On the public citation graph

Identification of mtROS-sensitive processes in activated CD4 + T cells

0 signed · 168 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1522-2683(19991201)20:18<3551::aid-elps3551>3.0.co;2-2openalex-snapshot
Probability-based protein identification by searching sequence databases using mass spectrometry data
inferredcites →https://doi.org/10.1002/eji.201646599openalex-snapshot
Survival of mature T cells in the periphery is intrinsically dependent on GIMAP1 in mice
inferredcites →https://doi.org/10.1002/stem.5530110814openalex-snapshot
Granulocyte-Macrophage colony stimulating factor and interleukin 3: Target cells and kinetics of response in vivo
inferredcites →https://doi.org/10.1016/b978-0-12-405882-8.00003-9openalex-snapshot
Peroxiredoxins as Preferential Targets in H2O2-Induced Signaling
inferredcites →https://doi.org/10.1016/j.abb.2004.05.024openalex-snapshot
Redox regulation of protein-tyrosine phosphatases
inferredcites →https://doi.org/10.1016/j.abb.2016.12.003openalex-snapshot
Peroxiredoxin 6 in the repair of peroxidized cell membranes and cell signaling
inferredcites →https://doi.org/10.1016/j.bbabio.2013.03.009openalex-snapshot
Molecular mechanisms of superoxide production by complex III: A bacterial versus human mitochondrial comparative case study
inferredcites →https://doi.org/10.1016/j.bbabio.2019.148133openalex-snapshot
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III
inferredcites →https://doi.org/10.1016/j.bbadis.2020.165716openalex-snapshot
Unraveling the role of thiosulfate sulfurtransferase in metabolic diseases
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.03.003openalex-snapshot
Manganese superoxide dismutase: A regulator of T cell activation-induced oxidative signaling and cell death
inferredcites →https://doi.org/10.1016/j.bbamcr.2013.10.020openalex-snapshot
T cell activation induces CuZn superoxide dismutase (SOD)-1 intracellular re-localization, production and secretion
inferredcites →https://doi.org/10.1016/j.bbrc.2004.06.040openalex-snapshot
Expression cloning of oligomerization-activated genes with cell-proliferating potency by pseudotype retrovirus vector
inferredcites →https://doi.org/10.1016/j.bbrc.2007.05.019openalex-snapshot
The distribution of the DEK protein in mammalian chromatin
inferredcites →https://doi.org/10.1016/j.bcp.2012.01.027openalex-snapshot
Thiostrepton is an inducer of oxidative and proteotoxic stress that impairs viability of human melanoma cells but not primary melanocytes
inferredcites →https://doi.org/10.1016/j.biocel.2018.03.019openalex-snapshot
Peroxiredoxin 2 mediates insulin sensitivity of skeletal muscles through regulation of protein tyrosine phosphatase oxidation
inferredcites →https://doi.org/10.1016/j.ceca.2017.01.007openalex-snapshot
Crosstalk between calcium and reactive oxygen species signaling in cancer
inferredcites →https://doi.org/10.1016/j.cell.2016.11.012openalex-snapshot
Structure of Mammalian Respiratory Supercomplex I 1 III 2 IV 1
inferredcites →https://doi.org/10.1016/j.celrep.2012.10.009openalex-snapshot
T cell Activation Is Driven by an ADP-Dependent Glucokinase Linking Enhanced Glycolysis with Mitochondrial Reactive Oxygen Species Generation
inferredcites →https://doi.org/10.1016/j.celrep.2016.03.009openalex-snapshot
The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency
inferredcites →https://doi.org/10.1016/j.febslet.2005.03.027openalex-snapshot
Human mitochondrial peroxiredoxin 5 protects from mitochondrial DNA damages induced by hydrogen peroxide
inferredcites →https://doi.org/10.1016/j.febslet.2011.01.046openalex-snapshot
NDUFB7 and NDUFA8 are located at the intermembrane surface of complex I
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2012.08.001openalex-snapshot
Peroxiredoxin 1 functions as a signal peroxidase to receive, transduce, and transmit peroxide signals in mammalian cells
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2014.11.013openalex-snapshot
The basics of thiols and cysteines in redox biology and chemistry
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2015.01.032openalex-snapshot
Composition of the redox environment of the endoplasmic reticulum and sources of hydrogen peroxide
inferredcites →https://doi.org/10.1016/j.gene.2018.04.048openalex-snapshot
MYH9: Structure, functions and role of non-muscle myosin IIA in human disease
inferredcites →https://doi.org/10.1016/j.gep.2011.05.001openalex-snapshot
Expression of Crip2, a LIM-domain-only protein, in the mouse cardiovascular system under physiological and pathological conditions
inferredcites →https://doi.org/10.1016/j.immuni.2005.02.004openalex-snapshot
Granzyme A Induces Caspase-Independent Mitochondrial Damage, a Required First Step for Apoptosis
inferredcites →https://doi.org/10.1016/j.immuni.2007.01.008openalex-snapshot
Formins Regulate the Actin-Related Protein 2/3 Complex-Independent Polarization of the Centrosome to the Immunological Synapse
inferredcites →https://doi.org/10.1016/j.immuni.2011.09.021openalex-snapshot
The Transcription Factor Myc Controls Metabolic Reprogramming upon T Lymphocyte Activation
inferredcites →https://doi.org/10.1016/j.immuni.2012.10.020openalex-snapshot
Mitochondria Are Required for Antigen-Specific T Cell Activation through Reactive Oxygen Species Signaling
inferredcites →https://doi.org/10.1016/j.immuni.2014.04.006openalex-snapshot
Downmodulation of Tumor Suppressor p53 by T Cell Receptor Signaling Is Critical for Antigen-Specific CD4+ T Cell Responses
inferredcites →https://doi.org/10.1016/j.immuni.2017.03.019openalex-snapshot
Glutathione Primes T Cell Metabolism for Inflammation
inferredcites →https://doi.org/10.1016/j.it.2018.01.005openalex-snapshot
Reactive Oxygen Species: Involvement in T Cell Signaling and Metabolism
inferredcites →https://doi.org/10.1016/j.jmb.2008.04.076openalex-snapshot
Crystal Structure of Metastasis-Associated Protein S100A4 in the Active Calcium-Bound Form
inferredcites →https://doi.org/10.1016/j.mad.2008.01.006openalex-snapshot
Changes in dihydrolipoamide dehydrogenase expression and activity during postnatal development and aging in the rat brain
inferredcites →https://doi.org/10.1016/j.neulet.2007.12.068openalex-snapshot
Silencing of peroxiredoxin 3 and peroxiredoxin 5 reveals the role of mitochondrial peroxiredoxins in the protection of human neuroblastoma SH-SY5Y cells toward MPP+
inferredcites →https://doi.org/10.1016/j.redox.2014.08.006openalex-snapshot
Examination of bioenergetic function in the inner mitochondrial membrane peptidase 2-like (Immp2l) mutant mice
inferredcites →https://doi.org/10.1016/j.redox.2018.101087openalex-snapshot
Quantifying changes in the bacterial thiol redox proteome during host-pathogen interaction
inferredcites →https://doi.org/10.1016/j.redox.2019.101141openalex-snapshot
Mitochondrial superoxide disrupts the metabolic and epigenetic landscape of CD4+ and CD8+ T-lymphocytes
inferredcites →https://doi.org/10.1016/j.redox.2019.101255openalex-snapshot
Mitochondria as central hub of the immune system
inferredcites →https://doi.org/10.1016/s0021-9258(18)89034-2openalex-snapshot
Identification of the binding site on cytochrome c1 for cytochrome c.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80547-4openalex-snapshot
Chaperone Activity with a Redox Switch
inferredcites →https://doi.org/10.1016/s0165-2478(97)85307-2openalex-snapshot
The complexity of a κ promoter: Three interdependent costimulatory sites 5′ of the decamer
inferredcites →https://doi.org/10.1016/s0165-2478(97)85309-6openalex-snapshot
Pre-exposure to oxidative stress decreases the NF-κB dependent transcription in T lymphocytes
inferredcites →https://doi.org/10.1016/s0165-2478(97)87147-7openalex-snapshot
Pre-exposure to oxidative stress decreases the NF-κB dependent transcription in T lymphocytes
inferredcites →https://doi.org/10.1016/s0891-5849(02)01000-6openalex-snapshot
Inhibition of PTPs by H2O2 regulates the activation of distinct MAPK pathways
inferredcites →https://doi.org/10.1021/acs.chemrestox.8b00353openalex-snapshot
Glutamine-451 Confers Sensitivity to Oxidative Inhibition and Heme-Thiolate Sulfenylation of Cytochrome P450 4B1
inferredcites →https://doi.org/10.1021/bi800282dopenalex-snapshot
Cysteine pKa Depression by a Protonated Glutamic Acid in Human DJ-1
inferredcites →https://doi.org/10.1021/ic200267xopenalex-snapshot
Oxidation of Zinc–Thiolate Complexes of Biological Interest by Hydrogen Peroxide: A Theoretical Study
inferredcites →https://doi.org/10.1021/pr401179vopenalex-snapshot
Proteomic Quantification and Site-Mapping of S -Nitrosylated Proteins Using Isobaric iodoTMT Reagents
inferredcites →https://doi.org/10.1038/emboj.2009.101openalex-snapshot
Prdx1 inhibits tumorigenesis via regulating PTEN/AKT activity
inferredcites →https://doi.org/10.1038/emboj.2011.289openalex-snapshot
Calcium microdomains at the immunological synapse: how ORAI channels, mitochondria and calcium pumps generate local calcium signals for efficient T‐cell activation
inferredcites →https://doi.org/10.1038/nature03587openalex-snapshot
Regulation of PDGF signalling and vascular remodelling by peroxiredoxin II
inferredcites →https://doi.org/10.1038/nature14427openalex-snapshot
Structure of the human 80S ribosome
inferredcites →https://doi.org/10.1038/nature19364openalex-snapshot
Ionic immune suppression within the tumour microenvironment limits T cell effector function
inferredcites →https://doi.org/10.1038/ncomms12886openalex-snapshot
Dynamic actin cycling through mitochondrial subpopulations locally regulates the fission–fusion balance within mitochondrial networks
inferredcites →https://doi.org/10.1038/ncomms14816openalex-snapshot
Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease
inferredcites →https://doi.org/10.1038/onc.2012.624openalex-snapshot
Role for Prdx1 as a specific sensor in redox-regulated senescence in breast cancer
inferredcites →https://doi.org/10.1038/s41467-016-0009-6openalex-snapshot
In situ click chemistry generation of cyclooxygenase-2 inhibitors
inferredcites →https://doi.org/10.1038/s41467-017-02694-8openalex-snapshot
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species
inferredcites →https://doi.org/10.1038/s41467-018-04686-8openalex-snapshot
Mitochondrial reactive oxygen species regulate the induction of CD8+ T cells by plasmacytoid dendritic cells
inferredcites →https://doi.org/10.1038/s41586-018-0061-yopenalex-snapshot
Structure of the alternative complex III in a supercomplex with cytochrome oxidase
inferredcites →https://doi.org/10.1038/s41586-019-1785-zopenalex-snapshot
Bile acid metabolites control TH17 and Treg cell differentiation
inferredcites →https://doi.org/10.1038/s41594-018-0073-1openalex-snapshot
Cryo-EM structures of complex I from mouse heart mitochondria in two biochemically defined states
inferredcites →https://doi.org/10.1038/srep36741openalex-snapshot
LUC7L3/CROP inhibits replication of hepatitis B virus via suppressing enhancer II/basal core promoter activity
inferredcites →https://doi.org/10.1042/bj20040485openalex-snapshot
Superoxide production by NADH:ubiquinone oxidoreductase (complex I) depends on the pH gradient across the mitochondrial inner membrane
inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot
How mitochondria produce reactive oxygen species
inferredcites →https://doi.org/10.1073/pnas.0400782101openalex-snapshot
A gene atlas of the mouse and human protein-encoding transcriptomes
inferredcites →https://doi.org/10.1073/pnas.040461197openalex-snapshot
Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase
inferredcites →https://doi.org/10.1073/pnas.0604571103openalex-snapshot
T cell surface redox levels determine T cell reactivity and arthritis susceptibility
inferredcites →https://doi.org/10.1073/pnas.0610618104openalex-snapshot
Cryptic proteolytic activity of dihydrolipoamide dehydrogenase
inferredcites →https://doi.org/10.1073/pnas.0812149106openalex-snapshot
Quantifying the global cellular thiol–disulfide status
inferredcites →https://doi.org/10.1073/pnas.1101747108openalex-snapshot
Cysteine-rich intestinal protein 2 ( CRIP2 ) acts as a repressor of NF-κB–mediated proangiogenic cytokine transcription to suppress tumorigenesis and angiogenesis
inferredcites →https://doi.org/10.1073/pnas.111163698openalex-snapshot
Exploring the DNA-binding specificities of zinc fingers with DNA microarrays
inferredcites →https://doi.org/10.1073/pnas.1806833115openalex-snapshot
Oxidative stress is tightly regulated by cytochrome c phosphorylation and respirasome factors in mitochondria
inferredcites →https://doi.org/10.1073/pnas.1936213100openalex-snapshot
Control of Bcl-2 expression by reactive oxygen species
inferredcites →https://doi.org/10.1073/pnas.95.7.3478openalex-snapshot
Thiolate ligands in metallothionein confer redox activity on zinc clusters
inferredcites →https://doi.org/10.1073/pnas.97.9.4567openalex-snapshot
Uncovering the [2Fe2S] domain movement in cytochrome bc 1 and its implications for energy conversion
inferredcites →https://doi.org/10.1074/jbc.271.8.4138openalex-snapshot
Activation of Mitogen-activated Protein Kinase by H2O2
inferredcites →https://doi.org/10.1074/jbc.274.17.11693openalex-snapshot
Inhibition of T Cell Signaling by Mitogen-activated Protein Kinase-targeted Hematopoietic Tyrosine Phosphatase (HePTP)
inferredcites →https://doi.org/10.1074/jbc.m001901200openalex-snapshot
The Cytochrome bc 1 and Cytochromec Oxidase Complexes Associate to Form a Single Supracomplex in Yeast Mitochondria
inferredcites →https://doi.org/10.1074/jbc.m005957200openalex-snapshot
Redox Switch of Hsp33 Has a Novel Zinc-binding Motif
inferredcites →https://doi.org/10.1074/jbc.m113.476895openalex-snapshot
Mitochondria-derived Hydrogen Peroxide Selectively Enhances T Cell Receptor-initiated Signal Transduction
inferredcites →https://doi.org/10.1074/jbc.m114.575308openalex-snapshot
Mitochondria Are Gate-keepers of T Cell Function by Producing the ATP That Drives Purinergic Signaling
inferredcites →https://doi.org/10.1074/jbc.m115.663906openalex-snapshot
Selective Sensitization of Zinc Finger Protein Oxidation by Reactive Oxygen Species through Arsenic Binding
inferredcites →https://doi.org/10.1074/jbc.m116.774174openalex-snapshot
The KIM-family protein-tyrosine phosphatases use distinct reversible oxidation intermediates: Intramolecular or intermolecular disulfide bond formation
inferredcites →https://doi.org/10.1074/jbc.m209681200openalex-snapshot
Effect of Cytochrome c on the Generation and Elimination of O 2⨪ and H2O2 in Mitochondria
inferredcites →https://doi.org/10.1074/jbc.m307818200openalex-snapshot
Thioredoxin 2, an Oxidative Stress-induced Protein, Contains a High Affinity Zinc Binding Site
inferredcites →https://doi.org/10.1074/jbc.m310341200openalex-snapshot
Characterization of Superoxide-producing Sites in Isolated Brain Mitochondria
inferredcites →https://doi.org/10.1074/jbc.m407715200openalex-snapshot
Complex III Releases Superoxide to Both Sides of the Inner Mitochondrial Membrane
inferredcites →https://doi.org/10.1074/jbc.m803028200openalex-snapshot
The Redox Environment in the Mitochondrial Intermembrane Space Is Maintained Separately from the Cytosol and Matrix
inferredcites →https://doi.org/10.1074/jbc.r111.283432openalex-snapshot
Peroxiredoxin Functions as a Peroxidase and a Regulator and Sensor of Local Peroxides
inferredcites →https://doi.org/10.1074/jbc.r113.462929openalex-snapshot
Oxidant Sensing by Reversible Disulfide Bond Formation
inferredcites →https://doi.org/10.1074/jbc.r113.467738openalex-snapshot
The Redox Biochemistry of Protein Sulfenylation and Sulfinylation
inferredcites →https://doi.org/10.1083/jcb.141.1.143openalex-snapshot
The 13-kD FK506 Binding Protein, FKBP13, Interacts with a Novel Homologue of the Erythrocyte Membrane Cytoskeletal Protein 4.1
inferredcites →https://doi.org/10.1083/jcb.200105148openalex-snapshot
Filamin A, the Arp2/3 complex, and the morphology and function of cortical actin filaments in human melanoma cells
inferredcites →https://doi.org/10.1084/jem.20010659openalex-snapshot
Discrete Generation of Superoxide and Hydrogen Peroxide by T Cell Receptor Stimulation
inferredcites →https://doi.org/10.1084/jem.20100031openalex-snapshot
Regulation of T cell receptor signaling by activation-induced zinc influx
inferredcites →https://doi.org/10.1089/15230860152542916openalex-snapshot
Oxidation of Zinc Finger Transcription Factors: Physiological Consequences
inferredcites →https://doi.org/10.1089/ars.2006.8.835openalex-snapshot
Zinc Center as Redox Switch—New Function for an Old Motif
inferredcites →https://doi.org/10.1089/ars.2008.2269openalex-snapshot
Zinc Fingers as Biologic Redox Switches?
inferredcites →https://doi.org/10.1089/ars.2009.3021openalex-snapshot
Redox Control Systems in the Nucleus: Mechanisms and Functions
inferredcites →https://doi.org/10.1089/ars.2010.3773openalex-snapshot
Are Zinc-Finger Domains of Protein Kinase C Dynamic Structures That Unfold by Lipid or Redox Activation?
inferredcites →https://doi.org/10.1089/ars.2012.4845openalex-snapshot
Mitochondrial Respiratory Supercomplex Association Limits Production of Reactive Oxygen Species from Complex I
inferredcites →https://doi.org/10.1089/ars.2012.5156openalex-snapshot
Thiol–Disulfide Exchange in Signaling: Disulfide Bonds As a Switch
inferredcites →https://doi.org/10.1091/mbc.e12-12-0862openalex-snapshot
Protein import and oxidative folding in the mitochondrial intermembrane space of intact mammalian cells
inferredcites →https://doi.org/10.1093/hmg/ddr440openalex-snapshot
Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIle mutation causing hypertrophic cardiomyopathy
inferredcites →https://doi.org/10.1093/jb/mvs006openalex-snapshot
Regulation of intracellular signalling through cysteine oxidation by reactive oxygen species
inferredcites →https://doi.org/10.1093/nar/gkl229openalex-snapshot
Applications for protein sequence-function evolution data: mRNA/protein expression analysis and coding SNP scoring tools
inferredcites →https://doi.org/10.1093/nar/gky1038openalex-snapshot
PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools
inferredcites →https://doi.org/10.1093/nar/gky1106openalex-snapshot
The PRIDE database and related tools and resources in 2019: improving support for quantification data
inferredcites →https://doi.org/10.1093/nar/gky1131openalex-snapshot
STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a124277openalex-snapshot
Acidic Regions of Cytochrome c1 Are Essential for Ubiquinol-Cytochrome c Reductase Activity in Yeast Cells Lacking the Acidic QCR6 Protein1
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a133901openalex-snapshot
Identity of the Heme-Not-Containing Protein in Bovine Heart Cytochrome c1 Preparation with the Protein Mediating c1-c Complex Formation—A Protein with High Glutamic Acid Content1
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a135409openalex-snapshot
Dissociation of Bovine Cytochrome c1 Subcomplex and the Status of Cysteine Residues in the Subunits1
inferredcites →https://doi.org/10.1101/gr.772403openalex-snapshot
PANTHER: A Library of Protein Families and Subfamilies Indexed by Function
inferredcites →https://doi.org/10.1111/j.1523-1755.2004.00491.xopenalex-snapshot
Reactive oxygen species amplify protein kinase C signaling in high glucose-induced fibronectin expression by human peritoneal mesothelial cells
inferredcites →https://doi.org/10.1111/jnc.12117openalex-snapshot
Mitochondrial peroxiredoxin‐5 as potential modulator of mitochondria‐ ER crosstalk in MPP +‐induced cell death
inferredcites →https://doi.org/10.1126/science.1085643openalex-snapshot
A Zinc Clasp Structure Tethers Lck to T Cell Coreceptors CD4 and CD8
inferredcites →https://doi.org/10.1128/jvi.00332-19openalex-snapshot
Modulation of Sialic Acid Dependence Influences the Central Nervous System Transduction Profile of Adeno-associated Viruses
inferredcites →https://doi.org/10.1128/jvi.00662-19openalex-snapshot
The Interferon-Inducible Proteoglycan Testican-2/SPOCK2 Functions as a Protective Barrier against Virus Infection of Lung Epithelial Cells
inferredcites →https://doi.org/10.1128/jvi.01559-12openalex-snapshot
Peroxiredoxin II Regulates Effector and Secondary Memory CD8+T Cell Responses
inferredcites →https://doi.org/10.1128/mcb.14.8.5099openalex-snapshot
Molecular Cloning of a Novel Human cDNA Encoding a Zinc Finger Protein That Binds to the Interleukin-3 Promoter
inferredcites →https://doi.org/10.1134/s1990747807020018openalex-snapshot
Hydrogen peroxide and peroxiredoxins in redox regulation of intracellular signaling
inferredcites →https://doi.org/10.1146/annurev.pharmtox.47.120505.105110openalex-snapshot
Targeting Antioxidants to Mitochondria by Conjugation to Lipophilic Cations
inferredcites →https://doi.org/10.1155/2016/6762343openalex-snapshot
Roles of Zinc Signaling in the Immune System
inferredcites →https://doi.org/10.1155/2018/9086947openalex-snapshot
Hydroxytyrosol Ameliorates Endothelial Function under Inflammatory Conditions by Preventing Mitochondrial Dysfunction
inferredcites →https://doi.org/10.1158/0008-5472.can-09-2587openalex-snapshot
Myeloid-Derived Suppressor Cells Inhibit T-Cell Activation by Depleting Cystine and Cysteine
inferredcites →https://doi.org/10.1172/jci122899openalex-snapshot
Thioredoxin-1 confines T cell alloresponse and pathogenicity in graft-versus-host disease
inferredcites →https://doi.org/10.1172/jci129388openalex-snapshot
Loss of ARPC1B impairs cytotoxic T lymphocyte maintenance and cytolytic activity
inferredcites →https://doi.org/10.1186/s12865-016-0151-2openalex-snapshot
Metallothionein regulates intracellular zinc signaling during CD4+ T cell activation
inferredcites →https://doi.org/10.1186/s12881-018-0521-0openalex-snapshot
Bilateral giant retinal tears in Osteogenesis Imperfecta
inferredcites →https://doi.org/10.1186/s12881-018-0709-3openalex-snapshot
Expanding the clinical phenotype of IARS2-related mitochondrial disease
inferredcites →https://doi.org/10.1186/s12929-015-0138-yopenalex-snapshot
“Down syndrome: an insight of the disease”
inferredcites →https://doi.org/10.1186/s12929-015-0194-3openalex-snapshot
T cells and reactive oxygen species
inferredcites →https://doi.org/10.1210/en.2010-0044openalex-snapshot
RhoA and DIAPH1 Mediate Adrenocorticotropin-Stimulated Cortisol Biosynthesis by Regulating Mitochondrial Trafficking
inferredcites →https://doi.org/10.1242/jcs.200006openalex-snapshot
The T cell IFT20 interactome reveals new players in immune synapse assembly
inferredcites →https://doi.org/10.1242/jcs.233783openalex-snapshot
Condensin II protein dysfunction impacts mitochondrial respiration and stress response
inferredcites →https://doi.org/10.1371/journal.pgen.1007051openalex-snapshot
Condensin II and GAIT complexes cooperate to restrict LINE-1 retrotransposition in epithelial cells
inferredcites →https://doi.org/10.1371/journal.pone.0023846openalex-snapshot
Impaired OXPHOS Complex III in Breast Cancer
inferredcites →https://doi.org/10.1371/journal.pone.0068667openalex-snapshot
Ribosomal Proteins RPL37, RPS15 and RPS20 Regulate the Mdm2-p53-MdmX Network
inferredcites →https://doi.org/10.1371/journal.pone.0170347openalex-snapshot
Death of Monocytes through Oxidative Burst of Macrophages and Neutrophils: Killing in Trans
inferredcites →https://doi.org/10.1371/journal.pone.0179159openalex-snapshot
Polyamine transporter potABCD is required for virulence of encapsulated but not nonencapsulated Streptococcus pneumoniae
inferredcites →https://doi.org/10.1515/hsz-2014-0280openalex-snapshot
Enzymatic control of cysteinyl thiol switches in proteins
inferredcites →https://doi.org/10.15252/embj.2018100300openalex-snapshot
Long‐term expanding human airway organoids for disease modeling
inferredcites →https://doi.org/10.15252/embj.2018100871openalex-snapshot
Redox signals at the ER–mitochondria interface control melanoma progression
inferredcites →https://doi.org/10.15252/embj.2019102817openalex-snapshot
Respiratory supercomplexes act as a platform for complex III‐mediated maturation of human mitochondrial complexes I and IV
inferredcites →https://doi.org/10.18632/oncotarget.11216openalex-snapshot
MetAP1 and MetAP2 drive cell selectivity for a potent anti-cancer agent in synergy, by controlling glutathione redox state
inferredcites →https://doi.org/10.18632/oncotarget.16486openalex-snapshot
A highly conserved redox-active Mx(2)CWx(6)R motif regulates Zap70 stability and activity
inferredcites →https://doi.org/10.2174/187153009788452390openalex-snapshot
T-Lymphocytes: A Target for Stimulatory and Inhibitory Effects of Zinc Ions
inferredcites →https://doi.org/10.3109/10715762.2012.752078openalex-snapshot
Reversible inactivation of dihydrolipoamide dehydrogenase by mitochondrial hydrogen peroxide
inferredcites →https://doi.org/10.3389/fimmu.2018.01075openalex-snapshot
Metabolic Reprogramming in Modulating T Cell Reactive Oxygen Species Generation and Antioxidant Capacity
inferredcites →https://doi.org/10.3389/fimmu.2018.02638openalex-snapshot
Role of Mechanotransduction and Tension in T Cell Function
inferredcites →https://doi.org/10.3389/fimmu.2018.02994openalex-snapshot
CD6, a Rheostat-Type Signalosome That Tunes T Cell Activation
inferredcites →https://doi.org/10.3389/fncel.2015.00336openalex-snapshot
SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis
inferredcites →https://doi.org/10.3389/fncel.2015.00427openalex-snapshot
Extracellular proteolysis in structural and functional plasticity of mossy fiber synapses in hippocampus
inferredcites →https://doi.org/10.3390/antiox8020032openalex-snapshot
Chronic Inhibition of Mitochondrial Dihydrolipoamide Dehydrogenase (DLDH) as an Approach to Managing Diabetic Oxidative Stress
inferredcites →https://doi.org/10.3390/molecules23071615openalex-snapshot
Characterization of Small Molecules Inhibiting the Pro-Angiogenic Activity of the Zinc Finger Transcription Factor Vezf1
inferredcites →https://doi.org/10.4049/jimmunol.0901662openalex-snapshot
Mitochondrial Reactive Oxygen Species Control T Cell Activation by Regulating IL-2 and IL-4 Expression: Mechanism of Ciprofloxacin-Mediated Immunosuppression
inferredcites →https://doi.org/10.4049/jimmunol.1600868openalex-snapshot
Hydrogen Peroxide Triggers a Dual Signaling Axis To Selectively Suppress Activated Human T Lymphocyte Migration
inferredcites →https://doi.org/10.4049/jimmunol.164.4.2170openalex-snapshot
Displacement of Linker for Activation of T Cells from the Plasma Membrane Due to Redox Balance Alterations Results in Hyporesponsiveness of Synovial Fluid T Lymphocytes in Rheumatoid Arthritis
inferredcites →https://doi.org/10.4049/jimmunol.174.2.953openalex-snapshot
Tristetraprolin Down-Regulates IL-2 Gene Expression through AU-Rich Element-Mediated mRNA Decay
inferredcites →https://doi.org/10.4049/jimmunol.1801629openalex-snapshot
IL-3 Receptor Expression on Activated Human Th Cells Is Regulated by IL-4, and IL-3 Synergizes with IL-4 to Enhance Th2 Cell Differentiation
inferredcites →https://doi.org/10.4049/jimmunol.181.9.6491openalex-snapshot
Zinc Signals Are Essential for Lipopolysaccharide-Induced Signal Transduction in Monocytes
inferredcites →https://doi.org/10.4110/in.2018.18.e14openalex-snapshot
The Role of Reactive Oxygen Species in Regulating T Cell-mediated Immunity and Disease
inferredcites →https://doi.org/10.4110/in.2018.18.e27openalex-snapshot
Damage-Associated Molecular Patterns in Inflammatory Diseases
inferredcites →https://doi.org/10.5483/bmbrep.2019.52.5.097openalex-snapshot
Neuronal function and dysfunction of CYFIP2: from actin dynamics to early infantile epileptic encephalopathy
inferredcites →https://doi.org/10.7554/elife.33057openalex-snapshot
ZFP36 RNA-binding proteins restrain T cell activation and anti-viral immunity
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.