Evolution in Neuromodulation—The Differential Roles of Acetylcholine in Higher Order Association vs. Primary Visual Cortices

Alzheimer's Disease and Senile Dementia: Loss of Neurons in the Basal Forebrain

Whitehouse, P., Price, D., Struble, R., Clark, A., Coyle, J., & DeLong, M. R. (1982) · Science · doi:10.1126/science.7058341 · Cited by 3,627 · see citing works

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685 · see citing works

Cellular basis of working memory

Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663 · see citing works

Top-Down Versus Bottom-Up Control of Attention in the Prefrontal and Posterior Parietal Cortices

Buschman, T. J., & Miller, E. K. (2007) · Science · doi:10.1126/science.1138071 · Cited by 2,380 · see citing works

Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6)

Mesulam, M. M., Mufson, E. J., Wainer, B. H., & Levey, A. I. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90108-2 · Cited by 2,329 · see citing works

Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey

Mesulam, M. ‐., Mufson, E. J., Levey, A. I., & Wainer, B. H. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902140206 · Cited by 1,962 · see citing works

Neural mechanisms of spatial selective attention in areas V1, V2, and V4 of macaque visual cortex

Luck, S. J., Chelazzi, L., Hillyard, S. A., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.1.24 · Cited by 1,615 · see citing works

Cognitive Deficit Caused by Regional Depletion of Dopamine in Prefrontal Cortex of Rhesus Monkey

Brozoski, T. J., Brown, R. M., Rosvold, H. E., & Goldman, P. S. (1979) · Science · doi:10.1126/science.112679 · Cited by 1,500 · see citing works

Acetylcholine receptors containing the β2 subunit are involved in the reinforcing properties of nicotine

Picciotto, M. R., Zoli, M., Rimondini, R., Léna, C., Marubio, L. M., Pich, E. M., Fuxe, K., & Changeux, J.-P. (1998) · Nature · doi:10.1038/34413 · Cited by 1,320 · see citing works

Selective gating of visual signals by microstimulation of frontal cortex

Moore, T., & Armstrong, K. M. (2003) · Nature · doi:10.1038/nature01341 · Cited by 1,156 · see citing works

Prevalence of smoking among psychiatric outpatients

(1986) · American Journal of Psychiatry · doi:10.1176/ajp.143.8.993 · Cited by 1,058 · see citing works

Attention Increases Sensitivity of V4 Neurons

Reynolds, J. H., Pasternak, T., & Desimone, R. (2000) · Neuron · doi:10.1016/s0896-6273(00)81206-4 · Cited by 1,017 · see citing works

Modulation of visual cortical plasticity by acetylcholine and noradrenaline

Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858 · see citing works

β-Amyloid1–42 Binds to α7 Nicotinic Acetylcholine Receptor with High Affinity

Wang, H.-Y., Lee, D. H. S., D’Andrea, M. R., Peterson, P. A., Shank, R. P., & Reitz, A. B. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.8.5626 · Cited by 818 · see citing works

Donepezil Improves Cognition and Global Function in Alzheimer Disease A 15-Week, Double-blind, Placebo-Controlled Study

Rogers, S. L. (1998) · Archives of Internal Medicine · doi:10.1001/archinte.158.9.1021 · Cited by 770 · see citing works

Stress weakens prefrontal networks: molecular insults to higher cognition

Arnsten, A. F. T. (2015) · Nature Neuroscience · doi:10.1038/nn.4087 · Cited by 752 · cited 1× · see citing works

Spatial attention decorrelates intrinsic activity fluctuations in macaque area V4

Mitchell, J. F., Sundberg, K. A., & Reynolds, J. H. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.013 · Cited by 710 · see citing works

Differential attention-dependent response modulation across cell classes in macaque visual area V4

Mitchell, J. F., Sundberg, K. A., & Reynolds, J. H. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.018 · Cited by 665 · see citing works

Prefrontal Acetylcholine Release Controls Cue Detection on Multiple Timescales

Parikh, V., Kozak, R., Martinez, V., & Sarter, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.025 · Cited by 623 · see citing works

Localization of function within the dorsolateral prefrontal cortex of the rhesus monkey

Goldman, P. S., & Rosvold, H. E. (1970) · Experimental Neurology · doi:10.1016/0014-4886(70)90222-0 · Cited by 581 · see citing works

Turning of nerve growth cones induced by neurotransmitters

Zheng, J. Q., Felder, M., Connor, J. A., & Poo, M.-M. (1994) · Nature · doi:10.1038/368140a0 · Cited by 580 · see citing works

Pedunculopontine Nucleus Region Deep Brain Stimulation in Parkinson Disease: Surgical Anatomy and Terminology

Hamani, C., Aziz, T. Z., Bloem, B. R., Brown, P., Chabardès, S., Coyne, T. J., Foote, K. D., García‐Rill, E., Hirsch, É. C., Lozano, A. M., et al. (2016) · Stereotactic and Functional Neurosurgery · doi:10.1159/000449010 · Cited by 571 · see citing works

Static and Dynamic Cognitive Deficits in Childhood Preceding Adult Schizophrenia: A 30-Year Study

Reichenberg, A., Caspi, A., Harrington, H., Houts, R., Keefe, R. S. E., Murray, R. M., Poulton, R., & Moffitt, T. E. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.09040574 · Cited by 557 · see citing works

Differential regulation of neocortical synapses by neuromodulators and activity

Gil, Z., Connors, B. W., & Amitai, Y. (1997) · Neuron · doi:10.1016/s0896-6273(00)80380-3 · Cited by 553 · see citing works

Neuromodulation and cortical function: modeling the physiological basis of behavior

Hasselmo, M. E. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00113-t · Cited by 552 · see citing works

Neuromodulation of thought: flexibilities and vulnerabilities in prefrontal cortical network synapses

Arnsten, A. F. T., Wang, M. J., & Paspalas, C. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.038 · Cited by 538 · see citing works

Fast modulation of visual perception by basal forebrain cholinergic neurons

Pinto, L., Goard, M. J., Estandian, D., Xu, M., Kwan, A. C., Lee, S.-H., Harrison, T. C., Feng, G., & Dan, Y. (2013) · Nature Neuroscience · doi:10.1038/nn.3552 · Cited by 529 · see citing works

Retinal waves coordinate patterned activity throughout the developing visual system

Ackman, J. B., Burbridge, T. J., & Crair, M. C. (2012) · Nature · doi:10.1038/nature11529 · Cited by 525 · see citing works

Basal forebrain circuit for sleep-wake control

Xu, M., Chung, S., Zhang, S., Zhong, P., Ma, C., Chang, W.-C., Weissbourd, B., Sakai, N., Luo, L., Nishino, S., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4143 · Cited by 514 · see citing works

NMDA Receptors Subserve Persistent Neuronal Firing during Working Memory in Dorsolateral Prefrontal Cortex

Wang, M., Yang, Y., Wang, C.-J., Gamo, N. J., Jin, L. E., Mazer, J. A., Morrison, J. H., Wang, X.-J., & Arnsten, A. F. T. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.032 · Cited by 489 · see citing works

Basal forebrain lesions in monkeys disrupt attention but not learning and memory [published erratum appears in J Neurosci 1995 Mar;15(3): following table of contents]

Voytko, M. L., Olton, D. S., Richardson, R., Gorman, L. K., Tobin, J., & Price, D. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-01-00167.1994 · Cited by 483 · see citing works

Laminar selectivity of the cholinergic suppression of synaptic transmission in rat hippocampal region CA1: computational modeling and brain slice physiology

Hasselmo, M., & Schnell, E. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03898.1994 · Cited by 466 · see citing works

Acetylcholine contributes through muscarinic receptors to attentional modulation in V1

Herrero, J. L., Roberts, M. J., Delicato, L. S., Gieselmann, M. A., Dayan, P., & Thiele, A. (2008) · Nature · doi:10.1038/nature07141 · Cited by 459 · see citing works

Intracellular accumulation of β-amyloid1–42 in neurons is facilitated by the α7 nicotinic acetylcholine receptor in Alzheimer’s disease

Nagele, R. G., D’Andrea, M. R., Anderson, W. J., & Wang, H.-Y. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00460-2 · Cited by 456 · see citing works

Initial phase 2 trial of a nicotinic agonist in schizophrenia

Freedman, R., Olincy, A., Buchanan, R. W., Harris, J. G., Gold, J. M., Johnson, L., Allensworth, D., Guzman-Bonilla, A., Clement, B., Ball, M. P., et al. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.07071135 · Cited by 426 · see citing works

Destruction and Creation of Spatial Tuning by Disinhibition: GABA_ABlockade of Prefrontal Cortical Neurons Engaged by Working Memory

Rao, S. G., Williams, G. V., & Goldman-Rakic, P. S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00485.2000 · Cited by 407 · see citing works

Analysis of the delayed-alternation deficit produced by dorsolateral prefrontal lesions in the rhesus monkey.

Goldman, P. S., Rosvold, H. E., Vest, B., & Galkin, T. W. (1971) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0031649 · Cited by 381 · see citing works

Lynx1, a Cholinergic Brake, Limits Plasticity in Adult Visual Cortex

Morishita, H., Miwa, J. M., Heintz, N., & Hensch, T. K. (2010) · Science · doi:10.1126/science.1195320 · Cited by 365 · see citing works

Cholinergic suppression specific to intrinsic not afferent fiber synapses in rat piriform (olfactory) cortex

Hasselmo, M. E., & Bower, J. M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1222 · Cited by 358 · see citing works

Correlated discharges among putative pyramidal neurons and interneurons in the primate prefrontal cortex.

Constantinidis, C., & Goldman-Rakic, P. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00188.2002 · Cited by 337 · see citing works

Isodirectional Tuning of Adjacent Interneurons and Pyramidal Cells During Working Memory: Evidence for Microcolumnar Organization in PFC

Rao, S. G., Williams, G. V., & Goldman, P. S. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.4.1903 · Cited by 335 · see citing works

Short-term memory in the rhesus monkey: Disruption from the anti-cholinergic scopolamine

Bartus, R. T., & Johnson, H. R. (1976) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(76)90286-0 · Cited by 334 · see citing works

Gain Modulation by Nicotine in Macaque V1

Disney, A. A., Aoki, C., & Hawken, M. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.034 · Cited by 331 · see citing works

Dynamic shifts of visual receptive fields in cortical area MT by spatial attention

Womelsdorf, T., Anton-Erxleben, K., Pieper, F., & Treue, S. (2006) · Nature Neuroscience · doi:10.1038/nn1748 · Cited by 317 · see citing works

NEURAL INPUTS INTO THE NUCLEUS BASALIS OF THE SUBSTANTIA INNOMINATA (Ch4) IN THE RHESUS MONKEY

Mesulam, M. M., & Mufson, E. J. (1984) · Brain · doi:10.1093/brain/107.1.253 · Cited by 316 · see citing works

Interdigitation of Contralateral and Ipsilateral Columnar Projections to Frontal Association Cortex in Primates

Goldman, P. S., & Schwartz, M. L. (1982) · Science · doi:10.1126/science.6177037 · Cited by 313 · see citing works

Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey

Steriade, M., Paré, D., Parent, A., & Smith, Y. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90006-1 · Cited by 313 · see citing works

Intrinsic circuit organization of the major layers and sublayers of the dorsolateral prefrontal cortex in the rhesus monkey

Kritzer, M. F., & Goldman‐Rakic, P. S. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590109 · Cited by 300 · see citing works

Cortical projection patterns of magnocellular basal nucleus subdivisions as revealed by anterogradely transportedPhaseolus vulgaris leucoagglutinin

Luiten, P. G. M., Gaykema, R. P. A., Traber, J., & Spencer, D. G. (1987) · Brain Research · doi:10.1016/0006-8993(87)91014-6 · Cited by 295 · see citing works

Decreased protein level of nicotinic receptor α7 subunit in the frontal cortex from schizophrenic brain

Guan, Z., Zhang, X., Blennow, K., & Nordberg, A. K. (1999) · Neuroreport · doi:10.1097/00001756-199906030-00028 · Cited by 286 · see citing works

Development of prestriate visual projections in the monkey and human fetal cerebrum revealed by transient cholinesterase staining

Kostovic, I., & Rakic, P. (1984) · The Journal of Neuroscience · doi:10.1523/jneurosci.04-01-00025.1984 · Cited by 270 · see citing works

Transient cholinesterase staining in the mediodorsal nucleus of the thalamus and its connections in the developing human and monkey brain

Kostovic, I., & Goldman‐Rakic, P. S. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902190405 · Cited by 260 · see citing works

Association of m1 and m2 muscarinic receptor proteins with asymmetric synapses in the primate cerebral cortex: morphological evidence for cholinergic modulation of excitatory neurotransmission.

Mrzljak, L., Levey, A. I., & Goldman-Rakic, P. S. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.11.5194 · Cited by 256 · see citing works

Selective Cholinergic Modulation of Cortical GABAergic Cell Subtypes

Kawaguchi, Y. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.3.1743 · Cited by 250 · see citing works

Septal Cholinergic Neuromodulation Tunes the Astrocyte-Dependent Gating of Hippocampal NMDA Receptors to Wakefulness

Papouin, T., Dunphy, J. M., Tolman, M., Dineley, K. T., & Haydon, P. G. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.021 · Cited by 243 · see citing works

An atlas of the regional and laminar distribution of choline acetyltransferase immunoreactivity in rat cerebral cortex

Lysakowski, A., Wainer, B. H., Bruce, G., & Hersh, L. B. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90180-2 · Cited by 239 · see citing works

A functional role of cholinergic innervation to neurons in the cat visual cortex

Sato, H., Hata, Y., Masui, H., & Tsumoto, T. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.4.765 · Cited by 228 · see citing works

Sequential interplay of nicotinic and GABAergic signaling guides neuronal development

Liu, Z., Neff, R. A., & Berg, D. K. (2006) · Science · doi:10.1126/science.1134246 · Cited by 227 · see citing works

Multiple Muscarinic Acetylcholine Receptor Subtypes Modulate Striatal Dopamine Release, as Studied with M₁–M₅Muscarinic Receptor Knock-Out Mice

Zhang, W., Yamada, M., Gomeza, J., Basile, A. S., & Wess, J. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06347.2002 · Cited by 224 · see citing works

Cortical input to the basal forebrain

Záborszky, L., Gaykema, R. P. A., Swanson, D. J., & Cullinan, W. E. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00049-3 · Cited by 221 · see citing works

Chapter 5: The organization of central cholinergic systems and their functional importance in sleep-waking states

Jones, B. E. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)62381-x · Cited by 212 · see citing works

Removal of Cholinergic Input to Rat Posterior Parietal Cortex Disrupts Incremental Processing of Conditioned Stimuli

Bucci, D. J., Holland, P. C., & Gallagher, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-19-08038.1998 · Cited by 205 · see citing works

A specialized NMDA receptor function in layer 5 recurrent microcircuitry of the adult rat prefrontal cortex

Wang, H., Stradtman, G. G., Wang, X.-J., & Gao, W.-J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804318105 · Cited by 199 · see citing works

Fast Synaptic Signaling by Nicotinic Acetylcholine and Serotonin 5-HT3Receptors in Developing Visual Cortex

Roerig, B., Nelson, D. A., & Katz, L. C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08353.1997 · Cited by 192 · see citing works

Nicotinic acetylcholine receptor β2 subunits in the medial prefrontal cortex control attention

Guillem, K., Bloem, B., Poorthuis, R. B., Loos, M., Smit, A. B., Maskos, U., Spijker, S., & Mansvelder, H. D. (2011) · Science · doi:10.1126/science.1207079 · Cited by 191 · see citing works

Cortical cholinergic signaling controls the detection of cues

Gritton, H. J., Howe, W. M., Mallory, C. S., Hetrick, V. L., Berke, J. D., & Sarter, M. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1516134113 · Cited by 191 · see citing works

Local Infusion of Scopolamine Into Intraparietal Cortex Slows Covert Orienting in Rhesus Monkeys

Davidson, M. C., & Marrocco, R. T. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.3.1536 · Cited by 188 · see citing works

Nicotinic α7 receptors enhance NMDA cognitive circuits in dorsolateral prefrontal cortex

Yang, Y., Paspalas, C. D., Jin, L. E., Picciotto, M. R., Arnsten, A. F. T., & Wang, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307849110 · Cited by 188 · see citing works

Differential cholinergic innervation within functional subdivisions of the human cerebral cortex: A choline acetyltransferase study

Mesulam, M. ‐., Hersh, L. B., Mash, D. C., & Geula, C. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903180308 · Cited by 188 · see citing works

Diversity and distribution of nicotinic acetylcholine receptors in the locus ceruleus neurons

Léna, C., d’Exaerde, A. D. K., Cordero‐Erausquin, M., Novère, N. G. L., Jiménez, M. D. M. A., & Changeux, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12126 · Cited by 181 · see citing works

Layer-Specific Modulation of the Prefrontal Cortex by Nicotinic Acetylcholine Receptors

Poorthuis, R. B., Bloem, B., Schak, B., Wester, J., de Kock, C. P. J., & Mansvelder, H. D. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhr390 · Cited by 176 · see citing works

Specialized Representations of Value in the Orbital and Ventrolateral Prefrontal Cortex: Desirability versus Availability of Outcomes

Rudebeck, P. H., Saunders, R. C., Lundgren, D. A., & Murray, E. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.042 · Cited by 170 · see citing works

Horizontal synaptic connections in monkey prefrontal cortex: An in vitro electrophysiological study

Gonzalez-Burgos, G. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.1.82 · Cited by 169 · see citing works

Specializations of the granular prefrontal cortex of primates: Implications for cognitive processing

Elston, G. N., Benavides‐Piccione, R., Elston, A., Zietsch, B., Defelipe, J., Manger, P., Casagrande, V., & Kaas, J. H. (2006) · The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology · doi:10.1002/ar.a.20278 · Cited by 167 · see citing works

Cholinergic modulation of a specific memory function of prefrontal cortex

Croxson, P. L., Kyriazis, D. A., & Baxter, M. G. (2011) · Nature Neuroscience · doi:10.1038/nn.2971 · Cited by 166 · see citing works

Acetylcholine stimulates cortical precursor cell proliferation in vitro via muscarinic receptor activation and MAP kinase phosphorylation

Ma, W., Maric, D., Li, B., Hu, Q., Andreadis, J. D., Grant, G. M., Liu, Q., Shaffer, K. M., Chang, Y. H., Zhang, L., et al. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00010.x · Cited by 161 · see citing works

Regional distribution of nicotinic receptors during prenatal development of human brain and spinal cord

Hellström-Lindahl, E., Gorbounova, O., Seiger, Å., Mousavi, M., & Nordberg, A. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00046-7 · Cited by 159 · see citing works

Mechanisms of Activation of Glutamate Receptors and the Time Course of Excitatory Synaptic Currents

Edmonds, B. W., Gibb, A. J., & Colquhoun, D. (1995) · Annual Review of Physiology · doi:10.1146/annurev.ph.57.030195.002431 · Cited by 157 · see citing works

Laminar Organization of Attentional Modulation in Macaque Visual Area V4

Nandy, A. S., Nassi, J. J., & Reynolds, J. H. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.029 · Cited by 155 · see citing works

Decreased cortical muscarinic receptors define a subgroup of subjects with schizophrenia

Scarr, E., Cowie, T., Kanellakis, S., Sundram, S., Pantelis, C., & Dean, B. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.28 · Cited by 149 · see citing works

Prenatal and adolescent exposure to tobacco smoke modulates the development of white matter microstructure

Jacobsen, L. K., Picciotto, M. R., Heath, C. J., Frost, S. J., Tsou, K. A., Dwan, R. A., Jackowski, M. P., Constable, R. T., & Mencl, W. E. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2402-07.2007 · Cited by 147 · see citing works

Correlated Variability in Laminar Cortical Circuits

Hansen, B. J., Chelaru, M. I., & Dragoi, V. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.029 · Cited by 146 · see citing works

Gender-specific effects of prenatal and adolescent exposure to tobacco smoke on auditory and visual attention

Jacobsen, L. K., Slotkin, T. A., Mencl, W. E., Frost, S. J., & Pugh, K. R. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301398 · Cited by 144 · see citing works

Area-Specific Features of Pyramidal Neurons—a Comparative Study in Mouse and Rhesus Monkey

Gilman, J. P., Medalla, M., & Luebke, J. I. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw062 · Cited by 140 · see citing works

Randomized, Double-Blind, Placebo-Controlled Study of Encenicline, an α7 Nicotinic Acetylcholine Receptor Agonist, as a Treatment for Cognitive Impairment in Schizophrenia

Keefe, R., Meltzer, H., Dgetluck, N., Gawryl, M., Koenig, G., Moebius, H., Lombardo, I., & Hilt, D. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.176 · Cited by 139 · see citing works

Developmental regulation of nicotinic acetylcholine receptors within midbrain dopamine neurons

Azam, L., Chen, Y., & Leslie, F. M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.11.011 · Cited by 138 · see citing works

Effects of Intracortical Infusion of Anticholinergic Drugs on Neuronal Plasticity in Kitten Striate Cortex

Gu, Q., & Singer, W. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00514.x · Cited by 137 · see citing works

Muscarinic Signaling in the Brain

Thiele, A. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170433 · Cited by 136 · see citing works

Glutamatergic Synapse Formation is Promoted by α7-Containing Nicotinic Acetylcholine Receptors

Lozada, A. F., Wang, X., Gounko, N. V., Massey, K. A., Duan, J., Liu, Z., & Berg, D. K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6246-11.2012 · Cited by 134 · see citing works

Prefrontal cortical projections to the cholinergic neurons in the basal forebrain

Gaykema, R. P. A., Weeghel, R. V., Hersh, L. B., & Luiten, P. G. M. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903030405 · Cited by 134 · see citing works

Cholinergic enhancement of direction selectivity in the visual cortex of the cat

Murphy, P. C., & Sillito, A. M. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90170-s · Cited by 130 · see citing works

Visual Circuit Development Requires Patterned Activity Mediated by Retinal Acetylcholine Receptors

Burbridge, T. J., Xu, H., Ackman, J. B., Ge, X., Zhang, Y., Ye, M.-J., Zhou, Z., Xu, J., Contractor, A., & Crair, M. C. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.051 · Cited by 130 · see citing works

Prefrontal cortical modulation of acetylcholine release in posterior parietal cortex

Nelson, C. L., Sarter, M., & Bruno, J. P. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.12.007 · Cited by 128 · see citing works

Regulation of α7Nicotinic Acetylcholine Receptors in the Developing Rat Somatosensory Cortex by Thalamocortical Afferents

Broide, R. S., Robertson, R. T., & Leslie, F. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-09-02956.1996 · Cited by 123 · see citing works

Nucleus basalis of Meynert neuronal activity during a delayed response task in monkey

Richardson, R. T., & DeLong, M. R. (1986) · Brain Research · doi:10.1016/0006-8993(86)91529-5 · Cited by 122 · see citing works

Direct excitation of parvalbumin‐positive interneurons by M 1 muscarinic acetylcholine receptors: roles in cellular excitability, inhibitory transmission and cognition

Yi, F., Ball, J., Stoll, K., Satpute, V. C., Mitchell, S., Pauli, J. L., Holloway, B. B., Johnston, A. D., Nathanson, N. M., Deisseroth, K. A., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.275453 · Cited by 118 · see citing works

Influence of Highly Distinctive Structural Properties on the Excitability of Pyramidal Neurons in Monkey Visual and Prefrontal Cortices

Amatrudo, J. M., Weaver, C. M., Crimins, J. L., Hof, P. R., Rosene, D. L., & Luebke, J. I. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2581-12.2012 · Cited by 111 · see citing works

Functional Nicotinic Acetylcholine Receptor Expression in Stem and Progenitor Cells of the Early Embryonic Mouse Cerebral Cortex

Atluri, P., Fleck, M. W., Shen, Q., Mah, S. J., Stadfelt, D., Barnes, W., Goderie, S. K., Temple, S., & Schneider, A. S. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0453 · Cited by 110 · see citing works

Nicotine activates immature “silent” connections in the developing hippocampus

Maggi, L., Magueresse, C. L., Changeux, J., & Cherubini, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437947100 · Cited by 109 · see citing works

Muscarinic acetylcholine receptors in macaque V1 are most frequently expressed by parvalbumin‐immunoreactive neurons

Disney, A. A., & Aoki, C. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21616 · Cited by 109 · see citing works

Developmental Excitation of Corticothalamic Neurons by Nicotinic Acetylcholine Receptors

Kassam, S. M., Herman, P. M., Goodfellow, N. M., Alves, N. C., & Lambe, E. K. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2645-08.2008 · Cited by 100 · see citing works

Neural interaction between the basal forebrain and functionally distinct prefrontal cortices in the rhesus monkey

Ghashghaei, H. T., & Barbas, H. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00585-6 · Cited by 100 · see citing works

Differential expression of muscarinic acetylcholine receptors across excitatory and inhibitory cells in visual cortical areas V1 and V2 of the macaque monkey

Disney, A. A., Domakonda, K. V., & Aoki, C. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21096 · Cited by 99 · see citing works

Alterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors

Ballesteros-Yáñez, I., Benavides-Piccione, R., Bourgeois, J.-P., Changeux, J.-P., & DeFelipe, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006269107 · Cited by 96 · see citing works

Calcium Imaging of Basal Forebrain Activity during Innate and Learned Behaviors

Harrison, T. C., Pinto, L., Brock, J. R., & Dan, Y. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00036 · Cited by 96 · see citing works

Layer-specific cholinergic control of human and mouse cortical synaptic plasticity

Verhoog, M. B., Obermayer, J., Kortleven, C., Wilbers, R., Wester, J., Baayen, J. C., de Kock, C. P. J., Meredith, R. M., & Mansvelder, H. D. (2016) · Nature Communications · doi:10.1038/ncomms12826 · Cited by 95 · see citing works

Impact of smoking abstinence on working memory neurocircuitry in adolescent daily tobacco smokers

Jacobsen, L. K., Mencl, W. E., Constable, R. T., Westerveld, M., & Pugh, K. R. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0797-9 · Cited by 93 · see citing works

The cholinergic innervation develops early and rapidly in the rat cerebral cortex: a quantitative immunocytochemical study

Mechawar, N., & Descarries, L. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00389-x · Cited by 91 · see citing works

α7 Nicotinic Acetylcholine Receptors Occur at Postsynaptic Densities of AMPA Receptor-Positive and -Negative Excitatory Synapses in Rat Sensory Cortex

Levy, R. B., & Aoki, C. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05001.2002 · Cited by 88 · see citing works

Acetylcholine-induced inhibition in the cat visual cortex is mediated by a GABAergic mechanism

Müller, C. M., & Singer, W. (1989) · Brain Research · doi:10.1016/0006-8993(89)90837-8 · Cited by 87 · see citing works

Selective removal of cholinergic neurons in the basal forebrain alters cued target detection

Chiba, A. A., Bushnell, P. J., Oshiro, W. M., & Gallagher, M. (1999) · NeuroReport · doi:10.1097/00001756-199909290-00044 · Cited by 83 · see citing works

NR2A-Containing NMDARs in the Prefrontal Cortex Are Required for Working Memory and Associated with Age-Related Cognitive Decline

McQuail, J. A., Beas, B. S., Kelly, K. B., Simpson, K. L., Frazier, C. J., Setlow, B., & Bizon, J. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2332-16.2016 · Cited by 80 · see citing works

Nicotinic α5 Subunits Drive Developmental Changes in the Activation and Morphology of Prefrontal Cortex Layer VI Neurons

Bailey, C. D. C., Alves, N. C., Nashmi, R., De Biasi, M., & Lambe, E. K. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.09.011 · Cited by 69 · see citing works

Disposed to Distraction: Genetic Variation in the Cholinergic System Influences Distractibility But Not Time-on-Task Effects

Berry, A. S., Demeter, E., Sabhapathy, S., English, B. A., Blakely, R., Sarter, M. F., & Lustig, C. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00607 · Cited by 66 · see citing works

Induction of Dendritic Spines by 2-Containing Nicotinic Receptors

Lozada, A. F., Wang, X., Gounko, N. V., Massey, K. A., Duan, J., Liu, Z., & Berg, D. K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6247-11.2012 · Cited by 65 · see citing works

Cholinergic Enhancement Increases the Effects of Voluntary Attention but Does Not Affect Involuntary Attention

Rokem, A., Landau, A. N., Garg, D., Prinzmetal, W., & Silver, M. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.118 · Cited by 65 · see citing works

A Randomized Trial to Assess the Efficacy and Safety of ABT-126, a Selective α7 Nicotinic Acetylcholine Receptor Agonist, in the Treatment of Cognitive Impairment in Schizophrenia

Haig, G. M., Bain, E., Robieson, W., Baker, J. D., & Othman, A. A. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.15010093 · Cited by 61 · see citing works

Distribution and effects of the muscarinic receptor subtypes in the primary visual cortex

Groleau, M., Kang, J. I., Huppé‐Gourgues, F., & Vaucher, E. (2015) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2015.00010 · Cited by 60 · see citing works

Distribution of choline acetyltransferase-immunoreactive axons in monkey frontal cortex

Lewis, D. A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90126-9 · Cited by 59 · see citing works

Cortico-thalamic connectivity is vulnerable to nicotine exposure during early postnatal development through α4/β2/α5 nicotinic acetylcholine receptors

Heath, C. J., King, S. L., Gotti, C., Marks, M. J., & Picciotto, M. R. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.130 · Cited by 59 · see citing works

Acetylcholinesterase in the human frontal associative cortex during the period of cognitive development: early laminar shifts and late innervation of pyramidal neurons

Kostović, I., Škavić, J., & Strinović, D. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90795-1 · Cited by 58 · see citing works

Contribution of Cholinergic and GABAergic Mechanisms to Direction Tuning, Discriminability, Response Reliability, and Neuronal Rate Correlations in Macaque Middle Temporal Area

Thiele, A., Herrero, J. L., Distler, C., & Hoffmann, K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0554-12.2012 · Cited by 57 · see citing works

Cholinergic suppression of visual responses in primate V1 is mediated by GABAergic inhibition

Disney, A. A., Aoki, C., & Hawken, M. J. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00188.2012 · Cited by 57 · see citing works

Muscarinic Receptors in Brain Stem and Mesopontine Cholinergic Arousal Functions

Yeomans, J. S. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-23274-9_11 · Cited by 51 · see citing works

Targeting Prefrontal Cortical Systems for Drug Development: Potential Therapies for Cognitive Disorders

Arnsten, A. F. T., & Wang, M. (2016) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103617 · Cited by 50 · see citing works

The design of novel muscarinic partial agonists that have functional selectivity in pharmacological preparations in vitro and reduced side-effect profile in vivo

Freedman, S. B., Dawson, G. R., Iversen, L. L., et al. (1993) · Life Sciences · doi:10.1016/0024-3205(93)90306-n · Cited by 48 · see citing works

Is There a Canonical Cortical Circuit for the Cholinergic System? Anatomical Differences Across Common Model Systems

Coppola, J. J., & Disney, A. A. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00008 · Cited by 48 · see citing works

Modulation-Specific and Laminar-Dependent Effects of Acetylcholine on Visual Responses in the Rat Primary Visual Cortex

Soma, S., Shimegi, S., Suematsu, N., Tamura, H., & Sato, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068430 · Cited by 46 · see citing works

Whole-Brain Monosynaptic Afferent Inputs to Basal Forebrain Cholinergic System

Hu, R. K., Jin, S., He, X., Xu, F., & Hu, J. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00098 · Cited by 46 · see citing works

Nicotinic α4β2 Cholinergic Receptor Influences on Dorsolateral Prefrontal Cortical Neuronal Firing during a Working Memory Task

Sun, Y.-A., Yang, Y., Galvin, V., Yang, S.-T., Arnsten, A., & Wang, M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0364-17.2017 · Cited by 46 · see citing works

Selective expression of m2 muscarinic receptor in the parvocellular channel of the primate visual cortex.

Mrzljak, L., Levey, A. I., & RAKIC, P. T. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.14.7337 · Cited by 43 · see citing works

Regulation of glutamate synapses by nicotinic acetylcholine receptors in auditory cortex

Metherate, R., & Hsieh, C. Y. (2003) · Neurobiology of Learning and Memory · doi:10.1016/s1074-7427(03)00062-5 · Cited by 41 · see citing works

Expression of m1‐type muscarinic acetylcholine receptors by parvalbumin‐immunoreactive neurons in the primary visual cortex: A comparative study of rat, guinea pig, ferret, macaque, and human

Disney, A. A., & Reynolds, J. H. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23456 · Cited by 40 · cited 1× · see citing works

Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotype

Fernández‐Jaén, A., López‐Martín, S., Albert, J., Fernández-Mayoralas, D. M., Fernández‐Perrone, A. L., de la Peña, M. J., Calleja‐Pérez, B., Rodríguez, M. R., López-Arribas, S., & Jareño, N. M. (2015) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2015.07.005 · Cited by 40 · see citing works

Association of the Nicotinic Receptor α7 Subunit Gene (CHRNA7) with Schizophrenia and Visual Backward Masking

Bakanidze, G., Roinishvili, M., Chkonia, E. D., Kitzrow, W., Richter, S., Neumann, K., Herzog, M. H., Brand, A., & Puls, I. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00133 · Cited by 38 · see citing works

Effects of neonatal monocular and binocular enucleation on transient acetylcholinesterase activity in developing rat visual cortex

Robertson, R. T., Fogolin, R. P., Tijerina, A. A., & Yu, J. Z. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90152-0 · Cited by 33 · see citing works

Muscarinic Attenuation of Mnemonic Rule Representation in Macaque Dorsolateral Prefrontal Cortex during a Pro- and Anti-Saccade Task

Major, A. J., Vijayraghavan, S., & Everling, S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2454-15.2015 · Cited by 32 · see citing works

Nicotinic acetylcholine receptor-mediated release of [3H]norepinephrine from developing and adult rat hippocampus: direct and indirect mechanisms

Leslie, F. M., Gallardo, K. A., & Park, M. K. (2002) · Neuropharmacology · doi:10.1016/s0028-3908(02)00019-9 · Cited by 32 · see citing works

Postsynaptic muscarinic M1 receptors activate prefrontal cortical EEG of C57BL/6J mouse

Douglas, C. L., Baghdoyan, H. A., & Lydic, R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00318.2002 · Cited by 30 · see citing works

Muscarinic acetylcholine receptors are expressed by most parvalbumin‐immunoreactive neurons in area <scp>MT</scp> of the macaque

Disney, A. A., Alasady, H. A., & Reynolds, J. H. (2014) · Brain and Behavior · doi:10.1002/brb3.225 · Cited by 28 · see citing works

Functional and laminar dissociations between muscarinic and nicotinic cholinergic neuromodulation in the tree shrew primary visual cortex

Bhattacharyya, A., Bießmann, F., Veit, J., Kretz, R., & Rainer, G. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08052.x · Cited by 24 · see citing works

Cholinergic Overstimulation Attenuates Rule Selectivity in Macaque Prefrontal Cortex

Major, A. J., Vijayraghavan, S., & Everling, S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3198-17.2017 · Cited by 22 · see citing works

High-Affinity Nicotinic Receptors Modulate Spontaneous Cortical Up States In Vitro

Sigalas, C., Rigas, P., Tsakanikas, P., & Skaliora, I. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5222-14.2015 · Cited by 21 · see citing works

Impaired functional organization in the visual cortex of muscarinic receptor knock-out mice

Groleau, M., Nguyen, H. N., Vanni, M. P., Huppé‐Gourgues, F., Casanova, C., & Vaucher, E. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.016 · Cited by 20 · see citing works

COMT genotype is associated with differential expression of muscarinic M1 receptors in human cortex

Dean, B., & Scarr, E. (2016) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32440 · Cited by 18 · see citing works

Muscarine-binding sites localized to cortical dopamine terminals

Liskowsky, D. R., & Potter, L. T. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90169-7 · Cited by 15 · see citing works

Pharmacological Differences Between Rat Frontal Cortex and Hippocampus in the Nicotinic Modulation of Noradrenaline Release Implicate Distinct Receptor Subtypes

Kennett, A., Heal, D. J., & Wonnacott, S. (2012) · Nicotine & Tobacco Research · doi:10.1093/ntr/nts128 · Cited by 15 · see citing works

Evidence that perihypoglossal neurons involved in vestibular-auditory and gaze control functions respond to nerve growth factor

Sukhov, R. R., Cayouette, M. H., Radeke, M. J., Feinstein, S. C., Blumberg, D., Rosenthal, A., Price, D. L., & Koliatsos, V. E. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970630)383:2 · Cited by 11 · see citing works

Premature Aging Phenotype in Mice Lacking High-Affinity Nicotinic Receptors: Region-Specific Changes in Layer V Pyramidal Cell Morphology

Konsolaki, E., & Skaliora, I. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu019 · Cited by 9 · see citing works

Development of prefrontal cortex

Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378 · see citing works

Dynamic Changes in Human Brain Connectivity Following Ultrasound NeuromodulationPreprint

Atkinson-Clément, C., Alkhawashki, M., Gatica, M., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4667550/v1 · Cited by 1 · see citing works

The use of muscarinic toxins in the study of muscarinic receptors

Jerusalinsky, D. A., Harvey, A. R., Karlsson, E., et al. (1997) · Life Sciences · doi:10.1016/s0024-3205(97)00061-1 · Cited by 7 · see citing works

Prospects of neuromodulation for chronic pain

Isagulyan, E. D., Mikhailova, V. A., Aslakhanova, K. S., & Slavin, K. V. (2021) · Brain Disorders · doi:10.1016/j.dscb.2021.100027 · Cited by 4 · see citing works

Practical Tips in Neuromodulation for Pain

Bendersky, D. (2018) · Anaesthesia & Critical Care Medicine Journal · doi:10.23880/accmj-16000134

PO001 / #500 A NEW BREAKTHROUGH NEUROMODULATION METHOD: ELECTRO-IONIC MODULATION (EIM)

Soybaş, Z., Şimşek, S., Erol, F. M. B., et al. (2022) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2022.08.176