Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action.

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作者： Francesco,Bedogni ^[1] ; Riccardo L,Rossi ^[2] ; Francesco,Galli ^[3] ; Clementina,Cobolli Gigli ^[1] ; Anna,Gandaglia ^[1] ; Charlotte,Kilstrup-Nielsen ^[4] ; Nicoletta,Landsberger ^[5]

作者单位： San Raffaele Rett Research Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan 20132, Italy; Laboratory of Genetic and Epigenetic Control of Gene Expression, Department of Theoretical and Applied Sciences, Division of Biomedical Research, University of Insubria, Busto Arsizio 21052, Italy. ^[1] Fondazione Istituto Nazionale Genetica Molecolare, Milan 20122, Italy. ^[2] San Raffaele Rett Research Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan 20132, Italy. ^[3] Laboratory of Genetic and Epigenetic Control of Gene Expression, Department of Theoretical and Applied Sciences, Division of Biomedical Research, University of Insubria, Busto Arsizio 21052, Italy. ^[4] San Raffaele Rett Research Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan 20132, Italy; Laboratory of Genetic and Epigenetic Control of Gene Expression, Department of Theoretical and Applied Sciences, Division of Biomedical Research, University of Insubria, Busto Arsizio 21052, Italy. Electronic address: landsben@uninsubria.it. ^[5]

关键词 MeCP2 Molecular genetics Pathway enrichment analysis Perturbation in gene expression Rett syndrome Structure and function

主题词动物(Animals);计算生物学(Computational Biology);基因表达调控, 发育期(Gene Expression Regulation, Developmental);人类(Humans);甲基-CpG-结合蛋白质2(Methyl-CpG-Binding Protein 2);Rett综合征(Rett Syndrome);信号传导(Signal Transduction)

DOI 10.1016/j.neubiorev.2014.01.011

PMID 24594195

发布时间 2022-01-29

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