Makenzie A Tharpe
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Researcher
Also affiliated: Clemson University (2024)
Graduate Student Researcher
Research Areas
Biography and Research Information
OverviewAI-generated summary
Makenzie A Tharpe's research focuses on the impact of nutrient deficiencies on cellular metabolism, particularly within muscle cells. In recent work, Tharpe investigated how iron depletion affects energy metabolism in C2C12 myoblast cells, observing impairments in mitochondrial complex I activity and specific protein level reductions. Further studies explored the consequences of folate deficiency and the loss of the SHMT2 enzyme, noting impacts on protein levels associated with oxidative phosphorylation, folate transport, and mitochondrial dynamics in the same cell line. These studies contribute to understanding the molecular mechanisms underlying metabolic dysfunction under specific nutritional stress conditions. Tharpe collaborates with Joanna Fiddler and Abigail L Zirbel at the University of Arkansas at Fayetteville, with whom they have co-authored three publications.
Metrics
- h-index: 1
- Publications: 3
- Citations: 1
Selected Publications
-
Loss of SHMT2 and Folate Deficiency Impair Protein Levels Involved in Oxidative Phosphorylation, Folate Transport, and Mitochondrial Dynamics in Mouse C2C12 Myoblast Cells (2025)
-
Marginal Iron Depletion Impairs Mitochondrial Complex I Activity and Reduces NDUFB8 and ISCU Protein Levels in Mouse C2C12 Myoblast Cells (2025)
Collaboration Network
Top Collaborators
- Marginal Iron Depletion Impairs Mitochondrial Complex I Activity and Reduces NDUFB8 and ISCU Protein Levels in Mouse C2C12 Myoblast Cells
- Loss of SHMT2 and Folate Deficiency Impair Protein Levels Involved in Oxidative Phosphorylation, Folate Transport, and Mitochondrial Dynamics in Mouse C2C12 Myoblast Cells
- Marginal Iron Depletion Impairs Mitochondrial Complex I Activity and Reduces NDUFB8 and ISCU Protein Levels in Mouse C2C12 Myoblast Cells
- Loss of SHMT2 and Folate Deficiency Impair Protein Levels Involved in Oxidative Phosphorylation, Folate Transport, and Mitochondrial Dynamics in Mouse C2C12 Myoblast Cells
- Marginal Iron Depletion Impairs Mitochondrial Complex I Activity and Reduces NDUFB8 and ISCU Protein Levels in Mouse C2C12 Myoblast Cells
Similar Researchers
Based on overlapping research topics