Complete list of significant, differentially abundant proteins identified in Mecp2 Jae/y cortex. List of 465 significant proteins/PTMs with UniProt accession identity, number (#) of peptides quantified, WT and Mecp2 Jae/y relative abundances, fold change expression (represented as Mecp2 Jae/y relative abundance/WT relative abundance), p-value, subcellular location, putative function, and hyperlink are provided. File format: Microsoft Excel spreadsheet. (XLS 302Â 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...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
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. ...
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 ...
List of significant genes and proteins that are CNS cell type-specific. Each individual tab represen...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
Abstract Background Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutatio...
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...
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...
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...
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. ...
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 ...
List of significant genes and proteins that are CNS cell type-specific. Each individual tab represen...
Gene size and fold change expression breakdown for CNS cell type-specific DE genes. Significant DE g...
Abstract Background Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutatio...
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...
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...
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...