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An integrative view of mammalian seasonal neuroendocrinology

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inferredcites →https://doi.org/10.1002/(sici)1097-4695(19980905)36:3<410::aid-neu8>3.0.co;2-zopenalex-snapshot
Photoperiod regulates neuronal bromodeoxyuridine labeling in the brain of a seasonally breeding mammal
inferredcites →https://doi.org/10.1002/cne.22606openalex-snapshot
Anatomical characterization of the neuropeptide S system in the mouse brain by in situ hybridization and immunohistochemistry
inferredcites →https://doi.org/10.1002/cne.24026openalex-snapshot
Coordinated seasonal regulation of metabolic and reproductive hypothalamic peptides in the desert jerboa
inferredcites →https://doi.org/10.1002/glia.23125openalex-snapshot
A sweet taste receptor‐dependent mechanism of glucosensing in hypothalamic tanycytes
inferredcites →https://doi.org/10.1007/978-1-4614-6199-9_13openalex-snapshot
Sex Steroid Regulation of Kisspeptin Circuits
inferredcites →https://doi.org/10.1007/978-3-642-82870-6openalex-snapshot
Circannual Rhythms
inferredcites →https://doi.org/10.1007/bf02245542openalex-snapshot
Photoperiod: Its importance as an impeller of pineal and seasonal reproductive rhythms
inferredcites →https://doi.org/10.1007/s00018-017-2667-xopenalex-snapshot
The impact of thyroid hormone in seasonal breeding has a restricted transcriptional signature
inferredcites →https://doi.org/10.1007/s00428-014-1602-xopenalex-snapshot
Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors
inferredcites →https://doi.org/10.1007/s00429-015-1101-0openalex-snapshot
Sensitivity to the photoperiod and potential migratory features of neuroblasts in the adult sheep hypothalamus
inferredcites →https://doi.org/10.1007/s00429-017-1478-zopenalex-snapshot
Seasonal reorganization of hypothalamic neurogenic niche in adult sheep
inferredcites →https://doi.org/10.1007/s00441-003-0789-yopenalex-snapshot
Ultrastructural localization of vimentin immunoreactivity and gene expression in tanycytes and their alterations in hamsters kept under different photoperiods
inferredcites →https://doi.org/10.1016/0016-6480(73)90130-5openalex-snapshot
Seasonal variation in LH and FSH of bilaterally castrated snowshoe hares
inferredcites →https://doi.org/10.1016/0016-6480(79)90012-1openalex-snapshot
The structure and function of the pars tuberalis of the vertebrate adenohypophysis
inferredcites →https://doi.org/10.1016/0197-0186(94)90100-7openalex-snapshot
Melatonin receptors: Localization, molecular pharmacology and physiological significance
inferredcites →https://doi.org/10.1016/0303-7207(82)90104-6openalex-snapshot
Actions of dopamine on prolactin secretion and cyclic AMP metabolism in ovine pituitary cells
inferredcites →https://doi.org/10.1016/0304-3940(86)90210-7openalex-snapshot
Change in duration of the nighttime melatonin peak may be a signal driving photoperiodic responses in the Djungarian hamster (Phodopus sungorus)
inferredcites →https://doi.org/10.1016/0378-4320(92)90004-wopenalex-snapshot
Maternal transfer of photoperiodic information in rodents
inferredcites →https://doi.org/10.1016/j.bbi.2016.12.013openalex-snapshot
A seasonal switch in histone deacetylase gene expression in the hypothalamus and their capacity to modulate nuclear signaling pathways
inferredcites →https://doi.org/10.1016/j.cell.2005.07.011openalex-snapshot
Decoding Dopamine Signaling
inferredcites →https://doi.org/10.1016/j.cell.2006.03.017openalex-snapshot
Circannual Control of Hibernation by HP Complex in the Brain
inferredcites →https://doi.org/10.1016/j.celrep.2014.10.006openalex-snapshot
Tissue-Specific Posttranslational Modification Allows Functional Targeting of Thyrotropin
inferredcites →https://doi.org/10.1016/j.celrep.2017.03.004openalex-snapshot
Single-Cell RNA-Seq Reveals Hypothalamic Cell Diversity
inferredcites →https://doi.org/10.1016/j.cophys.2018.04.006openalex-snapshot
Seasonal physiology: making the future a thing of the past
inferredcites →https://doi.org/10.1016/j.cub.2006.07.025openalex-snapshot
Kisspeptin Mediates the Photoperiodic Control of Reproduction in Hamsters
inferredcites →https://doi.org/10.1016/j.cub.2008.06.076openalex-snapshot
Ancestral TSH Mechanism Signals Summer in a Photoperiodic Mammal
inferredcites →https://doi.org/10.1016/j.cub.2008.07.040openalex-snapshot
New Insights into Ancient Seasonal Life Timers
inferredcites →https://doi.org/10.1016/j.cub.2010.02.066openalex-snapshot
Identification of Eya3 and TAC1 as Long-Day Signals in the Sheep Pituitary
inferredcites →https://doi.org/10.1016/j.cub.2010.10.048openalex-snapshot
A Molecular Switch for Photoperiod Responsiveness in Mammals
inferredcites →https://doi.org/10.1016/j.cub.2010.10.050openalex-snapshot
Adaptive Divergence in the Thyroid Hormone Signaling Pathway in the Stickleback Radiation
inferredcites →https://doi.org/10.1016/j.cub.2010.11.038openalex-snapshot
Acute Induction of Eya3 by Late-Night Light Stimulation Triggers TSHβ Expression in Photoperiodism
inferredcites →https://doi.org/10.1016/j.cub.2014.05.024openalex-snapshot
A Circannual Clock Drives Expression of Genes Central for Seasonal Reproduction
inferredcites →https://doi.org/10.1016/j.cub.2015.01.074openalex-snapshot
Functional Divergence of Type 2 Deiodinase Paralogs in the Atlantic Salmon
inferredcites →https://doi.org/10.1016/j.cub.2015.09.014openalex-snapshot
Binary Switching of Calendar Cells in the Pituitary Defines the Phase of the Circannual Cycle in Mammals
inferredcites →https://doi.org/10.1016/j.expneurol.2004.12.021openalex-snapshot
Neurogenesis in the ependymal layer of the adult rat 3rd ventricle
inferredcites →https://doi.org/10.1016/j.mce.2013.10.015openalex-snapshot
Cellular mechanisms and integrative timing of neuroendocrine control of GnRH secretion by kisspeptin
inferredcites →https://doi.org/10.1016/j.molmet.2017.08.015openalex-snapshot
Amino acid sensing in hypothalamic tanycytes via umami taste receptors
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2016.02.008openalex-snapshot
Hypothalamic neurogenesis persists in the aging brain and is controlled by energy-sensing IGF-I pathway
inferredcites →https://doi.org/10.1016/j.neuroscience.2010.11.022openalex-snapshot
Characterization of Kiss1 neurons using transgenic mouse models
inferredcites →https://doi.org/10.1016/j.tig.2017.11.003openalex-snapshot
Epigenetic Regulation of Biological Rhythms: An Evolutionary Ancient Molecular Timer
inferredcites →https://doi.org/10.1016/j.tins.2012.08.005openalex-snapshot
A vitamin for the brain
inferredcites →https://doi.org/10.1016/j.tins.2012.12.008openalex-snapshot
Hypothalamic tanycytes: potential roles in the control of feeding and energy balance
inferredcites →https://doi.org/10.1016/j.ydbio.2006.06.006openalex-snapshot
Dopachrome tautomerase (Dct) regulates neural progenitor cell proliferation
inferredcites →https://doi.org/10.1016/j.yfrne.2010.03.001openalex-snapshot
Gonadotropin-inhibitory hormone (GnIH) and its control of central and peripheral reproductive function
inferredcites →https://doi.org/10.1016/j.yfrne.2014.12.002openalex-snapshot
Neural mechanisms controlling seasonal reproduction: Principles derived from the sheep model and its comparison with hamsters
inferredcites →https://doi.org/10.1016/j.ygcen.2010.11.006openalex-snapshot
The hypophysial pars tuberalis transduces photoperiodic signals via multiple pathways and messenger molecules
inferredcites →https://doi.org/10.1016/j.ygcen.2012.03.010openalex-snapshot
Conservation of the photoperiodic neuroendocrine axis among vertebrates: Evidence from the teleost fish, Gasterosteus aculeatus
inferredcites →https://doi.org/10.1016/j.ygcen.2015.05.009openalex-snapshot
Comparative analysis reveals the underlying mechanism of vertebrate seasonal reproduction
inferredcites →https://doi.org/10.1016/j.ygcen.2016.02.020openalex-snapshot
Expression of regulatory neuropeptides in the hypothalamus of red deer (Cervus elaphus) reveals anomalous relationships in the seasonal control of appetite and reproduction
inferredcites →https://doi.org/10.1016/j.ygcen.2017.05.011openalex-snapshot
Signaling pathways to and from the hypophysial pars tuberalis, an important center for the control of seasonal rhythms
inferredcites →https://doi.org/10.1016/j.ygcen.2017.06.029openalex-snapshot
The pars tuberalis: The site of the circannual clock in mammals?
inferredcites →https://doi.org/10.1016/j.yhbeh.2006.06.004openalex-snapshot
Driving reproduction: RFamide peptides behind the wheel
inferredcites →https://doi.org/10.1016/s0074-7696(05)47003-5openalex-snapshot
Hypothalamic Tanycytes: A Key Component of Brain–Endocrine Interaction
inferredcites →https://doi.org/10.1016/s0306-4522(99)00383-8openalex-snapshot
Definitive evidence for the existence of morphological plasticity in the external zone of the median eminence during the rat estrous cycle: implication of neuro-glio-endothelial interactions in gonadotropin-releasing hormone release
inferredcites →https://doi.org/10.1038/416854aopenalex-snapshot
Dominant role of the niche in melanocyte stem-cell fate determination
inferredcites →https://doi.org/10.1038/nature02117openalex-snapshot
Light-induced hormone conversion of T4 to T3 regulates photoperiodic response of gonads in birds
inferredcites →https://doi.org/10.1038/nature06738openalex-snapshot
Thyrotrophin in the pars tuberalis triggers photoperiodic response
inferredcites →https://doi.org/10.1038/ncomms3049openalex-snapshot
α-Tanycytes of the adult hypothalamic third ventricle include distinct populations of FGF-responsive neural progenitors
inferredcites →https://doi.org/10.1038/ncomms3108openalex-snapshot
The saccus vasculosus of fish is a sensor of seasonal changes in day length
inferredcites →https://doi.org/10.1038/nn.3079openalex-snapshot
Tanycytes of the hypothalamic median eminence form a diet-responsive neurogenic niche
inferredcites →https://doi.org/10.1038/nn.4462openalex-snapshot
Molecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes
inferredcites →https://doi.org/10.1038/nn.4495openalex-snapshot
A molecular census of arcuate hypothalamus and median eminence cell types
inferredcites →https://doi.org/10.1038/s41598-017-17920-yopenalex-snapshot
Downregulation of Deiodinase 3 is the earliest event in photoperiodic and photorefractory activation of the gonadotropic axis in seasonal hamsters
inferredcites →https://doi.org/10.1038/s41598-018-24381-4openalex-snapshot
Pineal-dependent increase of hypothalamic neurogenesis contributes to the timing of seasonal reproduction in sheep
inferredcites →https://doi.org/10.1038/s41598-019-40019-5openalex-snapshot
Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
inferredcites →https://doi.org/10.1038/srep29689openalex-snapshot
Orchestration of gene expression across the seasons: Hypothalamic gene expression in natural photoperiod throughout the year in the Siberian hamster
inferredcites →https://doi.org/10.1038/srep36057openalex-snapshot
Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
inferredcites →https://doi.org/10.1046/j.1365-2826.2000.00570.xopenalex-snapshot
Seasonal Changes in the Expression of Neuropeptide Y and Pro‐Opiomelanocortin mRNA in the Arcuate Nucleus of the Ovariectomized Ewe: Relationship to the Seasonal Appetite and Breeding Cycles
inferredcites →https://doi.org/10.1046/j.1365-2826.2001.00611.xopenalex-snapshot
Photoperiodic Regulation of Prolactin Gene Expression in the Syrian Hamster by a Pars Tuberalis-Derived Factor
inferredcites →https://doi.org/10.1046/j.1365-2826.2003.01060.xopenalex-snapshot
MT1 Melatonin Receptor mRNA Expressing Cells in the Pars Tuberalis of the European Hamster: Effect of Photoperiod
inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00746.xopenalex-snapshot
Seasonal regulation of food intake and body weight in the male Siberian hamster: studies of hypothalamic orexin (hypocretin), neuropeptide Y (NPY) andpro‐opiomelanocortin (POMC)
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.02079.xopenalex-snapshot
Neuromedin U and Neuromedin U receptor‐2 expression in the mouse and rat hypothalamus: effects of nutritional status
inferredcites →https://doi.org/10.1071/rd9920001openalex-snapshot
Seasonal prolactin secretion and its role in seasonal reproduction: a review
inferredcites →https://doi.org/10.1073/pnas.0808952105openalex-snapshot
Involvement of thyrotropin in photoperiodic signal transduction in mice
inferredcites →https://doi.org/10.1073/pnas.1310643110openalex-snapshot
Reversible DNA methylation regulates seasonal photoperiodic time measurement
inferredcites →https://doi.org/10.1073/pnas.1702943114openalex-snapshot
Maternal photoperiod programs hypothalamic thyroid status via the fetal pituitary gland
inferredcites →https://doi.org/10.1073/pnas.212517599openalex-snapshot
Temporal expression of seven clock genes in the suprachiasmatic nucleus and the pars tuberalis of the sheep: Evidence for an internal coincidence timer
inferredcites →https://doi.org/10.1073/pnas.69.9.2734openalex-snapshot
Circadian Surfaces and the Diversity of Possible Roles of Circadian Organization in Photoperiodic Induction
inferredcites →https://doi.org/10.1089/thy.2014.0169openalex-snapshot
A Thyroid Hormone Challenge in Hypothyroid Rats Identifies T3 Regulated Genes in the Hypothalamus and in Models with Altered Energy Balance and Glucose Homeostasis
inferredcites →https://doi.org/10.1095/biolreprod.113.112185openalex-snapshot
Hypothalamic Distribution, Adenohypophyseal Receptor Expression, and Ligand Functionality of RFamide-Related Peptide 3 in the Mare During the Breeding and Nonbreeding Seasons1
inferredcites →https://doi.org/10.1095/biolreprod25.1.85openalex-snapshot
Mechanism for Delay of First Ovulation in Lambs Born in the Wrong Season (Fall)1
inferredcites →https://doi.org/10.1095/biolreprod27.3.580openalex-snapshot
Alterations in the Control of Luteinizing Hormone Pulse Frequency Underlie the Seasonal Variation in Estradiol Negative Feedback in the Ewe1
inferredcites →https://doi.org/10.1095/biolreprod34.4.664openalex-snapshot
Maternal Transfer of Photoperiodic Information Influences the Photoperiodic Response of Prepubertal Djungarian Hamsters (Phodopus Sungorus Sungorus)1
inferredcites →https://doi.org/10.1095/biolreprod36.5.1333openalex-snapshot
Reproductive refractoriness of the ewe to inductive photoperiod is not caused by inappropriate secretion of melatonin
inferredcites →https://doi.org/10.1095/biolreprod50.4.965openalex-snapshot
Photoperiodic Synchronization of a Circannual Reproductive Rhythm in Sheep: Identification of Season-Specific Time Cues1
inferredcites →https://doi.org/10.1096/fj.08-121467openalex-snapshot
Egr1 involvement in evening gene regulation by melatonin
inferredcites →https://doi.org/10.1096/fj.13-229559openalex-snapshot
TSH restores a summer phenotype in photoinhibited mammals via the RF‐amides RFRP3 and kisspeptin
inferredcites →https://doi.org/10.1098/rspb.1982.0030openalex-snapshot
Photoperiodism in Japanese quail: the termination of seasonal breeding by photorefractoriness
inferredcites →https://doi.org/10.1098/rspb.2010.0396openalex-snapshot
Seasonal regulation of reproduction: altered role of melatonin under naturalistic conditions in hamsters
inferredcites →https://doi.org/10.1101/gad.938601openalex-snapshot
Hedgehog signaling in animal development: paradigms and principles
inferredcites →https://doi.org/10.1111/ejn.14287openalex-snapshot
A Kiss to drive rhythms in reproduction
inferredcites →https://doi.org/10.1111/j.1365-2826.1991.tb00231.xopenalex-snapshot
Pathways to the Secretion of Adrenocorticotropin: A View from the Portal*
inferredcites →https://doi.org/10.1111/j.1365-2826.1994.tb00580.xopenalex-snapshot
Photoperiodically‐lnduced Cycles in the Secretion of Prolactin in Hypothalamo‐Pituitary Disconnected Rams: Evidence for Translation of the Melatonin Signal in the Pituitary Gland
inferredcites →https://doi.org/10.1111/j.1365-2826.1995.tb00802.xopenalex-snapshot
Evidence that Melatonin Acts in the Pituitary Gland through a Dopamine‐independent Mechanism to Mediate Effects of Daylength on the Secretion of Prolactin in the Ram
inferredcites →https://doi.org/10.1111/j.1365-2826.2005.01389.xopenalex-snapshot
Regulation of MT1 Melatonin Receptor Expression in the Foetal Rat Pituitary
inferredcites →https://doi.org/10.1111/j.1365-2826.2007.01564.xopenalex-snapshot
Does a Melatonin‐Dependent Circadian Oscillator in the Pars Tuberalis Drive Prolactin Seasonal Rhythmicity?
inferredcites →https://doi.org/10.1111/j.1365-2826.2008.01721.xopenalex-snapshot
The Regulation of Seasonal Changes in Food Intake and Body Weight
inferredcites →https://doi.org/10.1111/j.1365-2826.2011.02250.xopenalex-snapshot
Melatonin‐Dependent Timing of Seasonal Reproduction by the Pars Tuberalis: Pivotal Roles for Long Daylengths and Thyroid Hormones
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06455.xopenalex-snapshot
Photoperiodic regulation of retinoic acid signaling in the hypothalamus
inferredcites →https://doi.org/10.1111/j.1600-079x.1994.tb00127.xopenalex-snapshot
Are the annual reproductive and body weight rhythms in the male European hamster (Cricetus cricetus) dependent upon a photoperiodically entrained circannual clock?
inferredcites →https://doi.org/10.1111/j.1600-079x.2007.00476.xopenalex-snapshot
Adaptations for life in the Arctic: evidence that melatonin rhythms in reindeer are not driven by a circadian oscillator but remain acutely sensitive to environmental photoperiod
inferredcites →https://doi.org/10.1111/j.1600-079x.2007.00511.xopenalex-snapshot
Keeping track of time under ice and snow in a sub‐arctic lake: plasma melatonin rhythms in Arctic charr overwintering under natural conditions
inferredcites →https://doi.org/10.1111/jne.12013openalex-snapshot
Circannual Variation in Thyroid Hormone Deiodinases in a Short‐Day Breeder
inferredcites →https://doi.org/10.1111/jne.12116openalex-snapshot
Neuromedin U Partly Mimics Thyroid‐Stimulating Hormone and Triggers W nt/β‐Catenin Signalling in the Photoperiodic Response of F 344 Rats
inferredcites →https://doi.org/10.1111/jne.12289openalex-snapshot
Somatostatin Agonist Pasireotide Promotes a Physiological State Resembling Short‐Day Acclimation in the Photoperiodic Male Siberian Hamster (Phodopus sungorus)
inferredcites →https://doi.org/10.1111/jne.12293openalex-snapshot
Evidence for Changes in Numbers of Synaptic Inputs onto KNDy and GnRH Neurones during the Preovulatory LH Surge in the Ewe
inferredcites →https://doi.org/10.1111/jne.12631openalex-snapshot
Neuroendocrine correlates of the critical day length response in the Soay sheep
inferredcites →https://doi.org/10.1111/jne.12640openalex-snapshot
Photoperiod and thyroid hormone regulate expression of l ‐dopachrome tautomerase (Dct), a melanocyte stem‐cell marker, in tanycytes of the ovine hypothalamus
inferredcites →https://doi.org/10.1111/jne.12679openalex-snapshot
Maternal photoperiodic programming enlightens the internal regulation of thyroid‐hormone deiodinases in tanycytes
inferredcites →https://doi.org/10.1111/jne.12680openalex-snapshot
A unifying hypothesis for control of body weight and reproduction in seasonally breeding mammals
inferredcites →https://doi.org/10.1111/jne.12694openalex-snapshot
A brief history of circannual time
inferredcites →https://doi.org/10.1126/science.1115360openalex-snapshot
Neurogenesis in the Hypothalamus of Adult Mice: Potential Role in Energy Balance
inferredcites →https://doi.org/10.1126/science.1132009openalex-snapshot
Characterizing a Mammalian Circannual Pacemaker
inferredcites →https://doi.org/10.1126/science.148.3677.1609openalex-snapshot
Pineal Gland: Influence on Gonads of Male Hamsters
inferredcites →https://doi.org/10.1126/science.249.4971.906openalex-snapshot
Endogenous Reproductive Rhythms in a Tropical Bird
inferredcites →https://doi.org/10.1126/science.aao0318openalex-snapshot
Diurnal transcriptome atlas of a primate across major neural and peripheral tissues
inferredcites →https://doi.org/10.1139/z94-123openalex-snapshot
The pineal gland signals autumn to reindeer (Rangifer tarandus tarandus) exposed to the continuous daylight of the Arctic summer
inferredcites →https://doi.org/10.1152/ajpregu.00191.2015openalex-snapshot
Somatostatin receptor activation is involved in the control of daily torpor in a seasonal mammal
inferredcites →https://doi.org/10.1152/ajpregu.00424.2002openalex-snapshot
Photoperiod effects on gene expression for hypothalamic appetite-regulating peptides and food intake in the ram
inferredcites →https://doi.org/10.1152/ajpregu.1985.249.1.r111openalex-snapshot
Pineal gland influences period of circannual rhythms of ground squirrels
inferredcites →https://doi.org/10.1152/ajpregu.2000.278.1.r271openalex-snapshot
Photoperiod regulates arcuate nucleus POMC, AGRP, and leptin receptor mRNA in Siberian hamster hypothalamus
inferredcites →https://doi.org/10.1152/physrev.2000.80.4.1523openalex-snapshot
Prolactin: Structure, Function, and Regulation of Secretion
inferredcites →https://doi.org/10.1159/000332822openalex-snapshot
Gonadotropin-Inhibitory Hormone Is a Hypothalamic Peptide That Provides a Molecular Switch between Reproduction and Feeding
inferredcites →https://doi.org/10.1177/002215540205001209openalex-snapshot
The mt1 Melatonin Receptor and RORβ Receptor Are Co-localized in Specific TSH-immunoreactive Cells in the Pars Tuberalis of the Rat Pituitary
inferredcites →https://doi.org/10.1177/074873001129001980openalex-snapshot
Mammalian Photoperiodic System: Formal Properties and Neuroendocrine Mechanisms of Photoperiodic Time Measurement
inferredcites →https://doi.org/10.1177/074873001129002079openalex-snapshot
Photoperiodic Control of Seasonality in Birds
inferredcites →https://doi.org/10.1177/0748730410361918openalex-snapshot
Differential Regulation of Kiss1 Expression by Melatonin and Gonadal Hormones in Male and Female Syrian Hamsters
inferredcites →https://doi.org/10.1177/0748730411420062openalex-snapshot
Seasonal Changes in Cell Proliferation in the Adult Sheep Brain and Pars Tuberalis
inferredcites →https://doi.org/10.1177/0748730411420812openalex-snapshot
Hypothesis
inferredcites →https://doi.org/10.1177/0748730413487974openalex-snapshot
Exogenous T 3 Elicits Long Day–Like Alterations in Testis Size and the RFamides Kisspeptin and Gonadotropin-Inhibitory Hormone in Short-Day Siberian Hamsters
inferredcites →https://doi.org/10.1177/0748730413498561openalex-snapshot
Photoperiod Can Entrain Circannual Rhythms in Pinealectomized European Hamsters
inferredcites →https://doi.org/10.1177/0748730418766601openalex-snapshot
Melatonin-independent Photoperiodic Entrainment of the Circannual TSH Rhythm in the Pars Tuberalis of the European Hamster
inferredcites →https://doi.org/10.1177/074873099129000731openalex-snapshot
Seasonal and Daily Variations in Plasma Melatonin in the High-Arctic Svalbard Ptarmigan ( Lagopus mutus hyperboreus )
inferredcites →https://doi.org/10.1210/edrv-6-4-564openalex-snapshot
Dopamine: A Prolactin-Inhibiting Hormone*
inferredcites →https://doi.org/10.1210/edrv.23.1.0455openalex-snapshot
Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases
inferredcites →https://doi.org/10.1210/en.132.1.285openalex-snapshot
Prolonged exposure to melatonin leads to time-dependent sensitization of adenylate cyclase and down-regulates melatonin receptors in pars tuberalis cells from ovine pituitary
inferredcites →https://doi.org/10.1210/en.137.9.4018openalex-snapshot
The ovine pars tuberalis secretes a factor(s) that regulates gene expression in both lactotropic and nonlactotropic pituitary cells
inferredcites →https://doi.org/10.1210/en.143.8.3083openalex-snapshot
Photoperiodic Regulation of Leptin Resistance in the Seasonally Breeding Siberian Hamster (Phodopus sungorus)
inferredcites →https://doi.org/10.1210/en.2003-0322openalex-snapshot
Evidence that Thyroid Hormones Act in the Ventromedial Preoptic Area and the Premammillary Region of the Brain to Allow the Termination of the Breeding Season in the Ewe
inferredcites →https://doi.org/10.1210/en.2003-0838openalex-snapshot
Photoperiodic Regulation of Hypothalamic Retinoid Signaling: Association of Retinoid X Receptor γ with Body Weight
inferredcites →https://doi.org/10.1210/en.2004-0366openalex-snapshot
Seasonal Morphological Changes in the Neuro-Glial Interaction between Gonadotropin-Releasing Hormone Nerve Terminals and Glial Endfeet in Japanese Quail
inferredcites →https://doi.org/10.1210/en.2004-1452openalex-snapshot
Photoperiodic Regulation of Histamine H3 Receptor and VGF Messenger Ribonucleic Acid in the Arcuate Nucleus of the Siberian Hamster
inferredcites →https://doi.org/10.1210/en.2005-0132openalex-snapshot
Photorefractoriness in Mammals: Dissociating a Seasonal Timer from the Circadian-Based Photoperiod Response
inferredcites →https://doi.org/10.1210/en.2005-0323openalex-snapshot
Differential Regulation of KiSS-1 mRNA Expression by Sex Steroids in the Brain of the Male Mouse
inferredcites →https://doi.org/10.1210/en.2006-0606openalex-snapshot
Melatonin Regulates Type 2 Deiodinase Gene Expression in the Syrian Hamster
inferredcites →https://doi.org/10.1210/en.2007-0038openalex-snapshot
VGF-Derived Peptide, TLQP-21, Regulates Food Intake and Body Weight in Siberian Hamsters
inferredcites →https://doi.org/10.1210/en.2007-0316openalex-snapshot
Hypothalamic Thyroid Hormone Catabolism Acts as a Gatekeeper for the Seasonal Control of Body Weight and Reproduction
inferredcites →https://doi.org/10.1210/en.2007-0848openalex-snapshot
RFamide-Related Peptide Gene Is a Melatonin-Driven Photoperiodic Gene
inferredcites →https://doi.org/10.1210/en.2008-0575openalex-snapshot
Potent Action of RFamide-Related Peptide-3 on Pituitary Gonadotropes Indicative of a Hypophysiotropic Role in the Negative Regulation of Gonadotropin Secretion
inferredcites →https://doi.org/10.1210/en.2008-0834openalex-snapshot
Identification of Melatonin-Regulated Genes in the Ovine Pituitary Pars Tuberalis, a Target Site for Seasonal Hormone Control
inferredcites →https://doi.org/10.1210/en.2009-0609openalex-snapshot
Impact of Melatonin and Molecular Clockwork Components on the Expression of Thyrotropin β-Chain (Tshb) and the Tsh Receptor in the Mouse Pars Tuberalis
inferredcites →https://doi.org/10.1210/en.2011-1039openalex-snapshot
Melatonin Controls Photoperiodic Changes in Tanycyte Vimentin and Neural Cell Adhesion Molecule Expression in the Djungarian Hamster (Phodopus sungorus)
inferredcites →https://doi.org/10.1210/en.2011-1110openalex-snapshot
Identification, Expression, and Physiological Functions of Siberian Hamster Gonadotropin-Inhibitory Hormone
inferredcites →https://doi.org/10.1210/en.2011-1249openalex-snapshot
Effects of Manipulating Hypothalamic Triiodothyronine Concentrations on Seasonal Body Weight and Torpor Cycles in Siberian Hamsters
inferredcites →https://doi.org/10.1210/en.2011-1622openalex-snapshot
Stimulatory Effect of RFRP-3 on the Gonadotrophic Axis in the Male Syrian Hamster: The Exception Proves the Rule
inferredcites →https://doi.org/10.1210/en.2011-1792openalex-snapshot
Photoperiod Regulates Vitamin A and Wnt/β-Catenin Signaling in F344 Rats
inferredcites →https://doi.org/10.1210/en.2011-2049openalex-snapshot
Development, Sex Steroid Regulation, and Phenotypic Characterization of RFamide-Related Peptide (Rfrp) Gene Expression and RFamide Receptors in the Mouse Hypothalamus
inferredcites →https://doi.org/10.1210/en.2012-2051openalex-snapshot
Induction of the Metabolic Regulator Txnip in Fasting-Induced and Natural Torpor
inferredcites →https://doi.org/10.1210/en.2014-1030openalex-snapshot
Physiological Roles of Gonadotropin-Inhibitory Hormone Signaling in the Control of Mammalian Reproductive Axis: Studies in the NPFF1 Receptor Null Mouse
inferredcites →https://doi.org/10.1210/en.2015-1708openalex-snapshot
Photoperiodic and Diurnal Regulation of WNT Signaling in the Arcuate Nucleus of the Female Djungarian Hamster, Phodopus sungorus
inferredcites →https://doi.org/10.1210/en.2015-1854openalex-snapshot
No Evidence That RFamide-Related Peptide 3 Directly Modulates LH Secretion in the Ewe
inferredcites →https://doi.org/10.1210/en.2016-1689openalex-snapshot
Roles of RFRP-3 in the daily and seasonal regulation of reproductive activity in female Syrian hamsters
inferredcites →https://doi.org/10.1210/en.2018-00389openalex-snapshot
KNDy Cells Revisited
inferredcites →https://doi.org/10.1210/en.2018-00653openalex-snapshot
The Gonadotropin-Releasing Hormone Pulse Generator
inferredcites →https://doi.org/10.1210/endo-101-3-818openalex-snapshot
The Endocrine Control of Seasonal Reproductive Function in the Ewe: A Marked Change in Response to the Negative Feedback Action of Estradiol on Luteinizing Hormone Secretion12
inferredcites →https://doi.org/10.1210/endo-113-4-1261openalex-snapshot
Antigonadal Effects of Timed Melatonin Infusion in Pinealectomized Male Djungarian Hamsters (Phodopus sungorus sungorus): Duration is the Critical Parameter*
inferredcites →https://doi.org/10.1210/endo-113-6-2276openalex-snapshot
Pineal Melatonin Secretion Drives the Reproductive Response to Daylength in the Ewe*
inferredcites →https://doi.org/10.1210/endo-125-1-384openalex-snapshot
Prenatal Photoperiod Influences Neonatal Prolactin Secretion in the Sheep*
inferredcites →https://doi.org/10.1210/er.2017-00235openalex-snapshot
The Versatile Tanycyte: A Hypothalamic Integrator of Reproduction and Energy Metabolism
inferredcites →https://doi.org/10.1210/me.2012-1366openalex-snapshot
Npas4Is Activated by Melatonin, and Drives the Clock GeneCry1in the Ovine Pars Tuberalis
inferredcites →https://doi.org/10.1242/dev.116947openalex-snapshot
Ezh2 represses the basal cell lineage during lung endoderm development
inferredcites →https://doi.org/10.1242/jeb.163741openalex-snapshot
Waiting for the sun: The circannual program of reindeer is delayed by the recurrence of rhythmical melatonin secretion after the arctic night
inferredcites →https://doi.org/10.1371/journal.pgen.1004574openalex-snapshot
Dopamine Signaling Leads to Loss of Polycomb Repression and Aberrant Gene Activation in Experimental Parkinsonism
inferredcites →https://doi.org/10.1371/journal.pgen.1005287openalex-snapshot
Npvf: Hypothalamic Biomarker of Ambient Temperature Independent of Nutritional Status
inferredcites →https://doi.org/10.1371/journal.pgen.1005378openalex-snapshot
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
inferredcites →https://doi.org/10.1371/journal.pone.0021351openalex-snapshot
Thyroid Hormone Signalling Genes Are Regulated by Photoperiod in the Hypothalamus of F344 Rats
inferredcites →https://doi.org/10.1371/journal.pone.0062003openalex-snapshot
Hypothalamic Ventricular Ependymal Thyroid Hormone Deiodinases Are an Important Element of Circannual Timing in the Siberian Hamster (Phodopus sungorus)
inferredcites →https://doi.org/10.1371/journal.pone.0109755openalex-snapshot
Efficient Gene Targeting in Golden Syrian Hamsters by the CRISPR/Cas9 System
inferredcites →https://doi.org/10.1371/journal.pone.0172724openalex-snapshot
Hypothalamic over-expression of VGF in the Siberian hamster increases energy expenditure and reduces body weight gain
inferredcites →https://doi.org/10.1371/journal.pone.0187953openalex-snapshot
Aggregate-level lead exposure, gun violence, homicide, and rape
inferredcites →https://doi.org/10.1523/jneurosci.09-12-04122.1989openalex-snapshot
Hypothalamic expression of a novel gene product, VGF: immunocytochemical analysis
inferredcites →https://doi.org/10.1523/jneurosci.2437-12.2013openalex-snapshot
Fgf10-Expressing Tanycytes Add New Neurons to the Appetite/Energy-Balance Regulating Centers of the Postnatal and Adult Hypothalamus
inferredcites →https://doi.org/10.1530/jme-15-0224openalex-snapshot
Thyroid hormone and vitamin D regulate VGF expression and promoter activity
inferredcites →https://doi.org/10.1530/joe-14-0141openalex-snapshot
Clocks for all seasons: unwinding the roles and mechanisms of circadian and interval timers in the hypothalamus and pituitary
inferredcites →https://doi.org/10.1530/joe-18-0177openalex-snapshot
How can a binary switch within the pars tuberalis control seasonal timing of reproduction?
inferredcites →https://doi.org/10.1530/jrf.0.0800159openalex-snapshot
Photoperiodic history and a changing melatonin pattern can determine the neuroendocrine response of the ewe to daylength
inferredcites →https://doi.org/10.1530/jrf.0.0980625openalex-snapshot
Evidence for a circannual rhythm of reproduction and prolactin secretion in a seasonally breeding macropodid marsupial, the Bennett's wallaby ( Macropus rufogriseus rufogriseus )
inferredcites →https://doi.org/10.1530/revreprod/1.3.153openalex-snapshot
The pars tuberalis of the pituitary: a gateway for neuroendocrine output
inferredcites →https://doi.org/10.1677/joe.0.1070211openalex-snapshot
Influences of thyroidectomy and thyroxine replacement on photoperiodically controlled reproduction in quail
inferredcites →https://doi.org/10.1677/joe.0.1370457openalex-snapshot
Dopamine D1 receptor analogues act centrally to stimulate prolactin secretion in ewes
inferredcites →https://doi.org/10.3109/07420528.2012.754450openalex-snapshot
Photoperiodic Variation in CD45-Positive Cells and Cell Proliferation in the Mediobasal Hypothalamus of the Soay Sheep
inferredcites →https://doi.org/10.3109/07420528.2013.852104openalex-snapshot
2-Arachidonoyl glycerol sensitizes the pars distalis and enhances forskolin-stimulated prolactin secretion in Syrian hamsters
inferredcites →https://doi.org/10.3389/fendo.2014.00019openalex-snapshot
Thyroid Hormone and Seasonal Rhythmicity
inferredcites →https://doi.org/10.3389/fendo.2018.00662openalex-snapshot
How to Contribute to the Progress of Neuroendocrinology: Discovery of GnIH and Progress of GnIH Research
inferredcites →https://doi.org/10.3389/fendo.2019.00183openalex-snapshot
Functional Implications of RFRP-3 in the Central Control of Daily and Seasonal Rhythms in Reproduction
inferredcites →https://doi.org/10.3389/fneur.2017.00079openalex-snapshot
Tanycytes As Regulators of Seasonal Cycles in Neuroendocrine Function
inferredcites →https://doi.org/10.3389/fnins.2014.00115openalex-snapshot
Universality and diversity in the signal transduction pathway that regulates seasonal reproduction in vertebrates
inferredcites →https://doi.org/10.3389/fnins.2015.00387openalex-snapshot
Hypothalamic tanycytes—masters and servants of metabolic, neuroendocrine, and neurogenic functions
inferredcites →https://doi.org/10.7554/elife.02439openalex-snapshot
Distinct and separable roles for EZH2 in neurogenic astroglia
inferredcites →https://doi.org/10.7554/elife.35656openalex-snapshot
Estrogenic-dependent glutamatergic neurotransmission from kisspeptin neurons governs feeding circuits in females

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4017417openalex-extracted
The Effect of Month and Breed on Plasma Acth Concentrations in Equids
inferred← citeshttps://doi.org/10.1002/2211-5463.13350openalex-snapshot
Comparative transcriptomics of the Djungarian hamster hypothalamus during short photoperiod acclimation and spontaneous torpor
inferred← citeshttps://doi.org/10.1002/9781119709268.rook087openalex-snapshot
Acquired Disorders of Hair
inferred← citeshttps://doi.org/10.1002/jez.2666openalex-snapshot
Evolution in reproductive tempo and investment across the Peromyscus radiation
inferred← citeshttps://doi.org/10.1002/jnr.24606openalex-snapshot
Circadian rhythms in the mouse reproductive axis during the estrous cycle and pregnancy
inferred← citeshttps://doi.org/10.1002/mnfr.202300035openalex-snapshot
Photoperiod‐Dependent Effects of Grape‐Seed Proanthocyanidins on Adipose Tissue Metabolic Markers in Healthy Rats
inferred← citeshttps://doi.org/10.1007/7854_2019_115openalex-snapshot
Circadian Regulation of the Brain and Behavior: A Neuroendocrine Perspective
inferred← citeshttps://doi.org/10.1007/s00359-023-01677-zopenalex-snapshot
A clock for all seasons in the subterranean
inferred← citeshttps://doi.org/10.1007/s00359-026-01844-yopenalex-snapshot
Conserved communication between the pars tuberalis and mediobasal hypothalamus in the Golden hamster and Svalbard ptarmigan: a genome enabled ligand-receptor pairing analysis
inferred← citeshttps://doi.org/10.1007/s00360-020-01280-7openalex-snapshot
Predictive and reactive changes in antioxidant defence system in a heterothermic rodent
inferred← citeshttps://doi.org/10.1007/s00360-025-01636-xopenalex-snapshot
Perspective: rheostasis revisited—hibernation and tanycytes
inferred← citeshttps://doi.org/10.1007/s00360-026-01700-0openalex-snapshot
Seasonal fluctuations in the hypothalamic irisin and its correlation with the hypothalamic-pituitary-gonadal -axis activity in male rhesus monkeys (Macaca mulatta)
inferred← citeshttps://doi.org/10.1007/s00418-022-02079-zopenalex-snapshot
Seasonal vascular plasticity in the mediobasal hypothalamus of the adult ewe
inferred← citeshttps://doi.org/10.1007/s00441-023-03799-xopenalex-snapshot
Unique morphology and photoperiodically regulated activity of neurosecretory canopy cells in the pond snail Lymnaea stagnalis
inferred← citeshttps://doi.org/10.1007/s10142-025-01562-9openalex-snapshot
Transcriptome analysis of the hypothalamus and testes in Brandt’s Vole: new insights into mechanisms of photoperiodic plasticity in postnatal testicular development
inferred← citeshttps://doi.org/10.1007/s10641-024-01645-9openalex-snapshot
Effect of photoperiod on the anxiety of zebrafish
inferred← citeshttps://doi.org/10.1016/b978-0-12-819975-6.00021-2openalex-snapshot
Melatonin and the circadian system: Keys for health with a focus on sleep
inferred← citeshttps://doi.org/10.1016/b978-0-12-820093-3.00004-6openalex-snapshot
Organization of the mammalian hypothalamus-pituitary axes
inferred← citeshttps://doi.org/10.1016/b978-0-12-820107-7.00015-xopenalex-snapshot
Arcuate nucleus, median eminence, and hypophysial pars tuberalis
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.02.005openalex-snapshot
Thyroid hormone and hypothalamic stem cells in seasonal functions
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.02.009openalex-snapshot
Thyroid hormone regulation of adult neural stem cell fate: A comparative analysis between rodents and primates
inferred← citeshttps://doi.org/10.1016/j.anbehav.2023.08.007openalex-snapshot
Early life events, but not response to a short photoperiod, correlate with foraging behaviour of Siberian hamsters
inferred← citeshttps://doi.org/10.1016/j.animal.2025.101508openalex-snapshot
CRISPR-Cas9 gene-editing to assess the role of RF-amide−related peptide 3 in ovine seasonal breeding
inferred← citeshttps://doi.org/10.1016/j.brainres.2020.146725openalex-snapshot
Effect of postnatal photoperiod on DNA methylation dynamics in the mouse brain
inferred← citeshttps://doi.org/10.1016/j.coemr.2020.01.001openalex-snapshot
Endocrine drivers of photoperiod response
inferred← citeshttps://doi.org/10.1016/j.cveq.2026.07.006openalex-snapshot
The Influence of Season on Endocrine Testing in Equids
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2024.103811openalex-snapshot
Warm spells in winter affect the equilibrium between winter phenotypes
inferred← citeshttps://doi.org/10.1016/j.mce.2019.110687openalex-snapshot
Temporal organization of pineal melatonin signaling in mammals
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110825openalex-snapshot
Circuit-level analysis identifies target genes of sex steroids in ewe seasonal breeding
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110876openalex-snapshot
Pleiotropic effects of proopiomelanocortin and VGF nerve growth factor inducible neuropeptides for the long-term regulation of energy balance
inferred← citeshttps://doi.org/10.1016/j.mce.2024.112216openalex-snapshot
Photoperiod, but not progesterone, has a strong impact upon the transcriptome of the medio-basal hypothalamus in female goats and ewes
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2025.106403openalex-snapshot
Concerning the circadian rhythms of prolactin, its secretion timing, and regulation of the affiliative mind
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2025.121494openalex-snapshot
How the brain adapts to nature's rhythms: a year of neuroimaging in a seasonal mammal
inferred← citeshttps://doi.org/10.1016/j.tem.2025.10.005openalex-snapshot
Tanycytes: bloodhounds of the metabolic brain
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.08.031openalex-snapshot
No evidence that Spexin impacts LH release and seasonal breeding in the ewe
inferred← citeshttps://doi.org/10.1016/j.tvjl.2022.105857openalex-snapshot
The effect of month and breed on plasma adrenocorticotropic hormone concentrations in equids
inferred← citeshttps://doi.org/10.1016/j.ygcen.2020.113620openalex-snapshot
Central and peripheral actions of melatonin on reproduction in seasonal and continuous breeding mammals
inferred← citeshttps://doi.org/10.1016/j.ygcen.2021.113853openalex-snapshot
Field study reveals morphological and neuroendocrine correlates of seasonal breeding in female water voles, Arvicola terrestris
inferred← citeshttps://doi.org/10.1016/j.yhbeh.2022.105215openalex-snapshot
A cross-taxonomic perspective on the integration of temperature cues in vertebrate seasonal neuroendocrine pathways
inferred← citeshttps://doi.org/10.1038/s41398-021-01494-5openalex-snapshot
Enlightened: addressing circadian and seasonal changes in photoperiod in animal models of bipolar disorder
inferred← citeshttps://doi.org/10.1038/s41467-020-18061-zopenalex-snapshot
Circadian clock mechanism driving mammalian photoperiodism
inferred← citeshttps://doi.org/10.1038/s41559-020-01356-1openalex-snapshot
Seasonal variation in UVA light drives hormonal and behavioural changes in a marine annelid via a ciliary opsin
inferred← citeshttps://doi.org/10.1038/s41598-025-27059-wopenalex-snapshot
Non-seasonal breeding appears dominant with incomplete penetrance in Australian Basenji dogs
inferred← citeshttps://doi.org/10.1071/an19418openalex-snapshot
Animal responses to environmental variation: physiological mechanisms in ecological models of performance in deer (Cervidae)
inferred← citeshttps://doi.org/10.1080/07420528.2023.2288223openalex-snapshot
SAD rats: Effects of short photoperiod and carbohydrate consumption on sleep, liver steatosis, and the gut microbiome in diurnal grass rats
inferred← citeshttps://doi.org/10.1080/09291016.2026.2720341openalex-snapshot
Photoperiodic regulation of reproduction in livestock: chronobiological mechanisms, management implications and future perspectives
inferred← citeshttps://doi.org/10.1080/26895293.2024.2393847openalex-snapshot
Cashmere cyclic growth affected by different photoperiods alters DNA methylation patterns
inferred← citeshttps://doi.org/10.1093/icb/icac035openalex-snapshot
Sex-Differences in Phenology: A Tinbergian Perspective
inferred← citeshttps://doi.org/10.1093/icb/icac064openalex-snapshot
Revisiting TSHβ’s Role in Avian Seasonal Reproduction, Insights, and Challenges from Mammalian Models
inferred← citeshttps://doi.org/10.1093/icb/icac121openalex-snapshot
Vertebrate Phenological Plasticity: From Molecular Mechanisms to Ecological and Evolutionary Implications
inferred← citeshttps://doi.org/10.1096/fj.202000961ropenalex-snapshot
Thyroid hormone receptors are required for the melatonin‐dependent control of Rfrp gene expression in mice
inferred← citeshttps://doi.org/10.1096/fj.202100162ropenalex-snapshot
Mechanisms of temperature modulation in mammalian seasonal timing
inferred← citeshttps://doi.org/10.1098/rspb.2025.1611openalex-snapshot
The fish pituitary directly responds to daylength and drives seasonality
inferred← citeshttps://doi.org/10.1101/2021.01.20.427447openalex-snapshot
Food and temperature change photoperiodic responses in two vole species: different roles for hypothalamic genes
inferred← citeshttps://doi.org/10.1101/2025.11.06.687099openalex-snapshot
Splicing of a core clock gene regulates seasonal adaptations by a winter gating mechanism
inferred← citeshttps://doi.org/10.1111/1749-4877.12613openalex-snapshot
Hibernation with rhythmicity: the circadian clock and hormonal adaptations of the hibernating Asiatic toads (Bufo gargarizans)
inferred← citeshttps://doi.org/10.1111/age.13138openalex-snapshot
Combined approaches identify known and novel genes associated with sheep litter size and non‐seasonal breeding
inferred← citeshttps://doi.org/10.1111/brv.12959openalex-snapshot
Programmed ageing: decline of stem cell renewal, immunosenescence, and Alzheimer's disease
inferred← citeshttps://doi.org/10.1111/exd.14130openalex-snapshot
Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
inferred← citeshttps://doi.org/10.1111/jnc.15218openalex-snapshot
Tanycytes: Gateway to the hungry brain
inferred← citeshttps://doi.org/10.1111/jne.12775openalex-snapshot
Discontinuity in the molecular neuroendocrine response to increasing daylengths in Ile‐de‐France ewes: Is transient Dio2 induction a key feature of circannual timing?
inferred← citeshttps://doi.org/10.1111/jne.13124openalex-snapshot
GnRH and the photoperiodic control of seasonal reproduction: Delegating the task to kisspeptin and RFRP ‐3
inferred← citeshttps://doi.org/10.1111/jne.13198openalex-snapshot
Impact of food restriction on the medio‐basal hypothalamus of intact ewes as revealed by a large‐scale transcriptomics study
inferred← citeshttps://doi.org/10.1111/jpi.12711openalex-snapshot
Photoperiod integration in C3H rd1 mice
inferred← citeshttps://doi.org/10.1111/jpi.12996openalex-snapshot
Melatonin and Seasonal Synchrony in Mammals
inferred← citeshttps://doi.org/10.1111/mec.16467openalex-snapshot
Differential temperature effects on photoperiodism in female voles: A possible explanation for declines in vole populations
inferred← citeshttps://doi.org/10.1126/sciadv.aed4249openalex-snapshot
Splicing of a core circadian clock gene regulates seasonal adaptations by a winter gating mechanism
inferred← citeshttps://doi.org/10.1134/s0006297921100126openalex-snapshot
Comparative Analysis and Identification of Differentially Expressed microRNAs in the Hypothalamus of Kazakh Sheep Exposed to Different Photoperiod Conditions
inferred← citeshttps://doi.org/10.1139/cjz-2024-0180openalex-snapshot
Altered gene expression related to fuel use and sensory capacity in tanycytes throughout the hibernation season in the golden hamster
inferred← citeshttps://doi.org/10.1146/annurev-vision-100820-094018openalex-snapshot
An Expanding Role for Nonvisual Opsins in Extraocular Light Sensing Physiology
inferred← citeshttps://doi.org/10.1159/000526188openalex-snapshot
Mapping the Pattern of Essential Neuroendocrine Cells Related to Puberty and VA Opsin Expression Provides Further Insight in the Photoreceptive Regulation of the Brain-Pituitary-Gonadal Axis in Atlantic Salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1177/07487304221085105openalex-snapshot
Daylength Shapes Entrainment Patterns to Artificial Photoperiods in a Subterranean Rodent
inferred← citeshttps://doi.org/10.1186/s12711-024-00910-wopenalex-snapshot
Integration of selective sweeps across the sheep genome: understanding the relationship between production and adaptation traits
inferred← citeshttps://doi.org/10.1186/s12862-025-02440-5openalex-snapshot
Functional mutations in the thyroid-stimulating hormone receptor in natural stickleback populations at sites identical to human disease-causing mutations
inferred← citeshttps://doi.org/10.1186/s12983-021-00391-3openalex-snapshot
Polymorphism of winter phenotype in Siberian hamster: consecutive litters do not differ in photoresponsiveness but prolonged acclimation to long photoperiod inhibits winter molt
inferred← citeshttps://doi.org/10.1210/endocr/bqad076openalex-snapshot
Novel Candidate Regulators and Developmental Trajectory of Pituitary Thyrotropes
inferred← citeshttps://doi.org/10.1242/jeb.230987openalex-snapshot
Gonads or body? Differences in gonadal and somatic photoperiodic growth response in two vole species
inferred← citeshttps://doi.org/10.1242/jeb.242792openalex-snapshot
Photoperiod is involved in the regulation of seasonal breeding in male water voles (Arvicola terrestris)
inferred← citeshttps://doi.org/10.1242/jeb.243030openalex-snapshot
Food and temperature change photoperiodic responses in two vole species
inferred← citeshttps://doi.org/10.1242/jeb.247224openalex-snapshot
c-fos induction in the choroid plexus, tanycytes and pars tuberalis is an early indicator of spontaneous arousal from torpor in a deep hibernator
inferred← citeshttps://doi.org/10.1242/jeb.250390openalex-snapshot
Polyphenisms in the reproductive response of male quail to short days are driven by testosterone-independent uncoupling in the photoperiodic TSH-DIO2/DIO3 pathway
inferred← citeshttps://doi.org/10.1242/jeb.251702openalex-snapshot
Continuous sampling of cerebrospinal fluid from the third ventricle of the hypothalamus to identify accumulating or depleting metabolites during hibernation
inferred← citeshttps://doi.org/10.1371/journal.pone.0309591openalex-snapshot
Seasonal changes in activity of hypothalamic thyroid hormone system in different winter phenotypes of Djungarian hamster (Phodopus sungorus)
inferred← citeshttps://doi.org/10.1530/biosciprocs.10.006openalex-snapshot
Models of embryonic diapause in Carnivora
inferred← citeshttps://doi.org/10.1530/joe-19-0302openalex-snapshot
Direct effects of the light environment on daily neuroendocrine control
inferred← citeshttps://doi.org/10.1530/joe-19-0502openalex-snapshot
What can seasonal models teach us about energy balance?
inferred← citeshttps://doi.org/10.18502/ijrm.v13i11.7967openalex-snapshot
The effect of seasonality on reproductive outcome of patients undergoing intracytoplasmic sperm injection: A descriptive cross-sectional study
inferred← citeshttps://doi.org/10.22541/au.164864478.83493348/v1openalex-snapshot
Food and temperature change photoperiodic responses in two vole species: different roles for Tshβ, Kisspeptin and Rfrp3
inferred← citeshttps://doi.org/10.29261/pakvetj/2023.051openalex-snapshot
Age-Related Gross and Histomorphometrical Dynamics of Pineal Gland (Epiphysis cereberi) Associated with Melatonin Profile in Beetal Goat (Capra aegagrus hircus) of Pakistan
inferred← citeshttps://doi.org/10.31857/s0320972521100122openalex-snapshot
Сравнительный анализ и идентификация дифференциально экспрессируемых микроРНК в гипоталамусе овец казахской породы, помещенных в различные фотопериодические условия
inferred← citeshttps://doi.org/10.32604/biocell.2023.044630openalex-snapshot
The regulatory role of melatonin in pituitary thyroid-stimulating hormone synthesis through casein kinase 1α
inferred← citeshttps://doi.org/10.3389/fendo.2019.00401openalex-snapshot
Tanycytes and the Control of Thyrotropin-Releasing Hormone Flux Into Portal Capillaries
inferred← citeshttps://doi.org/10.3389/fendo.2019.00901openalex-snapshot
Maternal Photoperiodic Programming: Melatonin and Seasonal Synchronization Before Birth
inferred← citeshttps://doi.org/10.3389/fendo.2020.00303openalex-snapshot
Hypothalamic–Pituitary–Thyroid Axis Crosstalk With the Hypothalamic–Pituitary–Gonadal Axis and Metabolic Regulation in the Eurasian Tree Sparrow During Mating and Non-mating Periods
inferred← citeshttps://doi.org/10.3389/fendo.2020.603538openalex-snapshot
Differential Regulation of the Expression of the Two Thyrotropin Beta Subunit Paralogs by Salmon Pituitary Cells In Vitro
inferred← citeshttps://doi.org/10.3389/fendo.2020.605111openalex-snapshot
Effects of Melatonin on Anterior Pituitary Plasticity: A Comparison Between Mammals and Teleosts
inferred← citeshttps://doi.org/10.3389/fendo.2021.731966openalex-snapshot
Unconventional Actions of Glycoprotein Hormone Subunits: A Comprehensive Review
inferred← citeshttps://doi.org/10.3389/fendo.2022.974518openalex-snapshot
Photoperiods induced the circRNA differential expression in the thyroid gland of OVX+E2 ewes
inferred← citeshttps://doi.org/10.3389/fendo.2026.1794734openalex-snapshot
The cAMP signaling pathway mediates photoperiod-induced follicle development in striped hamsters (Cricetulus barabensis) supported by association analyses
inferred← citeshttps://doi.org/10.3389/fevo.2021.735487openalex-snapshot
Interdependence of Thyroid and Corticosteroid Signaling in Vertebrate Developmental Transitions
inferred← citeshttps://doi.org/10.3389/fnins.2025.1589156openalex-snapshot
The ventral premammillary nucleus at the interface of environmental cues and social behaviors
inferred← citeshttps://doi.org/10.3389/fphys.2020.623665openalex-snapshot
The Torpid State: Recent Advances in Metabolic Adaptations and Protective Mechanisms†
inferred← citeshttps://doi.org/10.3389/fphys.2021.738471openalex-snapshot
Telling the Seasons Underground: The Circadian Clock and Ambient Temperature Shape Light Exposure and Photoperiodism in a Subterranean Rodent
inferred← citeshttps://doi.org/10.3389/fphys.2022.785706openalex-snapshot
Seasonality in Biological Rhythms in Scandinavian brown Bears
inferred← citeshttps://doi.org/10.3390/ani15010011openalex-snapshot
The Response of the miRNA Profiles of the Thyroid Gland to the Artificial Photoperiod in Ovariectomized and Estradiol-Treated Ewes
inferred← citeshttps://doi.org/10.3390/antiox13010072openalex-snapshot
Cherries with Different Geographical Origins Regulate Neuroprotection in a Photoperiod-Dependent Manner in F344 Rats
inferred← citeshttps://doi.org/10.3390/genes13040606openalex-snapshot
Transcriptome Analysis Revealed Long Non-Coding RNAs Associated with mRNAs in Sheep Thyroid Gland under Different Photoperiods
inferred← citeshttps://doi.org/10.3390/ijms24021008openalex-snapshot
Photoperiodic Remodeling of Adiposity and Energy Metabolism in Non-Human Mammals
inferred← citeshttps://doi.org/10.3390/ijms241713255openalex-snapshot
Brain Dopamine–Clock Interactions Regulate Cardiometabolic Physiology: Mechanisms of the Observed Cardioprotective Effects of Circadian-Timed Bromocriptine-QR Therapy in Type 2 Diabetes Subjects
inferred← citeshttps://doi.org/10.5772/intechopen.88766openalex-snapshot
Heart Rate Variability as Biomarker for Prognostic of Metabolic Disease
inferred← citeshttps://doi.org/10.5935/1984-0063.20200005openalex-snapshot
XV Latin-American Symposium on Chronobiology
inferred← citeshttps://doi.org/10.5935/1984-0063.20200006openalex-snapshot
Circadian modulation of motivation-related behavior
inferred← citeshttps://doi.org/10.5935/1984-0063.20200007openalex-snapshot
From the ruler to the smartphone tasks applied to identify sleep deprivation
inferred← citeshttps://doi.org/10.5935/1984-0063.20200008openalex-snapshot
The effect of pubertal development on the sleep-wake cycle
inferred← citeshttps://doi.org/10.5935/1984-0063.20200009openalex-snapshot
Shift work-related health problems: causes, effects, and light-based interventions
inferred← citeshttps://doi.org/10.5935/1984-0063.20200010openalex-snapshot
The impact of training shifts in dancers’ chronotype and sleep patterns
inferred← citeshttps://doi.org/10.5935/1984-0063.20200011openalex-snapshot
Characterization of the circadian expression profile of clock genes in Aag2 cell line infected and uninfected by Dengue 2 virus (DENV2)
inferred← citeshttps://doi.org/10.5935/1984-0063.20200012openalex-snapshot
Social modulation on daily variability in electric behavior
inferred← citeshttps://doi.org/10.5935/1984-0063.20200013openalex-snapshot
Electrocortical temporal complexity during wakefulness and sleep: an updated account
inferred← citeshttps://doi.org/10.5935/1984-0063.20200014openalex-snapshot
Fetal programming of adipose tissue function by gestational chronodisruption
inferred← citeshttps://doi.org/10.5935/1984-0063.20200015openalex-snapshot
Annual variation of daily activity patterns and its dependence on photoperiod: a quick overview
inferred← citeshttps://doi.org/10.5935/1984-0063.20200016openalex-snapshot
Different latitude influences the habitat and reproductive patterns of Pinnipeds
inferred← citeshttps://doi.org/10.5935/1984-0063.20200018openalex-snapshot
Chikungunya infection modulates the locomotor/flight activity of Aedes aegypti
inferred← citeshttps://doi.org/10.5935/1984-0063.20200019openalex-snapshot
Sleep and maternal behavior in the postpartum rat after haloperidol and midazolam treatments
inferred← citeshttps://doi.org/10.5935/1984-0063.20200020openalex-snapshot
Chronobiology in the wild: toolkit to study daily rhythms in free-living animals
inferred← citeshttps://doi.org/10.5935/1984-0063.20200021openalex-snapshot
What, how and (especially) when: chronoparmacological approach in cancer therapies
inferred← citeshttps://doi.org/10.70675/2422e4e4ze082z46d5z917dzee728d3ee71dopenalex-snapshot
Integrating reproduction and energy metabolism : a round way trip via RF-amide peptides
inferred← citeshttps://doi.org/10.70675/6d5212ddzd1fcz4605z9e7az0c9212990874openalex-snapshot
Régulation saisonnière de la plasticité cellulaire de l'hypothalamus mediobasal chez la brebis
inferred← citeshttps://doi.org/10.70675/754567e3z7b5dz421ezbbf3z0c0e80ec28beopenalex-snapshot
Rôle de la rétine dans les fonctions non-visuelles : traitement des informations relatives à la photopériode et impact de la lumière bleue sur le comportement.
inferred← citeshttps://doi.org/10.70675/7ed6cd19zbb1ez457cz8a6fz6be68cc17460openalex-snapshot
Régulations saisonnière et olfactive de la reproduction chez le campagnol terrestre (Arvicola terrestris)
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