ライフサイエンスコーパス: postpubertal

1 rowth period), and approximately 9.5 months (postpubertal).

2 ed barrier recovery in comparison with adult postpubertal (11 wk) males.

3 ndividuals exhibit latently expressed (i.e., postpubertal) above normal activity levels of hepatic mu

4 (Quebec), Canada, among previously inactive postpubertal adolescents aged 14 to 18 years (Tanner sta

5 ition, as a possible substrate for peri- and postpubertal advances in cognitive capacity.

6 Records of 1,326 postpubertal and 196 prepubertal patients currently more

7 boys (mean age, 4 years) and 49 testes in 25 postpubertal boys (mean age, 14 years) with color and po

8 pearance of ERalpha-negative preneoplasia in postpubertal Brca1 mutant mice.

9 Estradiol activated behavior in postpubertal, but not prepubertal, males.

10 th-retarded and normally sized, and pre- and postpubertal children.

11 prefrontal activity changes during peri- and postpubertal cortical maturation is largely unknown.

12 of germ cells generates a predisposition to postpubertal cyclin D2-driven initiation of full mitotic

13 at juvenile (day 20), prepubertal (day 30), postpubertal (day 56), and adult (day 90) ages (N = 115)

14 ale, rats exposed to prenatal stress develop postpubertal deficits in cognitive behaviors supported b

15 he mammary gland during a critical window in postpubertal development imparts a long-lasting protecti

16 atal development whereas they increased over postpubertal development in females.

17 Flow was detected in five and three postpubertal epididymides with power and color Doppler U

18 udies demonstrating increased risk linked to postpubertal exposures such as pesticides, plastics, ele

19 ding of the interaction between prenatal and postpubertal factors in the development of germ cell can

20 oximately 30% of the subjects in a sample of postpubertal female patients with mild-to-moderate, non-

21 using cultured anterior pituitary cells from postpubertal female rats and immortalized alphaT3-1 and

22 Moreover, higher trait anxiety in postpubertal females was mediated by elevated perfusion

23 ulcerative colitis), especially pubertal and postpubertal girls.

24 is partially reversed by prepubertal but not postpubertal gonadectomy.

25 seful predictors of calcium retention during postpubertal growth, calcium balance, bio-chemical marke

26 ith frontal cortex function were assessed in postpubertal (> 60 days) normal or gonadectomized male a

27 Patients with microalbuminuria and 25 yr of postpubertal IDDM have low risk of progression to advanc

28 Gonadectomized pre- and postpubertal male hamsters (Mesocricetus auratus) were t

29 udies have shown that removal of androgen in postpubertal male mice produces an increase in size and

30 ogen deprivation, provided by castration, in postpubertal male mice.

31 ing Acact-/- with AKR (ald/ald) mice yielded postpubertal male offspring characterized by adrenocorti

32 ICD therapy is indicated for PP in postpubertal males and in females >/= 30 years with the

33 r complete adrenocortical lipid depletion in postpubertal males, which appears to be androgen depende

34 iate mating behavior was similar in pre- and postpubertal males.

35 Among 618 postpubertal men, 157 recovered testicular function and

36 g activation in neurons from prepubertal and postpubertal mice of both sexes.

37 of VGlut1 and PSD95 proteins were higher in postpubertal monkeys and positively predicted activity-d

38 s are a rare group of tumours, distinct from postpubertal paediatric and adult tumours of this region

39 etection of epididymal flow is infrequent in postpubertal patients but appears comparable with both t

40 Densitometric measurements of postpubertal patients diagnosed with IgE-CMA (group I, n

41 d administration of dopamine agonists in the postpubertal period (D1 priming).

42 order are of particular interest because the postpubertal period is a critical one for the developmen

43 cardiographic investigation of children with postpubertal persistence of T-wave inversion at preparti

44 % in pubertal rats; this increased to 19% in postpubertal rats.

45 we compared CRF receptor binding in pre- and postpubertal rats.

46 95+) puncta, on PV interneurons was lower in postpubertal relative to prepubertal monkeys.

47 ct; evidence in support of the importance of postpubertal risk comes from three case/control studies

48 e relative importance of intrauterine versus postpubertal risk factors has continued.

49 e results suggest that TGFalpha may regulate postpubertal, sex differentiation in ventricular and per

50 alysis and morphological traits arising from postpubertal sexual dimorphism.

51 flow in 20 prepubertal testes and in all 49 postpubertal testes.

52 power than with color Doppler US in pre- and postpubertal testes.

53 in 22 of 24 prepubertal testes and in all 49 postpubertal testes.

54 Conversely, in postpubertal Tg glands, reduced ERalpha expression faile

55 However, in glands from postpubertal Tg mice, a pathway switch occurred and acti

56 Beginning in postpubertal virgin animals, low levels of transgene exp

57 Among 708 postpubertal women, 110 recovered normal ovarian functio