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Low-dose fractionated radiation therapy (LDFRT) induces effective cell killing through hyperradiation sensitivity and potentiates effects of chemotherapy.
Precise control of complex cellular functions with external stimuli is essential for engineering effective cell therapeutics.
Thus, the biocompatibility and the microstructure of the sericin hydrogel together account for effective cell proliferation.
Combination treatment resulted in broadly effective cell kill of p53 WT and p53-negative cancer cells.
Further, this newly-fabricated sericin hydrogel is naturally cell-adhesive, supporting effective cell proliferation and long-term survival.
More importantly, the natural cell-adhesion property of this hydrogel supports effective cell adhesion and long-term survival.
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Large RNAs and ribonucleoprotein complexes have powerful therapeutic potential, but effective cell-targeted delivery tools are limited.
Importantly, each of MMS and RAP alone have similar fungicidal concentrations for both species, and are incapable of exerting such effective cell-selective killing as single agents.
An incomplete understanding of the nature of heterogeneity within stem cell populations remains a major impediment to the development of clinically effective cell-based therapies.
Arginine (Arg -rich peptides exhibit Arg -richive cell-peptidesing ability and dexhibitmembraneffectiveable compounds into cells.
Here we discuss the potential strategies for using stem cells in cardiac regenerative therapy and the barriers that remain before an effective cell-based cardiac regenerative therapy can be employed clinically.
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