about
Regulation of the hypothalamic-pituitary-adrenal axis circadian rhythm by endocannabinoids is sexually diergic.Investigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) studLong-acting progestin-only contraceptives impair endometrial vasculature by inhibiting uterine vascular smooth muscle cell survival.Vasopressin does not mediate hypersensitivity of the hypothalamic pituitary adrenal axis during chronic stressParental pre-pregnancy BMI is a dominant early-life risk factor influencing BMI of offspring in adulthood.Interaction of bovine estrogen receptor with immobilized zinc.Proteasome-dependent down-regulation of activated nuclear hippocampal glucocorticoid receptors determines dynamic responses to corticosterone.Maternal and umbilical cord androgen concentrations do not predict digit ratio (2D:4D) in girls: a prospective cohort study.Circulating maternal testosterone concentrations at 18 weeks of gestation predict circulating levels of antimüllerian hormone in adolescence: a prospective cohort study.Prenatal determinants of uterine volume and ovarian reserve in adolescence.Gonadectomy reverses the sexually diergic patterns of circadian and stress-induced hypothalamic-pituitary-adrenal axis activity in male and female rats.In vitro and in vivo responses of doxorubicin ion exchange microspheres to hyperthermia.Postnatal masculinization alters the HPA axis phenotype in the adult female rat.Organizational role for testosterone and estrogen on adult hypothalamic-pituitary-adrenal axis activity in the male rat.Gonadal steroid replacement reverses gonadectomy-induced changes in the corticosterone pulse profile and stress-induced hypothalamic-pituitary-adrenal axis activity of male and female rats.The relationship between maternal and umbilical cord androgen levels and polycystic ovary syndrome in adolescence: a prospective cohort study.Organizational role for pubertal androgens on adult hypothalamic-pituitary-adrenal sensitivity to testosterone in the male rat.Corticosterone levels in the brain show a distinct ultradian rhythm but a delayed response to forced swim stress.Corticosteroids mediate fast feedback of the rat hypothalamic-pituitary-adrenal axis via the mineralocorticoid receptor.Effect of the glucocorticoid receptor antagonist Org 34850 on basal and stress-induced corticosterone secretion.Diurnal variation in the responsiveness of the hypothalamic-pituitary-adrenal axis of the male rat to noise stress.Circadian variation in basal plasma corticosterone and adrenocorticotropin in the rat: sexual dimorphism and changes across the estrous cycle.Clinical, ultrasound and biochemical features of polycystic ovary syndrome in adolescents: implications for diagnosisPregnenolone synthesis from cholesterol and hydroxycholesterols by mitochondria from ovaries following the stimulation of immature rats with pregnant mare's serum gonadotropin and human choriogonadotropinThe hypothalamic-pituitary-adrenal axis in rat pregnancy and lactation: circadian variation and interrelationship of plasma adrenocorticotropin and corticosteroneProduction rate, metabolic clearance rate and uterine extraction of corticosterone during rat pregnancy
P50
Q34244358-36CD73F2-6E2A-4614-A4BF-CC18A42E1F2AQ35137486-836EC7AE-5368-4F70-8798-4E4297CE947BQ35549107-BD5B4929-1880-42B8-A755-4525BD7A0A17Q37038298-8FEBC457-7A97-4438-A82B-CA9781125882Q37345467-48113BF9-F1FA-4282-9014-983594802AC0Q42006646-1BF257CF-5C6F-48D1-A1E4-75076E4D7B6AQ42517359-FC1B08C0-862D-4448-ABC9-81AEF667DF23Q43124820-BCD9C770-3F45-410F-B06C-31F8D272F5F9Q43162857-6FC9F698-732D-46F3-8515-E9566D83BE42Q43257233-124ECC51-0EC6-40FB-8D22-7F300A2A3F16Q44930675-B6F3E3D3-F11B-4F5A-B6CB-A84610A5DDC2Q45091532-C4B1948C-E069-46AA-AE5E-FE67CA515B0DQ45195674-E5FDD249-20CA-4803-A417-E0EFA38FE97FQ45206357-A5CEEC15-0116-474A-BC7E-55D5BFB7842CQ45236145-34BA84B0-9AD2-4236-B83E-FF13F1D6A766Q45945634-786A3E0E-3866-4AA3-B78B-1827F9723775Q46031600-C090E4D4-9133-4180-A92E-52DC31AC7FC4Q46690290-4B517DCF-C6D1-411F-B238-51BF036C1A4FQ46694906-72F0192C-853A-4E2F-ADDC-D113637C7F48Q46957564-7277221F-295E-4E1A-BA01-7BA355D72572Q48497047-752D6688-1D1A-49B4-B0B5-B75C8C843F13Q48632395-668B7A00-A167-45B0-B32A-AE436ED5FB76Q59619161-3F279428-3B4F-4525-849A-170709776357Q69406036-873EDD40-7DBE-4D97-A514-8B9CA5CE5706Q72458659-4BA43042-5680-4B11-B393-939BE238A595Q72814897-5E9EBF14-5A2A-409B-839C-11B42DE33214
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Helen C. Atkinson
@ast
Helen C. Atkinson
@en
Helen C. Atkinson
@es
Helen C. Atkinson
@nl
Helen C. Atkinson
@sl
type
label
Helen C. Atkinson
@ast
Helen C. Atkinson
@en
Helen C. Atkinson
@es
Helen C. Atkinson
@nl
Helen C. Atkinson
@sl
prefLabel
Helen C. Atkinson
@ast
Helen C. Atkinson
@en
Helen C. Atkinson
@es
Helen C. Atkinson
@nl
Helen C. Atkinson
@sl
P1053
B-9246-2015
P106
P1153
7101883673
P21
P31
P3829
P496
0000-0002-2172-3780