Unraveling the complexity of neurodegeneration in brains of subjects with Down syndrome: Insights from proteomics

Author:

Perluigi Marzia1,Di Domenico Fabio1,Buttterfield D. Allan23

Affiliation:

1. Department of Biochemical Sciences; Sapienza University of Rome; Rome Italy

2. Center of Membrane Sciences; Department of Chemistry; University of Kentucky; Lexington KY USA

3. Sanders-Brown Center on Aging; Department of Chemistry; University of Kentucky; Lexington KY USA

Publisher

Wiley

Subject

Clinical Biochemistry

Reference129 articles.

1. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype;Korenberg;Am. J. Hum. Genet.,1990

2. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group;Antonarakis;N. Engl. J. Med.,1991

3. Molecular mapping of twenty-four features of Down syndrome on chromosome 21;Delabar;Eur. J. Hum. Genet.,1993

4. Down syndrome phenotypes: the consequences of chromosomal imbalance;Korenberg;Proc. Natl. Acad. Sci. USA,1994

5. Differential gene expression studies to explore the molecular pathophysiology of Down syndrome;Antonarakis;Brain Res Brain Res Rev,2001

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