What is he best known for?
The fields of study he is best known for:
Michael B. Yaffe mostly deals with Cell biology, Biochemistry, Phosphorylation, Signal transduction and Kinase.
He interconnects DNA damage, G2-M DNA damage checkpoint, Cell cycle, Polo-like kinase and Binding site in the investigation of issues within Cell biology.
His work carried out in the field of Binding site brings together such families of science as Protein structure and Nuclear export signal.
His Phosphorylation study combines topics in areas such as Sequence motif, Computational biology and Mitosis.
His Signal transduction research is multidisciplinary, relying on both Autocrine signalling and Endosome.
His Kinase research integrates issues from NADPH oxidase and COS cells, Transfection.
His most cited work include:
- Scansite 2.0: proteome-wide prediction of cell signaling interactions using short sequence motifs (1384 citations)
- The structural basis for 14-3-3:phosphopeptide binding specificity. (1375 citations)
- RNF8 Transduces the DNA-Damage Signal via Histone Ubiquitylation and Checkpoint Protein Assembly. (859 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Cell biology, Biochemistry, Phosphorylation, Kinase and Signal transduction.
His Cell biology research incorporates elements of G2-M DNA damage checkpoint, Cell cycle, Transcription factor and DNA damage.
His study looks at the relationship between DNA damage and fields such as Cancer research, as well as how they intersect with chemical problems.
His Phosphorylation study frequently draws parallels with other fields, such as Binding site.
His Kinase research focuses on Computational biology and how it relates to Genetics.
The various areas that Michael B. Yaffe examines in his Mitosis study include Cytokinesis, PLK1 and Polo-like kinase.
He most often published in these fields:
- Cell biology (38.81%)
- Biochemistry (19.92%)
- Phosphorylation (16.43%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (38.81%)
- Coagulopathy (5.95%)
- Fibrinolysis (5.34%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cell biology, Coagulopathy, Fibrinolysis, Tissue plasminogen activator and Internal medicine.
His Cell biology study integrates concerns from other disciplines, such as Cell cycle and DNA damage.
His Coagulopathy study also includes
- Respiratory failure and related Pulmonary function testing and Mechanical ventilation,
- Intensive care medicine together with Global health and Animal data.
His Fibrinolysis research incorporates themes from Thrombin and Plasmin.
His Internal medicine research includes themes of Gastroenterology and Oncology.
His study in Phosphorylation is interdisciplinary in nature, drawing from both Tyrosine, Mutant and PLK1.
Between 2018 and 2021, his most popular works were:
- Tissue plasminogen activator (tPA) treatment for COVID-19 associated acute respiratory distress syndrome (ARDS): A case series. (261 citations)
- Tissue plasminogen activator (tPA) treatment for COVID-19 associated acute respiratory distress syndrome (ARDS): A case series. (261 citations)
- ISTH interim guidance on recognition and management of coagulopathy in COVID-19: A comment. (106 citations)
In his most recent research, the most cited papers focused on:
Michael B. Yaffe focuses on Tissue plasminogen activator, Coagulopathy, Cell biology, Fibrinolysis and Pneumonia.
His Tissue plasminogen activator research includes elements of Proinflammatory cytokine, Ex vivo, Plasmin and Urokinase.
The study incorporates disciplines such as Disseminated intravascular coagulation, Virology and Respiratory failure in addition to Coagulopathy.
His Cell biology study incorporates themes from Cancer cell, Cell cycle and Bromodomain.
The concepts of his Fibrinolysis study are interwoven with issues in Plasminogen activator, ARDS, Thrombin and Pharmacology.
His Signal transduction research is multidisciplinary, incorporating perspectives in Mutant, Kinase, Actin cytoskeleton and Phosphorylation.
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