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Single‐Vesicle Electrochemistry Following Repetitive Stimulation Reveals a Mechanism for Plasticity Changes with Iron Deficiency
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.201404744openalex-snapshot
Nanoelectrode for Amperometric Monitoring of Individual Vesicular Exocytosis Inside Single Synapses
inferredcites →https://doi.org/10.1002/ange.201504839openalex-snapshot
Quantitative Measurement of Transmitters in Individual Vesicles in the Cytoplasm of Single Cells with Nanotip Electrodes
inferredcites →https://doi.org/10.1002/anie.201404744openalex-snapshot
Nanoelectrode for Amperometric Monitoring of Individual Vesicular Exocytosis Inside Single Synapses
inferredcites →https://doi.org/10.1002/anie.201504839openalex-snapshot
Quantitative Measurement of Transmitters in Individual Vesicles in the Cytoplasm of Single Cells with Nanotip Electrodes
inferredcites →https://doi.org/10.1002/anie.202200716openalex-snapshot
Single‐Vesicle Electrochemistry Following Repetitive Stimulation Reveals a Mechanism for Plasticity Changes with Iron Deficiency
inferredcites →https://doi.org/10.1002/cbic.202000622openalex-snapshot
Electrochemical Quantification of Neurotransmitters in Single Live Cell Vesicles Shows Exocytosis is Predominantly Partial
inferredcites →https://doi.org/10.1007/s10534-012-9550-xopenalex-snapshot
Iron deficiency on neuronal function
inferredcites →https://doi.org/10.1016/0006-8993(94)90827-3openalex-snapshot
Actions of (±)-7-hydroxy-N,N-dipropylaminotetralin (7-OH-DPAT) on dopamine synthesis in limbic and extrapyramidal regions of rat brain
inferredcites →https://doi.org/10.1016/0167-4889(85)90159-4openalex-snapshot
Relationship between dopamine content and its secretion in PC12 cells as a function of cell growth
inferredcites →https://doi.org/10.1016/0304-4157(90)90007-yopenalex-snapshot
Receptor-effector coupling by G proteins
inferredcites →https://doi.org/10.1016/j.brs.2017.01.078openalex-snapshot
Impaired rTMS-induced short-term neuroplasticity in restless legs syndrome: a pilot study
inferredcites →https://doi.org/10.1016/j.conb.2018.06.013openalex-snapshot
Synaptic plasticity in human cortical circuits: cellular mechanisms of learning and memory in the human brain?
inferredcites →https://doi.org/10.1016/j.jpeds.2011.12.011openalex-snapshot
Iron Deficiency in Infancy is Associated with Altered Neural Correlates of Recognition Memory at 10 Years
inferredcites →https://doi.org/10.1016/j.neubiorev.2015.09.020openalex-snapshot
Molecular regulation of dendritic spine dynamics and their potential impact on synaptic plasticity and neurological diseases
inferredcites →https://doi.org/10.1016/j.pharmthera.2004.10.012openalex-snapshot
Modulation of neurotransmitter release by the second messenger-activated protein kinases: Implications for presynaptic plasticity
inferredcites →https://doi.org/10.1016/j.sleep.2004.01.011openalex-snapshot
Motor cortex excitability in restless legs syndrome
inferredcites →https://doi.org/10.1016/j.sleep.2007.11.012openalex-snapshot
Abnormally increased CSF 3-Ortho-methyldopa (3-OMD) in untreated restless legs syndrome (RLS) patients indicates more severe disease and possibly abnormally increased dopamine synthesis
inferredcites →https://doi.org/10.1016/j.sleep.2016.08.019openalex-snapshot
In search of alternatives to dopaminergic ligands for the treatment of restless legs syndrome: iron, glutamate, and adenosine
inferredcites →https://doi.org/10.1016/j.trechm.2019.02.014openalex-snapshot
Analytical Techniques: Shedding Light upon Nanometer-Sized Secretory Vesicles
inferredcites →https://doi.org/10.1016/j.yexcr.2010.12.006openalex-snapshot
Iron chelation down-regulates dopamine transporter expression by decreasing mRNA stability and increasing endocytosis in N2a cells
inferredcites →https://doi.org/10.1016/s1474-4422(14)70117-6openalex-snapshot
The role of iron in brain ageing and neurodegenerative disorders
inferredcites →https://doi.org/10.1017/s0033583516000081openalex-snapshot
The evidence for open and closed exocytosis as the primary release mechanism
inferredcites →https://doi.org/10.1017/s0954579415000061openalex-snapshot
Early life nutrition and neural plasticity
inferredcites →https://doi.org/10.1021/acs.accounts.6b00331openalex-snapshot
Quantitative Chemical Measurements of Vesicular Transmitters with Electrochemical Cytometry
inferredcites →https://doi.org/10.1021/cb400665fopenalex-snapshot
Actin Controls the Vesicular Fraction of Dopamine Released During Extended Kiss and Run Exocytosis
inferredcites →https://doi.org/10.1021/cn900040eopenalex-snapshot
Only a Fraction of Quantal Content is Released During Exocytosis as Revealed by Electrochemical Cytometry of Secretory Vesicles
inferredcites →https://doi.org/10.1038/s41539-019-0048-yopenalex-snapshot
Is plasticity of synapses the mechanism of long-term memory storage?
inferredcites →https://doi.org/10.1038/sj.npp.1301559openalex-snapshot
Synaptic Plasticity: Multiple Forms, Functions, and Mechanisms
inferredcites →https://doi.org/10.1073/pnas.1910859116openalex-snapshot
Plasticity in exocytosis revealed through the effects of repetitive stimuli affect the content of nanometer vesicles and the fraction of transmitter released
inferredcites →https://doi.org/10.1073/pnas.73.7.2424openalex-snapshot
Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor.
inferredcites →https://doi.org/10.1083/jcb.110.5.1693openalex-snapshot
Biogenesis of synaptic vesicle-like structures in a pheochromocytoma cell line PC-12.
inferredcites →https://doi.org/10.1083/jcb.201810054openalex-snapshot
Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity
inferredcites →https://doi.org/10.1091/mbc.e13-05-0289openalex-snapshot
Protein kinase C activation decreases peripheral actin network density and increases central nonmuscle myosin II contractility in neuronal growth cones
inferredcites →https://doi.org/10.1093/brain/awp125openalex-snapshot
Altered dopaminergic profile in the putamen and substantia nigra in restless leg syndrome
inferredcites →https://doi.org/10.1093/jn/127.12.2282openalex-snapshot
In Vivo Dopamine Metabolism Is Altered in Iron-Deficient Anemic Rats
inferredcites →https://doi.org/10.1093/sleep/29.12.1595openalex-snapshot
Increasing Cortical Excitability: A Possible Explanation For The Proconvulsant Role Of Sleep Deprivation
inferredcites →https://doi.org/10.1093/sleep/29.6.770openalex-snapshot
Absence of Postexercise and Delayed Facilitation of Motor Cortex Excitability in Restless Legs Syndrome: Evidence of Altered Cortical Plasticity?
inferredcites →https://doi.org/10.1096/fj.202000167rropenalex-snapshot
Brain iron deficiency and affected contextual fear memory in mice with conditional Ferroportin1 ablation in the brain
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03547.xopenalex-snapshot
Regulation of striatal tyrosine hydroxylase phosphorylation by acute and chronic haloperidol
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04175.xopenalex-snapshot
Down‐regulation of dopamine transporter by iron chelationin vitrois mediated by altered trafficking, not synthesis
inferredcites →https://doi.org/10.1111/j.1748-1716.2007.01805.xopenalex-snapshot
The PC12 cell as model for neurosecretion
inferredcites →https://doi.org/10.1111/j.1749-6632.1990.tb31991.xopenalex-snapshot
Dopamine Autoreceptorsa Biochemical, Pharmacological, and Morphological Studies
inferredcites →https://doi.org/10.1124/jpet.108.138586openalex-snapshot
Antipsychotic-Like Properties of Phosphodiesterase 4 Inhibitors: Evaluation of 4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone (RO-20-1724) with Auditory Event-Related Potentials and Prepulse Inhibition of Startle
inferredcites →https://doi.org/10.1124/pr.116.013342openalex-snapshot
Synaptic Vesicle-Recycling Machinery Components as Potential Therapeutic Targets
inferredcites →https://doi.org/10.1126/science.285.5435.1870openalex-snapshot
Long-Term Potentiation--A Decade of Progress?
inferredcites →https://doi.org/10.1146/annurev.neuro.23.1.649openalex-snapshot
Synaptic Plasticity and Memory: An Evaluation of the Hypothesis
inferredcites →https://doi.org/10.1155/2018/3419871openalex-snapshot
The Role of fMRI in the Assessment of Neuroplasticity in MS: A Systematic Review
inferredcites →https://doi.org/10.1159/000314341openalex-snapshot
Gestational and Neonatal Iron Deficiency Alters Apical Dendrite Structure of CA1 Pyramidal Neurons in Adult Rat Hippocampus
inferredcites →https://doi.org/10.1177/15648265070284s409openalex-snapshot
Iron Deficiency and Child Development
inferredcites →https://doi.org/10.1182/blood-2008-10-183582openalex-snapshot
Unraveling a novel Rac1-mediated signaling pathway that regulates cofilin dephosphorylation and secretion in thrombin-stimulated platelets
inferredcites →https://doi.org/10.1523/jneurosci.0164-07.2007openalex-snapshot
Changes in Synaptic Morphology Accompany Actin Signaling during LTP
inferredcites →https://doi.org/10.1523/jneurosci.18-15-05575.1998openalex-snapshot
D 2 -Like Dopamine Autoreceptor Activation Reduces Quantal Size in PC12 Cells
inferredcites →https://doi.org/10.1523/jneurosci.2883-07.2007openalex-snapshot
Sustained Arc/Arg3.1 Synthesis Controls Long-Term Potentiation Consolidation through Regulation of Local Actin Polymerization in the Dentate GyrusIn Vivo
inferredcites →https://doi.org/10.1523/jneurosci.5351-12.2013openalex-snapshot
cAMP-Mediated Stabilization of Fusion Pores in Cultured Rat Pituitary Lactotrophs
inferredcites →https://doi.org/10.1590/s1807-59322011001300002openalex-snapshot
Long-term potentiation and long-term depression: a clinical perspective
inferredcites →https://doi.org/10.3390/ijms21249519openalex-snapshot
Mass Spectrometric Imaging of Plasma Membrane Lipid Alteration Correlated with Amperometrically Measured Activity-Dependent Plasticity in Exocytosis
inferredcites →https://doi.org/10.3390/ph12030126openalex-snapshot
Multilevel Impacts of Iron in the Brain: The Cross Talk between Neurophysiological Mechanisms, Cognition, and Social Behavior
inferredcites →https://doi.org/10.3390/ph14020095openalex-snapshot
Mechanisms of Intranasal Deferoxamine in Neurodegenerative and Neurovascular Disease
inferredcites →https://doi.org/10.3945/an.110.000190openalex-snapshot
The Role of Iron in Learning and Memory
inferredcites →https://doi.org/10.3945/jn.108.095224openalex-snapshot
Dopamine D2 Receptor Expression Is Altered by Changes in Cellular Iron Levels in PC12 Cells and Rat Brain Tissue
inferredcites →https://doi.org/10.4103/1673-5374.162698openalex-snapshot
A useful electroencephalography (EEG) marker of brain plasticity: delta waves
inferredcites →https://doi.org/10.7554/elife.41711openalex-snapshot
Fusion pore regulation by cAMP/Epac2 controls cargo release during insulin exocytosis
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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