Match tier
Listed
Presence
Current · Arkansas
Last published
2022
Sources
OpenAlex · ORCID
Refreshed
2026-10-08
D
Dakota L. Pouncey
Breast Imaging
Also affiliated: National Institutes of Health (2017); University of Arkansas Medical Center (2016); National Institute of Allergy and Infectious Diseases (2017); Arkansas Children's Nutrition Center (2016); Arkansas Children's Research Institute (2016)
6 h-index
11 pubs
201 cited
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Dakota L. Pouncey's research focuses on the metabolic pathways of anticoagulants, specifically investigating novel reductive elimination pathways for 10-hydroxywarfarin. This work contributes to understanding drug metabolism and pharmacokinetics. Pouncey also has a publication in phylogenomics, examining the evolutionary relationships within the hard pines (Pinus subsection Ponderosae). Scholarship metrics include an h-index of 6 with 11 total publications and 194 total citations. Key collaborators include Grover P. Miller and Dustyn A. Barnette, with whom Pouncey has shared publications, as well as Julia Lefler and Hassan Karemera.
Metrics
- h-index: 6
- Publications: 11
- Citations: 201
Positions
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Breast Imaging publications 2014–2022University of Arkansas for Medical Sciences Institution web page
Selected Publications
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Discovery of Novel Reductive Elimination Pathway for 10-Hydroxywarfarin (2022)
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Phylogenomics in the Hard Pines (Pinus subsection Ponderosae; Pinaceae) Confirms Paraphyly in Pinus ponderosa, and Places Pinus jeffreyi with the California Big Cone Pines (2021)
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Significance of Competing Metabolic Pathways for 5F-APINACA Based on Quantitative Kinetics (2020)
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Novel isomeric metabolite profiles correlate with warfarin metabolism phenotype during maintenance dosing in a pilot study of 29 patients (2018)
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Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases (2017)
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MicroRNAs Modulate Pathogenesis Resulting from Chlamydial Infection in Mice (2016)
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Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells (2015)
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Warfarin Metabolite Profiles Reveal the Importance of Factors on Patient Dose‐Responses to Anticoagulant Therapy (2015)
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Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites (2014)
Collaboration Network
Top Collaborators
Grover P. Miller
University of Arkansas for Medical Sciences
7 shared publications
In database
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
- Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
- Novel isomeric metabolite profiles correlate with warfarin metabolism phenotype during maintenance dosing in a pilot study of 29 patients
- Significance of Competing Metabolic Pathways for 5F-APINACA Based on Quantitative Kinetics
Showing 5 of 7 shared publications
Jessica H. Hartman
University of Arkansas for Medical Sciences (US)
4 shared publications
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
- Novel isomeric metabolite profiles correlate with warfarin metabolism phenotype during maintenance dosing in a pilot study of 29 patients
- Warfarin Metabolite Profiles Reveal the Importance of Factors on Patient Dose‐Responses to Anticoagulant Therapy
Gunnar Boysen
University of Arkansas for Medical Sciences
4 shared publications
In database
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
- Novel isomeric metabolite profiles correlate with warfarin metabolism phenotype during maintenance dosing in a pilot study of 29 patients
- Significance of Competing Metabolic Pathways for 5F-APINACA Based on Quantitative Kinetics
- Warfarin Metabolite Profiles Reveal the Importance of Factors on Patient Dose‐Responses to Anticoagulant Therapy
Eugene S. Smith
Central Arkansas Veterans Healthcare System (US)
2 shared publications
- Novel isomeric metabolite profiles correlate with warfarin metabolism phenotype during maintenance dosing in a pilot study of 29 patients
- Warfarin Metabolite Profiles Reveal the Importance of Factors on Patient Dose‐Responses to Anticoagulant Therapy
Robert Nshimiyimana
Hendrix College (US)
2 shared publications
- Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
Linda P. Desrochers
Hendrix College
2 shared publications
In database
- Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
Thomas E. Goodwin
Hendrix College
2 shared publications
In database
- Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
Dustyn A. Barnette
University of Arkansas for Medical Sciences
2 shared publications
In database
- Stereospecific Metabolism of R- and S-Warfarin by Human Hepatic Cytosolic Reductases
- Discovery of Novel Reductive Elimination Pathway for 10-Hydroxywarfarin
C. Preston Pugh
University of Arkansas for Medical Sciences
1 shared publication
In database
- Multiple UDP-glucuronosyltransferases in human liver microsomes glucuronidate both R- and S-7-hydroxywarfarin into two metabolites
April C.L. Bostian
University of Arkansas for Medical Sciences
1 shared publication
In database
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
Leena Maddukuri
University of Arkansas for Medical Sciences
1 shared publication
In database
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
Megan R. Reed
University of Arkansas for Medical Sciences
1 shared publication
In database
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
Tatsiana Savenka
University of Arkansas for Medical Sciences (US)
1 shared publication
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
Lauren Evoy Davis
University of Arkansas for Medical Sciences (US)
1 shared publication
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
Robert L. Eoff
University of Arkansas for Medical Sciences
1 shared publication
In database
- Kynurenine Signaling Increases DNA Polymerase Kappa Expression and Promotes Genomic Instability in Glioblastoma Cells
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