James J. Greenhaw
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Also affiliated: United States Food and Drug Administration (2011–2024); Center for Drug Evaluation and Research (2020); University of Miami (2003); University of Tennessee Health Science Center (2001–2003); PAREXEL International (United States) (2012); University of Memphis (1990)
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
James Greenhaw's research focuses on the pharmacokinetic analysis of substances in animal models, particularly Sprague-Dawley rats. His recent work, published in 2024, investigated the pharmacokinetics of nicotine and its metabolites under various administration routes, including nose-only inhalation, oral gavage, and intravenous infusion in male rats. Greenhaw has published 37 papers with a total of 871 citations, reflecting a scholarly h-index of 19. He collaborates with several colleagues at the National Center for Toxicological Research, including Matthew Bryant, Xiaobo He, Seonggi Min, and Florence McLellen, with whom he shares one publication each.
Metrics
- h-index: 19
- Publications: 37
- Citations: 886
Selected Publications
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Pharmacokinetic analysis of nicotine and its metabolites (cotinine and trans-3′-hydroxycotinine) in male Sprague-Dawley rats following nose-only inhalation, oral gavage, and intravenous infusion of nicotine (2024)
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Hepatic Transcript Profiles of Cytochrome P450 Genes Predict Sex Differences in Drug Metabolism (2020)
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A randomized controlled laboratory study on the long-term effects of methylphenidate on cardiovascular function and structure in rhesus monkeys (2018)
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Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes (2018)
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Drug-Induced Liver Injury in Children: Clinical Observations, Animal Models, and Regulatory Status (2017)
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Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria (2016)
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Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children (2015)
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Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis (2014)
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Identification of a metabolic biomarker panel in rats for prediction of acute and idiosyncratic hepatotoxicity (2014)
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Detection of hepatotoxicity potential with metabolite profiling (metabolomics) of rat plasma (2014)
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Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics (2014)
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Study Protocol Preparation, Review, and Approval (2013)
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Good Laboratory Practices (2013)
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Introduction (2013)
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Final Report, Study Close-Out, and Conclusions (2013)
Collaboration Network
Top Collaborators
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice
Showing 5 of 19 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
Showing 5 of 14 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
Showing 5 of 13 shared publications
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice
- Evaluating effects of penicillin treatment on the metabolome of rats
- Hepatic Transcript Profiles of Cytochrome P450 Genes Predict Sex Differences in Drug Metabolism
- Identification of a metabolic biomarker panel in rats for prediction of acute and idiosyncratic hepatotoxicity
Showing 5 of 6 shared publications
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Detection of hepatotoxicity potential with metabolite profiling (metabolomics) of rat plasma
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Mouse Liver Protein Sulfhydryl Depletion after Acetaminophen Exposure
- A randomized controlled laboratory study on the long-term effects of methylphenidate on cardiovascular function and structure in rhesus monkeys
Showing 5 of 6 shared publications
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Evaluating effects of penicillin treatment on the metabolome of rats
- Identification of a metabolic biomarker panel in rats for prediction of acute and idiosyncratic hepatotoxicity
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Detection of hepatotoxicity potential with metabolite profiling (metabolomics) of rat plasma
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice
- Evaluating effects of penicillin treatment on the metabolome of rats
- Identification of a metabolic biomarker panel in rats for prediction of acute and idiosyncratic hepatotoxicity
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
- Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice
- Evaluating effects of penicillin treatment on the metabolome of rats
- Identification of a metabolic biomarker panel in rats for prediction of acute and idiosyncratic hepatotoxicity
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
- Introduction
- Good Laboratory Practices
- Final Report, Study Close-Out, and Conclusions
- Study Protocol Preparation, Review, and Approval
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Pharmacokinetic analysis of nicotine and its metabolites (cotinine and trans-3′-hydroxycotinine) in male Sprague-Dawley rats following nose-only inhalation, oral gavage, and intravenous infusion of nicotine
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Hepatic Transcript Profiles of Cytochrome P450 Genes Predict Sex Differences in Drug Metabolism
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Pharmacokinetic analysis of nicotine and its metabolites (cotinine and trans-3′-hydroxycotinine) in male Sprague-Dawley rats following nose-only inhalation, oral gavage, and intravenous infusion of nicotine
- Study Start Through End of In-Life
- Study Protocol Preparation, Review, and Approval
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
- Mechanisms for epigallocatechin gallate induced inhibition of drug metabolizing enzymes in rat liver microsomes
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