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Role of norepinephrine in the regulation of rapid eye movement sleep
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Outgoing claims: the papers this work cites, builds on, or argues with.
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A Review of REM Sleep Deprivation
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Subregional organization of preoptic area /anterior hypothalamic projections to arousal-related monoaminergic cell groups
inferredcites →https://doi.org/10.1002/aja.1001810106openalex-snapshot
Immunocytochemical study using a GABA antiserum for the demonstration of inhibitory neurons in the rat locus ceruleus
inferredcites →https://doi.org/10.1002/cne.901570105openalex-snapshot
Catecholamine‐containing neurons of the nucleus locus coeruleus in the cat
inferredcites →https://doi.org/10.1002/cne.902950311openalex-snapshot
Immunohistochemical study of choline acetyltransferase‐immunoreactive processes and cells innervating the pontomedullary reticular formation in the rat
inferredcites →https://doi.org/10.1002/neu.480050605openalex-snapshot
Activity patterns of catecholamine‐containing pontine neurons in the dorso‐lateral tegmentum of unrestrained cats
inferredcites →https://doi.org/10.1002/syn.1109openalex-snapshot
GABAergic neurons in prepositus hypoglossi regulate REM sleep by its action on locus coeruleus in freely moving rats
inferredcites →https://doi.org/10.1007/3-540-05462-6_2openalex-snapshot
The role of monoamines and acetylcholine-containing neurons in the regulation of the sleep-waking cycle
inferredcites →https://doi.org/10.1007/978-1-4757-4669-3openalex-snapshot
Brainstem Control of Wakefulness and Sleep
inferredcites →https://doi.org/10.1007/978-3-540-68706-1_1483openalex-snapshot
Rapid Eye Movement Sleep
inferredcites →https://doi.org/10.1007/bf00431640openalex-snapshot
Effet de la chlorimipramine sur l'activit� de pointes �Ponto-G�niculo-Occipitales� (PGO) du babouin Papio hamadryas
inferredcites →https://doi.org/10.1007/s004210100383openalex-snapshot
REM sleep and catecholamine excretion: a study in elite athletes
inferredcites →https://doi.org/10.1016/0006-8993(69)90285-6openalex-snapshot
Differential effects of sodium butyrate and physostigmine upon the activities of para-sleep in acute brain stem preparations
inferredcites →https://doi.org/10.1016/0006-8993(75)90369-8openalex-snapshot
Sleep cycle control and cholinergic mechanisms: Differential effects of carbachol injections at pontine brain stem sites
inferredcites →https://doi.org/10.1016/0006-8993(77)90083-xopenalex-snapshot
Evidence for norepinephrine-mediated collateral inhibition of locus coeruleus neurons
inferredcites →https://doi.org/10.1016/0006-8993(77)90948-9openalex-snapshot
Effects of locus coeruleus lesions upon cerebral monoamine content, sleep-wakefulness states and the response to amphetamine in the cat
inferredcites →https://doi.org/10.1016/0006-8993(79)91072-2openalex-snapshot
Effects of intraventricular injection of 6-hydroxydopamine in the developing kitten. 1. On the sleepwaking cycles
inferredcites →https://doi.org/10.1016/0006-8993(81)90397-8openalex-snapshot
Effects of locus coeruleus lesions upon sleeping and waking in the rabbit
inferredcites →https://doi.org/10.1016/0006-8993(81)90752-6openalex-snapshot
Are the gigantocellular tegmental field neurons responsible for paradoxical sleep?
inferredcites →https://doi.org/10.1016/0006-8993(82)91252-5openalex-snapshot
Slow rhythmic rate fluctuations of cat midbrain reticular neurons in synchronized sleep and waking
inferredcites →https://doi.org/10.1016/0006-8993(83)90590-5openalex-snapshot
Kainic acid lesions of gigantocellular tegmental field (FTG) neurons does not abolish REM sleep
inferredcites →https://doi.org/10.1016/0006-8993(84)90354-8openalex-snapshot
Site-specific enhancement and suppression of desynchronized sleep signs following cholinergic stimulation of three brainstem regions
inferredcites →https://doi.org/10.1016/0006-8993(86)90137-xopenalex-snapshot
Pontine neuronal response to local cholinergic infusion: Relation to REM sleep
inferredcites →https://doi.org/10.1016/0006-8993(86)90288-xopenalex-snapshot
Correlational analysis of central noradrenergic neuronal activity and sympathetic tone in behaving cats
inferredcites →https://doi.org/10.1016/0006-8993(90)90581-uopenalex-snapshot
Changes in pontine unit activity with REM sleep deprivation
inferredcites →https://doi.org/10.1016/0006-8993(91)90100-aopenalex-snapshot
REM sleep deprivation reduces auditory evoked inhibition of dorsolateral pontine neurons
inferredcites →https://doi.org/10.1016/0006-8993(91)91064-8openalex-snapshot
Cholinergic antagonists and REM sleep generation
inferredcites →https://doi.org/10.1016/0006-8993(96)00256-9openalex-snapshot
Chronic low-amplitude electrical stimulation of the laterodorsal tegmental nucleus of freely moving cats increases REM sleep
inferredcites →https://doi.org/10.1016/0013-4694(82)90042-6openalex-snapshot
Alterations in the sleep-waking cycle induced by cooling of the locus coeruleus area
inferredcites →https://doi.org/10.1016/0013-4694(84)90007-5openalex-snapshot
Study of sleep-wakefulness states by computer graphics and cluster analysis before and after lesions of the pontine tegmentum in the cat
inferredcites →https://doi.org/10.1016/0013-4694(86)90095-7openalex-snapshot
Behavioral states in the chronic medullary and midpontine cat
inferredcites →https://doi.org/10.1016/0014-2999(80)90346-5openalex-snapshot
Prazosin increases paradoxical sleep
inferredcites →https://doi.org/10.1016/0014-2999(84)90048-7openalex-snapshot
Sleep: Neurotransmitters and neuromodulators
inferredcites →https://doi.org/10.1016/0014-2999(88)90061-1openalex-snapshot
GABAA and GABAB receptors in locus coeruleus: effects of blockers
inferredcites →https://doi.org/10.1016/0091-3057(83)90272-1openalex-snapshot
Dopamine metabolism and receptor sensitivity in rat brain after REM sleep deprivation
inferredcites →https://doi.org/10.1016/0091-3057(91)90424-zopenalex-snapshot
Effect of REM sleep deprivation on rat brain acetylcholinesterase
inferredcites →https://doi.org/10.1016/0091-3057(93)90251-nopenalex-snapshot
Rapid eye movement sleep deprivation increases chloride-sensitive Mg-ATPase activity in the rat brain
inferredcites →https://doi.org/10.1016/0149-7634(94)00043-zopenalex-snapshot
Neuronal activity in the peribrachial area: Relationship to behavioral state control
inferredcites →https://doi.org/10.1016/0168-0102(95)00998-1openalex-snapshot
Mild electrical stimulation of pontine tegmentum around locus coeruleus reduces rapid eye movement sleep in rats
inferredcites →https://doi.org/10.1016/0168-0102(95)93696-yopenalex-snapshot
Rapid eye movement sleep deprivation decreases membrane fluidity in the rat brain
inferredcites →https://doi.org/10.1016/0169-328x(94)00253-bopenalex-snapshot
Localization of NMDA receptor subunit mRNAs in the rat locus coeruleus
inferredcites →https://doi.org/10.1016/0169-328x(94)90135-xopenalex-snapshot
Localization of GABAA receptor subunit mRNAs in the rat locus coeruleus
inferredcites →https://doi.org/10.1016/0301-0082(86)90008-0openalex-snapshot
Single unit activity of locus coeruleus neurons in behaving animals
inferredcites →https://doi.org/10.1016/0304-3940(79)91508-8openalex-snapshot
Elimination of paradoxical sleep by lesions of the pontine gigantocellular tegmental field in the cat
inferredcites →https://doi.org/10.1016/0304-3940(90)90576-uopenalex-snapshot
Enhancement of acetylcholine release during paradoxical sleep in the dorsal tegmental field of the cat brain stem
inferredcites →https://doi.org/10.1016/0304-3940(91)90401-eopenalex-snapshot
Short-term REM sleep deprivation increases acetylcholinesterase activity in the medulla of rats
inferredcites →https://doi.org/10.1016/0306-4522(86)90280-0openalex-snapshot
Autoradiographic localization of M1 and M2 muscarine receptors in the rat brain
inferredcites →https://doi.org/10.1016/0306-4522(86)90281-2openalex-snapshot
Actions of acetylcholine and nicotine on rat locus coeruleus neurons in vitro
inferredcites →https://doi.org/10.1016/0306-4522(91)90002-6openalex-snapshot
Paradoxical sleep and its chemical/structural substrates in the brain
inferredcites →https://doi.org/10.1016/0306-4522(93)90433-gopenalex-snapshot
Effect of rapid eye movement sleep deprivation on rat brain monoamine oxidases
inferredcites →https://doi.org/10.1016/0306-4522(94)00333-zopenalex-snapshot
Possible mechanism of rapid eye movement sleep deprivation induced increase in NaK ATPase activity
inferredcites →https://doi.org/10.1016/0306-4522(94)00481-jopenalex-snapshot
Afferent projections to the rat locus coeruleus demonstrated by retrograde and anterograde tracing with cholera-toxin B subunit and Phaseolus vulgaris leucoagglutinin
inferredcites →https://doi.org/10.1016/0306-4522(96)00177-7openalex-snapshot
Alterations in synaptosomal calcium concentrations after rapid eye movement sleep deprivation in rats
inferredcites →https://doi.org/10.1016/0361-9230(80)90184-7openalex-snapshot
Acetylcholinesterase and catecholamine distribution in the locus ceruleus of the rat
inferredcites →https://doi.org/10.1016/0361-9230(86)90019-5openalex-snapshot
Comparison of rostro-caudal brain stem influence on preoptic neurons and cortical EEG
inferredcites →https://doi.org/10.1016/s0006-8993(00)02013-8openalex-snapshot
Monoamines and sleep: microdialysis findings in pons and amygdala
inferredcites →https://doi.org/10.1016/s0079-6123(08)63799-1openalex-snapshot
Afferent regulation of locus coeruleus neurons: anatomy, physiology and pharmacology
inferredcites →https://doi.org/10.1016/s0079-6123(08)63833-9openalex-snapshot
Effects of local pontine injection of noradrenergic agents on desynchronized sleep of the cat
inferredcites →https://doi.org/10.1016/s0168-0102(99)00013-9openalex-snapshot
Role of GABA-A receptor in the preoptic area in the regulation of sleep–wakefulness and rapid eye movement sleep
inferredcites →https://doi.org/10.1016/s0169-328x(98)00088-6openalex-snapshot
REM sleep deprivation increases the levels of tyrosine hydroxylase and norepinephrine transporter mRNA in the locus coeruleus
inferredcites →https://doi.org/10.1016/s0197-0186(99)00025-xopenalex-snapshot
Norepinephrine induced alpha-adrenoceptor mediated increase in rat brain Na-K ATPase activity is dependent on calcium ion
inferredcites →https://doi.org/10.1016/s0197-0186(99)00121-7openalex-snapshot
Uncompetitive stimulation of rat brain Na-K ATPase activity by rapid eye movement sleep deprivation
inferredcites →https://doi.org/10.1016/s0304-3940(97)13410-3openalex-snapshot
GABA in locus coeruleus regulates spontaneous rapid eye movement sleep by acting on GABAA receptors in freely moving rats
inferredcites →https://doi.org/10.1016/s0306-4522(01)00062-8openalex-snapshot
Interactions between cholinergic and GABAergic neurotransmitters in and around the locus coeruleus for the induction and maintenance of rapid eye movement sleep in rats
inferredcites →https://doi.org/10.1016/s0306-4522(96)00549-0openalex-snapshot
GABA release in the locus coeruleus as a function of sleep/wake state
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Cholinergic and non-cholinergic afferents of the caudolateral parabrachial nucleus: a role in the long-term enhancement of rapid eye movement sleep
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Role of wake inducing brain stem area on rapid eye movement sleep regulation in freely moving cats
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Identification of sleep-promoting neurons in vitro
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Electrophysiological evidence that noradrenergic neurons of the rat locus coeruleus are tonically inhibited by GABA during sleep
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Norepinephrine‐Stimulated Increase in Na+,K+‐ATPaseActivity in the Rat Brain Is Mediated Throughα1A‐Adrenoceptor Possibly by Dephosphorylation of the Enzyme
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Sleep Deprivation in the Rat: V. Energy Use and Mediation
inferredcites →https://doi.org/10.1093/sleep/20.9.757openalex-snapshot
Contributions of the Pedunculopontine Region to Normal and Altered REM Sleep
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Effects of Methoxamine and a-Adrenoceptor Antagonists, Prazosin and Yohimbine, on the Sleep-Wake Cycle of the Rat
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Effect of REM sleep deprivation on molecular forms of acetylcholinesterase in rats
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Localization of muscarinic receptor subtypes in brain stem areas regulating sleep
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Alpha-2 adrenoceptor mediated paradoxical (REM) sleep inhibition in the cat
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BRAIN MECHANISMS OF SLEEP
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Effect of rapid eye movement sleep deprivation on rat brain Na‐K ATPase activity
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THE RETICULAR FORMATION REVISITED
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Tyrosine hydroxylase activity in rat brain following “REM” sleep deprivation
inferredcites →https://doi.org/10.1126/science.1094539openalex-snapshot
Sleep Cycle Oscillation: Reciprocal Discharge by Two Brainstem Neuronal Groups
inferredcites →https://doi.org/10.1126/science.1135627openalex-snapshot
Neuronal excitability modulation over the sleep cycle: a structural and mathematical model
inferredcites →https://doi.org/10.1126/science.118.3062.273openalex-snapshot
Regularly Occurring Periods of Eye Motility, and Concomitant Phenomena, During Sleep
inferredcites →https://doi.org/10.1126/science.159.3810.112openalex-snapshot
Increased Turnover of Cerebral Norepinephrine during Rebound of Paradoxical Sleep in the Rat
inferredcites →https://doi.org/10.1126/science.274.5290.1211openalex-snapshot
Neuronal Gene Expression in the Waking State: A Role for the Locus Coeruleus
inferredcites →https://doi.org/10.1126/science.3775363openalex-snapshot
The Brain Nucleus Locus Coeruleus: Restricted Afferent Control of a Broad Efferent Network
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Central Catecholamine Neuron Systems: Anatomy and Physiology of the Norepinephrine and Epinephrine Systems
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Noradrenergic activity in rat brain during rapid eye movement sleep deprivation and rebound sleep
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Invited Review: How sleep deprivation affects gene expression in the brain: a review of recent findings
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Selective firing by cat pontine brain stem neurons in desynchronized sleep.
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Actions of neurotransmitters on pontine medical reticular formation neurons of the cat
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Nucleus locus ceruleus: new evidence of anatomical and physiological specificity
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Pedunculopontine Nucleus Region Deep Brain Stimulation in Parkinson Disease: Surgical Anatomy and Terminology
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Principles And Practice Of Sleep Medicine
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Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle
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GABA-mediated inhibition of locus coeruleus from the dorsomedial rostral medulla
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Innervation of Histaminergic Tuberomammillary Neurons by GABAergic and Galaninergic Neurons in the Ventrolateral Preoptic Nucleus of the Rat
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Differential c-Fos Expression in Cholinergic, Monoaminergic, and GABAergic Cell Groups of the Pontomesencephalic Tegmentum after Paradoxical Sleep Deprivation and Recovery
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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How microglia sense and regulate neuronal activity
inferred← citeshttps://doi.org/10.1002/jnr.24838openalex-snapshot
Rapid eye movement sleep deprivation impairs neuronal plasticity and reduces hippocampal neuronal arborization in male albino rats: Noradrenaline is involved in the process
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Rapid eye movement sleep deprivation induced gene regulation for modulation of noradrenaline level in brain regions of rats: Implications with chronic sleep‐loss associated pathophysiological conditions
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Locus Coeruleus and Adrenergic Modulation of Rapid Eye Movement Sleep
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Pharmacology of Sleep and PTSD: Prazosin - An Alpha-1 Adrenoreceptor Antagonist Approach to Post-traumatic Stress Disorder Pharmacotherapy
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Pharmacologic Treatment of PTSD
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Regulation of Brain Na-K ATPase Activity by Noradrenaline with Particular Reference to Normal and Altered Rapid Eye Movement Sleep
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Sleep Phenotypes in Zebrafish
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Association Between Ageing and REM Sleep Loss: Noradrenaline Acting as a Mediator
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Effect of paradoxical sleep deprivation on oxidative stress parameters in brain regions of adult and old rats
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Mechanism of noradrenaline-induced stimulation of Na–K ATPase activity in the rat brain: implications on REM sleep deprivation-induced increase in brain excitability
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Rapid Eye Movement Sleep Deprivation Associated Increase in Na-K ATPase Activity in the Rat Brain is Due to Noradrenaline Induced α1-Adrenoceptor Mediated Increased α-Subunit of the Enzyme
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Interplay Between Vestibular Dysfunction and Sleep Disorders
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REM sleep deprivation induces changes of Down Regulatory Antagonist Modulator (DREAM) expression in the ventrobasal thalamic nuclei of Sprague–Dawley rats
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A Review of Sleep Disturbances among Infants and Children with Neurodevelopmental Disorders
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Basic Pharmacologic Mechanisms of Sleep
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Role of alpha and beta adrenoceptors in locus coeruleus stimulation-induced reduction in rapid eye movement sleep in freely moving rats
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Sleep and sleep regulation in the ferret (Mustela putorius furo)
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Intermittent hypoxia and sleep restriction: Motor, cognitive and neurochemical alterations in rats
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Neurochemical and electrophysiological changes induced by paradoxical sleep deprivation in rats
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REM sleep deprivation of rats induces acute phase response in liver
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A Parallel Group Placebo Controlled Study of Prazosin for Trauma Nightmares and Sleep Disturbance in Combat Veterans with Post-Traumatic Stress Disorder
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Mechanism of noradrenaline-induced α1-adrenoceptor mediated regulation of Na-K ATPase subunit expression in Neuro-2a cells
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The moderating effect of cortisol and dehydroepiandrosterone on the relation between sleep and depression or burnout
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Terpenoids derived from Semen Ziziphi Spinosae oil enhance sleep by modulating neurotransmitter signaling in mice
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Glymphatic dysfunction mediates altered regional neural abilities in night-shift nurses: A multimodal neuroimaging and transcriptomic study
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Cetacean sleep: An unusual form of mammalian sleep
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Noradrenaline acting on α1-adrenoceptor mediates REM sleep deprivation-induced increased membrane potential in rat brain synaptosomes
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REM sleep deprivation-induced noradrenaline stimulates neuronal and inhibits glial Na–K ATPase in rat brain: In vivo and in vitro studies
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GABA in pedunculo pontine tegmentum regulates spontaneous rapid eye movement sleep by acting on GABAA receptors in freely moving rats
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Modulation of dopamine from ventral tegmental area neurons by the LC-REM-OFF and PPT-REM-ON neurons in REMS regulation in freely moving rats
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Cytomorphometric changes in rat brain neurons after rapid eye movement sleep deprivation
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Increased apoptosis in rat brain after rapid eye movement sleep loss
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Stimulatory role of calcium in rapid eye movement sleep deprivation–induced noradrenaline-mediated increase in Na-K-ATPase activity in rat brain
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The neurobiological characteristics of rapid eye movement (REM) sleep are candidate endophenotypes of depression, schizophrenia, mental retardation and dementia
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Noradrenaline involvement in basic and higher integrated REM sleep processes
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Activation of inactivation process initiates rapid eye movement sleep
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Distinct behavioral and neurochemical alterations induced by intermittent hypoxia or paradoxical sleep deprivation in rats
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Sleep-stage-specific regulation of plasma catecholamine concentration
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Rapid eye movement sleep loss associated cytomorphometric changes and neurodegeneration
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REM sleep loss increases brain excitability: Role of noradrenalin and its mechanism of action
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Obstructive sleep apnea and cancer: Epidemiologic links and theoretical biological constructs
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Trauma associated sleep disorder: A parasomnia induced by trauma
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The roles of dopamine and serotonin, and of their receptors, in regulating sleep and waking
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Neuronal models of REM-sleep control: evolving concepts
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REM-sleep loss, oxidative damage, and apoptosis
inferred← citeshttps://doi.org/10.1017/cbo9780511921179.038openalex-snapshot
The role of REM sleep in maintaining neuronal excitability and its possible mechanism of action
inferred← citeshttps://doi.org/10.1017/s1092852920001121openalex-snapshot
Prazosin for treatment of post-traumatic stress disorder: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1038/s41598-018-33069-8openalex-snapshot
Bidirectional and context-dependent changes in theta and gamma oscillatory brain activity in noradrenergic cell-specific Hypocretin/Orexin receptor 1-KO mice
inferred← citeshttps://doi.org/10.1073/pnas.1310692110openalex-snapshot
Nonequilibrium landscape theory of neural networks
inferred← citeshttps://doi.org/10.1093/hmg/ddaa084openalex-snapshot
Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader–Willi syndrome
inferred← citeshttps://doi.org/10.1098/rsif.2016.0902openalex-snapshot
An integrated modelling framework for neural circuits with multiple neuromodulators
inferred← citeshttps://doi.org/10.1101/809822openalex-snapshot
The paternally imprinted gene Snord116 regulates cortical neuronal activity
inferred← citeshttps://doi.org/10.1111/ejn.15136openalex-snapshot
Pathophysiology linking depression and type 2 diabetes: Psychotherapy, physical exercise, and fecal microbiome transplantation as damage control
inferred← citeshttps://doi.org/10.1111/j.1365-2869.2008.00731.xopenalex-snapshot
Prazosin modulates rapid eye movement sleep deprivation‐induced changes in body temperature in rats
inferred← citeshttps://doi.org/10.1111/j.1365-2869.2009.00781.xopenalex-snapshot
Endogenous ouabain-like compounds in locus coeruleus modulate rapid eye movement sleep in rats
inferred← citeshttps://doi.org/10.1111/j.1479-8425.2005.00176_3.xopenalex-snapshot
Free Communication Abstracts
inferred← citeshttps://doi.org/10.1111/jnc.16116openalex-snapshot
Noradrenaline enhances Na‐K ATPase subunit expression by HuR ‐induced mRNA stabilization and their transportation to the cell surface through PLC and PKC mediated pathway: Implications with REMS ‐loss associated disorders
inferred← citeshttps://doi.org/10.1152/jn.01355.2005openalex-snapshot
Oscillatory and Intrinsic Membrane Properties of Guinea Pig Nucleus Prepositus Hypoglossi Neurons In Vitro
inferred← citeshttps://doi.org/10.1176/appi.ajp.2013.12081133openalex-snapshot
A Trial of Prazosin for Combat Trauma PTSD With Nightmares in Active-Duty Soldiers Returned From Iraq and Afghanistan
inferred← citeshttps://doi.org/10.1186/1744-9081-6-62openalex-snapshot
Cytomorphometric changes in the dorsal raphe neurons after rapid eye movement sleep deprivation are mediated by noradrenalin in rats
inferred← citeshttps://doi.org/10.1523/jneurosci.4015-04.2005openalex-snapshot
Direct and Indirect Inhibition by Catecholamines of Hypocretin/Orexin Neurons
inferred← citeshttps://doi.org/10.21236/ada622633openalex-snapshot
Prazosin Augmentation of Outpatient Treatment of Alcohol Use Disorders in Active Duty Soldiers with and without PTSD
inferred← citeshttps://doi.org/10.2147/nss.s140621openalex-snapshot
Relevance of deprivation studies in understanding rapid eye movement sleep
inferred← citeshttps://doi.org/10.2174/1570159x13666150414185737openalex-snapshot
REM sleep and its Loss-Associated Epigenetic Regulation with Reference to Noradrenaline in Particular
inferred← citeshttps://doi.org/10.2174/1871527321666220512092718openalex-snapshot
A Review on Pathophysiological Aspects of Sleep Deprivation
inferred← citeshttps://doi.org/10.3389/fneur.2016.00025openalex-snapshot
Rapid Eye Movement Sleep Deprivation Induces Neuronal Apoptosis by Noradrenaline Acting on Alpha1 Adrenoceptor and by Triggering Mitochondrial Intrinsic Pathway
inferred← citeshttps://doi.org/10.3389/fnmol.2017.00067openalex-snapshot
Transcriptome Analysis Reveals Altered Expression of Memory and Neurotransmission Associated Genes in the REM Sleep Deprived Rat Brain
inferred← citeshttps://doi.org/10.3389/fnmol.2019.00007openalex-snapshot
Noradrenaline Acting on Alpha1 Adrenoceptor as well as by Chelating Iron Reduces Oxidative Burden on the Brain: Implications With Rapid Eye Movement Sleep
inferred← citeshttps://doi.org/10.4103/2224-4018.154288openalex-snapshot
Targeting modulation of noradrenalin release in the brain for amelioration of REMS loss-associated effects
inferred← citeshttps://doi.org/10.54254/2753-8818/2025.22940openalex-snapshot
The Influence of PTSD on Circadian Rhythm
inferred← citeshttps://doi.org/10.5772/17435openalex-snapshot
Noradrenergic Mechanisms in Parkinson’s Disease and L-DOPA-Induced Dyskinesia: Hypothesis and Evidences from Behavioural and Biochemical Studies
inferred← citeshttps://doi.org/10.58837/chula.the.2019.366openalex-snapshot
Alteration levels of monoamine neurotransmitter related with non-motor symptoms and their fluctuation patterns during on/off periods in Parkinsons patients
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