On the public citation graph

Modulation of ERK1/MAPK3 potentiates ERK nuclear signalling, facilitates neuronal cell survival and improves memory in mouse models of neurodegenerative disorders

https://doi.org/10.1101/496141
0 signed · 58 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hipo.22769openalex-snapshot
C hronic impairment of ERK signaling in glutamatergic neurons of the forebrain does not affect spatial memory retention and LTP in the same manner as acute blockade of the ERK pathway
inferredcites →https://doi.org/10.1007/978-1-60761-795-2_12openalex-snapshot
Lentiviral Vectors to Study the Differential Function of ERK1 and ERK2 MAP Kinases
inferredcites →https://doi.org/10.1007/978-1-62703-251-3_17openalex-snapshot
The MPTP/Probenecid Model of Progressive Parkinson’s Disease
inferredcites →https://doi.org/10.1007/978-1-62703-791-4_9openalex-snapshot
Behavioral Methods for the Study of the Ras–ERK Pathway in Memory Formation and Consolidation: Passive Avoidance and Novel Object Recognition Tests
inferredcites →https://doi.org/10.1007/s007020100016openalex-snapshot
Phosphorylated mitogen-activated protein kinase (MAPK/ERK-P), protein kinase of 38 kDa (p38-P), stress-activated protein kinase (SAPK/JNK-P), and calcium/calmodulin-dependent kinase II (CaM kinase II) are differentially expressed in tau deposits in neurons and glial cells in tauopathies
inferredcites →https://doi.org/10.1016/bs.acr.2018.02.004openalex-snapshot
Extracellular-Regulated Kinases: Signaling From Ras to ERK Substrates to Control Biological Outcomes
inferredcites →https://doi.org/10.1016/j.bbr.2006.12.004openalex-snapshot
Sex differences in behavior and striatal ascorbate release in the 140 CAG knock-in mouse model of Huntington's disease
inferredcites →https://doi.org/10.1016/j.biopsych.2014.04.002openalex-snapshot
Derangement of Ras-Guanine Nucleotide-Releasing Factor 1 (Ras-GRF1) and Extracellular Signal-Regulated Kinase (ERK) Dependent Striatal Plasticity in L-DOPA-Induced Dyskinesia
inferredcites →https://doi.org/10.1016/j.biopsych.2016.06.016openalex-snapshot
Severe Intellectual Disability and Enhanced Gamma-Aminobutyric Acidergic Synaptogenesis in a Novel Model of Rare RASopathies
inferredcites →https://doi.org/10.1016/j.brainresbull.2011.07.021openalex-snapshot
Gene expression and behaviour in mouse models of HD
inferredcites →https://doi.org/10.1016/j.celrep.2015.10.009openalex-snapshot
Coordinated Regulation of Synaptic Plasticity at Striatopallidal and Striatonigral Neurons Orchestrates Motor Control
inferredcites →https://doi.org/10.1016/j.coph.2006.08.012openalex-snapshot
ERK2: a logical AND gate critical for drug-induced plasticity?
inferredcites →https://doi.org/10.1016/j.expneurol.2016.05.008openalex-snapshot
Cognitive training modifies disease symptoms in a mouse model of Huntington's disease
inferredcites →https://doi.org/10.1016/j.nbd.2017.10.015openalex-snapshot
cJun N-terminal kinase (JNK) mediates cortico-striatal signaling in a model of Parkinson's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2014.11.005openalex-snapshot
ERK (MAPK) does not phosphorylate tau under physiological conditions in vivo or in vitro
inferredcites →https://doi.org/10.1016/j.neuroscience.2015.04.026openalex-snapshot
Neuroprotective and anti-inflammatory properties of a novel non-thiazolidinedione PPARγ agonist in vitro and in MPTP-treated mice
inferredcites →https://doi.org/10.1016/j.nlm.2013.06.013openalex-snapshot
Molecular and cellular mechanisms of dopamine-mediated behavioral plasticity in the striatum
inferredcites →https://doi.org/10.1016/s0002-9440(10)63445-1openalex-snapshot
Okadaic-Acid-Induced Inhibition of Protein Phosphatase 2A Produces Activation of Mitogen-Activated Protein Kinases ERK1/2, MEK1/2, and p70 S6, Similar to That in Alzheimer's Disease
inferredcites →https://doi.org/10.1016/s0169-328x(02)00488-6openalex-snapshot
Up-regulation of mitogen-activated protein kinases ERK1/2 and MEK1/2 is associated with the progression of neurofibrillary degeneration in Alzheimer’s disease
inferredcites →https://doi.org/10.1016/s0306-4522(02)00205-1openalex-snapshot
Subacute systemic 3-nitropropionic acid intoxication induces a distinct motor disorder in adult C57Bl/6 mice: behavioural and histopathological characterisation
inferredcites →https://doi.org/10.1016/s0896-6273(02)00716-xopenalex-snapshot
Knockout of ERK1 MAP Kinase Enhances Synaptic Plasticity in the Striatum and Facilitates Striatal-Mediated Learning and Memory
inferredcites →https://doi.org/10.1038/2836openalex-snapshot
The MAPK cascade is required for mammalian associative learning
inferredcites →https://doi.org/10.1038/36849openalex-snapshot
A role for the Ras signalling pathway in synaptic transmission and long-term memory
inferredcites →https://doi.org/10.1038/76095openalex-snapshot
Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
inferredcites →https://doi.org/10.1038/nn.2709openalex-snapshot
Caspase-3 triggers early synaptic dysfunction in a mouse model of Alzheimer's disease
inferredcites →https://doi.org/10.1038/nrn1346openalex-snapshot
MAPK cascade signalling and synaptic plasticity
inferredcites →https://doi.org/10.1038/nrn3200openalex-snapshot
The ageing cortical synapse: hallmarks and implications for cognitive decline
inferredcites →https://doi.org/10.1038/tp.2012.58openalex-snapshot
Environmental enrichment rescues female-specific hyperactivity of the hypothalamic-pituitary-adrenal axis in a model of Huntington's disease
inferredcites →https://doi.org/10.1074/jbc.272.31.19103openalex-snapshot
A Requirement for the Mitogen-activated Protein Kinase Cascade in Hippocampal Long Term Potentiation
inferredcites →https://doi.org/10.1074/jbc.m408127200openalex-snapshot
Increased tau Phosphorylation in Apolipoprotein E4 Transgenic Mice Is Associated with Activation of Extracellular Signal-regulated Kinase
inferredcites →https://doi.org/10.1093/hmg/11.6.633openalex-snapshot
Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice
inferredcites →https://doi.org/10.1093/hmg/8.1.115openalex-snapshot
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse
inferredcites →https://doi.org/10.1093/hmg/9.4.503openalex-snapshot
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice
inferredcites →https://doi.org/10.1111/j.1601-183x.2006.00230.xopenalex-snapshot
Mitogen‐activated protein kinase/extracellular regulated kinase signalling and memory stabilization: a review
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07367.xopenalex-snapshot
ERK and cell death: ERK1/2 in neuronal death
inferredcites →https://doi.org/10.1111/j.1750-3639.2001.tb00387.xopenalex-snapshot
Phosphorylated Map Kinase (ERK1, ERK2) Expression is Associated with Early Tau Deposition in Neurones and Glial Cells, but not with Increased Nuclear DNA Vulnerability and Cell Death, in Alzheimer Disease, Pick's Disease, Progressive Supranuclear Palsy and Corticobasal Degeneration
inferredcites →https://doi.org/10.1126/science.1095760openalex-snapshot
Independent Cellular Processes for Hippocampal Memory Consolidation and Reconsolidation
inferredcites →https://doi.org/10.1126/science.6610213openalex-snapshot
Dopaminergic Neurotoxicity of 1-Methyl-4-Phenyl-1,2,5,6-Tetrahydropyridine in Mice
inferredcites →https://doi.org/10.1146/annurev-neuro-070815-014015openalex-snapshot
Alzheimer's Disease Mechanisms and Emerging Roads to Novel Therapeutics
inferredcites →https://doi.org/10.1186/jbiol38openalex-snapshot
ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially
inferredcites →https://doi.org/10.1371/journal.pone.0003873openalex-snapshot
The N-Terminal Domain of ERK1 Accounts for the Functional Differences with ERK2
inferredcites →https://doi.org/10.1371/journal.pone.0049838openalex-snapshot
Comprehensive Behavioral and Molecular Characterization of a New Knock-In Mouse Model of Huntington’s Disease: zQ175
inferredcites →https://doi.org/10.1371/journal.pone.0050717openalex-snapshot
Characterization of Neurophysiological and Behavioral Changes, MRI Brain Volumetry and 1H MRS in zQ175 Knock-In Mouse Model of Huntington's Disease
inferredcites →https://doi.org/10.1371/journal.pone.0164072openalex-snapshot
A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the HdhQ111 Mouse Model of Huntington’s Disease
inferredcites →https://doi.org/10.1523/eneuro.0149-16.2017openalex-snapshot
Activation of Ras-ERK Signaling and GSK-3 by Amyloid Precursor Protein and Amyloid Beta Facilitates Neurodegeneration in Alzheimer’s Disease
inferredcites →https://doi.org/10.1523/jneurosci.13-10-04181.1993openalex-snapshot
Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid
inferredcites →https://doi.org/10.1523/jneurosci.21-12-04125.2001openalex-snapshot
Beta-amyloid activates the mitogen-activated protein kinase cascade via hippocampal alpha7 nicotinic acetylcholine receptors: In vitro and in vivo mechanisms related to Alzheimer's disease.
inferredcites →https://doi.org/10.1523/jneurosci.3571-14.2015openalex-snapshot
Clathrin-Independent Trafficking of AMPA Receptors
inferredcites →https://doi.org/10.3233/jhd-170275openalex-snapshot
Modulating Neurotrophin Receptor Signaling as a Therapeutic Strategy for Huntington’s Disease
inferredcites →https://doi.org/10.3389/fnagi.2015.00245openalex-snapshot
Hippocampal Injections of Oligomeric Amyloid β-peptide (1–42) Induce Selective Working Memory Deficits and Long-lasting Alterations of ERK Signaling Pathway
inferredcites →https://doi.org/10.3389/fnbeh.2011.00079openalex-snapshot
Ras?ERK Signaling in Behavior: Old Questions and New Perspectives
inferredcites →https://doi.org/10.3389/fnbeh.2011.00084openalex-snapshot
ERK Pathway Activation Bidirectionally Affects Visual Recognition Memory and Synaptic Plasticity in the Perirhinal Cortex
inferredcites →https://doi.org/10.3389/fnbeh.2014.00135openalex-snapshot
Mood disorders in Huntington's disease: from behavior to cellular and molecular mechanisms
inferredcites →https://doi.org/10.3389/fnbeh.2015.00361openalex-snapshot
Cognitive Training at a Young Age Attenuates Deficits in the zQ175 Mouse Model of HD
inferredcites →https://doi.org/10.3389/neuro.02.001.2010openalex-snapshot
A simple role for BDNF in learning and memory?
inferredcites →https://doi.org/10.7554/elife.17111openalex-snapshot
Impairment of cocaine-mediated behaviours in mice by clinically relevant Ras-ERK inhibitors

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/slct.74510openalex-snapshot
Integrating Network Pharmacology and Molecular Docking to Uncover Neuroprotective Phytochemicals From Symplocos racemosa Roxb. in Mitigating Alzheimer's Disease
inferred← citeshttps://doi.org/10.1101/801563openalex-snapshot
Overlap in synaptic neurological condition susceptibility pathways and the neural pannexin 1 interactome revealed by bioinformatics analyses
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.