Match tier
Listed
Presence
Current · Arkansas
Last published
2026
Sources
OpenAlex · ORCID
Refreshed
2026-10-05
S
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Stuart B. Berryhill's research investigates the biological mechanisms underlying bone health and disease, with a recent focus on the role of autophagy in bone mass regulation. His work has explored how genetic factors, such as GATA4, influence osteoblast function and osteoclast differentiation, impacting bone resorption. Berryhill has also examined the potential of novel biomaterials, like polyurethane scaffolds incorporating nanohydroxyapatite and decellularized bone, for bone regeneration applications. His publications include studies on the impact of chaperone-mediated autophagy loss on cancellous bone mass in mice and the comparative efficacy of genetic engineering techniques like CRISPR interference versus Cre-loxP systems. He has collaborated with researchers at the University of Arkansas for Medical Sciences, including Melda Onal, Dominique J. Laster, Julie Crawford, and Nisreen Akel, on multiple projects.
Metrics
- h-index: 4
- Publications: 6
- Citations: 56
Selected Publications
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Combined senolytics induce varied phenotypic and functional responses on senescent phenotypes of mesenchymal stromal cell populations (2026)
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Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice (2024)
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CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system (2023)
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Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass (2022)
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Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold (2019)
Collaboration Network
Top Collaborators
Nisreen Akel
University of Arkansas for Medical Sciences
3 shared publications
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
Dominique J. Laster
University of Arkansas for Medical Sciences
3 shared publications
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
Julie Crawford
University of Arkansas for Medical Sciences
3 shared publications
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
Melda Onal
University of Arkansas for Medical Sciences
3 shared publications
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
James A. Hendrixson
University of Arkansas for Medical Sciences
2 shared publications
In database
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
Austin Bow
University of Tennessee at Knoxville (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Steven D. Newby
University of Tennessee at Knoxville (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Rebecca E. Rifkin
University of Tennessee at Knoxville (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Bailey K. Jackson
University of Arkansas at Little Rock
1 shared publication
In database
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Alicia Adina Matavosian
University of Tennessee at Knoxville (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Christopher Griffin
University of Arkansas at Little Rock (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
William J. King
University of Arkansas at Little Rock (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Karrer M. Alghazali
University of Arkansas at Little Rock (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Anwer Mhannawee
University of Arkansas at Little Rock (US)
1 shared publication
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Roy Morello
University of Arkansas for Medical Sciences
1 shared publication
In database
- Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
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