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Mecp2 truncation in male mice promotes affiliative social behavior

Mouse models of Rett syndrome, with targeted mutations in the Mecp2 gene, show a high degree of phenotypic consistency with the clinical syndrome. In addition to severe and age-specific regression in motor and cognitive abilities, a variety of studies have demonstrated that Mecp2 mutant mice display...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Behav Genet
Asıl Yazarlar: Pearson, B.L., Defensor, E.B., Pobbe, R.L.H., Yamamoto, L.H.L., Bolivar, V.J., Blanchard, D.C., Blanchard, R.J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5843946/
https://ncbi.nlm.nih.gov/pubmed/21909962
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-011-9501-2
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