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Dynamic action of neurometals at the synapse
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1997)7:6<666::aid-hipo8>3.0.co;2-copenalex-snapshot
Suppression of long-term potentiation in hippocampal slices by copper
inferredcites →https://doi.org/10.1002/bies.10193openalex-snapshot
Complexity of calcium signaling in synaptic spines
inferredcites →https://doi.org/10.1002/jnr.20714openalex-snapshot
Inhibition of presynaptic activity by zinc released from mossy fiber terminals during tetanic stimulation
inferredcites →https://doi.org/10.1002/jnr.21233openalex-snapshot
Role of zinc influx via AMPA/kainate receptor activation in metabotropic glutamate receptor‐mediated calcium release
inferredcites →https://doi.org/10.1002/jnr.21449openalex-snapshot
Negative modulation of presynaptic activity by zinc released from schaffer collaterals
inferredcites →https://doi.org/10.1002/jnr.21732openalex-snapshot
Attenuation of hippocampal mossy fiber long‐term potentiation by low micromolar concentrations of zinc
inferredcites →https://doi.org/10.1002/jnr.22456openalex-snapshot
Zinc signaling through glucocorticoid and glutamate signaling in stressful circumstances
inferredcites →https://doi.org/10.1007/bf00592566openalex-snapshot
Histochemical demonstration of heavy metals
inferredcites →https://doi.org/10.1007/s00232-005-0804-1openalex-snapshot
Contrasting Effects of Cd2+ and Co2+ on the Blocking/Unblocking of Human Cav3 Channels
inferredcites →https://doi.org/10.1007/s00232-008-9148-yopenalex-snapshot
Effects of Copper on T-Type Ca2+ Channels in Mouse Spermatogenic Cells
inferredcites →https://doi.org/10.1007/s00424-010-0809-1openalex-snapshot
Glutamate receptors, neurotoxicity and neurodegeneration
inferredcites →https://doi.org/10.1007/s00702-004-0124-0openalex-snapshot
Trace and major elements in whole blood, serum, cerebrospinal fluid and urine of patients with Parkinson?s disease
inferredcites →https://doi.org/10.1007/s00775-007-0330-yopenalex-snapshot
Thionein/metallothionein control Zn(II) availability and the activity of enzymes
inferredcites →https://doi.org/10.1007/s101620010082openalex-snapshot
Zinc Inhibition of Group I mGluR-Mediated Calcium Homeostasis in Auditory Neurons
inferredcites →https://doi.org/10.1007/s10534-008-9186-zopenalex-snapshot
Molecular aspects of human cellular zinc homeostasis: redox control of zinc potentials and zinc signals
inferredcites →https://doi.org/10.1007/s12035-010-8158-9openalex-snapshot
Zinc Signaling in the Hippocampus and Its Relation to Pathogenesis of Depression
inferredcites →https://doi.org/10.1016/0006-8993(82)90067-1openalex-snapshot
Ionic mechanisms of cholinergic excitation in mammalian hippocampal pyramidal cells
inferredcites →https://doi.org/10.1016/0028-3908(95)00109-jopenalex-snapshot
Structure and function of the NMDA receptor channel
inferredcites →https://doi.org/10.1016/0166-2236(93)90081-vopenalex-snapshot
Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation
inferredcites →https://doi.org/10.1016/0270-9139(91)90052-wopenalex-snapshot
Role of extracellular zinc and copper on metallothionein regulation in cultured rat hepatocytes*1
inferredcites →https://doi.org/10.1016/0301-0082(94)90082-5openalex-snapshot
Modulation of inhibitory and excitatory amino acid receptor ion channels by zinc
inferredcites →https://doi.org/10.1016/0896-6273(90)90199-popenalex-snapshot
Zinc has opposite effects on NMDA and Non-NMDA receptors expressed in xenopus oocytes
inferredcites →https://doi.org/10.1016/0896-6273(94)90269-0openalex-snapshot
The role of Ca2+ channels in hippocampal mossy fiber synaptic transmission and long-term potentiation
inferredcites →https://doi.org/10.1016/j.abb.2007.02.017openalex-snapshot
The zinc/thiolate redox biochemistry of metallothionein and the control of zinc ion fluctuations in cell signaling
inferredcites →https://doi.org/10.1016/j.aca.2008.08.018openalex-snapshot
Speciation analysis of selected metals and determination of their total contents in paired serum and cerebrospinal fluid samples: An approach to investigate the permeability of the human blood-cerebrospinal fluid-barrier
inferredcites →https://doi.org/10.1016/j.brainres.2004.01.013openalex-snapshot
Hippocampal mossy fiber calcium transients are maintained during long-term potentiation and are inhibited by endogenous zinc
inferredcites →https://doi.org/10.1016/j.brainres.2005.04.006openalex-snapshot
Tetanically released zinc inhibits hippocampal mossy fiber calcium, zinc and synaptic responses
inferredcites →https://doi.org/10.1016/j.brainres.2010.01.085openalex-snapshot
Zinc differentially acts on components of long-term potentiation at hippocampal CA1 synapses
inferredcites →https://doi.org/10.1016/j.brainresrev.2008.10.003openalex-snapshot
Zinc and cortical plasticity
inferredcites →https://doi.org/10.1016/j.brainresrev.2009.09.003openalex-snapshot
Insight into zinc signaling from dietary zinc deficiency
inferredcites →https://doi.org/10.1016/j.cccn.2003.12.008openalex-snapshot
Peripheral markers of blood–brain barrier damage
inferredcites →https://doi.org/10.1016/j.ejphar.2004.07.015openalex-snapshot
Amino terminal domain regulation of NMDA receptor function
inferredcites →https://doi.org/10.1016/j.expneurol.2005.08.030openalex-snapshot
Concentrations of extracellular free zinc (pZn)e in the central nervous system during simple anesthetization, ischemia and reperfusion
inferredcites →https://doi.org/10.1016/j.jtemb.2005.03.003openalex-snapshot
Advances in metallothionein structure and functions
inferredcites →https://doi.org/10.1016/j.jtemb.2007.05.001openalex-snapshot
Elemental profile of cerebrospinal fluid in patients with Parkinson's disease
inferredcites →https://doi.org/10.1016/j.mam.2005.07.013openalex-snapshot
Relevance, essentiality and toxicity of trace elements in human health
inferredcites →https://doi.org/10.1016/j.mcn.2006.11.018openalex-snapshot
ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis
inferredcites →https://doi.org/10.1016/j.nbd.2003.12.016openalex-snapshot
The blood–brain barrier: an overview
inferredcites →https://doi.org/10.1016/j.neuint.2006.12.001openalex-snapshot
Copper and zinc as modulators of neuronal excitability in a physiologically significant concentration range
inferredcites →https://doi.org/10.1016/j.neuint.2010.07.010openalex-snapshot
Zinc-mediated attenuation of hippocampal mossy fiber long-term potentiation induced by forskolin
inferredcites →https://doi.org/10.1016/j.neuro.2007.06.005openalex-snapshot
Manganese inhibits NMDA receptor channel function: Implications to psychiatric and cognitive effects
inferredcites →https://doi.org/10.1016/j.neuropharm.2008.07.046openalex-snapshot
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
inferredcites →https://doi.org/10.1016/j.neuroscience.2008.01.061openalex-snapshot
Zinc at glutamatergic synapses
inferredcites →https://doi.org/10.1016/j.neuroscience.2008.10.009openalex-snapshot
Positive modulation of long-term potentiation at hippocampal CA1 synapses by low micromolar concentrations of zinc
inferredcites →https://doi.org/10.1016/j.neuroscience.2010.04.017openalex-snapshot
Increases in extracellular zinc in the amygdala in acquisition and recall of fear experience and their roles in response to fear
inferredcites →https://doi.org/10.1016/j.nurt.2008.05.001openalex-snapshot
Therapeutics for Alzheimer's Disease Based on the Metal Hypothesis
inferredcites →https://doi.org/10.1016/j.pharmthera.2005.11.004openalex-snapshot
Zinc and copper: Pharmacological probes and endogenous modulators of neuronal excitability
inferredcites →https://doi.org/10.1016/s0006-8993(01)02022-4openalex-snapshot
Cadmium toxicity in synaptic neurotransmission in the brain
inferredcites →https://doi.org/10.1016/s0006-8993(96)01009-8openalex-snapshot
The effects of copper ions on glutamate receptors in cultured rat cortical neurons
inferredcites →https://doi.org/10.1016/s0006-8993(98)00881-6openalex-snapshot
In vivo stimulation-induced release of manganese in rat amygdala
inferredcites →https://doi.org/10.1016/s0074-7742(08)60279-2openalex-snapshot
Neurobiology of Zinc and Zinc-Containing Neurons
inferredcites →https://doi.org/10.1016/s0165-0173(00)00044-8openalex-snapshot
Movement of zinc and its functional significance in the brain
inferredcites →https://doi.org/10.1016/s0165-0173(02)00234-5openalex-snapshot
Manganese action in brain function
inferredcites →https://doi.org/10.1016/s0165-0270(03)00173-0openalex-snapshot
Methods for studying synaptosomal copper release
inferredcites →https://doi.org/10.1016/s0165-6147(00)01541-8openalex-snapshot
Zn2+: a novel ionic mediator of neural injury in brain disease
inferredcites →https://doi.org/10.1016/s0166-2236(00)01610-6openalex-snapshot
Ca2+–Zn2+ permeable AMPA or kainate receptors: possible key factors in selective neurodegeneration
inferredcites →https://doi.org/10.1016/s0301-0082(98)00095-1openalex-snapshot
Group I metabotropic glutamate receptors: implications for brain diseases
inferredcites →https://doi.org/10.1016/s0896-6273(00)80763-1openalex-snapshot
Identification and Mechanism of Action of Two Histidine Residues Underlying High-Affinity Zn2+ Inhibition of the NMDA Receptor
inferredcites →https://doi.org/10.1016/s0896-6273(00)81149-6openalex-snapshot
The Actions of Synaptically Released Zinc at Hippocampal Mossy Fiber Synapses
inferredcites →https://doi.org/10.1038/308734a0openalex-snapshot
Release of endogenous Zn2+ from brain tissue during activity
inferredcites →https://doi.org/10.1038/328640a0openalex-snapshot
Micromolar concentrations of Zn2+ antagonize NMDA and GABA responses of hippocampal neurons
inferredcites →https://doi.org/10.1038/377115a0openalex-snapshot
Contrasting properties of two forms of long-term potentiation in the hippocampus
inferredcites →https://doi.org/10.1073/pnas.0605390103openalex-snapshot
Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity
inferredcites →https://doi.org/10.1073/pnas.0610923104openalex-snapshot
Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology
inferredcites →https://doi.org/10.1073/pnas.1031598100openalex-snapshot
Modulation of mitochondrial function by endogenous Zn 2+ pools
inferredcites →https://doi.org/10.1073/pnas.96.4.1716openalex-snapshot
Elimination of zinc from synaptic vesicles in the intact mouse brain by disruption of the ZnT 3 gene
inferredcites →https://doi.org/10.1074/jbc.m108808200openalex-snapshot
Zinc Inhibition of cAMP Signaling
inferredcites →https://doi.org/10.1074/jbc.m111263200openalex-snapshot
Growth Inhibitory Factor Prevents Neurite Extension and the Death of Cortical Neurons Caused by High Oxygen Exposure through Hydroxyl Radical Scavenging
inferredcites →https://doi.org/10.1089/ars.2006.8.1419openalex-snapshot
Zinc Coordination Environments in Proteins as Redox Sensors and Signal Transducers
inferredcites →https://doi.org/10.1093/clinchem/32.12.2187openalex-snapshot
Concentrations of zinc, iron, molybdenum, arsenic, and lithium in cerebrospinal fluid of patients with brain tumors.
inferredcites →https://doi.org/10.1101/lm.80705openalex-snapshot
A model of bidirectional synaptic plasticity: From signaling network to channel conductance
inferredcites →https://doi.org/10.1111/j.1460-9568.1996.tb01189.xopenalex-snapshot
Copper Modulation of NMDA Responses in Mouse and Rat Cultured Hippocampal Neurons
inferredcites →https://doi.org/10.1111/j.1471-4159.2004.02587.xopenalex-snapshot
Zinc inhibits glutamate release via activation of pre‐synaptic KATP channels and reduces ischaemic damage in rat hippocampus
inferredcites →https://doi.org/10.1111/j.1471-4159.2007.04825.xopenalex-snapshot
IP3 receptor/Ca2+ channel: from discovery to new signaling concepts
inferredcites →https://doi.org/10.1111/j.1474-9726.2007.00283.xopenalex-snapshot
Calcium homeostasis and modulation of synaptic plasticity in the aged brain
inferredcites →https://doi.org/10.1113/jphysiol.1987.sp016883openalex-snapshot
Permeation and block of N‐methyl‐D‐aspartic acid receptor channels by divalent cations in mouse cultured central neurones.
inferredcites →https://doi.org/10.1113/jphysiol.1988.sp017078openalex-snapshot
The role of divalent cations in the N‐methyl‐D‐aspartate responses of mouse central neurones in culture.
inferredcites →https://doi.org/10.1113/jphysiol.2002.020172openalex-snapshot
Zn 2+ currents are mediated by calcium‐permeable AMPA/Kainate channels in cultured murine hippocampal neurones
inferredcites →https://doi.org/10.1124/mol.51.6.1015openalex-snapshot
Differential Sensitivity of RecombinantN-Methyl-d-Aspartate Receptor Subtypes to Zinc Inhibition
inferredcites →https://doi.org/10.1124/mol.63.3.463openalex-snapshot
Calmodulin-Regulated Adenylyl Cyclases: Cross-Talk and Plasticity in the Central Nervous System
inferredcites →https://doi.org/10.1126/science.1350109openalex-snapshot
Microdomains of High Calcium Concentration in a Presynaptic Terminal
inferredcites →https://doi.org/10.1152/ajpcell.00541.2007openalex-snapshot
Insights into Zn2+ homeostasis in neurons from experimental and modeling studies
inferredcites →https://doi.org/10.1152/jn.1999.81.2.781openalex-snapshot
Selective Induction of LTP and LTD by Postsynaptic [Ca2+]i Elevation
inferredcites →https://doi.org/10.1248/jhs.47.520openalex-snapshot
Significance of Transferrin in Iron Delivery to the Brain
inferredcites →https://doi.org/10.1248/yakushi.124.577openalex-snapshot
Essential Trace Metals and Brain Function
inferredcites →https://doi.org/10.1254/jphs.09033scopenalex-snapshot
Modulation of the Substance P Release From Cultured Rat Primary Afferent Neurons by Zinc Ions
inferredcites →https://doi.org/10.1358/dnp.2006.19.8.1021492openalex-snapshot
Therapeutic Treatments for Alzheimer's Disease Based on Metal Bioavailability
inferredcites →https://doi.org/10.1523/jneurosci.1258-06.2006openalex-snapshot
Zinc Modulates Bidirectional Hippocampal Plasticity by Effects on NMDA Receptors
inferredcites →https://doi.org/10.1523/jneurosci.23-17-06847.2003openalex-snapshot
Evidence for Chelatable Zinc in the Extracellular Space of the Hippocampus, But Little Evidence for Synaptic Release of Zn
inferredcites →https://doi.org/10.1523/jneurosci.3699-04.2005openalex-snapshot
NMDA Receptor Activation Mediates Copper Homeostasis in Hippocampal Neurons
inferredcites →https://doi.org/10.1529/biophysj.106.103333openalex-snapshot
Zn2+ Sensitivity of High- and Low-Voltage Activated Calcium Channels
inferredcites →https://doi.org/10.3109/10408447509079857openalex-snapshot
Pekmeability Changes in the Blood-Brain Barrier: Causes and Consequences
inferredcites →https://doi.org/10.3233/jad-2006-102-309openalex-snapshot
Blood-brain barrier flux of aluminum, manganese, iron and other metals suspected to contribute to metal-induced neurodegeneration
inferredcites →https://doi.org/10.4061/2011/491597openalex-snapshot
Insight into Glutamate Excitotoxicity from Synaptic Zinc Homeostasis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118697191.ch10openalex-snapshot
Ligand Design to Target and Modulate Metal–Protein Interactions in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1002/cbdv.71623openalex-snapshot
Metal Ions in Longgu (Fossilized Bone) as a Natural Synergistic Network for Multi‐Target Therapy in Psychiatric Disorders
inferred← citeshttps://doi.org/10.1002/jnr.23143openalex-snapshot
Copper signaling in the mammalian nervous system: Synaptic effects
inferred← citeshttps://doi.org/10.1007/978-1-0716-1546-1_7openalex-snapshot
Molecular Insights into the Effect of Metals on Amyloid Aggregation
inferred← citeshttps://doi.org/10.1007/s10534-014-9790-zopenalex-snapshot
Abnormal metal levels in the primary visual pathway of the DBA/2J mouse model of glaucoma
inferred← citeshttps://doi.org/10.1007/s10534-014-9791-yopenalex-snapshot
Interaction of metal ions with neurotransmitter receptors and potential role in neurodiseases
inferred← citeshttps://doi.org/10.1016/bs.aiip.2023.01.005openalex-snapshot
Heavy metal pollutants: The hidden pervasive threat to honey bees and other pollinators
inferred← citeshttps://doi.org/10.1016/j.aca.2014.06.037openalex-snapshot
Three-dimensional printed sample load/inject valves enabling online monitoring of extracellular calcium and zinc ions in living rat brains
inferred← citeshttps://doi.org/10.1016/j.aca.2016.11.052openalex-snapshot
Using on-line solid phase extraction for in vivo speciation of diffusible ferrous and ferric iron in living rat brain extracellular fluid
inferred← citeshttps://doi.org/10.1016/j.anbehav.2026.123519openalex-snapshot
Associative learning in bumble bees is disrupted by high trace metal concentrations
inferred← citeshttps://doi.org/10.1016/j.bbapap.2014.11.005openalex-snapshot
Calcium binding to gatekeeper residues flanking aggregation-prone segments underlies non-fibrillar amyloid traits in superoxide dismutase 1 (SOD1)
inferred← citeshttps://doi.org/10.1016/j.bbr.2022.114163openalex-snapshot
Zinc Supplement Reverses Short-Term Memory Deficit in Sodium Benzoate-Induced Neurotoxicity in Male Wistar Rats by Enhancing Anti-Oxidative Capacity Via Nrf 2 Up-Regulation
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.03.012openalex-snapshot
Affinity of copper and zinc ions to proteins and peptides related to neurodegenerative conditions (Aβ, APP, α-synuclein, PrP)
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.04.004openalex-snapshot
Metal ions as modulators of protein conformation and misfolding in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.ccr.2021.213790openalex-snapshot
Metal ion coordination in peptide fragments of neurotrophins: A crucial step for understanding the role and signaling of these proteins in the brain
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.134089openalex-snapshot
Honey bees cannot sense harmful concentrations of metal pollutants in food
inferred← citeshttps://doi.org/10.1016/j.chroma.2013.12.047openalex-snapshot
A high-throughput microdialysis–parallel solid phase extraction–inductively coupled plasma mass spectrometry hyphenated system for continuous monitoring of extracellular metal ions in living rat brain
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2026.09.010openalex-snapshot
High levels of copper lead to cognitive impairment in major depressive disorder by inhibiting lncRNA NEAT1 and mitochondrial autophagy
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2015.11.006openalex-snapshot
Cognitive impairment in amyotrophic lateral sclerosis, clues from the SOD1 mouse
inferred← citeshttps://doi.org/10.1016/j.neuint.2013.01.023openalex-snapshot
The missing link in the amyloid cascade of Alzheimer’s disease – Metal ions
inferred← citeshttps://doi.org/10.1017/erm.2014.11openalex-snapshot
Copper as a key regulator of cell signalling pathways
inferred← citeshttps://doi.org/10.1021/acschemneuro.4c00280openalex-snapshot
Interplay between Copper, Phosphatidylserine, and α-Synuclein Suggests a Link between Copper Homeostasis and Synaptic Vesicle Cycling
inferred← citeshttps://doi.org/10.1021/acschemneuro.7b00121openalex-snapshot
Kinetic Analysis Reveals the Identity of Aβ-Metal Complex Responsible for the Initial Aggregation of Aβ in the Synapse
inferred← citeshttps://doi.org/10.1021/ar300074topenalex-snapshot
Therapeutic Redistribution of Metal Ions To Treat Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1021/cn300237ropenalex-snapshot
The Molecular Basis of Memory. Part 2: Chemistry of the Tripartite Mechanism
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Dynamics of ZnII Binding as a Key Feature in the Formation of Amyloid Fibrils by Aβ11-28
inferred← citeshttps://doi.org/10.1038/s41392-019-0063-8openalex-snapshot
History and progress of hypotheses and clinical trials for Alzheimer’s disease
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Misfolded proteins in Alzheimer's disease and type II diabetes
inferred← citeshttps://doi.org/10.1039/c2mt20018jopenalex-snapshot
Proposed glucocorticoid-mediated zinc signaling in the hippocampus
inferred← citeshttps://doi.org/10.1039/c3mt20106fopenalex-snapshot
Electroanalysis of the interaction between (−)-epigallocatechin-3-gallate (EGCG) and amyloid-β in the presence of copper
inferred← citeshttps://doi.org/10.1039/c3mt20231copenalex-snapshot
Copper modulates the large dense core vesicle secretory pathway in PC12 cells
inferred← citeshttps://doi.org/10.1039/c3mt20264jopenalex-snapshot
d-Histidine and l-histidine attenuate zinc-induced neuronal death in GT1-7 cells
inferred← citeshttps://doi.org/10.1039/c3mt20269kopenalex-snapshot
Synaptic Zn2+ homeostasis and its significance
inferred← citeshttps://doi.org/10.1039/c6mt00125dopenalex-snapshot
Iron accumulates in the primate choroid of the eye with aging as revealed with synchrotron X-ray fluorescence microscopy
inferred← citeshttps://doi.org/10.1039/c7mt00046dopenalex-snapshot
Cross talk between neurometals and amyloidogenic proteins at the synapse and the pathogenesis of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1039/d0dt01138jopenalex-snapshot
X1INH, an improved next-generation affinity-optimized hydrazonic ligand, attenuates abnormal copper( i )/copper( ii )-α-Syn interactions and affects protein aggregation in a cellular model of synucleinopathy
inferred← citeshttps://doi.org/10.1039/d4tb01093kopenalex-snapshot
A smart adaptable metal sequestering peptide conjugate to modulate Aβ fibrillar aggregation
inferred← citeshttps://doi.org/10.1042/ebc20160073openalex-snapshot
The zinc paradigm for metalloneurochemistry
inferred← citeshttps://doi.org/10.1074/jbc.m113.470740openalex-snapshot
Calcium Ions Promote Superoxide Dismutase 1 (SOD1) Aggregation into Non-fibrillar Amyloid
inferred← citeshttps://doi.org/10.1074/jbc.m114.570382openalex-snapshot
Novel Zinc-binding Site in the E2 Domain Regulates Amyloid Precursor-like Protein 1 (APLP1) Oligomerization
inferred← citeshttps://doi.org/10.1080/00218839.2023.2186018openalex-snapshot
Effects of octopamine on memory retention under chemical stress: a behavioral study on honey bees
inferred← citeshttps://doi.org/10.1101/2023.01.25.525351openalex-snapshot
Aluminium alters excitability by inhibiting calcium, sodium and potassium currents in bovine chromaffin cells
inferred← citeshttps://doi.org/10.1111/ejn.13104openalex-snapshot
Copper enhances cellular and network excitabilities, and improves temporal processing in the rat hippocampus
inferred← citeshttps://doi.org/10.1111/ejn.14575openalex-snapshot
Elevated zinc transporter ZnT3 in the dentate gyrus of mast cell‐deficient mice
inferred← citeshttps://doi.org/10.1111/jnc.14716openalex-snapshot
Copper and zinc ions govern the trans‐directed dimerization of APP family members in multiple ways
inferred← citeshttps://doi.org/10.1152/jn.00631.2013openalex-snapshot
In vivo and in vitro analyses of amygdalar function reveal a role for copper
inferred← citeshttps://doi.org/10.1155/2016/2680409openalex-snapshot
The Therapeutic Potential of Rosemary (Rosmarinus officinalis) Diterpenes for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1155/bca/4226220openalex-snapshot
Semax, a Copper Chelator Peptide, Decreases the Cu(II)‐Catalyzed ROS Production and Cytotoxicity of aβ by Metal Ion Stripping and Redox Silencing
inferred← citeshttps://doi.org/10.1242/jeb.241869openalex-snapshot
Metal pollutants have additive negative effects on honey bee cognition
inferred← citeshttps://doi.org/10.1371/journal.pone.0090070openalex-snapshot
Neuroprotective Copper Bis(thiosemicarbazonato) Complexes Promote Neurite Elongation
inferred← citeshttps://doi.org/10.1515/hsz-2024-0054openalex-snapshot
Zinc and copper effect mechanical cell adhesion properties of the amyloid precursor protein
inferred← citeshttps://doi.org/10.1523/jneurosci.0180-14.2014openalex-snapshot
Amyloid Precursor Protein Dimerization and Synaptogenic Function Depend on Copper Binding to the Growth Factor-Like Domain
inferred← citeshttps://doi.org/10.3389/fnagi.2014.00015openalex-snapshot
Increased metal content in the TDP-43A315T transgenic mouse model of frontotemporal lobar degeneration and amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.3389/fncel.2017.00297openalex-snapshot
Zinc as a Neuromodulator in the Central Nervous System with a Focus on the Olfactory Bulb
inferred← citeshttps://doi.org/10.3389/fneur.2018.00333openalex-snapshot
Prognostic Value of Serum Copper for Post-Stroke Clinical Recovery: A Pilot Study
inferred← citeshttps://doi.org/10.3389/fnins.2016.00233openalex-snapshot
Metal Ion Toxins and Brain Aquaporin-4 Expression: An Overview
inferred← citeshttps://doi.org/10.3389/fnmol.2017.00021openalex-snapshot
Structure and Synaptic Function of Metal Binding to the Amyloid Precursor Protein and its Proteolytic Fragments
inferred← citeshttps://doi.org/10.3390/biom12081015openalex-snapshot
The Role of Metals in the Neuroregenerative Action of BDNF, GDNF, NGF and Other Neurotrophic Factors
inferred← citeshttps://doi.org/10.3390/ijms141122067openalex-snapshot
The Molecular Mechanisms of Zinc Neurotoxicity and the Pathogenesis of Vascular Type Senile Dementia
inferred← citeshttps://doi.org/10.3390/ijms21207625openalex-snapshot
Development of Conformational Antibodies to Detect Bcl-xL’s Amyloid Aggregates in Metal-Induced Apoptotic Neuroblastoma Cells
inferred← citeshttps://doi.org/10.3390/molecules24162940openalex-snapshot
Complex of EGCG with Cu(II) Suppresses Amyloid Aggregation and Cu(II)-Induced Cytotoxicity of α-Synuclein
inferred← citeshttps://doi.org/10.3390/nu12082473openalex-snapshot
Food in Chronic Pain: Friend or Foe?
inferred← citeshttps://doi.org/10.3934/neuroscience.2021005openalex-snapshot
The biological pathways of Alzheimer disease: a review
inferred← citeshttps://doi.org/10.4018/978-1-5225-5282-6.ch008openalex-snapshot
Zinc and Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.4061/2011/292593openalex-snapshot
Glutamate‐Mediated Primary Somatosensory Cortex Excitability Correlated with Circulating Copper and Ceruloplasmin
inferred← citeshttps://doi.org/10.70675/96ecf2bfz4f00z4f48z990dz819088a03509openalex-snapshot
Impacts of metallic pollutants on honey bees : from the colony to the brain
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