ATP-Mediated Glia Signaling

The Gap Junction Communication Channel

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Glutamate Induces Calcium Waves in Cultured Astrocytes: Long-Range Glial Signaling

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Glutamate-mediated astrocyte–neuron signalling

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Glutamate neurotoxicity in cortical cell culture

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Differentiated Rat Glial Cell Strain in Tissue Culture

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Prostaglandins stimulate calcium-dependent glutamate release in astrocytes

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Regulation and Kinetics of the Actin-Myosin-ATP Interaction

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The Function of Myosin and Myosin Light Chain Kinase Phosphorylation in Smooth Muscle

Kamm, K. E., & Stull, J. T. (1985) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.25.040185.003113 · Cited by 1,064

Direct Signaling from Astrocytes to Neurons in Cultures of Mammalian Brain Cells

Nedergaard, M. (1994) · Science · doi:10.1126/science.8134839 · Cited by 1,016

Astrocyte-mediated potentiation of inhibitory synaptic transmission

Kang, J., Jiang, L., Goldman, S. A., & Nedergaard, M. (1998) · Nature Neuroscience · doi:10.1038/3684 · Cited by 870

Pannexins, distant relatives of the connexin family with specific cellular functions?

D’hondt, C., Ponsaerts, R., SMEDT, H. D., Bultynck, G., & Himpens, B. (2009) · BioEssays · doi:10.1002/bies.200800236 · Cited by 153

Purinergic transmission in the central nervous system

North, R. A., & Verkhratsky, A. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-006-0060-y · Cited by 150

Deep Brain Stimulation Results in Local Glutamate and Adenosine Release

Tawfik, V. L., Chang, S.-Y., Hitti, F. L., Roberts, D. W., Leiter, J. C., Jovanovic, S., & Lee, K. H. (2010) · Neurosurgery · doi:10.1227/01.neu.0000371988.73620.4c · Cited by 154

Diversity in protein–protein interactions of connexins: emerging roles

Hervé, J., Bourmeyster, N., & Sarrouilhe, D. (2004) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2003.10.022 · Cited by 144

Introduction to Purinergic Signalling in the Brain

Burnstock, G. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-4719-7_1 · Cited by 142

The birth and postnatal development of purinergic signalling

Burnstock, G., Fredholm, B. B., North, R. A., & Verkhratsky, A. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02114.x · Cited by 142

Connexins in the Heart: Regulation, Function and Involvement in Cardiac Disease

Rodríguez‐Sinovas, A., Sánchez, J. A., Valls-Lacalle, L., Consegal, M., & González, I. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094413 · Cited by 142

A role for Connexin43 during neurodevelopment

Wiencken‐Barger, A. E., Djukic, B., Casper, K. B., & McCarthy, K. D. (2007) · Glia · doi:10.1002/glia.20484 · Cited by 145

Homeostatic function of astrocytes: Ca2+ and Na+ signalling

Parpura, V., & Verkhratsky, A. (2012) · Translational Neuroscience · doi:10.2478/s13380-012-0040-y · Cited by 142

Reduced Expression of P2Y1 Receptors in Connexin43-Null Mice Alters Calcium Signaling and Migration of Neural Progenitor Cells

Scemes, E., Duval, N., & Meda, P. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-36-11444.2003 · Cited by 133

Regulation of the blood?biliary barrier: interaction between gap and tight junctions in hepatocytes

Kojima, T., Yamamoto, T., Murata, M., Chiba, H., Kokai, Y., & Sawada, N. (2003) · Medical Molecular Morphology · doi:10.1007/s00795-003-0220-5 · Cited by 125

Glial modulation of synaptic transmission in culture

Araque, A., & Perea, G. (2004) · Glia · doi:10.1002/glia.20026 · Cited by 123

Protection after stroke: cellular effectors of neurovascular unit integrity

Posada‐Duque, R., Barreto, G. E., & Cardona‐Gómez, G. P. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00231 · Cited by 122

The modulatory effects of connexin 43 on cell death/survival beyond cell coupling

Rodríguez‐Sinovas, A., Cabestrero, A., López, D., Torre, I., Morente, M., Abellán, A., Miró‐Casas, E., Ruiz‐Meana, M., & David Garcia-dorado, A. (2007) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2007.03.003 · Cited by 123

Pathways of neuron-astrocyte interactions and their possible role in neuroprotection

Kirchhoff, F., Dringen, R., & Giaume, C. (2001) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s004060170036 · Cited by 121

P2X and P2Y purinoreceptors mediate ATP-evoked calcium signalling in optic nerve glia in situ

James, G., & Butt, A. M. (2001) · Cell Calcium · doi:10.1054/ceca.2001.0232 · Cited by 117

Control of cell proliferation by neurotransmitters in the developing vertebrate retina

Martins, R. A. P., & Pearson, R. A. (2007) · Brain Research · doi:10.1016/j.brainres.2007.04.076 · Cited by 126

Ionotropic receptors in neuronal–astroglial signalling: What is the role of “excitable” molecules in non-excitable cells

Lalo, U., Pankratov, Y., Parpura, V., & Verkhratsky, A. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.09.007 · Cited by 123

Anti-Depressant Fluoxetine Reveals its Therapeutic Effect Via Astrocytes

Kinoshita, M., Hirayama, Y., Fujishita, K., Shibata, K., Shinozaki, Y., Shigetomi, E., Takeda, A., Le, H. P. N., Hayashi, H., Hiasa, M., et al. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.05.036 · Cited by 117

Ion Channels and Electrophysiological Properties of Astrocytes: Implications for Emergent Stimulation Technologies

McNeill, J., Rudyk, C., Hildebrand, M. E., & Salmaso, N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.644126 · Cited by 130

Dysfunctional serotonergic neuron-astrocyte signaling in depressive-like states

González-Arias, C., Sánchez-Ruiz, A., Esparza, J., Sánchez‐Puelles, C., Arancibia, L., Ramírez‐Franco, J., Gobbo, D., Kirchhoff, F., & Perea, G. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02269-8 · Cited by 124

The (Multiple) Realization of Psychological and other Properties in the Sciences

Aizawa, K., & Gillett, C. (2009) · Mind & Language · doi:10.1111/j.1468-0017.2008.01359.x · Cited by 115

Synaptic P2X receptors

Robertson, S. J., Ennion, S. J., Evans, R. J., & Edwards, F. A. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00222-1 · Cited by 112

Receptors, Ion Channels, and Signaling Mechanisms Underlying Microglial Dynamics

Madry, C., & Attwell, D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.r115.637157 · Cited by 109

The inflammasome pathway is amplified and perpetuated in an autocrine manner through connexin43 hemichannel mediated ATP release

Mugisho, O. O., Green, C. R., Kho, D. T., Zhang, J., Graham, E. S., Acosta, M. L., & Rupenthal, I. D. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.11.015 · Cited by 108

Light-Driven ATP Transmembrane Transport Controlled by DNA Nanomachines

Li, P., Xie, G., Liu, P., Kong, X., Song, Y., Wen, L., & Jiang, L. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b10527 · Cited by 108

Neuronal soma–satellite glial cell interactions in sensory ganglia and the participation of purinergic receptors

Gu, Y., Chen, Y., Zhang, X., Li, G.-W., Wang, C., & Huang, L.-Y. M. (2010) · Neuron Glia Biology · doi:10.1017/s1740925x10000116 · Cited by 106

Adhesive properties of connexin hemichannels

Cotrina, M. L., Lin, J. H.-C., & Nedergaard, M. (2008) · Glia · doi:10.1002/glia.20728 · Cited by 106

The role of nucleotides in the neuron–glia communication responsible for the brain functions

Inoue, K., Koizumi, S., & Tsuda, M. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04824.x · Cited by 105

Astrocytic control of synaptic transmission and plasticity: a target for drugs of abuse?

Haydon, P. G., Blendy, J. A., Moss, S. J., & Jackson, F. R. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.050 · Cited by 103

Calcium homeostasis modulator (CALHM) ion channels

Ma, Z., Tanis, J. E., Taruno, A., & Foskett, J. K. (2015) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-015-1757-6 · Cited by 101

The role of intracellular calcium stores in synaptic plasticity and memory consolidation

Baker, K., Edwards, T. M., & Rickard, N. S. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.04.011 · Cited by 99

Rapidly exchanging Ca2+ stores in neurons: molecular, structural and functional properties

Meldolesi, J. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(01)00004-1 · Cited by 100

Modulation of intercellular calcium signaling in astrocytes by extracellular calcium and magnesium

Stout, C. E., & Charles, A. C. (2003) · Glia · doi:10.1002/glia.10257 · Cited by 101

Morphine-Induced Chemotaxis and Brain-Derived Neurotrophic Factor Expression in Microglia

Takayama, N., & Ueda, H. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3170-04.2005 · Cited by 97

A Quantitative Model of Purinergic Junctional Transmission of Calcium Waves in Astrocyte Networks

Bennett, M. R., Farnell, L., & Gibson, W. G. (2005) · Biophysical Journal · doi:10.1529/biophysj.105.062968 · Cited by 101

Ion changes and signalling in perisynaptic glia

Deitmer, J. W., & Rose, C. R. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.10.006 · Cited by 98

Synchronization of Ca2+ oscillations: involvement of ATP release in astrocytes

Koizumi, S. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07438.x · Cited by 100

Copper in Human Health and Disease: A Comprehensive Review

Binesh, A., & Venkatachalam, K. (2024) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70052 · Cited by 101

Neuroendocrine Regulation of Puberty

Ojeda, S. R., & Bilger, M. (2000) · Humana Press eBooks · doi:10.1007/978-1-59259-707-9_12 · Cited by 93

Astrocytic Atrophy Following Status Epilepticus Parallels Reduced Ca2+ Activity and Impaired Synaptic Plasticity in the Rat Hippocampus

Plata, A., Lebedeva, A., Denisov, P., Nosova, O., Postnikova, T. Y., Pimashkin, A. S., Brazhe, A., Zaitsev, A. V., Rusakov, D. A., & Semyanov, A. V. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00215 · Cited by 89

Inflammatory Mechanisms of Neurodegeneration in Toxin-Based Models of Parkinson's Disease

Litteljohn, D., Mangano, E. N., Clarke, M., Bobyn, J., Moloney, K., & Hayley, S. P. (2010) · Parkinson s Disease · doi:10.4061/2011/713517 · Cited by 98

ATP Signaling in Brain: Release, Excitotoxicity and Potential Therapeutic Targets

Cisneros-Mejorado, A., Pérez‐Samartín, A., Gottlieb, M., & Matute, C. (2014) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-014-0092-3 · Cited by 93

Role of Astrocytes in Matching Blood Flow to Neuronal Activity

Jakovčević, D., & Harder, D. R. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(06)79004-4 · Cited by 90

Communication between astrocytes and neurons: a complex language

Perea, G., & Araque, A. (2002) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(02)00007-4 · Cited by 92

Components of Astrocytic Intercellular Calcium Signaling

Scemes, E. (2000) · Molecular Neurobiology · doi:10.1385/mn:22:1-3:167 · Cited by 90

Connexin 43 mimetic peptides inhibit spontaneous epileptiform activity in organotypic hippocampal slice cultures

Samoilova, M., Wentlandt, K., Adamchik, Y., Velumian, A. A., & Carlen, P. L. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.01.005 · Cited by 86

Alteration of purinergic P2X4 and P2X7 receptor expression in rats with temporal-lobe epilepsy induced by pilocarpine

Doná, F., Ulrich, H., Persike, D. S., Conceição, I. M., Blini, J. P., Cavalheiro, É. A., & Fernandes, M. J. D. S. (2008) · Epilepsy Research · doi:10.1016/j.eplepsyres.2008.10.008 · Cited by 87

Introduction to Purinergic Signalling in the Brain

Burnstock, G. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-30651-9_1 · Cited by 85

Deep Brain Stimulation: Are Astrocytes a Key Driver Behind the Scene?

Fenoy, A. J., Goetz, L., Chabardès, S., & Xia, Y. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12223 · Cited by 88

Astroglia: Important mediators of traumatic brain injury

Floyd, C. L., & Lyeth, B. G. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)61005-4 · Cited by 80

Tonabersat Prevents Inflammatory Damage in the Central Nervous System by Blocking Connexin43 Hemichannels

Kim, Y., Griffin, J. M., Nor, M. N. M., Zhang, J., Freestone, P. S., Danesh-Meyer, H. V., Rupenthal, I. D., Acosta, M. L., Nicholson, L. F. B., O’Carroll, S. J., et al. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0536-9 · Cited by 81

Luteinizing hormone-releasing hormone (LHRH) neurons: Mechanism of pulsatile LHRH release

Terasawa, E. (2001) · Vitamins and hormones · doi:10.1016/s0083-6729(01)63004-8 · Cited by 81

Connexins, cell motility, and the cytoskeleton

Olk, S., Zoidl, G., & Dermietzel, R. (2009) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20404 · Cited by 80

Equine sweating and anhidrosis Part 1 – equine sweating

Jenkinson, D. M., Elder, H. Y., & Bovell, D. L. (2006) · Veterinary Dermatology · doi:10.1111/j.1365-3164.2006.00545.x · Cited by 79

Where the thoughts dwell: The physiology of neuronal–glial “diffuse neural net”

Verkhratsky, A., Parpura, V., & Rodriguez, J. J. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.05.002 · Cited by 83

Subunit-specific Coupling between γ-Aminobutyric Acid Type A and P2X2 Receptor Channels

Boué‐Grabot, É., Toulmé, E., Emerit, M. B., & Garret, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m410223200 · Cited by 79

Purinergic signaling in neural development

Zimmermann, H. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.02.007 · Cited by 77

Cx32 Formation and/or Cx32-Mediated Intercellular Communication Induces Expression and Function of Tight Junctions in Hepatocytic Cell Line

Kojima, T., Spray, D. C., Kokai, Y., Chiba, H., Mochizuki, Y., & Sawada, N. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5511 · Cited by 77

Sub‐micromolar increase in [Ca2+]i triggers delayed exocytosis of ATP in cultured astrocytes

Pryazhnikov, E., & Khiroug, L. S. (2007) · Glia · doi:10.1002/glia.20590 · Cited by 77

EphrinBs Regulate d-Serine Synthesis and Release in Astrocytes

Zhuang, Z.-Y., Yang, B., Theus, M. H., Sick, J. T., Bethea, J. R., Sick, T. J., & Liebl, D. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0481-10.2010 · Cited by 77

Characteristics of subepithelial fibroblasts as a mechano-sensor in the intestine: cell-shape-dependent ATP release and P2Y1 signaling

Furuya, K., Sokabe, M., & Furuya, S. (2005) · Journal of Cell Science · doi:10.1242/jcs.02453 · Cited by 77

ATP Triggers Intracellular Ca2+ Release in Type II Cells of the Rat Carotid Body

Xu, J., Tse, F. W., & Tse, A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.039735 · Cited by 74

The purinergic neurotransmitter revisited: A single substance or multiple players?

Mutafova–Yambolieva, V. N., & Durnin, L. (2014) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2014.05.012 · Cited by 78

Morphological and physiological interactions of NG2‐glia with astrocytes and neurons

Wigley, R., Hamilton, N., Nishiyama, A., Kirchhoff, F., & Butt, A. M. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00729.x · Cited by 75

Expression and function of astrocytic gap junctions in aging

Cotrina, M. L., Gao, Q., Lin, J. H.-C., & Nedergaard, M. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02258-2 · Cited by 72

Recent Patents on Novel P2X7 Receptor Antagonists and their Potential for Reducing Central Nervous System Inflammation

Friedle, S. A., Curet, M., & Watters, J. J. (2009) · Recent Patents on CNS Drug Discovery · doi:10.2174/157488910789753530 · Cited by 74

ATP‐induced, sustained calcium signalling in cultured rat cortical astrocytes: evidence for a non‐capacitative, P2X7‐like‐mediated calcium entry

Nobile, M., Monaldi, I., Alloisio, S., Cugnoli, C., & Ferroni, S. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)00129-7 · Cited by 70

Neuroglial ATP release through innexin channels controls microglial cell movement to a nerve injury

Samuels, S. E., Lipitz, J. B., Dahl, G., & Muller, K. J. (2010) · The Journal of General Physiology · doi:10.1085/jgp.201010476 · Cited by 70

Neuroinflammation contributes to autophagy flux blockage in the neurons of rostral ventrolateral medulla in stress-induced hypertension rats

Du, D., Hu, L., Wu, J., Wu, Q. J., Cheng, W., Guo, Y., Guan, R., Wang, Y., Chen, X., Yan, X., et al. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0942-2 · Cited by 69

P2X receptor-mediated excitatory synaptic currents in somatosensory cortex

Pankratov, Y. V., Lalo, U., Krishtal, O., & Verkhratsky, A. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00233-1 · Cited by 69

Chronic psychotropic drug treatment causes differential expression of connexin 43 and GFAP in frontal cortex of rats.

Fatemi, S., Folsom, T., Reutiman, T. J., Pandian, T., Braun, N. N., & Haug, K. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.05.016 · Cited by 72

Contribution of Glial-Neuronal Interactions to the Neuroendocrine Control of Female Puberty

Ojeda, S., Lomniczi, A., & Sandau, U. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07515.x · Cited by 64

ATP, glia and central respiratory control

Erlichman, J. S., Leiter, J. C., & Gourine, A. V. (2010) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2010.06.009 · Cited by 65

Enhanced astroglial Ca2+ signaling increases excitatory synaptic strength in the epileptic brain

Álvarez‐Ferradas, C., Morales, J. C., Wellmann, M., Nualart, F., Roncagliolo, M., Fuenzalida, M., & Bonansco, C. (2015) · Glia · doi:10.1002/glia.22817 · Cited by 66

Cellular injury induces activation of MAPK via P2Y receptors

Yang, L., Cranson, D., & Trinkaus‐Randall, V. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10774 · Cited by 66

Early P2X7R-related astrogliosis in autoimmune encephalomyelitis.

Grygorowicz, T., Wełniak-Kamińska, M., & Strużyńska, L. (2016) · Molecular and cellular neurosciences · doi:10.1016/j.mcn.2016.02.003 · Cited by 60

How do taste cells lacking synapses mediate neurotransmission? CALHM 1, a voltage‐gated ATP channel

Taruno, A., Matsumoto, I., Ma, Z., Marambaud, P., & Foskett, J. K. (2013) · BioEssays · doi:10.1002/bies.201300077 · Cited by 62

Potentiation by ATP of lipopolysaccharide-stimulated nitric oxide production in cultured astrocytes

Murakami, K., Nakamura, Y., & Yoneda, Y. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00804-7 · Cited by 62

Purinergic receptors modulate MAP kinases and transcription factors that control microglial inflammatory gene expression

Potucek, Y., Crain, J. M., & Watters, J. J. (2006) · Neurochemistry International · doi:10.1016/j.neuint.2006.04.005 · Cited by 61

Spatiotemporal characteristics of calcium dynamics in astrocytes

Kang, M., & Othmer, H. G. (2009) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.3206698 · Cited by 67

Mathematical model of morphogen electrophoresis through gap junctions

Esser, A. T., Smith, K. C., Weaver, J. C., & Levin, M. G. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20870 · Cited by 64

Ectopic vesicular neurotransmitter release along sensory axons mediates neurovascular coupling via glial calcium signaling

Thyssen, A., Hirnet, D., Wolburg, H., Schmalzing, G., Deitmer, J. W., & Lohr, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003501107 · Cited by 61

New insights into purinergic receptor signaling in neuronal differentiation, neuroprotection, and brain disorders

Majumder, P., Trujillo, C. A., Lopes, C. G., Resende, R. R., Gomes, K. N., Yuahasi, K. K., Britto, L. R. G., & Ulrich, H. (2007) · Purinergic Signalling · doi:10.1007/s11302-007-9074-y · Cited by 64

Ciliary beat co-ordination by calcium

Schmid, A., & Salathe, M. A. (2011) · Biology of the Cell · doi:10.1042/bc20100120 · Cited by 60

Imaging of cortical astrocytes using 2-photon laser scanning microscopy in the intact mouse brain

Tian, G.-F., Takano, T., Lin, J. H.-C., Wang, X., Bekar, L. K., & Nedergaard, M. (2006) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2006.07.001 · Cited by 62

P2X7 receptor differentially modulates astroglial apoptosis and clasmatodendrosis in the rat brain following status epilepticus

Kim, J., Ryu, H. J., Yeo, S., & Kang, T. (2010) · Hippocampus · doi:10.1002/hipo.20850 · Cited by 60

Glia, sympathetic activity and cardiovascular disease

Marina, N., Teschemacher, A. G., Kasparov, S., & Gourine, A. V. (2016) · Experimental Physiology · doi:10.1113/ep085713 · Cited by 60

Regulation of cell-to-cell communication mediated by astrocytic ATP in the CNS

Koizumi, S., Fujishita, K., & Inoue, K. (2005) · Purinergic Signalling · doi:10.1007/s11302-005-6321-y · Cited by 58

Long‐lasting modulation of synaptic input to Purkinje neurons by Bergmann glia stimulation in rat brain slices

Brockhaus, J., & Deitmer, J. W. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.028423 · Cited by 59

Müller Cell Ca2+ Waves Evoked by Purinergic Receptor Agonists in Slices of Rat Retina

Li, Y., Holtzclaw, L. A., & Russell, J. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.986 · Cited by 58

Increase of intracellular Ca2+ by P2X and P2Y receptor-subtypes in cultured cortical astroglia of the rat

Fischer, W., Appelt, K., Grohmann, M., Franke, H., Nörenberg, W., & Illés, P. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.026 · Cited by 57

Retinovascular physiology and pathophysiology: New experimental approach/new insights

Puro, D. G. (2012) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2012.01.001 · Cited by 57

Altered Kir and gap junction channels in temporal lobe epilepsy

Bedner, P., & Steinhäuser, C. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.01.011 · Cited by 56

Rho-family GTPases modulate Ca2+-dependent ATP release from astrocytes

Blum, A. E., Joseph, S. M., Przybylski, R. J., & Dubyak, G. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00175.2008 · Cited by 56

Morphology and Properties of Astrocytes

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