What is he best known for?
The fields of study he is best known for:
His main research concerns Cell biology, Cell cycle, Cyclin-dependent kinase 1, Cyclin-dependent kinase and Kinase.
He has researched Cell biology in several fields, including CHEK1, Biochemistry and Proliferating cell nuclear antigen.
His biological study spans a wide range of topics, including Molecular biology and Cell growth.
His Cyclin-dependent kinase study integrates concerns from other disciplines, such as Phosphatase, CDC25A and Cyclin-dependent kinase 2.
He combines subjects such as Phosphorylation and Cyclin with his study of Kinase.
In his work, G1/S transition and Cancer research is strongly intertwined with Centrosome, which is a subfield of Phosphorylation.
His most cited work include:
- Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. (1152 citations)
- CDC25 phosphatases in cancer cells: key players? Good targets? (530 citations)
- The when and wheres of CDC25 phosphatases. (350 citations)
What are the main themes of his work throughout his whole career to date?
Bernard Ducommun focuses on Cell biology, Cell cycle, Biochemistry, Mitosis and Cdc25.
His studies deal with areas such as Cyclin-dependent kinase 1, Cyclin-dependent kinase and CHEK1 as well as Cell biology.
His study looks at the relationship between Cyclin-dependent kinase 1 and topics such as Cyclin-dependent kinase 7, which overlap with Cyclin-dependent kinase complex.
His Cell cycle study incorporates themes from Multicellular organism, Cancer research, Tumor spheroid and Cell growth.
His research in Mitosis focuses on subjects like DNA damage, which are connected to Downregulation and upregulation.
His Cdc25 research incorporates themes from HeLa and CDC25A.
He most often published in these fields:
- Cell biology (59.28%)
- Cell cycle (36.60%)
- Biochemistry (27.84%)
What were the highlights of his more recent work (between 2013-2020)?
- Cell biology (59.28%)
- Spheroid (11.86%)
- Tumor spheroid (12.89%)
In recent papers he was focusing on the following fields of study:
Cell biology, Spheroid, Tumor spheroid, Cell and Cancer research are his primary areas of study.
When carried out as part of a general Cell biology research project, his work on Phosphorylation is frequently linked to work in Micronucleus test, therefore connecting diverse disciplines of study.
The Spheroid study combines topics in areas such as Biophysics, Cell growth and Biomedical engineering.
His Cytoskeleton study in the realm of Cell connects with subjects such as Dynamics.
His studies in Cancer research integrate themes in fields like Cancer, Cell cycle, Cell cycle checkpoint, Breast cancer cells and Cluster analysis.
His research in Cell cycle intersects with topics in Probabilistic logic and Simulation.
Between 2013 and 2020, his most popular works were:
- Short and long time effects of low temperature Plasma Activated Media on 3D multicellular tumor spheroids. (87 citations)
- Low-temperature plasma-induced antiproliferative effects on multi-cellular tumor spheroids (52 citations)
- Low-temperature plasma-induced antiproliferative effects on multi-cellular tumor spheroids (52 citations)
In his most recent research, the most cited papers focused on:
Bernard Ducommun mostly deals with Cell biology, Spheroid, Cell, Cell growth and Phosphorylation.
He conducts interdisciplinary study in the fields of Cell biology and Histone code through his research.
Within one scientific family, Bernard Ducommun focuses on topics pertaining to Biophysics under Spheroid, and may sometimes address concerns connected to Cancer, In vitro, Characterization and Cancer cell.
His work in Cell growth covers topics such as Cell culture which are related to areas like Proliferation index and Catalase.
Bernard Ducommun has included themes like Tumor spheroid, Nanotechnology, DNA damage, Reactive oxygen species and Growth inhibition in his Phosphorylation study.
His work deals with themes such as Apoptosis, Programmed cell death, Toxicology and Cysteine, which intersect with DNA damage.
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