官方服务：
资源简介：
Explore the pathogenesis and inheritance of Rett syndrome
应用场景：
创建时间：
2018-07-27
相关数据集
Integrated gene expression and alternative splicing analysis in human and mouse models of Rett Syndrome.
The folder "Homo_sapiens" contains 8 subfolders. Each of them is an individual input Bioproject downloaded from SRA and reanalized with the same transcriptomic pipeline in order to compute:1) Differen
DataCite Commons2024-07-19 更新130
Inhibition of BET proteins rescues neural defects in Rett syndrome [RNA-seq]
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder caused by mutations in the methyl-CpG binding protein 2 (MeCP2). Cellular heterogeneity in the brain confounds the understanding of
NIAID Data Ecosystem80
Additional file 2: of RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome
List of significant genes (pÂ
DataCite Commons2024-12-18 更新60
Isogenic Pairs of Wild Type and Mutant Induced Pluripotent Stem Cell (iPSC) Lines from Rett Syndrome Patients as In Vitro Disease Model
Rett syndrome (RTT) is an autism spectrum developmental disorder caused by mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene. Excellent RTT mouse models have been created to study th
NIAID Data Ecosystem80
VPA alleviates neurological deficits and restores gene expression in a mouse model of Rett syndrome. Mus musculus
Rett syndrome (RTT) is a devastating neurodevelopmental disorder that occurs once in every 10,000-15,000 live female births. Despite intensive research, no effective cure is yet available. Valproic ac
NIAID Data Ecosystem60
