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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100
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
MECP2 MRD genetic variant data in CSV
MECP2 genetic variant data from the Maastricht Rett database (MRD) in CSV format. FAIR machine-readable metadata is available at:http://purl.org/biosemantics-lumc/rettbase/fdp
DataCite Commons2020-08-26 更新60
Middle East & Africa Rett syndrome Market
The Middle East & Africa Rett syndrome report provides a detailed analysis of emerging investment pockets, highlighting current and future market trends. It offers strategic insights into capital flow
IMR REPORTS80
Swapping the DNA binding domain of MeCP2 with that of MBD2 to abolish binding to non-CG methlyation results in RTT-like phenotypes in mice [ATAC-seq]
Mutations in the MECP2 gene cause the profound neurological disorder Rett syndrome. MeCP2 protein is an epigenetic reader that recruits the NCOR1/2 corepressor complexes to methylated cytosine in its
NIAID Data Ecosystem80
