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Astrocyte-targeted therapies for AD aim to prevent the transformation of reactive astrocytes into type A1 astrocytes and encompass strategies such as stem cell therapy, pharmacological interventions, and gene-editing technologies ( Nurr1 and Foxa2 , contributes to therapeutic improvement (Tsai, 2018)

Not only the limited cultivation time previously described, but also the restriction to those cells that can easily be accessed from humans and readily cultivated confines the spectrum of target cells available for disease modeling

Your journey will be unique, but heres a general idea of what you can expect and what might influence your progress