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Links from GEO DataSets

Items: 14

1.

Neuronal DNA damage response-associated dysregulation of signalling pathways and cholesterol metabolism at th earliest stages of Alzheimer-type pathology

(Submitter supplied) High levels of oxidative stress and an associated neuronal DDR occur at the earliest stages of Alzheimer pathology (low Braak stage), and is associated with cognitive impairment. The aim of the present study was to combine immuno-LCM and microarray analysis to characterize the neuronal transcriptome at low Braak stages (Braak 0-II), with respect to the neuronal DDR, in post-mortem human frontal cortex derived from the Medical Research Council Cognitive Function and Ageing Study (MRC-CFAS).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE66333
ID:
200066333
2.

Type 2 Diabetes Mellitus is Associated with Transcriptome Alterations in Cortical Neurones and Associated Neurovascular Unit Cells in the Ageing Brain

(Submitter supplied) Type 2 diabetes mellitus (T2D), characterised by peripheral insulin resistance, is a risk factor for dementia. In addition to its contribution to small and large vessel disease, T2D may directly damage cells of the brain neurovascular unit. In this study, we investigated the transcriptomic changes in cortical neurones, and associated astrocytes and endothelial cells of the neurovascular unit, in the ageing brain
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
33 Samples
Download data: CEL
Series
Accession:
GSE161355
ID:
200161355
3.

Microarray analysis of the astrocyte transcriptome in the ageing brain: relationship to Alzheimer's pathology and ApoE genotype

(Submitter supplied) Astrocyte dysfunction impacts their normal function, including neuronal support, thereby contributing to neurodegenerative pathologies including Alzheimer's disease (AD). Therefore to understand the role of astrocytes in the pathogenesis of age-related disorders we analysed the gene expression profile of astrocytes with respect to Alzheimer-type pathology. The aim of the present study was to combine immuno-LCM and microarray analysis to characterise the astrocyte transcriptome at different Braak stages, and with respect to ApoE genotype, in post-mortem human temporal cortex sampled dervied from the Medical Research Council Cognitive Function and Ageing Study (MRC-CFAS).
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4135
Platform:
GPL570
18 Samples
Download data: CEL
Series
Accession:
GSE29652
ID:
200029652
4.
Full record GDS4135

Postmortem temporal cortex from Medical Research Council Cognitive Function and Ageing Study (MRC-CFAS) cohort: astrocytes

Analysis of GFAP+ astrocytes representing different Braak stages and ApoE genotypes, in post-mortem temporal cortex samples. Astrocytes synthesize ApoE, which is involved in the astrocytic clearance of aggregated β-amyloid plaques. Results provide insight into role of ApoE in Alzheimer's pathology.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state, 2 genotype/variation sets
Platform:
GPL570
Series:
GSE29652
18 Samples
Download data: CEL
DataSet
Accession:
GDS4135
ID:
4135
5.

REST and Stress Resistance in Aging and Alzheimer’s Disease

(Submitter supplied) Comparison of the gene expression profiles of adult human brain samples from frontal cortical regions, including samples from young, middle aged, normal aged.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5204
Platform:
GPL570
41 Samples
Download data: CEL
Series
Accession:
GSE53890
ID:
200053890
6.
Full record GDS5204

Age effect on normal adult brain: frontal cortical region

Analysis of postmortem neuropathologically normal brain samples from the frontal cortical regions of young, middle aged, normal aged and extremely aged adults. Results provide insight into molecular mechanisms of aging in frontal cortical regions of the brain.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 4 age, 2 gender sets
Platform:
GPL570
Series:
GSE53890
41 Samples
Download data: CEL
7.

Candesartan neuroprotection on Rat Primary cerebellar granule cells (CGCs)

(Submitter supplied) Neuronal cultures were treated with candesartan at neuroprotective concentrations followed by excitotoxic glutamate amounts. Candesartan significantly reduced glutamate-induced inflammation. To provide mechanistic insight into the potential targets and pathways that may underlie these benefits, we performed genome wide expression profile analysis and evaluated the data by Ingenuity Pathway Analysis (IPA) and Gene Set Enrichment Analysis (GSEA). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
16 Samples
Download data: CEL, CHP
Series
Accession:
GSE67036
ID:
200067036
8.

Microarray analyses of laser-captured hippocampus reveal distinct gray and white matter signatures associated with incipient Alzheimer’s disease

(Submitter supplied) Alzheimer's disease (AD) is a devastating neurodegenerative disorder that threatens to reach epidemic proportions as our population ages. Although much research has examined molecular pathways associated with AD, relatively few studies have focused on critical early stages. Our prior microarray study correlated gene expression in human hippocampus with AD markers. Results suggested a new model of early-stage AD in which pathology spreads along myelinated axons, orchestrated by upregulated transcription and epigenetic factors related to growth and tumor suppression (Blalock et al., 2004). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4136
Platform:
GPL570
30 Samples
Download data: CEL
Series
Accession:
GSE28146
ID:
200028146
9.
Full record GDS4136

Various stages of Alzheimer's disease: laser-captured hippocampal CA1 gray matter

Analysis of laser-captured hippocampal CA1 gray matter from FFPE hippocampal sections of subjects at varying stages (incipient, moderate, severe) of Alzheimer’s disease (AD). Results provide insight into gray matter-specific molecular mechanisms underlying AD.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 19 age, 4 disease state sets
Platform:
GPL570
Series:
GSE28146
30 Samples
Download data: CEL
10.

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
11.
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
12.

Evaluation of gene expression profile in postmortem brain with Alzheimer´s disease-type neuropathological changes

(Submitter supplied) Unravel the mechanisms underlying brain aging and Alzheimer´s disease (AD) has been difficult because of complexity of the networks that drive these aging-related changes. Analysis of the gene expression in the brain is a valuable tool to study the function of the brain under normal and pathological conditions. Gene microarray technology allows massively parallel analysis of most genes expressed in a tissue, and therefore is an important research tool that potentially can provide the investigative power needed to address the complexity of brain aging and neurodegenerative processes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1930
128 Samples
Download data
Series
Accession:
GSE13214
ID:
200013214
13.

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
14.

Transcriptomic Profiling Reveals Discrete Poststroke Dementia Neuronal and Gliovascular Signatures

(Submitter supplied) Around 25% of stroke survivors over 65 years old develop progressive cognitive decline more than 3 months post-stroke, with features of vascular dementia. Poststroke dementia (PSD) is associated with pathology in frontal brain regions, in particular dorsal lateral prefrontal cortex (DLPFC) neurons and white matter, remote from the infarct, implicating damage to anterior cognitive circuits (ACC) involved in impaired executive function. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL23038 GPL23159
100 Samples
Download data: CEL, CHP
Series
Accession:
GSE186798
ID:
200186798
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