What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Cell biology, Cyclin-dependent kinase, Cyclin A, Cyclin D and Cyclin A2.
His biological study spans a wide range of topics, including Cell cycle and Cyclin.
His study in Cyclin is interdisciplinary in nature, drawing from both Kinase and Cyclin-dependent kinase 2.
His Cyclin-dependent kinase research focuses on Restriction point in particular.
His Cyclin A research is multidisciplinary, incorporating perspectives in Cyclin-dependent kinase 1, Cyclin-dependent kinase complex, Molecular biology and Cyclin B.
His Cyclin D study incorporates themes from Cyclin E, Cyclin binding and Cyclin D3.
His most cited work include:
- CDK inhibitors: positive and negative regulators of G1-phase progression (5228 citations)
- Inhibitors of mammalian G1 cyclin-dependent kinases. (2903 citations)
- Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals (1974 citations)
What are the main themes of his work throughout his whole career to date?
James M. Roberts spends much of his time researching Cell biology, Cyclin-dependent kinase, Cyclin E, Cell cycle and Cyclin.
The Cell biology study combines topics in areas such as Molecular biology, Cell division, Cyclin A and Cyclin-dependent kinase 2.
His Cyclin A study combines topics from a wide range of disciplines, such as Cyclin-dependent kinase 1, Cyclin A2, Polo-like kinase and Cyclin D.
As part of the same scientific family, James M. Roberts usually focuses on Cyclin A2, concentrating on Cyclin-dependent kinase complex and intersecting with Cyclin-dependent kinase 3.
His study looks at the intersection of Cyclin-dependent kinase and topics like Cytoplasm with Tyrosine kinase.
James M. Roberts has included themes like Progenitor cell, Cancer research, Cell growth and Cellular differentiation in his Cell cycle study.
He most often published in these fields:
- Cell biology (57.89%)
- Cyclin-dependent kinase (33.33%)
- Cyclin E (29.82%)
What were the highlights of his more recent work (between 2007-2014)?
- Cell biology (57.89%)
- Cell cycle (28.95%)
- Cyclin-dependent kinase (33.33%)
In recent papers he was focusing on the following fields of study:
James M. Roberts mostly deals with Cell biology, Cell cycle, Cyclin-dependent kinase, Cyclin A and Cancer research.
Specifically, his work in Cell biology is concerned with the study of Kinase.
His work on Restriction point as part of general Cell cycle research is frequently linked to Cell fate determination, thereby connecting diverse disciplines of science.
His biological study spans a wide range of topics, including Cytoplasm, Carcinogenesis, Tyrosine kinase, Kinase activity and Leukemia.
His Cyclin A study combines topics in areas such as Cyclin-dependent kinase 1, Cyclin A2, Tissue homeostasis, Polo-like kinase and Cyclin D.
Cyclin E is closely connected to Cyclin B in his research, which is encompassed under the umbrella topic of Cyclin A2.
Between 2007 and 2014, his most popular works were:
- CDK inhibitors: cell cycle regulators and beyond. (794 citations)
- Cyclin I activates Cdk5 and regulates expression of Bcl-2 and Bcl-XL in postmitotic mouse cells (82 citations)
- Separation of telomerase functions by reverse genetics (78 citations)
In his most recent research, the most cited papers focused on:
His primary areas of investigation include Cell biology, Cell cycle, Cyclin A, Cyclin-dependent kinase and Cyclin D.
His Cell biology research is multidisciplinary, incorporating perspectives in Cellular differentiation, Cyclin-dependent kinase 1, Histone deacetylase, Cyclin D1 and Telomerase reverse transcriptase.
His Cyclin-dependent kinase 1 research includes elements of Restriction point, Tissue homeostasis and Polo-like kinase.
His research on Cyclin D1 focuses in particular on Cyclin E.
His work deals with themes such as Molecular biology, Cyclin A2 and Cyclin B, which intersect with Cyclin D.
His Cyclin A2 study frequently draws parallels with other fields, such as Kinase.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
