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Whether GIP receptors in muscle tissue contribute to muscle pain is not well studied
not surprising for a molecule as CD26 that was originally described as a surface marker of T lymphocytes [13]
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Nanomedicine platforms, engineered with precise control over size, surface chemistry, and drug release kinetics, can enhance the bioavailability and tumor-specific delivery of immunotherapeutic agents while minimizing systemic toxicity ( To distinguish from the broadly discussed literature on sarcoma nanomedicine, the main contribution of this mini-review is specifically focused on the precise intersection of engineered nanoplatforms and translational barriers
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