U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

Neurod2 RNA-Seq

(Submitter supplied) Neurod2 expression was knocked down in primary cortical neurons from mouse and RNA-Seq was performed.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TXT
Series
Accession:
GSE131494
ID:
200131494
2.

NeuroD2 ChIP-SEQ from embryonic cortex

(Submitter supplied) NeuroD2 targets were identified from embryonic day 14.5 cerebral cortex tissue.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
5 Samples
Download data: BED, WIG
Series
Accession:
GSE67539
ID:
200067539
3.

Molecular alterations in the motor and somatosensory areas of the juvenile NeuroD2 deficient mouse

(Submitter supplied) We found morphofunctional alterations in the neocortex of NeuroD2 deficient mice that were associated with autism/schizophrenia-like behaviors. Thus we asked what are the NeuroD2 target genes that are modified in NeuroD2 deficient mice. In particular it was interesting to determine which genes could be related with morphofunctional alterations and autism/schizophrenia
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE110491
ID:
200110491
4.

NeuroD2 ChIP-SEQ from postnatal cortex

(Submitter supplied) NeuroD2 targets were identified from postnatal day 0 cerebral cortex tissue.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
5 Samples
Download data: TXT, WIG
Series
Accession:
GSE84895
ID:
200084895
5.

Whole genome bisulfite sequencing of mouse neural progenitor cells and neurons from the mouse cerebral cortex at day 15.5 of embryonic development

(Submitter supplied) Global changes in DNA methylation occur during mammalian development but may be more limited during differentiation of cell lineages. The extent and specific nature of methylation changes at the time when neural progenitor cells in the brain cease proliferation and commit to become differentiated cortical neurons remains unknown. Here, we have used whole genome bisulfite sequencing to quantitate a level of modified bisulfite-resistant cytosines (5-methylcytosine and 5-hydroxymethylcytosine) at base resolution in differentiating neurons and their progenitors isolated from mouse brain at the peak of embryonic neurogenesis. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: BEDGRAPH
Series
Accession:
GSE101090
ID:
200101090
6.

H3K27ac ChIP upon NeuroD1 overexpression

(Submitter supplied) Cell-fate specification relies on a close cooperation of distinct transcription factors and their crosstalk with the epigenetic landscape during embryonic development. NeuroD1 is known to be essential for eliciting neurogenesis and is able to reprogram other cell types into neurons. Despite progress, its global impact on the epigenome and cooperativity with other transcription factors during neurogenesis remains unknown. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
7 Samples
Download data: CSV
Series
Accession:
GSE168853
ID:
200168853
7.

NeuroD1 reprograms chromatin and transcription factor landscapes to induce the neuronal program

(Submitter supplied) Cell fate specification relies on the action of critical transcription factors that become available at distinct stages of embryonic development. One such factor is NeuroD1, which is essential for eliciting the neuronal development program and possesses the ability to reprogram other cell types into neurons. Given this capacity, it is important to understand its targets and the mechanism underlying neuronal specification. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
7 Samples
Download data: TXT, WIG, XLSX
Series
Accession:
GSE65072
ID:
200065072
8.

Genetic and epigenetic determinants of neurogenesis and myogenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL1261 GPL11002 GPL9250
33 Samples
Download data: BAM, BEDGRAPH, CEL, MAP
Series
Accession:
GSE34908
ID:
200034908
9.

Genetic and epigenetic determinants of neurogenesis and myogenesis [expression profiling]

(Submitter supplied) The regulatory networks of differentiation programs have been partly characterized; however, the molecular mechanisms of lineage-specific gene regulation by highly similar transcription factors remain largely unknown. Here we compare the genome-wide binding and transcription profiles of NEUROD2-mediated neurogenesis with MYOD-mediated myogenesis. We demonstrate that NEUROD2 and MYOD bind a shared CAGCTG E-box motif and E-box motifs specific for each factor: CAGGTG for MYOD and CAGATG for NEUROD2. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
24 Samples
Download data: CEL
Series
Accession:
GSE34907
ID:
200034907
10.

Genetic and epigenetic determinants of neurogenesis and myogenesis [ChIP-seq]

(Submitter supplied) The regulatory networks of differentiation programs have been partly characterized; however, the molecular mechanisms of lineage-specific gene regulation by highly similar transcription factors remain largely unknown. Here we compare the genome-wide binding and transcription profiles of NEUROD2-mediated neurogenesis with MYOD-mediated myogenesis. We demonstrate that NEUROD2 and MYOD bind a shared CAGCTG E-box motif and E-box motifs specific for each factor: CAGGTG for MYOD and CAGATG for NEUROD2. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9250 GPL11002
9 Samples
Download data: BAM, BEDGRAPH, MAP
Series
Accession:
GSE34906
ID:
200034906
11.

Integrative genomic analysis of early neurogenesis reveals a temporal genetic program for differentiation and specification of preplate and Cajal-Retzius neurons

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL17021 GPL13112
43 Samples
Download data
Series
Accession:
GSE166015
ID:
200166015
12.

Integrative genomic analysis of early neurogenesis reveals a temporal genetic program for differentiation and specification of preplate and Cajal-Retzius neurons [scRNA-Seq]

(Submitter supplied) Neurogenesis in the developing neocortex begins with the generation of the preplate, which consists of early-born neurons including Cajal-Retzius (CR) cells and subplate neurons. Here, utilizing the Ebf2-EGFP transgenic mouse in which EGFP initially labels the preplate neurons then persists in CR cells, we reveal the dynamic transcriptome profiles of early neurogenesis and CR cell differentiation. Genome-wide RNA-seq and ChIP-seq analyses at multiple early neurogenic stages have revealed the temporal gene expression dynamics of early neurogenesis and distinct histone modification patterns in early differentiating neurons. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
8 Samples
Download data: MTX, TSV
Series
Accession:
GSE166014
ID:
200166014
13.

Integrative genomic analysis of early neurogenesis reveals a temporal genetic program for differentiation and specification of preplate and Cajal-Retzius neurons [RNA-Seq]

(Submitter supplied) Neurogenesis in the developing neocortex begins with the generation of the preplate, which consists of early-born neurons including Cajal-Retzius (CR) cells and subplate neurons. Here, utilizing the Ebf2-EGFP transgenic mouse in which EGFP initially labels the preplate neurons then persists in CR cells, we reveal the dynamic transcriptome profiles of early neurogenesis and CR cell differentiation. Genome-wide RNA-seq and ChIP-seq analyses at multiple early neurogenic stages have revealed the temporal gene expression dynamics of early neurogenesis and distinct histone modification patterns in early differentiating neurons. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: CSV
Series
Accession:
GSE166012
ID:
200166012
14.

Integrative genomic analysis of early neurogenesis reveals a temporal genetic program for differentiation and specification of preplate and Cajal-Retzius neurons [ChIP-Seq]

(Submitter supplied) Neurogenesis in the developing neocortex begins with the generation of the preplate, which consists of early-born neurons including Cajal-Retzius (CR) cells and subplate neurons. Here, utilizing the Ebf2-EGFP transgenic mouse in which EGFP initially labels the preplate neurons then persists in CR cells, we reveal the dynamic transcriptome profiles of early neurogenesis and CR cell differentiation. Genome-wide RNA-seq and ChIP-seq analyses at multiple early neurogenic stages have revealed the temporal gene expression dynamics of early neurogenesis and distinct histone modification patterns in early differentiating neurons. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
23 Samples
Download data: BED
Series
Accession:
GSE166011
ID:
200166011
15.

Cell type-specific alternative splicing during mammalian neuronal differentiation

(Submitter supplied) Alternative precursor-mRNA splicing (AS) is a key regulation of gene expression and protein diversity. AS is highly happened in the nervous system and misregulation of AS caused neurological diseases. In current research, we identified and validated the differential AS events from purified neural progenitor cells (NPCs) and neurons. Our data demonstrated a systematic characterization of AS events between endogenous NPCs and neurons, which may serve as a useful resource for further investigations.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE96950
ID:
200096950
16.

Identification of TIA1 mRNA targets during human neuronal development

(Submitter supplied) Background: Neuronal development is a tightly controlled process involving multi-layered regulatory mechanisms. While transcriptional pathways regulating neurodevelopment are well characterized, post-transcriptional programs are still poorly understood. TIA1 is an RNA-binding protein that can regulate splicing, stability, or translation of target mRNAs, and has been shown to play critical roles in neurodevelopment. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
27 Samples
Download data: CSV
Series
Accession:
GSE166306
ID:
200166306
17.

STAU2 Binds a Complex RNA Cargo that Changes Temporally With Production of Diverse Intermediate Progenitors During Mouse Corticogenesis

(Submitter supplied) The double-stranded RNA binding protein (RBP) STAU2 displays temporally regulated associations with RNA determinants that contribute to IPC and cortical lamination during corticogenesis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
24 Samples
Download data: CSV
Series
Accession:
GSE163378
ID:
200163378
18.

Loss of BAF complex in developing cortex perturbs radial neuronal migration in a WNT signaling-dependent manner

(Submitter supplied) We performed RNA-Seq from postnatal cortical tissue at stage P1 from controls and BAF double knock-out (dcKO) mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: TXT
Series
Accession:
GSE175362
ID:
200175362
19.

Epigenetic regulation by BAF (mSWI/SNF) complexes limits neural stem cell proliferation by suppressing Wnt signaling in late cortical neurogenesis

(Submitter supplied) We have analyzed changes in gene expression, histone 3 lysine 4 dimethyl (H3K4me2) and histone 3 lysine 37 trimethyl (H3K27me3) levels in the embryonic cortex at E17.5 resulting from conditional deletion of BAF complex - i.e., double knockout of BAF155 and BAF170, in late cortical progenitors utilizing Cre expression under human GFAP (hGFAP) promoter (dcKO_hGFAP-Cre). Moreover, we also analyzed gene expression in WT E17.5 cortex treated with vehicle and Wnt inhibitor together with that of in dcKO_hGFAP-Cre cortex treated with Wnt inhibitor. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
36 Samples
Download data: TXT, XLS
Series
Accession:
GSE106711
ID:
200106711
20.

Tissue-wide Mechanisms Overrule Cell-intrinsic Gene Function in Radial Neuronal Migration

(Submitter supplied) The mammalian neocortex is composed of diverse neuronal and glial cell classes that broadly arrange in six distinct laminae. Cortical layers emerge during development and defects in the developmental programs that orchestrate cortical lamination are associated with neurodevelopmental diseases. The developmental principle of cortical layer formation is based on concerted radial projection neuron migration, from their birthplace to their final target position. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
97 Samples
Download data: TAB, XLSX
Series
Accession:
GSE200604
ID:
200200604
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=3|qty=3|blobid=MCID_672d88fbfa580660f37a03aa|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center