Madeline G. Amos Data-verified
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Researcher
unknown
Research Areas
Biography and Research Information
OverviewAI-generated summary
Madeline G. Amos studies the molecular mechanisms underlying muscle wasting conditions. Her research has investigated the role of PGC-1α, a key regulator of mitochondrial biogenesis, in mitigating cancer cachexia in mice. In a 2022 publication, Amos and collaborators demonstrated that overexpression of PGC-1α was insufficient to prevent cancer-associated muscle loss in both male and female mouse models. This work contributes to the understanding of metabolic dysregulation in disease states. Amos has a h-index of 2, with 3 total publications and 37 citations. She has collaborated with several researchers at the University of Arkansas at Fayetteville, including Nicholas P. Greene, Megan E. Rosa‐Caldwell, Tyrone A. Washington, and Ana Regina Cabrera, on shared publications.
Metrics
- h-index: 2
- Publications: 3
- Citations: 37
Selected Publications
-
PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice (2022)
Collaboration Network
Top Collaborators
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
- PGC-1α overexpression is not sufficient to mitigate cancer cachexia in either male or female mice
Similar Researchers
Based on overlapping research topics