DENDRITIC SPINE PATHOLOGIES IN HIPPOCAMPAL PYRAMIDAL NEURONS FROM RETT SYNDROME BRAIN AND AFTER EXPRESSION OF RETT-ASSOCIATED MECP2 MUTATIONS

Rett syndrome (RTT) is an X chromosome-linked neurodevelopmental disorder associated with the characteristic neuropathology of dendritic spines common in diseases presenting with mental retardation (MR). Here, we present the first quantitative analyses of dendritic spine density in postmortem brain...

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Bibliografiset tiedot
Päätekijät: Chapleau, Christopher A., Calfa, Gaston D., Lane, Meredith C., Albertson, Asher J., Larimore, Jennifer L., Kudo, Shinichi, Armstrong, Dawna L., Percy, Alan K., Pozzo-Miller, Lucas
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2722110/
https://ncbi.nlm.nih.gov/pubmed/19442733
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2009.05.001
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