List of significant genes and proteins that are CNS cell type-specific. Each individual tab represents one expression data set, with each containing respective gene/protein name and identity, FPKM or relative peptide abundance, fold change expression, estimated size, p-, and/or q-value (FDR), and which CNS cell population each gene/protein belongs to. File format: Microsoft Excel spreadsheet. (XLS 213Â kb
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
List of 77 gene-protein matches (gene expression p < 0.05, protein expression p < 0.1). Information ...
Complete list of significant, differentially expressed (DE) genes identified in Mecp2 Jae/y cortex. ...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
Complete list of significant, differentially abundant proteins identified in Mecp2 Jae/y cortex. Lis...
List of all pathways identified in proteomics and RNA-Seq data sets. Pathways identified in either t...
List of significant genes (p < 0.05) identified as RTT hits along with references. Information on ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Principal components analysis (PCA) was carried out on the top 5000 most variable genes as defined b...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Table S2. List of siRNA targets resulting in negative differential circularity. Primary microglia we...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
List of 77 gene-protein matches (gene expression p < 0.05, protein expression p < 0.1). Information ...
Complete list of significant, differentially expressed (DE) genes identified in Mecp2 Jae/y cortex. ...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
Complete list of significant, differentially abundant proteins identified in Mecp2 Jae/y cortex. Lis...
List of all pathways identified in proteomics and RNA-Seq data sets. Pathways identified in either t...
List of significant genes (p < 0.05) identified as RTT hits along with references. Information on ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Principal components analysis (PCA) was carried out on the top 5000 most variable genes as defined b...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Table S2. List of siRNA targets resulting in negative differential circularity. Primary microglia we...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...