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Pluripotent Nontumorigenic Adipose Tissue-Derived Muse Cells have Immunomodulatory Capacity Mediated by Transforming Growth Factor-β1

The secretome of MUSE cells contains factors that may play a role in regulation of stemness, apoptosis and immunomodulation

Human adipose tissue possesses a unique population of pluripotent stem cells with nontumorigenic and low telomerase activities: potential implications in regenerative medicine

Functional melanocytes are readily reprogrammable from multilineage-differentiating stress-enduring (muse) cells, distinct stem cells in human fibroblasts

Isolation, culture and evaluation of multilineage-differentiating stress-enduring (Muse) cells

Multilineage-differentiating stress-enduring (Muse) cells are a primary source of induced pluripotent stem cells in human fibroblasts

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Macrophage- and pluripotent-like reparative Muse cells are unique endogenous stem cells distinct from other somatic stem cells

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Unique multipotent cells in adult human mesenchymal cell populations

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Nose-to-brain delivery of human muse cells enhances structural and functional recovery in the murine ischemic stroke model

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