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Basal forebrain cholinergic signalling: development, connectivity and roles in cognition
Open accessAbstract
Acetylcholine plays an essential role in fundamental aspects of cognition. Studies that have mapped the activity and functional connectivity of cholinergic neurons have shown that the axons of basal forebrain cholinergic neurons innervate the pallium with far more topographical and functional organization than was historically appreciated. Together with the results of studies using new probes that allow release of acetylcholine to be detected with high spatial and temporal resolution, these findings have implicated cholinergic networks in 'binding' diverse behaviours that contribute to cognition. Here, we review recent findings on the developmental origins, connectivity and function of cholinergic neurons, and explore the participation of cholinergic signalling in the encoding of cognition-related behaviours.
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“ACh signaling is essential for neuronal development, where it plays a trophic role in establishing and maintaining neuronal connectivity [111, 112].”
From Adolescent nicotine exposure and persistent neurocircuitry changes: unveiling lifelong psychiatric risks (2025) · cites this paper as [111]
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Cites
The cholinergic hypothesis of geriatric memory dysfunction
Bartus, R. T., Dean, R. L., Beer, B., & Lippa, A. S. (1982) · Science · doi:10.1126/science.7046051 · Cited by 5,545
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
Theta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332
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
The role of acetylcholine in learning and memory
Hasselmo, M. E. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.09.002 · Cited by 1,693
Alzheimer's disease: Targeting the Cholinergic System
H. Ferreira-Vieira, T., M. Guimaraes, I., R. Silva, F., & M. Ribeiro, F. (2016) · Current Neuropharmacology · doi:10.2174/1570159x13666150716165726 · Cited by 1,551
Molecular diversity and specializations among the cells of the adult mouse brain
Saunders, A., Macosko, E. Z., Wysoker, A., Goldman, M., Krienen, F. M., de Rivera, H., Bien, E., Baum, M., Bortolin, L., Wang, S., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.028 · Cited by 1,531
Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior
Picciotto, M. R., Higley, M. J., & Mineur, Y. S. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.036 · Cited by 1,404
Human Memory and the Cholinergic System
Drachman, D. A. (1974) · Archives of Neurology · doi:10.1001/archneur.1974.00490320001001 · Cited by 1,398
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Nicotinic Acetylcholine Receptors and Nicotinic Cholinergic Mechanisms of the Central Nervous System
Dani, J. A., & Bertrand, D. (2007) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.47.120505.105214 · Cited by 1,197
A long, remarkable journey: Tangential migration in the telencephalon
Marín, Ó., & Rubenstein, J. L. R. (2001) · Nature reviews. Neuroscience · doi:10.1038/35097509 · Cited by 1,077
Cholinergic systems in mammalian brain and spinal cord
WOOLF, N. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90006-m · Cited by 948
Brain nicotinic acetylcholine receptors: native subtypes and their relevance
Gotti, C., Zoli, M., & Clementi, F. (2006) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2006.07.004 · Cited by 882
Sussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873
Basal Forebrain Cholinergic Circuits and Signaling in Cognition and Cognitive Decline
Ballinger, E. C., Ananth, M. R., Talmage, D. A., & Role, L. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.006 · Cited by 763
Self-citationSingle-cell transcriptomic profiling of the aging mouse brain
Ximerakis, M., Lipnick, S. L., Innes, B. T., Simmons, S. K., Adiconis, X., Dionne, D., Mayweather, B. A., Nguyen, L., Niziolek, Z., Ozek, C., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0491-3 · Cited by 736
Diversity and Pattern in the Developing Spinal Cord
Tanabe, Y., & Jessell, T. M. (1996) · Science · doi:10.1126/science.274.5290.1115 · Cited by 718
Organization of cerebral cortical afferent systems in the rat. II. Magnocellular basal nucleus
Saper, C. B. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902220302 · Cited by 703
Nicotinic acetylcholine involvement in cognitive function in animals
Levin, E. D., & Simon, B. B. (1998) · Psychopharmacology · doi:10.1007/s002130050667 · Cited by 675
THE ACTION OF CERTAIN ESTERS AND ETHERS OF CHOLINE, AND THEIR RELATION TO MUSCARINE
Dale, H. H. (1914) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)08268-0 · Cited by 658
A third vesicular glutamate transporter expressed by cholinergic and serotoninergic neurons
Gras, C., Herzog, E., Bellenchi, G. C., Bernard, V., Ravassard, P., Pohl, M., Gasnier, B., Giros, B., & El Mestikawy, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05442.2002 · Cited by 639
Muscarinic acetylcholine receptors: mutant mice provide new insights for drug development
Wess, J., Eglen, R. M., & Gautam, D. (2007) · Nature Reviews Drug Discovery · doi:10.1038/nrd2379 · Cited by 637
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
Katz, B., & Miledi, R. (1965) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1965.0016 · Cited by 609
Molecular architecture of the developing mouse brain
La Manno, G., Siletti, K., Furlan, A., Gyllborg, D., Vinsland, E., Mossi Albiach, A., Mattsson Langseth, C., Khven, I., Lederer, A. R., Dratva, L. M., et al. (2021) · Nature · doi:10.1038/s41586-021-03775-x · Cited by 563
Flames, N., Pla, R., Gelman, D. M., Rubenstein, J. L. R., Puelles, L., & Marín, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2750-07.2007 · Cited by 560
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
Hippocampal theta activity following selective lesion of the septal cholinergic systeM
Lee, M., Chrobak, J. J., Attila Gabor, S. I. K., Wiley, R. G., & Buzsáki, G. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90341-7 · Cited by 496
Developmental diversification of cortical inhibitory interneurons
Mayer, C., Hafemeister, C., Bandler, R. C., Machold, R., Batista Brito, R., Jaglin, X., Allaway, K., Butler, A., Fishell, G., & Satija, R. (2018) · Nature · doi:10.1038/nature25999 · Cited by 492
Molecular characterization of selectively vulnerable neurons in Alzheimer’s disease
Leng, K., Li, E., Eser, R., Piergies, A., Sit, R., Tan, M., Neff, N., Li, S. H., Rodriguez, R. D., Suemoto, C. K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00764-7 · Cited by 485
Improved CUT&RUN chromatin profiling tools
Meers, M. P., Bryson, T. D., Henikoff, J. G., & Henikoff, S. (2019) · eLife · doi:10.7554/elife.46314 · Cited by 474
The ins and outs of the striatum: Role in drug addiction
Yager, L. M., Garcia, A. F., Wunsch, A. M., & Ferguson, S. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.033 · Cited by 467
The hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430
Kosaka, T., Tauchi, M., & Dahl, J. L. (1988) · Experimental Brain Research · doi:10.1007/bf00247609 · Cited by 417
Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFR
Marvin, J. S., Scholl, B., Wilson, D. E., Podgorski, K., Kazemipour, A., Müller, J. A., Schoch, S., Quiroz, F. J. U., Rebola, N., Bao, H., et al. (2018) · Nature Methods · doi:10.1038/s41592-018-0171-3 · Cited by 412
An optimized acetylcholine sensor for monitoring in vivo cholinergic activity
Jing, M., Li, Y., Zeng, J., Huang, P., Skirzewski, M., Kljakic, O., Peng, W., Qian, T., Tan, K., Zou, J., et al. (2020) · Nature Methods · doi:10.1038/s41592-020-0953-2 · Cited by 408
Vandecasteele, M., Varga, V., Berényi, A., Papp, E., Barthó, P., Venance, L., Freund, T. F., & Buzsáki, G. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411233111 · Cited by 406
Central Cholinergic Neurons Are Rapidly Recruited by Reinforcement Feedback
Hangya, B., Ranade, S. P., Lorenc, M., & Kepecs, A. (2015) · Cell · doi:10.1016/j.cell.2015.07.057 · Cited by 399
A genetically encoded fluorescent acetylcholine indicator for in vitro and in vivo studies
Jing, M., Zhang, P., Wang, G., Feng, J., Mesik, L., Zeng, J., Jiang, H., Wang, S., Looby, J. C., Guagliardo, N. A., et al. (2018) · Nature Biotechnology · doi:10.1038/nbt.4184 · Cited by 392
Self-citationMotor neurons and the generation of spinal motor neuron diversity
Stifani, N. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00293 · Cited by 389
Cholinergic circuitry of the human nucleus basalis and its fate in Alzheimer's disease
Mesulam, M. M. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23415 · Cited by 382
Mineur, Y. S., Obayemi, A., Wigestrand, M. B., Fote, G. M., Calarco, C. A., Li, A. M., & Picciotto, M. R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219731110 · Cited by 375
Liu, A. K. L., Chang, R. C., Pearce, R. K. B., & Gentleman, S. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1392-5 · Cited by 365
A genetically encoded fluorescent sensor for in vivo imaging of GABA
Marvin, J. S., Shimoda, Y., Magloire, V., Leite, M., Kawashima, T., Jensen, T. P., Kolb, I., Knott, E. L., Novák, O., Podgorski, K., et al. (2019) · Nature Methods · doi:10.1038/s41592-019-0471-2 · Cited by 362
Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers
Storm, E. E., Garel, S., Borello, U., Hébert, J. M., Martı́nez, S., McConnell, S. K., Martin, G. R., & Rubenstein, J. L. R. (2006) · Development · doi:10.1242/dev.02324 · Cited by 361
The ventral pallidum: Subregion-specific functional anatomy and roles in motivated behaviors
Root, D. H., Meléndez, R. I., Záborszky, L., & Napier, T. C. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.03.005 · Cited by 359
Eckenstein, F., & Baughman, R. W. (1984) · Nature · doi:10.1038/309153a0 · Cited by 356
Thiele, A., & Bellgrove, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.008 · Cited by 350
Large-scale two-photon calcium imaging in freely moving mice
Zong, W., Obenhaus, H. A., Skytøen, E. R., Eneqvist, H., de Jong, N. L., do Vale, R. D., Jorge, M., Moser, M., & Moser, E. I. (2022) · Cell · doi:10.1016/j.cell.2022.02.017 · Cited by 344
Phasic acetylcholine release and the volume transmission hypothesis: time to move on
Sarter, M. F., Parikh, V., & Howe, W. M. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2635 · Cited by 340
Klinkenberg, I., Sambeth, A., & Blokland, A. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.033 · Cited by 335
Extended Amygdala and Basal Forebrain
Alheid, G. F. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07082.x · Cited by 334
Preissl, S., Fang, R., Huang, H., Zhao, Y., Raviram, R., Gorkin, D. U., Zhang, Y., Sos, B. C., Afzal, V., Dickel, D. E., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0079-3 · Cited by 332
Ren, J., Qin, C., Hu, F., Tan, J., Qiu, L., Zhao, S., Feng, G., & Luo, M. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.038 · Cited by 315
Intravenous nicotine in Alzheimer's disease: a pilot study
NEWHOUSE, P. A., Sunderland, T., Tariot, P. N., Blumhardt, C. L., Weingartner, H., Mellow, A. M., & Murphy, D. L. (1988) · Psychopharmacology · doi:10.1007/bf00174504 · Cited by 308
Human cholinergic basal forebrain: chemoanatomy and neurologic dysfunction
Mufson, E. J., Ginsberg, S. D., Ikonomović, M. D., & DeKosky, S. T. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(03)00068-1 · Cited by 295
Functional consequences of neuropeptide and small-molecule co-transmission
Nusbaum, M. P., Blitz, D. M., & Marder, E. E. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.56 · Cited by 289
DNA methylation atlas of the mouse brain at single-cell resolution
Liu, H., Zhou, J., Tian, W., Luo, C., Bartlett, A., Aldridge, A., Lucero, J., Osteen, J. K., Nery, J. R., Chen, H., et al. (2021) · Nature · doi:10.1038/s41586-020-03182-8 · Cited by 289
Energy matters: presynaptic metabolism and the maintenance of synaptic transmission
Li, S., & Sheng, Z. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00535-8 · Cited by 285
Záborszky, L., Csordás, A., Mosca, K., Kim, J., Gielow, M. R., Vadász, C., & Nádasdy, Z. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht210 · Cited by 284
Jones, B. E. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0444-2 · Cited by 283
Dalley, J. W., McGaughy, J., O'Connell, M. T., Cardinal, R. N., Levita, L., & Robbins, T. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-13-04908.2001 · Cited by 277
Mechanisms and functions of GABA co-release
Tritsch, N. X., Granger, A. J., & Sabatini, B. L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2015.21 · Cited by 276
Entorhinal cortex dysfunction in Alzheimer's disease
Igarashi, K. M. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.11.006 · Cited by 276
Neural Circuit Motifs in Valence Processing
Tye, K. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.001 · Cited by 268
Increases in cortical acetylcholine release during sustained attention performance in rats
Himmelheber, A. M., Sarter, M., & Bruno, J. P. (2000) · Cognitive Brain Research · doi:10.1016/s0926-6410(00)00012-4 · Cited by 261
Early emergence of cortical interneuron diversity in the mouse embryo
Mi, D., Li, Z., Lim, L., Li, M., Moissidis, M., Yang, Y., Gao, T., Hu, T. X., Pratt, T., Price, D. J., et al. (2018) · Science · doi:10.1126/science.aar6821 · Cited by 259
Rethinking the Pedunculopontine Nucleus: From Cellular Organization to Function
Mena‐Segovia, J., & Bolam, J. P. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.027 · Cited by 257
Ginsberg, S. D., Che, S., Wuu, J., Counts, S., & Mufson, E. J. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03764.x · Cited by 253
Mufson, E. J., Bothwell, M. A., Hersh, L. B., & Kordower, J. H. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902850204 · Cited by 245
The Input-Output Relationship of the Cholinergic Basal Forebrain
Gielow, M. R., & Záborszky, L. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.060 · Cited by 243
Jones, C. K., Byun, N. E., & Bubser, M. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.199 · Cited by 241
Umbriaco, D., Watkins, K. C., Descarries, L., Cozzari, C., & Hartman, B. K. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903480304 · Cited by 237
Zhao, Y., Marín, O., Hermesz, E., Powell, A., Flames, N., Palkovits, M., Rubenstein, J. L. R., & Westphal, H. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1537759100 · Cited by 227
Dual-transmitter neurons: functional implications of co-release and co-transmission
Vaaga, C. E., Borisovska, M., & Westbrook, G. L. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.04.010 · Cited by 221
Aghourian, M., Legault-Denis, C., Soucy, J.-P., Rosa-Neto, P., Gauthier, S., Kostikov, A., Gravel, P., & Bédard, M.-A. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.183 · Cited by 220
Neuronal and Extraneuronal Nicotinic Acetylcholine Receptors
Zoli, M., Pucci, S., Vilella, A., & Gotti, C. (2018) · Current Neuropharmacology · doi:10.2174/1570159x15666170912110450 · Cited by 219
Cholinergic modulation of hippocampal network function
Ruivo, L. M. T.-G., & Mellor, J. R. (2013) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2013.00002 · Cited by 214
An action potential initiation mechanism in distal axons for the control of dopamine release
Liu, C., Cai, X., Ritzau-Jost, A., Kramer, P. F., Li, Y., Khaliq, Z. M., Hallermann, S., & Kaeser, P. S. (2022) · Science · doi:10.1126/science.abn0532 · Cited by 213
Eiden, L. E. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.70062227.x · Cited by 209
Systematic Regional Variations in the Loss of Cortical Cholinergic Fibers in Alzheimer's Disease
Geula, C., & Mesulam, M.-M. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.2.165 · Cited by 202
Cortical cholinergic fibers in aging and Alzheimer's disease: A morphometric study
Geula, C., & Mesulam, M. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90399-0 · Cited by 202
Specific basal forebrain-cortical cholinergic circuits coordinate cognitive operations
Záborszky, L., Gombkoto, P., Varsanyi, P., Gielow, M. R., Poe, G., Role, L. W., Ananth, M., Rajebhosale, P., Talmage, D. A., Hasselmo, M. E., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1676-18.2018 · Cited by 202
Self-citationCorelease of acetylcholine and GABA from cholinergic forebrain neurons
Saunders, A., Granger, A. J., & Sabatini, B. L. (2015) · eLife · doi:10.7554/elife.06412 · Cited by 200
Co-release of acetylcholine and GABA by the starburst amacrine cells
O'Malley, D., Sandell, J. H., & Masland, R. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-04-01394.1992 · Cited by 195
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
Cholinergic regulation of mood: from basic and clinical studies to emerging therapeutics
Dulawa, S. C., & Janowsky, D. S. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0219-x · Cited by 187
Amilhon, B., Lepicard, È., Renoir, T., Mongeau, R., Popa, D., Poirel, O., Miot, S., Gras, C., Gardier, A. M., Gallego, J., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5196-09.2010 · Cited by 186
Jiang, L., Kundu, S., Lederman, J., López‐Hernández, G. Y., Ballinger, E. C., Wang, S., Talmage, D. A., & Role, L. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.028 · Cited by 186
Self-citationMolecular basis of muscarinic receptor function
Wess, J. (1993) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(93)90049-p · Cited by 182
Regulation of synaptic transmission and plasticity by neuronal nicotinic acetylcholine receptors
McKay, B. E., Placzek, A. N., & Dani, J. A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.001 · Cited by 181
Ruivo, L. M. T.-G., Baker, K. L., Conway, M. W., Kinsley, P. J., Gilmour, G., Phillips, K. G., Isaac, J. T. R., Lowry, J. P., & Mellor, J. R. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.085 · Cited by 181
Cholinergic interneurons mediate fast VGluT3-dependent glutamatergic transmission in the striatum
Higley, M. J., Gittis, A. H., Oldenburg, I. A., Balthasar, N., Seal, R. P., Edwards, R. H., Lowell, B. B., Kreitzer, A. C., & Sabatini, B. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019155 · Cited by 175
The Basal Forebrain Cholinergic Projection System in Mice
Záborszky, L., van den Pol, A. N., & Gyengési, E. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10028-7 · Cited by 173
Cell type-specific long-range connections of basal forebrain circuit
Do, J. P. H., Xu, M., Lee, S., Chang, W.-C., Zhang, S., Chung, S., Yung, T. J., Fan, J. L., Miyamichi, K., Luo, L., et al. (2016) · eLife · doi:10.7554/elife.13214 · Cited by 173
Co-transmission of acetylcholine and GABA regulates hippocampal states
Takács, V. T., Cserép, C., Schlingloff, D., Pósfai, B., Szőnyi, A., Sos, K. E., Környei, Z., Dénes, Á., Gulyás, A. I., Freund, T. F., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05136-1 · Cited by 169
Complete morphologies of basal forebrain cholinergic neurons in the mouse
Wu, H., Williams, J., & Nathans, J. (2014) · eLife · doi:10.7554/elife.02444 · Cited by 167
Berse, B., & Blusztajn, J. K. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.38.22101 · Cited by 164
The acetylcholine receptor at the neuromuscular junction
Peper, K., Bradley, R. J., & Dreyer, F. (1982) · Physiological Reviews · doi:10.1152/physrev.1982.62.4.1271 · Cited by 164
Alkaslasi, M. R., Piccus, Z. E., Hareendran, S., Silberberg, H., Chen, L., Zhang, Y., Petros, T. J., & Le Pichon, C. E. (2021) · Nature Communications · doi:10.1038/s41467-021-22691-2 · Cited by 163
Muscarinic Signaling in the Brain
Thiele, A. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170433 · Cited by 155
Flandin, P., Zhao, Y., Vogt, D., Jeong, J., Long, J., Potter, G., Westphal, H., & Rubenstein, J. L. R. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.020 · Cited by 155
Howe, W. M., Gritton, H. J., Lusk, N. A., Roberts, E. A., Hetrick, V. L., Berke, J. D., & Sarter, M. F. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2737-16.2017 · Cited by 155
Co-release of acetylcholine and gamma-aminobutyric acid by a retinal neuron
O'Malley, D. M., & Masland, R. H. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.9.3414 · Cited by 150
Spatiotemporally heterogeneous coordination of cholinergic and neocortical activity
Lohani, S., Moberly, A. H., Benisty, H., Landa, B., Jing, M., Li, Y., Higley, M. J., & Cardin, J. A. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01202-6 · Cited by 150
Time of origin of cholinergic neurons in the rat basal forebrain
Semba, K., & Fibiger, H. C. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902690107 · Cited by 149
Koh, S., & Loy, R. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-09-02999.1989 · Cited by 147
Diffuse Cortical Projection Systems: Anatomical Organization and Role in Cortical Function
Saper, C. B. (1987) · Comprehensive physiology · doi:10.1002/cphy.cp010506 · Cited by 146
Cholinergic modulation of spatial learning, memory and navigation
Solari, N., & Hangya, B. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14089 · Cited by 146
Lawson, V. H., & Bland, B. H. (1993) · Experimental Neurology · doi:10.1006/exnr.1993.1047 · Cited by 144
Cholinergic modulation of striatal microcircuits
Abudukeyoumu, N., Hernández-Flores, T., Garcia-Munoz, M., & Arbuthnott, G. W. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13949 · Cited by 144
Bloem, B., Schoppink, L., Rotaru, D. C., Faiz, A., Hendriks, P., Mansvelder, H. D., van de Berg, W. D. J., & Wouterlood, F. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3011-14.2014 · Cited by 143
Alifragis, P., Liapi, A., & Parnavelas, J. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1245-04.2004 · Cited by 143
Cellular, Synaptic and Network Effects of Acetylcholine in the Neocortex
Colangelo, C., Shichkova, P., Keller, D. X., Markram, H., & Ramaswamy, S. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00024 · Cited by 143
Petrou, M., Frey, K. A., Kilbourn, M. R., Scott, P. J. H., Raffel, D. M., Bohnen, N. I., Müller, M. L. T. M., Albin, R. L., & Koeppe, R. A. (2014) · Journal of Nuclear Medicine · doi:10.2967/jnumed.113.124792 · Cited by 142
Fisher, A. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07507.x · Cited by 140
Fragkouli, A., van Wijk, N. V., Lopes, R., Kessaris, N., & Pachnis, V. (2009) · Development · doi:10.1242/dev.038083 · Cited by 135
Turrini, P., Casu, M. A., Wong, T. P., De Koninck, Y., Ribeiro-da-Silva, A., & Cuello, A. C. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00172-5 · Cited by 135
Cholinergic Modulation of Glial Function During Aging and Chronic Neuroinflammation
Gamage, R. V., Wagnon, I. M., Rossetti, I., Childs, R., Niedermayer, G., Chesworth, R., & Gyengési, E. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.577912 · Cited by 134
Majdi, A., Sadigh‐Eteghad, S., Aghsan, S. R., Farajdokht, F., Vatandoust, S. M., Abbas-Abad, A. N., & Mahmoudi, J. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0089 · Cited by 130
Cholinergic shaping of neural correlations
Minces, V. H., Pinto, L., Dan, Y., & Chiba, A. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621493114 · Cited by 129
Impact of Basal Forebrain Cholinergic Inputs on Basolateral Amygdala Neurons
Ünal, Ç. T., Paré, D., & Záborszky, L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2706-14.2015 · Cited by 124
Granger, A. J., Wang, W., Robertson, K., El-Rifai, M., Zanello, A. F., Bistrong, K., Saunders, A., Chow, B. W., Nuñez, V., Turrero García, M., et al. (2020) · eLife · doi:10.7554/elife.57749 · Cited by 124
Acetylcholine, a New Active Principle of Ergot
Ewins, A. J. (1914) · Biochemical Journal · doi:10.1042/bj0080044 · Cited by 122
A regulatory network to segregate the identity of neuronal subtypes.
Lee, S., Lee, B., Joshi, K., Pfaff, S. L., Lee, J. W., & Lee, S.-K. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.03.021 · Cited by 122
Pax6 influences the time and site of origin of glial precursors in the ventral neural tube.
Sun, T., Pringle, N., Hardy, A. P., Richardson, W., & Smith, H. (1998) · Molecular and cellular neurosciences · doi:10.1006/mcne.1998.0711 · Cited by 121
Cho, H.-H., Cargnin, F., Kim, Y., Lee, B., Kwon, R.-J., Nam, H., Shen, R., Barnes, A. P., Lee, J. W., Lee, S., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004280 · Cited by 116
Involvement of the cholinergic system in conditioning and perceptual memory
Robinson, L., Platt, B., & Riedel, G. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.01.055 · Cited by 115
Cholinergic Modulation of Neuroinflammation: Focus on α7 Nicotinic Receptor
Piovesana, R., Intriago, M. S. S., Dini, L., & Tata, A. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094912 · Cited by 115
Cholinergic suppression of hippocampal sharp-wave ripples impairs working memory
Zhang, Y., Cao, L., Varga, V., Jing, M., Karadas, M., Li, Y., & Buzsáki, G. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2016432118 · Cited by 111
Chandler, D. J., & Waterhouse, B. D. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00020 · Cited by 110
Transcriptional mechanisms controlling motor neuron diversity and connectivity
di Sanguinetto, S. D. T., Dasen, J. S., & Arber, S. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.04.002 · Cited by 109
Retinoids control anterior and dorsal properties in the developing forebrain.
Halilagic, A., Ribes, V., Ghyselinck, N., Zile, M., Dollé, P., & Studer, M. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2006.11.021 · Cited by 106
Cholinergic regulation of fear learning and extinction
Wilson, M. A., & Fadel, J. R. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23840 · Cited by 106
Kramer, P. F., Brill-Weil, S. G., Cummins, A. C., Zhang, R., Camacho-Hernandez, G. A., Newman, A. H., Eldridge, M. A. G., Averbeck, B. B., & Khaliq, Z. M. (2022) · Neuron · doi:10.1016/j.neuron.2022.07.011 · Cited by 104
Basal forebrain cholinergic system in the dementias: Vulnerability, resilience, and resistance
Geula, C., Dunlop, S. R., Ayala, I., Kawles, A. S., Flanagan, M. E., Gefen, T., & Mesulam, M. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15471 · Cited by 102
Cotransmission of acetylcholine and GABA
Granger, A. J., Mulder, N., Saunders, A. B., & Sabatini, B. L. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.031 · Cited by 101
Wang, Y., Wang, X., Lu, J.-J., Li, Q., Gao, C., Liu, X.-H., Sun, Y., Yang, M., Lim, Y. P., Evin, G. M., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2733-10.2011 · Cited by 99
Mori, T., Yuxing, Z., Takaki, H., Takeuchi, M., Iseki, K., Hagino, S., Kitanaka, J., Takemura, M., Misawa, H., Ikawa, M., et al. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03415.x · Cited by 99
Schmitz, T. W., Mur, M., Aghourian, M., Bédard, M., & Spreng, R. N. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.001 · Cited by 99
Díaz‐García, C. M., Lahmann, C., Martínez‐François, J. R., Li, B., Koveal, D., Nathwani, N., Rahman, M., Keller, J. P., Marvin, J. S., Looger, L. L., et al. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24433 · Cited by 99
The nicotinic acetylcholine receptor: From molecular biology to cognition
Changeux, J., Corringer, P., & Maskos, U. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.03.024 · Cited by 98
An essential role of acetylcholine-glutamate synergy at habenular synapses in nicotine dependence
Frahm, S., Antolin-Fontes, B., Görlich, A., Zander, J.-F., Ahnert-Hilger, G., & Ibañez-Tallon, I. (2015) · eLife · doi:10.7554/elife.11396 · Cited by 98
Borden, P. M., Zhang, P., Shivange, A. V., Marvin, J. S., Cichon, J., Dan, C., Podgorski, K., Figueiredo, A. M. P. D., Novák, O., Tanimoto, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.07.939504 · Cited by 98
Laszlovszky, T., Schlingloff, D., Hegedüs, P., Freund, T. F., Gulyás, A. I., Kepecs, Á., & Hangya, B. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0648-0 · Cited by 98
Crouse, R. B., Kim, K. K. O., Batchelor, H. M., Girardi, E., Kamaletdinova, R., Chan, J., Rajebhosale, P., Pittenger, S. T., Role, L. W., Talmage, D. A., et al. (2020) · eLife · doi:10.7554/elife.57335 · Cited by 98
Self-citationTrkAGene Ablation in Basal Forebrain Results in Dysfunction of the Cholinergic Circuitry
Sanchez‐Ortiz, E., Yui, D., Song, D., Li, Y., Rubenstein, J. L. R., Reichardt, L. F., & Parada, L. F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6314-11.2012 · Cited by 94
Intermediate targets in formation of topographic projections: inputs from the thalamocortical system
Garel, S., & Rubenstein, J. L. R. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.014 · Cited by 89
Regulation of neuronal nicotinic receptor traffic and expression
Gaimarri, A., Moretti, M., Riganti, L., Zanardi, A., Clementi, F., & Gotti, C. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.02.005 · Cited by 89
Poulin, A. N., Guerci, A., Mestikawy, S. E., & Semba, K. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21081 · Cited by 87
A Central Role for Mixed Acetylcholine/GABA Transmission in Direction Coding in the Retina
Sethuramanujam, S., McLaughlin, A. J., deRosenroll, G., Hoggarth, A., Schwab, D. J., & Awatramani, G. B. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.041 · Cited by 86
Furusho, M., Ono, K., Takebayashi, H., Masahira, N., Kagawa, T., Ikeda, K., & Ikenaka, K. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.01.031 · Cited by 85
Obermayer, J., Luchicchi, A., Heistek, T. S., de Kloet, S. F., Terra, H., Bruinsma, B., Mnie-Filali, O., Kortleven, C., Galakhova, A. A., Khalil, A. J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13244-9 · Cited by 83
Motor neurons and oligodendrocytes arise from distinct cell lineages by progenitor recruitmentPreprint
Ravanelli, A. M., & Appel, B. (2015) · Genes & Development · doi:10.1101/gad.271312.115 · Cited by 82
The role of basal forebrain cholinergic neurons in fear and extinction memory
Knox, D. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.001 · Cited by 81
Extensive and spatially variable within-cell-type heterogeneity across the basolateral amygdala
O’Leary, T. P., Sullivan, K. E., Wang, L., Clements, J., Lemire, A. L., & Cembrowski, M. S. (2020) · eLife · doi:10.7554/elife.59003 · Cited by 81
Isoform cell-type specificity in the mouse primary motor cortex
Booeshaghi, A. S., Yao, Z., van Velthoven, C. T. J., Smith, K. A., Tasic, B., Zeng, H., & Pachter, L. S. (2021) · Nature · doi:10.1038/s41586-021-03969-3 · Cited by 81
Elshatory, Y. M., & Gan, L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5730-07.2008 · Cited by 80
Endogenous FGF-2 Is Important for Cholinergic Sprouting in the Denervated Hippocampus
Fagan, A. M., Suhr, S. T., Lucidi‐Phillipi, C. A., Peterson, D. A., Holtzman, D. M., & Gage, F. H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02499.1997 · Cited by 79
Aitta‐aho, T., Hay, Y. A., Phillips, B. U., Saksida, L. M., Bussey, T. J., Paulsen, O., & Apergis‐Schoute, J. (2018) · Current Biology · doi:10.1016/j.cub.2018.06.064 · Cited by 79
The role of acetylcholine in negative encoding bias: Too much of a good thing?
Mineur, Y. S., & Picciotto, M. R. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.14641 · Cited by 78
THE PROBLEMS OF NEURONS WITH LONG AXONS
Cavanagh, J. (1984) · The Lancet · doi:10.1016/s0140-6736(84)92457-7 · Cited by 72
Target selectivity of septal cholinergic neurons in the medial and lateral entorhinal cortex
Desikan, S., Koser, D. E., Neitz, A., & Monyer, H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716531115 · Cited by 72
Fritz, H.-C., Ray, N. J., Dyrba, M., Sorg, C., Teipel, S. J., & Grothe, M. J. (2018) · Human Brain Mapping · doi:10.1002/hbm.24417 · Cited by 71
Diverse Spatiotemporal Scales of Cholinergic Signaling in the Neocortex
Disney, A. A., & Higley, M. J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1306-19.2019 · Cited by 71
NKX2-1 Is Required in the Embryonic Septum for Cholinergic System Development, Learning, and Memory
Magno, L., Barry, C., Schmidt‐Hieber, C., Theodotou, P., Häusser, M., & Kessaris, N. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.07.053 · Cited by 69
Upmanyu, N., Jin, J., Emde, H. V. D., Ganzella, M., Bösche, L., Malviya, V. N., Zhuleku, E., Politi, A. Z., Ninov, M., Silbern, I., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.02.008 · Cited by 69
Central cholinergic regulation of respiration: nicotinic receptors
Shao, X. M., & Feldman, J. L. (2009) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.88 · Cited by 68
Ma, X., Zhang, Y., Wang, L., Li, N., Barkai, E., Zhang, X., Lin, L., & Xu, J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1568-19.2020 · Cited by 68
Wong, D. F., Kuwabara, H., Horti, A. G., Roberts, J., Nandi, A., Cascella, N. G., Brašić, J. R., Weerts, E. M., Kitzmiller, K., Phan, J.-A., et al. (2018) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyy021 · Cited by 66
Interneuron Types and Their Circuits in the Basolateral Amygdala
Hájos, N. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.687257 · Cited by 66
Cantero, J. L., Atienza, M., Lage, C., Záborszky, L., Vilaplana, E., López‐García, S., Pozueta, A., Rodríguez‐Rodríguez, E., Blesa, R., Alcolea, D. A., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz224 · Cited by 65
A Review of the Cholinergic System and Therapeutic Approaches to Treat Brain Disorders
Bertrand, D., & Wallace, T. L. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_141 · Cited by 65
Cholinergic double duty: cue detection and attentional control
Sarter, M., & Lustig, C. (2019) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2018.12.026 · Cited by 64
Robert, B., Kimchi, E. Y., Watanabe, Y., Chakoma, T. L., Jing, M., Li, Y., & Polley, D. B. (2021) · eLife · doi:10.7554/elife.69514 · Cited by 64
Silberberg, S. N., Taher, L., Lindtner, S., Sandberg, M., Nord, A. S., Vogt, D., Mckinsey, G. L., Hoch, R., Pattabiraman, K., Zhang, D., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.027 · Cited by 62
PET Imaging of Cholinergic Neurotransmission in Neurodegenerative Disorders
Tiepolt, S., Meyer, P., Patt, M., Deuther‐Conrad, W., Hesse, S., Barthel, H., & Sabri, O. (2022) · Journal of Nuclear Medicine · doi:10.2967/jnumed.121.263198 · Cited by 61
Bone morphogenetic protein 9 induces the transcriptome of basal forebrain cholinergic neurons
G.‐Coviella, I. L., Follettie, M. T., Mellott, T. J., Kovacheva, V., Slack, B. E., Diesl, V., Berse, B., Thies, R. S., & Blusztajn, J. K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502097102 · Cited by 60
Case, D. T., Burton, S. D., Gedeon, J. Y., Williams, S.-P. G., Urban, N. N., & Seal, R. P. (2017) · Nature Communications · doi:10.1038/s41467-017-00765-4 · Cited by 58
Molecularly defined and functionally distinct cholinergic subnetworks
Li, X., Yu, H., Zhang, B., Li, L., Chen, W., Yu, Q., Huang, X., Xiao, K., Wang, Y., Jing, W., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.08.025 · Cited by 58
Hollera, T., Berse, B., Cermak, J. M., Diebler, M., & Blusztajn, J. K. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12808-1 · Cited by 55
Nerve growth factor is primarily produced by GABAergic neurons of the adult rat cortex
Biane, J. S., Conner, J. M., & Tuszynski, M. H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00220 · Cited by 55
Chen, L., Chatterjee, M., & Li, J. Y. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3742-10.2010 · Cited by 54
Lhx6 and Lhx8: cell fate regulators and beyond
Zhou, C., Yang, G., Chen, M., He, L., Xiang, L., Ricupero, C. L., Mao, J. J., & Ling, J. (2015) · The FASEB Journal · doi:10.1096/fj.14-267500 · Cited by 54
Kondo, H., & Záborszky, L. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.23967 · Cited by 54
Chavez, C. M., & Záborszky, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw091 · Cited by 54
Hillmer, A. T., Li, S., Zheng, M., Scheunemann, M., Lin, S.-F., Nabulsi, N., Holden, D., Pracitto, R., Labaree, D. C., Ropchan, J. R., et al. (2017) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-017-3621-8 · Cited by 54
The homeobox genes Lhx7 and Gbx1 are expressed in the basal forebrain cholinergic system
Asbreuk, C. H. J., van Schaick, H. S. A., Cox, J. J., Kromkamp, M., Smidt, M. P., & Burbach, J. P. H. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00466-3 · Cited by 53
Nilbratt, M., Porras, O. H., Marutle, A., Hovatta, O., & Nordberg, A. K. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00916.x · Cited by 52
Nonomura, T., Nishio, C., Lindsay, R. M., & Hatanaka, H. (1995) · Brain Research · doi:10.1016/0006-8993(95)00357-v · Cited by 51
The Role of p75NTRin Cholinergic Basal Forebrain Structure and Function
Boskovic, Z., Alfonsi, F., Rumballe, B. A., Fonseka, S., Windels, F., & Coulson, E. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2364-14.2014 · Cited by 51
Slomianka, L., & Geneser, F. A. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903120404 · Cited by 51
Patterning, Regionalization, and Cell Differentiation in the Forebrain
Marín, Ó., & Rubenstein, J. L. R. (2002) · Elsevier eBooks · doi:10.1016/b978-012597951-1/50007-x · Cited by 50
Berse, B., López-Coviella, I., & Blusztajn, J. K. (1999) · Biochemical Journal · doi:10.1042/bj3420301 · Cited by 50
Kimes, A. S., Chefer, S. I., Matochik, J. A., Contoreggi, C. S., Vaupel, D. B., Stein, E. A., & Mukhin, A. G. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.015 · Cited by 49
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 49
Organizational principles of amygdalar input-output neuronal circuits
Huang, L., Chen, Y., Jin, S., Lin, L., Duan, S., Si, K., Gong, W., & Zhu, J. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01262-3 · Cited by 49
Zhu, F., Elnozahy, S., Lawlor, J., & Kuchibhotla, K. V. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01289-5 · Cited by 49
Investigating striatal function through cell-type-specific manipulations
Kreitzer, A. C., & Berke, J. D. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.018 · Cited by 48
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Metadata
- Authors
- Ananth, M. R., Rajebhosale, P., Kim, R., Talmage, D. A., & Role, L. W.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Ananth, Mala R.
- Role, Lorna W.
- Venue
- Nature Reviews Neuroscience
- Published
- 2023-02-23
- Volume
- 24
- Issue
- 4
- Pages
- 233-251
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC10439770
- OpenAlex
- W4321610346
- Semantic Scholar
- 87c380ffb1b9cea07172adcaa43cedaefb324e5a
- Cited by
- 148
- References
- 268
- Citations by year
- 2026: 44 · 2025: 63 · 2024: 36 · 2023: 5
- FWCI
- 5.70
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (1zians009424-02, ZIA NS009424)
- National Institute of Neurological Disorders and Stroke
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- basal forebrain cholinergic neurons, acetylcholine, cholinergic neurotransmission, cognitive behavior
- MeSH terms
- Acetylcholine, Cognition, Humans, Signal Transduction, Cholinergic Agents, Basal Forebrain
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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