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Links from GEO DataSets

Items: 20

1.

Next Generation Sequencing Facilitates Comparisons of Control and Schizophrenia-Patient derived hiPSC-derived neurons

(Submitter supplied) Cell-based models of many neurological and psychiatric diseases, established by reprogramming patient somatic cells into human induced pluripotent stem cells (hiPSCs), have now been reported. While numerous reports have demonstrated that neuronal cells differentiated from hiPSCs are electrophysiologically active mature neurons, the “age” of these cells relative to cells in the human brain remains unresolved. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
11 Samples
Download data: TXT
2.

Next Generation Sequencing Compares Effects of microRNA-9 perturbation in control and SZ hiPSC NPCs

(Submitter supplied) To follow-up findings that miR-9 was abundantly expressed in control NPCs, significantly down-regulated in a subset of SZ NPCs, and that miR-9 levels/activity, neural migration and diagnosis were strongly correlated, we tested the effect of manipulating miR-9 at cellular, proteomic and transcriptomic levels. Unexpectedly, proteomic- and RNAseq-based analysis revealed that these effects were mediated primarily by small changes in expression of indirect miR-9 targets, rather than large changes in direct miR-9 targets; these indirect targets are enriched for migration-associated genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
16 Samples
Download data: TXT
3.

Dysregulation of miRNA-9 in a subset of schizophrenia patient-derived neural progenitor cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
39 Samples
Download data
Series
Accession:
GSE80163
ID:
200080163
4.

Next Generation Sequencing Facilitates Comparisons of Control and Schizophrenia-Patient derived hiPSC-derived NPCs

(Submitter supplied) Cell-based models of many neurological and psychiatric diseases, established by reprogramming patient somatic cells into human induced pluripotent stem cells (hiPSCs), have now been reported. While numerous reports have demonstrated that neuronal cells differentiated from hiPSCs are electrophysiologically active mature neurons, the “age” of these cells relative to cells in the human brain remains unresolved. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TXT
5.

MicroRNA profiling of neurons generated using induced pluripotent stem cells derived from patients with schizophrenia and 22q11.2 deletion

(Submitter supplied) We are using induced pluripotent stem cell (iPSC) technology to study neuropsychiatric disorders associated with 22q11.2 microdeletions (del), the most common known schizophrenia (SZ) -associated genetic factor. Several genes in the deleted region have been implicated; one of the more promising candidates is DGCR8, which codes for a protein involved in microRNA (miRNA) biogenesis. We carried out miRNA expression profiling (miRNA-seq) on neurons generated from iPSCs derived from controls and SZ patients with 22q11.2 del.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
16 Samples
Download data: XLS
Series
Accession:
GSE65367
ID:
200065367
6.

Comparing Control and Schizophrenic hiPSC-derived NPCs

(Submitter supplied) Cell-based models of many neurological and psychiatric diseases, established by reprogramming patient somatic cells into human induced pluripotent stem cells (hiPSCs), have now been reported. While numerous reports have demonstrated that neuronal cells differentiated from hiPSCs are electrophysiologically active mature neurons, the “age” of these cells relative to cells in the human brain remains unresolved. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
24 Samples
Download data: CEL, TXT
Series
Accession:
GSE40102
ID:
200040102
7.

Transcriptional consequences of manipulating the candidate schizophrenia susceptibility gene miR-137 in human neural progenitor cells

(Submitter supplied) In the largest published genome-wide association study (GWAS) of schizophrenia to date (PGC1), the most significant association (P = 1.6 X 10-11) was observed at an intronic variant (rs1625579) within the MIR137 host gene (MIR137HG). In this study we have performed genome-wide RNA profiling of a human foetal neural progenitor cell line following miR-137 manipulation, in order to identify gene expression changes through which genetic variation at the MIR137HG locus could confer susceptibility to schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE49793
ID:
200049793
8.

MicroRNA profiling during neural differentiation of induced pluripotent stem cells

(Submitter supplied) MicroRNAs (miRNA) play an essential role in the regulation of gene expression, influence signaling networks responsible for several cellular processes like differentiation of pluripotent stem cells. Despite several studies on the neurogenesis process, no global analysis of microRNA expression during differentiation of induced pluripotent stem cells (iPSC) to neuronal stem cells (NSC) has been done. Therefore we compared the profile of microRNA expression in iPSC lines and in NSC lines derived from them, using microarray-based analysis. Two different protocols for NSC formation were used: direct and two-step via neural rosette formation. We confirmed the new associations of previously described miRNAs in regulation of NSC differentiation from iPSC. We discovered upregulation of miR-10 family, miR-30 family and miR-9 family and downregulation of miR-302 and miR-515 family. Moreover we showed that miR-10 family play a crucial role in the negative regulation of genes expression belonging to signaling pathways involved in neural differentiation: WNT signaling pathway, focal adhesion, signaling pathways regulating pluripotency of stem cells.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19117
8 Samples
Download data: CEL
Series
Accession:
GSE134061
ID:
200134061
9.

Deconvolution of Transcriptional Networks Identifies TCF4 as a Master Regulator in Schizophrenia

(Submitter supplied) We report the data generated upon knockdown of TCF4 in hiPSC-derived neural progenitor cells and glutamatergic neurons.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
23 Samples
Download data: TXT
10.

Transcriptome of iPSC-derived Cerebral Organoids with Heterozygous Knockout in CHD8

(Submitter supplied) CHD8 (chromodomain helicase DNA binding protein 8), which codes for a member of the CHD family of ATP-dependent chromatin-remodeling factors, is the most commonly mutated gene in autism spectrum disorders (ASD) identified in exome-sequencing studies. Loss of function mutations in the gene have also been found in schizophrenia (SZ) and intellectual disabilities, and affects cancer cell proliferation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
11.

Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with signatures from post mortem adult brains

(Submitter supplied) Whereas highly penetrant variants have proven well-suited to human induced pluripotent stem cell (hiPSC)-based models, the power of hiPSC-based studies to resolve the much smaller effects of common variants within the size of cohorts that can be realistically assembled remains uncertain. In developing a large case/control schizophrenia (SZ) hiPSC-derived cohort of neural progenitor cells and neurons, we identified and accounted for a variety of technical and biological sources of variation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
94 Samples
Download data: CSV
12.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL25480 GPL16791
5718 Samples
Download data
Series
Accession:
GSE119291
ID:
200119291
13.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [RNA-seq]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
44 Samples
Download data: TXT
14.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA207]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
380 Samples
Download data
Series
Accession:
GSE119289
ID:
200119289
15.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA206]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
380 Samples
Download data
Series
Accession:
GSE119288
ID:
200119288
16.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA205]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
380 Samples
Download data
Series
Accession:
GSE119287
ID:
200119287
17.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA204]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
380 Samples
Download data
Series
Accession:
GSE119286
ID:
200119286
18.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA203]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
380 Samples
Download data
Series
Accession:
GSE119285
ID:
200119285
19.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA202]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
378 Samples
Download data
Series
Accession:
GSE119284
ID:
200119284
20.

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia [MSA201]

(Submitter supplied) Integration of in silico and in vitro approaches to design and conduct transcriptomic drug screening in patient-derived neural cells, in order to survey novel pathologies and points of intervention in schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25480
378 Samples
Download data
Series
Accession:
GSE119283
ID:
200119283
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