ライフサイエンスコーパス: masculine

1 males, toward perceiving the walkers as more masculine.

2 testes acts early in life to make the brain masculine.

3 ps, we show that FSD is associated with more masculine androgen profiles.

4 suggest that estrogen is necessary for full masculine AR expression in the song system and that the

5 els between morphology and the expression of masculine behavior exist for the POA, whereas other rela

6 All wild-type mice showed normal masculine behavior, including mounts and pelvic thrusts

7 to estrogens during development can enhance masculine behaviors in adult females and reduce expressi

8 ng originated in the negative charge and 4-5 masculine bend in the reduced isoalloxazine ring of FAD,

9 fection produces inflammation and HCC with a masculine bias.

10 of penis size on attractiveness with a more masculine body shape (i.e., greater shoulder-to-hip rati

11 rformance), that wielding power performed in masculine but not feminine ways increases testosterone.

12 been shown to play a role in maintaining the masculine character of many of these sex differences, bu

13 ates of recurrent ACS and MACE compared with masculine characteristics.

14 Yet, ERalphaKO males given APO showed masculine copulatory behavior and chemoinvestigatory beh

15 ved both feminine (cytochrome P450 4a14) and masculine (cytochrome P450 4a12 and trefoil factor 3) ge

16 The present results indicate that masculine development of AR expression begins in area X

17 tion maintain that ovarian estrogen prevents masculine development of the copulatory system in birds,

18 t steroid hormones play a role in the normal masculine development of the song system.

19 Attempts to prevent masculine development through various estrogen receptor

20 metabolites of testicular secretions causing masculine development.

21 kB as a candidate factor that contributes to masculine differentiation of HVC because of its Z-linkag

22 s is the fact that "signals" inherent in the masculine episodic and female continuous growth hormone

23 Whereas renaturalization of the masculine episodic GH profile restored normal male-like

24 owth hormone-devoid interpulse period in the masculine episodic profile can explain the complete repr

25 P450 isoform in male rats, is induced by the masculine "episodic" secretory growth hormone profile.

26 Enhancing masculine facial characteristics increased both perceive

27 We used GEOS-Chem simulations (2x2.5 masculine grid resolution) to estimate annual O3 exposur

28 nd reductions in the pulse amplitudes of the masculine growth hormone profile as the cause for the di

29 Similarly, perceptions that masculine males look aggressive increase strongly with d

30 anes cause significantly more deaths than do masculine-named hurricanes.

31 acts during fetal and neonatal life to cause masculine neural development.

32 ether it was performed in gender-stereotyped masculine or feminine ways.

33 , are expressed at higher levels and trigger masculine patterns of development.

34 neural song circuit on the right had a more masculine phenotype than that on the left.

35 We observed that restoration of the normal masculine plasma growth hormone pulse in hypophysectomiz

36 ly dimorphic behaviors: estrogen sets up the masculine repertoire of sexual and territorial behaviors

37 splays are relatively common features of the masculine reproductive behavior in birds.

38 More masculine right 2D:4D and 3D:4D ratios were correlated w

39 ecessarily adhere to stereotypical images of masculine self-dependence.

40 ted close attention to current PSA, had high masculine self-esteem and little distress from sexual dy

41 We find that AR mutant males exhibit masculine sexual and territorial displays, but they have

42 atment of adult mice with androgens promotes masculine sexual behavior in both sexes.

43 velopment or adulthood for the expression of masculine sexual behavior in mice.

44 w the ERalpha is not required for display of masculine sexual behavior.

45 ine content in brain regions associated with masculine sexual behavior.

46 Serotonin (5-HT) is generally inhibitory to masculine sexual behavior.

47 idence suggesting that 5-HT is inhibitory to masculine sexual behavior.

48 n derived from testicular androgens promotes masculine sexual differentiation of neuroanatomy and sex

49 development would prevent the development of masculine song systems, zebra finches were treated embry

50 f parents to have comparatively larger, more masculine sons, and smaller, more feminine daughters, an

51 minority groups, women who harbored implicit masculine stereotypes about engineering reported less co

52 use both sides of the song circuit were more masculine than that of females, diffusible factors such

53 emale mice with XY sex chromosomes were more masculine than XX mice in the density of vasopressin-imm

54 n and women preferred female candidates with masculine voices.

55 Likewise, men preferred men with masculine voices.

56 and female leaders with lower-pitched (i.e., masculine) voices are generally preferred by both men an

57 petition (wielding power) in stereotypically masculine vs. feminine ways.