Complete list of significant, differentially expressed (DE) genes identified in Mecp2 Jae/y cortex. NCBI gene names with WT and Mecp2 Jae/y FPKM values, Log2 fold change expression, and q-value (FDR) are provided for each identified DE gene. File format: Microsoft Excel spreadsheet. (XLS 84Â 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...
Principal components analysis (PCA) was carried out on the top 5000 most variable genes as defined b...
List of significant genes (p < 0.05) identified as RTT hits along with references. Information on ...
List of 77 gene-protein matches (gene expression p < 0.05, protein expression p < 0.1). Information ...
Complete list of significant, differentially abundant proteins identified in Mecp2 Jae/y cortex. Lis...
List of significant genes and proteins that are CNS cell type-specific. Each individual tab represen...
List of all pathways identified in proteomics and RNA-Seq data sets. Pathways identified in either t...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
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...
Intestinal MECP2 deletion using the villin-Cre Tg mouse. Immunofluorescence was performed to detect ...
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...
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...
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...
List of significant genes (p < 0.05) identified as RTT hits along with references. Information on ...
List of 77 gene-protein matches (gene expression p < 0.05, protein expression p < 0.1). Information ...
Complete list of significant, differentially abundant proteins identified in Mecp2 Jae/y cortex. Lis...
List of significant genes and proteins that are CNS cell type-specific. Each individual tab represen...
List of all pathways identified in proteomics and RNA-Seq data sets. Pathways identified in either t...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
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...
Intestinal MECP2 deletion using the villin-Cre Tg mouse. Immunofluorescence was performed to detect ...
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...
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...
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...