Culturing human pluripotent stem cells with caudalizing morphogens and SMAD inhibitors to generate spinal cord neural stem cells.
Tunicate extracellular matrix and fish skin collagen replace costly mammalian sources to reduce environmental harm while maintaining cell proliferation.
Curved microwells guide stem cell aggregation into uniform spheroids, addressing the difficulty of replicating inner ear structure in hearing loss models.
CD51 negative selection isolates living neuronal cells using magnetic beads to label non-neuronal contaminants.
Differentiating human pluripotent stem cells into brain pericyte-like cells resolves scalability and marker expression contradictions for BBB models.
Virtual electrowetting electrodes replace physical structures to resolve the contradiction between manipulation flexibility and device complexity.
A culture medium containing GSK3β, BMP, and TGF-β inhibitors induces pluripotent stem cells into a differentiation-promoted state.
KU-60019 accelerates cell maturation to reveal neurodegenerative phenotypes within seven days, bypassing the decades required for natural aging.