On the public citation graph

A Novel Thioredoxin-Mediated Mechanism in Autism Spectrum Disorder

0 signed · 98 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9781118553480.ch04openalex-extracted
Oxidative Stress in Neurodegenerative Diseases
inferredcites →https://doi.org/10.1002/advs.202205783openalex-extracted
The NO Answer for Autism Spectrum Disorder
inferredcites →https://doi.org/10.1002/mas.21413openalex-extracted
Mass spectrometry analysis of nitrotyrosine‐containing proteins
inferredcites →https://doi.org/10.1007/s00406-004-0456-7openalex-extracted
Increased oxidative stress and altered activities of erythrocyte free radical scavenging enzymes in autism
inferredcites →https://doi.org/10.1007/s11307-015-0926-5openalex-extracted
Baseline [18F]FMISO μPET as a Predictive Biomarker for Response to HIF-1α Inhibition Combined with 5-FU Chemotherapy in a Human Colorectal Cancer Xenograft Model
inferredcites →https://doi.org/10.1007/s12031-021-01792-zopenalex-extracted
Regional Differences in S-Nitrosylation in the Cortex, Striatum, and Hippocampus of Juvenile Male Mice
inferredcites →https://doi.org/10.1007/s12031-023-02166-3openalex-extracted
Nitric Oxide Synthase Inhibition Prevents Cell Proliferation in Glioblastoma
inferredcites →https://doi.org/10.1007/s12035-019-01742-2openalex-extracted
Oxidative Stress in Autism Spectrum Disorder
inferredcites →https://doi.org/10.1007/s12311-012-0355-9openalex-extracted
Consensus Paper: Pathological Role of the Cerebellum in Autism
inferredcites →https://doi.org/10.1016/0891-0618(96)00148-2openalex-extracted
Nitric oxide neurotoxicity
inferredcites →https://doi.org/10.1016/j.ab.2013.12.025openalex-extracted
Activity assays of mammalian thioredoxin and thioredoxin reductase: Fluorescent disulfide substrates, mechanisms, and use with tissue samples
inferredcites →https://doi.org/10.1016/j.apsb.2023.07.010openalex-extracted
Oxidative stress, the blood–brain barrier and neurodegenerative diseases: The critical beneficial role of dietary antioxidants
inferredcites →https://doi.org/10.1016/j.bbagen.2015.09.010openalex-extracted
Nitric oxide and the thioredoxin system: a complex interplay in redox regulation
inferredcites →https://doi.org/10.1016/j.ceb.2005.02.004openalex-extracted
Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins
inferredcites →https://doi.org/10.1016/j.cell.2010.01.009openalex-extracted
Inactivation of Peroxiredoxin I by Phosphorylation Allows Localized H2O2 Accumulation for Cell Signaling
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.04.029openalex-extracted
Nuclear and cytoplasmic peroxiredoxin-1 differentially regulate NF-κB activities
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2013.07.036openalex-extracted
The thioredoxin antioxidant system
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2014.05.011openalex-extracted
Protective effects of the thioredoxin and glutaredoxin systems in dopamine-induced cell death
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2015.01.014openalex-extracted
The overexpression and nuclear translocation of Trx-1 during hypoxia confers on HepG2 cells resistance to DDP, and GL-V9 reverses the resistance by suppressing the Trx-1/Ref-1 axis
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2022.06.007openalex-extracted
A cross-talk between nitric oxide and the glutamatergic system in a Shank3 mouse model of autism
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2022.11.035openalex-extracted
The contribution of an imbalanced redox signalling to neurological and neurodegenerative conditions
inferredcites →https://doi.org/10.1016/j.ijdevneu.2014.11.007openalex-extracted
Thioredoxin: A novel, independent diagnosis marker in children with autism
inferredcites →https://doi.org/10.1016/j.niox.2023.09.003openalex-extracted
Effects of Extended-Release 7-Nitroindazole Gel Formulation Treatment on the Behavior of Shank3 Mouse Model of Autism
inferredcites →https://doi.org/10.1016/j.pathophys.2006.05.007openalex-extracted
Oxidative stress in autism
inferredcites →https://doi.org/10.1016/j.pharmthera.2021.107939openalex-extracted
Novel treatments for autism spectrum disorder based on genomics and systems biology
inferredcites →https://doi.org/10.1016/j.plefa.2005.06.002openalex-extracted
Increased excretion of a lipid peroxidation biomarker in autism
inferredcites →https://doi.org/10.1016/j.pnpbp.2017.11.016openalex-extracted
PSD95: A synaptic protein implicated in schizophrenia or autism?
inferredcites →https://doi.org/10.1016/j.redox.2018.01.008openalex-extracted
13 reasons why the brain is susceptible to oxidative stress
inferredcites →https://doi.org/10.1016/j.redox.2020.101567openalex-extracted
The role of nitric oxide in brain disorders: Autism spectrum disorder and other psychiatric, neurological, and neurodegenerative disorders
inferredcites →https://doi.org/10.1016/j.redox.2022.102347openalex-extracted
The antioxidant enzyme Peroxiredoxin-1 controls stroke-associated microglia against acute ischemic stroke
inferredcites →https://doi.org/10.1016/j.redox.2023.102983openalex-extracted
Shank3 ameliorates neuronal injury after cerebral ischemia/reperfusion via inhibiting oxidative stress and inflammation
inferredcites →https://doi.org/10.1016/j.tips.2017.06.001openalex-extracted
Targeting the Thioredoxin System for Cancer Therapy
inferredcites →https://doi.org/10.1038/mp.2011.57openalex-extracted
SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism
inferredcites →https://doi.org/10.1038/nn1770openalex-extracted
Time to give up on a single explanation for autism
inferredcites →https://doi.org/10.1038/npp.2012.174openalex-extracted
Neuroinflammation and Autism: Toward Mechanisms and Treatments
inferredcites →https://doi.org/10.1038/npre.2010.4200.1openalex-extracted
Molecular Evaluation of exons 8 and 22 of the SHANK3 gene in Autism Spectrum Disorders
inferredcites →https://doi.org/10.1038/nrd1330openalex-extracted
Neurodegenerative diseases and oxidative stress
inferredcites →https://doi.org/10.1038/nrn1537openalex-extracted
Iron, brain ageing and neurodegenerative disorders
inferredcites →https://doi.org/10.1038/nrn2851openalex-extracted
Behavioural phenotyping assays for mouse models of autism
inferredcites →https://doi.org/10.1038/s12276-020-00498-3openalex-extracted
Deficiency of peroxiredoxin 2 exacerbates angiotensin II-induced abdominal aortic aneurysm
inferredcites →https://doi.org/10.1038/s41380-018-0113-6openalex-extracted
Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function
inferredcites →https://doi.org/10.1038/s41398-019-0388-7openalex-extracted
S-nitrosylation of E3 ubiquitin-protein ligase RNF213 alters non-canonical Wnt/Ca+2 signaling in the P301S mouse model of tauopathy
inferredcites →https://doi.org/10.1038/s41398-021-01578-2openalex-extracted
Proteomics of autism and Alzheimer’s mouse models reveal common alterations in mTOR signaling pathway
inferredcites →https://doi.org/10.1038/s41398-022-01890-5openalex-extracted
Arsenic alters nitric oxide signaling similar to autism spectrum disorder and Alzheimer’s disease-associated mutations
inferredcites →https://doi.org/10.1038/s41598-019-42068-2openalex-extracted
Inhibition of the thioredoxin system by PX-12 (1-methylpropyl 2-imidazolyl disulfide) impedes HIV-1 infection in TZM-bl cells
inferredcites →https://doi.org/10.1038/s41598-020-70383-6openalex-extracted
Systems biology reveals reprogramming of the S-nitroso-proteome in the cortical and striatal regions of mice during aging process
inferredcites →https://doi.org/10.1038/s41598-023-50248-4openalex-extracted
Mutations associated with autism lead to similar synaptic and behavioral alterations in both sexes of male and female mouse brain
inferredcites →https://doi.org/10.1038/s44220-023-00195-wopenalex-extracted
Symptom dimensions of resting-state electroencephalographic functional connectivity in autism
inferredcites →https://doi.org/10.1038/sj.cdd.4401818openalex-extracted
Involvement of glutaredoxin-1 and thioredoxin-1 in β-amyloid toxicity and Alzheimer's disease
inferredcites →https://doi.org/10.1038/tp.2016.181openalex-extracted
Impaired GABA synthesis, uptake and release are associated with depression-like behaviors induced by chronic mild stress
inferredcites →https://doi.org/10.1046/j.1432-1327.2000.01597.xopenalex-extracted
Glutathione metabolism in brain
inferredcites →https://doi.org/10.1073/pnas.94.8.3633openalex-extracted
AP-1 transcriptional activity is regulated by a direct association between thioredoxin and Ref-1
inferredcites →https://doi.org/10.1074/jbc.271.32.19180openalex-extracted
S-Nitrosoglutathione Is Cleaved by the Thioredoxin System with Liberation of Glutathione and Redox Regulating Nitric Oxide
inferredcites →https://doi.org/10.1074/jbc.274.31.21645openalex-extracted
Identification of Thioredoxin-binding Protein-2/Vitamin D3 Up-regulated Protein 1 as a Negative Regulator of Thioredoxin Function and Expression
inferredcites →https://doi.org/10.1074/jbc.m000835200openalex-extracted
Thioredoxin Facilitates the Induction of Heme Oxygenase-1 in Response to Inflammatory Mediators
inferredcites →https://doi.org/10.1074/jbc.m112.355875openalex-extracted
Thioredoxin Reductase Linked to Cytoskeleton by Focal Adhesion Kinase Reverses Actin S-Nitrosylation and Restores Neutrophil β2 Integrin Function
inferredcites →https://doi.org/10.1080/00207454.2020.1713776openalex-extracted
3-Nitrotyrosine: a versatile oxidative stress biomarker for major neurodegenerative diseases
inferredcites →https://doi.org/10.1089/ars.2006.8.1723openalex-extracted
Thioredoxin-1 and Posttranslational Modifications
inferredcites →https://doi.org/10.1089/ars.2007.9.25openalex-extracted
Thioredoxin and Related Molecules–From Biology to Health and Disease
inferredcites →https://doi.org/10.1089/ars.2010.3474openalex-extracted
Significance of Brain Tissue Oxygenation and the Arachidonic Acid Cascade in Stroke
inferredcites →https://doi.org/10.1089/ars.2010.3831openalex-extracted
Thioredoxin 1-Mediated Post-Translational Modifications: Reduction, Transnitrosylation, Denitrosylation, and Related Proteomics Methodologies
inferredcites →https://doi.org/10.1089/ars.2015.6378openalex-extracted
TrxR1 as a Potent Regulator of the Nrf2-Keap1 Response System
inferredcites →https://doi.org/10.1089/ars.2016.6925openalex-extracted
Redox Signaling Mediated by Thioredoxin and Glutathione Systems in the Central Nervous System
inferredcites →https://doi.org/10.1093/toxsci/kfh050openalex-extracted
Thioredoxin and Its Role in Toxicology
inferredcites →https://doi.org/10.1093/toxsci/kfs271openalex-extracted
Increased Nuclear Thioredoxin-1 Potentiates Cadmium-Induced Cytotoxicity
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.03907.xopenalex-extracted
Oxidative stress and neurodegeneration: where are we now?
inferredcites →https://doi.org/10.1111/jnc.13581openalex-extracted
Dissecting the role of redox signaling in neuronal development
inferredcites →https://doi.org/10.11138/fneur/2015.30.3.159openalex-extracted
Why is nitric oxide important for our brain?
inferredcites →https://doi.org/10.1126/sciadv.ade0764openalex-extracted
Mechanistic insight into female predominance in Alzheimer’s disease based on aberrant protein S-nitrosylation of C3
inferredcites →https://doi.org/10.1126/science.1158265openalex-extracted
Regulated Protein Denitrosylation by Cytosolic and Mitochondrial Thioredoxins
inferredcites →https://doi.org/10.1128/mcb.25.5.1980-1988.2005openalex-extracted
Cytoplasmic Thioredoxin Reductase Is Essential for Embryogenesis but Dispensable for Cardiac Development
inferredcites →https://doi.org/10.1136/jmg.2008.060871openalex-extracted
Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist
inferredcites →https://doi.org/10.1146/annurev-pharmtox-010818-021856openalex-extracted
Modulating NRF2 in Disease: Timing Is Everything
inferredcites →https://doi.org/10.1146/annurev.bi.64.070195.000525openalex-extracted
SUPEROXIDE RADICAL AND SUPEROXIDE DISMUTASES
inferredcites →https://doi.org/10.1155/2014/164938openalex-extracted
Potential Role of Selenoenzymes and Antioxidant Metabolism in relation to Autism Etiology and Pathology
inferredcites →https://doi.org/10.1155/2014/590808openalex-extracted
Thioredoxin System Regulation in the Central Nervous System: Experimental Models and Clinical Evidence
inferredcites →https://doi.org/10.1155/2021/6685204openalex-extracted
Oxidative Stress as a Common Key Event in Developmental Neurotoxicity
inferredcites →https://doi.org/10.1179/1743132812y.0000000073openalex-extracted
Oxidative stress and inflammation biomarkers in the blood of patients with Huntington’s disease
inferredcites →https://doi.org/10.1186/s13045-018-0575-7openalex-extracted
Inhibition of thioredoxin activates mitophagy and overcomes adaptive bortezomib resistance in multiple myeloma
inferredcites →https://doi.org/10.1186/s43045-020-00021-4openalex-extracted
Thioredoxin level and inflammatory markers in children with autism spectrum disorders
inferredcites →https://doi.org/10.1371/journal.pone.0052788openalex-extracted
N-Methyl-D-Aspartate Receptor-Dependent Denitrosylation of Neuronal Nitric Oxide Synthase Increase the Enzyme Activity
inferredcites →https://doi.org/10.1371/journal.pone.0108346openalex-extracted
Disturbed Flow Enhances Inflammatory Signaling and Atherogenesis by Increasing Thioredoxin-1 Level in Endothelial Cell Nuclei
inferredcites →https://doi.org/10.15252/msb.202211267openalex-extracted
A metabolic map of the DNA damage response identifies PRDX1 in the control of nuclear ROS scavenging and aspartate availability
inferredcites →https://doi.org/10.3389/fnagi.2021.717263openalex-extracted
Expression of the Excitatory Postsynaptic Scaffolding Protein, Shank3, in Human Brain: Effect of Age and Alzheimer’s Disease
inferredcites →https://doi.org/10.3390/antiox11112161openalex-extracted
The Role of the Thioredoxin System in Brain Diseases
inferredcites →https://doi.org/10.3390/antiox12051078openalex-extracted
The Importance of Thioredoxin-1 in Health and Disease
inferredcites →https://doi.org/10.3390/antiox9111151openalex-extracted
The NRF2, Thioredoxin, and Glutathione System in Tumorigenesis and Anticancer Therapies
inferredcites →https://doi.org/10.3390/biomedicines10071757openalex-extracted
The Thioredoxin System of Mammalian Cells and Its Modulators
inferredcites →https://doi.org/10.3390/biomedicines8050124openalex-extracted
Sex Differences in Biological Processes and Nitrergic Signaling in Mouse Brain
inferredcites →https://doi.org/10.3390/brainsci11060677openalex-extracted
Systems Biology Reveals S-Nitrosylation-Dependent Regulation of Mitochondrial Functions in Mice with Shank3 Mutation Associated with Autism Spectrum Disorder
inferredcites →https://doi.org/10.3390/cancers2020209openalex-extracted
Thioredoxin and Cancer: A Role for Thioredoxin in all States of Tumor Oxygenation
inferredcites →https://doi.org/10.3390/ijms18122772openalex-extracted
Nrf2, the Master Regulator of Anti-Oxidative Responses
inferredcites →https://doi.org/10.3390/ijms21113948openalex-extracted
Low Doses of Arsenic in a Mouse Model of Human Exposure and in Neuronal Culture Lead to S-Nitrosylation of Synaptic Proteins and Apoptosis via Nitric Oxide
inferredcites →https://doi.org/10.3390/molecules24081583openalex-extracted
Oxidative Stress: A Key Modulator in Neurodegenerative Diseases
inferredcites →https://doi.org/10.3390/oxygen3010004openalex-extracted
The Role of Oxidative Stress in Autism Spectrum Disorder: A Narrative Literature Review
inferredcites →https://doi.org/10.3791/55718openalex-extracted
Novel Object Recognition Test for the Investigation of Learning and Memory in Mice
inferredcites →https://doi.org/10.3969/j.issn.1673-5374.2012.05.009openalex-extracted
Oxidative stress in neurodegenerative diseases.
inferredcites →https://doi.org/10.7150/thno.85460openalex-extracted
Nuclear translocation of thioredoxin-1 promotes colorectal cancer development via modulation of the IL-6/STAT3 signaling axis through interaction with STAT3
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.