Proteomics Study of Peripheral Blood Mononuclear Cells in Down Syndrome Children

Down syndrome (DS) is the most common chromosomal disorder and the leading genetic cause of intellectual disability in humans, which results from the triplication of chromosome 21. To search for biomarkers for the early detection and exploration of the disease mechanisms, here, we investigated the p...

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Detalles Bibliográficos
Autores principales: Lanzillotta, Chiara, Greco, Viviana, Valentini, Diletta, Villani, Alberto, Folgiero, Valentina, Caforio, Matteo, Locatelli, Franco, Pagnotta, Sara, Barone, Eugenio, Urbani, Andrea, Di Domenico, Fabio, Perluigi, Marzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696178/
https://www.ncbi.nlm.nih.gov/pubmed/33187268
http://dx.doi.org/10.3390/antiox9111112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696178/
https://www.ncbi.nlm.nih.gov/pubmed/33187268
http://dx.doi.org/10.3390/antiox9111112

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