What is he best known for?
The fields of study he is best known for:
Robert G. Hawley mainly investigates Molecular biology, Haematopoiesis, Bone marrow, Viral vector and Gene.
His Molecular biology study combines topics from a wide range of disciplines, such as Embryonic stem cell, Cellular differentiation, Mutant, Signal transduction and Stem cell.
His study in Haematopoiesis is interdisciplinary in nature, drawing from both Cell culture and Transplantation.
Robert G. Hawley combines subjects such as Cancer research, Thrombopoietin and Megakaryocyte with his study of Bone marrow.
His biological study spans a wide range of topics, including Enhancer, Promoter, Transgene and Green fluorescent protein.
Gene is a subfield of Genetics that Robert G. Hawley studies.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Versatile retroviral vectors for potential use in gene therapy. (647 citations)
- Inhibition of nuclear hormone receptor activity by calreticulin (335 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Molecular biology, Haematopoiesis, Stem cell, Cancer research and Cell biology.
The Molecular biology study combines topics in areas such as Gene expression, Mutant, Green fluorescent protein, Gene and Long terminal repeat.
His studies in Haematopoiesis integrate themes in fields like Cell culture, Progenitor cell, Myeloid, Bone marrow and Transplantation.
Robert G. Hawley interconnects Genetic enhancement, Immunology and Virology in the investigation of issues within Stem cell.
As a member of one scientific family, Robert G. Hawley mostly works in the field of Genetic enhancement, focusing on Viral vector and, on occasion, Transgene.
His research in Cell biology intersects with topics in Endothelial stem cell, Embryonic stem cell, Cellular differentiation and Adult stem cell.
He most often published in these fields:
- Molecular biology (39.59%)
- Haematopoiesis (36.73%)
- Stem cell (31.43%)
What were the highlights of his more recent work (between 2010-2019)?
- Cancer research (31.84%)
- Gene (22.45%)
- Promoter (9.39%)
In recent papers he was focusing on the following fields of study:
Robert G. Hawley mainly investigates Cancer research, Gene, Promoter, Parkinson's disease and Carfilzomib.
The study incorporates disciplines such as Autophagy, Apoptosis, Signal transduction and Ectopic expression in addition to Cancer research.
Specifically, his work in Gene is concerned with the study of Transcription factor.
His biological study deals with issues like Regulatory sequence, which deal with fields such as Molecular biology.
As a part of the same scientific family, Robert G. Hawley mostly works in the field of Sequestosome 1, focusing on Autophagosome and, on occasion, Computational biology.
He has included themes like BECN1 and Programmed cell death in his Computational biology study.
Between 2010 and 2019, his most popular works were:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Identification of an ABCB1 (P-glycoprotein)-positive carfilzomib-resistant myeloma subpopulation by the pluripotent stem cell fluorescent dye CDy1. (58 citations)
- Identification of an ABCB1 (P-glycoprotein)-positive carfilzomib-resistant myeloma subpopulation by the pluripotent stem cell fluorescent dye CDy1. (58 citations)
In his most recent research, the most cited papers focused on:
Robert G. Hawley mostly deals with Cancer research, Autophagy, Carfilzomib, Proteasome inhibitor and Parkinson's disease.
His studies deal with areas such as Computational biology and Programmed cell death as well as Autophagy.
His work deals with themes such as Cytotoxic T cell, Cancer stem cell, Pharmacology and Induced pluripotent stem cell, which intersect with Carfilzomib.
His Parkinson's disease study incorporates themes from ATG5, Pathogenesis, Real-time polymerase chain reaction, Gene and Promoter.
His Gene study improves the overall literature in Genetics.
His Sequestosome 1 research is multidisciplinary, incorporating elements of MAP1LC3B, Autophagosome, Physiology and Initiation factor.
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