What is he best known for?
The fields of study he is best known for:
David H. Sherr spends much of his time researching Aryl hydrocarbon receptor, Transcription factor, Cancer research, Receptor and Cell biology.
His work deals with themes such as Carcinogenesis, Inflammation, Signal transduction and Immune system, which intersect with Aryl hydrocarbon receptor.
David H. Sherr has researched Transcription factor in several fields, including Molecular biology, Apoptosis and Immunology.
The Cancer research study combines topics in areas such as Cell culture, Regulation of gene expression and NF-κB.
His research integrates issues of Gut flora, Fatty acid synthase, Pharmacology and Fatty liver in his study of Receptor.
His research in Cell biology intersects with topics in T cell and Cell growth.
His most cited work include:
- Fas(CD95)/FasL interactions required for programmed cell death after T-cell activation (1417 citations)
- Inhibition of NF-kappaB/Rel induces apoptosis of murine B cells. (564 citations)
- The aryl hydrocarbon receptor interacts with c-Maf to promote the differentiation of type 1 regulatory T cells induced by IL-27 (507 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Aryl hydrocarbon receptor, Cell biology, Molecular biology, Immunology and B cell.
His studies deal with areas such as Receptor, Cancer research, Signal transduction and Cell growth as well as Aryl hydrocarbon receptor.
David H. Sherr interconnects Apoptosis, Cell culture, Induced pluripotent stem cell and Endogeny in the investigation of issues within Cell biology.
The concepts of his Apoptosis study are interwoven with issues in Endocrinology and Internal medicine.
His study in Molecular biology is interdisciplinary in nature, drawing from both T cell, Antibody, Hapten, Antigen and Naive B cell.
David H. Sherr combines subjects such as Regulation of gene expression and NF-κB with his study of Transcription factor.
He most often published in these fields:
- Aryl hydrocarbon receptor (34.78%)
- Cell biology (33.54%)
- Molecular biology (31.06%)
What were the highlights of his more recent work (between 2016-2021)?
- Aryl hydrocarbon receptor (34.78%)
- Cancer research (27.33%)
- Neuroscience (3.11%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Aryl hydrocarbon receptor, Cancer research, Neuroscience, Cancer and Metastasis.
His work deals with themes such as Receptor, Internal medicine, Kidney disease, Uremia and Immunotherapy, which intersect with Aryl hydrocarbon receptor.
His Receptor research includes elements of Translational science and Pharmacology.
His Cancer research research is multidisciplinary, incorporating elements of Cell, Gene knockdown, Carcinogen, Cancer stem cell and Transcription factor.
Transcription factor is a subfield of Biochemistry that David H. Sherr studies.
His Induced pluripotent stem cell study combines topics in areas such as Regulation of gene expression and Cell biology.
Between 2016 and 2021, his most popular works were:
- Gut Microbiota-Derived Tryptophan Metabolites Modulate Inflammatory Response in Hepatocytes and Macrophages. (139 citations)
- Control of tumor-associated macrophages and T cells in glioblastoma via AHR and CD39. (96 citations)
- Targeting STUB1–tissue factor axis normalizes hyperthrombotic uremic phenotype without increasing bleeding risk (26 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Aryl hydrocarbon receptor, Cancer research, Neuroscience, Receptor and Political science.
His work carried out in the field of Aryl hydrocarbon receptor brings together such families of science as CCL2, Gut flora, Small hairpin RNA, Viral replication and CYP1B1.
His research in Gut flora focuses on subjects like Inflammation, which are connected to Pharmacology.
His studies deal with areas such as Cancer, Metastasis and Cell, Matrigel as well as Small hairpin RNA.
He interconnects Cell growth, WNT5A, Cancer stem cell, CD24 and Catenin in the investigation of issues within CYP1B1.
He has included themes like Endocrinology, Kidney disease and Antithrombotic in his Cancer research study.
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