What is he best known for?
The fields of study he is best known for:
His primary areas of study are Cell biology, Phosphorylation, Molecular biology, Biochemistry and Cyclin-dependent kinase 2.
His work is dedicated to discovering how Cell biology, Cell cycle are connected with Mitosis and Nuclear protein and other disciplines.
His Phosphorylation research is multidisciplinary, relying on both Tyrosine, Transcription factor and Kinase.
The Molecular biology study combines topics in areas such as Epidermal growth factor, Ubiquitin, Gene product, Gene expression and Cyclin E.
The study incorporates disciplines such as Protein-Serine-Threonine Kinases and Akt/PKB signaling pathway in addition to Cyclin-dependent kinase 2.
Tony Hunter combines subjects such as Wee1 and Protein tyrosine phosphatase with his study of Protein phosphorylation.
His most cited work include:
- The Protein Kinase Complement of the Human Genome (6034 citations)
- The protein kinase family: conserved features and deduced phylogeny of the catalytic domains. (4213 citations)
- Oncogenic kinase signalling. (3069 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cell biology, Molecular biology, Biochemistry, Phosphorylation and Kinase.
As a part of the same scientific study, Tony Hunter usually deals with the Cell biology, concentrating on Cell cycle and frequently concerns with Mitosis.
His Molecular biology study deals with RNA intersecting with Messenger RNA.
Tony Hunter interconnects Tyrosine and Histidine in the investigation of issues within Phosphorylation.
His Protein tyrosine phosphatase research is multidisciplinary, incorporating elements of Phosphatase and Receptor tyrosine kinase.
His MAP2K7 study incorporates themes from c-Raf and MAP kinase kinase kinase.
He most often published in these fields:
- Cell biology (39.90%)
- Molecular biology (32.63%)
- Biochemistry (29.24%)
What were the highlights of his more recent work (between 2012-2021)?
- Cell biology (39.90%)
- Phosphorylation (26.66%)
- Biochemistry (29.24%)
In recent papers he was focusing on the following fields of study:
Tony Hunter mostly deals with Cell biology, Phosphorylation, Biochemistry, Cancer research and Kinase.
The various areas that he examines in his Cell biology study include SUMO protein, Ubiquitin, Genetics and Transcription.
His biological study focuses on Protein phosphorylation.
His biological study deals with issues like Tyrosine phosphorylation, which deal with fields such as Protein tyrosine phosphatase.
His Kinase research incorporates themes from Histidine kinase, Cell cycle and Isozyme.
His work focuses on many connections between Protein kinase C and other disciplines, such as Mutation, that overlap with his field of interest in Molecular biology.
Between 2012 and 2021, his most popular works were:
- Vitamin D Receptor-Mediated Stromal Reprogramming Suppresses Pancreatitis and Enhances Pancreatic Cancer Therapy (532 citations)
- An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma (341 citations)
- A framework for advancing our understanding of cancer-associated fibroblasts (332 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Phosphorylation, Biochemistry, Cell biology, Kinase and Protein phosphorylation.
His Phosphorylation research includes elements of Signal transduction, Nucleoside-diphosphate kinase and Histidine.
His work deals with themes such as Cell cycle checkpoint, Transcription factor, Ubiquitin ligase and DNA damage, which intersect with Cell biology.
His work carried out in the field of Kinase brings together such families of science as Autophagy, Cancer, Cell cycle, Cancer research and Phosphoglycerate kinase 1.
As part of one scientific family, Tony Hunter deals mainly with the area of Cancer, narrowing it down to issues related to the Gene, and often Molecular biology.
His Protein phosphorylation study combines topics in areas such as Tyrosine, Protein tyrosine phosphatase, Posttranslational modification, Proteins metabolism and Expanded genetic code.
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