コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 was observed earlier in female offspring (at sexual maturation).
2 nutritional status has a powerful effect on sexual maturation.
3 ing crosses were smaller before the onset of sexual maturation.
4 before a YP-mediated yellowing reoccurs upon sexual maturation.
5 tion may play an overlooked role in parasite sexual maturation.
6 hment of critical weight (CW), pupation, and sexual maturation.
7 consistent with a role in the regulation of sexual maturation.
8 g which Nos1 activity shaped minipuberty and sexual maturation.
9 ies into growth, lean mass and the timing of sexual maturation.
10 used by the neuroendocrine brain to control sexual maturation.
11 closion and continues through the process of sexual maturation.
12 ery 6 months from 11 years of age until full sexual maturation.
13 and kinematics in a species, either side of sexual maturation.
14 accelerates development, resulting in faster sexual maturation.
15 related phenotypes, in particular the age of sexual maturation.
16 hysiological sexual dimorphisms that precede sexual maturation.
17 th the male and hermaphrodite pattern before sexual maturation.
18 GH resistance in humans that may occur after sexual maturation.
19 mRNA, decreases in male mice at the time of sexual maturation.
20 induced either at postnatal day 10 or after sexual maturation.
21 opment in a progression that correlates with sexual maturation.
22 of males and females undergoing their first sexual maturation.
23 nge in brain electrophysiology is related to sexual maturation.
24 ion of LepR from Kiss1 neurons would prevent sexual maturation.
25 ed the ability of exogenous leptin to induce sexual maturation.
26 r common genetic variants influencing female sexual maturation.
27 rocess that requires conserved regulators of sexual maturation.
28 ay favor slower childhood growth but earlier sexual maturation.
29 and/or action is a developmental disorder of sexual maturation.
30 rogram by which the brain controls mammalian sexual maturation.
31 We used established criteria to determine sexual maturation.
32 to loss of height, osteoporosis, and delayed sexual maturation.
33 ypothalamus controls the advent of mammalian sexual maturation.
34 icular degeneration in males beginning after sexual maturation.
35 t 5-7 weeks of age, possibly coincident with sexual maturation.
36 hormone (LHRH), the neuropeptide controlling sexual maturation.
38 elopmental transition from juvenile stage to sexual maturation, also regulates light avoidance in Dro
39 Mice carrying the transgene exhibit delayed sexual maturation and a diminished reproductive capacity
41 dietary intake of fat and cholesterol and of sexual maturation and body mass index (BMI) on LDL-C wer
42 ductal elongation and side branching during sexual maturation and early pregnancy, but failed to dev
43 n's metabolic effects.SIGNIFICANCE STATEMENT Sexual maturation and fertility are dispensable at the i
44 thalamic-pituitary-gonadal axis, controlling sexual maturation and fertility in diverse species from
47 matic investment in health, such that faster sexual maturation and higher parity increases risk of di
50 We conclude that IGF1 may coregulate female sexual maturation and longevity; wild-derived strains ca
51 uration; and Nrip1 is involved in regulating sexual maturation and may affect longevity by regulating
52 ng new avenues to develop methods to control sexual maturation and mitigate associated detrimental ef
53 s1(hrGFP) neurons, a population critical for sexual maturation and positive estrogen feedback in fema
56 lts reveal that miR-7a2 critically regulates sexual maturation and reproductive function by interconn
57 veal that miR-7a2 is a critical regulator of sexual maturation and reproductive function, as mice lac
58 530 M. nattereri males, we compare rates of sexual maturation and the temporal distribution of phase
59 ges (classification method for the degree of sexual maturation) and showed noticeable sex-specific di
60 ed strains carry specific alleles that delay sexual maturation; and Nrip1 is involved in regulating s
61 nutritional status, and delayed skeletal and sexual maturation are common in children with sickle cel
62 thways that control growth and the timing of sexual maturation are conserved through evolution, and s
63 n mice resulted in dose-dependent defects in sexual maturation as well as in olfaction, hearing, and
67 leghorn chickens (Gallus gallus domesticus) sexual maturation brings about permanent female gravidit
68 ienced a limited period of starvation during sexual maturation but not when females had unlimited acc
69 RANKL-deficient mice develop normally during sexual maturation, but fail to form lobuloalveolar struc
70 Little is known about GnRH release during sexual maturation, but it is assumed to be minimal befor
74 tal hypothalamic gliogenesis markedly alters sexual maturation by preventing this recruitment, a proc
77 calcin) and postmenarcheal age (a measure of sexual maturation) described 75% of the variability in c
78 behavioral deficits were absent before full sexual maturation, despite some slight forebrain structu
79 sformed FM, SAT, and VAT, adjusting for age, sexual maturation, extended BMI percentile, and race-by-
80 iated regulation of blood pressure, but upon sexual maturation, female rats would have lower resting
82 aged 13 to 19 years; Tanner stage 4 and 5 of sexual maturation), half of whom were exposed prenatally
83 ied 10 men (age, 27 to 57 years) with normal sexual maturation, idiopathic infertility, sexual dysfun
84 tion, but they can replace each other during sexual maturation if necessary to generate robust male-s
86 l development is divided into five stages of sexual maturation in boys and girls according to the sta
87 ression in ovary and testis increased during sexual maturation in cells with a known secretory role,
91 ed age-related brain changes coinciding with sexual maturation in the males of the facultatively euso
92 rs of this superfamily are key in triggering sexual maturation in vertebrates but also regulate repro
93 ssing the unresolved matter of the timing of sexual maturation in western Atlantic bluefin tuna (ABFT
94 tify genetic loci/genes that regulate female sexual maturation, including loci that mediate lifespan
95 nover and energy homeostasis with growth and sexual maturation, integrating both metabolic and develo
98 worm, Platynereis dumerilii, a species where sexual maturation is tightly regulated by both metabolic
99 cturally similar to MC4R and which regulates sexual maturation, linear growth rate, and lean mass acc
100 GF1 have significantly delayed age of female sexual maturation, measured by vaginal patency (VP).
104 maize requires the selective elimination and sexual maturation of floral organs in an initially bisex
105 sensitivity of the female morphs and faster sexual maturation of the male mimic increases the freque
107 ment during minipuberty reversed deficits in sexual maturation, olfaction, and cognition in Nos1 muta
111 sed the influence of parental weight status, sexual maturation, race-ethnicity, and energy expenditur
113 ssemination of pollen and sperm can begin at sexual maturation, release of seeds and larvae is delaye
114 rmonal and metabolic changes associated with sexual maturation, reproduction, aging, and calorie rest
115 our results support the relationship between sexual maturation, skin physiology, and the skin microbi
116 romone signaling controls female schistosome sexual maturation, suggesting avenues for therapeutic in
117 y, p130 expression in testis correlates with sexual maturation, suggesting p130 is important for the
118 of human MKRN3 delays aspects of C. elegans sexual maturation, suggesting the conservation of Makori
120 tering developmental trajectory with delayed sexual maturation, the ependymal region has fewer sensor
121 t evidence that MC3R regulates the timing of sexual maturation, the rate of linear growth and the acc
123 o-neuron cell fate switch occurs during male sexual maturation under the cell-autonomous control of t
124 pulation play a role in leptin regulation of sexual maturation via actions on AVPV kisspeptin/tyrosin
131 leptin levels in these individuals promotes sexual maturation, which requires the pulsatile, coordin
132 ct on gene expression was not apparent until sexual maturation, which suggested that estrogen respons
133 educed expression of the ManR at the time of sexual maturation will increase the potency of LH in viv
134 ion about the bird's internal state, such as sexual maturation, with song learning and production.