Match tier
Listed
Presence
Current · Arkansas
Last published
2026
Sources
OpenAlex · ORCID
Refreshed
2026-10-05
Biography and Research Information
OverviewAI-generated summary
Kelly J. Davis studies the cellular mechanisms of brain injury and recovery, with a recent focus on the cerebellum. Their work investigates the dual roles of apoptosis and cell survival pathways in Purkinje cells following transient global ischemia. This research examines the balance between cell death and survival mechanisms that occur four days after the ischemic event, utilizing animal models to understand these complex biological processes. Davis has one publication and collaborates with researchers at the National Center for Toxicological Research, including Angel Paredes, Ada G Cino Ozuna, and Zhen He.
Metrics
- h-index: 36
- Publications: 79
- Citations: 5,941
Positions
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Senior Staff Pathologist 2009–presentToxicologic Pathology Associates Pathology ORCID
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Senior Staff Pathologist publications 2026National Center for Toxicological Research ORCID
Selected Publications
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Dual Characteristics of Apoptosis and Survival in Cerebellar Purkinje Cells Four Days After Transient Global Ischemia (2026)
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Unexpected Consequences: A Rare Mycotic Pseudoaneurysm After Salmonella Gastroenteritis (2025)
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The incorporation of MALDI mass spectrometry imaging in studies to identify markers of toxicity following in utero opioid exposures in mouse fetuses (2024)
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Biodistribution and toxic potential of silver nanoparticles when introduced to the female rat reproductive tract (2024)
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90-day nose-only inhalation toxicity study of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in Sprague-Dawley rats (2021)
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Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice (2021)
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14-Day Nose-Only Inhalation Toxicity and Haber’s Rule Study of NNK in Sprague-Dawley Rats (2021)
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Toxicokinetic and Genotoxicity Study of NNK in Male Sprague Dawley Rats Following Nose-Only Inhalation Exposure, Intraperitoneal Injection, and Oral Gavage (2021)
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In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver (2016)
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Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice (2016)
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Proteomic analysis of acetaminophen-induced hepatotoxicity and identification of heme oxygenase 1 as a potential plasma biomarker of liver injury (2016)
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In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver (2016)
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In vivo genotoxicity of estragole in male F 344 rats (2014)
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Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats (2014)
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Early biomarkers of doxorubicin-induced heart injury in a mouse model (2014)
Collaboration Network
Top Collaborators
Michelle E. Bishop
National Center for Toxicological Research
7 shared publications
In database
- In vivo genotoxicity of estragole in male F 344 rats
- In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver
- Toxicokinetic and Genotoxicity Study of NNK in Male Sprague Dawley Rats Following Nose-Only Inhalation Exposure, Intraperitoneal Injection, and Oral Gavage
- Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats
- 14-Day Nose-Only Inhalation Toxicity and Haber’s Rule Study of NNK in Sprague-Dawley Rats
Showing 5 of 7 shared publications
Sherry M. Lewis
National Center for Toxicological Research
6 shared publications
In database
- Development of doxorubicin-induced chronic cardiotoxicity in the B6C3F1 mouse model
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Toxicokinetic and Genotoxicity Study of NNK in Male Sprague Dawley Rats Following Nose-Only Inhalation Exposure, Intraperitoneal Injection, and Oral Gavage
- 14-Day Nose-Only Inhalation Toxicity and Haber’s Rule Study of NNK in Sprague-Dawley Rats
Showing 5 of 6 shared publications
Mason G. Pearce
National Center for Toxicological Research
5 shared publications
In database
- In vivo genotoxicity of estragole in male F 344 rats
- Toxicokinetic and Genotoxicity Study of NNK in Male Sprague Dawley Rats Following Nose-Only Inhalation Exposure, Intraperitoneal Injection, and Oral Gavage
- Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats
- 14-Day Nose-Only Inhalation Toxicity and Haber’s Rule Study of NNK in Sprague-Dawley Rats
- 90-day nose-only inhalation toxicity study of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in Sprague-Dawley rats
Mugimane G. Manjanatha
National Center for Toxicological Research
5 shared publications
In database
- In vivo genotoxicity of estragole in male F 344 rats
- In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver
- Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats
- Biodistribution and toxic potential of silver nanoparticles when introduced to the female rat reproductive tract
- In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver
Xi Yang
National Center for Toxicological Research (US)
4 shared publications
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Proteomic analysis of acetaminophen-induced hepatotoxicity and identification of heme oxygenase 1 as a potential plasma biomarker of liver injury
- Mouse Liver Protein Sulfhydryl Depletion after Acetaminophen Exposure
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
William F. Salminen
National Center for Toxicological Research (US)
4 shared publications
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Proteomic analysis of acetaminophen-induced hepatotoxicity and identification of heme oxygenase 1 as a potential plasma biomarker of liver injury
- Mouse Liver Protein Sulfhydryl Depletion after Acetaminophen Exposure
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
Varsha G. Desai
National Center for Toxicological Research
4 shared publications
In database
- Development of doxorubicin-induced chronic cardiotoxicity in the B6C3F1 mouse model
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice
Carrie L. Moland
National Center for Toxicological Research
4 shared publications
In database
- Development of doxorubicin-induced chronic cardiotoxicity in the B6C3F1 mouse model
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice
Taewon Lee
Korea University (KR)
4 shared publications
- Development of doxorubicin-induced chronic cardiotoxicity in the B6C3F1 mouse model
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice
Levan Muskhelishvili
National Center for Toxicological Research (US)
4 shared publications
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Mouse Liver Protein Sulfhydryl Depletion after Acetaminophen Exposure
- Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice
James C. Fuscoe
National Center for Toxicological Research
4 shared publications
In database
- Development of doxorubicin-induced chronic cardiotoxicity in the B6C3F1 mouse model
- Early biomarkers of doxorubicin-induced heart injury in a mouse model
- Sex-related differential susceptibility to doxorubicin-induced cardiotoxicity in B6C3F1 mice
- Doxorubicin‐induced delayed‐onset subclinical cardiotoxicity in mice
Wei Ding
National Center for Toxicological Research (US)
4 shared publications
- In vivo genotoxicity of estragole in male F 344 rats
- Toxicokinetic and Genotoxicity Study of NNK in Male Sprague Dawley Rats Following Nose-Only Inhalation Exposure, Intraperitoneal Injection, and Oral Gavage
- Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats
- 90-day nose-only inhalation toxicity study of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in Sprague-Dawley rats
Lascelles E. Lyn‐Cook
National Center for Toxicological Research
4 shared publications
In database
- In vivo genotoxicity of estragole in male F 344 rats
- In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver
- Sex-specific dose-response analysis of genotoxicity in cyproterone acetate-treated F344 rats
- In Vivo Alkaline Comet Assay and Enzyme-modified Alkaline Comet Assay for Measuring DNA Strand Breaks and Oxidative DNA Damage in Rat Liver
James J. Greenhaw
National Center for Toxicological Research
3 shared publications
In database
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Mouse Liver Protein Sulfhydryl Depletion after Acetaminophen Exposure
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
Richard D. Beger
National Center for Toxicological Research
3 shared publications
In database
- Proteomic analysis of acetaminophen-induced hepatotoxicity and identification of heme oxygenase 1 as a potential plasma biomarker of liver injury
- Comprehensive analysis of alterations in lipid and bile acid metabolism by carbon tetrachloride using integrated transcriptomics and metabolomics
- The incorporation of MALDI mass spectrometry imaging in studies to identify markers of toxicity following in utero opioid exposures in mouse fetuses
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