On the public citation graph
E3-Specific Degrader Discovery by Dynamic Tracing of Substrate Receptor Abundance
0 signed · 95 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.
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known work and none has been retracted — and get a dated CiteStamped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/jssc.200500116openalex-snapshot
Two‐dimensional separation of peptides using RP‐RP‐HPLC system with different pH in first and second separation dimensions
inferredcites →https://doi.org/10.1002/pmic.201000722openalex-snapshot
Reversed‐phase chromatography with multiple fraction concatenation strategy for proteome profiling of human MCF10A cells
inferredcites →https://doi.org/10.1007/978-1-4939-9145-7_7openalex-snapshot
Locus-Specific Knock-In of a Degradable Tag for Target Validation Studies
inferredcites →https://doi.org/10.1016/j.cell.2013.02.024openalex-snapshot
Cand1 Promotes Assembly of New SCF Complexes through Dynamic Exchange of F Box Proteins
inferredcites →https://doi.org/10.1016/j.cell.2017.10.016openalex-snapshot
Composition and Regulation of the Cellular Repertoire of SCF Ubiquitin Ligases
inferredcites →https://doi.org/10.1016/j.cell.2019.11.031openalex-snapshot
Proteolysis-Targeting Chimeras as Therapeutics and Tools for Biological Discovery
inferredcites →https://doi.org/10.1016/j.celrep.2019.09.079openalex-snapshot
Aryl Sulfonamides Degrade RBM39 and RBM23 by Recruitment to CRL4-DCAF15
inferredcites →https://doi.org/10.1016/j.chembiol.2021.01.005openalex-snapshot
Chemoproteomics-enabled discovery of covalent RNF114-based degraders that mimic natural product function
inferredcites →https://doi.org/10.1016/j.chembiol.2021.04.002openalex-snapshot
An E3 ligase guide to the galaxy of small-molecule-induced protein degradation
inferredcites →https://doi.org/10.1016/j.molcel.2019.07.013openalex-snapshot
Plasticity of the Cullin-RING Ligase Repertoire Shapes Sensitivity to Ligand-Induced Protein Degradation
inferredcites →https://doi.org/10.1016/j.molcel.2019.12.013openalex-snapshot
PIKES Analysis Reveals Response to Degraders and Key Regulatory Mechanisms of the CRL4 Network
inferredcites →https://doi.org/10.1016/j.str.2019.10.005openalex-snapshot
Structural Basis and Kinetic Pathway of RBM39 Recruitment to DCAF15 by a Sulfonamide Molecular Glue E7820
inferredcites →https://doi.org/10.1016/s1097-2765(00)80156-2openalex-snapshot
Ubiquitination and Degradation of the Substrate Recognition Subunits of SCF Ubiquitin–Protein Ligases
inferredcites →https://doi.org/10.1021/acschembio.5b00216openalex-snapshot
Selective Small Molecule Induced Degradation of the BET Bromodomain Protein BRD4
inferredcites →https://doi.org/10.1021/acschembio.8b00692openalex-snapshot
Quantitative Live-Cell Kinetic Degradation and Mechanistic Profiling of PROTAC Mode of Action
inferredcites →https://doi.org/10.1021/jacs.1c00990openalex-snapshot
DCAF11 Supports Targeted Protein Degradation by Electrophilic Proteolysis-Targeting Chimeras
inferredcites →https://doi.org/10.1021/jacs.1c03980openalex-snapshot
Discovery of a Covalent FEM1B Recruiter for Targeted Protein Degradation Applications
inferredcites →https://doi.org/10.1038/nature17416openalex-snapshot
Cullin–RING ubiquitin E3 ligase regulation by the COP9 signalosome
inferredcites →https://doi.org/10.1038/nature18611openalex-snapshot
A novel cereblon modulator recruits GSPT1 to the CRL4CRBN ubiquitin ligase
inferredcites →https://doi.org/10.1038/nchembio.1858openalex-snapshot
Catalytic in vivo protein knockdown by small-molecule PROTACs
inferredcites →https://doi.org/10.1038/nchembio.2329openalex-snapshot
Structural basis of PROTAC cooperative recognition for selective protein degradation
inferredcites →https://doi.org/10.1038/nchembio.2363openalex-snapshot
Selective degradation of splicing factor CAPERα by anticancer sulfonamides
inferredcites →https://doi.org/10.1038/ncomms13166openalex-snapshot
Targeted inhibition of the COP9 signalosome for treatment of cancer
inferredcites →https://doi.org/10.1038/nmeth.1322openalex-snapshot
Universal sample preparation method for proteome analysis
inferredcites →https://doi.org/10.1038/nmeth.1638openalex-snapshot
A public genome-scale lentiviral expression library of human ORFs
inferredcites →https://doi.org/10.1038/nrm1547openalex-snapshot
Function and regulation of cullin–RING ubiquitin ligases
inferredcites →https://doi.org/10.1038/s41467-019-09358-9openalex-snapshot
Prospective discovery of small molecule enhancers of an E3 ligase-substrate interaction
inferredcites →https://doi.org/10.1038/s41573-021-00371-6openalex-snapshot
PROTAC targeted protein degraders: the past is prologue
inferredcites →https://doi.org/10.1038/s41586-020-2000-yopenalex-snapshot
NEDD8 nucleates a multivalent cullin–RING–UBE2D ubiquitin ligation assembly
inferredcites →https://doi.org/10.1038/s41586-020-2168-1openalex-snapshot
Multispecific drugs herald a new era of biopharmaceutical innovation
inferredcites →https://doi.org/10.1038/s41586-020-2374-xopenalex-snapshot
The CDK inhibitor CR8 acts as a molecular glue degrader that depletes cyclin K
inferredcites →https://doi.org/10.1038/s41588-020-0635-0openalex-snapshot
Selective Mediator dependence of cell-type-specifying transcription
inferredcites →https://doi.org/10.1038/s41589-019-0279-5openalex-snapshot
Electrophilic PROTACs that degrade nuclear proteins by engaging DCAF16
inferredcites →https://doi.org/10.1038/s41589-019-0294-6openalex-snapshot
BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design
inferredcites →https://doi.org/10.1038/s41589-019-0304-8openalex-snapshot
Harnessing the anti-cancer natural product nimbolide for targeted protein degradation
inferredcites →https://doi.org/10.1038/s41589-019-0362-yopenalex-snapshot
Development of targeted protein degradation therapeutics
inferredcites →https://doi.org/10.1038/s41589-019-0378-3openalex-snapshot
Structural complementarity facilitates E7820-mediated degradation of RBM39 by DCAF15
inferredcites →https://doi.org/10.1038/s41589-019-0411-6openalex-snapshot
Structural basis of indisulam-mediated RBM39 recruitment to DCAF15 E3 ligase complex
inferredcites →https://doi.org/10.1038/s41589-020-0469-1openalex-snapshot
Unifying principles of bifunctional, proximity-inducing small molecules
inferredcites →https://doi.org/10.1038/s41589-020-0594-xopenalex-snapshot
Rational discovery of molecular glue degraders via scalable chemical profiling
inferredcites →https://doi.org/10.1038/s41589-022-01177-2openalex-snapshot
Functional E3 ligase hotspots and resistance mechanisms to small-molecule degraders
inferredcites →https://doi.org/10.1073/pnas.1521738113openalex-snapshot
PROTAC-induced BET protein degradation as a therapy for castration-resistant prostate cancer
inferredcites →https://doi.org/10.1073/pnas.96.16.9124openalex-snapshot
Ubiquitin-dependent degradation of multiple F-box proteins by an autocatalytic mechanism
inferredcites →https://doi.org/10.1101/2022.08.15.503206openalex-snapshot
Proteome-scale induced proximity screens reveal highly potent protein degraders and stabilizers
inferredcites →https://doi.org/10.1126/sciadv.abd6263openalex-snapshot
Targeting oncoproteins with a positive selection assay for protein degraders
inferredcites →https://doi.org/10.1126/science.1075901openalex-snapshot
Role of Predicted Metalloprotease Motif of Jab1/Csn5 in Cleavage of Nedd8 from Cul1
inferredcites →https://doi.org/10.1126/science.1244851openalex-snapshot
Lenalidomide Causes Selective Degradation of IKZF1 and IKZF3 in Multiple Myeloma Cells
inferredcites →https://doi.org/10.1126/science.1244917openalex-snapshot
The Myeloma Drug Lenalidomide Promotes the Cereblon-Dependent Destruction of Ikaros Proteins
inferredcites →https://doi.org/10.1126/science.aal3755openalex-snapshot
Anticancer sulfonamides target splicing by inducing RBM39 degradation via recruitment to DCAF15
inferredcites →https://doi.org/10.1126/science.aao5902openalex-snapshot
Chemically induced proximity in biology and medicine
inferredcites →https://doi.org/10.1126/science.aat0572openalex-snapshot
Defining the human C2H2 zinc finger degrome targeted by thalidomide analogs through CRBN
inferredcites →https://doi.org/10.1146/annurev-biochem-090120-013613openalex-snapshot
Cullin-RING Ubiquitin Ligase Regulatory Circuits: A Quarter Century Beyond the F-Box Hypothesis
inferredcites →https://doi.org/10.3791/61787openalex-snapshot
High-Throughput Cellular Profiling of Targeted Protein Degradation Compounds Using HiBiT CRISPR Cell Lines
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.4654255openalex-extracted
Trim4 Promotes Small-Molecule-Induced CORO1A Neddylated-Degradation for Triple Negative Breast Cancer Therapy
inferred← citeshttps://doi.org/10.1002/ange.3307512openalex-snapshot
Proteomics‐Driven Strategies for Proximity‐Inducing Drug Discovery
inferred← citeshttps://doi.org/10.1002/anie.3307512openalex-snapshot
Proteomics‐Driven Strategies for Proximity‐Inducing Drug Discovery
inferred← citeshttps://doi.org/10.1002/mog2.70058openalex-snapshot
Molecular Glue Degraders Redefining Targeted Therapies From Discovery to Therapeutic Applications
inferred← citeshttps://doi.org/10.1002/wrna.1877openalex-snapshot
Challenges in Therapeutically Targeting the RNA ‐Recognition Motif
inferred← citeshttps://doi.org/10.1007/978-1-0716-5508-5_3openalex-snapshot
Utilization of Functional Degradation Pathways for the Characterization of Ubiquitin-Proteasome System Tool Compounds
inferred← citeshttps://doi.org/10.1016/b978-0-443-21816-3.00004-xopenalex-snapshot
Protease-mediated degradation
inferred← citeshttps://doi.org/10.1016/j.chembiol.2024.04.001openalex-snapshot
Molecular glues and induced proximity: An evolution of tools and discovery
inferred← citeshttps://doi.org/10.1016/j.chembiol.2024.10.007openalex-snapshot
Degradome analysis to identify direct protein substrates of small-molecule degraders
inferred← citeshttps://doi.org/10.1016/j.drudis.2025.104307openalex-snapshot
Modulating the phosphorylation status of target proteins through bifunctional molecules
inferred← citeshttps://doi.org/10.1016/j.drudis.2025.104480openalex-snapshot
Rational discovery of molecular glue degraders based on block chemistry
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118055openalex-snapshot
Global landscape of PROTAC: Perspectives from patents, drug pipelines, clinical trials, and licensing transactions
inferred← citeshttps://doi.org/10.1016/j.jddst.2026.109004openalex-snapshot
Next-generation PROTACs (proteolysis targeting chimeras) in oncology: Targeting the undruggable proteome
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.01.022openalex-snapshot
Cullin-RING ligases employ geometrically optimized catalytic partners for substrate targeting
inferred← citeshttps://doi.org/10.1016/j.molcel.2026.03.004openalex-snapshot
An interactome-based framework for DDB1- and CUL4-associated factor prioritization in targeted protein degradation
inferred← citeshttps://doi.org/10.1016/j.sbi.2024.102811openalex-snapshot
Emerging strategies for prospective discovery of molecular glue degraders
inferred← citeshttps://doi.org/10.1016/j.slasd.2023.12.008openalex-snapshot
Screening for molecular glues – Challenges and opportunities
inferred← citeshttps://doi.org/10.1016/j.tips.2023.08.007openalex-snapshot
Proteomic approaches advancing targeted protein degradation
inferred← citeshttps://doi.org/10.1016/j.xgen.2024.100651openalex-snapshot
Pooled endogenous protein tagging and recruitment for systematic profiling of protein function
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00800openalex-snapshot
Methods to Study the Molecular Mechanism and Drive the Design of Protein Degraders
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c00723openalex-snapshot
Targeted Protein Degradation: Current and Emerging Approaches for E3 Ligase Deconvolution
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c00949openalex-snapshot
Phenotypic Screening for Targeted Protein Degradation: Strategies, Challenges, and Emerging Opportunities
inferred← citeshttps://doi.org/10.1021/acscentsci.3c00395openalex-snapshot
Proximity-Based Modalities for Biology and Medicine
inferred← citeshttps://doi.org/10.1021/acschembio.4c00191openalex-snapshot
Extrapolating Lessons from Targeted Protein Degradation to Other Proximity-Inducing Drugs
inferred← citeshttps://doi.org/10.1021/jacs.2c11098openalex-snapshot
Advancing Targeted Protein Degradation via Multiomics Profiling and Artificial Intelligence
inferred← citeshttps://doi.org/10.1021/jacs.5c12299openalex-snapshot
From Serendipity to Strategy: Rationalizing Molecular Glue Discovery and Proximity-Induced Pharmacology through Chemical Biology
inferred← citeshttps://doi.org/10.1021/jacsau.4c00442openalex-snapshot
Paralogue-Selective Degradation of the Lysine Acetyltransferase EP300
inferred← citeshttps://doi.org/10.1038/s41467-024-49739-3openalex-snapshot
Alkylamine-tethered molecules recruit FBXO22 for targeted protein degradation
inferred← citeshttps://doi.org/10.1038/s41467-024-52966-3openalex-snapshot
Principles of paralog-specific targeted protein degradation engaging the C-degron E3 KLHDC2
inferred← citeshttps://doi.org/10.1038/s41467-026-72524-3openalex-snapshot
Cysteine availability tunes ubiquitin signaling via inverse stability of LRRC58 E3 ligase and its substrate CDO1
inferred← citeshttps://doi.org/10.1038/s41580-024-00729-9openalex-snapshot
Targeted protein degradation: from mechanisms to clinic
inferred← citeshttps://doi.org/10.1038/s41589-024-01590-9openalex-snapshot
Ubiquitin-specific proximity labeling for the identification of E3 ligase substrates
inferred← citeshttps://doi.org/10.1038/s41594-024-01257-yopenalex-snapshot
Noncanonical assembly, neddylation and chimeric cullin–RING/RBR ubiquitylation by the 1.8 MDa CUL9 E3 ligase complex
inferred← citeshttps://doi.org/10.1080/17460441.2024.2306845openalex-snapshot
Molecular glue degraders: exciting opportunities for novel drug discovery
inferred← citeshttps://doi.org/10.1126/sciadv.ado6492openalex-snapshot
Mechanism of degrader-targeted protein ubiquitinability
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3161717/v1openalex-snapshot
Pooled endogenous protein tagging and recruitment for scalable discovery of effectors for induced proximity therapeutics
inferred← citeshttps://doi.org/10.2147/ijgm.s502644openalex-snapshot
Systematic Analysis of E3 Ligase-Related Genes Identified UBE2L3 as a Prognostic Biomarker Associated With Drug Resistance in Acute Myeloid Leukemia
inferred← citeshttps://doi.org/10.3389/fnmol.2024.1370509openalex-snapshot
Targeted protein degradation in CNS disorders: a promising route to novel therapeutics?
inferred← citeshttps://doi.org/10.3390/ijms232315440openalex-snapshot
Targeted Protein Degradation: Clinical Advances in the Field of Oncology
inferred← citeshttps://doi.org/10.3390/plants13212997openalex-snapshot
Cullin-Conciliated Regulation of Plant Immune Responses: Implications for Sustainable Crop Protection
inferred← citeshttps://doi.org/10.7150/thno.97662openalex-snapshot
TRIM4 enhances small-molecule-induced neddylated-degradation of CORO1A for triple negative breast cancer therapy
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.