eScholarship
metadata only
Development and Optimization of FRET and BRET TORCAR Reporters
Mechanistic target of rapamycin complex 1 (mTORC1) integrates growth-factor, nutrient, energy, and stress signals to regulate cell growth and homeostasis. Because conventional endpoint assays cannot fully resolve the timing, subcellular organization, or cell-to-cell variability of mTORC1 signaling,
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Formal Modeling of mTOR Associated Biological Regulatory Network Reveals Novel Therapeutic Strategy for the Treatment of Cancer#1000749
- Structural Investigation of mTORC1 Regulation at the Lysosomal Membrane#1106912
- Circulatory onset governs blood stem cell development through mechanistic target of rapamycin signaling#635472
- Investigating the potential role of mechanistic target of rapamycin complex 1 (mTORC1) in regulating cell fate decisions in Dictyostelium discoideum#225003
- Compromised ESCRT signalling is sufficient for resistance to the Target of Rapamycin Complex inhibitor Torin1 in fission yeast#300688
Record · ID 1119910
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive