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Besides, senescence typically accompanies augmented p21CIP1 or p16INK4a expression, while quiescence is p27KIP1 dependent, and differentiation can involve multiple signaling pathways (e.g., Wnt/Notch/Hedgehog/p16 INK4a )
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These studies showcase the translation of UCN-based SMD platforms toward ultrasensitive clinical assays and point-of-care testing
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