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Links from GEO DataSets

Items: 20

1.

RNA-seq of SOX5 overexpressing primary human neuronal progenitors

(Submitter supplied) Purpose: The goal of this study was to assess gene expression changes in neurons overexpressing SOX5 using human primary neuronal culture system. Methods: 6 samples each from control GFP and SOX5 overexpressing neurons were used to isolate total RNA using miRNeasy kit, Qiagen. We performed rRNA-depleted 69bp paired end stranded RNA-seq on neurons overexpressing either GFP or SOX5 tagged with GFP. Overexpression of SOX5 in neurons validated that a significant proportion of Attenuated cortical patterning (ACP) genes are regulated by SOX5, and that predicted SOX5 targets exhibit a net downregulation, consist with its repressive function. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: R, TXT
2.

Transcriptomic analysis of autistic brain reveals convergent molecular pathology [high-throughput sequence data]

(Submitter supplied) Autism spectrum disorder (ASD) is a common, highly heritable neurodevelopmental condition characterized by marked genetic heterogeneity. Thus, a fundamental question is whether autism represents an aetiologically heterogeneous disorder in which the myriad genetic or environmental risk factors perturb common underlying molecular pathways in the brain. Here, we demonstrate consistent differences in transcriptome organization between autistic and normal brain by gene co-expression network analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9115
6 Samples
Download data: TXT
3.

Transcriptomic Analysis of Autism Brain Reveals Convergent Molecular Pathology [array data]

(Submitter supplied) Autism spectrum disorder (ASD) is a common, highly heritable neuro-developmental condition characterized by marked genetic heterogeneity. Thus, a fundamental question is whether autism represents an etiologically heterogeneous disorder in which the myriad genetic or environmental risk factors perturb common underlying molecular pathways in the brain. Here, we demonstrate consistent differences in transcriptome organization between autistic and normal brain by gene co-expression network analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
79 Samples
Download data: TXT
Series
Accession:
GSE28521
ID:
200028521
4.

Aberrant expression of lncRNAs in autistic brain

(Submitter supplied) To assess for the potential contribution of dysregulated long non-coding RNA expression in autism pathogenesis, we profiled lncRNAs and mRNAs from post mortem brain tissue from autism patients and age/sex matched controls
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array; Expression profiling by array
Platform:
GPL15314
8 Samples
Download data: TXT
Series
Accession:
GSE36315
ID:
200036315
5.

Transcriptomic signatures of risk genes implicated in psychiatric disorders during neuronal differentiation

(Submitter supplied) Susceptibility genes for Autism Spectrum Disorder (ASD), Fragile X Syndrome (FXS), monogenetic disorders with intellectual disabilities (ID) or schizophrenia (SCZ) converge on processes related to neuronal function and differentiation. Furthermore, ASD risk genes are enriched for FMRP (Fragile X Mental Retardation Protein) targets and for genes implicated in ID. In addition, a significant co-heritability was observed between ASD and SCZ. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
21 Samples
Download data: IDAT, TXT
Series
Accession:
GSE69838
ID:
200069838
6.

Autism-like phenotype and risk gene-RNA deadenylation by CPEB4 mis-splicing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL15207 GPL11180
71 Samples
Download data: CEL
Series
Accession:
GSE113842
ID:
200113842
7.

Genome-wide analysis of mRNA polyadenylation in Cortex/Striatum of CPEB4 modified mice [II]

(Submitter supplied) To test the mRNA polyadenylation status in brain of CPEB4 modified mice we performed poly(U)-chromatography on RNA purified from a pool of cortex and striatum tissues of control and TgCPEB4∆4 mice
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
18 Samples
Download data: CEL
Series
Accession:
GSE113840
ID:
200113840
8.

Genome-wide analysis of mRNA polyadenylation in Cortex/Striatum of CPEB4 modified mice [I]

(Submitter supplied) To test the mRNA polyadenylation status in brain of CPEB4 modified mice, we performed poly(U)-chromatography on RNA purified from a pool of cortex and striatum tissues of WT and CPEB4 KOGT/+ and CPEB4 KO
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
18 Samples
Download data: CEL
Series
Accession:
GSE113838
ID:
200113838
9.

Genome-wide analysis of mRNA polyadenylation in prefrontal cortex of idiopathic ASD patients

(Submitter supplied) The aim of this work was to test the mRNA polyadenylation status in the brain of autistic patients. We performed poly(U)-chromatography on RNA purified from post-mortem prefrontal cortex tissue of control and idiopathic ASD cases.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
27 Samples
Download data: CEL
Series
Accession:
GSE113834
ID:
200113834
10.

CPEB1 and CPEB4-associated mRNAs in mice striatum

(Submitter supplied) To identify CPEB1 and CPEB4 regulated RNA we performed CPEB1 and CPEB4 RNA immunoprecipitation (RIP) followed by microarray hybridization analysis with striatal (St) RNA from wild-type (WT) and R6/1 mice (HD mice).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
8 Samples
Download data: CEL
Series
Accession:
GSE113833
ID:
200113833
11.

Genome wide binding of trr (ChIP-seq) and expression analysis (RNA-seq) of trr- and G9a mutant fly heads

(Submitter supplied) trr ChIP-seq, trr RNA-seq, G9a RNA-seq
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13304 GPL11203
13 Samples
Download data: TXT, WIG
Series
Accession:
GSE89459
ID:
200089459
12.

Misregulation of an activity-dependent splicing network as a common mechanism underlying autism spectrum disorders

(Submitter supplied) A key challenge in understanding and ultimately treating autism is to identify common molecular mechanisms underlying this genetically heterogeneous disorder. Transcriptomic profiling of autistic brains has revealed correlated misregulation of the neuronal splicing regulator nSR100/SRRM4 and its target microexon splicing program in more than one-third of analyzed individuals. To investigate whether nSR100 misregulation is causally linked to autism, we generated mutant mice with reduced levels of this protein and its target splicing program. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TXT
Series
Accession:
GSE89984
ID:
200089984
13.

Expression of protein-coding genes and lncRNAs in brain and other human tissues

(Submitter supplied) We used microarray expression profiling to assess protein-coding and non-coding gene expression across 8 brain samples and 7 other human tissues.
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL20604
15 Samples
Download data: TXT
Series
Accession:
GSE81410
ID:
200081410
14.

Neural gene expression in Pten knock-in mice at 6-weeks of age

(Submitter supplied) The goal of this study was to assess the changes in the neural transcriptome of Ptenm3m4 mice, in order to better understand their ASD-related phenotypes. For our initial cellular and behavioral characterization of this mouse line, see Tilot, et al., Human Molecular Genetics, 2014
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
18 Samples
Download data: CSV, DIFF
Series
Accession:
GSE59318
ID:
200059318
15.

The human lncRNA GOMAFU suppresses neuronal interferon response pathways affected in schizophrenia

(Submitter supplied) Long noncoding RNAs (lncRNAs) play multifaceted roles in regulating molecular networks that underlie normal brain function and the complex etiology of neuropsychiatric disorders. One example is the human neuronal lncRNA GOMAFU, which was reported to display abnormal expression in schizophrenia (SCZ) postmortem brains, regulate alternative splicing of SCZ risk gene transcripts, and harbor genetic variates contributing to the risk of SCZ. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: TXT
Series
Accession:
GSE206720
ID:
200206720
16.

MiR-137 and GOMAFU form a novel non-coding RNA pathway to regulate human neuron differentiation and molecular networks affected in neuropsychiatric diseases

(Submitter supplied) Increasing evidence suggests important roles of long noncoding RNAs (lncRNAs) in normal neuron development and neuropsychiatric disorders that disturb early neurodevelopmental processes. One such lncRNA is GOMAFU, which displays aberrant expression in schizophrenia postmortem brains and is known to regulate SCZ-associated splice variants in developing human neurons. However, molecular mechanisms that control expression and biological function of GOMAFU in human neuron development remain elusive. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
17.

RNA-seq of poly(A)-/ribo- or poly(A)+ RNAs from mouse and rhesus ES cells

(Submitter supplied) We have used RNA-seq to examine circular RNAs from RNase R treated poly(A)-/ribo- RNAs in human embryonic stem cells
Organism:
Mus musculus; Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL13112 GPL14954
6 Samples
Download data: BW
Series
Accession:
GSE53942
ID:
200053942
18.

Mouse ES Timecourse

(Submitter supplied) High temporal resolution RNAseq timecourse of mouse ES differentiation Investigations of transcriptional responses during developmental transitions typically use time courses with intervals that are not commensurate with the timescales of known biological processes. Moreover, such experiments typically focus on protein-coding transcripts, ignoring the important impact of long noncoding RNAs. We evaluated coding and noncoding expression dynamics at unprecedented temporal resolution (6-hourly) in differentiating mouse embryonic stem cells and report the effects of increased temporal resolution on the characterization of the underlying molecular processes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
42 Samples
Download data: CSV
Series
Accession:
GSE75028
ID:
200075028
19.

RNA Sequencing of mouse Purkinje cells across postnatal development

(Submitter supplied) We analyzed Purkinje cell transcriptome dynamics in the developing mouse cerebellum during the first three postnatal weeks, a key developmental period equivalent to the third trimester in human cerebellar development. Our study represents the first detailed analysis of developmental Purkinje cell transcriptomes and provides a valuable dataset for gene network analyses and biological questions on genes implicated in cerebellar and Purkinje cell development.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
15 Samples
Download data: TXT
Series
Accession:
GSE86824
ID:
200086824
20.

Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder

(Submitter supplied) To investigate the cell types and driver genes perturbed by 16p11.2 deletions using cerebral organoids
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
71 Samples
Download data: XLSX
Series
Accession:
GSE200851
ID:
200200851
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