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Differential distribution of endoplasmic reticulum controls metabotropic signaling and plasticity at hippocampal synapses
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Actin-associated protein synaptopodin in the rat hippocampal formation: Localization in the spine neck and close association with the spine apparatus of principal neurons
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Mechanisms of synaptic depression triggered by metabotropic glutamate receptors
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A simple method for organotypic cultures of nervous tissue
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Ca2+ signaling in dendritic spines
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Activity-Dependent Plasticity of the NMDA-Receptor Fractional Ca2+ Current
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Nonlinear Regulation of Unitary Synaptic Signals by CaV2.3 Voltage-Sensitive Calcium Channels Located in Dendritic Spines
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The mGluR theory of fragile X mental retardation
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Differential plasma membrane distribution of metabotropic glutamate receptors mGluR1α, mGluR2 and mGluR5, relative to neurotransmitter release sites
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Local Calcium Release in Dendritic Spines Required for Long-Term Synaptic Depression
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Two Distinct Forms of Long-Term Depression Coexist in CA1 Hippocampal Pyramidal Cells
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Synergistic Release of Ca2+ from IP3-Sensitive Stores Evoked by Synaptic Activation of mGluRs Paired with Backpropagating Action Potentials
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Regulation of Dendritic Spine Morphology and Synaptic Function by Shank and Homer
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Ca2+ signaling in dendritic spines
inferredcites →https://doi.org/10.1038/1831592a0openalex-snapshot
Electron Microscopy of Synaptic Contacts on Dendrite Spines of the Cerebral Cortex
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Local calcium signalling by inositol-1,4,5-trisphosphate in Purkinje cell dendrites
inferredcites →https://doi.org/10.1038/35046067openalex-snapshot
Calcium stores regulate the polarity and input specificity of synaptic modification
inferredcites →https://doi.org/10.1038/361031a0openalex-snapshot
A synaptic model of memory: long-term potentiation in the hippocampus
inferredcites →https://doi.org/10.1038/nature04783openalex-snapshot
Experience-dependent and cell-type-specific spine growth in the neocortex
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Locally dynamic synaptic learning rules in pyramidal neuron dendrites
inferredcites →https://doi.org/10.1038/nn1747openalex-snapshot
Spine growth precedes synapse formation in the adult neocortex in vivo
inferredcites →https://doi.org/10.1038/nn736openalex-snapshot
Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons
inferredcites →https://doi.org/10.1073/pnas.0802940105openalex-snapshot
Optical induction of plasticity at single synapses reveals input-specific accumulation of αCaMKII
inferredcites →https://doi.org/10.1073/pnas.1832384100openalex-snapshot
Synaptopodin-deficient mice lack a spine apparatus and show deficits in synaptic plasticity
inferredcites →https://doi.org/10.1073/pnas.89.1.123openalex-snapshot
Intracellular injection of Ca2+ chelators blocks induction of long-term depression in rat visual cortex.
inferredcites →https://doi.org/10.1103/physreve.76.021922openalex-snapshot
Diffusion in a dendritic spine: The role of geometry
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04342.xopenalex-snapshot
Dynamic distribution of endoplasmic reticulum in hippocampal neuron dendritic spines
inferredcites →https://doi.org/10.1126/science.1096615openalex-snapshot
Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity
inferredcites →https://doi.org/10.1126/science.1114816openalex-snapshot
Neuronal Activity Regulates Diffusion Across the Neck of Dendritic Spines
inferredcites →https://doi.org/10.1126/science.272.5262.716openalex-snapshot
Direct Measurement of Coupling Between Dendritic Spines and Shafts
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New Attacks Breach Computer Codes
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Role for Rapid Dendritic Protein Synthesis in Hippocampal mGluR-Dependent Long-Term Depression
inferredcites →https://doi.org/10.1126/stke.2192004pl5openalex-snapshot
Imaging Calcium Concentration Dynamics in Small Neuronal Compartments
inferredcites →https://doi.org/10.1186/1475-925x-2-13openalex-snapshot
ScanImage: Flexible software for operating laser scanning microscopes
inferredcites →https://doi.org/10.1523/jneurosci.0176-06.2006openalex-snapshot
Two Coincidence Detectors for Spike Timing-Dependent Plasticity in Somatosensory Cortex
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Principles of Long-Term Dynamics of Dendritic Spines
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Dendritic spines of rat cerebellar Purkinje cells: serial electron microscopy with reference to their biophysical characteristics
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Induction of Hippocampal Long-Term Depression Requires Release of Ca2+from Separate Presynaptic and Postsynaptic Intracellular Stores
inferredcites →https://doi.org/10.1523/jneurosci.1749-06.2006openalex-snapshot
Spine Ca2+Signaling in Spike-Timing-Dependent Plasticity
inferredcites →https://doi.org/10.1523/jneurosci.22-06-02215.2002openalex-snapshot
Endosomal Compartments Serve Multiple Hippocampal Dendritic Spines from a Widespread Rather Than a Local Store of Recycling Membrane
inferredcites →https://doi.org/10.1523/jneurosci.2702-08.2008openalex-snapshot
Spine Neck Plasticity Controls Postsynaptic Calcium Signals through Electrical Compartmentalization
inferredcites →https://doi.org/10.1523/jneurosci.3091-06.2006openalex-snapshot
NMDA-Dependent, But Not Group I Metabotropic Glutamate Receptor-Dependent, Long-Term Depression at Schaffer Collateral–CA1 Synapses Is Associated with Long-Term Reduction of Release from the Rapidly Recycling Presynaptic Vesicle Pool
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Key Role of the Postsynaptic Density Scaffold Proteins Shank and Homer in the Functional Architecture of Ca 2+ Homeostasis at Dendritic Spines in Hippocampal Neurons
inferredcites →https://doi.org/10.1523/jneurosci.5528-08.2009openalex-snapshot
Synaptopodin Regulates Plasticity of Dendritic Spines in Hippocampal Neurons
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Hippocampal Long-Term Synaptic Plasticity and Signal Amplification of NMDA Receptors
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Dendritic Distribution of Autophagosomes Underlies Pathway-Selective Induction of LTD
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inferred← citeshttps://doi.org/10.1074/jbc.m112.376491openalex-snapshot
Balancing Arc Synthesis, mRNA Decay, and Proteasomal Degradation
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Synaptic anchoring of the endoplasmic reticulum depends on myosin V and caldendrin activity
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mir124-dependent tagging of glutamatergic synapses by synaptopodin controls non-uniform and input-specific homeostatic synaptic plasticity
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Compartment-specific tuning of hippocampal dendritic feature selectivity by intracellular Ca 2+ release
inferred← citeshttps://doi.org/10.1101/2021.12.30.474557openalex-snapshot
Properties and proximity proteomics of synaptopodin provide insight into the molecular organization of the spine apparatus of dendritic spines
inferred← citeshttps://doi.org/10.1101/2022.09.20.508741openalex-snapshot
Combined DiI and antibody labeling reveals complex dysgenesis of hippocampal spine synapses in a mouse model of Fragile X Syndrome
inferred← citeshttps://doi.org/10.1101/2024.02.16.580703openalex-snapshot
Epigenetic repression of cFos supports sequential formation of distinct spatial memories
inferred← citeshttps://doi.org/10.1101/2025.10.06.677012openalex-snapshot
Endoplasmic Reticulum Geometry Dictates Neuronal Bursting via Calcium Store Refill Rates
inferred← citeshttps://doi.org/10.1101/526509openalex-snapshot
Characterization of neuronal synaptopodin reveals a myosin V-dependent mechanism of synaptopodin clustering at the post-synaptic sites
inferred← citeshttps://doi.org/10.1101/538041openalex-snapshot
Freeze-frame imaging of synaptic activity using SynTagMA
inferred← citeshttps://doi.org/10.1101/cshperspect.a005686openalex-snapshot
Calcium Signaling in Dendritic Spines
inferred← citeshttps://doi.org/10.1101/pdb.top089714openalex-snapshot
Stimulating Neurons with Heterologously Expressed Light-Gated Ion Channels
inferred← citeshttps://doi.org/10.1109/bigdata50022.2020.9378053openalex-snapshot
NeuroKube: An Automated and Autoscaling Neuroimaging Reconstruction Framework using Cloud Native Computing and A.I.
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2010.07344.xopenalex-snapshot
Learning rules and persistence of dendritic spines
inferred← citeshttps://doi.org/10.1111/j.1476-5381.2011.01328.xopenalex-snapshot
Signalling pathways underlying structural plasticity of dendritic spines
inferred← citeshttps://doi.org/10.1111/jnc.14958openalex-snapshot
The endoplasmic reticulum acetyltransferases ATase1/NAT8B and ATase2/NAT8 are differentially regulated to adjust engagement of the secretory pathway
inferred← citeshttps://doi.org/10.1113/jp277726openalex-snapshot
Intracellular calcium stores mediate metaplasticity at hippocampal dendritic spines
inferred← citeshttps://doi.org/10.1113/jphysiol.2011.216564openalex-snapshot
Synaptically activated Ca2+ waves and NMDA spikes locally suppress voltage‐dependent Ca2+ signalling in rat pyramidal cell dendrites
inferred← citeshttps://doi.org/10.1117/12.2251227openalex-snapshot
Rapid imaging of mammalian brain slices with a compact light sheet fluorescent microscope
inferred← citeshttps://doi.org/10.1124/pr.110.003814openalex-snapshot
Endoplasmic Reticulum Ca2+ Handling in Excitable Cells in Health and Disease
inferred← citeshttps://doi.org/10.1126/science.aah5982openalex-snapshot
Ultrastructural evidence for synaptic scaling across the wake/sleep cycle
inferred← citeshttps://doi.org/10.1126/science.abm1670openalex-snapshot
Compartment-specific tuning of dendritic feature selectivity by intracellular Ca 2+ release
inferred← citeshttps://doi.org/10.1134/s0006297921060018openalex-snapshot
The Role of Stress-Induced Changes of Homer1 Expression in Stress Susceptibility
inferred← citeshttps://doi.org/10.1134/s0006350923020215openalex-snapshot
Two Subcompartments of the Smooth Endoplasmic Reticulum in Perisynaptic Astrocytic Processes: Ultrastructure and Distribution in Hippocampal and Neocortical Synapses
inferred← citeshttps://doi.org/10.1146/annurev-physiol-021113-170400openalex-snapshot
Plasticity of Dendritic Spines: Subcompartmentalization of Signaling
inferred← citeshttps://doi.org/10.1152/jn.00526.2011openalex-snapshot
Activity-dependent regulation of synaptic strength by PSD-95 in CA1 neurons
inferred← citeshttps://doi.org/10.1152/jn.00770.2013openalex-snapshot
Dendritic spine heterogeneity and calcium dynamics in basolateral amygdala principal neurons
inferred← citeshttps://doi.org/10.1152/physrev.00012.2013openalex-snapshot
Dendritic Spines: The Locus of Structural and Functional Plasticity
inferred← citeshttps://doi.org/10.1162/neco_a_00408openalex-snapshot
System Identification of mGluR-Dependent Long-Term Depression
inferred← citeshttps://doi.org/10.1177/1073858410386357openalex-snapshot
Dendritic Spine Plasticity: New Regulatory Roles of Dynamic Microtubules
inferred← citeshttps://doi.org/10.1177/1073858415613277openalex-snapshot
Roles of Calcium Stores and Store-Operated Channels in Plasticity of Dendritic Spines
inferred← citeshttps://doi.org/10.1177/1073858418769644openalex-snapshot
Dendritic Spine Elimination: Molecular Mechanisms and Implications
inferred← citeshttps://doi.org/10.1177/1073858418785334openalex-snapshot
Intracellular Ca 2+ Release and Synaptic Plasticity: A Tale of Many Stores
inferred← citeshttps://doi.org/10.1177/10738584261488785openalex-snapshot
Spatial Compartmentalization of the Neuronal Endoplasmic Reticulum: Structural Basis of Calcium Signaling and Cellular Homeostasis
inferred← citeshttps://doi.org/10.1177/25152564231185011openalex-snapshot
E-Syt1 Regulates Neuronal Activity-Dependent Endoplasmic Reticulum–Plasma Membrane Junctions and Surface Expression of AMPA Receptors
inferred← citeshttps://doi.org/10.1186/1750-1326-9-21openalex-snapshot
Ryanodine receptors: physiological function and deregulation in Alzheimer disease
inferred← citeshttps://doi.org/10.1186/1756-6606-4-30openalex-snapshot
Differential trafficking of AMPA receptors following activation of NMDA receptors and mGluRs
inferred← citeshttps://doi.org/10.1186/s12576-021-00819-9openalex-snapshot
Brain is modulated by neuronal plasticity during postnatal development
inferred← citeshttps://doi.org/10.1186/s13041-014-0060-3openalex-snapshot
Rapid regulation of endoplasmic reticulum dynamics in dendritic spines by NMDA receptor activation
inferred← citeshttps://doi.org/10.1186/s13041-021-00795-6openalex-snapshot
Prenatal treatment with rapamycin restores enhanced hippocampal mGluR-LTD and mushroom spine size in a Down’s syndrome mouse model
inferred← citeshttps://doi.org/10.1186/s13041-024-01089-3openalex-snapshot
Synaptopodin is required for long-term depression at Schaffer collateral-CA1 synapses
inferred← citeshttps://doi.org/10.1186/s40478-016-0311-xopenalex-snapshot
Rewiring neuronal microcircuits of the brain via spine head protrusions-a role for synaptopodin and intracellular calcium stores
inferred← citeshttps://doi.org/10.1242/jcs.230177openalex-snapshot
Myosin V regulates synaptopodin clustering and localization in the dendrites of hippocampal neurons
inferred← citeshttps://doi.org/10.1371/journal.pbio.1002181openalex-snapshot
Ryanodine Receptor Activation Induces Long-Term Plasticity of Spine Calcium Dynamics
inferred← citeshttps://doi.org/10.1371/journal.pbio.2006202openalex-snapshot
Fast calcium transients in dendritic spines driven by extreme statistics
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1000987openalex-snapshot
Lobe Specific Ca2+-Calmodulin Nano-Domain in Neuronal Spines: A Single Molecule Level Analysis
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004949openalex-snapshot
Control of Ca2+ Influx and Calmodulin Activation by SK-Channels in Dendritic Spines
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1010069openalex-snapshot
Calcium modeling of spine apparatus-containing human dendritic spines demonstrates an “all-or-nothing” communication switch between the spine head and dendrite
inferred← citeshttps://doi.org/10.1371/journal.pone.0024879openalex-snapshot
Functional Characterization of the Dendritically Localized mRNA Neuronatin in Hippocampal Neurons
inferred← citeshttps://doi.org/10.1371/journal.pone.0028380openalex-snapshot
Simulation of Postsynaptic Glutamate Receptors Reveals Critical Features of Glutamatergic Transmission
inferred← citeshttps://doi.org/10.1371/journal.pone.0071155openalex-snapshot
Long Lasting Protein Synthesis- and Activity-Dependent Spine Shrinkage and Elimination after Synaptic Depression
inferred← citeshttps://doi.org/10.1371/journal.pone.0090451openalex-snapshot
Characterization of Aromatase Expression in the Adult Male and Female Mouse Brain. I. Coexistence with Oestrogen Receptors α and β, and Androgen Receptors
inferred← citeshttps://doi.org/10.1371/journal.pone.0148310openalex-snapshot
The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
inferred← citeshttps://doi.org/10.1371/journal.pone.0158295openalex-snapshot
Extended Synaptotagmin (ESyt) Triple Knock-Out Mice Are Viable and Fertile without Obvious Endoplasmic Reticulum Dysfunction
inferred← citeshttps://doi.org/10.1371/journal.pone.0225394openalex-snapshot
Circadian clock regulates the shape and content of dendritic spines in mouse barrel cortex
inferred← citeshttps://doi.org/10.1371/journal.pone.0355625openalex-snapshot
Synaptopodin KO rat for assessing the dendritic spine apparatus and axonal cisternal organelle in synaptic plasticity, development, and behavior
inferred← citeshttps://doi.org/10.14201/gredos.110642openalex-snapshot
Plasticidad del sistema glutamatérgico en la vía olfatoria de roedores sometidos a deprivación sensorial. Estudio del receptor mGluR1a en el bulbo olfatorio
inferred← citeshttps://doi.org/10.1523/jneurosci.0175-20.2020openalex-snapshot
Mechanisms Underlying Long-Term Synaptic Zinc Plasticity at Mouse Dorsal Cochlear Nucleus Glutamatergic Synapses
inferred← citeshttps://doi.org/10.1523/jneurosci.0409-12.2012openalex-snapshot
Repetitive Magnetic Stimulation Induces Functional and Structural Plasticity of Excitatory Postsynapses in Mouse Organotypic Hippocampal Slice Cultures
inferred← citeshttps://doi.org/10.1523/jneurosci.0791-25.2025openalex-snapshot
Altered Structural Plasticity Mediated by mGlu and NMDA Receptors and Impaired Cognition in a Genetic ASD Model (Shank3 +/− Mice)
inferred← citeshttps://doi.org/10.1523/jneurosci.0807-25.2025openalex-snapshot
Activity Deprivation Modulates the Shank3/Homer1/mGluR5 Signaling Pathway to Enable Synaptic Upscaling
inferred← citeshttps://doi.org/10.1523/jneurosci.1157-19.2019openalex-snapshot
Pleiotropic Mitochondria: The Influence of Mitochondria on Neuronal Development and Disease
inferred← citeshttps://doi.org/10.1523/jneurosci.1466-21.2022openalex-snapshot
Stabilization of Spine Synaptopodin by mGluR1 Is Required for mGluR-LTD
inferred← citeshttps://doi.org/10.1523/jneurosci.2472-20.2021openalex-snapshot
Abl2:Cortactin Interactions Regulate Dendritic Spine Stability via Control of a Stable Filamentous Actin Pool
inferred← citeshttps://doi.org/10.1523/jneurosci.3210-10.2011openalex-snapshot
Removal of Synaptic Ca 2+ -Permeable AMPA Receptors during Sleep
inferred← citeshttps://doi.org/10.1523/jneurosci.4208-14.2015openalex-snapshot
Costimulation of AMPA and Metabotropic Glutamate Receptors Underlies Phospholipase C Activation by Glutamate in Hippocampus
inferred← citeshttps://doi.org/10.1523/jneurosci.4577-11.2012openalex-snapshot
Cholinergic Induction of Input-Specific Late-Phase LTP via Localized Ca2+Release in the Visual Cortex
inferred← citeshttps://doi.org/10.1523/jneurosci.5619-09.2010openalex-snapshot
Activation Conditions for the Induction of Metabotropic Glutamate Receptor-Dependent Long-Term Depression in Hippocampal CA1 Pyramidal Cells
inferred← citeshttps://doi.org/10.15252/embj.201694526openalex-snapshot
mGluR long‐term depression regulates GluA2 association with COPII vesicles and exit from the endoplasmic reticulum
inferred← citeshttps://doi.org/10.15252/embj.2020106523openalex-snapshot
Caldendrin and myosin V regulate synaptic spine apparatus localization via ER stabilization in dendritic spines
inferred← citeshttps://doi.org/10.15252/embj.2021109012openalex-snapshot
miR‐124‐dependent tagging of synapses by synaptopodin enables input‐specific homeostatic plasticity
inferred← citeshttps://doi.org/10.17577/ijertv9is020083openalex-snapshot
Review on Modelling Aspect of Ryanodine Receptor in CA1 Neuron
inferred← citeshttps://doi.org/10.20381/ruor-2709openalex-snapshot
The Role of LMO4 in the Regulation of Hippocampal and Amygdalar Synaptic Function
inferred← citeshttps://doi.org/10.2183/pjab.97.028openalex-snapshot
New insights into the regulation of synaptic transmission and plasticity by the endoplasmic reticulum and its membrane contacts
inferred← citeshttps://doi.org/10.31857/s0006302923020126openalex-snapshot
Two subcompartments of the smooth endoplasmic reticulum in perisynaptic astrocytic processes: ultrastructure and distribution in hippocampal and neocortical synapses
inferred← citeshttps://doi.org/10.31857/s0320972521060014openalex-snapshot
Роль изменений экспрессии Homer1 в чувствительности к стрессу
inferred← citeshttps://doi.org/10.3233/jad-240042openalex-snapshot
Evidence that Alzheimer’s Disease Is a Disease of Competitive Synaptic Plasticity Gone Awry
inferred← citeshttps://doi.org/10.3233/jhd-170266openalex-snapshot
Inhibition of TRPC1-Dependent Store-Operated Calcium Entry Improves Synaptic Stability and Motor Performance in a Mouse Model of Huntington’s Disease
inferred← citeshttps://doi.org/10.3389/fcell.2020.618733openalex-snapshot
Complex Interactions Between Membrane-Bound Organelles, Biomolecular Condensates and the Cytoskeleton
inferred← citeshttps://doi.org/10.3389/fcell.2021.680118openalex-snapshot
The Implication of STEP in Synaptic Plasticity and Cognitive Impairments in Alzheimer’s Disease and Other Neurological Disorders
inferred← citeshttps://doi.org/10.3389/fnana.2014.00064openalex-snapshot
Endoplasmic reticulum calcium stores in dendritic spines
inferred← citeshttps://doi.org/10.3389/fnana.2014.00141openalex-snapshot
Input transformation by dendritic spines of pyramidal neurons
inferred← citeshttps://doi.org/10.3389/fnbeh.2022.806356openalex-snapshot
The Intriguing Contribution of Hippocampal Long-Term Depression to Spatial Learning and Long-Term Memory
inferred← citeshttps://doi.org/10.3389/fncel.2017.00363openalex-snapshot
Store-Operated Calcium Entry Is Required for mGluR-Dependent Long Term Depression in Cortical Neurons
inferred← citeshttps://doi.org/10.3389/fncel.2021.652721openalex-snapshot
Sustained Hippocampal Synaptic Pathophysiology Following Single and Repeated Closed-Head Concussive Impacts
inferred← citeshttps://doi.org/10.3389/fncel.2021.695817openalex-snapshot
Astrocytic IP3Rs: Beyond IP3R2
inferred← citeshttps://doi.org/10.3389/fncel.2024.1482844openalex-snapshot
Synaptopodin: a key regulator of Hebbian plasticity
inferred← citeshttps://doi.org/10.3389/fncom.2016.00104openalex-snapshot
Depotentiation from Potentiated Synaptic Strength in a Tristable System of Coupled Phosphatase and Kinase
inferred← citeshttps://doi.org/10.3389/fncom.2018.00058openalex-snapshot
A Glutamatergic Spine Model to Enable Multi-Scale Modeling of Nonlinear Calcium Dynamics
inferred← citeshttps://doi.org/10.3389/fncom.2019.00038openalex-snapshot
Intrinsic Spine Dynamics Are Critical for Recurrent Network Learning in Models With and Without Autism Spectrum Disorder
inferred← citeshttps://doi.org/10.3389/fnmol.2012.00061openalex-snapshot
Ca2+ sensor proteins in dendritic spines: a race for Ca2+
inferred← citeshttps://doi.org/10.3389/fnsyn.2019.00005openalex-snapshot
Optical Quantal Analysis Using Ca2+ Indicators: A Robust Method for Assessing Transmitter Release Probability at Excitatory Synapses by Imaging Single Glutamate Release Events
inferred← citeshttps://doi.org/10.3389/fnsyn.2019.00019openalex-snapshot
Probing Single Synapses via the Photolytic Release of Neurotransmitters
inferred← citeshttps://doi.org/10.3390/biom14121617openalex-snapshot
Endoplasmic Reticulum Calcium Signaling in Hippocampal Neurons
inferred← citeshttps://doi.org/10.3390/biomedicines10112692openalex-snapshot
Combined DiI and Antibody Labeling Reveals Complex Dysgenesis of Hippocampal Dendritic Spines in a Mouse Model of Fragile X Syndrome
inferred← citeshttps://doi.org/10.3390/cells9010160openalex-snapshot
STIM Protein-NMDA2 Receptor Interaction Decreases NMDA-Dependent Calcium Levels in Cortical Neurons
inferred← citeshttps://doi.org/10.3390/cells9122577openalex-snapshot
Alterations of the Endoplasmic Reticulum (ER) Calcium Signaling Molecular Components in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ijms231710027openalex-snapshot
Interactions between the Polysialylated Neural Cell Adhesion Molecule and the Transient Receptor Potential Canonical Channels 1, 4, and 5 Induce Entry of Ca2+ into Neurons
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