Biography and Research Information
OverviewAI-generated summary
Stuart B. Berryhill's research focuses on the molecular mechanisms underlying bone health and age-related changes. His work has investigated the role of chaperone-mediated autophagy in bone mass, particularly in the context of cancellous bone. Recent publications include studies on the impact of autophagy loss on vertebral bone mass in female mice and the effect of chaperone-mediated autophagy loss on age-related bone loss in male mice. Berryhill has also explored advancements in genetic engineering techniques, specifically comparing CRISPR interference with the Cre-loxP system for cell type specificity. His research collaborations include work with Melda Onal, Dominique J. Laster, Julie Crawford, and Nisreen Akel at the University of Arkansas for Medical Sciences, with whom he has co-authored multiple publications. Berryhill's scholarship metrics include an h-index of 4 with 5 total publications and 52 total citations.
Metrics
- h-index: 4
- Publications: 5
- Citations: 52
Selected Publications
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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)
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
Ryan S. MacLeod
University of Arkansas for Medical Sciences (US)
1 shared publication
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
Milena Dimori
University of Arkansas for Medical Sciences
1 shared publication
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
Qiang Fu
University of Arkansas for Medical Sciences
1 shared publication
In database
- Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass
Alicen James
University of Arkansas for Medical Sciences (US)
1 shared publication
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
Qiang Fu
University of Arkansas for Medical Sciences (US)
1 shared publication
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
Jeff D. Thostenson
University of Arkansas for Medical Sciences
1 shared publication
In database
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
Intawat Nookaew
University of Arkansas for Medical Sciences
1 shared publication
In database
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
Charles A. O’Brien
University of Arkansas for Medical Sciences
1 shared publication
In database
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
A. Gordon James
University of Arkansas for Medical Sciences
1 shared publication
In database
- Loss of chaperone‐mediated autophagy does not alter age‐related bone loss in male mice
Similar Researchers
Based on overlapping research topics
Jacob Laster
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
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Teenamol E. Joseph
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
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Michela Palmieri
University of Arkansas for Medical Sciences
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Michael D. Yoder
University of Central Arkansas
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Julia Baranyk
University of Arkansas at Fayetteville
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Linda Hardy
University of Arkansas for Medical Sciences
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