Redox proteomics analysis of HNE-modified proteins in DS brain: clues for understanding development of Alzheimer disease

Down syndrome (DS) is the most common genetic cause of intellectual disability, due to partial or complete triplication of chromosome 21. DS subjects are characterized by a number of abnormalities including premature aging and development of Alzheimer’s disease (AD) neuropathology after approximatel...

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Detaylı Bibliyografya
Yayımlandı:Free Radic Biol Med
Asıl Yazarlar: Di Domenico, Fabio, Pupo, Gilda, Tramutola, Antonella, Giorgi, Alessandra, Schininà, Maria Eugenia, Coccia, Raffaella, Head, Elizabeth, Butterfield, D. Allan, Perluigi, Marzia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2014
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4686229/
https://ncbi.nlm.nih.gov/pubmed/24675226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.freeradbiomed.2014.03.027
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