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The neuro-hormonal control of rapid dynamic skin colour change in an amphibian during amplexusA review of factors influencing the stress response in Australian marsupialsMaximizing the reliability of non-invasive endocrine sampling in the tiger (Panthera tigris): environmental decay and intra-sample variation in faecal glucocorticoid metabolitesRepeated thermal stressor causes chronic elevation of baseline corticosterone and suppresses the physiological endocrine sensitivity to acute stressor in the cane toad (Rhinella marina).Prevalence and determinants of stereotypic behaviours and physiological stress among tigers and leopards in Indian zoos.Annual cycles of urinary reproductive steroid concentrations in wild and captive endangered Fijian ground frogs (Platymantis vitiana).Evaluating physiological stress in Sumatran tigers (Panthera tigris ssp. sumatrae) managed in Australian zoosSight of a predator induces a corticosterone stress response and generates fear in an amphibian.Acute thermal stressor increases glucocorticoid response but minimizes testosterone and locomotor performance in the cane toad (Rhinella marina)Over-wintering tadpoles of Mixophyes fasciolatus act as reservoir host for Batrachochytrium dendrobatidisAn introduced competitor elevates corticosterone responses of a Native Lizard (Varanus varius).Evaluation of physiological stress in Australian wildlife: Embracing pioneering and current knowledge as a guide to future research directions.Non-invasive reproductive and stress endocrinology in amphibian conservation physiology.Does physiological response to disease incur cost to reproductive ecology in a sexually dichromatic amphibian species?Repeatability of baseline corticosterone and acute stress responses to capture, and patterns of reproductive hormones in vitellogenic and non-vitellogenic female Fijian ground frog (Platymantis vitiana).Non-invasive evaluation of physiological stress in an iconic Australian marsupial: the Koala (Phascolarctos cinereus).Are baseline and short-term corticosterone stress responses in free-living amphibians repeatable?The effect of stress and stress hormones on dynamic colour-change in a sexually dichromatic Australian frog.Sexual dimorphism in baseline urinary corticosterone metabolites and their association with body-condition indices in a peri-urban population of the common Asian toad (Duttaphrynus melanostictus).Evaluating Stress Physiology and Parasite Infection Parameters in the Translocation of Critically Endangered Woylies (Bettongia penicillata).One size does not fit all: Monitoring faecal glucocorticoid metabolites in marsupials.Host stress physiology and Trypanosoma haemoparasite infection influence innate immunity in the woylie (Bettongia penicillata).Repeatability of baseline corticosterone and short-term corticosterone stress responses, and their correlation with testosterone and body condition in a terrestrial breeding anuran (Platymantis vitiana).Faecal cortisol metabolites in Bengal (Panthera tigris tigris) and Sumatran tigers (Panthera tigris sumatrae).Fecal glucocorticoid metabolite response of captive koalas (Phascolarctos cinereus) to visitor encounters.Faecal glucocorticoid metabolites and body temperature in Australian merino ewes (Ovis aries) during summer artificial insemination (AI) program.Sarcoptic mange in wombats-A review and future research directions.Individual variation and repeatability in urinary corticosterone metabolite responses to capture in the cane toad (Rhinella marina).Dose-response relationship of tryptophan with large neutral amino acids, and its impact on physiological responses in the chick model.Interrelationship among annual cycles of sex steroids, corticosterone and body condition in Nyctibatrachus humayuni.Interrelationship among steroid hormones, energetics and vocalisation in the Bombay night frog (Nyctibatrachus humayuni).Inverse urinary corticosterone and testosterone metabolite responses to different durations of restraint in the cane toad (Rhinella marina).Urinary corticosterone metabolites and chytridiomycosis disease prevalence in a free-living population of male Stony Creek frogs (Litoria wilcoxii).Urinary corticosterone metabolite responses to capture and captivity in the cane toad (Rhinella marina).Development of a model for investigation of perennial ryegrass toxicosis in sheepEvaluating physiological stress in Asiatic black bears (Ursus thibetanus) rescued from bile farms in VietnamTesting for Short- and Long-Term Thermal Plasticity in Corticosterone Responses of an Ectothermic VertebrateEffects of temperature on urinary corticosterone metabolite responses to short-term capture and handling stress in the cane toad (Rhinella marina)Physiological Stress in Rescued Wild Koalas Are Influenced by Habitat Demographics, Environmental Stressors, and Clinical InterventionMeasuring wool cortisol and progesterone levels in breeding maiden Australian merino sheep (Ovis aries)
P50
Q27322676-72870D14-B701-418D-9247-57B83A3678A5Q28601760-4642D02B-F401-4977-BA38-0F7AAF3E4D21Q28603278-F0E67D66-9035-47EA-B67C-B74823AD5B71Q30788303-F36381B9-C162-4E1D-AA49-8485AD302C8FQ30845490-9B14BE2B-CDD4-4C8E-8864-D03821945579Q33511397-72C932C0-611F-460B-A271-3C40C851F93BQ34047004-2258886E-2A48-4EC4-B2EE-49EBA8386EF6Q34979816-B3864D6B-05CB-475C-A871-95F9EE716CA8Q35124227-51CEF578-0107-4A7B-930F-27A33A7EB5E4Q35125256-09AB1713-714E-4013-8639-7A9F8CA8D90DQ35599186-6088290F-A629-4B9C-BE07-9F152D213192Q35873567-39DEDB25-81D1-486E-892F-C106693FE91CQ36725650-4C85BD4B-4E24-436B-8B23-194A0E5DD0E3Q39298197-42B6BFED-62B3-4A6C-B7FE-A311CEBCA82BQ39386211-61E2B9FB-327C-4566-B932-35A55F6EA0BEQ39435708-4396699F-558F-49AF-ADE1-65B449D4F367Q39539921-62B1FCCD-D8B6-4E36-AB0F-5E85C45ECBA8Q40099035-13F1C903-31A2-4309-9332-825660660F3FQ40323134-DEC5EEAD-101B-4E16-BFA2-C39E7E1C4B9EQ40327601-806006E5-F604-4ED3-BF88-EFE71F5C8A86Q40419011-B431A7FB-ECDA-439C-BA51-B3053D53A18DQ40645996-0E026519-D281-403A-AF88-C72EB286D829Q44904959-6D965886-73FE-482C-A7A4-1265A1C4DF2CQ46194219-ADBC3EB1-C6B0-4332-9FE9-D1E9032F2DD2Q46516138-D30A83FA-BC90-46FC-9445-9A5B0C3D7E53Q47704409-5CC41A05-50E3-40F4-A18A-5F59FBDDC009Q47833069-3EB30A37-DF02-48D7-A352-4054289EAF00Q48025491-CD353276-7ECA-48B9-9A87-EE55C896F42AQ50021298-1C79D7D2-3993-481D-9AC1-35E0405216A8Q50021305-6967C565-71A3-489D-A224-05B0F1C1F5B6Q51018206-35AE2670-492A-4C7B-8F24-9FAB30AB1580Q51171076-9685557A-5111-4313-B0C9-19FD424B3F8FQ51172956-85BA6EFC-EBC6-423A-8613-B9926C765EC6Q51438273-93E90F42-DAEB-4E05-8AE7-44383C05220AQ57625458-AD425F33-ED23-45AB-A25A-40CAE705481BQ60544448-F25015D1-C5B9-491F-B209-6578C0ADC3EFQ60544450-B2B3907E-0CB0-4E09-8A52-59EE6B940C07Q60544464-A0C03620-C20F-4EE4-AD37-707004FD58E4Q61806987-52AD1646-0EC4-4770-968D-1DB8E4474A65Q64068200-350BAAC0-E06E-4D49-9863-FB27318903FE
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Edward J Narayan
@ast
Edward J Narayan
@en
Edward J Narayan
@es
Edward J Narayan
@nl
type
label
Edward J Narayan
@ast
Edward J Narayan
@en
Edward J Narayan
@es
Edward J Narayan
@nl
prefLabel
Edward J Narayan
@ast
Edward J Narayan
@en
Edward J Narayan
@es
Edward J Narayan
@nl
P106
P1153
24725207800
P21
P31
P496
0000-0003-2719-0900