Apoptosis-based therapies
By John Calvin Reed. Nature reviews. Drug discovery, 2002
651 citations recorded by the source corpus.
Subfields: Hepatology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/33dd7022336845a151b478c9c47d6b7c9101195b
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In Hepatology
In Molecular Biology
Citations in the corpus
- Targeting proteases: successes, failures and future prospects (2006, background): “As such, preventing protease activation could be an attractive area for potential new therapeutics, and is particularly amenable to RNAi approache”
- Bcl-2 family proteins and cancer (2008, background): “…releasing proteins that participate in caspase activation (for example, cytochrome c) and that neutralize endogenous inhibitors of caspases (for example, SMAC; OMI/Htra2, which inhibit IAPs), as well as unleashing several mediators of Oncogene caspase-independent necrotic cell death (Reed, 2002).”
- Pre-B cell colony-enhancing factor inhibits neutrophil apoptosis in experimental inflammation and clinical sepsis. (2004, background): “marrow stores each day (60); an equal number die an apoptotic death, thus the numbers of circulating cells remain constant.”