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Links from GEO DataSets

Items: 8

1.

Expression data from post mortem Alzheimer's disease brains

(Submitter supplied) To identify molecular pathological alterations in AD brains, we performed interspecies comparative microarray analyses using RNAs prepared from postmortem human brain tissues donated for the Hisayama study and hippocampal RNAs from the triple-transgenic mouse model of AD (3xTg-AD) Three-way ANOVA of microarray data from frontal cortex, temporal cortex and hippocampus with presence/absence of AD and vascular dementia, and sex, as factors revealed that the gene expression profile is most significantly altered in the hippocampi of AD brains. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4758
Platform:
GPL6244
80 Samples
Download data: CEL, CHP
Series
Accession:
GSE36980
ID:
200036980
2.

Expression data from Alzheimer's disease model mouse

(Submitter supplied) To identify molecular pathological alterations in AD brains, we performed interspecies comparative microarray analyses using RNAs prepared from postmortem human brain tissues donated for the Hisayama study and hippocampal RNAs from the triple-transgenic mouse model of AD (3xTg-AD) Three-way ANOVA of microarray data from frontal cortex, temporal cortex and hippocampus with presence/absence of AD and vascular dementia, and sex, as factors revealed that the gene expression profile is most significantly altered in the hippocampi of AD brains. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE36981
ID:
200036981
3.
Full record GDS4758

Postmortem Alzheimer's disease brains: Hisayama study

Analysis of postmortem brain tissues (frontal cortex, temporal cortex, hippocampus) from male and female Hisayama residents pathologically diagnosed as having Alzheimer's disease (AD) or an AD-like disorder. Results provide insight into the molecular mechanisms underlying AD brain pathology.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 2 gender, 3 tissue sets
Platform:
GPL6244
Series:
GSE36980
79 Samples
Download data: CEL, CHP
4.

Genome-wide Mapping Implicates 5-Hydroxymethylcytosines in Diabetes and Alzheimer’s Disease

(Submitter supplied) Background: Diabetes mellitus (DM) is a recognized risk factor for dementias, including AD, increasing its odds by two-fold. Because DM is potentially modifiable risk factor, a greater understanding of the mechanisms linking DM to the clinical expression of AD may provide insights into much needed dementia therapeutics. Epigenetics offers a novel approach, and previously under-investigated 5-hydroxymethylcytosines (5hmC) is now emerging as a promising measure to investigate in diabetes related conditions. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24676
149 Samples
Download data: CSV
Series
Accession:
GSE203337
ID:
200203337
5.

Gene expression data from temporal cortex of young adult, old and AD-like Microcebus murinus

(Submitter supplied) Aging is the primary risk factor of neurodegenerative disorders such as Alzheimer's disease (AD). However, the molecular events occurring during brain aging are extremely complex and still largely unknown. For a better understanding of these age-associated modifications, animal models as close as possible to humans are needed. We thus analyzed the transcriptome of the temporal cortex of the primate Microcebus murinus using human oligonucleotide microarrays (Affymetrix). more...
Organism:
Microcebus murinus; Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4128
Platform:
GPL570
18 Samples
Download data: CEL, CHP
Series
Accession:
GSE21779
ID:
200021779
6.
Full record GDS4128

Model of cerebral aging and Alzheimer's disease: temporal cortex

Analysis of temporal cortex of young adult, old healthy, and Alzheimer’s disease (AD-like) animals. AD-like animals presented ß-amyloid plaques and cortical atrophy, which are signs of AD in humans. Results provided insight into molecular basis of physiological versus pathological brain aging.
Organism:
Homo sapiens; Microcebus murinus
Type:
Expression profiling by array, count, 2 age, 2 disease state, 2 gender sets
Platform:
GPL570
Series:
GSE21779
18 Samples
Download data: CEL, CHP
7.

Alzheimer's disease and the normal aged brain (steph-affy-human-433773)

(Submitter supplied) Information about the genes that are preferentially expressed during the course of Alzheimer’s disease (AD) could improve our understanding of the molecular mechanisms involved in the pathogenesis of this common cause of cognitive impairment in older persons, provide new opportunities in the diagnosis, early detection, and tracking of this disorder, and provide novel targets for the discovery of interventions to treat and prevent this disorder. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
161 Samples
Download data: CEL, CHP, XLS
Series
Accession:
GSE5281
ID:
200005281
8.

Transcriptome changes in the Alzheimer's middle temporal gyrus: importance of RNA metabolism and mitochondria-associated membrane (MAM) genes

(Submitter supplied) We used Illumina Human HT-12 v4 arrays to compare RNA expression of middle temporal gyrus (MTG; BA21) in Alzheimer’s Disease (AD = 97) and non-demented controls (ND = 98). A total of 938 transcripts were highly differentially expressed (adj p < 0.01; log2 Fold Change (FC) ≥ |0.500|, with 411 overexpressed and 527 underexpressed in AD. Our results correlated with expression profiling in neurons from AD and ND obtained by Laser Capture Microscopy in MTG from an independent dataset (log2 FC correlation: r = 0.504; p = 2.2e-16). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
195 Samples
Download data: TXT, XLSX
Series
Accession:
GSE132903
ID:
200132903
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