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1 rowth period), and approximately 9.5 months (postpubertal).
2 into three groups: prepubertal, pubertal and postpubertal.
3 ed barrier recovery in comparison with adult postpubertal (11 wk) males.
4 ndividuals exhibit latently expressed (i.e., postpubertal) above normal activity levels of hepatic mu
5  tetracycline antibiotic during the pubertal/postpubertal adolescent growth phase.
6  (Quebec), Canada, among previously inactive postpubertal adolescents aged 14 to 18 years (Tanner sta
7 ition, as a possible substrate for peri- and postpubertal advances in cognitive capacity.
8                             Records of 1,326 postpubertal and 196 prepubertal patients currently more
9 3PNs such shifts were most prominent between postpubertal and adult animals.
10 CP and IP L3PNs in the DLPFC of prepubertal, postpubertal, and adult macaque monkeys, and used laser
11  were most prominent between prepubertal and postpubertal animals, whereas for CP L3PNs such shifts w
12  social communication that are predictive of postpubertal behaviors.
13 boys (mean age, 4 years) and 49 testes in 25 postpubertal boys (mean age, 14 years) with color and po
14 olescent play, bridges the preweaning to the postpubertal brain by engaging the same neural networks
15 pearance of ERalpha-negative preneoplasia in postpubertal Brca1 mutant mice.
16              Estradiol activated behavior in postpubertal, but not prepubertal, males.
17 e duplication varies between prepubertal and postpubertal cases.
18 re detected between prepubertal and pubertal/postpubertal children.
19 th-retarded and normally sized, and pre- and postpubertal children.
20 uman-only ex vivo study, we demonstrate that postpubertal cisgender females have higher levels of CD1
21 ogeneous findings in prepubertal compared to postpubertal cohorts.
22 prefrontal activity changes during peri- and postpubertal cortical maturation is largely unknown.
23  of germ cells generates a predisposition to postpubertal cyclin D2-driven initiation of full mitotic
24  at juvenile (day 20), prepubertal (day 30), postpubertal (day 56), and adult (day 90) ages (N = 115)
25 ale, rats exposed to prenatal stress develop postpubertal deficits in cognitive behaviors supported b
26 he mammary gland during a critical window in postpubertal development imparts a long-lasting protecti
27 atal development whereas they increased over postpubertal development in females.
28 egression models were constructed to predict postpubertal dimensions relevant to ASD.
29 vocalizations that have predictive power for postpubertal dimensions relevant to ASD.
30          Flow was detected in five and three postpubertal epididymides with power and color Doppler U
31 udies demonstrating increased risk linked to postpubertal exposures such as pesticides, plastics, ele
32 ding of the interaction between prenatal and postpubertal factors in the development of germ cell can
33 oximately 30% of the subjects in a sample of postpubertal female patients with mild-to-moderate, non-
34 using cultured anterior pituitary cells from postpubertal female rats and immortalized alphaT3-1 and
35            Moreover, higher trait anxiety in postpubertal females was mediated by elevated perfusion
36 ulcerative colitis), especially pubertal and postpubertal girls.
37 is partially reversed by prepubertal but not postpubertal gonadectomy.
38 seful predictors of calcium retention during postpubertal growth, calcium balance, bio-chemical marke
39 ith frontal cortex function were assessed in postpubertal (> 60 days) normal or gonadectomized male a
40                                     However, postpubertal HFD resulted in a high degree of hepatic st
41 is relative to mice with shorter duration of postpubertal HFD.
42 erefore investigated OSR1/OSR1 expression in postpubertal human uteri, and the prenatal and postnatal
43  Patients with microalbuminuria and 25 yr of postpubertal IDDM have low risk of progression to advanc
44                      Gonadectomized pre- and postpubertal male hamsters (Mesocricetus auratus) were t
45 udies have shown that removal of androgen in postpubertal male mice produces an increase in size and
46 ogen deprivation, provided by castration, in postpubertal male mice.
47 ing Acact-/- with AKR (ald/ald) mice yielded postpubertal male offspring characterized by adrenocorti
48           ICD therapy is indicated for PP in postpubertal males and in females >/= 30 years with the
49 r complete adrenocortical lipid depletion in postpubertal males, which appears to be androgen depende
50 iate mating behavior was similar in pre- and postpubertal males.
51                                    Among 618 postpubertal men, 157 recovered testicular function and
52 g activation in neurons from prepubertal and postpubertal mice of both sexes.
53  of VGlut1 and PSD95 proteins were higher in postpubertal monkeys and positively predicted activity-d
54 s are a rare group of tumours, distinct from postpubertal paediatric and adult tumours of this region
55 etection of epididymal flow is infrequent in postpubertal patients but appears comparable with both t
56                Densitometric measurements of postpubertal patients diagnosed with IgE-CMA (group I, n
57 ge, 2-18 years; 28 prepubertal patients; 286 postpubertal patients; 260 female patients) were evaluat
58 ertal (postnatal day [PD] 21-30; PreP-S) and postpubertal (PD41-50; PostP-S) foot-shock and restraint
59 d administration of dopamine agonists in the postpubertal period (D1 priming).
60 order are of particular interest because the postpubertal period is a critical one for the developmen
61 females during preweaning, peripubertal, and postpubertal periods alters glucose homeostasis and diab
62 cardiographic investigation of children with postpubertal persistence of T-wave inversion at preparti
63 we compared CRF receptor binding in pre- and postpubertal rats.
64 % in pubertal rats; this increased to 19% in postpubertal rats.
65 izations predicted individual variability of postpubertal reciprocal social interaction and olfactory
66 95+) puncta, on PV interneurons was lower in postpubertal relative to prepubertal monkeys.
67 ct; evidence in support of the importance of postpubertal risk comes from three case/control studies
68 e relative importance of intrauterine versus postpubertal risk factors has continued.
69 ing homeostatic regulation of body weight in postpubertal rodents and humans.
70 e results suggest that TGFalpha may regulate postpubertal, sex differentiation in ventricular and per
71 alysis and morphological traits arising from postpubertal sexual dimorphism.
72 icrobiota on osteoimmune response effects in postpubertal skeletal development.
73 ectory, was associated with late pubertal or postpubertal stage before the pandemic (odds ratio [OR],
74  flow in 20 prepubertal testes and in all 49 postpubertal testes.
75 power than with color Doppler US in pre- and postpubertal testes.
76 in 22 of 24 prepubertal testes and in all 49 postpubertal testes.
77                               Conversely, in postpubertal Tg glands, reduced ERalpha expression faile
78                      However, in glands from postpubertal Tg mice, a pathway switch occurred and acti
79                                 Beginning in postpubertal virgin animals, low levels of transgene exp
80                                    Among 708 postpubertal women, 110 recovered normal ovarian functio