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Links from GEO DataSets

Items: 20

1.
Full record GDS2191

Bipolar disorder: orbitofrontal cortex

Analysis of postmortem orbitofrontal cortex from 10 adults with bipolar disorder. Results provide insight into the pathophysiology of the disease.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL96
Series:
GSE5389
21 Samples
Download data: CEL
DataSet
Accession:
GDS2191
ID:
2191
2.

Expression profiling of human adult postmortem brain tissue from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (dorsolateral prefrontal cortex and orbitofrontal cortex) from patients with bipolar disorder and matched healthy controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
82 Samples
Download data: CEL
Series
Accession:
GSE5392
ID:
200005392
3.

Adult postmortem brain tissue (orbitofrontal cortex) from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (orbitofrontal cortex) from patients with bipolar disorder and matched healthy controls. Orbitofrontal cortex tissue from a cohort of 30 subjects was investigated and the final analysis included 10 bipolar and 11 control subjects. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2191
Platform:
GPL96
21 Samples
Download data: CEL
Series
Accession:
GSE5389
ID:
200005389
4.

Adult postmortem brain tissue (dorsolateral prefrontal cortex) from subjects with bipolar disorder and healthy controls

(Submitter supplied) Bipolar affective disorder is a severe psychiatric disorder with a strong genetic component but unknown pathophysiology. We used microarray technology (Affymetrix HG-U133A GeneChips) to determine the expression of approximately 22 000 mRNA transcripts in post-mortem brain tissue (dorsolateral prefrontal cortex) from patients with bipolar disorder and matched healthy controls. A cohort of 70 subjects was investigated and the final analysis included 30 bipolar and 31 control subjects. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2190
Platform:
GPL96
61 Samples
Download data: CEL
Series
Accession:
GSE5388
ID:
200005388
5.
Full record GDS2190

Bipolar disorder: dorsolateral prefrontal cortex

Analysis of postmortem dorsolateral prefrontal cortex from 30 adults with bipolar disorder. Results provide insight into the pathophysiology of the disease.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL96
Series:
GSE5388
61 Samples
Download data: CEL
DataSet
Accession:
GDS2190
ID:
2190
6.

Comparison of post-mortem tissue from brain BA10 region between schizophrenic and control patients.

(Submitter supplied) Analysis of gene expression in two large schizophrenia cohorts identifies multiple changes associated with nerve terminal function. Schizophrenia is a severe psychiatric disorder with a world-wide prevalence of 1%. The pathophysiology of the illness is not understood, but is thought to have a strong genetic component with some environmental influences on aetiology. To gain further insight into disease mechanism, we used microarray technology to determine the expression of over 30 000 mRNA transcripts in post-mortem tissue from a brain region associated with the pathophysiology of the disease (Brodmann area 10: anterior prefrontal cortex) in 28 schizophrenic and 23 control patients.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4523
Platform:
GPL570
51 Samples
Download data: CEL
Series
Accession:
GSE17612
ID:
200017612
7.
Full record GDS4523

Schizophrenia: postmortem anterior prefrontal cortex

Analysis of post-mortem tissue from the anterior prefrontal cortex (Brodmann Area 10, BA10) of schizophrenic patients. The BA10 region mediates the negative pathophysiology of schizophrenia. Results provide insight into molecular mechanisms underlying the negative symptoms of schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 33 age, 2 disease state, 2 gender sets
Platform:
GPL570
Series:
GSE17612
51 Samples
Download data: CEL
DataSet
Accession:
GDS4523
ID:
4523
8.

Expression data from brain tissue of Rattus norvegicus treated with D-Serine

(Submitter supplied) d-serine is naturally present throughout the human body. It is also used as add-on therapy for treatment-refractory schizophrenia. d-Serine interacts with the strychnine-insensitive glycine binding site of NMDA receptor, and this interaction could lead to potentially toxic activity (i.e., excitotoxicity) in brain tissue. The transcriptomic changes that occur in the brain after d-serine exposure have not been fully explored. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS3643
Platform:
GPL1355
24 Samples
Download data: CEL
Series
Accession:
GSE10748
ID:
200010748
9.
Full record GDS3643

D-serine effect on the brain: dose response

Analysis of forebrains of animals treated with up to 500 mg/kg D-serine for 96 hours. D-serine is involved in many physiological processes through its interaction with the glycine binding site of the NMDA receptor. Results provide insight into the impact of D-serine exposure on neuronal functions.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 6 dose sets
Platform:
GPL1355
Series:
GSE10748
24 Samples
Download data: CEL
DataSet
Accession:
GDS3643
ID:
3643
10.

Expression profiling of human adult postmortem brain tissue from Down syndrome and healthy control subjects

(Submitter supplied) Down syndrome (DS) is the result of trisomy chromosome 21 but the mechanisms by which the genotype leads to the characteristic disease phenotype are unclear. We performed a microarray study using human adult brain tissue (dorsolateral prefrontal cortex) from DS subjects and healthy controls to characterise for the first time the human adult Down syndrome brain Keywords: disease state analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2941
Platform:
GPL96
15 Samples
Download data: CEL
Series
Accession:
GSE5390
ID:
200005390
11.
Full record GDS2941

Down syndrome: brain

Analysis of postmortem brains of individuals with Down syndrome. Results provide insight into the pathogenesis of Down syndrome.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL96
Series:
GSE5390
15 Samples
Download data: CEL
DataSet
Accession:
GDS2941
ID:
2941
12.

Comparison of post-mortem tissue from Brodman Brain BA22 region between schizophrenic and control patients

(Submitter supplied) Transcriptional analysis of the superior temporal cortex (BA22) in schizophrenia: Pathway insight into disease pathology and drug development Schizophrenia is a highly debilitating psychiatric disorder which is known to have heritable genetic and environmental components. To gain some insight into the mechanisms underpinning both positive and negative symptoms of the disease, we determined the genome wide expression of mRNA transcripts in post-mortem tissue from the superior temporal cortex (Brodmann Area 22, BA22) in schizophrenic and control patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4522
Platform:
GPL570
42 Samples
Download data: CEL
Series
Accession:
GSE21935
ID:
200021935
13.
Full record GDS4522

Schizophrenia: postmortem superior temporal cortex

Analysis of post-mortem tissue from the superior temporal cortex (Brodmann Area 22, BA22) of schizophrenic patients. The BA22 region mediates the positive pathophysiology of schizophrenia. Results provide insight into molecular mechanisms underlying the positive symptoms of schizophrenia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 30 age, 2 disease state, 2 gender sets
Platform:
GPL570
Series:
GSE21935
42 Samples
Download data: CEL
DataSet
Accession:
GDS4522
ID:
4522
14.

Distinctive transcriptome alterations of prefrontal pyramidal neurons in schizophrenia and schizoaffective disorder

(Submitter supplied) Schizophrenia is associated with alterations in working memory that reflect dysfunction of dorsolateral prefrontal cortex (DLPFC) circuitry. Working memory depends on the activity of excitatory pyramidal cells in DLPFC layer 3, and to a lesser extent in layer 5. Although many studies have profiled gene expression in DLPFC gray matter in schizophrenia, little is known about cell type-specific transcript expression in these two populations of pyramidal cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
208 Samples
Download data: CEL
Series
Accession:
GSE93987
ID:
200093987
15.

Human cerebellum, frontal cortex [BA4, BA9] and caudate nucleus HD tissue experiment

(Submitter supplied) Post mortem human brain tissue comparison between HD patients and controls from 3 brain regions - cerebellum, frontal cortex [BA4, BA9] and caudate nucleus. Gene expression analysed using linear models from LIMMA package in Bioconductor suite. Keywords: disease state analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL96 GPL97
404 Samples
Download data: CEL
Series
Accession:
GSE3790
ID:
200003790
16.

Influence of exhaustive endurance exercise on gene expression in peripheral blood

(Submitter supplied) cDNA microarray screening for gene expression changes in peripheral blood of eight half-marathon runners before (time point 0), immediately (time point 1) after and 24 h (time point 2) after exercise for details see publication: ... Keywords: repeat sample
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1962
8 Samples
Download data
Series
Accession:
GSE2532
ID:
200002532
17.

Expression profiling in monozygotic twins discordant for bipolar disorder

(Submitter supplied) To identify genes dysregulated in bipolar disorder (BD1) we carried out global gene expression profiling using whole-genome microarrays. To minimize genetic variation in gene expression levels between cases and controls we compared expression profiles in lymphoblastoid cell lines from monozygotic twin pairs discordant for the disease. We identified 82 genes that were differentially expressed by ≥ 1.3-fold in 3 BD1 cases compared to their co-twins, and which were statistically (p ≤ 0.05) differentially expressed between the groups of BD1 cases and controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2779
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE7036
ID:
200007036
18.
Full record GDS2779

Lymphoblastoid cell lines from monozygotic twin pairs discordant for bipolar disorder

Analysis of lymphoblastoid cell lines derived from 3 monozygotic twin pairs discordant for bipolar disorder. Results provide insight into the molecular pathogenesis of bipolar disorder.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 3 other sets
Platform:
GPL570
Series:
GSE7036
6 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS2779
ID:
2779
19.

Olanzapine vs. Saline rat pfc

(Submitter supplied) Male Sprague-Dawley albino rats (Charles River) initially weighting approximately 200 grams were randomly assigned to one of the following: 1) olanzapine (2 mg/kg/day, I.P.) (N=20) or 2) Saline (N=20) and administered olanzapine or saline for 21 days. Frontal cortex (N=4/group) was dissected and homogenized for microarray, QPCR and western blotting following previous methods (Fatemi et al. 2003; Brooks et al. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS2608
Platform:
GPL1355
8 Samples
Download data
Series
Accession:
GSE2547
ID:
200002547
20.
Full record GDS2608

Antipsychotic agent olanzapine effect on the brain frontal cortex

Analysis of brain frontal cortices of albino Sprague-Dawley males treated with olanzapine for 21 days. Olanzapine is a second generation antipsychotic agent. Results provide insight into the molecular basis of the clinical response to olanzapine.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL1355
Series:
GSE2547
8 Samples
Download data
DataSet
Accession:
GDS2608
ID:
2608
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