What is he best known for?
The fields of study he is best known for:
His main research concerns Receptor, Aryl hydrocarbon receptor, Internal medicine, Biochemistry and Cytosol.
His work deals with themes such as Exon, Stereochemistry, Binding site and Cell biology, which intersect with Receptor.
His studies deal with areas such as Xenobiotic and CYP1B1 as well as Aryl hydrocarbon receptor.
His study focuses on the intersection of Internal medicine and fields such as Endocrinology with connections in the field of Hydroxylation, 3,3'-Diindolylmethane and Microsome.
His research in Biochemistry is mostly concerned with Enzyme inducer.
The concepts of his Cytosol study are interwoven with issues in Inducer, Methylcholanthrene and Molecular biology.
His most cited work include:
- Role of Aryl Hydrocarbon Receptor-mediated Induction of the CYP1 Enzymes in Environmental Toxicity and Cancer (946 citations)
- Enzyme induction in the cytochrome P-450 system. (574 citations)
- Regulatory gene product of the Ah locus. Characterization of the cytosolic inducer-receptor complex and evidence for its nuclear translocation. (356 citations)
What are the main themes of his work throughout his whole career to date?
Allan B. Okey mainly investigates Receptor, Internal medicine, Biochemistry, Cytosol and Aryl hydrocarbon receptor.
His Receptor research is multidisciplinary, relying on both Cell culture, Nuclear receptor, Stereochemistry and Mechanism of action.
His Internal medicine study combines topics from a wide range of disciplines, such as Endocrinology and Downregulation and upregulation.
His studies in Cytosol integrate themes in fields like Benzopyrene, Molecular mass, Tetrachlorodibenzo-p-dioxin, Receptor complex and Steroid.
His research integrates issues of Molecular biology, Transcriptome, Toxicity and CYP1B1 in his study of Aryl hydrocarbon receptor.
In his work, Cell biology is strongly intertwined with Xenobiotic, which is a subfield of Toxicity.
He most often published in these fields:
- Receptor (48.85%)
- Internal medicine (32.06%)
- Biochemistry (29.01%)
What were the highlights of his more recent work (between 2008-2019)?
- Aryl hydrocarbon receptor (29.01%)
- Transcriptome (15.27%)
- Toxicity (23.66%)
In recent papers he was focusing on the following fields of study:
Allan B. Okey mostly deals with Aryl hydrocarbon receptor, Transcriptome, Toxicity, Gene and Molecular biology.
His work carried out in the field of Aryl hydrocarbon receptor brings together such families of science as Receptor, Xenobiotic and CYP1B1.
His Toxicity research includes themes of Cytochrome b5, type A, Microarray and Endocrinology.
His study in the field of Messenger RNA is also linked to topics like Chemokine receptor and Glutamate dehydrogenase 1.
His Messenger RNA study results in a more complete grasp of Biochemistry.
His Molecular biology study incorporates themes from Monooxygenase and Cycloheximide.
Between 2008 and 2019, his most popular works were:
- Systematic evaluation of medium-throughput mRNA abundance platforms. (61 citations)
- Aryl hydrocarbon receptor (AHR)-regulated transcriptomic changes in rats sensitive or resistant to major dioxin toxicities (49 citations)
- Hepatic transcriptomic responses to TCDD in dioxin-sensitive and dioxin-resistant rats during the onset of toxicity. (41 citations)
In his most recent research, the most cited papers focused on:
His primary areas of investigation include Aryl hydrocarbon receptor, Molecular biology, Transcriptome, Toxicity and Receptor.
His studies link CYP1B1 with Aryl hydrocarbon receptor.
His Molecular biology study integrates concerns from other disciplines, such as Aryl hydrocarbon receptor nuclear translocator, Messenger RNA and Methylcholanthrene.
To a larger extent, Allan B. Okey studies Biochemistry with the aim of understanding Messenger RNA.
His Transcriptome research incorporates themes from Microarray and Transactivation.
His work in Toxicity covers topics such as CYP1A2 which are related to areas like Xenobiotic, NFE2L2 and CYP2S1.
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