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Journal Highlights

Stem Cell Niche and Microenvironment
Pluripotent Stem Cells and Reprogramming
ImmunoMSC
Stem Cell-Based Regenerative Therapies
Organoids and 3D Stem Cell Cultures
Stem Cell Gene Editing and CRISPR
Hematopoietic Stem Cell Transplantation HSCT
Cancer Stem Cells and Tumorigenesis
Ethical, Regulatory, and Translational Issues
Biomaterial Support for Stem Cell Growth

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Stem Cell Gene Editing and CRISPR

Stem cell gene editing, particularly using CRISPR technology, has opened new frontiers in precision medicine. CRISPR allows for targeted modifications in stem cell DNA, enabling the correction of genetic defects at the source. This approach holds promise for treating inherited disorders, cancers, and other diseases. Combining gene editing with stem cells enhances the development of personalized therapies and disease models. Ongoing research focuses on improving safety, accuracy, and ethical oversight of these powerful tools.