Over the past two decades, induced pluripotent stem cells (iPSCs) have reshaped our understanding of ALS pathogenesis and emerged as a promising translational platform for therapy development.
First-pass extracted concept
induced pluripotent stem cells
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iPSCs
Evidence Snippets
We then discuss the challenges and opportunities for each model, including the use of induced pluripotent stem cells and incorporation of sensors and actuator modalities to enhance the capabilities of these models.
This review systematically reviews the research progress of stem cells in the treatment of AS in recent years, focusing on the mechanism of the main cell types such as ... induced pluripotent stem cells (iPSCs)...
Engineering of induced pluripotent stem cells for the efficient development of non-alloreactive, hypoimmunogenic CD8αβ CAR-T cells
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Recent clinical trial setbacks highlight the need for robust translational iPSC models that can better predict therapeutic response.
Induced pluripotent stem cells are presented as a promising translational platform for ALS therapy development.
Large iPSC patient cohorts, quantitative phenotyping, genetically informed patient stratification, and reverse translational research are beginning to close the gap between in vitro discovery and clinical testing in ALS.
Effective disease-modifying therapies for ALS remain elusive despite advances in iPSC and three-dimensional modeling.
Use of induced pluripotent stem cells and incorporation of sensors and actuator modalities are presented as opportunities to enhance gut-brain axis microfluidic models.
The review summarizes MSCs, iPSCs, and EPCs as stem-cell types relevant to atherosclerosis through regulation of lipid metabolism, inhibition of inflammation, repair of vascular endothelium, and stabilization of atherosclerotic plaque.
The paper concerns engineering induced pluripotent stem cells to enable efficient development of non-alloreactive, hypoimmunogenic CD8αβ CAR-T cells.