S. Lecker

Molecular Biology · 2001–2007

A researcher in the Science corpus: 7 papers; trusts 4 researchers and is trusted by 9 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 81 citations into it; #4,241 of 17,773 by trust here, #2,446 by citations
• Cell Biology — 25 citations into it; #1,848 of 2,073 by trust here, #1,127 by citations
• Epidemiology — 22 citations into it; #1,970 of 2,148 by trust here, #858 by citations
• Cellular and Molecular Neuroscience — 16 citations into it; #1,136 of 2,998 by trust here, #352 by citations

Whom S. Lecker trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. A. Goldberg
2. Eric H. Baehrecke
3. J. Adams
4. D. Glass
5. M. Glickman
6. J. Sacheck
7. D. Cai
8. Timothy R. Hughes
9. Masafumi Muratani
10. L. Hicke

Who trusts S. Lecker overall

1. M. Sandri
2. P. Bonaldo
3. J. Sacheck
4. E. Masiero
5. C. Mammucari
6. D. Glass
7. V. Romanello
8. A. Goldberg
9. S. Schiaffino
10. G. Milan

Papers from S. Lecker's perspective

Ordered by how strongly the researchers S. Lecker trusts endorse each paper. Same corpus, a different order for every researcher.

1. 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)
2. Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways (Nature Cell Biology)
3. Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo (Nature Cell Biology)
4. Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy. (Cell)
5. Functional discovery via a compendium of expression profiles. (Cell)
6. U Box Proteins as a New Family of Ubiquitin-Protein Ligases* (Journal of Biological Chemistry)
7. An integrated stress response regulates amino acid metabolism and resistance to oxidative stress. (Molecules and Cells)
8. The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors. (Molecules and Cells)
9. Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy (Science)
10. Regulation of insulin action and pancreatic β-cell function by mutated alleles of the gene encoding forkhead transcription factor Foxo1 (Nature Genetics)

Their papers

• Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy. (2004) — 2,963 citations
• FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells. (2007) — 1,513 citations
• Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy (2001) — 1,808 citations
• PGC-1α protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription (2006) — 1,031 citations
• Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression (2004) — 1,572 citations
• Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases (2007) — 599 citations
• Protein degradation by the ubiquitin-proteasome pathway in normal and disease states. (2006) — 1,185 citations