Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome

MECP2 loss-of-function mutations cause Rett syndrome, a neurodevelopmental disorder resulting from a disrupted brain transcriptome. How these transcriptional defects are decoded into a disease proteome remains unknown. We studied the proteome of Rett cerebrospinal fluid (CSF) to identify consensus R...

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Detalles Bibliográficos
Autores principales: Zlatic, Stephanie A., Duong, Duc, Gadalla, Kamal K.E., Murage, Brenda, Ping, Lingyan, Shah, Ruth, Fink, James J., Khwaja, Omar, Swanson, Lindsay C., Sahin, Mustafa, Rayaprolu, Sruti, Kumar, Prateek, Rangaraju, Srikant, Bird, Adrian, Tarquinio, Daniel, Carpenter, Randall, Cobb, Stuart, Faundez, Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437849/
https://www.ncbi.nlm.nih.gov/pubmed/36060065
http://dx.doi.org/10.1016/j.isci.2022.104966

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437849/
https://www.ncbi.nlm.nih.gov/pubmed/36060065
http://dx.doi.org/10.1016/j.isci.2022.104966

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