U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 10

1.

RNA-Seq analysis of Candida glabrata wild-type and Cghhf1Δhhf2Δ mutant in the presence and absence of methyl methanesulfonate (MMS).

(Submitter supplied) To determine the effect of lack of two Histone H4 genes, CgHHF1 and CgHHF2, on global transcriptional profile, and on transcriptional response towards MMS exposure, RNA-Seq analysis was conducted on log-phase grown Candida glabrata wild-type and Cghhf1∆2∆ cells in the presence and absence of MMS. Comparative transcriptome analysis of wild-type and Cghhf1∆2∆ cells displayed deregulation of 303 genes due to the loss of CgHHF1 and CgHHF2 genes. more...
Organism:
Nakaseomyces glabratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25492
8 Samples
Download data: TXT
Series
Accession:
GSE142737
ID:
200142737
2.

Multifactorial role of mitochondria in echinocandin tolerance revealed by transcriptome analysis of drug-tolerant cells

(Submitter supplied) This study compared the transcriptional response of Candida glabrata echinocandin tolerant cells relative to no treated controls.
Organism:
Nakaseomyces glabratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22777
1 Sample
Download data: CSV, XLSX
Series
Accession:
GSE178797
ID:
200178797
3.

Multifactorial role of mitochondria in echinocandin tolerance revealed by transcriptome analysis of drug-tolerant cells

(Submitter supplied) This study compared the transcriptional response of Candida glabrata micafungin exposed cells.
Organism:
Nakaseomyces glabratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28968
5 Samples
Download data: TXT, XLSX
Series
Accession:
GSE178656
ID:
200178656
4.

A new regulator in the crossroads of oxidative stress resistance and virulence in Candida glabrata: the transcription factor CgTog1

(Submitter supplied) The goals of this study are to compare C. glabrata transcriptome profiling (RNA-seq) upon exposure to hydrogen peroxide in order to assess the correspondent response. The role of the transcription factor Tog1 is clarified through comparison of the transcrptome profiles of WT and Tog1 mutant cells. mRNA profiles of WT and ∆tog1 were generated by deep sequencing, in duplicate, using Illumina HiSeq. The sequence reads that passed quality filters were analyzed with TopHat followed by HTSeq. more...
Organism:
Nakaseomyces glabratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26394
8 Samples
Download data: TXT
Series
Accession:
GSE148288
ID:
200148288
5.

Gene expression in Histone H1 variant deletion chicken DT40 mutant cell

(Submitter supplied) There are six histone H1 variant in chicken. 01H1/02H1/03H1/.10H1/H1L and H1R. In those variant we forcused on H1L and H1R those molecule were most similar H1 among six H1 variants. we established linker histone H1L and H1R deleted mutant in chicken B-cell derived DT40 cell and assay gene expression in normal condition in those mutant cells. The detail charactalization of those mutant cell was published in Takami et al., BBRC 268, 501-508 (2000) and Hashimoto et al., DNA repair (2007) Keywords: gene expression array-based, count
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
5 Samples
Download data
Series
Accession:
GSE5114
ID:
200005114
6.

Gene expression profiling of RPMI-grown and macrophage-internalized Candida glabrata wild-type, Cgrsc3-a∆ and Cgrtt109∆ cells.

(Submitter supplied) To delineate the interaction of Candida glabrata with host immune cells, we performed genome-wide transcriptional profiling analysis on THP-1 macrophage-internalized wild-type and chromatin remodeling defective mutant (Cgrsc3-a∆ and Cgrtt109∆) yeasts. Genes implicated in ergosterol biosynthesis, and high-affinity iron uptake and homeostasis were found to be down-regulated in C. glabrata wild-type and mutant cells upon macrophage internalization. more...
Organism:
Nakaseomyces glabratus CBS 138; Nakaseomyces glabratus
Type:
Expression profiling by array
Platform:
GPL15745
16 Samples
Download data: TXT
Series
Accession:
GSE38953
ID:
200038953
7.

Replication stress shapes a protective chromatin environment across fragile genomic regions

(Submitter supplied) Recent integrative epigenome analyses highlight the importance of functionally distinct chromatin states for gene regulation, cellular differentiation and accurate cell function. How these states are established and maintained is a matter of intense investigation. Here, we present evidence for DNA damage as an unexpected means to shape a protective chromatin environment at genomic regions of recurrent replication stress. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
36 Samples
Download data: BED, BW
Series
Accession:
GSE104800
ID:
200104800
8.

Response of Candida glabrata to environmental iron availability

(Submitter supplied) To examine the response of Candida glabrata cells to iron-depleted and iron-repleted environmental conditions, transcriptional profiling analysis was carried out on wild-type and Cghog1∆ cells grown either in presence of BPS or ferric chloride. Genes involved in iron transport and homeostasis, oxidative phosphorylation, amino acid metabolic process and chromatin silencing were found to be differentially regulated.
Organism:
Nakaseomyces glabratus CBS 138
Type:
Expression profiling by array
Platform:
GPL19118
12 Samples
Download data: TXT
Series
Accession:
GSE60741
ID:
200060741
9.

Unravelling adaptive mechanisms to H2O2 in Candida glabrata using laboratory adaptive evolution

(Submitter supplied) Transcriptome analysis of C. glabrata mutants evolved for improved tolerance to H2O2.
Organism:
Nakaseomyces glabratus
Type:
Expression profiling by array
Platform:
GPL23894
8 Samples
Download data: GPR
Series
Accession:
GSE102502
ID:
200102502
10.

Genomic targets sites of the Candida glabrata transcription factor Pdr1

(Submitter supplied) Pdr1 is the major regulator of azole resistance in the fungal pathogen Candida glabrata. Earlier experiments demonstrated that expression of Pdr1 itself is increased when cells lose their mitochondrial genome (rho0). Here we use chromatin immunoprecipitation coupled with highthroughput sequencing (ChIP-seq) to map the genomic binding sites for Pdr1 in both normal and rho0 cells. These data provide the first look at genes that are likely to represent the direct targets of Pdr1 in this important pathogen.
Organism:
Nakaseomyces glabratus CBS 138
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19002
9 Samples
Download data: WIG
Series
Accession:
GSE59839
ID:
200059839
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=7|qty=5|blobid=MCID_673cd69fc78220302e383a75|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center