New Insights Into Cholinergic Neuron Diversity

Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq

Zeisel, A., Muñoz-Manchado, A. B., Codeluppi, S., Lönnerberg, P., La Manno, G., Juréus, A., Marques, S., Munguba, H., He, L., Betsholtz, C., et al. (2015) · Science · doi:10.1126/science.aaa1934 · Cited by 3,124 · see citing works

Molecular Architecture of the Mouse Nervous System

Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,995 · 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

The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease

Hampel, H., Mesulam, M.-M., Cuello, A. C., Farlow, M. R., Giacobini, E., Grossberg, G. T., Khachaturian, A. S., Vergallo, A., Cavedo, E., Snyder, P. J., et al. (2018) · Brain · doi:10.1093/brain/awy132 · Cited by 1,918 · see citing works

Shared and distinct transcriptomic cell types across neocortical areas

Tasic, B., Yao, Z., Graybuck, L. T., Smith, K. A., Nguyen, T. N., Bertagnolli, D., Goldy, J., Garren, E., Economo, M. N., Viswanathan, S., et al. (2018) · Nature · doi:10.1038/s41586-018-0654-5 · Cited by 1,746 · see citing works

Adult mouse cortical cell taxonomy revealed by single cell transcriptomics

Tasic, B., Menon, V., Nguyen, T. N., Kim, T. K., Jarsky, T., Yao, Z., Levi, B., Gray, L. T., Sorensen, S. A., Dolbeare, T., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4216 · Cited by 1,714 · see citing works

Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons

Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420 · see citing works

The organization of the projection from the cerebral cortex to the striatum in the rat

McGeorge, A. J., & Faull, R. L. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90128-0 · Cited by 1,345 · see citing works

Basic Neurochemistry???Molecular, Cellular, and Medical Aspects

Long, D. M. (2006) · Neurosurgery Quarterly · doi:10.1097/01.wnq.0000203279.82150.41 · Cited by 1,288 · see citing works

Synaptic organisation of the basal ganglia

Bolam, J. P., Hanley, J. J., Booth, P. A. C., & Bevan, M. D. (2000) · Journal of Anatomy · doi:10.1046/j.1469-7580.2000.19640527.x · Cited by 950 · see citing works

Loss of <i>Nkx2.1</i> homeobox gene function results in a ventral to dorsal molecular respecification within the basal telencephalon: evidence for a transformation of the pallidum into the striatum

Sussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873 · see citing works

Topographical organization and relationship with ventral striatal compartments of prefrontal corticostriatal projections in the rat

Berendse, H. W., Graaf, Y. G.-D., & Groenewegen, H. J. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903160305 · Cited by 847 · see citing works

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 735 · see citing works

Origin and Molecular Specification of Striatal Interneurons

Marín, Ó., Anderson, S. A., & Rubenstein, J. L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06063.2000 · Cited by 627 · see citing works

Activity-Regulated Transcription: Bridging the Gap between Neural Activity and Behavior

Yap, E.-L., & Greenberg, M. E. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.013 · Cited by 626 · see citing works

Dopaminergic neurons inhibit striatal output through non-canonical release of GABA

Tritsch, N. X., Ding, J. B., & Sabatini, B. L. (2012) · Nature · doi:10.1038/nature11466 · Cited by 576 · 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

Delineation of multiple subpallial progenitor domains by the combinatorial expression of transcriptional codes

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 · see citing works

Acetylcholine-mediated modulation of striatal function

Calabresi, P., Centonze, D., Gubellini, P., Pisani, A., & Bernardi, G. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01501-5 · Cited by 440 · see citing works

The Striatum Organizes 3D Behavior via Moment-to-Moment Action Selection

Markowitz, J. E., Gillis, W. F., Beron, C. C., Neufeld, S. Q., Robertson, K., Bhagat, N. D., Peterson, R. E., Peterson, E., Hyun, M., Linderman, S. W., et al. (2018) · Cell · doi:10.1016/j.cell.2018.04.019 · Cited by 422 · see citing works

Activity-dependent homeostatic specification of transmitter expression in embryonic neurons

Borodinsky, L. N., Root, C. M., Cronin, J. A., Sann, S. B., Gu, X., & Spitzer, N. C. (2004) · Nature · doi:10.1038/nature02518 · Cited by 396 · see citing works

Integration of electrophysiological recordings with single-cell RNA-seq data identifies neuronal subtypes

Fuzik, J., Zeisel, A., Máté, Z., Calvigioni, D., Yanagawa, Y., Szabó, G., Linnarsson, S., & Harkany, T. (2016) · Nature Biotechnology · doi:10.1038/nbt.3443 · Cited by 386 · see citing works

<i>Lhx6</i>Activity Is Required for the Normal Migration and Specification of Cortical Interneuron Subtypes

Liodis, P., Denaxa, M., Grigoriou, M., Akufo-Addo, C., Yanagawa, Y., & Pachnis, V. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3055-06.2007 · Cited by 377 · see citing works

A Major External Source of Cholinergic Innervation of the Striatum and Nucleus Accumbens Originates in the Brainstem

Dautan, D., Huerta-Ocampo, I., Witten, I. B., Deisseroth, K. A., Bolam, J. P., Gerdjikov, T. V., & Mena‐Segovia, J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5071-13.2014 · Cited by 335 · see citing works

Intrinsic Membrane Properties Underlying Spontaneous Tonic Firing in Neostriatal Cholinergic Interneurons

Bennett, B. D., Callaway, J. C., & Wilson, C. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08493.2000 · Cited by 332 · see citing works

Generation of a whole-brain atlas for the cholinergic system and mesoscopic projectome analysis of basal forebrain cholinergic neurons

Li, X., Yu, B., Sun, Q., Zhang, Y., Ren, M., Zhang, X., Li, A., Yuan, J., Madisen, L., Luo, Q., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703601115 · Cited by 329 · see citing works

The Thalamostriatal Pathway and Cholinergic Control of Goal-Directed Action: Interlacing New with Existing Learning in the Striatum

Bradfield, L. A., Bertran‐Gonzalez, J., Chieng, B. C. H., & Balleine, B. W. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.039 · Cited by 307 · see citing works

The distribution of acetylcholine in the peripheral and the central nervous system

MacIntosh, F. C. (1941) · The Journal of Physiology · doi:10.1113/jphysiol.1941.sp003913 · Cited by 292 · see citing works

Genetic and activity-dependent mechanisms underlying interneuron diversity

Wamsley, B., & Fishell, G. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.30 · Cited by 290 · see citing works

GABAergic circuits mediate the reinforcement-related signals of striatal cholinergic interneurons

English, D. F., Ibáñez-Sandoval, O., Stark, E., Tecuapetla, F., Buzsáki, G., Deisseroth, K. A., Tepper, J. M., & Koós, T. Z. (2011) · Nature Neuroscience · doi:10.1038/nn.2984 · Cited by 288 · see citing works

Neurons in the Basal Forebrain Project to the Cortex in a Complex Topographic Organization that Reflects Corticocortical Connectivity Patterns: An Experimental Study Based on Retrograde Tracing and 3D Reconstruction

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 · see citing works

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 · see citing works

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 249 · see citing works

Striatal cholinergic interneuron regulation and circuit effects

Lim, S. A. O., Kang, U. J., & McGehee, D. S. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00022 · Cited by 236 · see citing works

Diversity of Interneurons in the Dorsal Striatum Revealed by Single-Cell RNA Sequencing and PatchSeq

Muñoz-Manchado, A. B., Bengtsson Gonzales, C., Zeisel, A., Munguba, H., Bekkouche, B., Skene, N. G., Lönnerberg, P., Ryge, J., Harris, K. D., Linnarsson, S., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.053 · Cited by 229 · see citing works

The LIM-homeobox gene <i>Lhx8</i> is required for the development of many cholinergic neurons in the mouse forebrain

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 · see citing works

Dopaminergic control of the striatum for high-level cognition

Cools, R. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.04.002 · Cited by 221 · see citing works

NKX2.1 specifies cortical interneuron fate by activatingLhx6

Du, T., Xu, Q., Ocbina, P. J. R., & Anderson, S. A. (2008) · Development · doi:10.1242/dev.015123 · Cited by 220 · see citing works

Heterogeneity and Diversity of Striatal GABAergic Interneurons: Update 2018

Tepper, J. M., Koós, T. Z., Ibáñez-Sandoval, O., Tecuapetla, F., Faust, T. W., & Assous, M. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00091 · Cited by 218 · see citing works

The vesicular glutamate transporter VGLUT3 synergizes striatal acetylcholine tone

Gras, C., Amilhon, B., Lepicard, È. M., Poirel, O., Vinatier, J., Herbin, M., Dumas, S., Tzavara, E. T., Wade, M. R., Nomikos, G. G., et al. (2008) · Nature Neuroscience · doi:10.1038/nn2052 · Cited by 211 · see citing works

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 205 · see citing works

Acetylcholine Elevation Relieves Cognitive Rigidity and Social Deficiency in a Mouse Model of Autism

Karvat, G., & Kimchi, T. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.274 · Cited by 203 · see citing works

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 · see citing works

The Striosome and Matrix Compartments of the Striatum: A Path through the Labyrinth from Neurochemistry toward Function

Brimblecombe, K. R., & Cragg, S. J. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00333 · Cited by 201 · see citing works

Corelease 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 · see citing works

Neuromodulation by acetylcholine: examples from schizophrenia and depression

Higley, M. J., & Picciotto, M. R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.06.004 · Cited by 184 · see citing works

A wide diversity of cortical GABAergic interneurons derives from the embryonic preoptic area

Gelman, D., Griveau, A., Dehorter, N., Teissier, A., Varela, C., Pla, R., Pierani, A., & Marín, O. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4068-11.2011 · Cited by 179 · see citing works

Functional Characterization of Intrinsic Cholinergic Interneurons in the Cortex

von Engelhardt, J., Eliava, M., Meyer, A. H., Rozov, A., & Monyer, H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4647-06.2007 · Cited by 177 · see citing works

Distinct Cortical-Thalamic-Striatal Circuits through the Parafascicular Nucleus

Mandelbaum, G., Taranda, J., Haynes, T. M., Hochbaum, D. R., Huang, K. W., Hyun, M., Venkataraju, K. U., Straub, C., Wang, W., Robertson, K., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.035 · Cited by 177 · see citing works

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 · see citing works

Control of Spontaneous Firing Patterns by the Selective Coupling of Calcium Currents to Calcium-Activated Potassium Currents in Striatal Cholinergic Interneurons

Goldberg, J. A., & Wilson, C. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2734-05.2005 · Cited by 172 · see citing works

Extrinsic Sources of Cholinergic Innervation of the Striatal Complex: A Whole-Brain Mapping Analysis

Dautan, D., Bay, H. H., Bolam, J. P., Gerdjikov, T. V., & Mena‐Segovia, J. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00001 · Cited by 172 · see citing works

Tuning of fast-spiking interneuron properties by an activity-dependent transcriptional switch

Dehorter, N., Ciceri, G., Bartolini, G., Lim, L., del Pino, I., & Marín, O. (2015) · Science · doi:10.1126/science.aab3415 · Cited by 169 · see citing works

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 · see citing works

Cortical Control of Striatal Dopamine Transmission via Striatal Cholinergic Interneurons

Kosillo, P., Zhang, Y.-F., Threlfell, S., & Cragg, S. J. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw252 · Cited by 164 · see citing works

Neural Stem Cells: Historical Perspective and Future Prospects

Breunig, J. J., Haydar, T. F., & RAKIC, P. T. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.005 · Cited by 161 · see citing works

Firing Properties of Anatomically Identified Neurons in the Medial Septum of Anesthetized and Unanesthetized Restrained Rats

Simon, A., Poindessous‐Jazat, F., Dutar, P., Epelbaum, J., & Bassant, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1401-06.2006 · Cited by 152 · see citing works

The fate of the brain cholinergic neurons in neurodegenerative diseases

Pepeu, G., & Giovannini, M. G. (2017) · Brain Research · doi:10.1016/j.brainres.2017.06.023 · Cited by 144 · see citing works

Origin and molecular specification of globus pallidus neurons

Nóbrega-Pereira, S., Gelman, D., Bartolini, G., Pla, R., Pierani, A., & Marín, O. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4023-09.2010 · Cited by 142 · see citing works

Cholinergic projections from the parabigeminal nucleus (Ch8) to the superior colliculus in the mouse: a combined analysis of horseradish peroxidase transport and choline acetyltransferase immunohistochemistry

Mufson, E. J., Martin, T. L., Mash, D. C., Wainer, B. H., & Mesulam, M. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)91114-5 · Cited by 141 · see citing works

Spontaneous firing and evoked pauses in the tonically active cholinergic interneurons of the striatum

Goldberg, J. A., & Reynolds, J. N. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.067 · Cited by 140 · see citing works

Centrality of Striatal Cholinergic Transmission in Basal Ganglia Function

Bonsi, P., Cuomo, D., Martella, G., Madeo, G., Schirinzi, T., Puglisi, F., Ponterio, G., & Pisani, A. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00006 · Cited by 140 · see citing works

Cortical and Thalamic Excitation Mediate the Multiphasic Responses of Striatal Cholinergic Interneurons to Motivationally Salient Stimuli

Doig, N. M., Magill, P. J., Apicella, P., Bolam, J. P., & Sharott, A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4627-13.2014 · Cited by 138 · see citing works

Cholinergic neuronal defect without cell loss in Huntington's disease

Smith, R. A., Chung, H., Rundquist, S., Maat–Schieman, M. L. C., Colgan, L. A., Englund, E. M., Liu, Y.-J., Roos, R. A. C., Faull, R. L. M., Brundin, P., et al. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl252 · Cited by 138 · see citing works

GABAergic inhibition in dual-transmission cholinergic and GABAergic striatal interneurons is abolished in Parkinson disease

Lozovaya, N., Eftekhari, S., Cloarec, R., Gouty‐Colomer, L., Dufour, A., Riffault, B., Billon-Grand, M., Pons-Bennaceur, A., Oumar, N., Burnashev, N., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03802-y · Cited by 137 · see citing works

Role of Striatal Cholinergic Interneurons in Set-Shifting in the Rat

Aoki, S., Liu, A. W., Zucca, A., Zucca, S., & Wickens, J. R. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0490-15.2015 · Cited by 136 · see citing works

LIM homeodomain transcription factor-dependent specification of bipotential MGE progenitors into cholinergic and GABAergic striatal interneurons

Fragkouli, A., van Wijk, N. V., Lopes, R., Kessaris, N., & Pachnis, V. (2009) · Development · doi:10.1242/dev.038083 · Cited by 135 · see citing works

Lhx6 directly regulates Arx and CXCR7 to determine cortical interneuron fate and laminar position

Vogt, D., Hunt, R. F., Mandal, S., Sandberg, M., Silberberg, S. N., Nagasawa, T., Yang, Z., Baraban, S. C., & Rubenstein, J. L. R. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.030 · Cited by 129 · see citing works

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 128 · see citing works

A Review of the Pedunculopontine Nucleus in Parkinson's Disease

French, I. T., & Muthusamy, K. A. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00099 · Cited by 126 · see citing works

Striatal Cholinergic Interneurons Control Motor Behavior and Basal Ganglia Function in Experimental Parkinsonism

Maurice, N., Liberge, M., Jaouen, F., Ztaou, S., Hanini, M., Camon, J., Deisseroth, K. A., Amalric, M., Goff, L. K., & Beurrier, C. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.034 · Cited by 125 · see citing works

Fate and freedom in developing neocortical circuits

Jabaudon, D. (2017) · Nature Communications · doi:10.1038/ncomms16042 · Cited by 125 · see citing works

Involvement of Striatal Cholinergic Interneurons and M1 and M4 Muscarinic Receptors in Motor Symptoms of Parkinson's Disease

Ztaou, S., Maurice, N., Camon, J., Guiraudie-Capraz, G., Goff, L. K., Beurrier, C., Liberge, M., & Amalric, M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0873-16.2016 · Cited by 123 · see citing works

Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions

Klug, J. R., Engelhardt, M. D., Cadman, C. N., Li, H., Smith, J. B., Ayala, S., Williams, E., Hoffman, H., & Jin, X. (2018) · eLife · doi:10.7554/elife.35657 · Cited by 122 · see citing works

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 120 · see citing works

Cholinergic connectivity: it's implications for psychiatric disorders

Scarr, E., Gibbons, A. S., Neo, J. H., Udawela, M., & Dean, B. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00055 · Cited by 117 · see citing works

Isl1 Directly Controls a Cholinergic Neuronal Identity in the Developing Forebrain and Spinal Cord by Forming Cell Type-Specific Complexes

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 · see citing works

Principles of Synaptic Organization of GABAergic Interneurons in the Striatum

Straub, C., Saulnier, J. L., Bègue, A., Feng, D. D., Huang, K. W., & Sabatini, B. L. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.007 · Cited by 116 · see citing works

The Neuron Identity Problem: Form Meets Function

Fishell, G., & Heintz, N. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.035 · Cited by 115 · see citing works

HCN2 Channels in Cholinergic Interneurons of Nucleus Accumbens Shell Regulate Depressive Behaviors

Cheng, J., Umschweif, G., Leung, J., Sagi, Y., & Greengard, P. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.018 · Cited by 110 · see citing works

The LIM homeobox gene, <i>L3/Lhx8</i>, is necessary for proper development of basal forebrain cholinergic neurons

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 · see citing works

Striatal cholinergic neurotransmission requires VGLUT3

Nelson, A. B., Bussert, T. G., Kreitzer, A. C., & Seal, R. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0901-14.2014 · Cited by 99 · see citing works

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 98 · see citing works

Neurons in the Ventral Striatum Exhibit Cell-Type-Specific Representations of Outcome during Learning

Atallah, H. E., McCool, A. D., Howe, M. W., & Graybiel, A. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.021 · Cited by 98 · see citing works

Role of Tonically Active Neurons in Primate Caudate in Reward-Oriented Saccadic Eye Movement

Shimo, Y., & Hikosaka, O. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07804.2001 · Cited by 97 · see citing works

Cholinergic systems and schizophrenia: primary pathology or epiphenomena?

Hyde, T. M., & Crook, J. M. (2001) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00101-6 · Cited by 97 · see citing works

Adult mouse basal forebrain harbors two distinct cholinergic populations defined by their electrophysiology

Ünal, Ç. T., Golowasch, J., & Záborszky, L. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00021 · Cited by 96 · see citing works

Timing of developmental sequences in different brain structures: physiological and pathological implications

Dehorter, N., Vinay, L., Hammond, C., & Ben‐Ari, Y. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08152.x · Cited by 93 · see citing works

Permissive corridor and diffusible gradients direct medial ganglionic eminence cell migration to the neocortex

Wichterle, H., Alvarez-Dolado, M., Erskine, L., & Alvarez-Buylla, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242721899 · Cited by 92 · see citing works

Enhanced flexibility of place discrimination learning by targeting striatal cholinergic interneurons

Okada, K., Nishizawa, K., Fukabori, R., Kai, N., Shiota, A., Ueda, M., Tsutsui, Y., Sakata, S., Matsushita, N., & Kobayashi, K. (2014) · Nature Communications · doi:10.1038/ncomms4778 · Cited by 90 · see citing works

The LIM-Homeobox GeneIslet-1Is Required for the Development of Restricted Forebrain Cholinergic Neurons

Elshatory, Y. M., & Gan, L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5730-07.2008 · Cited by 80 · see citing works

Pauses in Cholinergic Interneuron Activity Are Driven by Excitatory Input and Delayed Rectification, with Dopamine Modulation

Zhang, Y.-F., Reynolds, J. N. J., & Cragg, S. J. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.027 · Cited by 75 · see citing works

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 69 · see citing works

Developmental specification of forebrain cholinergic neurons

Allaway, K. C., & Machold, R. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2016.11.007 · Cited by 68 · see citing works

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 68 · see citing works

Spontaneous Synaptic Activation of Muscarinic Receptors by Striatal Cholinergic Neuron Firing

Mamaligas, A. A., & Ford, C. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.021 · Cited by 67 · see citing works

Roles of centromedian parafascicular nuclei of thalamus and cholinergic interneurons in the dorsal striatum in associative learning of environmental events

Yamanaka, K., Hori, Y., Minamimoto, T., Yamada, H., Matsumoto, N., Enomoto, K., Aosaki, T., Graybiel, A. M., & Kimura, M. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1713-z · Cited by 67 · see citing works

Dopamine neuron glutamate cotransmission evokes a delayed excitation in lateral dorsal striatal cholinergic interneurons

Chuhma, N., Mingote, S., Yetnikoff, L., Kalmbach, A., Ma, T. C., Ztaou, S., Siena, A.-C., Tepler, S., Poulin, J.-F., Ansorge, M. S., et al. (2018) · eLife · doi:10.7554/elife.39786 · Cited by 66 · see citing works

Choline transporter gene variation is associated with attention-deficit hyperactivity disorder

English, B. A., Hahn, M. K., Gizer, I., Mazei-Robison, M., Steele, A., Kurnik, D., Stein, M., Waldman, I., & Blakely, R. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9033-8 · Cited by 65 · see citing works

To move or to sense? Incorporating somatosensory representation into striatal functions

Robbe, D. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.04.009 · Cited by 64 · see citing works

Altered neurite morphology and cholinergic function of induced pluripotent stem cell-derived neurons from a patient with Kleefstra syndrome and autism

Nagy, J., Kobolák, J., Berzsenyi, S., Ábrahám, Z., Avci, H. X., Bock, I., Bekes, Z., Hodoscsek, B., Chandrasekaran, A., Téglási, A., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.144 · Cited by 61 · see citing works

Novel fast adapting interneurons mediate cholinergic‐induced fast GABAA inhibitory postsynaptic currents in striatal spiny neurons

Faust, T. W., Assous, M., Shah, F., Tepper, J. M., & Koós, T. Z. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12915 · Cited by 60 · see citing works

Pauses in cholinergic interneuron firing exert an inhibitory control on striatal output in vivo

Zucca, S., Zucca, A., Nakano, T., Aoki, S., & Wickens, J. R. (2018) · eLife · doi:10.7554/elife.32510 · Cited by 59 · see citing works

Compulsive Social Behavior Emerges after Selective Ablation of Striatal Cholinergic Interneurons

Martos, Y. V., Braz, B. Y., Beccaria, J. P., Murer, M. G., & Belforte, J. E. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3460-16.2017 · Cited by 58 · see citing works

Molecular control of two novel migratory paths for CGE-derived interneurons in the developing mouse brain

Touzot, A., Ruiz-Reig, N., Vitalis, T., & Studer, M. (2016) · Development · doi:10.1242/dev.131102 · Cited by 56 · see citing works

The Mouse Homeobox GeneGbx2Is Required for the Development of Cholinergic Interneurons in the Striatum

Chen, L., Chatterjee, M., & Li, J. Y. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3742-10.2010 · Cited by 54 · see citing works

Pedunculopontine Glutamatergic Neurons Provide a Novel Source of Feedforward Inhibition in the Striatum by Selectively Targeting Interneurons

Assous, M., Dautan, D., Tepper, J. M., & Mena‐Segovia, J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2913-18.2019 · Cited by 54 · see citing works

Different times of origin of choline acetyltransferase- and somatostatin-immunoreactive neurons in the rat striatum

Semba, K., Vincent, S., & Fibiger, H. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-10-03937.1988 · Cited by 53 · see citing works

Quantitative Imaging of Cholinergic Interneurons Reveals a Distinctive Spatial Organization and a Functional Gradient across the Mouse Striatum

Matamales, M., Götz, J., & Bertran‐Gonzalez, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157682 · Cited by 53 · see citing works

IHcurrent generates the afterhyperpolarisation following activation of subthreshold cortical synaptic inputs to striatal cholinergic interneurons

Oswald, M. J., Oorschot, D. E., Schulz, J. M., Lipski, J., & Reynolds, J. N. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.177600 · Cited by 52 · see citing works

OTX2 Transcription Factor Controls Regional Patterning within the Medial Ganglionic Eminence and Regional Identity of the Septum

Hoch, R. V., Lindtner, S., Price, J. D., & Rubenstein, J. L. R. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.06.043 · Cited by 48 · see citing works

Role of the Central Cholinergic System in the Therapeutics of Schizophrenia

Terry, A. V. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777247 · Cited by 48 · see citing works

Decoding brain state transitions in the pedunculopontine nucleus: cooperative phasic and tonic mechanisms

Petzold, A., Valencia, M., Pál, B. Z., & Mena‐Segovia, J. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00068 · Cited by 47 · see citing works

Central relaxin-3 receptor (RXFP3) activation increases ERK phosphorylation in septal cholinergic neurons and impairs spatial working memory

Albert‐Gascó, H., García-Avilés, Á., Moustafa, S., Sánchez‐Sarasúa, S., Gundlach, A. L., Olucha-Bordonau, F. E., & Sánchez‐Pérez, A. M. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1227-8 · Cited by 47 · see citing works

Cholinergic interneurons in the rat striatum modulate substitution of habits

Aoki, S., Liu, A. W., Akamine, Y., Zucca, A., Zucca, S., & Wickens, J. R. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13820 · Cited by 44 · see citing works

Transcription factor LIM homeobox 7 (Lhx7) maintains subtype identity of cholinergic interneurons in the mammalian striatum

Lopes, R., van Wijk, N. V., Neves, G., & Pachnis, V. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109251109 · Cited by 42 · see citing works

Striatal Cholinergic Interneurons Display Activity-Related Phosphorylation of Ribosomal Protein S6

Bertran‐Gonzalez, J., Chieng, B. C. H., Laurent, V., Valjent, E., & Balleine, B. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0053195 · Cited by 42 · see citing works

Molecular Mechanisms Controlling the Migration of Striatal Interneurons

Villar‐Cerviño, V., Kappeler, C., Pereira, S. N., Henkemeyer, M. J., Rago, L., Nieto, M. A., & Marín, Ó. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4317-14.2015 · Cited by 41 · see citing works

Fgf signaling controls the telencephalic distribution of Fgf-expressing progenitors generated in the rostral patterning center

Hoch, R. V., Clarke, J. A., & Rubenstein, J. L. R. (2015) · Neural Development · doi:10.1186/s13064-015-0037-7 · Cited by 40 · see citing works

Medial habenula cholinergic signaling regulates cocaine‐associated relapse‐like behavior

López, A. J., Jia, Y., White, A. O., Kwapis, J. L., Espinoza, M. E., Hwang, P. H., Campbell, R. R., Alaghband, Y., Chitnis, O., Matheos, D. P., et al. (2018) · Addiction Biology · doi:10.1111/adb.12605 · Cited by 40 · see citing works

Striatal Cholinergic Interneurons Modulate Spike-Timing in Striosomes and Matrix by an Amphetamine-Sensitive Mechanism

Crittenden, J. R., Lacey, C. J., Weng, F., Garrison, C. E., Gibson, D. J., Lin, Y., & Graybiel, A. M. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00020 · Cited by 39 · see citing works

Differences between Dorsal and Ventral Striatum in the Sensitivity of Tonically Active Neurons to Rewarding Events

Marche, K., Martel, A., & Apicella, P. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00052 · Cited by 39 · see citing works

Quantitative assessment of cell population diversity in single-cell landscapes

Liu, Q., Herring, C. A., Sheng, Q., Ping, J., Simmons, A. J., Chen, B., Banerjee, A., Li, W., Gu, G., Coffey, R. J., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2006687 · Cited by 39 · see citing works

An Activity-Dependent Retrograde Signal Induces the Expression of the High-Affinity Choline Transporter in Cholinergic Neurons

Krishnaswamy, A., & Cooper, E. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.025 · Cited by 37 · see citing works

Striatal cholinergic interneurons and D2 receptor-expressing GABAergic medium spiny neurons regulate tardive dyskinesia

Bordia, T., Zhang, D., Perez, X. A., & Quik, M. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.09.009 · Cited by 32 · see citing works

Tuning neural circuits by turning the interneuron knob

Dehorter, N., Marichal, N., Marín, Ó., & Berninger, B. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.12.009 · Cited by 32 · see citing works

Birth time/order-dependent neuron type specification

Kao, C.-F., & Lee, T. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.10.017 · Cited by 31 · see citing works

Single-Cell Gene Expression Analysis of Cholinergic Neurons in the Arcuate Nucleus of the Hypothalamus

Jeong, J. H., Woo, Y. J., Chua, S. C., & Jo, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162839 · Cited by 31 · see citing works

Striatal development involves a switch in gene expression networks, followed by a myelination event: Implications for neuropsychiatric disease

Novak, G., Fan, T., O’Dowd, B. F., & George, S. R. (2012) · Synapse · doi:10.1002/syn.21628 · Cited by 29 · see citing works

Pallial origin of basal forebrain cholinergic neurons in the nucleus basalis of Meynert and horizontal limb of the diagonal band nucleus

Pombero, A., Bueno, C., Saglietti, L., Rodenas, M., Guimerá, J., Bulfone, A., & Martı́nez, S. (2011) · Development · doi:10.1242/dev.069534 · Cited by 28 · see citing works

The Generation of Cortical Interneurons

Gelman, D. M., Marín, Ó., & Rubenstein, J. L. R. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0061 · Cited by 28 · see citing works

Different Subgroups of Cholinergic Neurons in the Basal Forebrain Are Distinctly Innervated by the Olfactory Regions and Activated Differentially in Olfactory Memory Retrieval

Zheng, Y., Feng, S., Zhu, X., Jiang, W., Wen, P., Ye, F., Rao, X., Jin, S., He, X., & Xu, F. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00099 · Cited by 26 · see citing works

Genomic analysis of transcriptional networks directing progression of cell states during MGE development

Sandberg, M., Taher, L., Hu, J., Black, B. L., Nord, A. S., & Rubenstein, J. L. R. (2018) · Neural Development · doi:10.1186/s13064-018-0119-4 · Cited by 26 · see citing works

The Embryonic Septum and Ventral Pallium, New Sources of Olfactory Cortex Cells

Ceci, M. L., Pedraza, M., & Carlos, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044716 · Cited by 25 · see citing works

Diverse populations of intrinsic cholinergic interneurons in the mouse olfactory bulb

Krosnowski, K. A., Ashby, S., Sathyanesan, A. G., Luo, W., Ogura, T., & Lin, W. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.04.024 · Cited by 23 · see citing works

Characterization of functional subgroups among genetically identified cholinergic neurons in the pedunculopontine nucleus

Baksa, B., Kovács, A., Bayasgalan, T., Szentesi, P., Kőszeghy, Á., Szűcs, P., & Pál, B. Z. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03025-4 · Cited by 23 · see citing works

Distinct migratory behaviors of striosome and matrix cells underlying the mosaic formation in the developing striatum

Hagimoto, K., Takami, S., Murakami, F., & Tanabe, Y. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24096 · Cited by 22 · see citing works

Synthesis, Storage and Release of Acetylcholine

Taylor, P., & Brown, J. H. (1999) · Cited by 21 · see citing works

Asynchronous Cholinergic Drive Correlates with Excitation-Inhibition Imbalance via a Neuronal Ca2+ Sensor Protein

Zhou, K., Cherra, S. J., Goncharov, A., & Jin, Y. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.043 · Cited by 19 · see citing works

Electrophysiological properties of basal forebrain cholinergic neurons identified by genetic and optogenetic tagging

López‐Hernández, G. Y., Ananth, M. R., Jiang, L., Ballinger, E. C., Talmage, D. A., & Role, L. W. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14073 · Cited by 17 · see citing works

Task‐dependent function of striatal cholinergic interneurons in behavioural flexibility

Okada, K., Nishizawa, K., Setogawa, S., Hashimoto, K., & Kobayashi, K. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13768 · Cited by 16 · see citing works

Parallel Emergence of a Compartmentalized Striatum with the Phylogenetic Development of the Cerebral Cortex

Hamasaki, T., & Goto, S. (2019) · Brain Science · doi:10.3390/brainsci9040090 · Cited by 6 · see citing works

A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain

Yao, Z., van Velthoven, C. T. J., Kunst, M., Zhang, M., McMillen, D., Lee, C., Jung, W., Goldy, J., Abdelhak, A., Aitken, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06812-z · Cited by 1,194 · see citing works

Neurodegenerative Disease: Roles for Sex, Hormones, and Oxidative Stress

Sumien, N., Cunningham, J. T., Davis, D., Engelland, R. E., Fadeyibi, O., Farmer, G. E., Mabry, S., Mensah-Kane, P., Trinh, O. T. P., Vann, P. H., et al. (2021) · Endocrinology · doi:10.1210/endocr/bqab185 · Cited by 102 · see citing works

Multienzyme chemiluminescent foldable biosensor for on-site detection of acetylcholinesterase inhibitors

Montali, L., Calabretta, M. M., Lopreside, A., D’Elia, M., Guardigli, M., & Michelini, E. (2020) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2020.112232 · Cited by 101 · see citing works

An Overview of 1,2,3-triazole-Containing Hybrids and Their Potential Anticholinesterase Activities

Khan, S. A., Akhtar, M. J., Gogoi, U., Meenakshi, D. U., & Das, A. (2023) · Pharmaceuticals · doi:10.3390/ph16020179 · Cited by 95 · see citing works

Brainstem Modulation of Large-Scale Intrinsic Cortical Activity Correlations

van den Brink, R. L., Pfeffer, T. A., & Donner, T. H. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00340 · Cited by 83 · see citing works

Heterogeneous pericoerulear neurons tune arousal and exploratory behaviours

Luskin, A. T., Li, L., Fu, X., Martin, M. M., Barcomb, K., Girven, K. S., Blackburn, T., Wells, B. A., Thai, S., Li, E. M., et al. (2025) · Nature · doi:10.1038/s41586-025-08952-w · Cited by 75 · see citing works

Local Thyroid Hormone Action in Brain Development

Alcaide, M. A., & Mayerl, S. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512352 · Cited by 70 · see citing works

Scientific review of the aesthetic uses of botulinum toxin type A

Park, M. Y., & Ahn, K. Y. (2021) · Archives of Craniofacial Surgery · doi:10.7181/acfs.2021.00003 · Cited by 66 · see citing works

Metabolic and Cellular Compartments of Acetyl-CoA in the Healthy and Diseased Brain

Jankowska-Kulawy, A., Klimaszewska-Łata, J., Gul-Hinc, S., Ronowska, A., & Szutowicz, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231710073 · Cited by 49 · see citing works

Striatal cholinergic transmission. Focus on nicotinic receptors’ influence in striatal circuits

Assous, M. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15135 · Cited by 50 · see citing works

Loss of primary cilia and dopaminergic neuroprotection in pathogenic LRRK2-driven and idiopathic Parkinson’s disease

Khan, S. S., Jaimon, E., Lin, Y.-E., Nikoloff, J., Tonelli, F., Alessi, D. R., & Pfeffer, S. R. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402206121 · Cited by 61 · see citing works

Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders

Poppi, L. A., Ho-Nguyen, K.-T., Shi, A., Daut, C. T., & Tischfield, M. A. (2021) · Cells · doi:10.3390/cells10040907 · Cited by 46 · see citing works

From Progenitors to Progeny: Shaping Striatal Circuit Development and Function

Knowles, R., Dehorter, N., & Ellender, T. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0620-21.2021 · Cited by 45 · see citing works

Dynamic regulation of the cholinergic system in the spinal central nervous system

Rima, M., Lattouf, Y., Younes, M. A., Bullier, E., Legendre, P., Mangin, J., & Hong, E. (2020) · Scientific Reports · doi:10.1038/s41598-020-72524-3 · Cited by 42 · see citing works

Recent advances in enzyme inhibition based-electrochemical biosensors for pharmaceutical and environmental analysis

Li, J., Chang, H., Zhang, N., He, Y., Zhang, D., Liu, B., & Fang, Y. (2022) · Talanta · doi:10.1016/j.talanta.2022.124092 · Cited by 38 · see citing works

Current Progress on Central Cholinergic Receptors as Therapeutic Targets for Alzheimer's Disease

Nagori, K., Pradhan, M., Sharma, M. K., Ajazuddin, M., Badwaik, H. R., & Nakhate, K. T. (2024) · Current Alzheimer Research · doi:10.2174/0115672050306008240321034006 · Cited by 37 · see citing works

A new advanced cellular model of functional cholinergic-like neurons developed by reprogramming the human SH-SY5Y neuroblastoma cell line

D’Aloia, A., Pastori, V., Blasa, S., Campioni, G., Peri, F., Sacco, E., Ceriani, M., Lecchi, M., & Costa, B. (2024) · Cell Death Discovery · doi:10.1038/s41420-023-01790-7 · Cited by 36 · see citing works

Therapeutic efficacy of Clompanus pubescens leaves fractions via downregulation of neuronal cholinesterases/Na+-K+ATPase/IL-1 β, and improving the neurocognitive and antioxidants status of streptozotocin-induced diabetic rats

Onikanni, S. A., Lawal, B., Oyinloye, B. E., Mostafa‐Hedeab, G., Alorabi, M., Cavalu, S. D., Olusola, A. O., Wang, C., & Batiha, G. E. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.112730 · Cited by 36 · see citing works

The cryptic gonadotropin-releasing hormone neuronal system of human basal ganglia

Skrapits, K., Sárvári, M., Farkas, I., Göcz, B., Takács, S., Rumpler, É., Váczi, V., Vastagh, C., Rácz, G., Matolcsy, A., et al. (2021) · eLife · doi:10.7554/elife.67714 · Cited by 35 · see citing works

Spectroscopic Determination of Acetylcholine (ACh): A Representative Review

Świt, P., Pollap, A., & Orzeł, J. (2023) · Topics in Current Chemistry · doi:10.1007/s41061-023-00426-9 · Cited by 29 · see citing works

Neurotransmitter signaling regulates distinct phases of multimodal human interneuron migration

Bajaj, S., Bagley, J. A., Sommer, C., Vértesy, Á., Wong, S. N., Krenn, V., Lévi‐Strauss, J., & Knoblich, J. A. (2021) · The EMBO Journal · doi:10.15252/embj.2021108714 · Cited by 27 · see citing works

Cholinergic blockade of neuroinflammation: from tissue to RNA regulators

Zorbaz, T., Madrer, N., & Soreq, H. (2022) · Neuronal Signaling · doi:10.1042/ns20210035 · Cited by 28 · see citing works

Ontogenetic rules for the molecular diversification of hypothalamic neurons

Benevento, M., Hökfelt, T. G. M., & Harkany, T. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00615-3 · Cited by 28 · see citing works

Rapid modulation of striatal cholinergic interneurons and dopamine release by satellite astrocytes

Stedehouder, J., Roberts, B. M., Raina, S., Bossi, S., Liu, A. K. L., Doig, N. M., McGerty, K., Magill, P. J., Parkkinen, L., & Cragg, S. J. (2024) · Nature Communications · doi:10.1038/s41467-024-54253-7 · Cited by 27 · see citing works

Quercetin-1,2,3-Triazole Hybrids as Multifunctional Anti-Alzheimer’s Agents

Carreiro, E. P., Costa, A. R., Antunes, C. M., Ernesto, S., Pinto, F. C., Rodrigues, B., & Burke, A. J. (2023) · Molecules · doi:10.3390/molecules28227495 · Cited by 24 · see citing works

Cholinergic signaling controls immune functions and promotes homeostasis

Wessler, I. K., & Kirkpatrick, C. J. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106345 · Cited by 23 · see citing works

A dynamical systems view of neuroethology: Uncovering stateful computation in natural behaviors

Robson, D. N., & Li, J. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.01.002 · Cited by 26 · see citing works

Developmental deficits of MGE-derived interneurons in the Cntnap2 knockout mouse model of autism spectrum disorder

Ahmed, N. Y., Knowles, R., Liu, L., Yan, Y., Li, X., Schümann, U., Wang, Y., Sontani, Y., Reynolds, N., Natoli, R., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1112062 · Cited by 22 · see citing works

Cadmium-promoted thyroid hormones disruption mediates ROS, inflammation, Aβ and Tau proteins production, gliosis, spongiosis and neurodegeneration in rat basal forebrain

Solà, E., Moyano, P. M., Flores, A., García, J. M., García, J., Anadón, M. J., Frejo, M. T., Pelayo, A., Fernández, M. D. L. C., & del Pino, J. (2023) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2023.110428 · Cited by 22 · see citing works

What’s wrong with the striatal cholinergic interneurons in Parkinson’s disease? Focus on intrinsic excitability

Tubert, C., & Murer, M. G. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14742 · Cited by 22 · see citing works

Endogenous Acetylcholine and Its Modulation of Cortical Microcircuits to Enhance Cognition

Venkatesan, S., Jeoung, H., Chen, T., Power, S. K., Liu, Y., & Lambe, E. K. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_138 · Cited by 21 · see citing works

Evaluation of eGFP expression in the ChAT-eGFP transgenic mouse brain

Gamage, R. V., Záborszky, L., Münch, G. W., & Gyengési, E. (2023) · BMC Neuroscience · doi:10.1186/s12868-023-00773-9 · Cited by 18 · see citing works

Targeting a vulnerable septum-hippocampus cholinergic circuit in a critical time window ameliorates tau-impaired memory consolidation

Wu, D., Yu, N., Gao, Y., Xiong, R., Liu, L., Lei, H., Jin, S., Liu, J., Liu, Y., Xie, J., et al. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00614-7 · Cited by 17 · see citing works

Brainstem noradrenergic neurons: Identifying a hub at the intersection of cognition, motility, and skeletal muscle regulation

Delbono, O., Wang, Z., & Messi, M. L. (2022) · Acta Physiologica · doi:10.1111/apha.13887 · Cited by 17 · see citing works

Lactiplantibacillus plantarum X7022 Plays Roles on Aging Mice with Memory Impairment Induced by D-Galactose Through Restoring Neuronal Damage, Relieving Inflammation and Oxidative Stress

Yin, D., Zhao, L. X., Deng, S., Xie, Y., Ro, K.-S., Yang, Z., Du, L., Xie, J., & Wei, D. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10208-w · Cited by 17 · see citing works

Er81 Transcription Factor Fine-Tunes Striatal Cholinergic Interneuron Activity and Drives Habit Formation

Ranjbar‐Slamloo, Y., Ahmed, N. Y., Abed, A. S. A., Gao, L., Sontani, Y., Rcom-H'cheo-Gauthier, A. N., Arabzadeh, E., & Dehorter, N. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0967-20.2021 · Cited by 14 · see citing works

Fetal blockade of nicotinic acetylcholine transmission causes autism-like impairment of biological motion preference in the neonatal chick

Matsushima, T., Miura, M., Patzke, N., Toji, N., Wada, K., Ogura, Y., Homma, K. J., Sgadó, P., & Vallortígara, G. (2022) · Cerebral Cortex Communications · doi:10.1093/texcom/tgac041 · Cited by 13 · see citing works

Development of a versatile LCM-Seq method for spatial transcriptomics of fluorescently tagged cholinergic neuron populations

Rumpler, É., Göcz, B., Skrapits, K., Sárvári, M., Takács, S., Farkas, I., Póliska, S., Papp, M., Solymosi, N., & Hrabovszky, E. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105121 · Cited by 11 · see citing works

Design, synthesis and biological evaluation of galantamine analogues for cognitive improvement in Alzheimer's disease

Li, M., Ma, C., Li, Y., Wang, H., Xiu, X., Zhao, X., Liu, P., Yang, H., & Cheng, M. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.117198 · Cited by 12 · see citing works

Extrinsic and intrinsic control of striatal cholinergic interneuron activity

Ratna, D., & Francis, T. C. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1528419 · Cited by 12 · see citing works

The integrated model of glutamate and dopamine hypothesis for schizophrenia: Prediction and personalized medicine for prevent potential treatment-resistant patients

Huang, L.-C., Lin, S., Tseng, H., Chen, K. C., & Yang, Y. K. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.110159 · Cited by 10 · see citing works

Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum

Shostak, D. M., Constantin, S., Flannery, J. C., & Wray, S. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1147554 · Cited by 10 · see citing works

Naringin and Naringenin: Potential Multi-Target Agents for Alzheimer’s Disease

Lu, J., Chen, J., Li, S., Pan, G.-J., Ou, Y., Yuan, L.-F., Jiang, J., Zeng, L., & Zhao, J. J. (2024) · Current Medical Science · doi:10.1007/s11596-024-2921-z · Cited by 9 · see citing works

Systematic Analysis of SH-SY5Y Differentiation Protocols and Neuronal Subtype Abundance

Prisacar, M., Esser, S., Hausherr, M., Karacora, B., Vyushkova, Y., Eisenacher, M., Grugel, R., Marcus, K., & Eggers, B. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01627-0 · Cited by 9 · see citing works

Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors

Caubit, X., Gubellini, P., Roubertoux, P. L., Carlier, M., Molitor, J., Chabbert, D., Metwaly, M., Salin, P., Fatmi, A., Belaïdouni, Y., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01865-6 · Cited by 10 · see citing works

Flavonoid-rich fractions of C. volubile and V. amygdalina alleviates arsenic-induced neurotoxicity by improving neurosignaling and antioxidant capacity in rats' brain

Ugbaja, R. N., Akinhanmi, T. F., Onunkwor, B. O., Ugwor, E. I., James, A. S., Babalola, A. A., Babayemi, D. O., Ezenandu, E. O., & Ugbaja, V. C. (2022) · Brain Disorders · doi:10.1016/j.dscb.2022.100050 · Cited by 9 · see citing works

Neuronal Transplantation for Alzheimer’s Disease and Prospects for Generating Exogenic Neurons as a Source of Cells for Implantation

Strell, P., Johnson, S. T., Carchi, C., & Low, W. C. (2023) · Cell Transplantation · doi:10.1177/09636897231164712 · Cited by 9 · see citing works

A visualized sensor based on layered double hydroxides with peroxidase-like activity for sensitive acetylcholinesterase assay

Cheng, H., Wang, Y., Wang, Y., Ge, L., Liu, X., & Li, F. (2023) · Analytical Methods · doi:10.1039/d3ay00776f · Cited by 9 · see citing works

The cholinergic basal forebrain and its role in neurodegeneration

Cykowski, M. D., & Masdeu, J. C. (2025) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaf112 · Cited by 8 · see citing works

Focal acetylcholinergic modulation of the human midcingulo‐insular network during attention: Meta‐analytic neuroimaging and behavioral evidence

Chakraborty, S., Lee, S. K., Arnold, S. M., Haast, R. A. M., KHAN, A. R., & Schmitz, T. W. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15990 · Cited by 8 · see citing works

Natural products as a source of cholinesterase inhibitors

de Oliveira, P. C. O., da Silva, G. M., Cass, Q. B., de Moraes, M. C., & Cardoso, C. L. (2024) · Pharmacological Research - Natural Products · doi:10.1016/j.prenap.2024.100099 · Cited by 8 · see citing works

Role of Bmal1 in mediating the cholinergic system to regulate the behavioral rhythm of nocturnal marine molluscs

Gao, X., Zhang, M., Lyu, M., Lin, S., Luo, X., You, W., & Ke, C. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.05.038 · Cited by 8 · see citing works

Mapping multi-regional functional connectivity of astrocyte-neuronal networks during behaviors

Wang, H., Huang, M., Yang, S., Xu, J., Li, J., Qin, H., Liang, S., Teng, T., Yang, C., Gong, M., et al. (2024) · Neurophotonics · doi:10.1117/1.nph.11.4.045010 · Cited by 7 · see citing works

Spatial multi-omics characterization of neuroblastoma reveals ferroptosis-associated metabolic features in high-risk tumors

Tu, C., Tan, C. W., Monkman, J. H., Almeida, A. C., Antonio-Carreon, G., Omer, N., Hull, G., Chung, K., Mehdi, A. M., Salerno, A., et al. (2026) · Genome Medicine · doi:10.1186/s13073-026-01622-0 · Cited by 7 · see citing works

Blackcurrant ( Ribes nigrum L.) improves cholinergic signaling and protects against chronic Scopolamine-induced memory impairment in mice

da Costa, P., Schetinger, M. R. C., Baldissarelli, J., Stefanello, N., Lopes, T. F., Reichert, K. P., Assmann, C. E., Bottari, N. B., Miron, V. V., Vargas, F. F. A., et al. (2024) · Journal of Psychopharmacology · doi:10.1177/02698811241273776 · Cited by 7 · see citing works

Camk2a-Cre and Tshz3 Expression in Mouse Striatal Cholinergic Interneurons: Implications for Autism Spectrum Disorder

Caubit, X., Arbeille, E., Chabbert, D., Desprez, F., Messak, I., Fatmi, A., Habermann, B. H., Gubellini, P., & Fasano, L. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.683959 · Cited by 7 · see citing works

What Is the Role of Thalamostriatal Circuits in Learning Vocal Sequences?

Xiao, L., & Roberts, T. F. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.724858 · Cited by 6 · see citing works

Neurochemical heterogeneity of ChAT-immunoreactive neurons in the basal forebrain cholinergic nuclei and striatum in reference to CGRP, CCK, and calcium-binding proteins

Meher, M. M., Afrin, M., Jahan, M. R., Nozaki, K., Masumoto, K., Yanai, A., & Islam, M. N. (2025) · Acta Histochemica · doi:10.1016/j.acthis.2025.152291 · Cited by 6 · see citing works

Resveratrol Mitigates Cognitive Impairments and Cholinergic Cell Loss in the Medial Septum in a Mouse Model of Gradual Cerebral Hypoperfusion

Fagerli, E. A., Jackson, C. W., Escobar, I., Ferrier, F. J., Lao, E. J. P., Saul, I., Gomez, J., Dave, K. R., Bracko, O., & Pérez‐Pinzón, M. A. (2024) · Antioxidants · doi:10.3390/antiox13080984 · Cited by 6 · see citing works

The Central Cholinergic Synapse: A Primer

Klein, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199670 · Cited by 5 · see citing works

Inverse expression of Ten3 and Lphn2 across the developing mouse brain suggests a global strategy for circuit assembly

Chon, U., Pederick, D. T., Song, J. H., Zhang, Y., Rana, I., & Luo, L. (2026) · Current Biology · doi:10.1016/j.cub.2026.04.037 · Cited by 5 · see citing works

P2X2 receptors supply extracellular choline as a substrate for acetylcholine synthesis

Maruyama, T., Mano, A., Ishii, T., Kakinuma, Y., & Kaneda, M. (2021) · FEBS Open Bio · doi:10.1002/2211-5463.13332 · Cited by 5 · see citing works

Striatal cholinergic interneurons exhibit compartment-specific anatomical and functional organization in the mouse

Hobel, Z. B., Yang, L.-T., Brechbill, T. R., Liu, Q., Goldberg, J. A., & Plotkin, J. L. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2519939123 · Cited by 4 · see citing works

Cocaine-induced gene regulation in D1 and D2 neuronal ensembles of the nucleus accumbens

Mews, P., Mason, A. V., Kirchner, E. G., Estill, M. S., & Nestler, E. J. (2025) · Communications Biology · doi:10.1038/s42003-025-08327-x · Cited by 7 · see citing works

TIGAR deficiency enhances skeletal muscle thermogenesis by increasing neuromuscular junction cholinergic signaling

Tang, Y., Zong, H., Kwon, H., Qiu, Y., Pessin, J. B., Wu, L., Buddo, K. A., Boykov, I. N., Schmidt, C. A., Lin, C., et al. (2022) · eLife · doi:10.7554/elife.73360 · Cited by 4 · see citing works

Acetylcholine Inhibits Spontaneous Firing Activity of Terminal Nerve GnRH Neurons in Medaka

Tanaka, A., Umatani, C., & Oka, Y. (2023) · ZOOLOGICAL SCIENCE · doi:10.2108/zs220070 · Cited by 4 · see citing works

Basal Forebrain Cholinergic Neurons Have Specific Characteristics during the Perinatal Period

Lozovaya, N., Moumen, A., & Hammond, C. (2024) · eNeuro · doi:10.1523/eneuro.0538-23.2024 · Cited by 4 · see citing works

Acetylcholine Neurons Become Cholinergic during Three Time Windows in the Developing Mouse Brain

Goral, R. O., Lamb, P. W., & Yakel, J. L. (2024) · eNeuro · doi:10.1523/eneuro.0542-23.2024 · Cited by 5 · see citing works

Cocaine-Induced Gene Regulation in D1 and D2 Neuronal Ensembles of the Nucleus Accumbens Revealed by Single-Cell RNA SequencingPreprint

Mews, P., Mason, A. V., Kirchner, E. G., Estill, M. S., & Nestler, E. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.19.599762 · Cited by 4 · see citing works

Regulation of neural stem cells by innervating neurons

Dittmann, N. L., Chen, L., & Voronova, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.16287 · Cited by 3 · see citing works

L-carnitine: new perspectives on the management of preterm infants

Sisi, M., Yong, L., Lixing, Q., Changsheng, G., Jin, Y., Hang, Z., Xing, C., & Heng, L. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1508441 · Cited by 3 · see citing works

Cholinergic Phenotypes of Acetyl-CoA with ATP-Citrate Lyase Link

Gul‐Hinc, S., Jankowska-Kulawy, A., & Szutowicz, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020782 · Cited by 3 · see citing works

The cholinergic synapses

Soreq, H., Bar, A., & Paldor, I. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19088-9.00003-2 · Cited by 3 · see citing works

Cerebellar defects are a primary pathology in mouse models of spinal muscular atrophy

Cottam, N. C., Dowling, M., Kong, L., Chan-Cortés, M. H., Charvet, C. J., Norzeron, N., Grover, C. J., Harrington, M. A., Sumner, C. J., & Sun, J. (2025) · Brain Pathology · doi:10.1111/bpa.70025 · Cited by 3 · see citing works

Immunohistochemical relationships of huntingtin-associated protein 1 with choline acetyltransferase in the forebrain cholinergic nuclei of adult mice

Meher, M. M., Islam, M. N., Yanai, A., Afrin, M., Jahan, M. R., Nozaki, K., Masumoto, K., & Shinoda, K. (2025) · Cell and Tissue Research · doi:10.1007/s00441-025-03996-w · Cited by 3 · see citing works

Cholinergic Deficiency in the Cholinergic System as a Pathogenetic Link in the Formation of Various Syndromes in COVID-19

Петрович, Л. С., Muzhenya, D. V., Рамазановна, Т. А., Уракова, Т. Ю., Сергеевич, Ш. Д., Thakushinov, I. A., TKHAKUSHINOV, R. A., Анатольевна, Т. Е., & Urakova, D. M. (2023) · The Chinese Journal of Physiology · doi:10.4103/cjop.cjop-d-22-00072 · Cited by 3 · see citing works

Cholinergic Receptor Muscarinic 1 Co-Localized with Mitochondria in Cultured Dorsal Root Ganglion Neurons, and Its Deletion Disrupted Mitochondrial Ultrastructure in Peripheral Neurons: Implications in Alzheimer’s Disease

Sabbir, M. G. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-230883 · Cited by 3 · see citing works

Gene and cell therapy for the nucleus basalis of Meynert with NGF in Alzheimer's disease

Eriksdotter, M., & Mitra, S. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819975-6.00012-1 · Cited by 3 · see citing works

Fetal imidacloprid causes ASD-like impairment of biological motion perception in neonatal chicksPreprint

Matsushima, T., Miura, M., Patzke, N., Toji, N., Wada, K., Ogura, Y., Homma, K. J., Sgadó, P., & Vallortígara, G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.19.492744 · Cited by 3 · see citing works

Establishing a 3D Spheroid Model of Cholinergic Neurons from SH-SY5Y Cells for Neurotoxicity Assessment

Franco-Campos, F., Fernández-Franzón, M., Rodríguez-Carrasco, Y., & Ruiz, M.-J. (2025) · Toxins · doi:10.3390/toxins17070336 · Cited by 2 · see citing works

The GPCR Smoothened on cholinergic interneurons modulates dopamine-associated acetylcholine dynamics, learning, and effort management

Uribe‐Cano, S., & Kottmann, A. H. (2026) · iScience · doi:10.1016/j.isci.2026.115324 · Cited by 2 · see citing works

The primary cilium of cholinergic neurons may be a linchpin in the progression of Parkinson’s Disease

Uribe‐Cano, S., & Kottmann, A. H. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2414226121 · Cited by 2 · see citing works

Pathogenic LRRK2 causes age-dependent and region-specific deficits in ciliation, innervation and viability of cholinergic neuronsPreprint

Brahmia, B., Naaldijk, Y., Sarkar, P., Parisiadou, L., & Hilfiker, S. (2024) · eLife · doi:10.7554/elife.101135.1 · Cited by 3 · see citing works

Testing a Choline Diet in Neuroligin-Deficient C. elegans to Reduce Repetitive Behavior in Autism

Balasingam, S., & Messenger, C. (2022) · Journal of Student Research · doi:10.47611/jsrhs.v11i3.2846 · Cited by 1 · see citing works

Altered striosome-matrix distribution and activity of striatal cholinergic interneurons in a model of autism-linked repetitive behaviors

Molitor, J., Graniou, J., Salin, P., Castets, F., Fatmi, A., Goff, L. K., Fasano, L., Caubit, X., & Gubellini, P. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03208-5 · Cited by 1 · see citing works

Nigral dopaminergic contact patterns related to striatal regions and cell types in male mice

Yang, Y., Karube, F., Kobayashi, K., & Fujiyama, F. (2025) · Neuroscience Research · doi:10.1016/j.neures.2025.105011 · Cited by 1 · see citing works

Mesoscopic analysis of GABAergic marker expression in acetylcholine neurons in the whole mouse brain

Goral, R. O., Roy, S., Co, C. A., Wine, R. N., Lamb, P. W., Turner, P. M., McBride, S. J., Usdin, T. B., & Yakel, J. L. (2025) · iScience · doi:10.1016/j.isci.2025.114531 · Cited by 1 · see citing works

Neuronal Subtype-Specific Expression of γ-Enolase: Its Role in Neuronal Differentiation

Horvat, S., Fonović, U. P., Zidar, N., Doljak, B., Kos, J., & Pišlar, A. H. (2026) · NeuroMolecular Medicine · doi:10.1007/s12017-025-08902-9 · Cited by 1 · see citing works

Choline supplementation partially reverses prefrontal neurochemical deficits induced by perinatal opioid exposure

Chen, S., Makela, A. G., Romanova, E. V., Reichelt, M., Cosby, K. L., Gibson, K., Bochenek, G., Hamilton, A., Sweedler, J. V., & Smith, B. L. (2026) · Scientific Reports · doi:10.1038/s41598-026-50469-3 · Cited by 1 · see citing works

Adult Neuronal Expression of the Alzheimer Risk Protein CD2AP is Enriched in NGF-Responsive Basal Forebrain Neurons, where it Collocates with Rab-5 EndosomesPreprint

Fitzsimons, L. A., Atif-Sheikh, M., Mueth, M. G., Rice, M., Howell, G. R., & Harrison, B. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.24.604961 · Cited by 1 · see citing works

Scopolamine-induced cholinergic disruption impairs temporal prediction in head-fixed micePreprint

Ujihara, Y., Yamada, K., Yamamoto, M., Hayashi, K., & Toda, K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.06.611607 · Cited by 2 · see citing works

Editorial: Mechanisms of cholinergic transmission in motivation and cognition

Francis, T. C., & Klawonn, A. M. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1586940 · Cited by 1 · see citing works

Visualized Sensor Based on Layered Double Hydroxides with Peroxidase-Like Activity for Sensitive Acetylcholinesterase AssayPreprint

Cheng, H., Wang, Y., Wang, Y., Ge, L., Liu, X., & Li, F. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4349444

Neurodegenerative diseases at the systems level

Sobti, N., & Bayraktar, G. (2023) · Journal of Student Research · doi:10.47611/jsr.v11i3.1644

CẬP NHẬT CÁC ỨNG DỤNG CỦA BOTULINUM TOXIN TYPE A TRONG LÂM SÀNG NGOẠI KHOA VÀ THẨM MỸ ÍT XÂM LẤN

Nguyễn, V. L., Lý, Q. H., Võ, T. H., Hà, T. T. M., & Nguyễn, H. G. (2023) · Tạp chí Y Dược học Cần Thơ · doi:10.58490/ctump.2023i67.2185

The Role of the Acetylcholine System and Its Components in the Development of Post-COVID Syndromes (Review)

Muzhenya, D. V., & Lysenkov, S. P. (2024) · Journal of Medical and Biological Research · doi:10.37482/2687-1491-z182

Pathogenic LRRK2 causes age-dependent and region-specific deficits in ciliation, innervation and viability of cholinergic neuronsPreprint

Brahmia, B., Naaldijk, Y., Sarkar, P., Parisiadou, L., & Hilfiker, S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.16.603799

Pathogenic LRRK2 causes age-dependent and region-specific deficits in ciliation, innervation and viability of cholinergic neuronsPreprint

Brahmia, B., Naaldijk, Y., Sarkar, P., Parisiadou, L., & Hilfiker, S. (2024) · eLife · doi:10.7554/elife.101135

Mouse Forebrain Region-specific Molecular Characteristics and Cholinergic Neurons Subtyping: An Integrated Analysis Based on Spatial Multi-omicsPreprint

Chen, Y., Han, M., Meng, J., Cao, D., Cheng, N., Luo, Q., Yang, J., & Zhang, G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.12.628119

Matrix-biased excitatory and inhibitory inputs to the striatum involving external segment of the globus pallidus

Karube, F., Kobayashi, K., & Fujiyama, F. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1706469

Developmental specification of forebrain cholinergic neurons

Allaway, K. C., & Machold, R. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2016.11.007 · Cited by 68 · see citing works

Editorial

Rétaux, S. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.05.001 · Cited by 1 · see citing works

Genetically tagging cholinergic diversity

Luo, J. K., & Pinto, L. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.009 · Cited by 1 · see citing works

Cholinergic interneurons in the dorsal and ventral striatum: anatomical and functional considerations in normal and diseased conditions

Gonzales, K. K., & Smith, Y. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12762 · Cited by 164 · see citing works

Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders

Poppi, L. A., Ho-Nguyen, K.-T., Shi, A., Daut, C. T., & Tischfield, M. A. (2021) · Cells · doi:10.3390/cells10040907 · Cited by 46 · see citing works