What is he best known for?
The fields of study he is best known for:
George E. Davis focuses on Cell biology, Tube morphogenesis, Integrin, Extracellular matrix and Molecular biology.
The various areas that George E. Davis examines in his Cell biology study include Endothelial stem cell, Tube formation, Pericyte and Morphogenesis.
His Tube morphogenesis research integrates issues from Lumen, CDC42, Matrix metalloproteinase and Intracellular.
His Integrin study combines topics from a wide range of disciplines, such as Cell adhesion and Cell adhesion molecule.
In his study, Sciatic nerve and Cell migration is inextricably linked to Matrix, which falls within the broad field of Extracellular matrix.
George E. Davis combines subjects such as Epitope and Binding site with his study of Molecular biology.
His most cited work include:
- Endothelial Extracellular Matrix: Biosynthesis, Remodeling, and Functions During Vascular Morphogenesis and Neovessel Stabilization (895 citations)
- Laminin promotes neuritic regeneration from cultured peripheral and central neurons. (649 citations)
- Proteolytic exposure of a cryptic site within collagen type IV is required for angiogenesis and tumor growth in vivo (437 citations)
What are the main themes of his work throughout his whole career to date?
George E. Davis mostly deals with Cell biology, Integrin, Extracellular matrix, Endothelial stem cell and Tube morphogenesis.
His Cell biology study integrates concerns from other disciplines, such as Tube formation, Angiogenesis and Matrix metalloproteinase.
His Integrin research includes elements of Fibronectin, Cell adhesion, Vascular smooth muscle and Intracellular.
His Extracellular matrix research is multidisciplinary, incorporating elements of Extracellular, Immunology, Basement membrane, Morphogenesis and Cytoskeleton.
His Endothelial stem cell study combines topics in areas such as Metalloproteinase and Fibrin.
His Tube morphogenesis study incorporates themes from Molecular biology, Pericyte and Endothelial cell morphogenesis.
He most often published in these fields:
- Cell biology (68.26%)
- Integrin (26.35%)
- Extracellular matrix (23.35%)
What were the highlights of his more recent work (between 2012-2020)?
- Cell biology (68.26%)
- Angiogenesis (14.37%)
- Endothelial stem cell (20.36%)
In recent papers he was focusing on the following fields of study:
George E. Davis spends much of his time researching Cell biology, Angiogenesis, Endothelial stem cell, Signal transduction and Tube morphogenesis.
His studies in Cell biology integrate themes in fields like Tube formation, Cytoskeleton and Cell polarity.
His Angiogenesis research includes themes of Endothelium and Pathology.
His Tube morphogenesis research incorporates elements of Pericyte and Stromal cell.
His work deals with themes such as Tissue engineering and Integrin, which intersect with Pericyte.
George E. Davis interconnects Extracellular and Basement membrane in the investigation of issues within Extracellular matrix.
Between 2012 and 2020, his most popular works were:
- Consensus guidelines for the use and interpretation of angiogenesis assays (194 citations)
- The Neuropilin 1 Cytoplasmic Domain Is Required for VEGF-A-Dependent Arteriogenesis (136 citations)
- State-of-the-Art Methods for Evaluation of Angiogenesis and Tissue Vascularization: A Scientific Statement From the American Heart Association (77 citations)
In his most recent research, the most cited papers focused on:
His primary areas of study are Cell biology, Angiogenesis, Cdc42 GTP-Binding Protein, Apical membrane and Cytoskeleton.
His primary area of study in Cell biology is in the field of Basement membrane assembly.
The concepts of his Angiogenesis study are interwoven with issues in Organ regeneration, In vivo and MAPK/ERK pathway.
His research in Cdc42 GTP-Binding Protein intersects with topics in Vasculogenesis, Cell adhesion and Filopodia.
His biological study spans a wide range of topics, including Acetylation, Tube formation, Tube morphogenesis and Tubulin, Microtubule.
His Cytoskeleton research is multidisciplinary, incorporating elements of RHOA and Small GTPase.
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