Brain-enriched microRNAs circulating in plasma as novel biomarkers for Rett syndrome

Rett syndrome (RTT) is a severe neurodevelopmental disorder caused by mutations in the X-linked gene MECP2 (methyl-CpG-binding protein 2). Minimally invasive and accurate biomarkers of disease progression and treatment response could facilitate screening of therapeutic compounds in animal models, en...

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Detalles Bibliográficos
Autores principales: Sheinerman, Kira, Djukic, Aleksandra, Tsivinsky, Vladimir G., Umansky, Samuil R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619658/
https://www.ncbi.nlm.nih.gov/pubmed/31291284
http://dx.doi.org/10.1371/journal.pone.0218623

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619658/
https://www.ncbi.nlm.nih.gov/pubmed/31291284
http://dx.doi.org/10.1371/journal.pone.0218623

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