home > bioproject > PRJDB3301
identifier PRJDB3301
type bioproject
sameAs
organism Mus musculus
title Small non-coding RNA sequencing of MeCP2-deficient cells
description Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked geneMECP2. However, molecular mechanisms of how MeCP2 deficiency leads to RTT pathogenesis are largely unknown. In this study, we performed the deep RNA sequencing using small non-coding RNA fraction from WT or MeCP2-KO neurons and WT or MeCP2 NSCs to identify microRNA that are regulated by MeCP2.
data type Transcriptome or Gene Expression
publication
properties 
{...}
dbXrefs
sra-run  DRR025058DRR025059DRR025060DRR025061DRR025062DRR025063DRR025064DRR025065DRR025066DRR025067 More
sra-submission  DRA002731
biosample  SAMD00022895SAMD00022896SAMD00022897SAMD00022898
sra-study  DRP002419
sra-sample  DRS016744DRS016745DRS016746DRS016747
sra-experiment  DRX022719DRX022720DRX022721DRX022722DRX022723DRX022724DRX022725DRX022726DRX022727DRX022728 More
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status public
visibility unrestricted-access
dateCreated 2014-11-11T04:09:27+09:00
dateModified 2014-12-08T01:30:13+09:00
datePublished 2014-12-08T01:30:13+09:00