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Links from GEO DataSets

Items: 20

1.

Expression data from wildtype and C. elegan mutants

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
20 Samples
Download data: CEL
Series
Accession:
GSE9967
ID:
200009967
2.

Expression data from wildtype and alb/cre liver-conditional Pdss2 knockout mutant mice

(Submitter supplied) Utilizing M. musculus as a model of mitochondrial dysfunction provides insight into cellular adaptations which occur as a consequence of genetic alterations causative of human disease. We characterized genome-wide expression profiles of liver-conditional knockout mice for Pdss2 compared with loxP controls. Our goal was to detect concordant changes among clusters of genes that comprise defined metabolic pathways utilizing gene set enrichment analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3454
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE10904
ID:
200010904
3.

Expression data from 2 wildtype and 8 C. elegans ETC mutants

(Submitter supplied) Utilizing C. elegans as a model of mitochondrial dysfunction provides insight into cellular adaptations which occur as a consequence of genetic alterations causative of human disease. We characterized genome-wide expression profiles of hypomorphic C. ele Our goal was to detect concordant changes among clusters of genes that comprise defined metabolic pathways utilizing gene set enrichment analysis. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Dataset:
GDS3453
Platform:
GPL200
10 Samples
Download data: CEL
Series
Accession:
GSE9897
ID:
200009897
4.

Expression data from wildtype and gas-1 mitochondrial mutant C. elegans

(Submitter supplied) Utilizing C. elegans as a model of mitochondrial dysfunction provides insight into cellular adaptations which occur as a consequence of genetic alterations causative of human disease. We characterized genome-wide expression profiles of hypomorhpic C. elegans mutants in nuclear-encoded subunits of respiratory chain complexes I, II and III. Our goal was to detect concordant changes among clusters of genes that comprise defined metabolic pathways utilizing gene set enrichment analysis. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Dataset:
GDS3452
Platform:
GPL200
10 Samples
Download data: CEL
Series
Accession:
GSE9896
ID:
200009896
5.
Full record GDS3454

Murine model of primary mitochondrial dysfunction

Analysis of hepatocytes from Pdss2 liver-specific knockouts. The mutant livers are depleted for Coenzyme Q (CoQ), a critical component of the mitochondrial respiratory chain. Results from this mammalian model of primary mitochondrial dysfunction are compared to nematode models (GDS3452 and GDS3453).
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE10904
6 Samples
Download data: CEL
6.
Full record GDS3453

Nematode models of primary mitochondrial dysfunction: complex I, II, and III mutants

Analysis of 8 different electron transport chain (ETC) subunit mutants (3 missense and 5 RNAi-induced) in complexes I, II, and III. Results from this validation set provide insight into the contributions of individual complexes or subunits to primary mitochondrial dysfunction.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 4 genotype/variation, 4 protocol sets
Platform:
GPL200
Series:
GSE9897
10 Samples
Download data: CEL
7.
Full record GDS3452

Nematode model of primary mitochondrial dysfunction: complex I mutants

Analysis of gas-1(fc21) electron transport chain complex I mutants. The gas-1(fc21) mutation affects the 49 kD subunit of complex I, decreasing the rate of complex I-dependent oxidative phosphorylation. Results provide insight into molecular mechanisms underlying primary mitochondrial disease .
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL200
Series:
GSE9896
10 Samples
Download data: CEL
8.

Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice

(Submitter supplied) To discern whether the same transcriptional signature of mitochondrial dysfunction previously reported in B6.Alb/cre,Pdss2loxP/loxP liver-conditional knockout mice (Peng, Falk et al. PLoS Genetics, 2008 [PMID 18437205]) was present regardless of Pdss2 mutation type, as well as to assess whether pharmacologic therapies modulate expression of particular pathways, genome-wide transcriptional profiling was performed in liver from B6.Pdss2(kd/kd) missense mutant mice on standard chow or supplemented long-term with either probucol or CoQ10.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
20 Samples
Download data: TXT
Series
Accession:
GSE27954
ID:
200027954
9.

RNA-sequencing of C.elegans isp-1 mutant and superoxide dismutase-isp-1 double mutants

(Submitter supplied) isp-1;sod double mutants have decreased lifespan, increased resistance to oxidative stress and slow physiologic rates. We performed RNA sequencing to compare gene expression between isp-1 mutants and isp-1;sod-3 and isp-1;sod-5 double mutants
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
12 Samples
Download data: TXT
Series
Accession:
GSE95240
ID:
200095240
10.

Role of mitochondrial unfolded protein response transcription fatcor ATFS-1 in lifespan of long-lived mitochondrial mutants

(Submitter supplied) In this work, we examined the effect of the transcription factor ATFS-1 in the long lifespan of the nuo-6 mitochondrial mutant. We also examined the effect of the hypoxia transcription factor hif-1. We sequenced both atfs-1 deletion mutants and atfs-1 gain-of-function point mutants in which the mitochondrial localization sequence of ATFS-1 is disrupted. Note that sequencing batch 2 was previously uploaded as part of GSE93724.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
43 Samples
Download data: TXT
Series
Accession:
GSE110984
ID:
200110984
11.

Expression Data of Reactive Oxygen Species Signalling in C. elegans

(Submitter supplied) We have shown that worms that possess mutations in two electron transport chain subunits live longer due to mtROS signalling. Wild type worms can also live longer by treatment with the pro-oxidant paraquat. Paraquat treatment is not additive to the mutations in the ETC subunits. We aimed to determine the underlying changes in gene expression that were common to both paraquat treatment and the two mutations. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Datasets:
GDS5193 GDS5194 GDS5195
Platform:
GPL200
22 Samples
Download data: CEL
Series
Accession:
GSE54024
ID:
200054024
12.
Full record GDS5195

nuo-6;ced-4 double mutation effect on young adults

Analysis of nuo-6;ced-4 double mutants. ced-4 mutation in the intrinsic apoptosis signaling pathway suppresses the longevity of electron transport chain mutant nuo-6. Results provide insight into molecular mechanisms underlying lifespan expansion.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 4 genotype/variation sets
Platform:
GPL200
Series:
GSE54024
13 Samples
Download data: CEL
13.
Full record GDS5194

isp-1;ced-4 double mutation effect on young adults

Analysis of isp-1;ced-4 double mutants. ced-4 mutation in the intrinsic apoptosis signaling pathway suppresses the longevity of electron transport chain mutant isp-1. Results provide insight into molecular mechanisms underlying lifespan expansion.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 4 genotype/variation sets
Platform:
GPL200
Series:
GSE54024
13 Samples
Download data: CEL
14.
Full record GDS5193

isp-1 and nuo-6 mutants and paraquat-treated wildtype young adults

Analysis of wildtype worms treated with the pro-oxidant paraquat and electron transport chain mutants isp-1 and nuo-6. Results provide insight into common molecular mechanisms underlying the increased longevity in all three conditions.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 3 genotype/variation, 3 protocol sets
Platform:
GPL200
Series:
GSE54024
13 Samples
Download data: CEL
15.

Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapy

(Submitter supplied) Microarray expression profiling has become a valuable tool in the evaluation of the genetic consequences of metabolic disease. Although 3’-biased gene expression microarray platforms were the first generation to have widespread availability, newer platforms are gradually emerging that have more up-to-date content and/or higher cost efficiency. Deciphering the relative strengths and weaknesses of these various platforms for metabolic pathway level analyses can be daunting. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS3616 GDS3618 GDS3619
4 related Platforms
18 Samples
Download data: CEL, TXT
Series
Accession:
GSE18677
ID:
200018677
16.
Full record GDS3619

Primary coenzyme Q deficient liver response to probucol (WG-6 2.0)

Analysis of livers from B6.Alb/cre,Pdss2(loxP/loxP) animals following treatment with probucol, an antioxidant/antihyperlipidemic agent. Results used to evaluate the performance of Illumina Mouse WG-6 in comparison to Affymetrix 430 2.0, and Affymetrix Gene 1.0 ST.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 gender, 4 individual sets
Platform:
GPL9526
Series:
GSE18677
6 Samples
Download data
17.
Full record GDS3618

Primary coenzyme Q deficient liver response to probucol (Gene 1.0 ST)

Analysis of livers from B6.Alb/cre,Pdss2(loxP/loxP) animals following treatment with probucol, an antioxidant/antihyperlipidemic agent. Results used to evaluate the performance of Affymetrix Gene 1.0 ST in comparison to Affymetrix 430 2.0, and Illumina Mouse WG-6.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 gender sets
Platform:
GPL9525
Series:
GSE18677
4 Samples
Download data: CEL
18.
Full record GDS3616

Primary coenzyme Q deficient liver response to probucol (430 2.0)

Analysis of livers from B6.Alb/cre,Pdss2(loxP/loxP) animals following treatment with probucol, an antioxidant/antihyperlipidemic agent. Results used to evaluate the performance of Affymetrix 430 2.0 in comparison to Affymetrix Gene 1.0 ST, and Illumina Mouse WG-6.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 gender sets
Platform:
GPL9523
Series:
GSE18677
4 Samples
Download data: CEL
19.

CEST-2.2 stimulates lipid metabolism and promotes longevity in mitochondrial mutant animals

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19757
19 Samples
Download data: BW, TSV
Series
Accession:
GSE168502
ID:
200168502
20.

CEST-2.2 stimulates lipid metabolism and promotes longevity in mitochondrial mutant animals (RNA-Seq)

(Submitter supplied) Intestine-specific transcriptome of wild-type. gas-1(fc21) and gas-1(fc21); cest-2.2 OE Caenorhaditis elegans in order to gain insight into how cest-2.2 overexpression ameliorates Complex I deficiency
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
15 Samples
Download data: FA, TSV, TXT, XLSX
Series
Accession:
GSE168501
ID:
200168501
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