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Links from GEO DataSets

Items: 20

1.
Full record GDS2144

Cochlear nucleus postnatal development

Analysis of cochlear nucleus (CN) at postnatal days 7 (P7), 14, and 21. Deprivation of auditory nerve input from P7 to P14 results in neuron death in the anteroventral CN. Results provide insight into the molecular basis underlying this critical period of susceptibility to loss of afferent input.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age sets
Platform:
GPL339
Series:
GSE2390
8 Samples
Download data: CEL
DataSet
Accession:
GDS2144
ID:
2144
2.

Postnatal Development of Mouse Cochlear Nucleus

(Submitter supplied) Developmental differences in gene expression in the postnatal mouse cochlear nucleus was analyzed at two or three ages using two different array platforms, the Affymetrix Mouse 430A GeneChip or the NIA 15K mouse cDNA microarray. These ages, P7, P14, and P21 parallel a critical period of neuron survival dependent on input from the auditory nerve. Keywords: parallel sample
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2144
Platforms:
GPL339 GPL236
18 Samples
Download data: CEL
Series
Accession:
GSE2390
ID:
200002390
3.

Activity Deprivation-Induced Transcriptional Changes in the P21 Cochlear Nucleus

(Submitter supplied) We analyzed whether cochlear removal-induced transcriptional changes in the cochlear nucleus (CN) were due to loss of electrical activity in the 8th nerve. Pharmacological activity blockade of the auditory nerve for 24 h resulted in similar expression changes for only a subset of genes. Thus, an additional factor not dependent on action potential-mediated signaling must also regulate transcriptional responses to deafferentation in the CN. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8321
6 Samples
Download data: CEL
Series
Accession:
GSE11726
ID:
200011726
4.

Gene Expression after Cochlear Removal in Cochlear Nucleus at P7 and P21

(Submitter supplied) Deprivation of peripheral nerve input by cochlear removal in young mice results in dramatic neuron death in the cochlear nucleus (CN). The same manipulation in older mice does not result in significant loss. The molecular basis of this critical period of vulnerability remains largely unknown. Here we identified genes regulated at early time points after cochlear removal at ages when neurons are vulnerable (postnatal day (P)7) or invulnerable (P21) to this challenge. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
44 Samples
Download data: CEL
Series
Accession:
GSE5394
ID:
200005394
5.

Selection of Neural Differentiation-Specific Genes by Comparing Profiles of Random Differentiation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2227
Platform:
GPL2987
21 Samples
Download data
Series
Accession:
GSE5459
ID:
200005459
6.

Guided differentiation of mouse embryonic stem cell

(Submitter supplied) The mouse embryonic stem cell’s differentiation was guided by several treatments, and each stage of differentiation was examined. Keywords: development stage
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2987
12 Samples
Download data
Series
Accession:
GSE3528
ID:
200003528
7.

Random differentiation of mouse embryonic stem cell

(Submitter supplied) Embryoid Bodies were dissociated and plated onto tissue culture dish in DMEM with fetal bovine serum and antibiotics for 4, 8, 12, 15, 21 day. Keywords: development stage
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2987
12 Samples
Download data
Series
Accession:
GSE3527
ID:
200003527
8.
Full record GDS2227

Guided differentiation into dopaminergic neurons and random differentiation into embryoid bodies

Comparison of cells induced to differentiate into dopaminergic neurons by guided differentiation (GD) to those induced to differentiate into embryoid bodies (EBs) by random differentiation (RD). Cells at 3 stages of differentiation in the GD model and days 4 to 21 EBs in the RD model compared.
Organism:
Mus musculus
Type:
Expression profiling by array, log ratio, 7 development stage, 2 growth protocol sets
Platform:
GPL2987
Series:
GSE5459
21 Samples
Download data
DataSet
Accession:
GDS2227
ID:
2227
9.

Rat Normal Cochlear Nucleus

(Submitter supplied) The cochlear nucleus is the first central pathway involved in the processing of peripheral auditory activity. It is heterogeneous in neuronal populations and physiologic responses and is organized in three major subdivisions: the anterior ventral cochlear nucleus (AVCN), the posterior ventral cochlear nucleus (PVCN) and the dorsal cochlear nucleus (DCN). Although each region demonstrates multiple cell types and functions, there are predominant populations of neurons in each region that underlie the principal role each subdivision plays in auditory processing. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by SAGE
Platform:
GPL23
3 Samples
Download data
Series
Accession:
GSE3628
ID:
200003628
10.

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
11.
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
12.

Aortas of mice on high fat diet

(Submitter supplied) Expression profiles in aortas isolated from mouse strains C3H.2/HeJ and C57.2Bl/6. Mice were were either on a high fat diet or normal diet for 0, 4, 10, 24, or 40 weeks. Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS735
Platform:
GPL891
54 Samples
Download data
Series
Accession:
GSE1560
ID:
200001560
13.
Full record GDS735

High fat diet effect on aorta: time course

Comparison of gene expression in aortas of C57BL/6 and C3H/HeJ fed identical high fat diets at 0, 4, 8, 24, and 40 weeks. C57BL/6 has a greater tendency than C3H/HeJ to develop atherosclerotic aortic lesions when both fed identical high fat diets.
Organism:
Mus musculus
Type:
Expression profiling by array, log ratio, 2 growth protocol, 2 strain, 5 time sets
Platform:
GPL891
Series:
GSE1560
54 Samples
Download data
DataSet
Accession:
GDS735
ID:
735
14.

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
15.
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
16.

Gene expression in FACS-purified cortical projection neurons

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL339 GPL1261
38 Samples
Download data: CEL, EXP
Series
Accession:
GSE17784
ID:
200017784
17.

FACS purified cortical projection neurons

(Submitter supplied) 3 subtypes of cortical projection neurons were purified by fluorescence-activated cell sorting at 4 different stages of development from mouse cortex. A detailed description of the data set is described in Arlotta, P et al (2005). Keywords = corticospinal motor neuron callosal corticotectal cortex development FACS
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1076
Platform:
GPL339
19 Samples
Download data: CEL, EXP
Series
Accession:
GSE2039
ID:
200002039
18.
Full record GDS1076

Corticospinal motor neuron development

Analysis of corticospinal motor neurons (CSMN) of C57BL/6 at embryonic day 18 to postnatal day 14. CSMN degeneration contributes to amyotrophic lateral sclerosis. CSMN compared to callosal projection and corticotectal projection neurons. Results provide insight into CSMN development.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 cell type, 4 development stage sets
Platform:
GPL339
Series:
GSE2039
19 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1076
ID:
1076
19.

Gene regulation in the hyperoxia mouse retina

(Submitter supplied) PURPOSE: Hyperoxia is toxic to photoreceptors, and this toxicity may be important in the progress of retinal dystrophies. This microarray study examines gene expression induced in the C57BL/6J mouse retina by hyperoxia over the 14-day period during which photoreceptors first resist, then succumb to, hyperoxia. METHODS: Young adult C57BL/6J mice were exposed to hyperoxia (75% oxygen) for up to 14 days. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE23437
ID:
200023437
20.

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
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