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Tau drives translational selectivity by interacting with ribosomal proteins

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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/cm.970080303openalex-snapshot
Phosphorylation determines two distinct species of tau in the central nervous system
inferredcites →https://doi.org/10.1007/978-3-319-89689-2_11openalex-snapshot
Lost in Translation: Evidence for Protein Synthesis Deficits in ALS/FTD and Related Neurodegenerative Diseases
inferredcites →https://doi.org/10.1007/s00401-001-0488-2openalex-snapshot
Cerebellar cortical tau pathology in progressive supranuclear palsy and corticobasal degeneration
inferredcites →https://doi.org/10.1007/s00401-015-1487-zopenalex-snapshot
PERK inhibition prevents tau-mediated neurodegeneration in a mouse model of frontotemporal dementia
inferredcites →https://doi.org/10.1007/s00401-018-1895-yopenalex-snapshot
Changes in proteome solubility indicate widespread proteostatic disruption in mouse models of neurodegenerative disease
inferredcites →https://doi.org/10.1007/s004010000333openalex-snapshot
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells
inferredcites →https://doi.org/10.1016/0006-8993(93)91385-6openalex-snapshot
Alz-50 immunohistochemistry in the normal sheep striatum: a light and electron microscope study
inferredcites →https://doi.org/10.1016/0169-328x(89)90060-0openalex-snapshot
Alzheimer's disease-associated reduction of polysomal mRNA translation
inferredcites →https://doi.org/10.1016/0197-4580(94)00175-zopenalex-snapshot
Ultrastructure of neurofibrillary tangles in the cerebral cortex of sheep
inferredcites →https://doi.org/10.1016/j.biopsych.2013.02.027openalex-snapshot
Allosteric Heat Shock Protein 70 Inhibitors Rapidly Rescue Synaptic Plasticity Deficits by Reducing Aberrant Tau
inferredcites →https://doi.org/10.1016/j.ceb.2017.02.010openalex-snapshot
An emerging role for the ribosome as a nexus for post-translational modifications
inferredcites →https://doi.org/10.1016/j.cell.2017.05.022openalex-snapshot
The Mammalian Ribo-interactome Reveals Ribosome Functional Diversity and Heterogeneity
inferredcites →https://doi.org/10.1016/j.celrep.2016.04.045openalex-snapshot
Interaction of tau with the RNA-Binding Protein TIA1 Regulates tau Pathophysiology and Toxicity
inferredcites →https://doi.org/10.1016/j.jmb.2012.02.003openalex-snapshot
DnaJA1 Antagonizes Constitutive Hsp70-Mediated Stabilization of Tau
inferredcites →https://doi.org/10.1016/j.juro.2011.09.142openalex-snapshot
Gene Expression Analysis of Urine Sediment: Evaluation for Potential Noninvasive Markers of Interstitial Cystitis/Bladder Pain Syndrome
inferredcites →https://doi.org/10.1016/j.revsto.2016.04.003openalex-snapshot
Le syndrome de Stevens-Johnson–toxic epidermal necrolysis (SJSTEN) lié à un insecticide : second cas dans la littérature et implications potentielles
inferredcites →https://doi.org/10.1016/s0021-9258(19)39286-5openalex-snapshot
Kinetic determination of the effects of ADP-ribosylation on the interaction of eukaryotic elongation factor 2 with ribosomes.
inferredcites →https://doi.org/10.1038/16729openalex-snapshot
Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase
inferredcites →https://doi.org/10.1038/nature11058openalex-snapshot
Sustained translational repression by eIF2α-P mediates prion neurodegeneration
inferredcites →https://doi.org/10.1038/nmeth.1314openalex-snapshot
SUnSET, a nonradioactive method to monitor protein synthesis
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nrm3993openalex-snapshot
The ribosome prophecy
inferredcites →https://doi.org/10.1038/s41593-017-0022-zopenalex-snapshot
Reducing the RNA binding protein TIA1 protects against tau-mediated neurodegeneration in vivo
inferredcites →https://doi.org/10.1073/pnas.1013063108openalex-snapshot
Inhibition of the interactions between eukaryotic initiation factors 4E and 4G impairs long-term associative memory consolidation but not reconsolidation
inferredcites →https://doi.org/10.1074/jbc.m115.682161openalex-snapshot
Requirement of Neuronal Ribosome Synthesis for Growth and Maintenance of the Dendritic Tree
inferredcites →https://doi.org/10.1074/jbc.m700906200openalex-snapshot
RAS/ERK Signaling Promotes Site-specific Ribosomal Protein S6 Phosphorylation via RSK and Stimulates Cap-dependent Translation
inferredcites →https://doi.org/10.1074/mcp.m115.050724openalex-snapshot
The Human Tau Interactome: Binding to the Ribonucleoproteome, and Impaired Binding of the Proline-to-Leucine Mutant at Position 301 (P301L) to Chaperones and the Proteasome
inferredcites →https://doi.org/10.1080/15476286.2015.1085149openalex-snapshot
Cis-regulatory RNA elements that regulate specialized ribosome activity
inferredcites →https://doi.org/10.1089/ars.2012.4984openalex-snapshot
FUsed in Sarcoma Is a Novel Regulator of Manganese Superoxide Dismutase Gene Transcription
inferredcites →https://doi.org/10.1093/bioinformatics/19.2.185openalex-snapshot
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
inferredcites →https://doi.org/10.1093/gerona/glu314openalex-snapshot
Intranasal Insulin Improves Age-Related Cognitive Deficits and Reverses Electrophysiological Correlates of Brain Aging
inferredcites →https://doi.org/10.1093/nar/gkn248openalex-snapshot
Comprehensive detection of human terminal oligo-pyrimidine (TOP) genes and analysis of their characteristics
inferredcites →https://doi.org/10.1093/nar/gkx1308openalex-snapshot
Oxidative stress damages rRNA inside the ribosome and differentially affects the catalytic center
inferredcites →https://doi.org/10.1101/lm.041947.116openalex-snapshot
Synaptic activation of ribosomal protein S6 phosphorylation occurs locally in activated dendritic domains
inferredcites →https://doi.org/10.1101/lm.044974.117openalex-snapshot
Synaptically driven phosphorylation of ribosomal protein S6 is differentially regulated at active synapses versus dendrites and cell bodies by MAPK and PI3K/mTOR signaling pathways
inferredcites →https://doi.org/10.1101/lm.1027208openalex-snapshot
De novo mRNA synthesis is required for both consolidation and reconsolidation of fear memories in the amygdala
inferredcites →https://doi.org/10.1111/acel.12057openalex-snapshot
mTOR regulates tau phosphorylation and degradation: implications for Alzheimer's disease and other tauopathies
inferredcites →https://doi.org/10.1111/bpa.12335openalex-snapshot
Altered Machinery of Protein Synthesis in Alzheimer's: From the Nucleolus to the Ribosome
inferredcites →https://doi.org/10.1111/j.1471-4159.2008.05470.xopenalex-snapshot
Forskolin induction of late‐LTP and up‐regulation of 5′ TOP mRNAs translation via mTOR, ERK, and PI3K in hippocampal pyramidal cells
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07057.xopenalex-snapshot
Proteomic characterization of lipid raft proteins in amyotrophic lateral sclerosis mouse spinal cord
inferredcites →https://doi.org/10.1126/science.1113694openalex-snapshot
Tau Suppression in a Neurodegenerative Mouse Model Improves Memory Function
inferredcites →https://doi.org/10.1126/science.6206567openalex-snapshot
Alzheimer's Disease Brain: Alterations in RNA Levels and in a Ribonuclease-Inhibitor Complex
inferredcites →https://doi.org/10.1128/mcb.21.24.8671-8683.2001openalex-snapshot
Amino Acid-Induced Translation of TOP mRNAs Is Fully Dependent on Phosphatidylinositol 3-Kinase-Mediated Signaling, Is Partially Inhibited by Rapamycin, and Is Independent of S6K1 and rpS6 Phosphorylation
inferredcites →https://doi.org/10.1136/jnnp.44.2.97openalex-snapshot
Alterations in protein synthetic capability of nerve cells in Alzheimer's disease.
inferredcites →https://doi.org/10.1159/000337230openalex-snapshot
Amyloid Oligomers Exacerbate Tau Pathology in a Mouse Model of Tauopathy
inferredcites →https://doi.org/10.1161/atvbaha.117.310035openalex-snapshot
Sex Chromosome Complement Defines Diffuse Versus Focal Angiotensin II–Induced Aortic Pathology
inferredcites →https://doi.org/10.1186/s40478-017-0489-6openalex-snapshot
Atypical, non-standard functions of the microtubule associated Tau protein
inferredcites →https://doi.org/10.1261/rna.1037108openalex-snapshot
All translation elongation factors and the e, f, and h subunits of translation initiation factor 3 are encoded by 5′-terminal oligopyrimidine (TOP) mRNAs
inferredcites →https://doi.org/10.1371/journal.pone.0008556openalex-snapshot
LDLR Expression and Localization Are Altered in Mouse and Human Cell Culture Models of Alzheimer's Disease
inferredcites →https://doi.org/10.1523/jneurosci.22-01-00133.2002openalex-snapshot
Neurodegeneration with Tau Accumulation in a Transgenic Mouse Expressing V337M Human Tau
inferredcites →https://doi.org/10.1523/jneurosci.2234-17.2017openalex-snapshot
FK506-Binding Protein 12.6/1b, a Negative Regulator of [Ca2+], Rescues Memory and Restores Genomic Regulation in the Hippocampus of Aging Rats
inferredcites →https://doi.org/10.1523/jneurosci.3029-15.2016openalex-snapshot
Pathological Tau Promotes Neuronal Damage by Impairing Ribosomal Function and Decreasing Protein Synthesis
inferredcites →https://doi.org/10.1523/jneurosci.3040-05.2005openalex-snapshot
Ribosome Dysfunction Is an Early Event in Alzheimer's Disease
inferredcites →https://doi.org/10.1523/jneurosci.3155-10.2010openalex-snapshot
Phosphorylation Dynamics Regulate Hsp27-Mediated Rescue of Neuronal Plasticity Deficits in Tau Transgenic Mice
inferredcites →https://doi.org/10.1523/jneurosci.3279-05.2005openalex-snapshot
Age-Dependent Neurofibrillary Tangle Formation, Neuron Loss, and Memory Impairment in a Mouse Model of Human Tauopathy (P301L)
inferredcites →https://doi.org/10.1523/jneurosci.4599-08.2009openalex-snapshot
Hippocampal and Cognitive Aging across the Lifespan: A Bioenergetic Shift Precedes and Increased Cholesterol Trafficking Parallels Memory Impairment
inferredcites →https://doi.org/10.1523/jneurosci.5397-12.2013openalex-snapshot
Tau Accumulation Activates the Unfolded Protein Response by Impairing Endoplasmic Reticulum-Associated Degradation
inferredcites →https://doi.org/10.3233/jad-150298openalex-snapshot
Identification of Novel Tau Interactions with Endoplasmic Reticulum Proteins in Alzheimer’s Disease Brain
inferredcites →https://doi.org/10.3389/fncel.2018.00220openalex-snapshot
The Involvement of Aβ42 and Tau in Nucleolar and Protein Synthesis Machinery Dysfunction
inferredcites →https://doi.org/10.3389/fnmol.2015.00075openalex-snapshot
Ribosomal Protein S6 Phosphorylation in the Nervous System: From Regulation to Function
inferredcites →https://doi.org/10.4161/21690731.2014.983402openalex-snapshot
Regulation of global and specific mRNA translation by the mTOR signaling pathway

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3751054openalex-extracted
A Complex Containing HNRNPA2B1 and N 6-Methyladenosine Modified Transcripts Mediates Actions of Toxic Tau Oligomers
inferred← citeshttps://doi.org/10.1002/alz.13784openalex-snapshot
The six brain‐specific TAU isoforms and their role in Alzheimer's disease and related neurodegenerative dementia syndromes
inferred← citeshttps://doi.org/10.1002/alz.70078openalex-snapshot
Insights into pathophysiology, biomarkers, and therapeutics in tauopathies: Proceedings of the Tau2024 Global Conference
inferred← citeshttps://doi.org/10.1002/alz.70339openalex-snapshot
Cell‐specific protein expression in Alzheimer's disease prefrontal cortex
inferred← citeshttps://doi.org/10.1002/alz.70852openalex-snapshot
Long‐read sequencing reveals genomic and epigenomic variation in the dark genome of human Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/bies.202200230openalex-snapshot
To aggregate or not to aggregate – Is it a matter of the ribosome?
inferred← citeshttps://doi.org/10.1002/cm.21781openalex-snapshot
Break and accelerator—The mechanics of Tau (and amyloid) toxicity
inferred← citeshttps://doi.org/10.1002/iub.70030openalex-snapshot
Tyrosine and Phenylalanine Activate Neuronal DNA Repair but Exhibit Opposing Effects on Global Transcription and Adult Female Mice Are Resilient to TyrRS / YARS1 Depletion
inferred← citeshttps://doi.org/10.1002/pmic.70018openalex-snapshot
Mining Alzheimer's Interactomes, Macromolecular Complexes and Pathways for Drug Discovery
inferred← citeshttps://doi.org/10.1007/s00221-020-05855-2openalex-snapshot
Comparison of proteome alterations during aging in the temporal lobe of humans and rhesus macaques
inferred← citeshttps://doi.org/10.1007/s10571-019-00741-0openalex-snapshot
Elucidating Critical Proteinopathic Mechanisms and Potential Drug Targets in Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s10571-020-00875-6openalex-snapshot
Mechanisms of Regulation and Diverse Activities of Tau-Tubulin Kinase (TTBK) Isoforms
inferred← citeshttps://doi.org/10.1007/s11033-023-08889-1openalex-snapshot
BANF1 promotes glutamate-induced apoptosis of HT-22 hippocampal neurons
inferred← citeshttps://doi.org/10.1007/s12035-022-02809-3openalex-snapshot
Tau Toxicity in Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s12272-026-01629-6openalex-snapshot
Integrative multi-omics analyses reveal nuclear noncoding RNA-mediated regulatory landscape in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.04.021openalex-snapshot
The pathophysiology of neurodegenerative disease: Disturbing the balance between phase separation and irreversible aggregation
inferred← citeshttps://doi.org/10.1016/j.abst.2025.12.004openalex-snapshot
Multi-omics integration and machine learning reveal biomarker networks and therapeutic targets in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bcp.2020.113945openalex-snapshot
Alzheimer’s disease beyond amyloid: Can the repetitive failures of amyloid-targeted therapeutics inform future approaches to dementia drug discovery?
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2020.12.015openalex-snapshot
De novo proteomic methods for examining the molecular mechanisms underpinning long-term memory
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2022.10.017openalex-snapshot
Posttranscriptional regulation of neurofilament proteins and tau in health and disease
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109035openalex-snapshot
SIRT6-CBP-dependent nuclear Tau accumulation and its role in protein synthesis
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.04.014openalex-snapshot
The science of puromycin: From studies of ribosome function to applications in biotechnology
inferred← citeshttps://doi.org/10.1016/j.ejphar.2026.179033openalex-snapshot
Ribosome impairment, tau alternative splicing, and stress granules: a convergent axis of neuronal vulnerability driving Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113180openalex-snapshot
The effects of mild closed head injuries on tauopathy and cognitive deficits in rodents: Primary results in wild type and rTg4510 mice, and a systematic review
inferred← citeshttps://doi.org/10.1016/j.expneurol.2021.113766openalex-snapshot
Effects of altered tau expression on dentate granule cell excitability in mice
inferred← citeshttps://doi.org/10.1016/j.expneurol.2023.114510openalex-snapshot
Experimental upregulation of developmentally downregulated ribosomal protein large subunits 7 and 7A promotes axon regeneration after injury in vivo
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104832openalex-snapshot
Co-expression network analysis of human tau-transgenic mice reveals protein modules associated with tau-induced pathologies
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115501openalex-snapshot
Structural evidence that RNA contributes to polymorphism of tau amyloid fibrils
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102132openalex-snapshot
RNA induces unique tau strains and stabilizes Alzheimer’s disease seeds
inferred← citeshttps://doi.org/10.1016/j.mad.2021.111594openalex-snapshot
Effect of age on the vascular proteome in middle cerebral arteries and mesenteric resistance arteries in mice
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.07.038openalex-snapshot
Interaction of tau with HNRNPA2B1 and N6-methyladenosine RNA mediates the progression of tauopathy
inferred← citeshttps://doi.org/10.1016/j.nbd.2020.104939openalex-snapshot
Tau-mediated dysregulation of RNA: Evidence for a common molecular mechanism of toxicity in frontotemporal dementia and other tauopathies
inferred← citeshttps://doi.org/10.1016/j.neuri.2021.100036openalex-snapshot
Neuronetworks: Analysis of brain pathology in Mucopolysaccharidoses – A systems biology approach
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2026.04.006openalex-snapshot
Predicted brain-regional gene expression patterns in individuals living with Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.neuron.2023.05.033openalex-snapshot
Increased G3BP2-Tau interaction in tauopathies is a natural defense against Tau aggregation
inferred← citeshttps://doi.org/10.1016/j.neuron.2026.08.032openalex-snapshot
Tau phosphorylation from neuronal adaptation to Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2022.07.015openalex-snapshot
Neuronal nuclear tau and neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2020.101892openalex-snapshot
Chronic PERK induction promotes Alzheimer-like neuropathology in Down syndrome: Insights for therapeutic intervention
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2023.102500openalex-snapshot
Selective neuronal vulnerability to deficits in RNA processing
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2025.102872openalex-snapshot
Translated retained intron 11 sequence confers pathological properties to Tau in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00476openalex-snapshot
Elucidation of the GSK3α Structure Informs the Design of Novel, Paralog-Selective Inhibitors
inferred← citeshttps://doi.org/10.1038/s41380-023-02088-xopenalex-snapshot
CPEB and translational control by cytoplasmic polyadenylation: impact on synaptic plasticity, learning, and memory
inferred← citeshttps://doi.org/10.1038/s41419-022-05324-4openalex-snapshot
Protein synthesis inhibition and loss of homeostatic functions in astrocytes from an Alzheimer’s disease mouse model: a role for ER-mitochondria interaction
inferred← citeshttps://doi.org/10.1038/s41419-024-06815-2openalex-snapshot
TauP301L disengages from the proteosome core complex and neurogranin coincident with enhanced neuronal network excitability
inferred← citeshttps://doi.org/10.1038/s41420-022-01186-zopenalex-snapshot
Overexpressing eukaryotic elongation factor 1 alpha (eEF1A) proteins to promote corticospinal axon repair after injury
inferred← citeshttps://doi.org/10.1038/s41467-023-40208-xopenalex-snapshot
Compilation of reported protein changes in the brain in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1038/s41598-020-61777-7openalex-snapshot
Tau protein- induced sequestration of the eukaryotic ribosome: Implications in neurodegenerative disease
inferred← citeshttps://doi.org/10.1038/s41598-021-84214-9openalex-snapshot
Whole genome methylation and transcriptome analyses to identify risk for cerebral palsy (CP) in extremely low gestational age neonates (ELGAN)
inferred← citeshttps://doi.org/10.1038/s41598-023-28081-6openalex-snapshot
Investigation of early molecular alterations in tauopathy with generative adversarial networks
inferred← citeshttps://doi.org/10.1074/jbc.ra120.015882openalex-snapshot
A combinatorial native MS and LC-MS/MS approach reveals high intrinsic phosphorylation of human Tau but minimal levels of other key modifications
inferred← citeshttps://doi.org/10.1093/bib/bbag275openalex-snapshot
Nonlinear kernel-based high-dimensional inference for set-based genetic association studies
inferred← citeshttps://doi.org/10.1093/braincomms/fcaa039openalex-snapshot
Passive immunotherapy for N-truncated tau ameliorates the cognitive deficits in two mouse Alzheimer’s disease models
inferred← citeshttps://doi.org/10.1101/2020.07.31.229583openalex-snapshot
Broad kinase inhibition mitigates early neuronal dysfunction and cognitive deficits in tauopathy
inferred← citeshttps://doi.org/10.1101/2020.08.09.243402openalex-snapshot
Susceptibility to gingipains and transcriptomic response to P. gingivalis highlights the ribosome, hypothalamus, and cholinergic neurons
inferred← citeshttps://doi.org/10.1101/2020.12.03.409334openalex-snapshot
A Complex Containing HNRNPA2B1 and N 6 -methyladenosine Modified Transcripts Mediates Actions of Toxic Tau Oligomers
inferred← citeshttps://doi.org/10.1101/2022.10.28.514304openalex-snapshot
Single-cell RNA-seq reveals alterations in peripheral CX3CR1 and nonclassical monocytes in familial tauopathy
inferred← citeshttps://doi.org/10.1101/2023.04.13.536828openalex-snapshot
Compilation of all known protein changes in the human Alzheimer’s disease brain
inferred← citeshttps://doi.org/10.1101/2025.03.28.645932openalex-snapshot
GVB+ neurons are resilient to tau-induced protein synthesis impairment
inferred← citeshttps://doi.org/10.1101/2025.04.17.649250openalex-snapshot
Mapping the spatiotemporal dynamics of de novo protein synthesis during long-term memory formation
inferred← citeshttps://doi.org/10.1101/2025.08.29.670302openalex-snapshot
Modified tau leads to neuronal and global ribosome dysfunction in C. elegans model of tauopathy
inferred← citeshttps://doi.org/10.1101/2025.10.15.682650openalex-snapshot
Elevation of the mechanically-sensitive protein emerin links nuclear mechanotransduction to tau-induced cytoskeletal remodeling in neurons
inferred← citeshttps://doi.org/10.1111/acel.14245openalex-snapshot
Pathogenic tau induces an adaptive elevation in mRNA translation rate at early stages of disease
inferred← citeshttps://doi.org/10.1111/cns.14304openalex-snapshot
Effects of heterologous human tau protein expression in yeast models of proteotoxic stress response
inferred← citeshttps://doi.org/10.1111/jfd.13346openalex-snapshot
Comparative proteomic analysis provides insight into the key proteins as potential targets underlying the effect of malachite green against Ichthyophthirius multifiliis
inferred← citeshttps://doi.org/10.1126/sciadv.aea8940openalex-snapshot
Neurons with granulovacuolar degeneration bodies are resilient to tau-induced protein synthesis impairment
inferred← citeshttps://doi.org/10.1155/2020/4505720openalex-snapshot
Differential Expression of mRNAs in Peripheral Blood Related to Prodrome and Progression of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.11648/j.ajep.20150406.15openalex-snapshot
Studies on Physicochemical Properties of Biofield Treated 2,4-Dichlorophenol
inferred← citeshttps://doi.org/10.1177/10738584231154551openalex-snapshot
Tau, RNA, and RNA-Binding Proteins: Complex Interactions in Health and Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1186/s12915-021-01132-yopenalex-snapshot
Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope
inferred← citeshttps://doi.org/10.1186/s13024-020-00389-1openalex-snapshot
FRET-based Tau seeding assay does not represent prion-like templated assembly of Tau filaments
inferred← citeshttps://doi.org/10.1186/s13024-020-00392-6openalex-snapshot
Deciphering cellular transcriptional alterations in Alzheimer’s disease brains
inferred← citeshttps://doi.org/10.1186/s13024-020-00405-4openalex-snapshot
Integrated analysis of the aging brain transcriptome and proteome in tauopathy
inferred← citeshttps://doi.org/10.1186/s13024-022-00526-yopenalex-snapshot
Alzheimer risk gene product Pyk2 suppresses tau phosphorylation and phenotypic effects of tauopathy
inferred← citeshttps://doi.org/10.1186/s13024-022-00572-6openalex-snapshot
Tau interactome and RNA binding proteins in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1186/s13024-023-00664-xopenalex-snapshot
Simple model systems reveal conserved mechanisms of Alzheimer’s disease and related tauopathies
inferred← citeshttps://doi.org/10.1186/s13073-023-01205-3openalex-snapshot
Single-cell RNA-seq reveals alterations in peripheral CX3CR1 and nonclassical monocytes in familial tauopathy
inferred← citeshttps://doi.org/10.1186/s40478-021-01208-4openalex-snapshot
Altered ribosomal function and protein synthesis caused by tau
inferred← citeshttps://doi.org/10.1186/s40478-022-01324-9openalex-snapshot
Differential protein expression in the hippocampi of resilient individuals identified by digital spatial profiling
inferred← citeshttps://doi.org/10.13023/etd.2019.368openalex-snapshot
Pathological Tau as a Cause, and Consequence, of Cellular Dysfunction
inferred← citeshttps://doi.org/10.13023/etd.2021.271openalex-snapshot
THE ROLE OF MICROTUBULE-ASSOCIATED PROTEIN TAU IN NEURONAL EXCITABILITY AND EPILEPTOGENESIS
inferred← citeshttps://doi.org/10.1371/journal.pone.0228771openalex-snapshot
Acute inhibition of the CNS-specific kinase TTBK1 significantly lowers tau phosphorylation at several disease relevant sites
inferred← citeshttps://doi.org/10.1523/eneuro.0255-20.2020openalex-snapshot
Donor-Specific Transcriptomic Analysis of Alzheimer's Disease-Associated Hypometabolism Highlights a Unique Donor, Ribosomal Proteins and Microglia
inferred← citeshttps://doi.org/10.1523/jneurosci.0391-19.2019openalex-snapshot
DrosophilaTau Negatively Regulates Translation and Olfactory Long-Term Memory, But Facilitates Footshock Habituation and Cytoskeletal Homeostasis
inferred← citeshttps://doi.org/10.1523/jneurosci.0435-21.2021openalex-snapshot
APOE4 Affects Basal and NMDAR-Mediated Protein Synthesis in Neurons by Perturbing Calcium Homeostasis
inferred← citeshttps://doi.org/10.1523/jneurosci.1727-25.2026openalex-snapshot
Progressive Supranuclear Palsy PERK Haplotype B Selectively Translates DLX1 Promoting Tau Toxicity
inferred← citeshttps://doi.org/10.1523/jneurosci.2324-22.2023openalex-snapshot
ZCCHC17 Modulates Neuronal RNA Splicing and Supports Cognitive Resilience in Alzheimer's Disease
inferred← citeshttps://doi.org/10.2174/0929866529666220905112156openalex-snapshot
Amplification of Amyloid Protein-induced Aggregation of the Eukaryotic Ribosome
inferred← citeshttps://doi.org/10.23889/suthesis.62147openalex-snapshot
Analysis of Adult Hippocampal Neurogenesis in Neurodegenerative disease
inferred← citeshttps://doi.org/10.3233/jad-215357openalex-snapshot
Transcriptome and Translatome Regulation of Pathogenesis in Alzheimer’s Disease Model Mice
inferred← citeshttps://doi.org/10.3389/ebm.2024.10057openalex-snapshot
Transcriptional-profile changes in the medial geniculate body after noise-induced tinnitus
inferred← citeshttps://doi.org/10.3389/fnagi.2021.650740openalex-snapshot
Stress Granules and Neurodegenerative Disorders: A Scoping Review
inferred← citeshttps://doi.org/10.3389/fncel.2020.594561openalex-snapshot
Cytoplasmic Expression of the ALS/FTD-Related Protein TDP-43 Decreases Global Translation Both in vitro and in vivo
inferred← citeshttps://doi.org/10.3389/fncel.2021.668500openalex-snapshot
Contribution of Energy Dysfunction to Impaired Protein Translation in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3389/fneur.2020.01056openalex-snapshot
Nuclear Transport Deficits in Tau-Related Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3389/fnins.2022.966877openalex-snapshot
Temporal Cortex Microarray Analysis Revealed Impaired Ribosomal Biogenesis and Hyperactivity of the Glutamatergic System: An Early Signature of Asymptomatic Alzheimer's Disease
inferred← citeshttps://doi.org/10.3389/fnins.2024.1372297openalex-snapshot
β-amyloid accumulation enhances microtubule associated protein tau pathology in an APPNL-G-F/MAPTP301S mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnmol.2021.623659openalex-snapshot
Targeted Quantification of Detergent-Insoluble RNA-Binding Proteins in Human Brain Reveals Stage and Disease Specific Co-aggregation in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fnmol.2021.742790openalex-snapshot
Tau Modulates mRNA Transcription, Alternative Polyadenylation Profiles of hnRNPs, Chromatin Remodeling and Spliceosome Complexes
inferred← citeshttps://doi.org/10.3389/fphar.2025.1600176openalex-snapshot
Distinct neuroprotective and anti-inflammatory effects of Kampo formulas ninjinyoeito and juzentaihoto in depression-like SAMP8 mice
inferred← citeshttps://doi.org/10.3390/biom10111487openalex-snapshot
Prion-Like Propagation Mechanisms in Tauopathies and Traumatic Brain Injury: Challenges and Prospects
inferred← citeshttps://doi.org/10.3390/biomedicines10020241openalex-snapshot
Tau mRNA Metabolism in Neurodegenerative Diseases: A Tangle Journey
inferred← citeshttps://doi.org/10.3390/biomedicines10081772openalex-snapshot
Proteomic Assessment of C57BL/6 Hippocampi after Non-Selective Pharmacological Inhibition of Nitric Oxide Synthase Activity: Implications of Seizure-like Neuronal Hyperexcitability Followed by Tauopathy
inferred← citeshttps://doi.org/10.3390/biomedicines13010029openalex-snapshot
Novel Role of Pin1-Cis P-Tau-ApoE Axis in the Pathogenesis of Preeclampsia and Its Connection with Dementia
inferred← citeshttps://doi.org/10.3390/cells11050840openalex-snapshot
What’s in a Gene? The Outstanding Diversity of MAPT
inferred← citeshttps://doi.org/10.3390/cells15151365openalex-snapshot
The Interactions of Tau, RNA, and Stress Granules in Neurodegenerative Disease: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/cells15171596openalex-snapshot
The Paradox of Tau and RNA-Binding Proteins: How Adaptive Stress Granule Regulation Becomes Pathological with Aging
inferred← citeshttps://doi.org/10.3390/ijms20143524openalex-snapshot
Proteomic Techniques to Examine Neuronal Translational Dynamics
inferred← citeshttps://doi.org/10.3390/ijms22031186openalex-snapshot
Broad Kinase Inhibition Mitigates Early Neuronal Dysfunction in Tauopathy
inferred← citeshttps://doi.org/10.3390/ijms23116039openalex-snapshot
Altered Brain Arginine Metabolism and Polyamine System in a P301S Tauopathy Mouse Model: A Time-Course Study
inferred← citeshttps://doi.org/10.3390/ijms26199741openalex-snapshot
Temporal Interactome Mapping of Human Tau in Drosophila Reveals Progressive Mitochondrial Engagement and Porin/VDAC1-Dependent Modulation of Toxicity
inferred← citeshttps://doi.org/10.3390/ijms27010455openalex-snapshot
Mutant Tau (P301L) Enhances Global Protein Translation in Differentiated SH-SY5Y Cells by Upregulating mTOR Signalling
inferred← citeshttps://doi.org/10.37247/pamb.1.2020.7openalex-snapshot
Proteomic Techniques to Examine Neuronal Translational Dynamics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13024037openalex-snapshot
Additional file 1 of Integrated analysis of the aging brain transcriptome and proteome in tauopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.14812347openalex-snapshot
Additional file 1 of Altered ribosomal function and protein synthesis caused by tau
inferred← citeshttps://doi.org/10.6084/m9.figshare.14812350openalex-snapshot
Additional file 2 of Altered ribosomal function and protein synthesis caused by tau
inferred← citeshttps://doi.org/10.6084/m9.figshare.14812353openalex-snapshot
Additional file 3 of Altered ribosomal function and protein synthesis caused by tau
inferred← citeshttps://doi.org/10.6084/m9.figshare.16599624openalex-snapshot
Additional file 3 of Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope
inferred← citeshttps://doi.org/10.6084/m9.figshare.16599642openalex-snapshot
Additional file 7 of Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope
inferred← citeshttps://doi.org/10.6084/m9.figshare.19695711openalex-snapshot
Additional file 1 of Alzheimer risk gene product Pyk2 suppresses tau phosphorylation and phenotypic effects of tauopathy
inferred← citeshttps://doi.org/10.64898/2026.01.12.699151openalex-snapshot
Tau-induced ribosomal collisions impair memory through the activation of the integrated stress response
inferred← citeshttps://doi.org/10.64898/2026.05.06.723176openalex-snapshot
High-throughput identification of protein turnover modulators in human neurons
inferred← citeshttps://doi.org/10.70675/623e7224z0cb0z47b1z8a22z549acf553ac0openalex-snapshot
Interaction entre la protéine Tau et la protéine p54nrb : effet sur la maturation des miARN au sein des paraspeckles
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