Neurotrophic effects of Cerebrolysin in the Mecp2(308/Y) transgenic model of Rett Syndrome

Rett syndrome is a childhood neurodevelopmental disorder caused by mutations in the gene encoding for methyl CpG binding protein (MeCP2). Neuropathological studies in patients with Rett syndrome and in MeCP2 mutant models have shown reduced dendritic arborization and abnormal neuronal packing. We ha...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Doppler, Edith, Rockenstein, Edward, Ubhi, Kiren, Inglis, Chandra, Mante, Michael, Adame, Anthony, Crews, Leslie, Hitzl, Monika, Moessler, Herbert, Masliah, Eliezer
格式: Artigo
語言:Inglês
出版: 2008
主題:
Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2732193/
https://ncbi.nlm.nih.gov/pubmed/18600331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-008-0407-x
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍