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Links from GEO DataSets

Items: 18

1.
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
2.

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
3.

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
4.

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
5.

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
6.
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
7.
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
8.

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
9.
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
10.

Age-related changes in the expression of schizophrenia susceptibility genes in the human prefrontal cortex

(Submitter supplied) The molecular basis of complex neuropsychiatric disorders most likely involves many genes. In recent years, specific genetic variations influencing risk for schizophrenia and other neuropsychiatric disorders have been reported. We have used custom DNA microarrays and qPCR to investigate the expression of putative schizophrenia susceptibility genes and related genes of interest in the normal human brain. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6893
72 Samples
Download data: TXT
Series
Accession:
GSE11546
ID:
200011546
11.

mRNA Sequencing Reveals Altered Synaptic Vesicular Transport in Post-Mortem Cerebellum

(Submitter supplied) Schizophrenia (SCZ) is a common, disabling mental illness with high heritability but complex, poorly understood genetic etiology. As the first phase of a genomic convergence analysis of SCZ, we generated 16.7 billion nucleotides of short read, shotgun sequences of cDNA from post-mortem cerebellar cortices of 14 patients and six matched controls. A rigorous analysis pipeline was developed for analysis of digital gene expression studies. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL7110
20 Samples
Download data
Series
Accession:
GSE12297
ID:
200012297
12.

Gene Expression Profiles in BA46 of Subjects with Schizophrenia and Matched Controls

(Submitter supplied) Results from clinical and imaging studies provide evidence for changes in schizophrenia with disease progression, however, the underlying molecular differences that may occur at different stages of illness have not been investigated. To test the hypothesis that the molecular basis for schizophrenia changes from early to chronic illness, we profiled genome-wide expression patterns in prefrontal cortex of schizophrenic subjects at different stages of illness, along with their age- and sex-matched controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
59 Samples
Download data: CEL
Series
Accession:
GSE21138
ID:
200021138
13.

An extreme human-specific delay in cortical synaptic development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca mulatta; Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL4134 GPL6244
21 Samples
Download data: CEL, TXT
Series
Accession:
GSE29140
ID:
200029140
14.

Identification of response genes upon neuronal activation in mouse cortical neurons

(Submitter supplied) We search for developmental changes specific to humans by examining gene expression profiles in the human, chimpanzee and rhesus macaque prefrontal and cerebellar cortex. In both brain regions, developmental patterns were more evolved in humans than in chimpanzees. The major human specific genes in prefrontal cortex was enriched in neuronal functions and regulated by several transcription factors, which were previously implicated in regulation of neuronal functions. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
9 Samples
Download data: TXT
Series
Accession:
GSE29139
ID:
200029139
15.

The mRNA expression patterns in macaque brains from prenatal to neonatal

(Submitter supplied) We search for developmental changes specific to humans by examining gene expression profiles in the human, chimpanzee and rhesus macaque prefrontal and cerebellar cortex. In both brain regions, developmental patterns were more evolved in humans than in chimpanzees. To distinguish whether the human specific developmental pattern represent novel human-specific developmental patterns or a shift in the timing of the existing patterns, we measured mRNA expression patterns in macaque brains from prenatal to neonatal. more...
Organism:
Macaca mulatta; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
12 Samples
Download data: CEL
Series
Accession:
GSE29138
ID:
200029138
16.

Gene expression in primate postnatal brain through lifespan

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca mulatta; Pan troglodytes; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
130 Samples
Download data: CEL
Series
Accession:
GSE22570
ID:
200022570
17.

Gene expression in primate postnatal brain through lifespan - cerebellar cortex

(Submitter supplied) We investigated molecular changes during human, chimpanzee, and rhesus macaque postnatal brain development at the transcriptome, proteome, and metabolome levels in two brain regions: the prefrontal cortex (PFC) that is involved in several human-specific cognitive processes, and the cerebellar cortex (CBC) that may be functionally more conserved. We find a nearly three-fold excess of human-specific gene expression changes in PFC compared to CBC. more...
Organism:
Homo sapiens; Macaca mulatta; Pan troglodytes
Type:
Expression profiling by array
Platform:
GPL6244
62 Samples
Download data: CEL
Series
Accession:
GSE22569
ID:
200022569
18.

Gene expression in primate postnatal brain through lifespan - prefrontal cortex

(Submitter supplied) We investigated molecular changes during human, chimpanzee, and rhesus macaque postnatal brain development at the transcriptome, proteome, and metabolome levels in two brain regions: the prefrontal cortex (PFC) that is involved in several human-specific cognitive processes, and the cerebellar cortex (CBC) that may be functionally more conserved. We find a nearly three-fold excess of human-specific gene expression changes in PFC compared to CBC. more...
Organism:
Pan troglodytes; Macaca mulatta; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
68 Samples
Download data: CEL, TSV
Series
Accession:
GSE22521
ID:
200022521
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