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- W4200346327 endingPage "13674" @default.
- W4200346327 startingPage "13674" @default.
- W4200346327 abstract "To date, gene therapy has employed viral vectors to deliver therapeutic genes. However, recent progress in molecular and cell biology has revolutionized the field of stem cells and gene therapy. A few years ago, clinical trials started using stem cell replacement therapy, and the induced pluripotent stem cells (iPSCs) technology combined with CRISPR-Cas9 gene editing has launched a new era in gene therapy for the treatment of neurological disorders. Here, we summarize the latest findings in this research field and discuss their clinical applications, emphasizing the relevance of recent studies in the development of innovative stem cell and gene editing therapeutic approaches. Even though tumorigenicity and immunogenicity are existing hurdles, we report how recent progress has tackled them, making engineered stem cell transplantation therapy a realistic option." @default.
- W4200346327 created "2021-12-31" @default.
- W4200346327 creator A5011909669 @default.
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- W4200346327 creator A5048934823 @default.
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- W4200346327 creator A5091455787 @default.
- W4200346327 date "2021-12-20" @default.
- W4200346327 modified "2023-10-17" @default.
- W4200346327 title "Induced Pluripotent Stem Cells (iPSCs) and Gene Therapy: A New Era for the Treatment of Neurological Diseases" @default.
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