1. Negah SS, Moradi HR, Forouzanfar F, Sahraian MA, Faraji M. The role of small extracellular vesicles derived from glial cells in the central nervous system under both normal and pathological conditions. Neurochemical Research. 2025; 50(2): 89. [ DOI:10.1007/s11064-025-04344-8] 2. Tondro G, Mohammadi A, Rajabzadeh G, Moradi HR, Negah SS. Niosomal Curcumin inhibited Gliomagenesis-Related markers in U87 cell line. 2023. [ DOI:10.21203/rs.3.rs-2817911/v1] 3. Palabaş T, Yılmaz E. Modulation of weak signal detection and transmission by an astrocyte in tripartite synapse model. Nonlinear Dynamics. 2025; 113(8): 8991-9004. [ DOI:10.1007/s11071-024-10758-w] 4. Boroomand M, Salehi E, Morady H, Rashidi M. Proective Effect of Frankincense Extract on the Histological Structure of Hippocampus and Cerebellum of Rats Exposed to Acrylamide. The Neuroscience Journal of Shefaye Khatam. 2024; 12(3): 64-76. [ DOI:10.61186/shefa.12.3.64] 5. Moradi HR, Taherianfard M, Rashidi M, Javid Z, Hesami SA. Protective effects of wheat sprout on acrylamide toxicity in the hippocampus structure and spatial learning and memory of rat. The Neuroscience Journal of Shefaye Khatam. 2023; 11(2): 10-9. [ DOI:10.61186/shefa.11.2.10] 6. Sahab-Negah S, Hajali V, Moradi HR, Gorji A. The impact of estradiol on neurogenesis and cognitive functions in Alzheimer's disease. Cellular and molecular neurobiology. 2020; 40(3): 283-99. [ DOI:10.1007/s10571-019-00733-0] 7. Tondro G, Rajabzade G, Mohammadi A, Moradi H, Sahab Negah S. Anti-inflammatory effects of nano-curcumin on a glioblastoma cell line. The Neuroscience Journal of Shefaye Khatam. 2022; 10(3): 48-56. [ DOI:10.52547/shefa.10.3.48] 8. Won W, Bhalla M, Lee J-H, Lee CJ. Astrocytes as Key Regulators of Neural Signaling in Health and Disease. Annual Review of Neuroscience. 2025; 48. [ DOI:10.1146/annurev-neuro-112723-035356] 9. Hajali V, Moradi HR, Sahab Negah S. Neurotransmitters Play as a Key Role in Adult Neurogenesis. The Neuroscience Journal of Shefaye Khatam. 2018; 6(4): 61-74. [ DOI:10.29252/shefa.6.4.61] 10. Moradi HR, Heydarian S, Abdollahinezhad S. Effects of Nanoplastics and Microplastics on the Health of the Peripheral and Central Nervous System. The Neuroscience Journal of Shefaye Khatam. 2024; 12(4): 97-110. [ DOI:10.61186/shefa.12.4.97] 11. Chi-Castañeda D, Suárez-Pozos E, Ortega A. Glial cells: mere passive contributors to brain function? : Frontiers Media SA; 2024. p. 1360462. [ DOI:10.3389/fncel.2023.1360462] 12. Monteiro-Pacheco A, Carvalho J, Pinto L, Canedo T. Adult astrocyte generation across health and disease: A systematic review. Neural Regeneration Research. 2026: 10.4103. [ DOI:10.4103/NRR.NRR-D-25-01229] 13. Lines J, Corkrum M, Aguilar J, Araque A. The duality of astrocyte neuromodulation: Astrocytes sense neuromodulators and are neuromodulators. Journal of Neurochemistry. 2025; 169(4): e70054. [ DOI:10.1111/jnc.70054] 14. Murphy-Royal C, Dupuis J, Groc L, Oliet SHR. Astroglial glutamate transporters in the brain: Regulating neurotransmitter homeostasis and synaptic transmission. Journal of Neuroscience Research. 2017; 95(11): 2140-51. [ DOI:10.1002/jnr.24029] 15. Wu J, Li R, Wang J, Zhu H, Ma Y, You C, et al. Reactive astrocytes in glioma: emerging opportunities and challenges. International journal of molecular sciences. 2025; 26(7): 2907. [ DOI:10.3390/ijms26072907] 16. Bernardinelli Y, Muller D, Nikonenko I. Astrocyte-Synapse Structural Plasticity. Neural Plasticity. 2014; 2014(1): 232105. [ DOI:10.1155/2014/232105] 17. Veiga A, Abreu DS, Dias JD, Azenha P, Barsanti S, Oliveira JF. Calcium-Dependent Signaling in Astrocytes: Downstream Mechanisms and Implications for Cognition. Journal of Neurochemistry. 2025; 169(2): e70019. [ DOI:10.1111/jnc.70019] 18. Khaksar Z, Moradi HR. Niacin (Vitamin B3) in Neurodegenerative Disorders: A Comprehensive Review of its Effects on Alzheimer's, Parkinson's, and Huntington's Diseases. The Neuroscience Journal of Shefaye Khatam. 2025: 0-. [ DOI:10.66224/shefa.14.2.67] 19. Khaksar Z, Morovvati H, Moradi HR, Sahab Negah S. The role of extracellular matrix in myelination and oligodendrogenesis of the central nervous system. The Neuroscience Journal of Shefaye Khatam. 2019; 7(2): 66-82. [ DOI:10.29252/shefa.7.2.66] 20. Moradi HR, Hajali V, Khaksar Z, Vafaee F, Forouzanfar F, Negah SS. The next step of neurogenesis in the context of Alzheimer's disease. Molecular Biology Reports. 2021; 48(7): 5647-60. [ DOI:10.1007/s11033-021-06520-9] 21. Menesse G, Millán AP, Torres JJ. Astrocyte-mediated higher-order control of synaptic plasticity. Communications Biology. 2026. [ DOI:10.1038/s42003-026-10044-y] 22. Hatashita Y, Inoue T. Recent optical approaches for anatomical and functional dissection of neuron-astrocyte circuitry. The Journal of Physiology. 2026; 604(4): 1547-57. [ DOI:10.1113/JP287485] 23. Herzberg W. Fibrillar astrocytes compared to protoplasmic astrocytes--electrophysiological function and model--REVIEW. Authorea Preprints. 2026. [ DOI:10.22541/au.177499347.77677626/v1] 24. Watanabe A, Guo C, Sjöström PJ. The developmental profile of visual cortex astrocytes. iScience. 2023; 26(6): 106828. [ DOI:10.1016/j.isci.2023.106828] 25. Covelo A, Araque A. Neuronal activity determines distinct gliotransmitter release from a single astrocyte. elife. 2018; 7: e32237. [ DOI:10.7554/eLife.32237] 26. Savtchouk I, Volterra A. Gliotransmission: beyond black-and-white. Journal of Neuroscience. 2018; 38(1): 14-25. [ DOI:10.1523/JNEUROSCI.0017-17.2017] 27. Li H, Zhao Y, Dai R, Geng P, Weng D, Wu W, et al. Astrocytes release ATP/ADP and glutamate in flashes via vesicular exocytosis. Molecular psychiatry. 2025; 30(6): 2475-2489. [ DOI:10.1038/s41380-024-02851-8] 28. Allen NJ, Eroglu C. Cell biology of astrocyte-synapse interactions. Neuron. 2017; 96(3): 697-708. [ DOI:10.1016/j.neuron.2017.09.056] 29. Andersen JV. The glutamate/GABA‐glutamine cycle: Insights, updates, and advances. Journal of Neurochemistry. 2025; 169(3): e70029. [ DOI:10.1111/jnc.70029] 30. Hayashi MK. Structure-function relationship of transporters in the glutamate-glutamine cycle of the central nervous system. International journal of molecular sciences. 2018; 19(4): 1177. [ DOI:10.3390/ijms19041177] 31. Tripodi F, Maffioli E, Sacchi S, Rabattoni V, Motta Z, Bearzi C, et al. Modulating the serine metabolism in human differentiated astrocytes: an integrated multi omics approach. Frontiers in Cellular Neuroscience. 2025; 19: 1616911. [ DOI:10.3389/fncel.2025.1616911] 32. Satake SI. Ethanol disrupts cerebellar synaptic modulation by enhancing EAAT4-mediated glutamate uptake. Communications Biology. 2026. [ DOI:10.1038/s42003-026-09978-0] 33. Provenzano F, Torazza C, Bonifacino T, Bonanno G, Milanese M. The key role of astrocytes in amyotrophic lateral sclerosis and their commitment to glutamate excitotoxicity. International journal of molecular sciences. 2023; 24(20): 15430. [ DOI:10.3390/ijms242015430] 34. Di Giovanni S. The neuronal-like behaviour of macrophages. Trends in Cell Biology. 2025. [ DOI:10.1016/j.tcb.2025.04.003] 35. Dias JD, Viana JF, Alves LS, Veiga A, Matos B, Machado JL, et al. AstroWars: the return of the astrocytic metabotropic glutamate receptor 5. The Journal of Physiology. 2026; 604(4): 1518-30. [ DOI:10.1113/JP288403] 36. Angulo MC. The Power of Neuroglia in Driving Brain Function. Neurochemical Research. 2025; 50(3): 184. [ DOI:10.1007/s11064-025-04437-4] 37. Doliwa M, Kuzniewska B, Nader K, Reniewicz P, Kaczmarek L, Michaluk P, et al. Astrocyte-Secreted Lcn2 Modulates Dendritic Spine Morphology. Cells. 2025; 14(3): 159. [ DOI:10.3390/cells14030159] 38. Gundersen V, Storm-Mathisen J, Bergersen LH. Neuroglial transmission. Physiological reviews. 2015; 95(3): 695-726. [ DOI:10.1152/physrev.00024.2014] 39. Henneberger C, Papouin T, Oliet SH, Rusakov DA. Long-term potentiation depends on release of D-serine from astrocytes. Nature. 2010; 463(7278): 232-6. [ DOI:10.1038/nature08673] 40. Sultan S, Li L, Moss J, Petrelli F, Cassé F, Gebara E, et al. Synaptic integration of adult-born hippocampal neurons is locally controlled by astrocytes. Neuron. 2015; 88(5): 957-72. [ DOI:10.1016/j.neuron.2015.10.037] 41. Koh W, Park M, Chun YE, Lee J, Shim HS, Park MG, et al. Astrocytes render memory flexible by releasing D-serine and regulating NMDA receptor tone in the hippocampus. Biological psychiatry. 2022; 15; 91(8): 740-752. [ DOI:10.1016/j.biopsych.2021.10.012] 42. Tapanes SA, Arizanovska D, Díaz MM, Folorunso OO, Harvey T, Brown SE, et al. Inhibition of glial D‐serine release rescues synaptic damage after brain injury. Glia. 2022; 70(6): 1133-52. [ DOI:10.1002/glia.24161] 43. Perez EJ, Tapanes SA, Loris ZB, Balu DT, Sick TJ, Coyle JT, et al. Enhanced astrocytic d-serine underlies synaptic damage after traumatic brain injury. The Journal of Clinical Investigation. 2017; 127(8): 3114-25. [ DOI:10.1172/JCI92300] 44. Corkrum M, Covelo A, Lines J, Bellocchio L, Pisansky M, Loke K, et al. Dopamine-evoked synaptic regulation in the nucleus accumbens requires astrocyte activity. Neuron. 2020; 105(6): 1036-47. e5. [ DOI:10.1016/j.neuron.2019.12.026] 45. Illes P, Rubini P, Ulrich H, Yin H-Y, Tang Y. Dysregulation of Astrocytic ATP/Adenosine Release in the Hippocampus Cause Cognitive and Affective Disorders: Molecular Mechanisms, Diagnosis, and Therapy. MedComm. 2025; 6(5): e70177. [ DOI:10.1002/mco2.70177] 46. Zhao YF, Verkhratsky A, Tang Y, Illes P. Astrocytes and major depression: The purinergic avenue. Neuropharmacology. 2022; 220: 109252. [ DOI:10.1016/j.neuropharm.2022.109252] 47. Li Y, Li L, Wu J, Zhu Z, Feng X, Qin L, et al. Activation of astrocytes in hippocampus decreases fear memory through adenosine A1 receptors. Elife. 2020; 9: e57155. [ DOI:10.7554/eLife.57155] 48. Verkhratsky A, Untiet V, Rose CR. Ionic signalling in astroglia beyond calcium. The Journal of Physiology. 2020; 598(9): 1655-1670. [ DOI:10.1113/JP277478] 49. McNeill J, Rudyk C, Hildebrand ME, Salmaso N. Ion channels and electrophysiological properties of astrocytes: implications for emergent stimulation technologies. Frontiers in Cellular Neuroscience. 2021; 15: 644126. [ DOI:10.3389/fncel.2021.644126] 50. Newman EA. New roles for astrocytes: regulation of synaptic transmission. Trends in neurosciences. 2003; 26(10): 536-42. [ DOI:10.1016/S0166-2236(03)00237-6] 51. Wang S, Wang B, Shang D, Zhang K, Yan X, Zhang X. Ion channel dysfunction in astrocytes in neurodegenerative diseases. Frontiers in Physiology. 2022; 13: 814285. [ DOI:10.3389/fphys.2022.814285] 52. Magistretti PJ, Allaman I. A cellular perspective on brain energy metabolism and functional imaging. Neuron. 2015; 86(4): 883-901. [ DOI:10.1016/j.neuron.2015.03.035] 53. Siervo M, Verdile G, Piknova B. Inorganic Nitrate Stores, Astrocyte Metabolism and Brain Health: An Emerging Paradigm. Nitric Oxide. 2025. [ DOI:10.1016/j.niox.2025.06.005] 54. Figley CR, Stroman PW. The role (s) of astrocytes and astrocyte activity in neurometabolism, neurovascular coupling, and the production of functional neuroimaging signals. European Journal of Neuroscience. 2011; 33(4): 577-88. [ DOI:10.1111/j.1460-9568.2010.07584.x] 55. Gao K, Cheung-Hoi Yu A. Glutamate, a Key for Astrocytes to Participate in Brain Function and Diseases. Neurochemical Research. 2025; 50(3): 1-7. [ DOI:10.1007/s11064-025-04418-7] 56. Haydon PG, Carmignoto G. Astrocyte Control of Synaptic Transmission and Neurovascular Coupling. Physiological Reviews. 2006; 86(3): 1009-31. [ DOI:10.1152/physrev.00049.2005] 57. Attwell D, Buchan AM, Charpak S, Lauritzen M, MacVicar BA, Newman EA. Glial and neuronal control of brain blood flow. Nature. 2010; 468(7321): 232-43. [ DOI:10.1038/nature09613] 58. Filosa JA, Blanco VM. Neurovascular coupling in the mammalian brain. Experimental Physiology. 2007; 92(4): 641-6. [ DOI:10.1113/expphysiol.2006.036368] 59. Christie IN, Theparambil SM, Braga A, Doronin M, Hosford PS, Brazhe A, et al. Astrocytes produce nitric oxide via nitrite reduction in mitochondria to regulate cerebral blood flow during brain hypoxia. Cell reports. 2023; (12): 113514. [ DOI:10.1016/j.celrep.2023.113514] 60. Lind B, Volterra A. Fast 3D imaging in the auditory cortex of awake mice reveals that astrocytes control neurovascular coupling responses at arteriole-capillary junctions. 2025. [ DOI:10.21203/rs.3.rs-6539397/v1] 61. Kim SK, Hayashi H, Ishikawa T, Shibata K, Shigetomi E, Shinozaki Y, et al. Cortical astrocytes rewire somatosensory cortical circuits for peripheral neuropathic pain. The Journal of clinical investigation. 2016; 126(5): 1983-97. [ DOI:10.1172/JCI82859] 62. Stogsdill JA, Eroglu C. The interplay between neurons and glia in synapse development and plasticity. Current opinion in neurobiology. 2017; 42: 1-8. [ DOI:10.1016/j.conb.2016.09.016] 63. Park J, Chung W-S. Astrocyte-dependent circuit remodeling by synapse phagocytosis. Current Opinion in Neurobiology. 2023; 81: 102732. [ DOI:10.1016/j.conb.2023.102732] 64. Kim N-S, Chung W-S. Astrocytes regulate neuronal network activity by mediating synapse remodeling. Neuroscience Research. 2023; 187: 3-13. [ DOI:10.1016/j.neures.2022.09.007] 65. Lawal O, Ulloa Severino FP, Eroglu C. The role of astrocyte structural plasticity in regulating neural circuit function and behavior. Glia. 2022; 70(8): 1467-83. [ DOI:10.1002/glia.24191] 66. Haim LB, Rowitch DH. Functional diversity of astrocytes in neural circuit regulation. Nature Reviews Neuroscience. 2017; 18(1): 31-41. [ DOI:10.1038/nrn.2016.159] 67. Farhy-Tselnicker I, Allen NJ. Astrocytes, neurons, synapses: a tripartite view on cortical circuit development. Neural development. 2018; 13: 1-12. [ DOI:10.1186/s13064-018-0104-y] 68. Stevens B. Neuron-Astrocyte Signaling in the Development and Plasticity of Neural Circuits. Neurosignals. 2008; 16(4): 278-88. [ DOI:10.1159/000123038] 69. Liu X, Ying J, Wang X, Zheng Q, Zhao T, Yoon S, et al. Astrocytes in neural circuits: key factors in synaptic regulation and potential targets for neurodevelopmental disorders. Frontiers in molecular neuroscience. 2021; 14: 729273. [ DOI:10.3389/fnmol.2021.729273] 70. Myer DJ, Gurkoff GG, Lee SM, Hovda DA, Sofroniew MV. Essential protective roles of reactive astrocytes in traumatic brain injury. Brain. 2006; 129(10): 2761-72. [ DOI:10.1093/brain/awl165] 71. Boghdadi AG, Teo L, Bourne JA. The Neuroprotective Role of Reactive Astrocytes after Central Nervous System Injury. Journal of Neurotrauma. 2020; 37(5): 681-691. [ DOI:10.1089/neu.2019.6938] 72. Yu G, Zhang Y, Ning B. Reactive astrocytes in central nervous system injury: subgroup and potential therapy. Frontiers in cellular neuroscience. 2021; 15: 792764. [ DOI:10.3389/fncel.2021.792764] 73. Ishii T, Takanashi Y, Sugita K, Miyazawa M, Yanagihara R, Yasuda K, et al. Endogenous reactive oxygen species cause astrocyte defects and neuronal dysfunctions in the hippocampus: a new model for aging brain. Aging cell. 2017; 16(1): 39-51. [ DOI:10.1111/acel.12523] 74. Liddelow SA, Barres BA. Reactive astrocytes: production, function, and therapeutic potential. Immunity. 2017; 46(6): 957-67. [ DOI:10.1016/j.immuni.2017.06.006] 75. Allen NJ, Bennett ML, Foo LC, Wang GX, Chakraborty C, Smith SJ, et al. Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors. Nature. 2012; 486(7403): 410-4. [ DOI:10.1038/nature11059] 76. Clarke LE, Liddelow SA, Chakraborty C, Münch AE, Heiman M, Barres BA. Normal aging induces A1-like astrocyte reactivity. Proceedings of the National Academy of Sciences. 2018; 115(8): E1896-E905. [ DOI:10.1073/pnas.1800165115] 77. Acosta C, Anderson HD, Anderson CM. Astrocyte dysfunction in Alzheimer disease. Journal of Neuroscience Research. 2017; 95(12): 2430-47. [ DOI:10.1002/jnr.24075] 78. Ramazi S, Arani F, Safaei A, Abbasi Z, Heidari Z, Ghasemian nafchi H, et al. The Role of astrocytes in the central nervous system: Physiological and pathophysiological conditions. The Neuroscience Journal of Shefaye Khatam. 2021; 9(2) :119-139. [ DOI:10.52547/shefa.9.2.119] 79. Yousefi A, Moradi HR, Khaksar Z, Abbasi S. Transplacental and lactational exposure to polystyrene nanoplastics induces structural and cellular alterations in the hippocampus of rat offspring. Neuroscience. 2026; 612:192-204. [ DOI:10.1016/j.neuroscience.2026.07.055] 80. Moradi HR, Khaksar Z, Alipour F, Fathollahi S, Taherianfard M, Rashidi M, Khodayari M. Zingiber officinale protects against acrylamide-induced spatial memory impairment, oxidative stress, and neurodegeneration in rats. Avicenna Journal of Phytomedicine. 2026:e27806. 81. Price BR, Norris CM, Sompol P, Wilcock DM. An emerging role of astrocytes in vascular contributions to cognitive impairment and dementia. Journal of Neurochemistry. 2018; 144(5): 644-650. [ DOI:10.1111/jnc.14273] 82. Lima A, Sardinha VM, Oliveira A, Reis M, Mota C, Silva M, et al. Astrocyte pathology in the prefrontal cortex impairs the cognitive function of rats. Molecular psychiatry. 2014; 19(7): 834-41. [ DOI:10.1038/mp.2013.182] 83. Craft S, Baker LD, Montine TJ, Minoshima S, Watson GS, Claxton A, et al. Intranasal insulin therapy for Alzheimer disease and amnestic mild cognitive impairment: a pilot clinical trial. Archives of neurology. 2012; 69(1): 29-38. [ DOI:10.1001/archneurol.2011.233] 84. Mecocci P, Polidori MC. Antioxidant clinical trials in mild cognitive impairment and Alzheimer's disease. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease. 2012; 1822(5): 631-8. [ DOI:10.1016/j.bbadis.2011.10.006] 85. Perea G, Araque A. Astrocytes potentiate transmitter release at single hippocampal synapses. Science. 2007; 317(5841): 1083-6. [ DOI:10.1126/science.1144640] 86. Pascual O, Casper KB, Kubera C, Zhang J, Revilla-Sanchez R, Sul J-Y, et al. Astrocytic purinergic signaling coordinates synaptic networks. Science. 2005; 310(5745): 113-6. [ DOI:10.1126/science.1116916] 87. Rothstein JD, Dykes-Hoberg M, Pardo CA, Bristol LA, Jin L, Kuncl RW, et al. Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron. 1996; 16(3): 675-86. [ DOI:10.1016/S0896-6273(00)80086-0] 88. Héja L, Barabás P, Nyitrai G, Kékesi KA, Lasztóczi B, Tőke O, et al. Glutamate uptake triggers transporter-mediated GABA release from astrocytes. PloS one. 2009; 4(9): e7153. [ DOI:10.1371/journal.pone.0007153] 89. Suzuki A, Stern SA, Bozdagi O, Huntley GW, Walker RH, Magistretti PJ, et al. Astrocyte-neuron lactate transport is required for long-term memory formation. Cell. 2011; 144(5): 810-23. [ DOI:10.1016/j.cell.2011.02.018] 90. Illes P. P2X7 receptors amplify CNS damage in neurodegenerative diseases. International Journal of Molecular Sciences. 2020; 21(17): 5996. [ DOI:10.3390/ijms21175996] 91. Khakh BS, McCarthy KD. Astrocyte calcium signaling: from observations to functions and the challenges therein. Cold Spring Harbor Perspectives in Biology. 2015; 7(4): a020404. [ DOI:10.1101/cshperspect.a020404] 92. Lin C-LG, Kong Q, Cuny GD, Glicksman MA. Glutamate transporter EAAT2: a new target for the treatment of neurodegenerative diseases. Future medicinal chemistry. 2012; 4(13): 1689-700. [ DOI:10.4155/fmc.12.122] 93. Araque A, Carmignoto G, Haydon PG, Oliet SH, Robitaille R, Volterra A. Gliotransmitters travel in time and space. Neuron. 2014; 81(4): 728-39. [ DOI:10.1016/j.neuron.2014.02.007] 94. Magistretti PJ, Allaman I. Lactate in the brain: from metabolic end-product to signalling molecule. Nature reviews neuroscience. 2018; 19(4): 235-49. [ DOI:10.1038/nrn.2018.19] 95. Liddelow SA, Guttenplan KA, Clarke LE, Bennett FC, Bohlen CJ, Schirmer L, et al. Neurotoxic reactive astrocytes are induced by activated microglia. Nature. 2017; 541(7638): 481-487. [ DOI:10.1038/nature21029] 96. Brown AM, Ransom BR. Astrocyte glycogen and brain energy metabolism. Glia. 2007; 55(12): 1263-71. [ DOI:10.1002/glia.20557] 97. Chung W-S, Baldwin KT, Allen NJ. Astrocyte regulation of synapse formation, maturation, and elimination. Cold Spring Harbor Perspectives in Biology. 2024; 16(8): a041352. [ DOI:10.1101/cshperspect.a041352] 98. Sofroniew MV. Astrocyte reactivity: subtypes, states, and functions in CNS innate immunity. Trends in immunology. 2020; 41(9): 758-70. [ DOI:10.1016/j.it.2020.07.004] 99. Giaume C. Astroglial Wiring is Adding Complexity to Neuroglial Networking. Front Neuroenergetics. 2010; 2. [ DOI:10.3389/fnene.2010.00129] 100. Stellwagen D, Malenka RC. Synaptic scaling mediated by glial TNF-alpha. Nature. 2006; 440(7087): 1054-9. [ DOI:10.1038/nature04671]
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