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Abnormal Expression of Synaptic Proteins and Neurotrophin-3 in the Down Syndrome Mouse Model Ts65Dn

Down Syndrome (DS) results from triplication of the whole or distal part of human chromosome 21. DS subjects suffer from deficits in learning and memory and cognitive functions in general, and, starting from early development, their brains show dendritic and spine structural alterations and cell los...

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Detalhes bibliográficos
Main Authors: Pollonini, Gabriella, Gao, Virginia, Rabe, Ausma, Palminiello, Sonia, Albertini, Giorgio, Alberini, Cristina M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2613315/
https://ncbi.nlm.nih.gov/pubmed/18703118
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2008.07.025
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