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Molecular responses of the Ts65Dn and Ts1Cje mouse models of Down syndrome to MK-801

Down syndrome, due to trisomy of human chromosome 21, is the most common genetic cause of intellectual disability. The Ts65Dn mouse model of Down syndrome is trisomic for orthologs of 94 chr21-encoded confirmed protein coding genes and displays a number of behavioral deficits. Recently, Ts65Dn mice...

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Detalhes bibliográficos
Main Authors: Siddiqui, Almas, Lacroix, Thomas, Stasko, Melissa R., Scott-McKean, Jonah J., Costa, Alberto C.S., Gardiner, Katheleen J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2677016/
https://ncbi.nlm.nih.gov/pubmed/19125866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2008.00428.x
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