ライフサイエンスコーパス: sex behavior

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1 e was anxiolytic but had no effect on female sex behavior.

2 sexually dimorphic adult phenotypes such as sex behavior.

3 y be critical for the control of anxiety and sex behaviors.

4 a 1 and beta have opposite effects on female sex behaviors.

5 hers, plays a small protective role in safer sex behavior among adolescents; this protective effect i

6 as a factor that can positively affect safer sex behavior among youth; however, the evidence linking

7 y age, in HIV prevalence, HIV awareness, and sex behaviors among MSM in 2014.

8 ion with one or both parents, measured safer sex behavior, and were published in English.

9 orphology of limbic regions involved in male sex behavior are larger in males than in females, and so

10 e statistically less likely to show complete sex behavior as compared to controls.

11 n, and oxytocin infused here promoted female sex behavior but had no effect on anxiety.

12 Finally, facilitation of sex behavior by D1-like agonists was blocked by the anti

13 Drug use, high-risk sex behaviors, depression, and unmet social needs interf

14 wing that a circuit controlling male-typical sex behavior exists in both sexes, with its activation i

15 This is indicative of maladaptive sex behavior following Meth and sex experience.

16 the regulation of gonadotropin secretion and sex behavior, GABAergic neuronal activity was about 2-fo

17 males masculinizes the POA and leads to male sex behavior in adults, thereby highlighting the pathway

18 erone can stimulate appreciable male-typical sex behavior in female mice.

19 fficient for facilitating the primary female sex behavior in laboratory animals, lordosis behavior.

20 GE(2)) mediates the masculinization of adult sex behavior in rats in response to the surge in serum t

21 Safer sex behavior, including use of contraceptives or condoms

22 ) after controlling for demographics, health/sex behaviors, medical comorbidities, cardiovascular ris

23 well analyzed neuroendocrine mechanisms for sex behavior, operating through a neural circuit that ha

24 ale and older; no significant differences in sex behaviors, residence of sex partners, or recent anti

25 les displayed equivalent frequencies of male sex behaviors toward an estrous female or a castrated ma

26 ion displayed equivalent frequencies of male sex behaviors when given testosterone after ovariectomy.

27 t-adolescent sexual communication with safer sex behavior, which was statistically heterogeneous (Q =

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