Francielly Morena da Silva Source Confirmed
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Post-Doctoral Fellow
University of Arkansas at Fayetteville
postdoc
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Biography and Research Information
OverviewAI-generated summary
Francielly Morena da Silva's research investigates molecular and physiological adaptations in skeletal muscle, particularly in the context of aging, disuse atrophy, and cancer cachexia. Her work has explored the temporal dynamics of muscle atrophy in female mice, noting potential differences in catabolic signaling compared to males. Da Silva has also examined the molecular signatures associated with exercise adaptation and aging, and the impact of circadian rhythms on inflammation-induced muscle atrophy. Her publications include studies on multi-transcriptome analysis to identify regulatory networks involved in muscle growth and the molecular landscape after exercise in humans. Da Silva collaborates with researchers at the University of Arkansas at Fayetteville, including Tyrone A. Washington, Ana Regina Cabrera, Eleanor R. Schrems, and Nicholas P. Greene, with whom she has co-authored numerous publications.
Metrics
- h-index: 10
- Publications: 38
- Citations: 358
Selected Publications
- Skeletal muscle methylome-transcriptome disruptions during the onset and progression of colorectal cancer-induced cachexia (2025) DOI
- The Age-Dependent Resident Myonuclear Multi-Omic Response to a Skeletal Muscle Hypertrophic Stimulus (2025) DOI
- Transcriptomic analysis demonstrates moderators of muscle quality are altered in age-related sarcopenic obesity (2025) DOI
- Promoting mitochondrial fusion is protective against cancer-induced muscle detriments in males and females (2025) DOI
- Global mitophagy inhibition via BNIP3 ablation is not sufficient to alleviate skeletal muscle impairments in male and female tumor-bearing mice (2025) DOI
- Myocellular adaptations to short‐term weighted wheel‐running exercise are largely conserved during C26‐tumour induction in male and female mice (2025) DOI
- The 24-hour molecular landscape after exercise in humans reveals MYC is sufficient for muscle growth (2024) DOI
- Transcriptional analysis of cancer cachexia: conserved and unique features across preclinical models and biological sex (2024) DOI
- Mitochondrial antioxidant SkQ1 attenuates C26 cancer-induced muscle wasting in males and improves muscle contractility in female tumor-bearing mice (2024) DOI
- Exploring heterogeneity: a dive into preclinical models of cancer cachexia (2024) DOI
- The 24-Hour Time Course of Integrated Molecular Responses to Resistance Exercise in Human Skeletal Muscle Implicates <i>MYC</i> as a Hypertrophic Regulator That is Sufficient for Growth (2024) DOI
- Supplemental table 6 (2023) DOI
- Supplemental table 1 (2023) DOI
- Supplemental table 3 (2023) DOI
- Supplemental table 2 (2023) DOI
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