| scholarly article | Q13442814 |
| P356 | DOI | 10.1210/EN.2008-1471 |
| P698 | PubMed publication ID | 19095740 |
| P50 | author | Pat Monaghan | Q20687752 |
| Karen A Spencer | Q52859036 | ||
| P2093 | author name string | Neil P Evans | |
| Patricia Monaghan | |||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1931-1934 | |
| P577 | publication date | 2008-12-18 | |
| P1433 | published in | Endocrinology | Q3054009 |
| P1476 | title | Postnatal stress in birds: a novel model of glucocorticoid programming of the hypothalamic-pituitary-adrenal axis | |
| P478 | volume | 150 |
| Q42281795 | A marker of biological age explains individual variation in the strength of the adult stress response. |
| Q33927390 | A mechanistic look at the effects of adversity early in life on cardiovascular disease risk during adulthood |
| Q46425798 | An experimental test of the effect of brood size on glucocorticoid responses, parental investment, and offspring phenotype |
| Q39173440 | Ancestry trumps experience: Transgenerational but not early life stress affects the adult physiological stress response |
| Q36154423 | Assessing the effects of repeated handling on the physiology and condition of semi-precocial nestlings |
| Q38419515 | Corticosterone exposure during development has sustained but not lifelong effects on body size and total and free corticosterone responses in the zebra finch |
| Q36418615 | Determinants and significance of corticosterone regulation in the songbird brain |
| Q38204152 | Development of food intake controls: neuroendocrine and environmental regulation of food intake during early life |
| Q55194781 | Developmental corticosterone treatment does not program immune responses in zebra finches (Taeniopygia guttata). |
| Q34835802 | Developmental post-natal stress can alter the effects of pre-natal stress on the adult redox balance |
| Q46440281 | Developmental programming of the HPA and HPG axes by early-life stress in male and female song sparrows. |
| Q37217545 | Developmental programming: cumulative effects of increased pre-hatching corticosterone levels and post-hatching unpredictable food availability on physiology and behaviour in adulthood |
| Q55412630 | Developmental stress increases reproductive success in male zebra finches. |
| Q38914530 | Developmental stress predicts social network position |
| Q93212735 | Developmental stress reduces body condition across avian life-history stages: A comparison of quantitative magnetic resonance data and condition indices |
| Q48704929 | Developmental stress, condition, and birdsong: a case study in song sparrows |
| Q51204103 | Does sex matter? Differential responses to corticosterone administration in the zebra finch. |
| Q61455469 | Does urbanization cause stress in wild birds during development? Insights from feather corticosterone levels in juvenile house sparrows (Passer domesticus) |
| Q57455205 | Early Life Stress Strengthens Trait Covariance: A Plastic Response That Results in Reduced Flexibility |
| Q35966477 | Early-Life Stress Triggers Juvenile Zebra Finches to Switch Social Learning Strategies |
| Q47755283 | Early-developmental stress, repeatability, and canalization in a suite of physiological and behavioral traits in female zebra finches |
| Q48127695 | Effect of isolation and conspecific presence in a novel environment on corticosterone concentrations in a social avian species, the zebra finch (Taeniopygia guttata). |
| Q47743458 | Effects of developmental conditions on glucocorticoid concentrations in adulthood depend on sex and foraging conditions |
| Q91317440 | Effects of experimental chronic traffic noise exposure on adult and nestling corticosterone levels, and nestling body condition in a free-living bird |
| Q90137019 | Effects of traffic noise exposure on corticosterone, glutathione and tonic immobility in chicks of a precocial bird |
| Q30446240 | Eggshell appearance does not signal maternal corticosterone exposure in Japanese quail: an experimental study with brown-spotted eggs |
| Q38801104 | Endocrine Flexibility: Optimizing Phenotypes in a Dynamic World? |
| Q51775211 | Environmental conditions shape the temporal pattern of investment in reproduction and survival. |
| Q46967392 | Environmentally relevant bouts of cooling stimulate corticosterone secretion in free-living eastern bluebird (Sialia sialis) nestlings: potential links between maternal behavior and corticosterone exposure in offspring |
| Q34489111 | Experimental food restriction reveals individual differences in corticosterone reaction norms with no oxidative costs |
| Q51455750 | Feather corticosterone of a nestling seabird reveals consequences of sex-specific parental investment. |
| Q37740308 | Flight performance in the altricial zebra finch: Developmental effects and reproductive consequences |
| Q55617900 | For better or worse: reduced adult lifespan following early-life stress is transmitted to breeding partners. |
| Q39448544 | Glucocorticoid programming of neuroimmune function. |
| Q91921033 | Glucocorticoids, male sexual signals, and mate choice by females: Implications for sexual selection |
| Q47703449 | Group housing during adolescence has long-term effects on the adult stress response in female, but not male, zebra finches (Taeniopygia guttata). |
| Q50738741 | HPA axis regulation, survival, and reproduction in free-living sparrows: Functional relationships or developmental correlations? |
| Q37034431 | Hand rearing affects emotional responses but not basic cognitive performance in European starlings |
| Q47729490 | High environmental ammonia exposure has developmental-stage specific and long-term consequences on the cortisol stress response in zebrafish |
| Q39767637 | Hormonal effects of maltreatment in Nazca booby nestlings: implications for the "cycle of violence". |
| Q51802850 | House sparrows mitigate growth effects of post-natal glucocorticoid exposure at the expense of longevity. |
| Q28079737 | How can we estimate natural selection on endocrine traits? Lessons from evolutionary biology |
| Q89124874 | Interactions of body temperature and nutritional status on hypothalamo-pituitary-adrenal axis activity in pre-thermoregulatory eastern bluebird chicks (Sialia sialis) |
| Q64922554 | Introduction to the Hypothalamic-Pituitary-Adrenal Axis: Healthy and Dysregulated Stress Responses, Developmental Stress and Neurodegeneration. |
| Q30462507 | Japanese quail's genetic background modulates effects of chronic stress on emotional reactivity but not spatial learning |
| Q35997033 | Long-Term and Transgenerational Effects of Stress Experienced during Different Life Phases in Chickens (Gallus gallus). |
| Q30356912 | Long-term effects of adolescent stress on neophobic behaviors in zebra finches are modulated by social context when in adulthood. |
| Q36123882 | Maternal and developmental immune challenges alter behavior and learning ability of offspring |
| Q46871654 | Melanin-based color of plumage: role of condition and of feathers' microstructure. |
| Q30831397 | Physical condition and stress levels during early development reflect feeding rates and predict pre- and post-fledging survival in a nearshore seabird |
| Q46851928 | Physiological flexibility in an avian range expansion |
| Q92111166 | Post-natal corticosterone exposure affects ornaments in adult male house sparrows (Passer domesticus) |
| Q89595675 | Post-natal corticosterone exposure downregulates the HPA axis through adulthood in a common passerine |
| Q92381814 | Post-natal glucocorticoid elevation affects GnRH-induced luteinizing hormone concentration in female house sparrows |
| Q37405529 | Pre- and Post-Natal Stress Programming: Developmental Exposure to Glucocorticoids Causes Long-Term Brain-Region Specific Changes to Transcriptome in the Precocial Japanese Quail |
| Q34068347 | Region-specific neural corticosterone patterns differ from plasma in a male songbird |
| Q48615168 | Regulation of the HPA axis is related to song complexity and measures of phenotypic quality in song sparrows |
| Q92718785 | Social experience during adolescence in female rats increases 50 kHz ultrasonic vocalizations in adulthood, without affecting anxiety-like behavior |
| Q46328954 | Song complexity, song rate, and variation in the adrenocortical stress response in song sparrows (Melospiza melodia). |
| Q51459359 | Stress exposure in early post-natal life reduces telomere length: an experimental demonstration in a long-lived seabird. |
| Q58493850 | Stress hormones, social associations and song learning in zebra finches |
| Q93025370 | Stress, Well-Being and Reproductive Success |
| Q30493345 | Stress, song and survival in sparrows |
| Q41546698 | Supplementary feeding increases nestling feather corticosterone early in the breeding season in house sparrows |
| Q38433663 | The influence of nest attendance and provisioning on nestling stress physiology in the Florida scrub-jay |
| Q26783187 | The positive and negative consequences of stressors during early life |
| Q38403924 | Time as tyrant: The minute, hour and day make a difference for corticosterone concentrations in wild nestlings. |
| Q92727900 | Under the weather: Corticosterone levels in wild nestlings are associated with ambient temperature and wind |
| Q58416590 | Variation in Reproductive Success Across Captive Populations: Methodological Differences, Potential Biases and Opportunities |
| Q45729825 | Vitamins, stress and growth: the availability of antioxidants in early life influences the expression of cryptic genetic variation |
| Q61373776 | Why are there associations between telomere length and behaviour? |
| Q37664903 | Wild jackdaws' reproductive success and their offspring's stress hormones are connected to provisioning rate and brood size, not to parental neophobia |
| Q55260778 | Young parents produce offspring with short telomeres: A study in a long-lived bird, the Black-browed Albatross (Thalassarche melanophrys). |
Search more.