Comprehensive Transcriptomic Investigation of Rett Syndrome Reveals Increasing Complexity Trends from Induced Pluripotent Stem Cells to Neurons with Implications for Enriched Pathways

[Image: see text] Rett syndrome (RTT) is a rare genetic neurodevelopmental disorder that has no cure apart from symptomatic treatments. While intense research efforts are required to fulfill this unmet need, the fundamental challenge is to obtain sufficient patient data. In this study, we used human...

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Detalles Bibliográficos
Autores principales: Odabasi, Yusuf Caglar, Yanasik, Sena, Saglam-Metiner, Pelin, Kaymaz, Yasin, Yesil-Celiktas, Ozlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666228/
https://www.ncbi.nlm.nih.gov/pubmed/38027357
http://dx.doi.org/10.1021/acsomega.3c06448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666228/
https://www.ncbi.nlm.nih.gov/pubmed/38027357
http://dx.doi.org/10.1021/acsomega.3c06448

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