Astrocyte reactivity and reactive astrogliosis: costs and benefits.
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[1] M. Nedergaard,et al. White matter astrocytes in health and disease , 2014, Neuroscience.
[2] Kara M. Smith,et al. Sex differences in Parkinson's disease and other movement disorders , 2014, Experimental Neurology.
[3] G. Gillies,et al. Sex differences in Parkinson’s disease , 2014, Frontiers in Neuroendocrinology.
[4] Milos Pekny,et al. The dual role of astrocyte activation and reactive gliosis , 2014, Neuroscience Letters.
[5] L. Alberghina,et al. Astrogliosis as a therapeutic target for neurodegenerative diseases , 2014, Neuroscience Letters.
[6] M. Cambron,et al. Astrocyte loss and astrogliosis in neuroinflammatory disorders , 2014, Neuroscience Letters.
[7] Y. Ao,et al. Heterogeneity of reactive astrocytes , 2014, Neuroscience Letters.
[8] S. Carmichael,et al. Astrocytic therapies for neuronal repair in stroke , 2014, Neuroscience Letters.
[9] B. MacVicar,et al. Microglial CR3 Activation Triggers Long-Term Synaptic Depression in the Hippocampus via NADPH Oxidase , 2014, Neuron.
[10] A. Verkhratsky,et al. Neuroglia in ageing and disease , 2014, Cell and Tissue Research.
[11] G. Knott,et al. Connexin 30 sets synaptic strength by controlling astroglial synapse invasion , 2014, Nature Neuroscience.
[12] Johan Liu,et al. HB‐EGF affects astrocyte morphology, proliferation, differentiation, and the expression of intermediate filament proteins , 2014, Journal of neurochemistry.
[13] E. Hol,et al. Acute isolation and transcriptome characterization of cortical astrocytes and microglia from young and aged mice , 2014, Neurobiology of Aging.
[14] M. Sofroniew,et al. Reactive Gliosis and the Multicellular Response to CNS Damage and Disease , 2014, Neuron.
[15] M. Faiz,et al. Synemin is expressed in reactive astrocytes and Rosenthal fibers in Alexander disease , 2014, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[16] D. Dietrich,et al. Synaptic integration by NG2 cells , 2013, Front. Cell. Neurosci..
[17] J. Yates,et al. Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor , 2013, Cell.
[18] C. Rose,et al. Astrocyte glutamine synthetase: pivotal in health and disease. , 2013, Biochemical Society transactions.
[19] Stephen J. Smith,et al. Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways , 2013, Nature.
[20] Beth Stevens,et al. TGF-β Signaling Regulates Neuronal C1q Expression and Developmental Synaptic Refinement , 2013, Nature Neuroscience.
[21] A. Prat,et al. Glial influence on the Blood Brain Barrier , 2013, Glia.
[22] E. Huang,et al. A Dramatic Increase of C1q Protein in the CNS during Normal Aging , 2013, The Journal of Neuroscience.
[23] B. Song,et al. Glial Scar Borders Are Formed by Newly Proliferated, Elongated Astrocytes That Interact to Corral Inflammatory and Fibrotic Cells via STAT3-Dependent Mechanisms after Spinal Cord Injury , 2013, The Journal of Neuroscience.
[24] M. Kubista,et al. Plasticity Response in the Contralesional Hemisphere after Subtle Neurotrauma: Gene Expression Profiling after Partial Deafferentation of the Hippocampus , 2013, PloS one.
[25] M. Iino,et al. Calcium-dependent N-cadherin up-regulation mediates reactive astrogliosis and neuroprotection after brain injury , 2013, Proceedings of the National Academy of Sciences.
[26] M. Nilsson,et al. Intermediate filaments are important for astrocyte response to oxidative stress induced by oxygen–glucose deprivation and reperfusion , 2013, Histochemistry and Cell Biology.
[27] E. Hol,et al. Reactive glia show increased immunoproteasome activity in Alzheimer's disease. , 2013, Brain : a journal of neurology.
[28] L. Tsai,et al. Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected]. , 2013, Cell stem cell.
[29] Fabian J Theis,et al. Live imaging of astrocyte responses to acute injury reveals selective juxtavascular proliferation , 2013, Nature Neuroscience.
[30] Johan Liu,et al. Bioactive 3D cell culture system minimizes cellular stress and maintains the in vivo‐like morphological complexity of astroglial cells , 2013, Glia.
[31] Michael Chen,et al. Forebrain engraftment by human glial progenitor cells enhances synaptic plasticity and learning in adult mice. , 2013, Cell stem cell.
[32] Y. Li,et al. Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis , 2013, Nature Neuroscience.
[33] R. Leak,et al. Astrocyte plasticity revealed by adaptations to severe proteotoxic stress , 2013, Cell and Tissue Research.
[34] A. Verkhratsky,et al. Neuroglia in Neurological Diseases , 2013 .
[35] A. Verkhratsky,et al. Peripheral Glial Cells , 2013 .
[36] Andrew W. Kraft,et al. Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice , 2013, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[37] R. Zorec,et al. Astrocytes Negatively Regulate Neurogenesis Through the Jagged1‐Mediated Notch Pathway , 2012, Stem cells.
[38] M. Selzer,et al. Scar-mediated inhibition and CSPG receptors in the CNS , 2012, Experimental Neurology.
[39] S. Strittmatter,et al. Axonal regeneration induced by blockade of glial inhibitors coupled with activation of intrinsic neuronal growth pathways , 2012, Experimental Neurology.
[40] S. Cullheim,et al. Reduced removal of synaptic terminals from axotomized spinal motoneurons in the absence of complement C3 , 2012, Experimental Neurology.
[41] Arne Schousboe,et al. Primary Cultures of Astrocytes: Their Value in Understanding Astrocytes in Health and Disease , 2012, Neurochemical Research.
[42] V. Gallo,et al. Experience-dependent regulation of NG2 progenitors in the developing barrel cortex , 2012, Nature Neuroscience.
[43] Eleonora Aronica,et al. Astrocyte immune responses in epilepsy , 2012, Glia.
[44] Giorgio Carmignoto,et al. Astrocyte calcium signaling and epilepsy , 2012, Glia.
[45] S. Bilbo,et al. Sex, glia, and development: Interactions in health and disease , 2012, Hormones and Behavior.
[46] Ivo D Dinov,et al. A role for ephrin-A5 in axonal sprouting, recovery, and activity-dependent plasticity after stroke , 2012, Proceedings of the National Academy of Sciences.
[47] A. Álvarez-Buylla,et al. Regional Astrocyte Allocation Regulates CNS Synaptogenesis and Repair , 2012, Science.
[48] Jeremy Seto,et al. Astrocyte-derived VEGF-A drives blood-brain barrier disruption in CNS inflammatory disease. , 2012, The Journal of clinical investigation.
[49] M. Kreft,et al. IFN-γ-induced increase in the mobility of MHC class II compartments in astrocytes depends on intermediate filaments , 2012, Journal of Neuroinflammation.
[50] Milos Pekny,et al. Modulation of Neural Plasticity as a Basis for Stroke Rehabilitation , 2012, Stroke.
[51] Ben A. Barres,et al. Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner , 2012, Neuron.
[52] B. Barres,et al. Genomic Analysis of Reactive Astrogliosis , 2012, The Journal of Neuroscience.
[53] E. Hol,et al. Differential cell proliferation in the cortex of the appsweps1de9 alzheimer's disease mouse model , 2012, Glia.
[54] Randy F. Stout,et al. Glial cells in (patho)physiology , 2012, Journal of neurochemistry.
[55] Fred H. Gage,et al. Local generation of glia is a major astrocyte source in postnatal cortex , 2012, Nature.
[56] S. Gold,et al. Sex-related factors in multiple sclerosis susceptibility and progression , 2012, Nature Reviews Neurology.
[57] M. Bennett,et al. The Role of Gap Junction Channels During Physiologic and Pathologic Conditions of the Human Central Nervous System , 2012, Journal of Neuroimmune Pharmacology.
[58] M. Götz,et al. Stab wound injury of the zebrafish telencephalon: A model for comparative analysis of reactive gliosis , 2012, Glia.
[59] M. Sofroniew,et al. Neurological diseases as primary gliopathies: a reassessment of neurocentrism , 2012, ASN neuro.
[60] T. Wieloch,et al. Levodopa Treatment Improves Functional Recovery After Experimental Stroke , 2012, Stroke.
[61] James C. Lee,et al. Role of Aβ-receptor for advanced glycation endproducts interaction in oxidative stress and cytosolic phospholipase A2 activation in astrocytes and cerebral endothelial cells , 2011, Neuroscience.
[62] M. Sands,et al. The Role of Attenuated Astrocyte Activation in Infantile Neuronal Ceroid Lipofuscinosis , 2011, The Journal of Neuroscience.
[63] Arne Klungland,et al. Glial-conditional deletion of aquaporin-4 (Aqp4) reduces blood–brain water uptake and confers barrier function on perivascular astrocyte endfeet , 2011, Proceedings of the National Academy of Sciences.
[64] M. Galea,et al. EphA4 Blockers Promote Axonal Regeneration and Functional Recovery Following Spinal Cord Injury in Mice , 2011, PloS one.
[65] Mark H. Ellisman,et al. Development of a Method for the Purification and Culture of Rodent Astrocytes , 2011, Neuron.
[66] M. Götz,et al. Genetic Deletion of Cdc42 Reveals a Crucial Role for Astrocyte Recruitment to the Injury Site In Vitro and In Vivo , 2011, The Journal of Neuroscience.
[67] J. Mendell,et al. Astrocytes from Familial and Sporadic ALS Patients are Toxic to Motor Neurons , 2011, Nature Biotechnology.
[68] T. Dick,et al. Functional regeneration of respiratory pathways after spinal cord injury , 2011, Nature.
[69] L. Garcia-Segura,et al. Sex differences in the inflammatory response of primary astrocytes to lipopolysaccharide , 2011, Biology of Sex Differences.
[70] S. Liebner,et al. Current concepts of blood-brain barrier development. , 2011, The International journal of developmental biology.
[71] O. Shupliakov,et al. A Pericyte Origin of Spinal Cord Scar Tissue , 2011, Science.
[72] S. Arnold,et al. Inducers of Chemical Hypoxia Act in a Gender- and Brain Region-Specific Manner on Primary Astrocyte Viability and Cytochrome c Oxidase , 2011, Neurotoxicity Research.
[73] W Noble,et al. Astrocytes are important mediators of Aβ-induced neurotoxicity and tau phosphorylation in primary culture , 2011, Cell Death and Disease.
[74] Matthew A. Hibbs,et al. Molecular clustering identifies complement and endothelin induction as early events in a mouse model of glaucoma. , 2011, The Journal of clinical investigation.
[75] E. Bradbury,et al. Manipulating the glial scar: Chondroitinase ABC as a therapy for spinal cord injury , 2011, Brain Research Bulletin.
[76] Magdalena Götz,et al. The stem cell potential of glia: lessons from reactive gliosis , 2011, Nature Reviews Neuroscience.
[77] J. Käs,et al. Reactive glial cells: increased stiffness correlates with increased intermediate filament expression , 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[78] Magdalena Götz,et al. In vivo fate mapping and expression analysis reveals molecular hallmarks of prospectively isolated adult neural stem cells. , 2010, Cell stem cell.
[79] Milos Pekny,et al. Defining cell populations with single-cell gene expression profiling: correlations and identification of astrocyte subpopulations , 2010, Nucleic acids research.
[80] Bengt R. Johansson,et al. Pericytes regulate the blood–brain barrier , 2010, Nature.
[81] Ben A. Barres,et al. Regulation of synaptic connectivity by glia , 2010, Nature.
[82] I. Módy,et al. Reducing excessive GABA-mediated tonic inhibition promotes functional recovery after stroke. , 2010, Nature.
[83] Anindita Dutta,et al. Cellular response after crush injury in adult zebrafish spinal cord , 2010, Developmental dynamics : an official publication of the American Association of Anatomists.
[84] H. Wolburg,et al. Astroglial structures in the zebrafish brain , 2010, The Journal of comparative neurology.
[85] C. Daniels,et al. Strategies for treatment in Alexander disease , 2010, Neurotherapeutics.
[86] Yanxin Zhao,et al. Targeting astrocytes for stroke therapy , 2010, Neurotherapeutics.
[87] M. Nedergaard,et al. Functions of astrocytes and their potential as therapeutic targets , 2010, Neurotherapeutics.
[88] B. Barres,et al. Astrocyte heterogeneity: an underappreciated topic in neurobiology , 2010, Current Opinion in Neurobiology.
[89] A. Messing,et al. Drug screening to identify suppressors of GFAP expression. , 2010, Human molecular genetics.
[90] M. Kreft,et al. Intermediate filaments attenuate stimulation‐dependent mobility of endosomes/lysosomes in astrocytes , 2010, Glia.
[91] V. Matyash,et al. Heterogeneity in astrocyte morphology and physiology , 2010, Brain Research Reviews.
[92] M. Faiz,et al. Attenuation of Reactive Gliosis Does Not Affect Infarct Volume in Neonatal Hypoxic-Ischemic Brain Injury in Mice , 2010, PloS one.
[93] Hajime Takano,et al. Selective induction of astrocytic gliosis generates deficits in neuronal inhibition , 2010, Nature Neuroscience.
[94] Y. Liu,et al. Glial fibrillary acidic protein-expressing neural progenitors give rise to immature neurons via early intermediate progenitors expressing both glial fibrillary acidic protein and neuronal markers in the adult hippocampus , 2010, Neuroscience.
[95] R. Sidman,et al. Communication via gap junctions underlies early functional and beneficial interactions between grafted neural stem cells and the host , 2010, Proceedings of the National Academy of Sciences.
[96] A. Buffo,et al. Astrocytes in the damaged brain: molecular and cellular insights into their reactive response and healing potential. , 2010, Biochemical pharmacology.
[97] M. Sofroniew,et al. Astrocytes: biology and pathology , 2009, Acta Neuropathologica.
[98] M. Sofroniew. Molecular dissection of reactive astrogliosis and glial scar formation , 2009, Trends in Neurosciences.
[99] M. Götz,et al. Conditional deletion of β1‐integrin in astroglia causes partial reactive gliosis , 2009, Glia.
[100] R. Bellamkonda,et al. Sustained delivery of thermostabilized chABC enhances axonal sprouting and functional recovery after spinal cord injury , 2009, Proceedings of the National Academy of Sciences.
[101] B. Song,et al. Reactive Astrocytes Form Scar-Like Perivascular Barriers to Leukocytes during Adaptive Immune Inflammation of the CNS , 2009, The Journal of Neuroscience.
[102] R. Roos,et al. The effect of mutant SOD1 dismutase activity on non-cell autonomous degeneration in familial amyotrophic lateral sclerosis , 2009, Neurobiology of Disease.
[103] Andrés Hurtado,et al. Transgenic inhibition of astroglial NF‐κB leads to increased axonal sparing and sprouting following spinal cord injury , 2009, Journal of neurochemistry.
[104] M. Chopp,et al. Neurorestorative therapies for stroke: underlying mechanisms and translation to the clinic , 2009, The Lancet Neurology.
[105] J. Cooper,et al. Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse , 2009, Experimental Neurology.
[106] D. Rempe,et al. The Janus-Faced Effects of Hypoxia on Astrocyte Function , 2009, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[107] V. Perry,et al. Microglial physiology: unique stimuli, specialized responses. , 2009, Annual review of immunology.
[108] J. Ojemann,et al. Uniquely Hominid Features of Adult Human Astrocytes , 2009, The Journal of Neuroscience.
[109] R. Koehler,et al. Astrocytes and the regulation of cerebral blood flow , 2009, Trends in Neurosciences.
[110] T. Takano,et al. Astrocytes and Ischemic Injury , 2009, Stroke.
[111] Michal Schwartz,et al. The bright side of the glial scar in CNS repair , 2009, Nature Reviews Neuroscience.
[112] A. T. Argaw,et al. VEGF-mediated disruption of endothelial CLN-5 promotes blood-brain barrier breakdown , 2009, Proceedings of the National Academy of Sciences.
[113] Karl H. Plate,et al. Angiogenesis after cerebral ischemia , 2009, Acta Neuropathologica.
[114] DelindaA . Johnson,et al. Nrf2 Activation in Astrocytes Protects against Neurodegeneration in Mouse Models of Familial Amyotrophic Lateral Sclerosis , 2008, The Journal of Neuroscience.
[115] Alexei Verkhratsky,et al. Neuroglia: the 150 years after , 2008, Trends in Neurosciences.
[116] M. Chopp,et al. Down‐regulation of neurocan expression in reactive astrocytes promotes axonal regeneration and facilitates the neurorestorative effects of bone marrow stromal cells in the ischemic rat brain , 2008, Glia.
[117] P. Greengard,et al. A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types , 2008, Cell.
[118] P. Greengard,et al. Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types , 2008, Cell.
[119] B. Barres. The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease , 2008, Neuron.
[120] S. Arnold,et al. Gender-specific regulation of mitochondrial fusion and fission gene transcription and viability of cortical astrocytes by steroid hormones. , 2008, Journal of molecular endocrinology.
[121] M. Kálmán,et al. Glial architecture of the ghost shark (Callorhinchus milii, Holocephali, Chondrichthyes) as revealed by different immunohistochemical markers. , 2008, Journal of experimental zoology. Part B, Molecular and developmental evolution.
[122] L. Hertz. Bioenergetics of cerebral ischemia: A cellular perspective , 2008, Neuropharmacology.
[123] D. Chen,et al. Abnormal reactivity of muller cells after retinal detachment in mice deficient in GFAP and vimentin. , 2008, Investigative ophthalmology & visual science.
[124] S. Akira,et al. STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury , 2008, The Journal of Neuroscience.
[125] M. Sur,et al. Tuned Responses of Astrocytes and Their Influence on Hemodynamic Signals in the Visual Cortex , 2008, Science.
[126] R. Dingledine,et al. Astrocytes in the Epileptic Brain , 2008, Neuron.
[127] Takahiro Takano,et al. Loss of Astrocytic Domain Organization in the Epileptic Brain , 2008, The Journal of Neuroscience.
[128] Magdalena Götz,et al. Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain , 2008, Proceedings of the National Academy of Sciences.
[129] P. Carmeliet,et al. Protective Role of Reactive Astrocytes in Brain Ischemia , 2008, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[130] D. Gutmann,et al. Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis , 2008, Nature Neuroscience.
[131] J. Silver,et al. CNS injury, glial scars, and inflammation: Inhibitory extracellular matrices and regeneration failure , 2008, Experimental Neurology.
[132] Y. Xing,et al. A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function , 2008, The Journal of Neuroscience.
[133] John D. Lambris,et al. The Classical Complement Cascade Mediates CNS Synapse Elimination , 2007, Cell.
[134] S. Goldman,et al. The Transcriptome and Metabolic Gene Signature of Protoplasmic Astrocytes in the Adult Murine Cortex , 2007, The Journal of Neuroscience.
[135] D. Rossi,et al. Astrocyte metabolism and signaling during brain ischemia , 2007, Nature Neuroscience.
[136] C. Iadecola,et al. Glial regulation of the cerebral microvasculature , 2007, Nature Neuroscience.
[137] P. Eriksson,et al. Increased Neurogenesis and Astrogenesis from Neural Progenitor Cells Grafted in the Hippocampus of GFAP−/−Vim−/− Mice , 2007, Stem cells.
[138] P. Magistretti,et al. Activity‐dependent regulation of energy metabolism by astrocytes: An update , 2007, Glia.
[139] W. Lamers,et al. Glutamine synthetase is essential in early mouse embryogenesis , 2007, Developmental dynamics : an official publication of the American Association of Anatomists.
[140] L. Olson,et al. Inhibiting Epidermal Growth Factor Receptor Improves Structural, Locomotor, Sensory, and Bladder Recovery from Experimental Spinal Cord Injury , 2007, The Journal of Neuroscience.
[141] E. Lane,et al. Intermediate filaments and stress. , 2007, Experimental cell research.
[142] Milos Pekny,et al. Attenuated glial reactions and photoreceptor degeneration after retinal detachment in mice deficient in glial fibrillary acidic protein and vimentin. , 2007, Investigative ophthalmology & visual science.
[143] M. Nilsson,et al. Enriched environment and astrocytes in central nervous system regeneration. , 2007, Journal of rehabilitation medicine.
[144] Hynek Wichterle,et al. Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons , 2007, Nature Neuroscience.
[145] Kevin Eggan,et al. Non–cell autonomous effect of glia on motor neurons in an embryonic stem cell–based ALS model , 2007, Nature Neuroscience.
[146] M. Pekny,et al. Synemin is expressed in reactive astrocytes in neurotrauma and interacts differentially with vimentin and GFAP intermediate filament networks , 2007, Journal of Cell Science.
[147] J. Mandell,et al. Molecular Mechanisms of Astrogliosis: New Approaches With Mouse Genetics , 2007, Journal of neuropathology and experimental neurology.
[148] Jerry Silver,et al. The role of extracellular matrix in CNS regeneration , 2007, Current Opinion in Neurobiology.
[149] J. Cooper,et al. Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis , 2007, Neurobiology of Disease.
[150] M. Kreft,et al. Cytoskeleton and Vesicle Mobility in Astrocytes , 2007, Traffic.
[151] J. Rothstein,et al. Mechanisms of Disease: astrocytes in neurodegenerative disease , 2006, Nature Clinical Practice Neurology.
[152] K. Houkin,et al. Intravenous administration of glial cell line‐derived neurotrophic factor gene‐modified human mesenchymal stem cells protects against injury in a cerebral ischemia model in the adult rat , 2006, Journal of neuroscience research.
[153] Milos Pekny,et al. Redefining the concept of reactive astrocytes as cells that remain within their unique domains upon reaction to injury , 2006, Proceedings of the National Academy of Sciences.
[154] D. Holtzman,et al. Matrix Metalloproteinases Expressed by Astrocytes Mediate Extracellular Amyloid-β Peptide Catabolism , 2006, The Journal of Neuroscience.
[155] M. Sofroniew,et al. Essential protective roles of reactive astrocytes in traumatic brain injury. , 2006, Brain : a journal of neurology.
[156] Tony Wyss-Coray,et al. Inflammation in Alzheimer disease: driving force, bystander or beneficial response? , 2006, Nature Medicine.
[157] O. Lindvall,et al. Intracerebral Infusion of Glial Cell Line–Derived Neurotrophic Factor Promotes Striatal Neurogenesis After Stroke in Adult Rats , 2006, Stroke.
[158] M. Fornerod,et al. Characterization of the Drosophila melanogaster genome at the nuclear lamina , 2006, Nature Genetics.
[159] Hideyuki Okano,et al. Conditional ablation of Stat3 or Socs3 discloses a dual role for reactive astrocytes after spinal cord injury , 2006, Nature Medicine.
[160] G. Kollias,et al. Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia , 2006, Science.
[161] A. Toutain,et al. Inborn error of amino acid synthesis: Human glutamine synthetase deficiency , 2006, Journal of Inherited Metabolic Disease.
[162] Christian Steinhäuser,et al. Astrocyte dysfunction in neurological disorders: a molecular perspective , 2006, Nature Reviews Neuroscience.
[163] M. Haber,et al. Reshaping neuron-glial communication at hippocampal synapses. , 2005, Neuron glia biology.
[164] George M. Smith,et al. Growth factor and cytokine regulation of chondroitin sulfate proteoglycans by astrocytes , 2005, Glia.
[165] Zhigang He,et al. EGFR Activation Mediates Inhibition of Axon Regeneration by Myelin and Chondroitin Sulfate Proteoglycans , 2005, Science.
[166] M. Sofroniew,et al. Reactive Astrocytes in Neural Repair and Protection , 2005, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[167] T. Takano,et al. An astrocytic basis of epilepsy , 2005, Nature Medicine.
[168] E. J. Green,et al. Inhibition of astroglial nuclear factor κB reduces inflammation and improves functional recovery after spinal cord injury , 2005, The Journal of experimental medicine.
[169] M. Nilsson,et al. Astrocyte activation and reactive gliosis , 2005, Glia.
[170] K. Willecke,et al. Emerging complexities in identity and function of glial connexins , 2005, Trends in Neurosciences.
[171] Milos Pekny,et al. Re-establishing the regenerative potential of central nervous system axons in postnatal mice , 2005, Journal of Cell Science.
[172] J. Hell,et al. Thrombospondins Are Astrocyte-Secreted Proteins that Promote CNS Synaptogenesis , 2005, Cell.
[173] W. Colledge. Faculty Opinions recommendation of Beta-lactam antibiotics offer neuroprotection by increasing glutamate transporter expression. , 2005 .
[174] N. Abbott. Dynamics of CNS Barriers: Evolution, Differentiation, and Modulation , 2005, Cellular and Molecular Neurobiology.
[175] P. Fisher,et al. β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression , 2005, Nature.
[176] M. Simard,et al. The neurobiology of glia in the context of water and ion homeostasis , 2004, Neuroscience.
[177] H. Liu,et al. Astrocytes in injured adult rat spinal cord may acquire the potential of neural stem cells , 2004, Neuroscience.
[178] Mary P Galea,et al. Axonal Regeneration and Lack of Astrocytic Gliosis in EphA4-Deficient Mice , 2004, The Journal of Neuroscience.
[179] M. Pekny,et al. Astrocyte intermediate filaments in CNS pathologies and regeneration , 2004, The Journal of pathology.
[180] M. Sofroniew,et al. GFAP-expressing progenitors are the principal source of constitutive neurogenesis in adult mouse forebrain , 2004, Nature Neuroscience.
[181] A. Reichenbach,et al. Astrocytes and Ependymal Glia , 2004 .
[182] B. MacVicar,et al. Calcium transients in astrocyte endfeet cause cerebrovascular constrictions , 2004, Nature.
[183] B. Barres,et al. Role for glia in synaptogenesis , 2004, Glia.
[184] P. Patterson,et al. Potent pro-inflammatory actions of leukemia inhibitory factor in the spinal cord of the adult mouse , 2004, Experimental Neurology.
[185] N. Sims,et al. Mitochondrial Glutathione: A Modulator of Brain Cell Death , 2004, Journal of bioenergetics and biomembranes.
[186] P. Carmeliet,et al. Under stress, the absence of intermediate filaments from Müller cells in the retina has structural and functional consequences , 2004, Journal of Cell Science.
[187] A. Yoshimura,et al. Socs3 deficiency in the brain elevates leptin sensitivity and confers resistance to diet-induced obesity , 2004, Nature Medicine.
[188] S. Paul,et al. Apolipoprotein E promotes astrocyte colocalization and degradation of deposited amyloid-β peptides , 2004, Nature Medicine.
[189] Mark Ellisman,et al. Absence of Glial Fibrillary Acidic Protein and Vimentin Prevents Hypertrophy of Astrocytic Processes and Improves Post-Traumatic Regeneration , 2004, The Journal of Neuroscience.
[190] J. O'Callaghan,et al. Induction of gp130-related Cytokines and Activation of JAK2/STAT3 Pathway in Astrocytes Precedes Up-regulation of Glial Fibrillary Acidic Protein in the 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Model of Neurodegeneration , 2004, Journal of Biological Chemistry.
[191] Mark Ellisman,et al. Maturation of astrocyte morphology and the establishment of astrocyte domains during postnatal hippocampal development , 2004, International Journal of Developmental Neuroscience.
[192] T. Horvath,et al. Disruption of neural signal transducer and activator of transcription 3 causes obesity, diabetes, infertility, and thermal dysregulation. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[193] Ngan B. Doan,et al. Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury , 2004, The Journal of Neuroscience.
[194] Jerry Silver,et al. Regeneration beyond the glial scar , 2004, Nature Reviews Neuroscience.
[195] M. Duchen,et al. β-Amyloid Peptides Induce Mitochondrial Dysfunction and Oxidative Stress in Astrocytes and Death of Neurons through Activation of NADPH Oxidase , 2004, The Journal of Neuroscience.
[196] S. Goldman,et al. New roles for astrocytes: Redefining the functional architecture of the brain , 2003, Trends in Neurosciences.
[197] D. Chen,et al. Robust neural integration from retinal transplants in mice deficient in GFAP and vimentin , 2003, Nature Neuroscience.
[198] A. Privat,et al. Axonal plasticity and functional recovery after spinal cord injury in mice deficient in both glial fibrillary acidic protein and vimentin genes , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[199] M. Duchen,et al. Changes in Intracellular Calcium and Glutathione in Astrocytes as the Primary Mechanism of Amyloid Neurotoxicity , 2003, The Journal of Neuroscience.
[200] Ulrich Dirnagl,et al. Ischemic tolerance and endogenous neuroprotection , 2003, Trends in Neurosciences.
[201] J. Neary,et al. Activation of Extracellular Signal-Regulated Kinase by Stretch-Induced Injury in Astrocytes Involves Extracellular ATP and P2 Purinergic Receptors , 2003, The Journal of Neuroscience.
[202] S. Carmichael,et al. Plasticity of Cortical Projections after Stroke , 2003, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[203] T. Deller,et al. Induction of STAT3 Signaling in Activated Astrocytes and Sprouting Septal Neurons Following Entorhinal Cortex Lesion in Adult Rats , 2002, Molecular and Cellular Neuroscience.
[204] James W. Fawcett,et al. Chondroitinase ABC promotes functional recovery after spinal cord injury , 2002, Nature.
[205] C. S. Ricard,et al. Differential gene expression in astrocytes from human normal and glaucomatous optic nerve head analyzed by cDNA microarray , 2002, Glia.
[206] M. Kálmán. GFAP expression withdraws—a trend of glial evolution? , 2002, Brain Research Bulletin.
[207] Mark Ellisman,et al. Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains , 2002, The Journal of Neuroscience.
[208] R. Hammer,et al. Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[209] V. Berezin,et al. Intermediate filaments regulate astrocyte motility , 2001, Journal of neurochemistry.
[210] F. Müller,et al. Effect of levodopa in combination with physiotherapy on functional motor recovery after stroke: a prospective, randomised, double-blind study , 2001, The Lancet.
[211] B. Barres,et al. Control of synapse number by glia. , 2001, Science.
[212] R. Dringen,et al. Metabolism and functions of glutathione in brain , 2000, Progress in Neurobiology.
[213] L. Eng,et al. Glial Fibrillary Acidic Protein: GFAP-Thirty-One Years (1969–2000) , 2000, Neurochemical Research.
[214] Xiao-ding Cao,et al. Dynamic expression of glial cell line‐derived neurotrophic factor after cerebral ischemia , 2000, Neuroreport.
[215] H. Yip,et al. Chondroitinase ABC promotes axonal regeneration of Clarke's neurons after spinal cord injury , 2000, Neuroreport.
[216] N. van Bruggen,et al. VEGF antagonism reduces edema formation and tissue damage after ischemia/reperfusion injury in the mouse brain. , 1999, The Journal of clinical investigation.
[217] C. Betsholtz,et al. Intermediate Filament Protein Partnership in Astrocytes* , 1999, The Journal of Biological Chemistry.
[218] J. Silver,et al. Robust Regeneration of Adult Sensory Axons in Degenerating White Matter of the Adult Rat Spinal Cord , 1999, The Journal of Neuroscience.
[219] Y. Mitsumoto,et al. Induction of glial cell line-derived neurotrophic factor receptor proteins in cerebral cortex and striatum after permanent middle cerebral artery occlusion in rats , 1999, Brain Research.
[220] L. Mucke,et al. Genetically-targeted and conditionally-regulated ablation of astroglial cells in the central, enteric and peripheral nervous systems in adult transgenic mice 1 Published on the World Wide Web on 7 June 1999. 1 , 1999, Brain Research.
[221] Clive N Svendsen,et al. Leukocyte Infiltration, Neuronal Degeneration, and Neurite Outgrowth after Ablation of Scar-Forming, Reactive Astrocytes in Adult Transgenic Mice , 1999, Neuron.
[222] U. Lendahl,et al. Abnormal Reaction to Central Nervous System Injury in Mice Lacking Glial Fibrillary Acidic Protein and Vimentin , 1999, The Journal of cell biology.
[223] K. Wisniewski,et al. Genotype-phenotype correlations in neuronal ceroid lipofuscinosis due to palmitoyl-protein thioesterase deficiency. , 1999, Molecular genetics and metabolism.
[224] O. Lindvall,et al. GDNF family ligands and receptors are differentially regulated after brain insults in the rat , 1999, The European journal of neuroscience.
[225] A. Reichenbach,et al. Microdomains for neuron–glia interaction: parallel fiber signaling to Bergmann glial cells , 1999, Nature Neuroscience.
[226] Alexander Sasha Rabchevsky,et al. A Role for Transforming Growth Factor α as an Inducer of Astrogliosis , 1998, The Journal of Neuroscience.
[227] A. Hamberger,et al. Altered taurine release following hypotonic stress in astrocytes from mice deficient for GFAP and vimentin. , 1998, Brain research. Molecular brain research.
[228] R. P. Stroemer,et al. Enhanced neocortical neural sprouting, synaptogenesis, and behavioral recovery with D-amphetamine therapy after neocortical infarction in rats. , 1998, Stroke.
[229] Steven Goldman,et al. Gap-junction-mediated propagation and amplification of cell injury , 1998, Nature Neuroscience.
[230] C. Justicia,et al. Epidermal growth factor receptor in proliferating reactive glia following transient focal ischemia in the rat brain , 1998, Glia.
[231] C. Betsholtz,et al. Impaired induction of blood‐brain barrier properties in aortic endothelial cells by astrocytes from GFAB‐deficient mice , 1998, Glia.
[232] Y. Ihara,et al. Diffuse plaques associated with astroglial amyloid β protein, possibly showing a disappearing stage of senile plaques , 1998, Acta Neuropathologica.
[233] R. Schmidt-Kastner,et al. Nestin expression in reactive astrocytes following focal cerebral ischemia in rats , 1997, Brain Research.
[234] B. Hoffer,et al. Glial Cell Line-Derived Neurotrophic Factor Protects against Ischemia-Induced Injury in the Cerebral Cortex , 1997, The Journal of Neuroscience.
[235] G. Kreutzberg,et al. Impaired neuroglial activation in interleukin‐6 deficient mice , 1997, Glia.
[236] G. Schneider,et al. Bcl-2 promotes regeneration of severed axons in mammalian CNS , 1997, Nature.
[237] A. Messing,et al. Conditional Ablation of Cerebellar Astrocytes in Postnatal Transgenic Mice , 1996, The Journal of Neuroscience.
[238] R. Kucherlapati,et al. GFAP Is Necessary for the Integrity of CNS White Matter Architecture and Long-Term Maintenance of Myelination , 1996, Neuron.
[239] R. Pearce,et al. Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[240] A. Brand,et al. Targeted ablation of glia disrupts axon tract formation in the Drosophila CNS. , 1995, Development.
[241] J. Jacobs,et al. Macrophages and glia participate in the removal of apoptotic neurons from the Drosophila embryonic nervous system , 1995, The Journal of comparative neurology.
[242] L. Peltonen,et al. Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis , 1995, Nature.
[243] R. Mrak,et al. Glial cytokines in Alzheimer's disease: review and pathogenic implications. , 1995, Human pathology.
[244] C. Winter,et al. A role for ciliary neurotrophic factor as an inducer of reactive gliosis, the glial response to central nervous system injury. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[245] J. Povlishock,et al. A new model for rapid stretch-induced injury of cells in culture: characterization of the model using astrocytes. , 1995, Journal of neurotrauma.
[246] C. Betsholtz,et al. Mice lacking glial fibrillary acidic protein display astrocytes devoid of intermediate filaments but develop and reproduce normally. , 1995, The EMBO journal.
[247] S. Itohara,et al. Mice devoid of the glial fibrillary acidic protein develop normally and are susceptible to scrapie prions , 1995, Neuron.
[248] C. Babinet,et al. Mice lacking vimentin develop and reproduce without an obvious phenotype , 1994, Cell.
[249] D. Turner,et al. Reactive astrocytes express the embryonic intermediate neurofilament nestin. , 1994, Neuroreport.
[250] L. Eng,et al. GFAP and Astrogliosis , 1994, Brain pathology.
[251] C. Finch,et al. Glial Fibrillary Acidic Protein: Regulation by Hormones, Cytokines, and Growth Factors , 1994, Brain pathology.
[252] V Balasingam,et al. Reactive astrogliosis in the neonatal mouse brain and its modulation by cytokines , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[253] M. Eddleston,et al. Molecular profile of reactive astrocytes—Implications for their role in neurologic disease , 1993, Neuroscience.
[254] S. Finkbeiner,et al. Glutamate induces calcium waves in cultured astrocytes: long-range glial signaling. , 1990, Science.
[255] P. Rakic. Specification of cerebral cortical areas. , 1988, Science.
[256] T. Kosaka,et al. Three‐dimensional structure of astrocytes in the rat dentate gyrus , 1986, The Journal of comparative neurology.
[257] K. McCarthy,et al. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue , 1980, The Journal of cell biology.
[258] J. Miller,et al. Fluid-percussion model of mechanical brain injury in the cat. , 1976, Journal of neurosurgery.
[259] W. Penfield,et al. EPILEPTOGENIC LESIONS OF THE BRAIN: A HISTOLOGIC STUDY , 1940 .
[260] D. Luciano,et al. Protective astrogenesis from the SVZ niche after injury is controlled by Notch modulator Thbs4. , 2016 .
[261] M. Ueffing,et al. The neuroprotective potential of retinal Müller glial cells. , 2014, Advances in experimental medicine and biology.
[262] A. Verkhratsky,et al. Glial physiology and pathophysiology , 2013 .
[263] A. Verkhratsky,et al. General Pathophysiology of Neuroglia , 2013 .
[264] A. Schousboe. Studies of Brain Metabolism: A Historical Perspective , 2012 .
[265] D. Hines,et al. Astroglial Metabolic Networks Sustain Hippocampal Synaptic Transmission , 2009 .
[266] Hideyuki Okano,et al. Spinal cord injury: emerging beneficial role of reactive astrocytes' migration. , 2008, The international journal of biochemistry & cell biology.
[267] S. Lipton,et al. Inflammatory mediators leading to protein misfolding and uncompetitive/fast off-rate drug therapy for neurodegenerative disorders. , 2007, International review of neurobiology.
[268] P. Luthert,et al. Glial remodeling and neural plasticity in human retinal detachment with proliferative vitreoretinopathy. , 2005, Investigative ophthalmology & visual science.
[269] M. C. Angulo,et al. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation , 2003, Nature Neuroscience.
[270] T. Wyss-Coray,et al. Adult mouse astrocytes degrade amyloid-beta in vitro and in situ. , 2003, Nature medicine.
[271] K. Wisniewski,et al. Infantile neuronal ceroid lipofuscinosis: no longer just a 'Finnish' disease. , 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
[272] F. Kirchhoff,et al. GFAP promoter‐controlled EGFP‐expressing transgenic mice: A tool to visualize astrocytes and astrogliosis in living brain tissue , 2001, Glia.
[273] D. Rodriguez,et al. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease , 2001, Nature Genetics.
[274] Alexander Sasha Rabchevsky,et al. A role for transforming growth factor alpha as an inducer of astrogliosis. , 1998, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[275] T. Beach,et al. Patterns of gliosis in alzheimer's disease and aging cerebrum , 1989, Glia.
[276] J. Booher,et al. Growth and cultivation of dissociated neurons and glial cells from embryonic chick, rat and human brain in flask cultures. , 1972, Neurobiology.