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Items: 1 to 20 of 353

1.

Characterization of the genes that were regulated by infection with enterotoxigenic E. coli (ETEC)

(Submitter supplied) In the present study, we investigated the pathogenicity of infection with enterotoxigenic E. coli (ETEC) using Caenorhabditis elegans as a model animal. The lifespan of the adult C. elegans infeted with ETEC was significantly longer than that of uninfected animals (control). Transcriptional profiling comparing infected- and uninfected animals suggested that genes related to the insulin-like peptide were upregulated by infection with ETEC.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22765
4 Samples
Download data: TXT
Series
Accession:
GSE247108
ID:
200247108
2.

Exploring the Impact of Cyclodipeptide on Fungal Metabolism: Insights into Membrane and Metabolic Responses

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans; Botrytis cinerea
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19757 GPL24810
10 Samples
Download data
Series
Accession:
GSE237226
ID:
200237226
3.

Exploring the Impact of Cyclodipeptide on Fungal Metabolism: Insights into Membrane and Metabolic Responses [C. elegans]

(Submitter supplied) This study investigates the effects of cyclodipeptide on fungal and nematode metabolism, specifically focusing on its impact on membrane composition and metabolic responses. Metabolomic profiles of treated and untreated fungal cultures were compared to unravel the molecular changes induced by cyclodipeptide, with a particular emphasis on membrane phospholipids such as monoolein and phosphatidyl ethanolamine, as well as other plasma membrane components like ergosterol and its derivative products. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
4 Samples
Download data: TXT
Series
Accession:
GSE237224
ID:
200237224
4.

Characterization of the genes that were regulated by feeding with C. acnes strains

(Submitter supplied) In the present study, we investigated the effect of Cutibacterium acnes on lifespan and susceptibility to infection with Staphylococcus aureus using Caenorhabditis elegans as a model animal. When adult C. elegans were fed C. acnes strains, the lifespan of the animals fed pathogenic C. acnes strain (HM-122) was significantly shorter than that of animals fed OP50 (control). In contrast, the lifespan of the animals fed commensal C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22765
3 Samples
Download data: TXT
Series
Accession:
GSE176406
ID:
200176406
5.

Nuclear receptor NHR-49 promotes peroxisome proliferation to compensate for aldehyde dehydrogenase deficiency in C. elegans

(Submitter supplied) The intracellular level of fatty aldehydes is tightly regulated to minimize the formation of toxic aldehyde adducts of cellular components. Accordingly, deficiency of a fatty aldehyde dehydrogenase FALDH causes the neurologic disorder Sjögren-Larsson syndrome (SLS) in humans. However, cellular responses to unresolved, elevated fatty aldehyde levels are poorly understood. Based on lipidomic and imaging analysis, we report that the loss of endoplasmic reticulum-, mitochondria- and peroxisomes-associated ALH-4, the C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
6 Samples
Download data: TSV
Series
Accession:
GSE162792
ID:
200162792
6.

Peroxisomal retrograde signaling in C. elegans

(Submitter supplied) Distinct retrograde signaling pathways have been identified for several cellular organelles. These pathways are important to maintain the function of these organelles in response to organelle-specific stress. Using Caenorhabditis elegans, we show for the first time that such a retrograde signaling also exists for peroxisomes. Analysis of the C. elegans transcriptome revealed that peroxisomal import stress caused by the knock-down of the peroxisomal matrix protein import receptor prx-5/PEX5 induces the compensatory up-regulation of genes involved in defense response and lipid metabolic processes, especially peroxisomal beta oxidation. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22765
6 Samples
Download data: TSV
Series
Accession:
GSE156318
ID:
200156318
7.

Lifespan and healthspan benefits of FW1256, a novel hydrogen sulfide donor compound, in C. elegans are independent from effects downstream of eat-2 mutation

(Submitter supplied) It has been suggested that hydrogen sulfide (H2S) may play a pivotal role in mediating some of these caloric restriction (CR)-associated benefits. We therefore explored whether a novel slow-releasing H2S donor compound, FW1256, mimics CR and reproduces CR-associated effects in normal feeding Caenorhabditis elegans. Using transcriptomics analysis via RNA sequencing, we determined sets of differentially expressed genes (DEG) for FW1256-exposed wild-type C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22765
12 Samples
Download data: CSV
Series
Accession:
GSE146412
ID:
200146412
8.

Next Generation Sequencing for Transcriptomes Analysis in GLP-1 Notch receptor ON and OFF genetic background

(Submitter supplied) Purpose: Ultilize the Next Generation Sequencing to determine the genes that are activated or repressed by GLP-1 Notch receptor in C. elegans germline. The list of genes generated from RNA-seq were intersected with the LAG-1 germline ChIP-seq data to identify direct transcriptional targets of the GLP-1/LAG-1 transcriptional complex in C. elegans germline stem cells. Methods: RNA isolated from hand dissected C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24892
10 Samples
Download data: XLS
Series
Accession:
GSE144229
ID:
200144229
9.

Next Generation Sequencing for Transcriptomes Analysis for LAG-1 time course by auxin treatment.

(Submitter supplied) Purpose: Ultilize Next Generation Sequencing to identify genes that are activated or repressed by LAG-1 (following auxin treatment to specifically deplete LAG-1 in C. elegans germline). The list of genes generated from RNA-seq identify primary and secondary targets of LAG-1 in C. elegans germline stem cells. Methods: RNA isolated from hand dissected C. elegans germline tumor (one day old adult animals) were used for RNA-seq library. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24892
16 Samples
Download data: XLS
Series
Accession:
GSE144227
ID:
200144227
10.

Genome-wide maps of chromatin state for LAG-1 in whole animals

(Submitter supplied) We report the application of conventional ChIP-seq analysis for LAG-1 chromatin state in whole animals. We identified 76 genes putatively regulated by LAG-1 that's overlapped by two independent antibodies (FLAG ab and GFP ab). These genes including previously known targets lst-1, sygl-1, and mir-61/250, supporting the success of the assay.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24892
4 Samples
Download data: XLS
Series
Accession:
GSE144225
ID:
200144225
11.

Genome-wide maps of chromatin state for LAG-1 in germline

(Submitter supplied) We report the application of conventional ChIP-seq analysis for LAG-1 chromatin state in germline. We identified 137 genes putatively regulated by LAG-1 that's overlapped by three independent biological replicates. These genes included previously known targets lst-1, sygl-1, and mir-61/250.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24892
4 Samples
Download data: XLS
Series
Accession:
GSE144223
ID:
200144223
12.

Characterization of the genes that were regulated by feeding with CBM 588

(Submitter supplied) In the present study, we investigated the effect of CBM 588 on lifespan and multiple-stress resistance using Caenorhabditis elegans as a model animal. When adult C. elegans were fed a standard diet of Escherichia coli OP50 or CBM 588, the lifespan of the animals fed CBM 588 was significantly longer than that of animals fed OP50. Moreover, the worms fed CBM 588 were more resistant to certain stressors, including infections with pathogenic bacteria, UV irradiation, and the metal stressor Cu2+. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
2 Samples
Download data: TXT
Series
Accession:
GSE123163
ID:
200123163
13.

Organismal sensitivity to environmental agents induced toxicity: A comparative ecotoxicogenomics approach

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans; Drosophila melanogaster
Type:
Expression profiling by array
Platforms:
GPL23371 GPL23370
24 Samples
Download data: TXT
Series
Accession:
GSE98166
ID:
200098166
14.

Organismal sensitivity to environmental agents induced toxicity: A comparative ecotoxicogenomics approach [Caenorhabditis elegans]

(Submitter supplied) To understand the role of genetic makeup in organismal tolerance/susceptibility we compared the Caenorhabditis elegans transcriptome profiles with those of Drosophila melanogaster. In this study, we exposed both organisms, to a synthetic chemical and evaluated their response at the transcriptome level, to gain insights to molecular players/pathways underlying organismal tolerance/susceptibility to xenobiotics
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL23371
12 Samples
Download data: TXT
Series
Accession:
GSE98165
ID:
200098165
15.

Neurohormonal signalling via a cytosolic sulfotransferase controls insulin sensitivity of C. elegans

(Submitter supplied) Insulin and insulin-like growth factor signalling regulates a broad spectrum of growth and metabolic responses to a variety of internal and environmental stimuli. Such responses can be tailored so that changes in insulin signalling result in distinct physiological responses to different stimuli. For example, the inhibition of insulin-like signalling is key in the responses of the nematode C. elegans to both osmotic stress and starvation, but these two stresses result in responses that are both physiologically and molecularly distinct. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
22 Samples
Download data: TXT
Series
Accession:
GSE111074
ID:
200111074
16.

Genome wide DNA 6mA methylome and transcriptome change upon mitochondrial stress in C.elegans

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL25147
12 Samples
Download data: XLSX
Series
Accession:
GSE118269
ID:
200118269
17.

Genome wide 6mA modification change upon mitochondial stress in C.elegans

(Submitter supplied) We discovered 364 peaks enrichment change in wild-type C.elegans genome by 6mA MeDIP-seq, which indicated those genes response to mitochondrial stress and may function in mitochondrial stress response.
Organism:
Caenorhabditis elegans
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL25147
4 Samples
Download data: XLSX
Series
Accession:
GSE118268
ID:
200118268
18.

Transcriptome wide change upon mitochondial stress in C.elegans

(Submitter supplied) We discovered 5446 genes expression change (4218 genes from P0 to F2) in wild-type C.elegans transcriptome compared to DAMT-1 mutant upon mitochondrial stress by RNA-seq, which indicated those genes response to mitochondrial stress and may function in mitochondrial stress response.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25147
8 Samples
Download data: XLSX
Series
Accession:
GSE118175
ID:
200118175
19.

Gene regulation by small RNAs and ADAR RNA editing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Third-party reanalysis; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL13657 GPL18245
32 Samples
Download data
Series
Accession:
GSE89890
ID:
200089890
20.

dsRNAs expressed in C. elegans development

(Submitter supplied) Cellular RNAs containing double-stranded RNA (dsRNA) structures are subject to A-to-I RNA editing by the adenosine deaminases that act on RNA (ADARs). While A-to-I editing can alter mRNA coding potential, most editing is observed in non-coding sequences, the function of which remains poorly characterized. Using a dsRNA immunoprecipitation and high-thoughput sequencing (dsRIP-Seq) approach, we identify 1523 expressed A-to-I edited regions and characterize their expression during Caenorhabditis elegans development. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
8 Samples
Download data: BED, BW, TXT
Series
Accession:
GSE79375
ID:
200079375
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