What is he best known for?
The fields of study he is best known for:
David D. Moore spends much of his time researching Nuclear receptor, Endocrinology, Internal medicine, Constitutive androstane receptor and Receptor. His work carried out in the field of Nuclear receptor brings together such families of science as Bile acid, Hepatocyte, Transactivation, Molecular biology and Regulator. His Bile acid study combines topics from a wide range of disciplines, such as Farnesoid X receptor, Pregnane X receptor and Cholestasis.
His Endocrinology research is multidisciplinary, incorporating perspectives in Regulation of gene expression, Liver X receptor beta and Cell biology. His Constitutive androstane receptor study integrates concerns from other disciplines, such as Jaundice, Sulfation, Xenobiotic, Bilirubin and Lithocholic acid. His Receptor research is multidisciplinary, incorporating elements of Hormone response element and Pharmacology.
His most cited work include:
- Preparation and Analysis of DNA (420 citations)
- Redundant Pathways for Negative Feedback Regulation of Bile Acid Production (398 citations)
- The Xenobiotic Compound 1,4-Bis(2-(3,5-Dichloropyridyloxy))Benzene Is an Agonist Ligand for the Nuclear Receptor CAR (343 citations)
What are the main themes of his work throughout his whole career to date?
Internal medicine, Endocrinology, Nuclear receptor, Receptor and Constitutive androstane receptor are his primary areas of study. Internal medicine is closely attributed to Gastroenterology in his work. In his study, Orphan receptor and Liver receptor homolog-1 is inextricably linked to Small heterodimer partner, which falls within the broad field of Endocrinology.
His work deals with themes such as Molecular biology, Cancer research, Cell biology and Transactivation, which intersect with Nuclear receptor. The concepts of his Constitutive androstane receptor study are interwoven with issues in Gene expression, Xenobiotic, Cytochrome P450, Pregnane X receptor and Pharmacology. His biological study spans a wide range of topics, including Farnesoid X receptor and Cholestasis.
He most often published in these fields:
- Internal medicine (36.09%)
- Endocrinology (30.45%)
- Nuclear receptor (23.68%)
What were the highlights of his more recent work (between 2017-2021)?
- Internal medicine (36.09%)
- Endocrinology (30.45%)
- Cell biology (11.65%)
In recent papers he was focusing on the following fields of study:
David D. Moore mostly deals with Internal medicine, Endocrinology, Cell biology, Cancer research and Constitutive androstane receptor. His Internal medicine study frequently draws connections between related disciplines such as Gastroenterology. His research on Endocrinology often connects related topics like Nuclear receptor.
His Cell biology research incorporates elements of Autophagy, Small intestine, Epigenomics, Gene and Enterohepatic circulation. His Cancer research research includes themes of Cancer, Protein kinase B, Inflammatory bowel disease and MAPK/ERK pathway. As a part of the same scientific family, David D. Moore mostly works in the field of Constitutive androstane receptor, focusing on Cytokine and, on occasion, Cytotoxic T cell.
Between 2017 and 2021, his most popular works were:
- miR-30a Remodels Subcutaneous Adipose Tissue Inflammation to Improve Insulin Sensitivity in Obesity (35 citations)
- MAPK4 overexpression promotes tumor progression via noncanonical activation of AKT/mTOR signaling (23 citations)
- Compensatory changes in CYP expression in three different toxicology mouse models: CAR-null, Cyp3a-null, and Cyp2b9/10/13-null mice (19 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Cell biology, Internal medicine, Cancer research, Autophagy and Heart failure. David D. Moore has included themes like White Adipocytes, Inflammasome, Liver cell, Gene product and Cell fate determination in his Cell biology study. His Endocrinology research extends to the thematically linked field of Internal medicine.
His studies deal with areas such as Proinflammatory cytokine, Inflammation and microRNA as well as Endocrinology. His work on Hepatocellular carcinoma as part of general Cancer research study is frequently connected to TGF alpha, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Autophagy research incorporates themes from Body weight and Brown adipose tissue, Brown Adipocytes.
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