Generation and characterization of a human neuronal in vitro model for Rett Syndrome using a direct reprogramming method
A Huber, V Sarne, AV Beribisky…�- Stem Cells and�…, 2024 - liebertpub.com
Rett Syndrome (RTT) is a severe neurodevelopmental disorder, afflicting 1 in 10,000 female
births. It is caused by mutations in the X-linked methyl-CpG-binding protein gene (MECP2)�…
births. It is caused by mutations in the X-linked methyl-CpG-binding protein gene (MECP2)�…
[HTML][HTML] GelMA hydrogel as a scaffold to enhance the survival and differentiation of human induced lateral ganglionic eminence precursor cells
L Nguyen, A McCaughey-Chapman…�- Journal of Neuroscience�…, 2024 - Elsevier
Cell reprogramming holds enormous potential to revolutionize our understanding of
neurological and neurodevelopmental disorders, as well as enhance drug discovery and�…
neurological and neurodevelopmental disorders, as well as enhance drug discovery and�…