A Comprehensive and Integrative Approach to MeCP2 Disease Transcriptomics

Mutations in MeCP2 result in a crippling neurological disease, but we lack a lucid picture of MeCP2′s molecular role. Individual transcriptomic studies yield inconsistent differentially expressed genes. To overcome these issues, we demonstrate a methodology to analyze all modern public data. We obta...

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Detalles Bibliográficos
Autores principales: Trostle, Alexander J., Li, Lucian, Kim, Seon-Young, Wang, Jiasheng, Al-Ouran, Rami, Yalamanchili, Hari Krishna, Liu, Zhandong, Wan, Ying-Wooi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049497/
https://www.ncbi.nlm.nih.gov/pubmed/36982190
http://dx.doi.org/10.3390/ijms24065122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049497/
https://www.ncbi.nlm.nih.gov/pubmed/36982190
http://dx.doi.org/10.3390/ijms24065122

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