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Research Areas
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Biography and Research Information
OverviewAI-generated summary
Dominique J. Laster's research investigates the biological mechanisms underlying bone health, with a recent focus on the role of autophagy. Laster's work has explored the impact of chaperone-mediated autophagy loss on bone mass, particularly in the context of aging and sex differences in mice. Publications include studies on the association between chaperone-mediated autophagy and low vertebral cancellous bone mass, and the lack of alteration in age-related bone loss in male mice following the loss of this process. Additionally, Laster has contributed to research on molecular biology techniques, specifically comparing CRISPR interference with the Cre-loxP system for enhanced cell type specificity. Scholarship metrics indicate an h-index of 3, with 3 total publications and 21 total citations. Laster has collaborated with researchers at the University of Arkansas for Medical Sciences, including Melda Onal, Julie Crawford, Nisreen Akel, and Stuart B. Berryhill, with whom multiple publications are shared.
Metrics
- h-index: 3
- Publications: 3
- Citations: 21
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
Stuart B. Berryhill
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
Julie Crawford
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Autophagy
Molecular Biology Techniques and Applications
Maria Jose Schuller-Almeida
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Molecular Biology Techniques and Applications
Teenamol E Jospeh
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Molecular Biology Techniques and Applications
Jacob Laster
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Molecular Biology Techniques and Applications
A. Gordon James
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Autophagy
Scott A. Stuart
University of Arkansas for Medical Sciences
Bone Metabolism and Diseases
Molecular Biology Techniques and Applications