What is he best known for?
The fields of study he is best known for:
- Gene
- DNA
- Internal medicine
Internal medicine, Endocrinology, Adipose tissue, White adipose tissue and Adipocyte are his primary areas of study.
His research in Internal medicine intersects with topics in Nuclear receptor and Cell biology.
His studies deal with areas such as Estrogen-related receptor gamma and Beta-3 adrenergic receptor as well as Endocrinology.
His study in Adipose tissue focuses on Lipolysis in particular.
His research in the fields of Thermogenin overlaps with other disciplines such as Cellular plasticity.
James G. Granneman interconnects Steatosis, AMP-activated protein kinase, AMPK, Insulin and Fatty liver in the investigation of issues within Adipocyte.
His most cited work include:
- In Vivo Identification of Bipotential Adipocyte Progenitors Recruited by β3-Adrenoceptor Activation and High-Fat Feeding (466 citations)
- PER2 controls lipid metabolism by direct regulation of PPARγ (288 citations)
- Molecular cloning and expression of the rat beta 3-adrenergic receptor. (278 citations)
What are the main themes of his work throughout his whole career to date?
James G. Granneman focuses on Internal medicine, Endocrinology, Adipose tissue, Cell biology and Adipocyte.
His Internal medicine study frequently links to other fields, such as Gene expression.
James G. Granneman works mostly in the field of Endocrinology, limiting it down to concerns involving Messenger RNA and, occasionally, Molecular biology and Gs alpha subunit.
The Adipose tissue study combines topics in areas such as Downregulation and upregulation, Mitochondrion and Denervation.
In general Cell biology study, his work on Lipid droplet and Kinase often relates to the realm of Population, thereby connecting several areas of interest.
James G. Granneman works mostly in the field of Adipocyte, limiting it down to topics relating to Lipolysis and, in certain cases, Intracellular and Organelle.
He most often published in these fields:
- Internal medicine (51.79%)
- Endocrinology (51.79%)
- Adipose tissue (36.61%)
What were the highlights of his more recent work (between 2017-2021)?
- Adipose tissue (36.61%)
- Cell biology (33.04%)
- Adipocyte (31.25%)
In recent papers he was focusing on the following fields of study:
James G. Granneman mainly investigates Adipose tissue, Cell biology, Adipocyte, Lipolysis and Lipid droplet.
His Brown adipose tissue study in the realm of Adipose tissue interacts with subjects such as Metabolic syndrome, Research areas and Group discussion.
His study looks at the relationship between Cell biology and topics such as White adipose tissue, which overlap with Adipogenesis and Stromal cell.
His work in Adipocyte tackles topics such as Proinflammatory cytokine which are related to areas like Cancer research, Downregulation and upregulation, Tumor progression, Bone marrow and Adipose tissue macrophages.
His Lipid droplet study incorporates themes from Lipid metabolism, Lung, Perilipin and Bioinformatics.
In the field of Endocrinology and Internal medicine James G. Granneman studies Carbohydrate metabolism.
Between 2017 and 2021, his most popular works were:
- Deconstructing Adipogenesis Induced by β3-Adrenergic Receptor Activation with Single-Cell Expression Profiling. (104 citations)
- Dynamic interactions of ABHD5 with PNPLA3 regulate triacylglycerol metabolism in brown adipocytes. (29 citations)
- Deciphering the Role of Lipid Droplets in Cardiovascular Disease: A Report From the 2017 National Heart, Lung, and Blood Institute Workshop. (29 citations)
In his most recent research, the most cited papers focused on:
- Gene
- DNA
- Internal medicine
His primary areas of investigation include Adipose tissue, Cell biology, Lipolysis, Adipogenesis and White adipose tissue.
His study in Adipose tissue is interdisciplinary in nature, drawing from both Lung, Lipid droplet and Disease.
His research on Cell biology often connects related topics like Adipose triglyceride lipase.
His Lipolysis research integrates issues from Inflammation, Triglyceride lipase, Fatty acid and Fatty liver.
His Adipogenesis research integrates issues from Cell, Cell type, Stromal cell, Adipocyte and Stem cell.
His White adipose tissue study combines topics in areas such as Receptor and STAT3.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
