ライフサイエンスコーパス: sexual maturation

1 was observed earlier in female offspring (at sexual maturation).

2 hysiological sexual dimorphisms that precede sexual maturation.

3 th the male and hermaphrodite pattern before sexual maturation.

4 GH resistance in humans that may occur after sexual maturation.

5 mRNA, decreases in male mice at the time of sexual maturation.

6 induced either at postnatal day 10 or after sexual maturation.

7 opment in a progression that correlates with sexual maturation.

8 of males and females undergoing their first sexual maturation.

9 nge in brain electrophysiology is related to sexual maturation.

10 ion of LepR from Kiss1 neurons would prevent sexual maturation.

11 ed the ability of exogenous leptin to induce sexual maturation.

12 r common genetic variants influencing female sexual maturation.

13 ay favor slower childhood growth but earlier sexual maturation.

14 and kinematics in a species, either side of sexual maturation.

15 and/or action is a developmental disorder of sexual maturation.

16 rogram by which the brain controls mammalian sexual maturation.

17 We used established criteria to determine sexual maturation.

18 to loss of height, osteoporosis, and delayed sexual maturation.

19 ypothalamus controls the advent of mammalian sexual maturation.

20 icular degeneration in males beginning after sexual maturation.

21 t 5-7 weeks of age, possibly coincident with sexual maturation.

22 hormone (LHRH), the neuropeptide controlling sexual maturation.

23 accelerates development, resulting in faster sexual maturation.

24 In this retrospective analysis, sexual maturation ages and reproductive hormone levels w

25 elopmental transition from juvenile stage to sexual maturation, also regulates light avoidance in Dro

26 Mice carrying the transgene exhibit delayed sexual maturation and a diminished reproductive capacity

27 dietary intake of fat and cholesterol and of sexual maturation and body mass index (BMI) on LDL-C wer

28 ductal elongation and side branching during sexual maturation and early pregnancy, but failed to dev

29 n's metabolic effects.SIGNIFICANCE STATEMENT Sexual maturation and fertility are dispensable at the i

30 thalamic-pituitary-gonadal axis, controlling sexual maturation and fertility in diverse species from

31 logical and psychological changes to achieve sexual maturation and fertility.

32 eptor for NPY-8, a neuropeptide required for sexual maturation and germ cell differentiation.

33 matic investment in health, such that faster sexual maturation and higher parity increases risk of di

34 ted estrogen levels and exhibited precocious sexual maturation and increased fecundity.

35 deficiency manifests as absent or incomplete sexual maturation and infertility.

36 We conclude that IGF1 may coregulate female sexual maturation and longevity; wild-derived strains ca

37 uration; and Nrip1 is involved in regulating sexual maturation and may affect longevity by regulating

38 In addition to mediating sexual maturation and reproduction through stimulation o

39 t developmental and life stage that leads to sexual maturation and reproductive capability.

40 lts reveal that miR-7a2 critically regulates sexual maturation and reproductive function by interconn

41 veal that miR-7a2 is a critical regulator of sexual maturation and reproductive function, as mice lac

42 ed strains carry specific alleles that delay sexual maturation; and Nrip1 is involved in regulating s

43 nutritional status, and delayed skeletal and sexual maturation are common in children with sickle cel

44 thways that control growth and the timing of sexual maturation are conserved through evolution, and s

45 Growth and sexual maturation assessed by Tanner staging and testicu

46 If ablations are performed before sexual maturation, attraction is unimpaired, demonstrati

47 In pubertal children, sexual maturation, BMI, dietary intervention (in girls),

48 leghorn chickens (Gallus gallus domesticus) sexual maturation brings about permanent female gravidit

49 ienced a limited period of starvation during sexual maturation but not when females had unlimited acc

50 RANKL-deficient mice develop normally during sexual maturation, but fail to form lobuloalveolar struc

51 Little is known about GnRH release during sexual maturation, but it is assumed to be minimal befor

52 In mice, Acrp30 levels increase during sexual maturation by 4-fold in males and 10-fold in fema

53 in GnRH signaling, such as the initiation of sexual maturation by kisspeptins.

54 time before or after adjustment for stage of sexual maturation by mixed linear model analysis.

55 Patients have absent or incomplete sexual maturation by the age of 18.

56 Normal sexual maturation depends on the migration of GnRH neuro

57 calcin) and postmenarcheal age (a measure of sexual maturation) described 75% of the variability in c

58 behavioral deficits were absent before full sexual maturation, despite some slight forebrain structu

59 Our results showed that sexual maturation had an impact on activities of enzymes

60 aged 13 to 19 years; Tanner stage 4 and 5 of sexual maturation), half of whom were exposed prenatally

61 ied 10 men (age, 27 to 57 years) with normal sexual maturation, idiopathic infertility, sexual dysfun

62 tion, but they can replace each other during sexual maturation if necessary to generate robust male-s

63 , the ablation of any of these classes after sexual maturation impairs attraction behavior.

64 the onset of puberty and a genetic basis for sexual maturation in humans.

65 ssing the unresolved matter of the timing of sexual maturation in western Atlantic bluefin tuna (ABFT

66 tify genetic loci/genes that regulate female sexual maturation, including loci that mediate lifespan

67 Hormonal control of sexual maturation is a common feature in animal developm

68 GF1 have significantly delayed age of female sexual maturation, measured by vaginal patency (VP).

69 ppearing at approximately 6 weeks of age, as sexual maturation occurred.

70 maize requires the selective elimination and sexual maturation of floral organs in an initially bisex

71 imals suggests that TIP39 may play a role in sexual maturation or gender-specific functions.

72 sed the influence of parental weight status, sexual maturation, race-ethnicity, and energy expenditur

73 nce that kisspeptin, a hormone that promotes sexual maturation, regulates metabolism.

74 ssemination of pollen and sperm can begin at sexual maturation, release of seeds and larvae is delaye

75 rmonal and metabolic changes associated with sexual maturation, reproduction, aging, and calorie rest

76 y, p130 expression in testis correlates with sexual maturation, suggesting p130 is important for the

77 minals or in the vicinity of LHRH perikarya, sexual maturation was accelerated.

78 When available, sexual maturation was noted.

79 Sexual maturation was the factor associated with the gre

80 postmenarcheal period and some indicators of sexual maturation were delayed.

81 leptin levels in these individuals promotes sexual maturation, which requires the pulsatile, coordin

82 ct on gene expression was not apparent until sexual maturation, which suggested that estrogen respons

83 educed expression of the ManR at the time of sexual maturation will increase the potency of LH in viv

84 ion about the bird's internal state, such as sexual maturation, with song learning and production.