel downstream regulators of male sexual behavior.

60 ssion of experience-induced reinforcement of sexual behavior.

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

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

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

64 rly and standard ART groups reported similar sexual behaviors.

65 obtain information on sociodemographics and sexual behaviors.

66 n first reported HPV detection and noncoital sexual behaviors.

67 ith HIV seroconversion, after adjustment for sexual behaviors.

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

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

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

71 ile providing guidance around reducing risky sexual behaviors.

72 973 to 2004, perhaps as a result of changing sexual behaviors.

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

74 s of persistent infection with posttreatment sexual behaviors.

75 4 signaling is necessary for male and female sexual behaviors.

76 y which hormones and other factors influence sexual behaviors.

77 etween the nervous system, genes, and innate sexual behaviors.

78 displayed appropriate gender-specific adult sexual behaviors.

79 ovide access to neural circuits that control sexual behaviors.

80 juvenile tail tips, and displaying defective sexual behaviors.

81 fied by sociodemographic characteristics and sexual behaviors.

82 or unreported sexual debut or nonpenetrative sexual behaviors.

83 Animals engaged in sexual behavior 1 hour before sacrifice.

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

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

86 12 months by year and stratified by sex and sexual behavior, age, and race/ethnicity.

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

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

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

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

91 Risky sexual behavior among Ethiopian university students, esp

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

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

94 health issues and for promoting responsible sexual behaviors among young people.

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

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

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

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

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

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

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

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

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

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

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

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

107 Sexual behavior and motivation were examined and compare

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

109 ferentiation of the body, also contribute to sexual behavior and neural development of both sexes.

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

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

112 underlying the reinforcing effects of female sexual behavior and raise the possibility that the alter

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

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

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

116 ribution of infectious stages on patterns of sexual behavior and the phase of epidemics is discussed.

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

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

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

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

121 res and circuits that would parallel that of sexual behaviors and peripheral organs has so far uncove

122 of the population, little is known about the sexual behaviors and sexual function of older people.

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

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

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

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

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

128 CDs), including compulsive gambling, buying, sexual behavior, and eating, can occur as a complication

129 r away from feeding directed behavior toward sexual behavior, and facilitates the formation of social

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

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

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

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

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

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

136 uences of these cues for female maternal and sexual behavior, and recent studies that explore the rol

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

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

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

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

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

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

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

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

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

146 The genetic mechanisms controlling sexual behavior are similar to those controlling body se

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

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

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

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

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

152 e as a possible contributing factor to risky sexual behavior associated with the contraction of HIV.

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

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

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

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

157 endogenous opioids in the brain area during sexual behavior but instead may contribute to the change

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

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

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

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

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

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

164 Experience with sexual behavior causes cross-sensitization of amphetamin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

182 egulation of developmental GnRH secretion or sexual behavior in adults, have not yet been explored.

183 Sexual behavior in Drosophila results from interactions

184 fruitless (fru) gene are key determinants of sexual behavior in Drosophila.

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

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

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

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

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

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

191 Challenges in the accurate measurement of sexual behavior in human immunodeficiency virus (HIV) pr

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

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

194 through which sexual experience facilitates sexual behavior in male rats.

195 ated with the development and integration of sexual behavior in mammals.

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

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

198 and is essential for the expression of male sexual behavior in rats.

199 a short discussion of hormones and feminine sexual behavior in some rodent species is followed by an

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

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

202 the pheromone cis-vaccenyl acetate modulates sexual behavior in the fly.

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

204 mption may partially defeminize adult female sexual behavior in the mouse.

205 , and incident infection was associated with sexual behavior in the past 30 days, namely having >1 ma

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

207 Sexual behaviors in a host population determine the succ

208 Sexual behaviors in animals are governed by inputs from

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

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

211 These regions are involved in the display of sexual behaviors in male green anoles as in many other v

212 C. elegans male sexual behaviors include chemotaxis and response to herm

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

214 tural reward behaviors, sucrose drinking and sexual behavior, increase levels of DeltaFosB in the NAc

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

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

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

218 meronasal organ (VNO) displayed male-typical sexual behavior indiscriminately toward female and male

219 Demographic and sexual behavior information was obtained from all partic

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

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

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

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

224 Examining global trends of adolescent sexual behavior is essential to inform clinical practice

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

226 In rats, female sexual behavior is regulated by a well defined limbic-hy

227 Sexual behavior is variable between individuals, ranging

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

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

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

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

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

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

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

235 is concern that self-reported information on sexual behavior may not be valid, especially if study pa

236 Sexual behavior may partly explain the observed associat

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

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

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

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

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

242 In a pretest for sexual behavior on the 10th day, there was no difference

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

244 , following different components of male rat sexual behavior or following control manipulations that

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

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

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

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

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

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

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

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

253 eral arousal but not specifically related to sexual behavior per se.

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

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

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

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

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

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

260 The increased exploration and sexual behavior recorded for amygdala-lesioned monkeys i

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

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

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

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

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

266 With changing sexual behaviors, SCCA incidence and patient demographic

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

268 =-0.43) crime conviction scores, lower risky sexual behavior scores (standardized estimate=-0.24), an

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

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

271 Exogenous opioids influence male rat sexual behavior, suggesting that endogenous opioid pepti

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

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

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

275 We investigated whether sexual behaviors that elevated the odds of oropharyngeal

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

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

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

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

280 y with a computer-assisted self-interview on sexual behavior used in 3 culturally and linguistically

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

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

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

284 Individual and couple-level sexual behavior was not associated with HCV infection.

285 Sexual behavior was significantly reduced in female mice

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

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

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

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

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

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

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

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

294 Specific sexual behaviors were associated with persistence, sugge

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

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

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

298 Indeed, ablations of the MPOA impair sexual behavior, whereas stimulation of the MPOA enhance

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

300 hormones as endocrine signals to synchronize sexual behavior with gamete maturation and as exogenous

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