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Links from GEO DataSets

Items: 9

1.

Protein KIC5 is a novel regulator of artemisinin stress response in the malaria parasite Plasmodium falciparum

(Submitter supplied) RNAseq data profiling the artemisinin-sensitive P. falciparum piggyBac mutant of the KIC5 gene (PF3D7_1138700, Kelch13 Interacting Candidate 5).
Organism:
Plasmodium falciparum; Plasmodium falciparum NF54
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL23997 GPL21298
20 Samples
Download data: XLSX
Series
Accession:
GSE205012
ID:
200205012
2.

A novel Modulator of Ring Stage Translation (MRST) gene alters artemisinin sensitivity in Plasmodium falciparum

(Submitter supplied) RNAseq data profiling the artemisinin-sensitive P. falciparum piggyBac mutant of the PF3D7_1136600 gene (conserved Plasmodium gene, unknown function)
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26920
20 Samples
Download data: XLSX
Series
Accession:
GSE223497
ID:
200223497
3.

Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL11248 GPL11250
101 Samples
Download data: GPR
Series
Accession:
GSE25883
ID:
200025883
4.

Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription (CGH)

(Submitter supplied) Artemisinin resistance in Plasmodium falciparum malaria has emerged in western Cambodia. This is a major threat to global plans to control and eliminate malaria as the artemisinins are a key component of antimalarial treatment throughout the world. Using DNA microarrays we identify key features of a transcriptional profile that are associated with the delayed parasite clearance phenotype. These include reduced expression of several basic metabolic and cellular pathways in the early stages, and increased expression of essentially all functionalities associated with protein metabolism in the later stages of P. more...
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by array
Platform:
GPL11250
10 Samples
Download data: GPR
Series
Accession:
GSE25879
ID:
200025879
5.

Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription (expression)

(Submitter supplied) Artemisinin resistance in Plasmodium falciparum malaria has emerged in western Cambodia. This is a major threat to global plans to control and eliminate malaria as the artemisinins are a key component of antimalarial treatment throughout the world. Using DNA microarrays we identify key features of a transcriptional profile that are associated with the delayed parasite clearance phenotype. These include reduced expression of several basic metabolic and cellular pathways in the early stages, and increased expression of essentially all functionalities associated with protein metabolism in the later stages of P. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL11248
91 Samples
Download data: GPR
Series
Accession:
GSE25878
ID:
200025878
6.

Plasmodium falciparum assocation study of artemisinin resistance

(Submitter supplied) A testing association of parasite genotypes with clinical resistance phenotype. Submission of genotypes from all microarray genotyped samples
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by genome tiling array
Platform:
GPL18484
516 Samples
Download data: FTR
Series
Accession:
GSE56390
ID:
200056390
7.

Global RNA expression profiling of k13-edited mutant and isogenic wild-type Plasmodium falciparum malaria parasites during the parasite's intra-erythrocytic developmental cycle and the parasite's response to dihydroartemisinin (DHA).

(Submitter supplied) K13 mutations are causal for artemisinin resistance in Plasmodium falciparum human malaria. The objective of our study is to characterize gene expression signatures associated with K13 mutations by comparing transcriptional profiles and response to DHA of K13 mutant (C580Y, R539T) and isogenic wild-type lines that were generated by zinc finger nuclease (ZFN) based editing in a long-term adapted (Dd2) and a contemporary laboratory-adapted clinical isolate (Cam3.II).
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL18893
156 Samples
Download data: GPR
Series
Accession:
GSE151189
ID:
200151189
8.

Transcriptome of ring-stage parasites responses to stress conditions upon knockdown of PfGCN5

(Submitter supplied) Purpose: this study is to analyze the change of overal transcriptome after three stress conditions in ring-stage Plasmodium falciparum before and after knockdown of PfGCN5 by TetR-DOZI system. Methods: In this study, the transcriptomes of a parasite line (TetR-PfGCN5::GFP) for knockdown (KD) of PfGCN5 by withdral of anhydrotetracycline (aTc) comparing to its control (TetR-PfGCN5::GFP with aTc) under three stress conditions [HS: heat shock, low-glucose starvation: L-Glu, and low dose of dihydroartemisinin (DHA) treatment] were analyzed at ring stage by RNAseq. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26920
22 Samples
Download data: XLSX
Series
Accession:
GSE221211
ID:
200221211
9.

Exceptionally high sequence-level variation in the transcriptome of Plasmodium falciparum

(Submitter supplied) Single-nucleotide variations (SNVs) in RNA, arising from co- and post-transcriptional phenomena including transcription errors and RNA-editing, are well studied in a range of organisms. In the malaria parasite Plasmodium falciparum, stage-specific and non-specific gene-expression variations accompany the parasite’s array of developmental and morphological phenotypes over the course of its complex life cycle. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL26920
14 Samples
Download data: SF, TXT
Series
Accession:
GSE179055
ID:
200179055
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