C. Sandri
Molecular Biology · 2004–2010
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 53 citations into it; #15,644 of 17,773 by trust here, #4,167 by citations
Whom C. Sandri trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts C. Sandri overall
Papers from C. Sandri's perspective
Ordered by how strongly the researchers C. Sandri trusts endorse each paper. Same corpus, a different order for every researcher.
- Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy. (Cell)
- Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo (Nature Cell Biology)
- The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors. (Molecules and Cells)
- Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy (Proceedings of the National Academy of Sciences of the United States of America)
- Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression (The FASEB Journal)
- IKKbeta/NF-kappaB activation causes severe muscle wasting in mice. (Cell)
- Trehalose, a Novel mTOR-independent Autophagy Enhancer, Accelerates the Clearance of Mutant Huntingtin and α-Synuclein* (Journal of Biological Chemistry)
- Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases (The FASEB Journal)
- Protein degradation by the ubiquitin-proteasome pathway in normal and disease states. (Journal of the American Society of Nephrology)
- PGC-1α protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription (Proceedings of the National Academy of Sciences of the United States of America)
Their papers
- FoxO3 controls autophagy in skeletal muscle in vivo. (2007) — 1,961 citations
- Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy. (2004) — 2,963 citations
- Mitochondrial fission and remodelling contributes to muscle atrophy (2010) — 598 citations