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HMSC transduced with lentiviral vectors to overexpress Ex-4 (MSC-Ex-4) maintained typical hMSC morphology, viability, and surface marker expression (CD44, CD73, CD90, and CD105), indicating that the genetic modification did not compromise stemness or core phenotypic characteristics [18, 26]

Unlike rigid docking approaches, MD explores a continuum of conformations, revealing transient and cryptic binding sites that might otherwise be missed

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