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Glutamate Induces Calcium Waves in Cultured Astrocytes: Long-Range Glial Signaling
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The Ca2+/Cl− dependent L‐[3H]glutamate binding: a new receptor or a particular transport process?
inferredcites →https://doi.org/10.1016/0166-2236(88)90183-xopenalex-snapshot
A new mechanism for glutamate receptor action: phosphoinositide hydrolysis
inferredcites →https://doi.org/10.1016/0166-2236(89)90133-1openalex-snapshot
Calcium oscillations in non-excitable cells
inferredcites →https://doi.org/10.1016/0304-3940(86)90537-9openalex-snapshot
Astrocyte glutamate receptor activation promotes inositol phospholipid turnover and calcium flux
inferredcites →https://doi.org/10.1016/0896-6273(89)90032-9openalex-snapshot
Intercellular signaling as visualized by endogenous calcium-dependent bioluminescence
inferredcites →https://doi.org/10.1016/0896-6273(89)90076-7openalex-snapshot
Glial and neuronal forms of the voltage-dependent sodium channel: characteristics and cell-type distribution
inferredcites →https://doi.org/10.1016/0896-6273(89)90121-9openalex-snapshot
Glutamate receptor subtypes may be classified into two major categories: A study on Xenopus oocytes injected with rat brain mRNA
inferredcites →https://doi.org/10.1016/s0021-9258(18)83166-0openalex-snapshot
Photochemically generated cytosolic calcium pulses and their detection by fluo-3
inferredcites →https://doi.org/10.1038/311656a0openalex-snapshot
Excitatory amino acids directly depolarize rat brain astrocytes in primary culture
inferredcites →https://doi.org/10.1038/319600a0openalex-snapshot
Repetitive transient rises in cytoplasmic free calcium in hormone-stimulated hepatocytes
inferredcites →https://doi.org/10.1038/325531a0openalex-snapshot
A new type of glutamate receptor linked to inositol phospholipid metabolism
inferredcites →https://doi.org/10.1038/329242a0openalex-snapshot
Membrane conductance oscillations in astrocytes induced by phorbol ester
inferredcites →https://doi.org/10.1038/334499a0openalex-snapshot
Regulation of calcium influx by second messengers in rat mast cells
inferredcites →https://doi.org/10.1038/335040a0openalex-snapshot
Repetitive spikes in cytoplasmic calcium evoked by histamine in human endothelial cells
inferredcites →https://doi.org/10.1038/336587a0openalex-snapshot
Opening of dihydropyridine calcium channels in skeletal muscle membranes by inositol trisphosphate
inferredcites →https://doi.org/10.1038/339378a0openalex-snapshot
Facilitation of voltage-gated ion channels in frog neuroglia by nerve impulses
inferredcites →https://doi.org/10.1038/339380a0openalex-snapshot
Multiple conductance channels in type-2 cerebellar astrocytes activated by excitatory amino acids
inferredcites →https://doi.org/10.1038/341197a0openalex-snapshot
Inositol phosphates and cell signalling
inferredcites →https://doi.org/10.1042/bj2410933openalex-snapshot
Sustained oscillations in extracellular calcium concentrations upon hormonal stimulation of perfused rat liver
inferredcites →https://doi.org/10.1073/pnas.85.11.4071openalex-snapshot
Applications of quantitative measurements for assessing glutamate neurotoxicity.
inferredcites →https://doi.org/10.1073/pnas.86.8.2708openalex-snapshot
Hepatocyte gap junctions are permeable to the second messenger, inositol 1,4,5-trisphosphate, and to calcium ions.
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Excitatory Amino Acid Agonist‐Antagonist Interactions at 2‐Amino‐4‐Phosphonobutyric Acid‐Sensitive Quisqualate Receptors Coupled to Phosphoinositide Hydrolysis in Slices of Rat Hippocampus
inferredcites →https://doi.org/10.1111/j.1749-6632.1986.tb27134.xopenalex-snapshot
The Neuronal Microenvironment: A Comparative View
inferredcites →https://doi.org/10.1126/science.2899909openalex-snapshot
Quinoxalinediones: Potent Competitive Non-NMDA Glutamate Receptor Antagonists
inferredcites →https://doi.org/10.1126/science.3291116openalex-snapshot
Specification of Cerebral Cortical Areas
inferredcites →https://doi.org/10.1126/science.6095454openalex-snapshot
Voltage-Dependent Calcium Channels in Glial Cells
inferredcites →https://doi.org/10.1523/jneurosci.03-06-01289.1983openalex-snapshot
Two types of astrocytes in cultures of developing rat white matter: differences in morphology, surface gangliosides, and growth characteristics
inferredcites →https://doi.org/10.1523/jneurosci.05-12-03295.1985openalex-snapshot
Pharmacological properties of gamma-aminobutyric acid-, glutamate-, and aspartate-induced depolarizations in cultured astrocytes
inferredcites →https://doi.org/10.1523/jneurosci.07-11-03600.1987openalex-snapshot
Cyclic AMP induces changes in distribution and transport of organelles within growth cones of Aplysia bag cell neurons
inferredcites →https://doi.org/10.1523/jneurosci.09-09-03169.1989openalex-snapshot
Calcium current in cortical astrocytes: induction by cAMP and neurotransmitters and permissive effect of serum factors
inferredcites →https://doi.org/10.1523/jneurosci.09-09-03230.1989openalex-snapshot
Quantitative physiological characterization of a quinoxalinedione non- NMDA receptor antagonist
inferredcites →https://doi.org/10.1523/jneurosci.10-04-01165.1990openalex-snapshot
Fluorescence measurement of changes in intracellular calcium induced by excitatory amino acids in cultured cortical astrocytes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5281/zenodo.1078207openalex-extracted
Finite Volume Model To Study The Effect Of Voltage Gated Ca2+ Channel On Cytosolic Calcium Advection Diffusion
inferred← citeshttps://doi.org/10.1001/archopht.117.11.1524openalex-snapshot
Nitric Oxide Mediates Excitotoxic and Anoxic Damage in Rat Retinal Ganglion Cells Cocultured With Astroglia
inferred← citeshttps://doi.org/10.1002/(sici)1096-9861(19970324)379:4<571::aid-cne8>3.0.co;2-#openalex-snapshot
Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain
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Regional and laminar specificity of kainate-stimulated cobalt uptake in the rat hippocampal formation
inferred← citeshttps://doi.org/10.1002/(sici)1097-0029(19990915)46:6<356::aid-jemt4>3.0.co;2-6openalex-snapshot
Confocal laser scanning microscopy of calcium dynamics in living cells
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Bcl-xl-Specific antibody labels activated microglia associated with Alzheimer's disease and other pathological states
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Altered gap junctional communication, intercellular signaling, and growth in cultured astrocytes deficient in connexin43
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Characterization of ryanodine receptors in oligodendrocytes, type 2 astrocytes, and O‐2A progenitors
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Role of intracellular Ca2 stores shaping normal activity in brain
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Localized calcium signaling in multinucleated osteoclasts
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Role of astroglia in estrogen regulation of synaptic plasticity and brain repair
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Prostaglandin E2 stimulates glutamate receptor-dependent astrocyte neuromodulation in cultured hippocampal cells
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Regional differences in glial cell modulation of synaptic transmission
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Octanol, a gap junction uncoupling agent, changes intracellular [H+] in rat astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199602)16:2<108::aid-glia3>3.0.co;2-#openalex-snapshot
P 2U nucleotide receptor activation in rat glial cell line induces [Ca 2+ ] i oscillations which depend on cytosolic pH
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199603)16:3<285::aid-glia11>3.0.co;2-wopenalex-snapshot
Nerve impulses increase glial intercellular permeability
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199604)16:4<296::aid-glia2>3.0.co;2-zopenalex-snapshot
Modulation of two functionally distinct Ca2 stores in astrocytes: Role of the plasmalemmal Na/Ca exchanger
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199608)17:4<274::aid-glia2>3.0.co;2-#openalex-snapshot
Electrical coupling among Bergmann glial cells and its modulation by glutamate receptor activation
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199704)19:4<343::aid-glia7>3.0.co;2-yopenalex-snapshot
Plasma albumin induces calcium waves in rat cortical astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199704)19:4<352::aid-glia8>3.0.co;2-zopenalex-snapshot
Abnormal calcium homeostasis in astrocytes from the trisomy 16 mouse
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199706)20:2<163::aid-glia8>3.0.co;2-aopenalex-snapshot
Bovine serum albumin and lysophosphatidic acid stimulate calcium mobilization and reversal of cAMP-induced stellation in rat spinal cord astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199707)20:3<184::aid-glia2>3.0.co;2-8openalex-snapshot
Expression of high-affinity neuronal and glial glutamate transporters in the rat optic nerve
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199708)20:4<299::aid-glia3>3.0.co;2-1openalex-snapshot
Gap junctions equalize intracellular Na+ concentration in astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199709)21:1<46::aid-glia5>3.0.co;2-#openalex-snapshot
Potassium homeostasis and glial energy metabolism
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199711)21:3<332::aid-glia8>3.0.co;2-6openalex-snapshot
Spontaneous intracellular calcium oscillations in cortical astrocytes from a patient with intractable childhood epilepsy (Rasmussen's Encephalitis)
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199712)21:4<380::aid-glia5>3.0.co;2-7openalex-snapshot
Glutamate receptor-mediated calcium responses in acutely isolated hippocampal astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199712)21:4<390::aid-glia6>3.0.co;2-7openalex-snapshot
Opposite influence of the metabotropic glutamate receptor subtypes mGlu3 and -5 on astrocyte proliferation in culture
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199801)22:1<19::aid-glia3>3.0.co;2-3openalex-snapshot
Fibroblast growth factor 2 (FGF-2) differentially regulates connexin (cx) 43 expression and function in astroglial cells from distinct brain regions
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<108::aid-glia11>3.0.co;2-vopenalex-snapshot
Dye coupling between spinal cord oligodendrocytes: Differences in coupling efficiency between gray and white matter
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<141::aid-glia13>3.0.co;2-ropenalex-snapshot
Visualization and functional blocking of gap junction hemichannels (connexons) with antibodies against external loop domains in astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<1::aid-glia1>3.0.co;2-aopenalex-snapshot
From neuro-glue (‘nervenkitt’) to glia: A prologue
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<39::aid-glia5>3.0.co;2-wopenalex-snapshot
Intercellular calcium waves in glia
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<50::aid-glia6>3.0.co;2-4openalex-snapshot
Intercellular calcium signaling and gap junctional communication in astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<85::aid-glia9>3.0.co;2-#openalex-snapshot
Heterotypic coupling between glial cells of the mammalian central nervous system
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199809)24:1<97::aid-glia10>3.0.co;2-topenalex-snapshot
Gap junction-mediated loops of neuronal-glial interactions
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N-acetylaspartylglutamate activates cyclic AMP-coupled metabotropic glutamate receptors in cerebellar astrocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199812)24:4<398::aid-glia5>3.0.co;2-ropenalex-snapshot
Inositol-trisphosphate-dependent intercellular calcium signaling in and between astrocytes and endothelial cells
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Late onset and increasing expression of the gap junction protein connexin30 in adult murine brain and long-term cultured astrocytes
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Seasonal changes in astrocytes parallel neuronal plasticity in the song control area HVc of the canary
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Glucocorticoids?potent modulators of astrocytic calcium signaling
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Intercellular Ca2+ waves induce temporally and spatially distinct intracellular Ca2+ oscillations in glia
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(199912)28:3<175::aid-glia1>3.0.co;2-7openalex-snapshot
Leech giant glial cell: functional role in a simple nervous system
inferred← citeshttps://doi.org/10.1002/(sici)1098-1136(200005)30:3<231::aid-glia3>3.0.co;2-1openalex-snapshot
Fibroblast growth factors-5 and -9 distinctly regulate expression and function of the gap junction protein connexin43 in cultured astroglial cells from different brain regions
inferred← citeshttps://doi.org/10.1002/(sici)1098-2779(1997)3:1<76::aid-mrdd10>3.0.co;2-oopenalex-snapshot
Potential therapeutic intervention following hypoxic-ischemic insult
inferred← citeshttps://doi.org/10.1002/1097-4652(200009)184:3<385::aid-jcp14>3.0.co;2-7openalex-snapshot
Calcium signaling induced by adhesion mediates protein tyrosine phosphorylation and is independent of pHi
inferred← citeshttps://doi.org/10.1002/1098-1136(20010101)33:1<12::aid-glia1002>3.0.co;2-vopenalex-snapshot
Traumatic injury of cultured astrocytes alters inositol (1,4,5)-trisphosphate-mediated signaling
inferred← citeshttps://doi.org/10.1002/1521-1878(200008)22:8<747::aid-bies8>3.0.co;2-0openalex-snapshot
Glial strategy for metabolic shuttling and neuronal function
inferred← citeshttps://doi.org/10.1002/1531-8249(200001)47:1<18::aid-ana6>3.0.co;2-nopenalex-snapshot
Meningeal cells can communicate with astrocytes by calcium signaling
inferred← citeshttps://doi.org/10.1002/9780470015902.a0000016.pub2openalex-snapshot
Astrocytes and Brain Signalling
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022540.pub2openalex-snapshot
Glioblastoma Models in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1002/9780470514696.ch11openalex-snapshot
The Triggering of Astrocytic Calcium Waves by NMDA‐Induced Neuronal Activation
inferred← citeshttps://doi.org/10.1002/9781118402061.ch1openalex-snapshot
History of Neuroscience and the Dawn of Research in Neuroglia
inferred← citeshttps://doi.org/10.1002/9783527651009.ch25openalex-snapshot
The Dynamics of Neuromodulation
inferred← citeshttps://doi.org/10.1002/9783527689620.ch4openalex-snapshot
Disinfectant Formulation Design
inferred← citeshttps://doi.org/10.1002/adma.202400346openalex-snapshot
Advances in Material‐Assisted Electromagnetic Neural Stimulation
inferred← citeshttps://doi.org/10.1002/adtp.202300083openalex-snapshot
Electrophoretic Delivery of Clinically Approved Anesthetic Drug for Chronic Pain Therapy
inferred← citeshttps://doi.org/10.1002/aja.1001920103openalex-snapshot
Voltage‐dependent ‐L‐type Ca2+ channels participate in regulating neural crest migration and differentiation
inferred← citeshttps://doi.org/10.1002/alz.71122openalex-snapshot
Astrocyte–vascular interplay in Alzheimer's disease pathology: Novel insights into stage‐specific biomarkers and therapeutic targets
inferred← citeshttps://doi.org/10.1002/bies.201600118openalex-snapshot
Lactate release from astrocytes to neurons contributes to cocaine memory formation
inferred← citeshttps://doi.org/10.1002/cne.20191openalex-snapshot
Oscillatory calcium responses mediated by P2Y2 purinergic receptors in terminal Schwann cells of longitudinal lanceolate endings isolated from rat vibrissae
inferred← citeshttps://doi.org/10.1002/cne.20567openalex-snapshot
Glial and neuronal connexin expression patterns in the rat spinal cord during development and following injury
inferred← citeshttps://doi.org/10.1002/cne.21756openalex-snapshot
A dual system of intercellular calcium signaling in glial nets associated with lanceolate sensory endings in rat vibrissae
inferred← citeshttps://doi.org/10.1002/cne.21873openalex-snapshot
Limited intravascular coupling in the rodent brainstem and retina supports a role for glia in regional blood flow
inferred← citeshttps://doi.org/10.1002/cne.903020414openalex-snapshot
On the organization of astrocytic gap junctions in rat brain as suggested by LM and EM immunohistochemistry of connexin43 expression
inferred← citeshttps://doi.org/10.1002/cne.903030305openalex-snapshot
Factors determining the morphology and distribution of astrocytes in the cat retina: A ‘contact‐spacing’ model of astrocyte interaction
inferred← citeshttps://doi.org/10.1002/cne.903180309openalex-snapshot
Light and electron immunocytochemical localization of AMPA‐selective glutamate receptors in the rat brain
inferred← citeshttps://doi.org/10.1002/cne.903330111openalex-snapshot
Glia cells of the monkey retina. I. Astrocytes
inferred← citeshttps://doi.org/10.1002/cne.903350209openalex-snapshot
Distribution of the mRNA for a metabotropic glutamate receptor (mGluR3) in the rat brain: An in situ hybridization study
inferred← citeshttps://doi.org/10.1002/cne.903500208openalex-snapshot
Cellular localization and laminar distribution of AMPA glutamate receptor subunits mRNAs and proteins in the rat cerebral cortex
inferred← citeshttps://doi.org/10.1002/cne.903620108openalex-snapshot
Metabotropic glutamate receptor mGluR5 subcellular distribution and developmental expression in hypothalamus
inferred← citeshttps://doi.org/10.1002/cphy.cp140101openalex-snapshot
Optical Methods in Cell Physiology
inferred← citeshttps://doi.org/10.1002/ddr.10206openalex-snapshot
Neurone‐to‐astrocyte communication by endogenous ATP in mixed culture of rat hippocampal neurones and astrocytes
inferred← citeshttps://doi.org/10.1002/glia.10016openalex-snapshot
Modifications in astrocyte morphology and calcium signaling induced by a brain capillary endothelial cell line
inferred← citeshttps://doi.org/10.1002/glia.10257openalex-snapshot
Modulation of intercellular calcium signaling in astrocytes by extracellular calcium and magnesium
inferred← citeshttps://doi.org/10.1002/glia.10283openalex-snapshot
Early loss of astrocytes after experimental traumatic brain injury
inferred← citeshttps://doi.org/10.1002/glia.10336openalex-snapshot
Electrophysiological and molecular evidence of L‐(Cav1), N‐ (Cav2.2), and R‐ (Cav2.3) type Ca2+ channels in rat cortical astrocytes
inferred← citeshttps://doi.org/10.1002/glia.1044openalex-snapshot
Modifications of retinal afferent activity induce changes in astroglial plasticity in the hamster circadian clock
inferred← citeshttps://doi.org/10.1002/glia.1108openalex-snapshot
Control of glial immune function by neurons
inferred← citeshttps://doi.org/10.1002/glia.20026openalex-snapshot
Glial modulation of synaptic transmission in culture
inferred← citeshttps://doi.org/10.1002/glia.20029openalex-snapshot
Astrocyte responses to neuronal activity
inferred← citeshttps://doi.org/10.1002/glia.20118openalex-snapshot
Cytoprotection against oxidative stress‐induced damage of astrocytes by extracellular ATP via P2Y1 receptors
inferred← citeshttps://doi.org/10.1002/glia.20157openalex-snapshot
Astrocytic contributions to bioenergetics of cerebral ischemia
inferred← citeshttps://doi.org/10.1002/glia.20213openalex-snapshot
Alterations in metabolism and gap junction expression may determine the role of astrocytes as “good samaritans” or executioners
inferred← citeshttps://doi.org/10.1002/glia.20367openalex-snapshot
Vesicular transmitter release from astrocytes
inferred← citeshttps://doi.org/10.1002/glia.20374openalex-snapshot
Astrocyte calcium waves: What they are and what they do
inferred← citeshttps://doi.org/10.1002/glia.20396openalex-snapshot
Astrocyte calcium elevations: Properties, propagation, and effects on brain signaling
inferred← citeshttps://doi.org/10.1002/glia.20415openalex-snapshot
Plasticity of perisynaptic astroglia during synaptogenesis in the mature rat hippocampus
inferred← citeshttps://doi.org/10.1002/glia.20543openalex-snapshot
Astrocyte control of the cerebrovasculature
inferred← citeshttps://doi.org/10.1002/glia.20564openalex-snapshot
Acute treatment with 17β‐estradiol attenuates astrocyte–astrocyte and astrocyte–neuron communication
inferred← citeshttps://doi.org/10.1002/glia.20627openalex-snapshot
Identification of a molecular target for glutamate regulation of astrocyte water permeability
inferred← citeshttps://doi.org/10.1002/glia.20809openalex-snapshot
Failure of Ca2+‐activated, CREB‐dependent transcription in astrocytes
inferred← citeshttps://doi.org/10.1002/glia.22288openalex-snapshot
Artifact versus reality—How astrocytes contribute to synaptic events
inferred← citeshttps://doi.org/10.1002/glia.22361openalex-snapshot
Fingolimod—A sphingosine‐like molecule inhibits vesicle mobility and secretion in astrocytes
inferred← citeshttps://doi.org/10.1002/glia.22422openalex-snapshot
The Importance of astrocyte‐derived purines in the modulation of sleep
inferred← citeshttps://doi.org/10.1002/glia.22425openalex-snapshot
Heterosynaptic long‐term depression mediated by ATP released from astrocytes
inferred← citeshttps://doi.org/10.1002/glia.22576openalex-snapshot
Corticosterone treatment results in enhanced release of peptidergic vesicles in astrocytes via cytoskeletal rearrangements
inferred← citeshttps://doi.org/10.1002/glia.22577openalex-snapshot
Traumatic scratch injury in astrocytes triggers calcium influx to activate the JNK/c-Jun/AP-1 pathway and switch on GFAP expression
inferred← citeshttps://doi.org/10.1002/glia.22821openalex-snapshot
Morphological plasticity of astroglia: Understanding synaptic microenvironment
inferred← citeshttps://doi.org/10.1002/glia.22920openalex-snapshot
Loose excitation–secretion coupling in astrocytes
inferred← citeshttps://doi.org/10.1002/glia.22975openalex-snapshot
Plasmalemmal and mitochondrial Na+‐Ca2+exchange in neuroglia
inferred← citeshttps://doi.org/10.1002/glia.22982openalex-snapshot
Spatio‐temporal characteristics of metabotropic glutamate receptor 5 traffic at or near the plasma membrane in astrocytes
inferred← citeshttps://doi.org/10.1002/glia.23143openalex-snapshot
An astroglial basis of major depressive disorder? An overview
inferred← citeshttps://doi.org/10.1002/glia.23181openalex-snapshot
Sensory response in host and engrafted astrocytes of adult brain in Vivo
inferred← citeshttps://doi.org/10.1002/glia.23609openalex-snapshot
Vascular endothelial growth factor increases the function of calcium‐impermeable AMPA receptor GluA2 subunit in astrocytes via activation of protein kinase C signaling pathway
inferred← citeshttps://doi.org/10.1002/glia.23613openalex-snapshot
Panglial gap junctions between astrocytes and olfactory ensheathing cells mediate transmission of Ca2+ transients and neurovascular coupling
inferred← citeshttps://doi.org/10.1002/glia.23940openalex-snapshot
Altered astrocytic function in experimental neuroinflammation and multiple sclerosis
inferred← citeshttps://doi.org/10.1002/glia.24011openalex-snapshot
Nicotine induces morphological and functional changes in astrocytes via nicotinic receptor activity
inferred← citeshttps://doi.org/10.1002/glia.24099openalex-snapshot
Assessment of astrocytes as a mediator of memory and learning in rodents
inferred← citeshttps://doi.org/10.1002/glia.24121openalex-snapshot
Astrocytes as essential time‐keepers of the central pacemaker
inferred← citeshttps://doi.org/10.1002/glia.440030503openalex-snapshot
The excitatory neurotransmitter glutamate causes filopodia formation in cultured hippocampal astrocytes
inferred← citeshttps://doi.org/10.1002/glia.440030612openalex-snapshot
Norepinephrine‐evoked calcium transients in cultured cerebral type 1 astroglia
inferred← citeshttps://doi.org/10.1002/glia.440040302openalex-snapshot
GABA release triggered by the activation of neuron‐like non‐NMDA receptors in cultured type 2 astrocytes is carrier‐mediated
inferred← citeshttps://doi.org/10.1002/glia.440040502openalex-snapshot
Excitatory amino acid receptors in primary cultures of glial cells from the retina
inferred← citeshttps://doi.org/10.1002/glia.440040503openalex-snapshot
Cerebral type 2 astroglia are heterogeneous with respect to their ability to respond to neuroligands linked to calcium mobilization
inferred← citeshttps://doi.org/10.1002/glia.440040504openalex-snapshot
Modulation of intracellular Ca++ in cultured astrocytes by influx through voltage‐activated Ca++ channels
inferred← citeshttps://doi.org/10.1002/glia.440050203openalex-snapshot
Spontaneous changes in intracellular calcium concentration in type I astrocytes from rat cerebral cortex in primary culture
inferred← citeshttps://doi.org/10.1002/glia.440050306openalex-snapshot
Agonist‐evoked Ca2+ transients in primary astroglial cultures–modulatory effects of valproic acid
inferred← citeshttps://doi.org/10.1002/glia.440060109openalex-snapshot
Type‐1 and type‐2 astrocytes are distinct targets for prostaglandins D2, E2, and F2α
inferred← citeshttps://doi.org/10.1002/glia.440060204openalex-snapshot
Glial response to dorsal root lesion in the irradiated spinal cord
inferred← citeshttps://doi.org/10.1002/glia.440060207openalex-snapshot
Postnatal development of dye‐coupling among astrocytes in rat visual cortex
inferred← citeshttps://doi.org/10.1002/glia.440060309openalex-snapshot
Heterogeneity in gap junction expression in astrocytes cultured from different brain regions
inferred← citeshttps://doi.org/10.1002/glia.440070203openalex-snapshot
Mechanisms of intercellular calcium signaling in glial cells studied with dantrolene and thapsigargin
inferred← citeshttps://doi.org/10.1002/glia.440070405openalex-snapshot
Independent changes of intracellular calcium and pH in identified leech glial cells
inferred← citeshttps://doi.org/10.1002/glia.440080305openalex-snapshot
Bergmann glia require continuous association with purkinje cells for normal phenotype expression
inferred← citeshttps://doi.org/10.1002/glia.440090206openalex-snapshot
Excitatory amino acid‐induced phosphoinositide hydrolysis in Müller glia
inferred← citeshttps://doi.org/10.1002/glia.440100209openalex-snapshot
Expression and regulation of a glutamate receptor subunit by bFGF in oligodendrocyte progenitors
inferred← citeshttps://doi.org/10.1002/glia.440100402openalex-snapshot
Synaptic transmission in the hippocampus: Critical role for glial cells
inferred← citeshttps://doi.org/10.1002/glia.440110205openalex-snapshot
Histamine and prostanoid receptors on glial cells
inferred← citeshttps://doi.org/10.1002/glia.440110211openalex-snapshot
Glutamate‐induced calcium signaling in astrocytes
inferred← citeshttps://doi.org/10.1002/glia.440110213openalex-snapshot
Neurotransmitter‐mediated signaling between axons and glial cells
inferred← citeshttps://doi.org/10.1002/glia.440110404openalex-snapshot
Astrocytes exhibit regional specificity in gap‐junction coupling
inferred← citeshttps://doi.org/10.1002/glia.440120104openalex-snapshot
Cortical type 2 astrocytes are not dye coupled nor do they express the major gap junction genes found in the central nervous system
inferred← citeshttps://doi.org/10.1002/glia.440120410openalex-snapshot
Cultured rat astrocytes possess Na+‐Ca2+ exchanger
inferred← citeshttps://doi.org/10.1002/glia.440130204openalex-snapshot
GFAP‐positive hippocampal astrocytes in situ respond to glutamatergic neuroligands with increases in [Ca2+]i
inferred← citeshttps://doi.org/10.1002/glia.440140104openalex-snapshot
Calcium waves in dissociated retinal glial (Müller) cells are evoked by release of calcium from intracellular stores
inferred← citeshttps://doi.org/10.1002/glia.440140205openalex-snapshot
AMPA‐type glutamate receptors in glial precursor cells of the rat corpus callosum: Ionic and pharmacological properties
inferred← citeshttps://doi.org/10.1002/glia.440140308openalex-snapshot
Calcium signaling in cultured rat oligodendrocytes
inferred← citeshttps://doi.org/10.1002/glia.440140405openalex-snapshot
Astrocytic gap junction removal, connexin43 redistribution, and epitope masking at excitatory amino acid lesion sites in rat brain
inferred← citeshttps://doi.org/10.1002/glia.440150212openalex-snapshot
Human epileptic astrocytes exhibit increased gap junction coupling
inferred← citeshttps://doi.org/10.1002/hbm.25087openalex-snapshot
Altered resting activity patterns and connectivity in individuals with complex regional pain syndrome
inferred← citeshttps://doi.org/10.1002/hipo.1031openalex-snapshot
Differential mechanisms of Ca2+ responses in glial cells evoked by exogenous and endogenous glutamate in rat hippocampus
inferred← citeshttps://doi.org/10.1002/hipo.1993.4500030714openalex-snapshot
Electrophysiologic characteristics of glial cells
inferred← citeshttps://doi.org/10.1002/hipo.450040105openalex-snapshot
Properties of GABA and glutamate responses in identified glial cells of the mouse hippocampal slice
inferred← citeshttps://doi.org/10.1002/hipo.450040313openalex-snapshot
Astrocytic dye coupling in rat hippocampus: Topography, developmental onset, and modulation by protein kinase C
inferred← citeshttps://doi.org/10.1002/j.2040-4603.1996.tb01751.xopenalex-snapshot
Optical Methods in Cell Physiology
inferred← citeshttps://doi.org/10.1002/jcb.10774openalex-snapshot
Cellular injury induces activation of MAPK via P2Y receptors
inferred← citeshttps://doi.org/10.1002/jcb.20258openalex-snapshot
P2Y receptors play a critical role in epithelial cell communication and migration
inferred← citeshttps://doi.org/10.1002/jcb.240460302openalex-snapshot
Bellini, carpaccio, and receptors in the central nervous system
inferred← citeshttps://doi.org/10.1002/jez.1402610306openalex-snapshot
Development of spinal motor networks in the chick embryo
inferred← citeshttps://doi.org/10.1002/jez.1402730205openalex-snapshot
Calcium oscillations and calcium waves coordinate rhythmic contractile activity within the stellate cell layer of medaka fish embryos
inferred← citeshttps://doi.org/10.1002/jlb.55.4.461openalex-snapshot
Slow calcium waves imaged in myeloid cells derived from neonatal cord blood
inferred← citeshttps://doi.org/10.1002/jnr.1141openalex-snapshot
Guanosine‐induced increase in free cytosolic calcium concentration in mouse astrocytes in primary cultures: Does it act on an A3 adenosine receptor?
inferred← citeshttps://doi.org/10.1002/jnr.20061openalex-snapshot
Ca 2+ ‐dependent glutamate release involves two classes of endoplasmic reticulum Ca 2+ stores in astrocytes
inferred← citeshttps://doi.org/10.1002/jnr.22060openalex-snapshot
CD38 regulation in activated astrocytes: Implications for neuroinflammation and HIV‐1 brain infection
inferred← citeshttps://doi.org/10.1002/jnr.22764openalex-snapshot
Role of gap junctions in chronic pain
inferred← citeshttps://doi.org/10.1002/jnr.24075openalex-snapshot
Astrocyte dysfunction in Alzheimer disease
inferred← citeshttps://doi.org/10.1002/jnr.24387openalex-snapshot
Does shuttling of glycogen‐derived lactate from astrocytes to neurons take place during neurotransmission and memory consolidation?
inferred← citeshttps://doi.org/10.1002/jnr.24699openalex-snapshot
Central nervous system‐infiltrated immune cells induce calcium increase in astrocytes via astroglial purinergic signaling
inferred← citeshttps://doi.org/10.1002/jnr.25042openalex-snapshot
Calcium signaling in individual APP/PS1 mouse dentate gyrus astrocytes increases ex vivo with Aβ pathology and age without affecting astrocyte network activity
inferred← citeshttps://doi.org/10.1002/jnr.25057openalex-snapshot
Altered basal ganglia infraslow oscillation and resting functional connectivity in complex regional pain syndrome
inferred← citeshttps://doi.org/10.1002/jnr.490360312openalex-snapshot
AMPA‐Selective glutamate receptor subunits in astroglial cultures
inferred← citeshttps://doi.org/10.1002/jnr.490400414openalex-snapshot
Long, interlaminar astroglial cell processes in the cortex of adult monkeys
inferred← citeshttps://doi.org/10.1002/jnr.490420102openalex-snapshot
Excitatory amino acid receptors in glia: Different subtypes for distinct functions?
inferred← citeshttps://doi.org/10.1002/mabi.201600059openalex-snapshot
Poly(3,4‐ethylenedioxythiophene):GlycosAminoGlycan Aqueous Dispersions: Toward Electrically Conductive Bioactive Materials for Neural Interfaces
inferred← citeshttps://doi.org/10.1002/neu.10019openalex-snapshot
Calcium oscillations in neocortical astrocytes under epileptiform conditions
inferred← citeshttps://doi.org/10.1002/neu.480250307openalex-snapshot
Nonlinear propagation of agonist‐induced cytoplasmic calcium waves in single astrocytes
inferred← citeshttps://doi.org/10.1002/neu.480280204openalex-snapshot
Evidence for glutamate‐mediated activation of hippocampal neurons by glial calcium waves
inferred← citeshttps://doi.org/10.1002/neu.480280404openalex-snapshot
Gap junctions are required for the propagation of spreading depression
inferred← citeshttps://doi.org/10.1002/nrc.10073openalex-snapshot
Possible involvement of nitric oxide in the modulation of photolytic flash‐induced intercellular calcium waves in cultured astrocytes
inferred← citeshttps://doi.org/10.1002/pmic.201800165openalex-snapshot
Proteins Regulating Microvesicle Biogenesis and Multidrug Resistance in Cancer
inferred← citeshttps://doi.org/10.1002/prot.20225openalex-snapshot
The effect of higher order RNA processes on changing patterns of protein domain selection: A developmentally regulated transcriptome of type 1 inositol 1,4,5‐trisphosphate receptors
inferred← citeshttps://doi.org/10.1002/smll.74843openalex-snapshot
Molecular Machines Enhance Insulin Release in Pancreatic Beta Cells
inferred← citeshttps://doi.org/10.1002/syn.890170406openalex-snapshot
Local communication within dendritic spines: Models of second messenger diffusion in granule cell spines of the mammalian olfactory bulb
inferred← citeshttps://doi.org/10.1002/wmts.48openalex-snapshot
Molecular biology of the InsP3Rs: focus on brain function in health and disease
inferred← citeshttps://doi.org/10.1006/cbir.1998.0391openalex-snapshot
GAP JUNCTIONAL COMMUNICATION IN THE DEVELOPING CENTRAL NERVOUS SYSTEM
inferred← citeshttps://doi.org/10.1006/cbir.1999.0393openalex-snapshot
DIVERSIFICATION OF GAP JUNCTION PROTEINS (CONNEXINS) IN THE CENTRAL NERVOUS SYSTEM AND THE CONCEPT OF FUNCTIONAL COMPARTMENTS
inferred← citeshttps://doi.org/10.1006/excr.2000.4902openalex-snapshot
Enhanced Calcium Transients in Glial Cells in Neonatal Cerebellar Cultures Derived from S100B Null Mice
inferred← citeshttps://doi.org/10.1006/exnr.1997.6467openalex-snapshot
Hippocampal Connexin 43 Expression in Human Complex Partial Seizure Disorder
inferred← citeshttps://doi.org/10.1006/exnr.2001.7712openalex-snapshot
Effective Reduction of Neuronal Death by Inhibiting Gap Junctional Intercellular Communication in a Rodent Model of Global Transient Cerebral Ischemia
inferred← citeshttps://doi.org/10.1006/frne.1997.0161openalex-snapshot
Peptide Receptors on Astrocytes
inferred← citeshttps://doi.org/10.1006/frne.2001.0226openalex-snapshot
Oxytocin-Secreting Neurons: A Physiological Model of Morphological Neuronal and Glial Plasticity in the Adult Hypothalamus
inferred← citeshttps://doi.org/10.1006/mcne.2001.1017openalex-snapshot
Atypical Neuroleptic Drugs Downregulate Dopamine Sensitivity in Rat Cortical and Striatal Astrocytes
inferred← citeshttps://doi.org/10.1006/meth.1998.0686openalex-snapshot
Functional Studies in Cultured Astrocytes
inferred← citeshttps://doi.org/10.1006/meth.1999.0774openalex-snapshot
Detecting Action Potentials in Neuronal Populations with Calcium Imaging
inferred← citeshttps://doi.org/10.1006/nbdi.1998.0197openalex-snapshot
Cloning and Expression of a P2yPurinoceptor from the Adult Bovine Corpus Callosum
inferred← citeshttps://doi.org/10.1006/nbdi.2000.0288openalex-snapshot
Source Localization and Possible Causes of Interictal Epileptic Activity in Tumor-Associated Epilepsy
inferred← citeshttps://doi.org/10.1006/scdb.2000.0214openalex-snapshot
Intercellular Ca2+signalling: the artery wall
inferred← citeshttps://doi.org/10.1007/0-387-23696-1_21openalex-snapshot
Hydrogen Sulfide as a Synaptic Modulator
inferred← citeshttps://doi.org/10.1007/1-4020-2541-6_20openalex-snapshot
Neural Plasticity and Cell Biology of Learning
inferred← citeshttps://doi.org/10.1007/1-4020-4456-9_5openalex-snapshot
Glutamate release from astrocytes: impact on neuronal function
inferred← citeshttps://doi.org/10.1007/112_2013_15openalex-snapshot
TRP Channels Coordinate Ion Signalling in Astroglia
inferred← citeshttps://doi.org/10.1007/11406501_2openalex-snapshot
Modeling IP3-Dependent Calcium Dynamics in Non-Excitable Cells
inferred← citeshttps://doi.org/10.1007/164_2018_203openalex-snapshot
N/OFQ-NOP System in Peripheral and Central Immunomodulation
inferred← citeshttps://doi.org/10.1007/3-211-27208-9_1openalex-snapshot
Depolarisation Phenomena in Traumatic and Ischaemic Brain Injury
inferred← citeshttps://doi.org/10.1007/3-540-45396-2_41openalex-snapshot
Nonlinear Waves on Stochastic Support: Calcium Waves in Astrocyte Syncytia
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