What is he best known for?
The fields of study he is best known for:
The scientist’s investigation covers issues in Osteoblast, Endocrinology, Internal medicine, Cellular differentiation and Cell biology.
His Osteoblast study combines topics in areas such as Osteocalcin, Gene expression and GPNMB.
His work is dedicated to discovering how Gene expression, Bone cell are connected with Osteopontin and other disciplines.
His Endocrinology research is multidisciplinary, incorporating perspectives in Agonist and Bone healing.
His study in Cell biology focuses on Extracellular matrix and Mesenchymal stem cell.
His Extracellular matrix research is multidisciplinary, incorporating elements of Cell growth and Calvaria.
His most cited work include:
- Progressive development of the rat osteoblast phenotype in vitro: Reciprocal relationships in expression of genes associated with osteoblast proliferation and differentiation during formation of the bone extracellular matrix (1407 citations)
- Relationship of cell growth to the regulation of tissue-specific gene expression during osteoblast differentiation. (812 citations)
- Factors that promote progressive development of the osteoblast phenotype in cultured fetal rat calvaria cells. (481 citations)
What are the main themes of his work throughout his whole career to date?
Thomas A. Owen mostly deals with Molecular biology, Osteoblast, Cell biology, Endocrinology and Internal medicine.
His studies in Molecular biology integrate themes in fields like Cellular differentiation, Complementary DNA, Northern blot, Regulation of gene expression and Response element.
His Osteoblast research incorporates themes from Bone cell, Phenotype, Gene expression, Gene and Osteocalcin.
Thomas A. Owen combines subjects such as Bone formation, Growth factor and Cell growth with his study of Cell biology.
Thomas A. Owen has included themes like Agonist, Receptor, Chondrocyte and CTGF in his Endocrinology study.
His work in the fields of Estrogen, Bone remodeling and Hormone overlaps with other areas such as Matrix gla protein.
He most often published in these fields:
- Molecular biology (43.33%)
- Osteoblast (37.78%)
- Cell biology (33.33%)
What were the highlights of his more recent work (between 2007-2020)?
- Osteoblast (37.78%)
- Receptor (10.00%)
- Cell biology (33.33%)
In recent papers he was focusing on the following fields of study:
Osteoblast, Receptor, Cell biology, Agonist and Molecular biology are his primary areas of study.
Thomas A. Owen merges many fields, such as Osteoblast and Hormone response element, in his writings.
His Receptor study incorporates themes from Osteocalcin, Endocrinology, Transcription and Vitamin D Response Element.
Thomas A. Owen works in the field of Cell biology, focusing on Bone cell in particular.
His research in Agonist intersects with topics in Prostaglandin E2 and Bone healing.
His Molecular biology research includes themes of SMAD binding, SMAD, Immediate early protein, Proto-oncogene tyrosine-protein kinase Src and Response element.
Between 2007 and 2020, his most popular works were:
- Osteoactivin, an anabolic factor that regulates osteoblast differentiation and function. (94 citations)
- The role of connective tissue growth factor (CTGF/CCN2) in skeletogenesis. (62 citations)
- 1α,25‐Dihydroxyvitamin D3 rapidly increases cytosolic calcium in clonal rat osteosarcoma cells lacking the vitamin D Receptor (60 citations)
In his most recent research, the most cited papers focused on:
Thomas A. Owen mainly investigates CTGF, Endocrinology, Cell biology, Osteoblast and Internal medicine.
The CTGF study combines topics in areas such as Molecular biology, Signal transduction, SMAD, Src family kinase and Response element.
His work deals with themes such as Osteocalcin, Receptor and Calcium metabolism, Calcium, which intersect with Endocrinology.
His work carried out in the field of Cell biology brings together such families of science as Biochemistry and Glycoprotein.
His study in Osteoblast is interdisciplinary in nature, drawing from both Chondrogenesis, Bone cell, GPNMB, Western blot and Retinoic acid.
His biological study spans a wide range of topics, including VDRE and Chondrocyte.
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