Norepinephrine, neurodevelopment and behavior

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

Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529 · see citing works

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 · see citing works

Orienting and reorienting: the locus coeruleus mediates cognition through arousal

Sara, S. J., & Bouret, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.011 · Cited by 1,056 · see citing works

Gating and Habituation of the Startle Reflex in Schizophrenic Patients

Braff, D. L. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820030038005 · Cited by 1,027 · see citing works

CATECHOLAMINES IN FETAL AND NEWBORN RAT BRAIN

Coyle, J. T., & Henry, D. P. (1973) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1973.tb04225.x · Cited by 782 · see citing works

Dopamine uptake through the norepinephrine transporter in brain regions with low levels of the dopamine transporter: evidence from knock-out mouse lines

Morón, J. A., Brockington, A., Wise, R. A., Rocha, B. A., & Hope, B. T. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-02-00389.2002 · Cited by 681 · see citing works

Ontogeny of monoamine neurons in the locus coeruleus, raphe nuclei and substantia nigra of the rat. I. Cell differentiation

Lauder, J. M., & Bloom, F. E. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901550407 · Cited by 658 · see citing works

Late prenatal ontogeny of central monoamine neurons in the rat: Fluorescence histochemical observations

Seiger, �., & Olson, L. (1973) · Anatomy and Embryology · doi:10.1007/bf00525058 · Cited by 652 · see citing works

Adrenergic pharmacology and cognition: Focus on the prefrontal cortex

Ramos, B. P., & Arnsten, A. F. T. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.11.006 · Cited by 641 · see citing works

Convergent regulation of locus coeruleus activity as an adaptive response to stress

Valentino, R. J., & Van Bockstaele, E. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.062 · Cited by 569 · see citing works

Role of Immediate-Early Genes in Synaptic Plasticity and Neuronal Ensembles Underlying the Memory Trace

Minatohara, K., Akiyoshi, M., & Okuno, H. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00078 · Cited by 507 · see citing works

Early prenatal ontogeny of central monoamine neurons in the rat: Fluorescence histochemical observations

Olson, L., & Seiger, �. (1972) · Anatomy and Embryology · doi:10.1007/bf00519099 · Cited by 501 · see citing works

Neuromelanin magnetic resonance imaging of locus ceruleus and substantia nigra in Parkinson's disease

Sasaki, M., Shibata, E., Tohyama, K., Takahashi, J., Otsuka, K., Tsuchiya, K., Takahashi, S., Ehara, S., Terayama, Y., & Sakai, A. (2006) · Neuroreport · doi:10.1097/01.wnr.0000227984.84927.a7 · Cited by 496 · see citing works

Influence of Neonatal Rearing Conditions on Stress‐Induced Adrenocorticotropin Responses and Norepinepherine Release in the Hypothalamic Paraventricular Nucleus

Liu, Caldji, Sharma, Plotsky, & Meaney (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00422.x · Cited by 451 · see citing works

Impaired prepulse inhibition of acoustic and tactile startle response in patients with Huntington's disease.

Swerdlow, N. R., Paulsen, J. S., BRAFF, D. L., Butters, N., Geyer, M. A., & Swenson, M. R. (1995) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.58.2.192 · Cited by 436 · see citing works

Sensorimotor gating in boys with Tourette's syndrome and ADHD: Preliminary results

Castellanos, F. X., Fine, E. J., Kaysen, D. L., Marsh, W., Rapoport, J. L., & Hallett, M. (1996) · Biological Psychiatry · doi:10.1016/0006-3223(95)00101-8 · Cited by 395 · see citing works

Reduced vas deferens contraction and male infertility in mice lacking P2X1 receptors

Mulryan, K., Gitterman, D. P., Lewis, C. J., Vial, C., LECKIE, B. J., Cobb, A. L., Brown, J. E., Conley, E. C., Buell, G. N., Pritchard, C. A., et al. (2000) · Nature · doi:10.1038/47495 · Cited by 392 · see citing works

Efferent projections of nucleus locus coeruleus: Topographic organization of cells of origin demonstrated by three-dimensional reconstruction

Loughlin, S. E., Foote, S. L., & Bloom, F. E. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90155-7 · Cited by 364 · see citing works

Sensorimotor gating deficits in adults with autism

Perry, W., Minassian, A., Lopez, B., Maron, L., & Lincoln, A. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.09.025 · Cited by 352 · see citing works

Neuromelanin in human dopamine neurons: Comparison with peripheral melanins and relevance to Parkinson's disease

Fedorow, H., Tribl, F., Halliday, G. M., Gerlach, M., Riederer, P. F., & Double, K. L. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.02.001 · Cited by 347 · see citing works

Impaired startle prepulse inhibition and habituation in patients with schizotypal personality disorder

Cadenhead, K. S., Geyer, M. A., & BRAFF, D. L. (1993) · American Journal of Psychiatry · doi:10.1176/ajp.150.12.1862 · Cited by 307 · see citing works

Up-regulation of GABAA receptor binding on neurons of the prefrontal cortex in schizophrenic subjects

Benes, F. M., Vincent, S. L., Marie, A. S., & Khan, Y. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00328-4 · Cited by 274 · see citing works

TYROSINE HYDROXYLASE IN RAT BRAIN: DEVELOPMENTAL CHARACTERISTICS

Coyle, J. T., & Axelrod, J. L. (1972) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1972.tb01431.x · Cited by 260 · see citing works

Locus coeruleus neuronal activity during the sleep-waking cycle in mice

Takahashi, K., Kayama, Y., Lin, J., & Sakai, K. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.009 · Cited by 251 · see citing works

Developmental origins of central norepinephrine neuron diversity

Robertson, S. D., Plummer, N. W., de Marchena, J., & Jensen, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3458 · Cited by 249 · see citing works

DSP-4: A novel compound with neurotoxic effects on noradrenergic neurons of adult and developing rats

Jaim-Etcheverry, G., & Zieher, L. M. (1980) · Brain Research · doi:10.1016/0006-8993(80)90049-9 · Cited by 231 · see citing works

DOPAMINE‐β‐HYDROXYLASE IN THE RAT BRAIN: DEVELOPMENTAL CHARACTERISTICS

Coyle, J. T., & Axelrod, J. L. (1972) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1972.tb01354.x · Cited by 230 · see citing works

Early-life stress disrupts attachment learning: the role of amygdala corticosterone, locus ceruleus corticotropin releasing hormone, and olfactory bulb norepinephrine

Moriceau, S., Shionoya, K., Jakubs, K., & Sullivan, R. M. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4106-09.2009 · Cited by 214 · see citing works

Evidence for a neurotrophic role of noradrenaline neurons in the postnatal development of rat cerebral cortex

Felten, D. L., Hallman, H., & Jonsson, G. (1982) · Journal of Neurocytology · doi:10.1007/bf01258008 · Cited by 211 · see citing works

Cyclic AMP is both a pro‐apoptotic and anti‐apoptotic second messenger

Insel, P. A., Zhang, L., Murray, F., Yokouchi, H., & Zambon, A. C. (2011) · Acta Physiologica · doi:10.1111/j.1748-1716.2011.02273.x · Cited by 204 · see citing works

Hindbrain noradrenergic A2 neurons: diverse roles in autonomic, endocrine, cognitive, and behavioral functions

Rinaman, L. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00556.2010 · Cited by 201 · see citing works

Synchronous Activity in Locus Coeruleus Results from Dendritic Interactions in Pericoerulear Regions

Ishimatsu, M., & Williams, J. T. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05196.1996 · Cited by 201 · see citing works

Raphe GABAergic Neurons Mediate the Acquisition of Avoidance after Social Defeat

Challis, C., Boulden, J., Veerakumar, A., Espallergues, J., Vassoler, F. M., Pierce, R. C., Beck, S. G., & Berton, O. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2383-13.2013 · Cited by 197 · see citing works

Activity of Raphé serotonergic neurons controls emotional behaviors

Teissier, A., Chemiakine, A., Inbar, B., Bagchi, S., Ray, R. S., Palmiter, R. D., Dymecki, S. M., Moore, H., & Ansorge, M. S. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.061 · Cited by 197 · see citing works

Electrical coupling synchronizes subthreshold activity in locus coeruleus neurons in vitro from neonatal rats

Christie, M. J., Williams, J., & North, R. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-10-03584.1989 · Cited by 195 · see citing works

Behavioral consequences of abnormal cortical development: insights into developmental disabilities

Berger-Sweeney, J. E. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(96)02251-6 · Cited by 190 · see citing works

Developing a neurobehavioral animal model of infant attachment to an abusive caregiver

Raineki, C., Moriceau, S., & Sullivan, R. M. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.12.019 · Cited by 190 · see citing works

The Development and Neurobiology of Infant Attachment and Fear

Landers, M. S., & Sullivan, R. M. (2012) · Developmental Neuroscience · doi:10.1159/000336732 · Cited by 180 · see citing works

Functional Evidence that BDNF Is an Anterograde Neuronal Trophic Factor in the CNS

Fawcett, J. P., Bamji, S. X., Causing, C. G., Aloyz, R. S., Ase, A. R., Reader, T. A., McLean, J. H., & Miller, F. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-08-02808.1998 · Cited by 173 · see citing works

Association of an odor with an activation of olfactory bulb noradrenergic β-receptors or locus coeruleus stimulation is sufficient to produce learned approach responses to that odor in neonatal rats.

Sullivan, R. M., Stackenwalt, G., Nasr, F., Lemon, C. H., & Wilson, D. A. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.5.957 · Cited by 169 · see citing works

Biochemical Aspects of Neurotransmission in the Developing Brain

Coyle, J. T. (1977) · International review of neurobiology · doi:10.1016/s0074-7742(08)60651-0 · Cited by 158 · see citing works

Comparison of the maturation of the adrenergic and serotonergic neurotransmitter systems in the brain: Implications for differential drug effects on juveniles and adults

Murrin, L. C., Sanders, J. D., & Bylund, D. B. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.01.028 · Cited by 152 · see citing works

Modification of postnatal development of neocortex in rat brain with experimental deprivation of locus coeruleus

Maeda, T., Tohyama, M., & Shimizu, N. (1974) · Brain Research · doi:10.1016/0006-8993(74)90261-3 · Cited by 146 · see citing works

Sexual dimorphism in locus coeruleus dendritic morphology: A structural basis for sex differences in emotional arousal

Bangasser, D. A., Zhang, X., Garachh, V., Hanhauser, E., & Valentino, R. J. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.02.037 · Cited by 144 · see citing works

Ontogeny of β-adrenergic receptors in rat cerebral cortex

Harden, T. K., Wolfe, B. B., Sporn, J., Perkins, J. P., & Molinoff, P. B. (1977) · Brain Research · doi:10.1016/0006-8993(77)90362-6 · Cited by 137 · see citing works

Postnatal development of electrical activity in the locus ceruleus

Nakamura, S., Kimura, F., & Sakaguchi, T. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.3.510 · Cited by 130 · see citing works

Ontogeny of β1- and β2-adrenergic receptors in rat cerebellum and cerebral cortex

Pittman, R. N., Minneman, K. P., & Molinoff, P. B. (1980) · Brain Research · doi:10.1016/0006-8993(80)90037-2 · Cited by 125 · see citing works

Prenatal stress induces long term stress vulnerability, compromising stress response systems in the brain and impairing extinction of conditioned fear after adult stress

Green, M. K., Rani, C. S. S., Joshi, A., Soto-Piña, A. E., Martinez, P. A., Frazer, A., Strong, R., & Morilak, D. A. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.041 · Cited by 124 · see citing works

Neuropeptide Y and Sympathetic Neurotransmissiona

Lundberg, J. M., Franco‐Cereceda, A., Lacroix, J., & Pernow, J. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb48930.x · Cited by 120 · see citing works

Predator stress engages corticotropin-releasing factor and opioid systems to alter the operating mode of locus coeruleus norepinephrine neurons

Curtis, A. L., Leiser, S. C., Snyder, K., & Valentino, R. J. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.020 · Cited by 120 · see citing works

Rodent model of infant attachment learning and stress

Moriceau, S., Roth, T. L., & Sullivan, R. M. (2010) · Developmental Psychobiology · doi:10.1002/dev.20482 · Cited by 119 · see citing works

DOPA decar☐ylase in the developing rat brain

Lamprecht, F., & Coyle, J. T. (1972) · Brain Research · doi:10.1016/0006-8993(72)90525-2 · Cited by 114 · see citing works

Activity of cat locus coeruleus noradrenergic neurons during the defense reaction.

Levine, E., Litto, W., & Jacobs, B. (1990) · Brain Research · doi:10.1016/0006-8993(90)90773-5 · Cited by 113 · see citing works

Growth Arrest and DNA-Damage-Inducible, Beta (GADD45b)-Mediated DNA Demethylation in Major Psychosis

Gavin, D. P., Sharma, R. P., Chase, K. A., Matrisciano, F., Dong, E., & Guidotti, A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.221 · Cited by 104 · see citing works

Opioid Inhibition in Locus Coeruleus

Travagli, R. A., Dunwiddie, T. V., & Williams, J. T. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.2.519 · Cited by 103 · see citing works

Alpha-2 adrenergic receptor development in rat CNS: an autoradiographic study

Happe, H. K., Coulter, C. L., Gerety, M. E., et al. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.09.004 · Cited by 101 · see citing works

Ontogeny of α1andα2-adrenoceptors in rat brain

Morris, M. J., Dausse, J., Devynck, M., et al. (1980) · Brain Research · doi:10.1016/0006-8993(80)91178-6 · Cited by 98 · see citing works

Expression of α2 adrenoceptors during rat brain development—II. α2C messenger RNA expression and [3H]rauwolscine binding

Winzer-Serhan, U. H., Raymon, H. K., Broide, R. S., Chen, Y., & Leslie, F. M. (1996) · Neuroscience · doi:10.1016/s0306-4522(96)00369-7 · Cited by 96 · see citing works

Elevated Norepinephrine may be a Unifying Etiological Factor in the Abuse of a Broad Range of Substances: Alcohol, Nicotine, Marijuana, Heroin, Cocaine, and Caffeine

Fitzgerald, P. J. (2013) · Substance Abuse Research and Treatment · doi:10.4137/sart.s13019 · Cited by 96 · see citing works

A qualitative and quantitative ultrastructural study of glial cells in the developing visual cortex of the rat

Parnavelas, J. G., Luder, R., Polland, S. G., Sullivan, K., & Lieberman, A. R. (1983) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1983.0022 · Cited by 96 · see citing works

Roles of glial cells in synapse development

Pfrieger, F. W. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0005-7 · Cited by 95 · see citing works

Persistent Stress-Induced Neuroplastic Changes in the Locus Coeruleus/Norepinephrine System

Borodovitsyna, O., Joshi, N., & Chandler, D. J. (2018) · Neural Plasticity · doi:10.1155/2018/1892570 · Cited by 95 · see citing works

Development and plasticity of the locus coeruleus: A review of recent physiological and pharmacological experimentation

Nakamura, S., & Sakaguchi, T. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90018-c · Cited by 94 · see citing works

The effect of neonatal 6‐hydroxydopamine treatment on synaptogenesis in the visual cortex of the rat

Blue, M. E., & Parnavelas, J. G. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902050211 · Cited by 93 · see citing works

The role of the noradrenergic system on the formation of synapses in the visual cortex of the rat

Parnavelas, J. G., & Blue, M. E. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90082-7 · Cited by 92 · see citing works

Manipulation of dorsal raphe serotonergic neurons modulates active coping to inescapable stress and anxiety-related behaviors in mice and rats

Nishitani, N., Nagayasu, K., Asaoka, N., Yamashiro, M., Andoh, C., Nagai, Y., Kinoshita, H., Kawai, H., Shibui, N., Liu, B., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0254-y · Cited by 92 · see citing works

Galanin in Ascending Systems: Focus on Coexistence with 5‐Hydroxytryptamine and Noradrenaline a

Hökfelt, T. G. M., Xu, Q., Shi, T.-J. S., HOLMBERG, K., & Zhang, X. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb10700.x · Cited by 91 · see citing works

Evidence for Functional Release of Endogenous Opioids in the Locus Ceruleus during Stress Termination

Curtis, A. L., Bello, N. T., & Valentino, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-13-j0001.2001 · Cited by 91 · see citing works

Association and linkage of α-2A adrenergic receptor gene polymorphisms with childhood ADHD

Park, L., Nigg, J., Waldman, I., Nummy, K., Huang-Pollock, C., Rappley, M., & Friderici, K. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001605 · Cited by 89 · see citing works

Control of 5-Hydroxytryptamine Release in the Dorsal Raphe Nucleus by the Noradrenergic System in Rat Brain. Role of α-Adrenoceptors

Bortolozzi, A. A., & Artigas, F. (2002) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300061 · Cited by 88 · see citing works

Maternal attenuation of hypothalamic paraventricular nucleus norepinephrine switches avoidance learning to preference learning in preweanling rat pups

Shionoya, K., Moriceau, S., Bradstock, P., & Sullivan, R. M. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.06.004 · Cited by 85 · see citing works

The involvement of the noradrenergic system arising from the locus coeruleus in the postnatal development of the cortex in rat brain

Wendlandt, S., Crow, T. J., & Stirling, R. V. (1977) · Brain Research · doi:10.1016/0006-8993(77)90355-9 · Cited by 83 · see citing works

Development of α‐Noradrenergic and Dopaminergic Receptor Systems Depends on Maturation of Their Presynaptic Nerve Terminals in the Rat Brain

Deskin, R., Seidler, F. J., Whitmore, W. L., et al. (1981) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1981.tb00419.x · Cited by 79 · see citing works

Neuroinflammation and Behavioral Abnormalities after Neonatal Terbutaline Treatment in Rats: Implications for Autism

Zerrate, M. C., Pletnikov, M. V., Connors, S. L., Vargas, D. L., Seidler, F. J., Zimmerman, A. W., Slotkin, T. A., & Pardo, C. A. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.121483 · Cited by 78 · see citing works

Ontogenesis of β-Adrenoceptor Signaling: Implications for Perinatal Physiology and for Fetal Effects of Tocolytic Drugs

Slotkin, T. A., Auman, J. T., & Seidler, F. J. (2003) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.048421 · Cited by 78 · see citing works

c-Fos importance for brain development

Velazquez, F. N., Caputto, B. L., & Boussin, F. D. (2015) · Aging · doi:10.18632/aging.100862 · Cited by 78 · see citing works

In utero beta 2 adrenergic agonist exposure and adverse neurophysiologic and behavioral outcomes

Witter, F. R., Zimmerman, A. W., Reichmann, J. P., & Connors, S. L. (2009) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2009.07.010 · Cited by 76 · see citing works

Enduring effects of infant memories: infant odor-shock conditioning attenuates amygdala activity and adult fear conditioning

Sevelinges, Y., Moriceau, S., Holman, P., Miner, C., Muzny, K., Gervais, R., Mouly, A.-M., & Sullivan, R. M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.04.025 · Cited by 74 · see citing works

Active sleep and its role in the prevention of apoptosis in the developing brain

Morrissey, M., Duntley, S. P., Anch, A. M., & Nonneman, R. J. (2004) · Medical Hypotheses · doi:10.1016/j.mehy.2004.01.014 · Cited by 71 · see citing works

Terbutaline Is a Developmental Neurotoxicant: Effects on Neuroproteins and Morphology in Cerebellum, Hippocampus, and Somatosensory Cortex

Rhodes, M. C., Seidler, F. J., Abdel-Rahman, A. A., Tate, C. A., Nyska, A., Rincavage, H. L., & Slotkin, T. A. (2004) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.060095 · Cited by 71 · see citing works

Pharmacological suppression of REM sleep prior to weaning counteracts the effectiveness of subsequent environmental enrichment on cortical growth in rats

Mirmiran, M., Uylings, H. B. M., & Corner, M. A. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90086-x · Cited by 64 · see citing works

Beta-2 adrenergic control of ornithine decarboxylase activity in brain regions of the developing rat.

Morris, G., & Slotkin, T. A. (1985) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21111-9 · Cited by 64 · see citing works

ERK Activation by G-protein-coupled Receptors in Mouse Brain Is Receptor Identity-specific

Vanhoose, A. M., Emery, M., Jimenez, L., & Winder, D. G. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m108309200 · Cited by 63 · see citing works

Stress : molecular genetic and neurobiological advances

McCarty, R. C. (1996) · Medical Entomology and Zoology · Cited by 59 · see citing works

Attenuation of α2A-adrenergic receptor expression in neonatal rat brain by RNA interference or antisense oligonucleotide reduced anxiety in adulthood

Shishkina, G. T., Kalinina, T., & Dygalo, N. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.015 · Cited by 59 · see citing works

Is Parkinson's Disease a Neurodevelopmental Disorder and Will Brain Organoids Help Us to Understand It?

Schwamborn, J. C. (2018) · Stem Cells and Development · doi:10.1089/scd.2017.0289 · Cited by 59 · see citing works

Mental Health in Children with Cerebral Palsy: Does Screening Capture the Complexity?

Bjørgaas, H. M., Elgen, I. B., Bøe, T., & Hysing, M. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/468402 · Cited by 58 · see citing works

Transient blockade of ERK phosphorylation in the critical period causes autistic phenotypes as an adult in mice

Yufune, S., Satoh, Y., Takamatsu, I., Ohta, H., Kobayashi, Y., Takaenoki, Y., Pagès, G., Pouysségur, J., Endo, S., & Kazama, T. (2015) · Scientific Reports · doi:10.1038/srep10252 · Cited by 57 · see citing works

Enduring Neurobehavioral Effects of Early Life Trauma Mediated Through Learning and Corticosterone Suppression

Moriceau, S. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/neuro.08.022.2009 · Cited by 57 · see citing works

Adult depression-like behavior, amygdala and olfactory cortex functions are restored by odor previously paired with shock during infant’s sensitive period attachment learning

Sevelinges, Y., Mouly, A.-M., Raineki, C., Moriceau, S., Forest, C., & Sullivan, R. M. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2010.07.005 · Cited by 56 · see citing works

Postnatal development of brain alpha1-adrenergic receptors: In vitro autoradiography with [125i]HEAT in normal rats and rats treated with alpha-difluoromethylornithine, a specific, irreversible inhibitor of ornithine decarboxylase

Jones, L. S., Gauger, L. L., Davis, J. N., Slotkin, T. A., & Bartolome, J. V. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90262-3 · Cited by 56 · see citing works

Targeting the noradrenergic system for anti-inflammatory and neuroprotective effects: implications for Parkinson's disease

Harkin, A., & O′Neill, E. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.235219 · Cited by 56 · see citing works

Child Development After Maternal Tocolysis with Beta-Sympathomimetic Drugs

Pitzer, M., Schmidt, M. H., Esser, G., et al. (2001) · Child Psychiatry & Human Development · doi:10.1023/a:1026419720410 · Cited by 55 · see citing works

The environmental enrichment effect upon cortical growth is neutralized by concomitant pharmacological suppression of active sleep in female rats

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