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Links from GEO DataSets

Items: 17

1.
Full record GDS2185

Runt-related transcription factor 2 null mutation effect on the embryonal bone (MG-U74B)

Analysis of embryonic day 14.5 humeri of runt-related transcription factor 2 (Runx2) deficient animals. Runx2 is an essential factor for skeletogenesis and heterozygous loss causes cleidocranial dysplasia. Results provide insight into the molecular mechanisms underlying skeletogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL82
Series:
GSE4911
4 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS2185
ID:
2185
2.

Expression data from mouse E14.5 wt and RUNX2 -/- humeri

(Submitter supplied) We used microarrays to identify genes differentially expressed between mouse RUNX2 -/- and wt embryonic humeri at stage E14.5 Keywords: wildtype versus knockout comparison
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS2184 GDS2185 GDS2186
Platforms:
GPL81 GPL82 GPL83
12 Samples
Download data: CEL, EXP
Series
Accession:
GSE4911
ID:
200004911
3.
Full record GDS2186

Runt-related transcription factor 2 null mutation effect on the embryonal bone (MG-U74C)

Analysis of embryonic day 14.5 humeri of runt-related transcription factor 2 (Runx2) deficient animals. Runx2 is an essential factor for skeletogenesis and heterozygous loss causes cleidocranial dysplasia. Results provide insight into the molecular mechanisms underlying skeletogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL83
Series:
GSE4911
4 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS2186
ID:
2186
4.
Full record GDS2184

Runt-related transcription factor 2 null mutation effect on the embryonal bone (MG-U74A)

Analysis of embryonic day 14.5 humeri of runt-related transcription factor 2 (Runx2) deficient animals. Runx2 is an essential factor for skeletogenesis and heterozygous loss causes cleidocranial dysplasia. Results provide insight into the molecular mechanisms underlying skeletogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE4911
4 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS2184
ID:
2184
5.

Mouse Retina P7 Rs1h KO versus Control

(Submitter supplied) Genome-wide expression profiling of the retinoschisin deficient retina in C57CL/6 mice. Keywords: Genetic modification
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2636
Platform:
GPL339
6 Samples
Download data
Series
Accession:
GSE5581
ID:
200005581
6.
Full record GDS2636

Retinoschisis model

Analysis of retinas from postnatal day 7 mutants lacking retinoschisin (RS1h), an animal model for retinoschisis (RS). RS is a recessive retinal dystrophy accompanied by macular disease often resulting in early-onset vision loss. Results provide insight into the pathogenesis of RS.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL339
Series:
GSE5581
6 Samples
Download data
DataSet
Accession:
GDS2636
ID:
2636
7.

Gene expression profile of Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP)

(Submitter supplied) Gene expression profile of Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) reveals murine targets for preclinical development of human prostate cancer therapy In this study, we have generated an open source TRAMP microarray dataset to identify differentially expressed genes from human prostate cancer that have concordant expression in TRAMP tumors, and thereby represent lead targets for preclinical therapy development. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE10525
ID:
200010525
8.

Regulation of 22q11 orthologous genes during mouse development

(Submitter supplied) 22q11-deletion syndrome (22q11DS) is a developmental anomaly caused by a microdeletion on human chromosome 22q11. Although mouse models indicated Tbx1 as the gene responsible of the syndrome, the phenotypic spectrum of del22q11 patients is complex suggesting that gene-gene and gene-environment interactions, probably during embryonic development, are crucial in delineating the pathogenesis of 22q11DS. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3634
14 Samples
Download data
Series
Accession:
GSE5050
ID:
200005050
9.

whole brains from nicotinic acetylcholine receptor subunit mutant mice and littermate controls

(Submitter supplied) Studies using mice with beta4 nicotinic acetylcholine receptor (nAChR) subunit deficiency (beta4-/- mice) helped reveal the roles of this subunit in bradycardiac response to vagal stimulation, nicotine-induced seizure activity and anxiety. In order to identify genes that might be related to beta4-containing nAChRs activity, we compared the mRNA expression profiles of brains from beta4-/- and wild-type mice using Affymetrix U74Avr2 microarray. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2309
Platform:
GPL81
11 Samples
Download data
Series
Accession:
GSE5320
ID:
200005320
10.
Full record GDS2309

Beta-4 nicotinic acetylcholine receptor subunit deficiency effect on the brain

Analysis of brains of beta-4 nicotinic acetylcholine receptor (nAChR) subunit null mutants. nAChRs are pentameric ion channels. Results provide insight into the molecular basis of the beta-4 subunit's role in the bradycardic response to vagal stimulation, nicotine-induced seizure, and anxiety.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE5320
11 Samples
Download data
DataSet
Accession:
GDS2309
ID:
2309
11.

Synaptic activity-regulated gene expression_embryonic day 18

(Submitter supplied) Activity-dependent changes in synapses rely on functional changes in resident proteins and on gene expression. We addressed the relationship between synapse activity and the expression of synaptic genes by comparing RNA levels in the neocortex of normal mice versus synaptically silent munc18-1 null mutants, using microarray expression analysis, quantitative PCR and Northern blotting. We hypothesized that genes under control of synaptic activity are differentially expressed between mutants and controls and found that few synaptic signaling genes were differentially expressed. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3106
11 Samples
Download data
Series
Accession:
GSE3639
ID:
200003639
12.

Synaptic activity-regulated gene expression_embryonic day 16

(Submitter supplied) Activity-dependent changes in synapses rely on functional changes in resident proteins and on gene expression. We addressed the relationship between synapse activity and the expression of synaptic genes by comparing RNA levels in the neocortex of normal mice versus synaptically silent munc18-1 null mutants, using microarray expression analysis, quantitative PCR and Northern blotting. We hypothesized that genes under control of synaptic activity are differentially expressed between mutants and controls and found that few synaptic signaling genes were differentially expressed. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3106
4 Samples
Download data
Series
Accession:
GSE3638
ID:
200003638
13.

Synaptic activity-regulated gene expression_embryonic day 14

(Submitter supplied) Activity-dependent changes in synapses rely on functional changes in resident proteins and on gene expression. We addressed the relationship between synapse activity and the expression of synaptic genes by comparing RNA levels in the neocortex of normal mice versus synaptically silent munc18-1 null mutants, using microarray expression analysis, quantitative PCR and Northern blotting. We hypothesized that genes under control of synaptic activity are differentially expressed between mutants and controls and found that few synaptic signaling genes were differentially expressed. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3106
6 Samples
Download data
Series
Accession:
GSE3637
ID:
200003637
14.

Laser microdissection and microarray analysis of the hippocampus of Rasgrf1 knockout mice

(Submitter supplied) We used manual macrodissection or laser capture microdissection (LCM) to isolate tissue sections of the hippocampus area of Ras-GRF1 wild type and knockout mice brains, and analyzed their transcriptional patterns using commercial oligonucleotide microarrays. Comparison between the transcriptomes of macrodissected and microdissected samples showed that the LCM samples allowed detection of significantly higher numbers of differentially expressed genes, with higher statistical rates of significance. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2816
Platform:
GPL339
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE8425
ID:
200008425
15.
Full record GDS2816

Ras-GRF1 deficiency effect on the hippocampus

Analysis of laser capture microdissected hippocampi of mutants lacking Ras-GRF1. Ras-GRF-1 is a guanine nucleotide exchange factor predominantly expressed in the central nervous system of mammals. Results provide insight into role of Ras-GRF1 in neural processes.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL339
Series:
GSE8425
6 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS2816
ID:
2816
16.

Glycoconjugate expression profiling in mouse postnatal cerebellar development

(Submitter supplied) We used a custom Affymetrix GeneChip, the "GLYCOv2" array, to measure differences in gene expression patterns from adult and postnatal day 7 (P7) mouse cerebellum RNA. Keywords = Cerebellum, microarray, development, glycoconjugates, glycosyltransferases, proteoglycans, gene expression Keywords: other
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1854
Platform:
GPL1420
6 Samples
Download data: CEL, EXP
Series
Accession:
GSE1712
ID:
200001712
17.
Full record GDS1854

Postnatal day 7 and adult cerebellum: glycoconjugate expression profile

Analysis of cerebellums of postnatal day 7 (P7) and adult animals using an array focusing on glycoconjugates. P7 was chosen for comparison as many differentiation events are peaking at this time. Glycoconjugates are widely distributed throughout the CNS and play an essential role in its development.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array, count, 2 age sets
Platform:
GPL1420
Series:
GSE1712
6 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1854
ID:
1854
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