What is he best known for?
The fields of study he is best known for:
Biochemistry, Pharmacology, Microsome, Metabolite and Acetaminophen are his primary areas of study.
His Biochemistry research incorporates themes from Molecular biology, Halothane and Drug.
His work carried out in the field of Pharmacology brings together such families of science as Gene expression profiling, Toxicity and Halothane hepatitis.
His studies in Microsome integrate themes in fields like Cytochrome, Antibody, Cysteine and Stereochemistry.
His Metabolite research includes themes of Chromatography, Chloroform and Phosgene.
In his study, Cytotoxic T cell is inextricably linked to Immunology, which falls within the broad field of Liver injury.
His most cited work include:
- Protective role of Kupffer cells in acetaminophen-induced hepatic injury in mice. (269 citations)
- Selective Protein Covalent Binding and Target Organ Toxicity (259 citations)
- Protection against acetaminophen-induced liver injury and lethality by interleukin 10: role of inducible nitric oxide synthase. (245 citations)
What are the main themes of his work throughout his whole career to date?
Lance R. Pohl mainly focuses on Biochemistry, Microsome, Immunology, Pharmacology and Metabolite.
Lance R. Pohl has researched Biochemistry in several fields, including Chromatography, Halothane and In vivo.
The study incorporates disciplines such as Isoflurane, Internal medicine, Hepatitis and Antibody, Hapten in addition to Halothane.
His Microsome study integrates concerns from other disciplines, such as Hydroxylation, Cytochrome, Stereochemistry and Metabolism.
He works mostly in the field of Immunology, limiting it down to concerns involving Liver injury and, occasionally, Acetaminophen.
The Pharmacology study combines topics in areas such as Enflurane and Toxicity.
He most often published in these fields:
- Biochemistry (40.91%)
- Microsome (26.62%)
- Immunology (18.18%)
What were the highlights of his more recent work (between 1997-2017)?
- Immunology (18.18%)
- Liver injury (12.34%)
- Acetaminophen (13.64%)
In recent papers he was focusing on the following fields of study:
Immunology, Liver injury, Acetaminophen, Pharmacology and Toxicity are his primary areas of study.
As part of one scientific family, Lance R. Pohl deals mainly with the area of Immunology, narrowing it down to issues related to the Drug, and often Immune system, Antigen and Function.
His Liver injury research includes elements of Acquired immune system, Eosinophilia and Antibody.
His work deals with themes such as Cell culture, Halothane, Natural killer cell and Hepatitis, which intersect with Pharmacology.
His Toxicity research is multidisciplinary, relying on both Heat shock protein, Toxicogenomics and Metabolite.
The concepts of his Glutathione study are interwoven with issues in Microsome, Stereochemistry and Metabolism.
Between 1997 and 2017, his most popular works were:
- Protective role of Kupffer cells in acetaminophen-induced hepatic injury in mice. (269 citations)
- Protection against acetaminophen-induced liver injury and lethality by interleukin 10: role of inducible nitric oxide synthase. (245 citations)
- Metabolic activation of diclofenac by human cytochrome P450 3A4: role of 5-hydroxydiclofenac. (152 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Liver injury, Acetaminophen, Pharmacology, Immunology and Interleukin.
His research in Liver injury intersects with topics in ALDH2, Acetylation and Toxicogenomics.
His studies deal with areas such as Metabolite, Enzyme, Hepatitis and Heat shock protein as well as Acetaminophen.
His Pharmacology research incorporates elements of Transcription factor, Gene expression, Gene expression profiling and Toxicity.
His study in Immunology is interdisciplinary in nature, drawing from both Confounding, Cytotoxic T cell and Drug.
His Interleukin study combines topics from a wide range of disciplines, such as Proteome, Cell growth, Drug development and Liver disease, Drug-induced liver disease.
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