On the public citation graph
c-Rel-Dependent Priming of Naive T Cells by Inflammatory Cytokines
0 signed · 133 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.
1 of the 63 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1016/s1074-7613(00)80103-x (notice 2009-04-17).
Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/eji.1830191114openalex-snapshot
Selective induction of growth factor production and growth factor receptor expression by different signals to a single t cell
inferredcites →https://doi.org/10.1002/eji.200324170openalex-snapshot
IL‐1 acts on antigen‐presenting cells to enhance the in vivo proliferation of antigen‐stimulated naive CD4 T cells via a CD28‐dependent mechanism that does not involve increased expression of CD28 ligands
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb01101.xopenalex-snapshot
The Rel subunit of NF‐kappaB‐like transcription factors is a positive and negative regulator of macrophage gene expression: distinct roles for Rel in different macrophage populations.
inferredcites →https://doi.org/10.1016/0952-7915(94)90120-1openalex-snapshot
CD28-B7 interactions in T-cell activation
inferredcites →https://doi.org/10.1016/j.immuni.2004.06.004openalex-snapshot
The Mitogen-Induced Increase in T Cell Size Involves PKC and NFAT Activation of Rel/NF-κB-Dependent c-myc Expression
inferredcites →https://doi.org/10.1016/j.immuni.2004.10.006openalex-snapshot
Toll-Dependent Control Mechanisms of CD4 T Cell Activation
inferredcites →https://doi.org/10.1016/j.it.2004.03.008openalex-snapshot
The two NF-κB activation pathways and their role in innate and adaptive immunity
inferredcites →https://doi.org/10.1016/s0008-8749(03)00114-xopenalex-snapshot
Selective loss of c-Rel compromises dendritic cell activation of T lymphocytes
inferredcites →https://doi.org/10.1016/s1074-7613(00)80103-xopenalex-snapshot
RETRACTED: Uncoupling IL-2 Signals that Regulate T Cell Proliferation, Survival, and Fas-Mediated Activation-Induced Cell Death
inferredcites →https://doi.org/10.1016/s1074-7613(01)00103-0openalex-snapshot
Early Transcription and Silencing of Cytokine Genes Underlie Polarization of T Helper Cell Subsets
inferredcites →https://doi.org/10.1016/s1074-7613(02)00272-8openalex-snapshot
Dendritic Cell Development and Survival Require Distinct NF-κB Subunits
inferredcites →https://doi.org/10.1016/s1074-7613(03)00053-0openalex-snapshot
The Survival of Antigen-Stimulated T Cells Requires NFκB-Mediated Inhibition of p73 Expression
inferredcites →https://doi.org/10.1016/s1471-4906(02)02264-0openalex-snapshot
It's all Rel-ative: NF-κB and CD28 costimulation of T-cell activation
inferredcites →https://doi.org/10.1038/32588openalex-snapshot
Dendritic cells and the control of immunity
inferredcites →https://doi.org/10.1038/86318openalex-snapshot
Gene regulation mediated by calcium signals in T lymphocytes
inferredcites →https://doi.org/10.1038/nature02761openalex-snapshot
Inferences, questions and possibilities in Toll-like receptor signalling
inferredcites →https://doi.org/10.1038/ni1004-971openalex-snapshot
The interface between innate and adaptive immunity
inferredcites →https://doi.org/10.1038/ni1008openalex-snapshot
Deletion of β-catenin impairs T cell development
inferredcites →https://doi.org/10.1038/ni1010openalex-snapshot
Upregulation of costimulatory molecules induced by lipopolysaccharide and double-stranded RNA occurs by Trif-dependent and Trif-independent pathways
inferredcites →https://doi.org/10.1038/ni949openalex-snapshot
Contribution of BCAP to maintenance of mature B cells through c-Rel
inferredcites →https://doi.org/10.1046/j.1365-3083.2003.01250.xopenalex-snapshot
Quantification of Cytokine Gene Expression Using an Economical Real‐Time Polymerase Chain Reaction Method Based on SYBR® Green I
inferredcites →https://doi.org/10.1073/pnas.0308231100openalex-snapshot
T cell receptor ζ reconstitution fails to restore responses of T cells rendered hyporesponsive by tumor necrosis factor α
inferredcites →https://doi.org/10.1073/pnas.092284399openalex-snapshot
Genomic expression programs and the integration of the CD28 costimulatory signal in T cell activation
inferredcites →https://doi.org/10.1073/pnas.230436397openalex-snapshot
Selective requirement for c-Rel during IL-12 P40 gene induction in macrophages
inferredcites →https://doi.org/10.1073/pnas.2433717100openalex-snapshot
CD4 T cell memory derived from young naive cells functions well into old age, but memory generated from aged naive cells functions poorly
inferredcites →https://doi.org/10.1073/pnas.97.3.1014openalex-snapshot
A nuclear export signal in the N-terminal regulatory domain of IκBα controls cytoplasmic localization of inactive NF-κB/IκBα complexes
inferredcites →https://doi.org/10.1074/jbc.c000916200openalex-snapshot
IκB Family Members Function by Different Mechanisms
inferredcites →https://doi.org/10.1074/jbc.m105865200openalex-snapshot
IκBβ, but Not IκBα, Functions as a Classical Cytoplasmic Inhibitor of NF-κB Dimers by Masking Both NF-κB Nuclear Localization Sequences in Resting Cells
inferredcites →https://doi.org/10.1074/jbc.m111559200openalex-snapshot
Characterization of the Nuclear Import and Export Functions of IκBε
inferredcites →https://doi.org/10.1084/jem.166.6.1774openalex-snapshot
Heterogeneity of helper/inducer T lymphocytes. I. Lymphokine production and lymphokine responsiveness.
inferredcites →https://doi.org/10.1084/jem.181.3.1091openalex-snapshot
FK506 inhibits antigen receptor-mediated induction of c-rel in B and T lymphoid cells.
inferredcites →https://doi.org/10.1084/jem.187.5.663openalex-snapshot
B Lymphocytes Differentially Use the Rel and Nuclear Factor κB1 (NF-κB1) Transcription Factors to Regulate Cell Cycle Progression and Apoptosis in Quiescent and Mitogen-activated Cells
inferredcites →https://doi.org/10.1084/jem.191.6.915openalex-snapshot
Activation-Induced Inhibition of Interleukin 6–Mediated T Cell Survival and Signal Transducer and Activator of Transcription 1 Signaling
inferredcites →https://doi.org/10.1093/intimm/11.3.361openalex-snapshot
c-Rel is crucial for lymphocyte proliferation but dispensable for T cell effector function
inferredcites →https://doi.org/10.1093/intimm/dxf055openalex-snapshot
c-Rel regulation of the cell cycle in primary mouse B lymphocytes
inferredcites →https://doi.org/10.1101/gad.13.4.400openalex-snapshot
Rel-dependent induction of A1 transcription is required to protect B cells from antigen receptor ligation-induced apoptosis
inferredcites →https://doi.org/10.1101/gad.9.16.1965openalex-snapshot
Mice lacking the c-rel proto-oncogene exhibit defects in lymphocyte proliferation, humoral immunity, and interleukin-2 expression.
inferredcites →https://doi.org/10.1126/science.278.5335.141openalex-snapshot
Evidence for a Role of CRM1 in Signal-Mediated Nuclear Protein Export
inferredcites →https://doi.org/10.1128/mcb.16.12.6736openalex-snapshot
CD28 Mediates a Potent Costimulatory Signal for Rapid Degradation of IκBβ Which Is Associated with Accelerated Activation of Various NF-κB/Rel Heterodimers
inferredcites →https://doi.org/10.1128/mcb.20.6.2269-2284.2000openalex-snapshot
Cytoplasmic Sequestration of Rel Proteins by IκBα Requires CRM1-Dependent Nuclear Export
inferredcites →https://doi.org/10.1128/mcb.21.14.4737-4747.2001openalex-snapshot
Postrepression Activation of NF-κB Requires the Amino-Terminal Nuclear Export Signal Specific to IκBα
inferredcites →https://doi.org/10.1128/mcb.21.14.4837-4846.2001openalex-snapshot
Cell-Specific Association and Shuttling of IκBα Provides a Mechanism for Nuclear NF-κB in B Lymphocytes
inferredcites →https://doi.org/10.1172/jci0215254openalex-snapshot
Critical roles of c-Rel in autoimmune inflammation and helper T cell differentiation
inferredcites →https://doi.org/10.1172/jci15254openalex-snapshot
Critical roles of c-Rel in autoimmune inflammation and helper T cell differentiation
inferredcites →https://doi.org/10.1189/jlb.1003456openalex-snapshot
TNFR1-induced sphingomyelinase activation modulates TCR signaling by impairing store-operated Ca2+ influx
inferredcites →https://doi.org/10.4049/jimmunol.157.3.1149openalex-snapshot
Differential regulation of c-Rel translocation in activated B and T cells
inferredcites →https://doi.org/10.4049/jimmunol.159.2.591openalex-snapshot
Inflammatory cytokines enhance the in vivo clonal expansion and differentiation of antigen-activated CD4+ T cells
inferredcites →https://doi.org/10.4049/jimmunol.162.2.766openalex-snapshot
Functional Characteristics and Survival Requirements of Memory CD4+ T Lymphocytes In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.162.6.3256openalex-snapshot
Inflammatory Cytokines Provide a Third Signal for Activation of Naive CD4+ and CD8+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.164.1.265openalex-snapshot
Functional Responses and Costimulator Dependence of Memory CD4+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.164.6.3157openalex-snapshot
The Role of High-Mobility Group I(Y) Proteins in Expression of IL-2 and T Cell Proliferation
inferredcites →https://doi.org/10.4049/jimmunol.166.9.5495openalex-snapshot
Prolonged Exposure of T Cells to TNF Down-Regulates TCRζ and Expression of the TCR/CD3 Complex at the Cell Surface
inferredcites →https://doi.org/10.4049/jimmunol.166.9.5688openalex-snapshot
Endotoxin-Induced Maturation of MyD88-Deficient Dendritic Cells
inferredcites →https://doi.org/10.4049/jimmunol.167.9.4948openalex-snapshot
c-Rel Is Required for the Protection of B Cells from Antigen Receptor-Mediated, But Not Fas-Mediated, Apoptosis
inferredcites →https://doi.org/10.4049/jimmunol.168.11.5521openalex-snapshot
Peptide Antigen Priming of Naive, But Not Memory, CD8 T Cells Requires a Third Signal That Can Be Provided by IL-12
inferredcites →https://doi.org/10.4049/jimmunol.168.6.2590openalex-snapshot
Cutting Edge: Identification of c-Rel-Dependent and -Independent Pathways of IL-12 Production During Infectious and Inflammatory Stimuli
inferredcites →https://doi.org/10.4049/jimmunol.168.8.3847openalex-snapshot
Molecular Mechanisms Underlying Differential Contribution of CD28 Versus Non-CD28 Costimulatory Molecules to IL-2 Promoter Activation
inferredcites →https://doi.org/10.4049/jimmunol.170.7.3724openalex-snapshot
c-Rel Is Required for Chromatin Remodeling Across the IL-2 Gene Promoter
inferredcites →https://doi.org/10.4049/jimmunol.172.9.5194openalex-snapshot
Inflammatory Cytokines Overcome Age-Related Defects in CD4 T Cell Responses In Vivo
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/eji.200939445openalex-snapshot
c‐Rel phenocopies PKCθ but not Bcl‐10 in regulating CD8+ T‐cell activation versus tolerance
inferred← citeshttps://doi.org/10.1007/s00262-008-0475-8openalex-snapshot
Danger signals and nonself entity of tumor antigen are both required for eliciting effective immune responses against HER-2/neu positive mammary carcinoma: implications for vaccine design
inferred← citeshttps://doi.org/10.1007/s10620-006-9406-8openalex-snapshot
Adacolumn Selective Leukocyte Adsorption Apheresis in Patients with Active Ulcerative Colitis: Clinical Efficacy, Effects on Plasma IL-8, and Expression of Toll-like Receptor 2 on Granulocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.62229-8openalex-snapshot
Inflammation in Bone Loss
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2017.07.007openalex-snapshot
NF-κB and the Transcriptional Control of Inflammation
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2021.02.003openalex-snapshot
Charting protein dephosphorylation triggered by Toll-like receptor (TLR) signaling in macrophages and its role in health and disease
inferred← citeshttps://doi.org/10.1016/j.cellimm.2015.04.007openalex-snapshot
Evolution of two prototypic T cell lineages
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114401openalex-snapshot
IRF4 impedes human CD8 T cell function and promotes cell proliferation and PD-1 expression
inferred← citeshttps://doi.org/10.1016/j.cyto.2011.08.014openalex-snapshot
Interferon regulatory factor-4 activates IL-2 and IL-4 promoters in cooperation with c-Rel
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.04.025openalex-snapshot
Contrasting effects of TNF and anti‐TNF on the activation of effector T cells and regulatory T cells in autoimmunity
inferred← citeshttps://doi.org/10.1016/j.jaci.2007.07.004openalex-snapshot
Defective T-cell activation caused by impairment of the TNF receptor 2 costimulatory pathway in common variable immunodeficiency
inferred← citeshttps://doi.org/10.1016/j.jaut.2008.04.012openalex-snapshot
Immune deficiency or hyperactivity-Nf-κb illuminates autoimmunity
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.111251openalex-snapshot
TNF-alpha: Roles in pathogenesis and therapeutics in cancer
inferred← citeshttps://doi.org/10.1016/j.tibs.2007.05.003openalex-snapshot
Diversity and regulation in the NF-κB system
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2021.12.009openalex-snapshot
Stabilin-1 mediates beneficial monocyte recruitment and tolerogenic macrophage programming during CVB3-induced viral myocarditis
inferred← citeshttps://doi.org/10.1038/cmi.2011.60openalex-snapshot
Peli: a family of signal-responsive E3 ubiquitin ligases mediating TLR signaling and T-cell tolerance
inferred← citeshttps://doi.org/10.1038/icb.2008.13openalex-snapshot
Influencing the fates of CD4 T cells on the path to memory: lessons from influenza
inferred← citeshttps://doi.org/10.1038/nature08068openalex-snapshot
Dual nature of the adaptive immune system in lampreys
inferred← citeshttps://doi.org/10.1038/ni.2090openalex-snapshot
The ubiquitin ligase Peli1 negatively regulates T cell activation and prevents autoimmunity
inferred← citeshttps://doi.org/10.1038/s41590-025-02138-2openalex-snapshot
Stepwise neofunctionalization of the NF-κB family member Rel during vertebrate evolution
inferred← citeshttps://doi.org/10.1038/s41598-019-53234-xopenalex-snapshot
Tumor necrosis factor induces rapid down-regulation of TXNIP in human T cells
inferred← citeshttps://doi.org/10.1038/sj.jid.5701064openalex-snapshot
Insights into Gene Modulation by Therapeutic TNF and IFNγ Antibodies: TNF Regulates IFNγ Production by T Cells and TNF-Regulated Genes Linked to Psoriasis Transcriptome
inferred← citeshttps://doi.org/10.1038/sj.onc.1209944openalex-snapshot
Unravelling the complexities of the NF-κB signalling pathway using mouse knockout and transgenic models
inferred← citeshttps://doi.org/10.1073/pnas.0803336105openalex-snapshot
Genomic expression profiling of TNF-α-treated BDC2.5 diabetogenic CD4 + T cells
inferred← citeshttps://doi.org/10.1093/infdis/jiy053openalex-snapshot
Identification and Characterization at the Single-Cell Level of Cytokine-Producing Circulating Cells in Children With Dengue
inferred← citeshttps://doi.org/10.1093/intimm/dxl007openalex-snapshot
IL-1β, but not IL-1α, is required for antigen-specific T cell activation and the induction of local inflammation in the delayed-type hypersensitivity responses
inferred← citeshttps://doi.org/10.1093/jimmun/vkaf096openalex-snapshot
RGS1 is an effective T-cell marker of acute myeloid leukemia remission after hematopoietic stem cell transplantation
inferred← citeshttps://doi.org/10.1101/2021.06.02.446831openalex-snapshot
CD4 + T cell lymphopenia and dysfunction in severe COVID-19 disease is autocrine TNF-α/TNFRI-dependent
inferred← citeshttps://doi.org/10.1101/cshperspect.a000182openalex-snapshot
Roles of the NF- B Pathway in Lymphocyte Development and Function
inferred← citeshttps://doi.org/10.1101/cshperspect.a000257openalex-snapshot
Selectivity of the NF- B Response
inferred← citeshttps://doi.org/10.1101/gad.351630.124openalex-snapshot
Selective regulation of a defined subset of inflammatory and immunoregulatory genes by an NF-κB p50–IκBζ pathway
inferred← citeshttps://doi.org/10.1111/j.0105-2896.2006.00388.xopenalex-snapshot
CD4+ T‐cell memory: generation and multi‐faceted roles for CD4+ T cells in protective immunity to influenza
inferred← citeshttps://doi.org/10.1111/j.1365-2567.2008.03034.xopenalex-snapshot
Depletion of γδ+ T cells increases CD4+ FoxP3 (T regulatory) cell response in coxsackievirus B3‐induced myocarditis
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2011.01091.xopenalex-snapshot
Dimer‐specific regulatory mechanisms within the NF‐κB family of transcription factors
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2012.01106.xopenalex-snapshot
NF‐κB function in B lymphocytes
inferred← citeshttps://doi.org/10.1111/jpi.12636openalex-snapshot
Immune‐pineal axis protects rat lungs exposed to polluted air
inferred← citeshttps://doi.org/10.1152/ajprenal.00381.2006openalex-snapshot
CD38 is required for priming by TNF-α: a mechanism for extracellular coordination of cell fate
inferred← citeshttps://doi.org/10.1155/2012/239368openalex-snapshot
A Key Role for NF-κB Transcription Factor c-Rel in T-Lymphocyte-Differentiation and Effector Functions
inferred← citeshttps://doi.org/10.1158/0008-5472.can-17-3962openalex-snapshot
A RIPK3-PGE2 Circuit Mediates Myeloid-Derived Suppressor Cell–Potentiated Colorectal Carcinogenesis
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-05-0259openalex-snapshot
Nuclear Factor-κB Dimer Exchange Promotes a p21waf1/cip1 Superinduction Response in Human T Leukemic Cells
inferred← citeshttps://doi.org/10.1159/000289200openalex-snapshot
T Cells as Sources and Targets of TNF: Implications for Immunity and Autoimmunity
inferred← citeshttps://doi.org/10.1159/000381382openalex-snapshot
Physiological Role of TNF in Mucosal Immunology: Regulation of T-Cell Function
inferred← citeshttps://doi.org/10.1164/rccm.202111-2493ocopenalex-snapshot
CD4+ T-Cell Dysfunction in Severe COVID-19 Disease Is Tumor Necrosis Factor-α/Tumor Necrosis Factor Receptor 1-Dependent.
inferred← citeshttps://doi.org/10.1177/1947601911421925openalex-snapshot
The c-Rel Transcription Factor in Development and Disease
inferred← citeshttps://doi.org/10.1201/9781420004274-11openalex-snapshot
NF- B in the Adaptive Immune System: Lymphocyte Survival and Function
inferred← citeshttps://doi.org/10.1201/9781420004274.ch7openalex-snapshot
NF-_B in the Adaptive Immune System
inferred← citeshttps://doi.org/10.1371/journal.pone.0005028openalex-snapshot
RNAi-Mediated c-Rel Silencing Leads to Apoptosis of B Cell Tumor Cells and Suppresses Antigenic Immune Response In Vivo
inferred← citeshttps://doi.org/10.1371/journal.pone.0024504openalex-snapshot
Inhibitor of Kappa B Epsilon (IκBε) Is a Non-Redundant Regulator of c-Rel-Dependent Gene Expression in Murine T and B Cells
inferred← citeshttps://doi.org/10.1517/14728222.11.2.111openalex-snapshot
NF-κB as a therapeutic target in autoimmune disease
inferred← citeshttps://doi.org/10.18632/aging.100522openalex-snapshot
Age-associated alterations in inducible gene transcription in human CD4+ T lymphocytes
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01718openalex-snapshot
A Dual Inhibitor of Cdc7/Cdk9 Potently Suppresses T Cell Activation
inferred← citeshttps://doi.org/10.3389/fimmu.2021.670776openalex-snapshot
LPSlow-Macrophages Alleviate the Outcome of Graft-Versus-Host Disease Without Aggravating Lymphoma Growth in Mice
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1042622openalex-snapshot
The dichotomous outcomes of TNFα signaling in CD4+ T cells
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1129191openalex-snapshot
NFκB signaling in T cell memory
inferred← citeshttps://doi.org/10.3390/biomedicines14020420openalex-snapshot
Identification and Mechanism Research of Oxidative Stress-Related Biomarkers in Oral Lichen Planus
inferred← citeshttps://doi.org/10.4049/jimmunol.1003988openalex-snapshot
Regulation of IFN-λ1 Promoter Activity (IFN-λ1/IL-29) in Human Airway Epithelial Cells
inferred← citeshttps://doi.org/10.4049/jimmunol.1003998openalex-snapshot
IL-1β and TGF-β Act Antagonistically in Induction and Differentially in Propagation of Human Proinflammatory Precursor CD4+ T Cells
inferred← citeshttps://doi.org/10.4049/jimmunol.1500286openalex-snapshot
Transmembrane TNF–TNFR2 Impairs Th17 Differentiation by Promoting Il2 Expression
inferred← citeshttps://doi.org/10.4049/jimmunol.178.11.6735openalex-snapshot
An Essential Role for TNF in Modulating Thresholds for Survival, Activation, and Tolerance of CD8+ T Cells
inferred← citeshttps://doi.org/10.4049/jimmunol.178.11.6777openalex-snapshot
Distinct Roles of Different NF-κB Subunits in Regulating Inflammatory and T Cell Stimulatory Gene Expression in Dendritic Cells
inferred← citeshttps://doi.org/10.4049/jimmunol.1801026openalex-snapshot
Costimulation through TLR2 Drives Polyfunctional CD8+ T Cell Responses
inferred← citeshttps://doi.org/10.4049/jimmunol.181.2.1272openalex-snapshot
Biphasic Regulation of Il2 Transcription in CD4+ T Cells: Roles for TNF-α Receptor Signaling and Chromatin Structure
inferred← citeshttps://doi.org/10.4049/jimmunol.2000039openalex-snapshot
IκBα Nuclear Export Enables 4-1BB–Induced cRel Activation and IL-2 Production to Promote CD8 T Cell Immunity
inferred← citeshttps://doi.org/10.4172/2157-7560.1000166openalex-snapshot
Interleukin-3 and Granulocyte-Macrophage Colony-Stimulating Factor Expression, a Biomarker of Memory CD8+ T Cell Immunity and Vaccine Efficacy
inferred← citeshttps://doi.org/10.5525/gla.thesis.74343openalex-snapshot
Investigating NF-κB ubiquitination: an in vitro study
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.