What is he best known for?
The fields of study he is best known for:
- Gene
- DNA
- Internal medicine
Myocyte, Cell biology, Internal medicine, Pathology and Cellular differentiation are his primary areas of study.
His Myocyte research includes elements of Ratón, Cell, Transplantation and DNA synthesis.
His Cell biology research incorporates themes from Embryonic stem cell, Cell growth and Anatomy.
His work carried out in the field of Internal medicine brings together such families of science as Endocrinology and Cardiology.
His Endocrinology research incorporates elements of Genetically modified mouse, Transgene and Gene expression.
His studies in Cellular differentiation integrate themes in fields like Molecular biology, Stem cell and Cellular cardiomyoplasty.
His most cited work include:
- Haematopoietic stem cells do not transdifferentiate into cardiac myocytes in myocardial infarcts (2036 citations)
- Human cardiovascular progenitor cells develop from a KDR + embryonic-stem-cell-derived population (1214 citations)
- Genetically selected cardiomyocytes from differentiating embronic stem cells form stable intracardiac grafts. (1130 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Cell biology, Internal medicine, Endocrinology, Genetically modified mouse and Transgene.
His research integrates issues of Cell cycle, In vitro and Embryonic stem cell in his study of Cell biology.
He has researched Embryonic stem cell in several fields, including Cell culture and Stem cell.
His studies deal with areas such as Immunology, Cellular differentiation and Transplantation as well as Stem cell.
He has included themes like Fibrosis and Gene expression in his Endocrinology study.
His research in Genetically modified mouse intersects with topics in Molecular biology, Fusion gene and Ratón.
He most often published in these fields:
- Cell biology (37.37%)
- Internal medicine (29.29%)
- Endocrinology (22.73%)
What were the highlights of his more recent work (between 2012-2021)?
- Cell biology (37.37%)
- Cell cycle (17.17%)
- Cyclin D2 (8.59%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Cell cycle, Cyclin D2, Internal medicine and Embryonic stem cell.
His Cell biology research includes themes of Cardiomyocyte proliferation and Transgene.
Loren J. Field studies Transgene, namely Genetically modified mouse.
His biological study spans a wide range of topics, including Endocrinology and Cardiology.
His research in Embryonic stem cell tackles topics such as Stem cell which are related to areas like Transplantation and Mice transgenic.
As a part of the same scientific study, Loren J. Field usually deals with the Induced pluripotent stem cell, concentrating on Cellular differentiation and frequently concerns with Cell growth.
Between 2012 and 2021, his most popular works were:
- Cardiomyocyte regeneration: A consensus statement (225 citations)
- Myocardial Polyploidization Creates a Barrier to Heart Regeneration in Zebrafish (111 citations)
- Parthenogenetic stem cells for tissue-engineered heart repair (82 citations)
In his most recent research, the most cited papers focused on:
- Gene
- DNA
- Internal medicine
His scientific interests lie mostly in Cell biology, Cell cycle, Cellular differentiation, Cell growth and Internal medicine.
The various areas that Loren J. Field examines in his Cell biology study include Embryonic stem cell, GLUT4 and Insulin Receptor Substrate Proteins, Insulin receptor.
His Cell cycle study combines topics from a wide range of disciplines, such as Cardiac function curve, Molecular biology, Bromodeoxyuridine and DNA synthesis.
The Cellular differentiation study combines topics in areas such as Cardiomyocyte proliferation and Stem cell.
His Cell growth study integrates concerns from other disciplines, such as Mesenchymal stem cell, Pathology, Neuroscience and Cell therapy.
His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Notch signaling pathway.
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