Research Areas
Biography and Research Information
OverviewAI-generated summary
Ashtyn Bell's research investigates molecular mechanisms related to DNA repair and protein function. Bell has published work examining the molecular mechanisms of E. coli MutS and the conservation of the insert-2 motif in Rev1, which confers an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis. Another publication details the binding of K2PtBr6 to lysozyme, and a separate project involved the development of a low-cost, Arduino-controlled fluorometer. Bell collaborates with researchers at the University of Arkansas for Medical Sciences, including Amit Ketkar, Robert L. Eoff, and Rehas S. Sewilam, as well as Julie Gunderson from Hendrix College, with whom Bell shares two publications. Bell's work has garnered 30 citations and an h-index of 2.
Metrics
- h-index: 2
- Publications: 4
- Citations: 30
Selected Publications
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Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis (2023)
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The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer (2021)
Collaboration Network
Top Collaborators
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- The Fluorino: A Low-Cost, Arduino-Controlled Fluorometer
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
- Conservation of the insert-2 motif confers Rev1 from different species with an ability to disrupt G-quadruplexes and stimulate translesion DNA synthesis
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