Quanyin Hu
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As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Articles
Scaffolds toughen bacteria-based therapy
Abstract References and Notes Information & Authors Metrics & Citations Check Access References Figures Tables Media Share Abstract Engineered cells can sense disease and deliver drugs at a site of pathology. These living therapeutics provide localized, self-sustaining responses to environmental changes, such as inflammation and pathogenic signals, that conventional drugs cannot offer (1, 2).
Peptide-Based PROTACs: Transitioning from Static Paradigm to a Dynamic Landscape within Targeted Protein Degradation Click to copy article link Article link copied!
1. Introduction Click to copy section linkSection link copied! By enabling catalytic degradation of disease-causing proteins rather than occupation-driven inhibition, proteolysis targeting chimeras (PROTACs) have expanded the therapeutic and conceptual view of pharmaceutical science. (1) The concept of PROTACs is inherently inclusive. Under the current research context, any molecular or supramolecular construct capable of catalyzing target protein degradation can fall under this scope.
Intracellular metal ion-based chemistry for programmed cell death
Intracellular metal ion-based chemistry for programmed cell death Intracellular metal ions play essential roles in multiple physiological processes, including catalytic action, diverse cellular processes, intracellular signaling, and electron transfer. It is crucial to maintain intracellular metal ion homeostasis which is achieved by the subtle balance of storage and release of metal ions intracellularly along with the influx and efflux of metal ions at the interface of the cell membrane.
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