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Author Details

James E Bradner
1995
262
106
PMIDPaper TitleJournal TitlePublished Year
37237081Genome-scale functional genomics identify genes preferentially essential for multiple myeloma cells compared to other neoplasias.Nat Cancer2023
37582753Diversity-oriented synthesis encoded by deoxyoligonucleotides.Nat Commun2023
37989745Author Correction: Diversity-oriented synthesis encoded by deoxyoligonucleotides.Nat Commun2023
36863346Discovery and characterization of a selective IKZF2 glue degrader for cancer immunotherapy.Cell Chem Biol2023
35226736BET-bromodomain and EZH2 inhibitor-treated chronic GVHD mice have blunted germinal centers with distinct transcriptomes.Blood2022
35994477A toolbox for class I HDACs reveals isoform specific roles in gene regulation and protein acetylation.PLoS Genet2022
35031563Inhibition of EZH2 transactivation function sensitizes solid tumors to genotoxic stress.Proc Natl Acad Sci U S A2022
34650218Selective targeting of MYC mRNA by stabilized antisense oligonucleotides.Oncogene2021
34107377The synergy of BET inhibitors with aurora A kinase inhibitors in MYCN-amplified neuroblastoma is heightened with functional TP53.Neoplasia2021
33547076Targeting oncoproteins with a positive selection assay for protein degraders.Sci Adv2021
33406420Functional Genomics Identify Distinct and Overlapping Genes Mediating Resistance to Different Classes of Heterobifunctional Degraders of Oncoproteins.Cell Rep2021
34396987BET bromodomain protein inhibition reverses chimeric antigen receptor extinction and reinvigorates exhausted T cells in chronic lymphocytic leukemia.J Clin Invest2021
34434504Correction: HDAC6 inhibitor WT161 downregulates growth factor receptors in breast cancer.Oncotarget2021
32948771Rapid and direct control of target protein levels with VHL-recruiting dTAG molecules.Nat Commun2020
32483291Selective Mediator dependence of cell-type-specifying transcription.Nat Genet2020
33016930Orally bioavailable CDK9/2 inhibitor shows mechanism-based therapeutic potential in MYCN-driven neuroblastoma.J Clin Invest2020
32620694Correction: Bromodomain and extraterminal protein inhibition blocks growth of triple-negative breast cancers through the suppression of aurora kinases.J Biol Chem2020
30664779Small-molecule targeting of brachyury transcription factor addiction in chordoma.Nat Med2019
31620231Dual Inhibition of TAF1 and BET Bromodomains from the BI-2536 Kinase Inhibitor Scaffold.ACS Med Chem Lett2019
30279226Small-molecule BCL6 inhibitor effectively treats mice with nonsclerodermatous chronic graft-versus-host disease.Blood2019
30630822Enhancer Domains in Gastrointestinal Stromal Tumor Regulate KIT Expression and Are Targetable by BET Bromodomain Inhibition.Cancer Res2019
31133746MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation.Nat Genet2019
31126889The BET inhibitor JQ1 attenuates double-strand break repair and sensitizes models of pancreatic ductal adenocarcinoma to PARP inhibitors.EBioMedicine2019
31431624PAX8 activates metabolic genes via enhancer elements in Renal Cell Carcinoma.Nature Communications2019
31260717Maintenance and enhancement of human peripheral blood mobilized stem/progenitor cell engraftment after ex vivo culture via an HDACi/SALL4 axis (3465).Exp Hematol2019
31160565Neuronal differentiation and cell-cycle programs mediate response to BET-bromodomain inhibition in MYC-driven medulloblastoma.Nat Commun2019
29581585The dTAG system for immediate and target-specific protein degradation.Nat Chem Biol2018
29892083Plasticity in binding confers selectivity in ligand-induced protein degradation.Nat Chem Biol2018
30503705Enhancer Architecture and Essential Core Regulatory Circuitry of Chronic Lymphocytic Leukemia.Cancer Cell2018
30397315A non-canonical SWI/SNF complex is a synthetic lethal target in cancers driven by BAF complex perturbation.Nat Cell Biol2018
30590042Non-overlapping Control of Transcriptome by Promoter- and Super-Enhancer-Associated Dependencies in Multiple Myeloma.Cell Rep2018
30431433Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma.Elife2018
30102854Structural and Atropisomeric Factors Governing the Selectivity of Pyrimido-benzodiazipinones as Inhibitors of Kinases and Bromodomains.ACS Chem Biol2018
29866822Gastrointestinal stromal tumor enhancers support a transcription factor network predictive of clinical outcome.Proc Natl Acad Sci U S A2018
29907650JAK2 is dispensable for maintenance of JAK2 mutant B-cell acute lymphoblastic leukemias.Genes Dev2018
30087114BET Bromodomain Inhibition Cooperates with PD-1 Blockade to Facilitate Antitumor Response in <i>Kras</i>-Mutant Non-Small Cell Lung Cancer.Cancer Immunol Res2018
30125504Structure-Guided Design and Development of Potent and Selective Dual Bromodomain 4 (BRD4)/Polo-like Kinase 1 (PLK1) Inhibitors.J Med Chem2018
29764999Targetable BET proteins- and E2F1-dependent transcriptional program maintains the malignancy of glioblastoma.Proc Natl Acad Sci U S A2018
29356495Translation Termination Factor GSPT1 Is a Phenotypically Relevant Off-Target of Heterobifunctional Phthalimide Degraders.ACS Chemical Biology2018
29142067JQ1 Induces DNA Damage and Apoptosis, and Inhibits Tumor Growth in a Patient-Derived Xenograft Model of Cholangiocarcinoma.Mol Cancer Ther2018
29444854BET bromodomain proteins regulate enhancer function during adipogenesis.Proceedings of the National Academy of Sciences of the United States of America2018
29760044NK Cells Mediate Synergistic Antitumor Effects of Combined Inhibition of HDAC6 and BET in a SCLC Preclinical Model.Cancer Res2018
29180399Diminished microRNA-29b level is associated with BRD4-mediated activation of oncogenes in cutaneous T-cell lymphoma.Blood2018
29302039Targeting the CoREST complex with dual histone deacetylase and demethylase inhibitors.Nat Commun2018
29258295Therapeutic targeting of ependymoma as informed by oncogenic enhancer profiling.Nature2018
29129717A Chemoproteomic Approach to Query the Degradable Kinome Using a Multi-kinase Degrader.Cell Chem Biol2018
29379199Enhancer invasion shapes MYCN-dependent transcriptional amplification in neuroblastoma.Nature Genetics2018
29511348Combined BET bromodomain and CDK2 inhibition in MYC-driven medulloblastoma.Oncogene2018
29251720Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation.Nat Chem Biol2018
29249691Dual Targeting of Oncogenic Activation and Inflammatory Signaling Increases Therapeutic Efficacy in Myeloproliferative Neoplasms.Cancer Cell2018
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Harvard Medical School
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Broad Institute
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Broad Institute of MIT and Harvard, USA Dana-Farber Cancer Institute
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Broad Institute of Harvard and MIT
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Memorial Sloan Kettering Cancer Center
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University of California san francisco
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Dana-Farber Cancer Institute, Harvard Medical School, Brigham and Women's Hospital
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Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard
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The University of Melbourne
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Novartis Institutes for BioMedical Research
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Dana-Farber Cancer Institute
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Broad Institute of Harvard and MIT
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Sanford Burnham Prebys Medical Discovery Institute
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CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
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Merck & Co.
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Broad Institute of MIT and Harvard
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The Jackson Laboratory Cancer Center
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