Ebert, Benjamin L.
Benjamin L. Ebert American oncologist
VIAF ID: 121115560 (Personal)
Permalink: http://viaf.org/viaf/121115560
Preferred Forms
- 100 0 _ ‡a Benjamin L. Ebert ‡c American oncologist
- 100 1 _ ‡a Ebert, Benjamin L.
- 100 1 _ ‡a Ebert, Benjamin L.
-
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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The AIM2 inflammasome exacerbates atherosclerosis in clonal haematopoiesis | |
Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia | |
Cancer therapy shapes the fitness landscape of clonal hematopoiesis | |
The CDK inhibitor CR8 acts as a molecular glue degrader that depletes cyclin K | |
Clonal hematopoiesis is associated with adverse outcomes in multiple myeloma patients undergoing transplant | |
Defining the human C2H2 zinc finger degrome targeted by thalidomide analogs through CRBN | |
Distinction of lymphoid and myeloid clonal hematopoiesis | |
A dominant-negative effect drives selection of TP53 missense mutations in myeloid malignancies | |
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles | |
Generations of physician-scientists | |
Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies | |
A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms | |
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection | |
The impact of the COVID-19 pandemic on cancer care | |
Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation | |
Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms. | |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes | |
The landscape of somatic copy-number alteration across human cancers | |
Metagene projection for cross-platform, cross-species characterization of global transcriptional states | |
miR-126 Regulates Distinct Self-Renewal Outcomes in Normal and Malignant Hematopoietic Stem Cells | |
Myelodysplastic syndromes, 2010: | |
PPM1D mutations are oncogenic drivers of de novo diffuse midline glioma formation | |
The Public Repository of Xenografts Enables Discovery and Randomized Phase II-like Trials in Mice | |
Rapid and deep-scale ubiquitylation profiling for biology and translational research | |
Recurrent genetic HLA loss in AML relapsed after matched unrelated allogeneic hematopoietic cell transplantation | |
Reversible ON- and OFF-switch chimeric antigen receptors controlled by lenalidomide | |
Small-molecule-induced polymerization triggers degradation of BCL6 |