Actions of norepinephrine in the cerebral cortex and thalamus: implications for function of the central noradrenergic system

Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle

Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960

Nucleus locus ceruleus: new evidence of anatomical and physiological specificity

Foote, S. L., Bloom, F. E., & Aston-Jones, G. (1983) · Physiological Reviews · doi:10.1152/physrev.1983.63.3.844 · Cited by 1,901

The functional states of the thalamus and the associated neuronal interplay.

Steriade, M., & Llinas, R. R. (1988) · Physiological Reviews · doi:10.1152/physrev.1988.68.3.649 · Cited by 1,746

Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone

Brown, D. A., & Adams, P. R. (1980) · Nature · doi:10.1038/283673a0 · Cited by 1,447

Electrophysiological properties of guinea‐pig thalamic neurones: an in vitro study.

Jahnsen, H., & Llinás, R. R. (1984) · Journal of Physiology · doi:10.1113/jphysiol.1984.sp015153 · Cited by 1,213

Ionic basis for the electro‐responsiveness and oscillatory properties of guinea‐pig thalamic neurones in vitro.

Jahnsen, H., & Llinas, R. H. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015154 · Cited by 1,081

Nonrepinephrine-containing locus coeruleus neurons in behaving rats exhibit pronounced responses to non-noxious environmental stimuli

Aston‐Jones, G., & Bloom, F. E. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00887.1981 · Cited by 1,072

Functional comparison of neurotransmitter receptor subtypes in mammalian central nervous system

Nicoll, R. A., Malenka, R. C., & Kauer, J. A. (1990) · Physiological Reviews · doi:10.1152/physrev.1990.70.2.513 · Cited by 857

Raphe unit activity in freely moving cats: correlation with level of behavioral arousal.

Trulson, M., & Jacobs, B. (1979) · Brain Research · doi:10.1016/0006-8993(79)90157-4 · Cited by 815

Control of the repetitive discharge of rat CA 1 pyramidal neurones in vitro.

Madison, D. V., & Nicoll, R. A. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015378 · Cited by 746

Reduced noradrenaline, but not dopamine and serotonin in motor thalamus of the MPTP primate: relation to severity of Parkinsonism

Pifl, C., Hornykiewicz, O., Blesa, J., Adánez, R., Cavada, C., & Obeso, J. A. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12162 · Cited by 42

Ketamine influences the locus coeruleus norepinephrine network, with a dependency on norepinephrine transporter genotype – a placebo controlled fMRI study

Liebe, T., Li, M., Čolić, L., Munk, M. H. J., Sweeney‐Reed, C. M., Woelfer, M., Kretzschmar, M., Steiner, J. H., von Düring, F., Behnisch, G., et al. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.09.001 · Cited by 45

Dopamine enhances the excitability of somatosensory thalamocortical neurons

Govindaiah, G., Wang, Y., & Cox, C. L. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.043 · Cited by 42

Correlation between Cortical State and Locus Coeruleus Activity: Implications for Sensory Coding in Rat Barrel Cortex

Fazlali, Z., Ranjbar‐Slamloo, Y., Adibi, M., & Arabzadeh, E. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00014 · Cited by 39

Frontal cortex ablation reversibly decreases striatal zif/268 and junB expression: Temporal correspondence with sensory neglect and its spontaneous recovery

Vargo, J. M., & Marshall, J. F. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199604)22:4 · Cited by 24

Distribution of the Noradrenaline Innervation and Adrenoceptors in the Macaque Monkey Thalamus

Pérez-Santos, I., Palomero‐Gallagher, N., Zilles, K., & Cavada, C. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab073 · Cited by 39

Subcellular targeting of kappa‐opioid receptors in the rat nucleus locus coeruleus

Reyes, B. A. S., Chavkin, C., & Bockstaele, E. J. V. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21880 · Cited by 37

Delayed motor learning in a 16p11.2 deletion mouse model of autism is rescued by locus coeruleus activation

Yin, X., Jones, N., Yang, J., Asraoui, N., Mathieu, M., Cai, L., & Chen, S. X. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00815-7 · Cited by 40

Reduction of adrenergic neurotransmission with clonidine aggravates spike-wave seizures and alters activity in the cortex and the thalamus in WAG/Rij rats

Sitnikova, E., & van Luijtelaar, G. (2004) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.11.004 · Cited by 36

Pedunculopontine nucleus: An integrative view with implications on Deep Brain Stimulation

Nowacki, A., Galati, S., Ai-Schlaeppi, J., Bassetti, C. L., Kaelin‐Lang, A., & Pollo, C. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.08.015 · Cited by 36

Galanin has REM-sleep deprivation-like effects on the sleep eeg in healthy young men

Murck, H., Antonijevic, I. A., Frieboes, R.-M., Maier, P., Schier, T., & Steiger, A. (1999) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(98)00059-4 · Cited by 36

New class of reduced computationally efficient neuronal models for large-scale simulations of brain dynamics

Komarov, M., Krishnan, G. P., Chauvette, S., Rulkov, N. F., Timofeev, I., & Bazhenov, M. (2017) · Journal of Computational Neuroscience · doi:10.1007/s10827-017-0663-7 · Cited by 38

Consequences of tuning network function by tonic and phasic locus coeruleus output and stress: Regulating detection and discrimination of peripheral stimuli

Devilbiss, D. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.06.015 · Cited by 33

Mechanisms underlying anticonvulsant and proconvulsant actions of norepinephrine

Ghasemi, M., & Mehranfard, N. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.05.015 · Cited by 35

Clinically Relevant Doses of Fluoxetine and Reboxetine Induce Changes in the TrkB Content of Central Excitatory Synapses

Wyneken, Ú., Sandoval, M., Sandoval, S., Jorquera, F., González, I., Vargas, F., Falcon, R., Monari, M., & Orrego, F. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301052 · Cited by 34

The beneficial effects of meditation: contribution of the anterior cingulate and locus coeruleus.

Craigmyle, N. A. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00731 · Cited by 32

Gene expression profile of neurodegeneration induced by 1B-adrenergic receptor overactivity: NMDA/GABAA dysregulation and apoptosis

Yun, J. S. (2003) · Brain · doi:10.1093/brain/awg277 · Cited by 32

α2-Adrenergic receptor-mediated modulation of calcium current in neocortical pyramidal neurons

Timmons, S. D., Geisert, E. E., Stewart, A. E., Lorenzon, N. M., & Foehring, R. C. (2004) · Brain Research · doi:10.1016/j.brainres.2004.04.025 · Cited by 34

Simplified dynamics in a model of noradrenergic modulation of cognitive performance

Gilzenrat, M. S., Holmes, B. D., Rajkowski, J., Aston‐Jones, G., & Cohen, J. D. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00055-2 · Cited by 31

Modulation of nicotine-induced attentional enhancement in rats by adrenoceptor antagonists

Hahn, B., & Stolerman, I. P. (2004) · Psychopharmacology · doi:10.1007/s00213-004-1969-5 · Cited by 32

Modulation of Prefrontal Cortex Slow Oscillations by Phasic Activation of the Locus Coeruleus

Durán, E., Yang, M., Neves, R. M., Logothetis, N. K., & Eschenko, O. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2020.11.028 · Cited by 28

Systemic Overexpression of the α1B‐Adrenergic Receptor in Mice: An Animal Model of Epilepsy

Kunieda, T., Zuscik, M. J., Boongird, A., Perez, D. M., Lüders, H. O., & Najm, I. (2002) · Epilepsia · doi:10.1046/j.1528-1157.2002.13202.x · Cited by 29

Enkephalin terminals form inhibitory-type synapses on neurons in the rat nucleus locus coeruleus that project to the medial prefrontal cortex

Bockstaele, E. J. V., Colago, E. E. O., & Pickel, V. M. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00432-7 · Cited by 28

Amplification and Suppression of Distinct Brainwide Activity Patterns by Catecholamines

van den Brink, R. L., Nieuwenhuis, S., & Donner, T. H. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0514-18.2018 · Cited by 27

Pro‐opiomelanocortin colocalizes with corticotropin‐ releasing factor in axon terminals of the noradrenergic nucleus locus coeruleus

Reyes, B. A. S., Glaser, J. D., Magtoto, R. L., & Bockstaele, E. J. V. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04744.x · Cited by 26

Use of Electron Microscopy in the Detection of Adrenergic Receptors

Aoki, C. J., Rodrigues, S. M., & Kurose, H. (2003) · Humana Press eBooks · doi:10.1385/1-59259-684-3:535 · Cited by 25

The Involvement of Noradrenaline in Rapid Eye Movement Sleep Mentation

Gottesmann, C. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00081 · Cited by 25

Dysfunctional Sensory Modalities, Locus Coeruleus, and Basal Forebrain: Early Determinants that Promote Neuropathogenesis of Cognitive and Memory Decline and Alzheimer’s Disease

Daulatzai, M. A. (2016) · Neurotoxicity Research · doi:10.1007/s12640-016-9643-3 · Cited by 27

Tracing of noradrenergic projections using manganese-enhanced MRI

Eschenko, O., Evrard, H., Neves, R. M., Beyerlein, M., Murayama, Y., & Logothetis, N. K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.031 · Cited by 22

Short-Term Effects of Chewing on Task Performance and Task-Induced Mydriasis: Trigeminal Influence on the Arousal Systems

Fantozzi, M. P. T., Cicco, V. D., Barresi, M., Cataldo, E., Faraguna, U., Bruschini, L., & Manzoni, D. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00068 · Cited by 22

Obstructive sleep apnea: re-evaluating our index of severity

Veasey, S. C. (2005) · Sleep Medicine · doi:10.1016/j.sleep.2005.08.012 · Cited by 22

General anaesthesia and electroencephalographic spindles

Sleigh, J. W., Scheib, C. M., & Sanders, R. D. (2011) · Trends in Anaesthesia and Critical Care · doi:10.1016/j.tacc.2011.10.001 · Cited by 22

State-dependent representation of stimulus-evoked activity in high-density recordings of neural cultures

Nieus, T. R., d’Andrea, V., Amin, H., Marco, S. D., Safaai, H., Maccione, A., Berdondini, L., & Panzeri, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-23853-x · Cited by 21

Activation of subthalamic alpha 2 noradrenergic receptors induces motor deficits as a consequence of neuronal burst firing

Delaville, C., Zapata, J., Cardoit, L., & Benazzouz, A. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.05.019 · Cited by 20

Trigeminal input, pupil size and cognitive performance: From oral to brain matter

Fantozzi, M. P. T., Cicco, V. D., Argento, S., Cicco, D. D., Barresi, M., Cataldo, E., Bruschini, L., D’Ascanio, P., Faraguna, U., & Manzoni, D. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147194 · Cited by 20

The path from trigeminal asymmetry to cognitive impairment: a behavioral and molecular study

Fantozzi, M. P. T., Lazzarini, G., Cicco, V. D., Briganti, A., Argento, S., Cicco, D. D., Barresi, M., Cataldo, E., Bruschini, L., D’Ascanio, P., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-82265-6 · Cited by 19

Whole-body biodistribution, radiation dosimetry estimates for the PET norepinephrine transporter probe (S,S)-[18F]FMeNER-D2 in non-human primates

Seneca, N. M., Andrée, B., Sjöholm, N., Schou, M., Pauli, S., Mozley, P. D., Stubbs, J. B., Liow, J., Sóvágó, J., Gulyás, B. Z., et al. (2005) · Nuclear Medicine Communications · doi:10.1097/01.mnm.0000171780.72908.e7 · Cited by 20

Activation of β-adrenoceptors opens calcium-activated potassium channels in astroglial cells

Muyderman, H., Sinclair, J., Jardemark, K. E., Hansson, E., & Nilsson, M. (2001) · Neurochemistry International · doi:10.1016/s0197-0186(00)00078-4 · Cited by 18

Noradrenergic enhancement of Ca2+ responses of basal dendrites in layer 5 pyramidal neurons of the prefrontal cortex

Barth, A. M., Vizi, E. S., & Lendvai, B. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.05.008 · Cited by 17

Columnar activity regulates astrocytic β-adrenergic receptor-like immunoreactivity in V1 of adult monkeys

Aoki, C. J., Lubin, M., & Fenstemaker, S. B. (1994) · Visual Neuroscience · doi:10.1017/s0952523800011214 · Cited by 16

Synergistic interactions between noradrenaline and glutamate in cytosolic calcium influx in cultured visual cortical neurons

Yang, B., Wang, Y., & Cynader, M. S. (1996) · Brain Research · doi:10.1016/0006-8993(96)00047-9 · Cited by 16

The Locus Coeruleus-Noradrenergic System and Stress: Implications for Post-Traumatic Stress Disorder

Berridge, C. W. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-329-9_10 · Cited by 15

Brainstem Influence on Thalamocortical Oscillations during Anesthesia Emergence

Scheib, C. M. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00066 · Cited by 16

Modelling Sleep and General Anaesthesia

SLEIGH, J. W., Voss, L. J., Steyn‐Ross, M. L., Steyn‐Ross, D. A., & Wilson, M. T. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0173-5_2 · Cited by 15

Adrenoceptor-induced changes of intracellular K+ and Ca2+ in astrocytes and neurons in rat cortical primary cultures

Muyderman, H., Hansson, E., & Nilsson, M. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00838-0 · Cited by 14

Mania: a Rational Neurobiology

Arnsten, A., & Manji, H. (2008) · Future Neurology · doi:10.2217/14796708.3.2.125 · Cited by 14

Neurophysiological actions of methylphenidate in the primary somatosensory cortex

Drouin, C., Wang, D. T., & Waterhouse, B. D. (2007) · Synapse · doi:10.1002/syn.20454 · Cited by 13

Wake‐promoting actions of noradrenergic α1‐ and β‐receptors within the lateral hypothalamic area

Schmeichel, B. E., & Berridge, C. W. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12084 · Cited by 11

Function and dysfunction of monoamine interactions in children and adolescents with AD/HD

Oades, R. D. (2006) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-7772-4_11 · Cited by 10

Combined Optogenetic Approaches Reveal Quantitative Dynamics of Endogenous Noradrenergic Transmission in the Brain

Nomura, S., Tricoire, L., Cohen, I., Kuhn, B., Lambolez, B., & Hepp, R. (2020) · iScience · doi:10.1016/j.isci.2020.101710 · Cited by 8

Chapter 2 Neurochemistry of cognition: serotonergic and adrenergic mechanisms

Ph, R., & Benoît, M. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88002-x · Cited by 11

Blocking Dopaminergic Signaling Soon after Learning Impairs Memory Consolidation in Guinea Pigs

Lee, K., & Chirwa, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135578 · Cited by 9

Synapse- and subtype-specific modulation of synaptic transmission by nicotinic acetylcholine receptors in the ventrobasal thalamus

Nagumo, Y., Takeuchi, Y., Imoto, K., & Miyata, M. (2010) · Neuroscience Research · doi:10.1016/j.neures.2010.12.002 · Cited by 9

Norepinephrine and serotonin axonal dynamics and clinical depression: a commentary on the interaction between serotonergic and noradrenergic axons during axonal regeneration

Harley, C. W. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00317-0 · Cited by 9

Zuclopenthixol facilitates memory retrieval in rats: possible involvement of noradrenergic and serotonergic mechanisms

Khalifa, A. E. (2003) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(03)00153-9 · Cited by 9

Olfaction modulates cortical arousal independent of perceived odor intensity and pleasantness

Yao, F., Chang, X., Zhou, B., & Zhou, W. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120843 · Cited by 9

On the Emergence of Tremor in Prodromal Parkinson’s Disease

Fearon, C., Lees, A. J., McKinley, J., McCarthy, A. J., Smyth, S., Farrell, M., & Lynch, T. (2020) · Journal of Parkinson s Disease · doi:10.3233/jpd-202322 · Cited by 8

N-methyl-d-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test

Schulz, S., Arning, L., Pinnow, M., Epplen, J. T., & Beste, C. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.02.024 · Cited by 8

Neuronal network modelling of the effects of anaesthetic agents on somatosensory pathways

Ting, C. H., Angel, A., & Linkens, D. A. (2003) · Biological Cybernetics · doi:10.1007/s00422-002-0346-x · Cited by 8

Noradrenaline Regulation of Brain-Body Communication

Fernandes, G., Lam, R. M., Park, J. H., Drummond, G. T., & Sur, M. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-89525-8_2 · Cited by 8

Spatiotemporal Organization of Prefrontal Norepinephrine Influences Neuronal Activity

Glaeser-Khan, S., Savalia, N. K., Cressy, J., Feng, J., Li, Y., Kwan, A. C., & Kaye, A. P. (2024) · eNeuro · doi:10.1523/eneuro.0252-23.2024 · Cited by 8

Effects of caffeine or RX821002 in rats with a neonatal ventral hippocampal lesion

Sandner, G., Angst, M.-J., Guiberteau, T., Guignard, B., & Nehlig, A. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00015 · Cited by 7

Endomorphin peptides: pharmacological and functional implications of these opioid peptides in the brain of mammals. Part one

Leff, P., Herrera, N., Matus-Ortega, M., Romero, L. P., Santillán, C. T., Juárez, A., & Palma, B. A. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 7

Ultrastructure of endomorphin‐1 immunoreactivity in the rat dorsal pontine tegmentum: Evidence for preferential targeting of peptidergic neurons in Barrington's nucleus rather than catecholaminergic neurons in the peri–locus coeruleus

Peoples, J. F., Wessendorf, M. W., Pierce, T. L., & Bockstaele, E. J. V. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10260 · Cited by 7

Death from Failed Protection? An Evolutionary-Developmental Theory of Sudden Infant Death Syndrome

Renz‐Polster, H., Blair, P. S., Ball, H. L., Jenni, O. G., & Bock, F. D. (2024) · Human Nature · doi:10.1007/s12110-024-09474-6 · Cited by 6

Learning-Induced Sequence Reactivation During Sharp-Wave Ripples: A Computational Study

Malerba, P., Tsimring, K., & Bazhenov, M. (2018) · Association for Women in Mathematics series · doi:10.1007/978-3-319-98684-5_11 · Cited by 6

Autophagy-Based Hypothesis on the Role of Brain Catecholamine Response During Stress

Limanaqi, F., Busceti, C. L., Biagioni, F., Fornai, F., & Puglisi‐Allegra, S. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.569248 · Cited by 6

The locus coeruleus–noradrenergic system and stress: modulation of arousal state and state-dependent behavioral processes

Berridge, C. W. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80025-2 · Cited by 6

Subanesthetic Ketamine Suppresses Locus Coeruleus–Mediated Alertness Effects: A 7T fMRI Study

Liebe, T., Danyeli, L. V., Şen, Z. D., Li, M., Kaufmann, J., & Walter, M. (2024) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyae022 · Cited by 5

A Mechanism for Nerve Cell Excitation by Norepinephrine via Alpha-1 Adrenoceptors: Inhibition of Potassium M-Current

Filippov, A. K., & Brown, D. A. (2012) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-012-9870-y · Cited by 5

Neuronal Nicotinic Receptors in Sleep-Related Epilepsy: Studies in Integrative Biology

Becchetti, A. (2012) · ISRN Biochemistry · doi:10.5402/2012/262941 · Cited by 6

Frontal noradrenergic and cholinergic transients exhibit distinct spatiotemporal dynamics during competitive decision-making

Wang, H., Ortega, H. K., Kelly, E. B., Indajang, J., Savalia, N. K., Glaeser-Khan, S., Feng, J., Li, Y., Kaye, A. P., & Kwan, A. C. (2025) · Science Advances · doi:10.1126/sciadv.adr9916 · Cited by 7

Sleep- and Wake-Like States in Small Networks In Vivo and In Vitro

McKillop, L. E., & Vyazovskiy, V. V. (2018) · Handbook of experimental pharmacology · doi:10.1007/164_2018_174 · Cited by 4

Optimization of Temporal Coding of Tactile Information in Rat Thalamus by Locus Coeruleus Activation

Rodenkirch, C., & Wang, Q. (2024) · Biology · doi:10.3390/biology13020079 · Cited by 3

Intraventricular insulin suppresses the acoustic startle response in rats

Thompson, S. C., Woods, S. C., Hendricks, S. E., Bell, S. M., & Figlewicz, D. P. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00260-7 · Cited by 3

Variations in Pupil Size Related to Memory for Recently Presented Words and Event Related Potentials

Kuipers, J.-R., & Phillips, W. A. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01638 · Cited by 3

A unified model library maps how neuromodulation reshapes the excitability landscape of neurons across the brain

Guarino, D., Carannante, I., & Alain Destexhe, A. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013765 · Cited by 6

Sensitivity of a model oscillator to shifts in the voltage-dependence of one or more ionic currents

Huang, I., Alonso, L. M., & Marder, E. (2026) · Journal of Neurophysiology · doi:10.1152/jn.00055.2026 · Cited by 1

α2-Adrenergic modulation of Ih in adult-born granule cells in the olfactory bulb

Hu, R., Shankar, J., Dong, G. Z., Villar, P. S., & Araneda, R. C. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1055569 · Cited by 1

Modeling and Parameter Analysis of Basic Single Channel Neuron Mass Model for SSVEP

Gao, D., Wang, Y., Fu, P., Qiu, J., & Li, H. (2025) · Sensors · doi:10.3390/s25061706 · Cited by 1

Circuit function is more robust to changes in synaptic than intrinsic conductancesPreprint

Fournier, Z., Alonso, L. M., & Marder, E. E. (2024) · eLife · doi:10.7554/elife.102938.1 · Cited by 1

Rhythmic circuit function is more robust to changes in synaptic than intrinsic conductancesPreprint

Fournier, Z., Alonso, L. M., & Marder, E. E. (2024) · eLife · doi:10.7554/elife.102938 · Cited by 1

Alpha-2 Adrenoceptors in the Paraventricular Thalamic Nucleus: Effects of Agonist Stimulation and Chronic Psychosocial Stress

Heilbronner, U. (2005) · doi:10.53846/goediss-3314

Neuronal Firing Pattern Modulation

Jones, S. W. (2001) · Encyclopedia of Life Sciences · doi:10.1038/npg.els.0000174

Pet imaging of two monoaminergic neurotransmitter systems in brain : studies of the norepinephrine transporter and dopamine D©ü receptor

Seneca, N. M. (2006) · Figshare

Characteristics of abnormal visual processing and recognition memory of affective pictures in PTSD

Borgelt, J. (2006)

Neuroanatomie und Neurophysiologie der zentralen noradrenergen und serotonergen Neuronensysteme

Baumgarten, H. G., & Grozdanovic, Z. (1996) · Springer eBooks · doi:10.1007/978-3-642-79855-9_3

Genetic Evidence for a Role of CREB in Sustained

Graves, L. A., Hellman, K. M., Veasey, S. C., Blendy, J. A., Pack, A. I., Rasch, B., Jan Born, A., Biron, D., Nagy, S., Tramm, N., et al. (2015)

A Mouse Model for Multiple System Atrophy

Perez, D. M. (2005) · Elsevier eBooks · doi:10.1016/b978-012088382-0/50051-7

Comparación del modelo de Cortínez y de Schnider en perfusión de propofol controlada por objetivo de 3 mcg/ml, a biofase, en voluntarios sanos

Avendaño, C. F., Cortínez, L. I., & Ramírez-Paesano, C. R. (2016) · Revista Española de Anestesiología y Reanimación · doi:10.1016/j.redar.2016.03.004

Comparison of the Cortínez and the Schnider models with a targeted effect-site TCI of 3mcg/ml in biophase in healthy volunteers

Avendaño, C. F., Cortínez, L. I., & Ramírez-Paesano, C. R. (2016) · Revista Española de Anestesiología y Reanimación (English Edition) · doi:10.1016/j.redare.2016.07.001

Comparison of Model and Schnider Cortínez Infusion of Propofol Target Controlled 3 Mcg/Ml, to Biophase in Healthy Volunteers

(2016) · Journal of Anesthesia & Critical Care Open Access · doi:10.15406/jaccoa.2016.06.00230

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The Sensitivity and Vulnerability of the Prefrontal Cortex to Changes in Daily Rhythms

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Serotonergic and Noradrenergic Neuromodulation in the Hippocampus and the Mechanism of Action of Antidepressants

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Anatomy and Physiology of the Nucleus Paragigantocellularis: Neural Regulation of Genital Reflexes in Male and Female Rats

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Neurochemical Transmission

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Altered listening changes the way we predict the auditory environment

Brinkmann, P. (2024) · doi:10.26481/dis.20240319pb

Rhythmic circuit function is more robust to changes in synaptic than intrinsic conductances

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Noradrenaline and serotonin selectively modulate thalamic burst firing by enhancing a hyperpolarization-activated cation current

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Noradrenergic modulation of firing pattern in guinea pig and cat thalamic neurons, in vitro

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Transient and long-lasting effects of iontophoretically administered norepinephrine on somatosensory cortical neurons in halothane-anesthetized cats

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Layer- and area-specific actions of norepinephrine on cortical synaptic transmission

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Norepinephrine Homogeneously Inhibits α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate- (AMPAR-) Mediated Currents in All Layers of the Temporal Cortex of the Rat

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