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Items: 1 to 20 of 30

1.

Expression data from Plasmodium falciparum

(Submitter supplied) Artemisinin and its derivatives exert the potent, antimalarial action, although the mechanisms by which these drugs inhibit the growth of mararia parasites is not fully understood. We used microarrays to detail the global gene expression change in early erythrocytic P. falciparum, and identified molecules that may contribute to the activity of dihydroartemisinin.
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
4 Samples
Download data: CEL
Series
Accession:
GSE160666
ID:
200160666
2.

Profiling γ-irradiated invasive Plasmodium falciparum merozoites using a systems biology approach

(Submitter supplied) Plasmodium falciparum malaria severely impacts human health. In order to broaden our understanding of merozoite invasion of erythrocytes which is responsible for clinical disease, a P. falciparum γ-irradiated "long-lived merozoite" (LLM) line was investigated. Cell-sieve purified LLM invaded human erythrocytes with an improved efficiency of 10- to 300-fold greater than wild-type (WT) parasites. A comparison of their genomes identified limited changes in the open reading frame of LLM; while only marginal differences were observed in the transcriptomes. more...
Organism:
Anopheles gambiae; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1321
32 Samples
Download data: CEL, CHP
Series
Accession:
GSE81818
ID:
200081818
3.

A High Parasite Density Environment Induces Transcriptional Changes and Cell Death in Plasmodium falciparum Blood Stages

(Submitter supplied) Transient regulation of Plasmodium numbers below the density that induces fever has been observed in chronic malaria infections in humans and this species transcending control cannot be explained by immunity alone. Using an in vitro system we have observed density dependent regulation of malaria parasitemia as a mechanism to possibly explain these in vivo observations. P. falciparum blood stages from a high but not low-density environment exhibited what appeared to be programmed changes during the late trophozoite and schizont stages of the intraerythrocytic cycle.
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
9 Samples
Download data: CEL, CSV
Series
Accession:
GSE91188
ID:
200091188
4.

Interactions of PfETRAMP14.1 with PfEMP1 and EXP-2 at the parasitophorous vacuolar membrane (PVM) of human malaria parasite Plasmodium falciparum

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum; Anopheles gambiae; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1321
23 Samples
Download data: CEL
Series
Accession:
GSE72448
ID:
200072448
5.

Interactions of PfETRAMP14.1 with PfEMP1 and EXP-2 at the parasitophorous vacuolar membrane (PVM) of human malaria parasite Plasmodium falciparum [LOW PARASITEMIA ANALYSIS]

(Submitter supplied) In our global differential gene expression analyses,ETRAMP14.1, an ETRAMP family member was found to be highly transcribed in vivo in severe Malaria patients from highly endemic Indian region. This study for the first time reports the interaction of ETRAMP14.1 with PfEMP1, EXP2 and Hsp70-1. Therefore, we propose that ETRAMP14.1 facilitate PfEMP1 to cross the PVM via transcolon machinery component EXP2.
Organism:
Homo sapiens; Anopheles gambiae; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1321
8 Samples
Download data: CEL
Series
Accession:
GSE72447
ID:
200072447
6.

Interactions of PfETRAMP14.1 with PfEMP1 and EXP-2 at the parasitophorous vacuolar membrane (PVM) of human malaria parasite Plasmodium falciparum [HIGH PARASITEMIA ANALYSIS]

(Submitter supplied) In our global differential gene expression analyses,ETRAMP14.1, an ETRAMP family member was found to be highly transcribed in vivo in severe Malaria patients from highly endemic Indian region. This study for the first time reports the interaction of ETRAMP14.1 with PfEMP1, EXP2 and Hsp70-1. Therefore, we propose that ETRAMP14.1 facilitate PfEMP1 to cross the PVM via transcolon machinery component EXP2.
Organism:
Plasmodium falciparum; Anopheles gambiae; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1321
15 Samples
Download data: CEL
Series
Accession:
GSE72446
ID:
200072446
7.

Gene profiling of P. falciparum and A. gambiae: an assessment of parasite maturation and of host response to infection

(Submitter supplied) Simultaneous analysis of Plasmodium falciparum and Anopheles gambiae gene expression: an assessment of parasite maturation and of the mosquito response to infection. Malaria is probably the most lethal and most prevalent parasitic disease in the world, causing more than one million deaths per year. In spite of intensive research, no vaccine exists and good vaccine candidates are still a necessity. Plasmodium sporozoites from mosquito midguts are not as infective as those from salivary glands, presenting a different type of motility which is presumably associated with their invasive capacity. more...
Organism:
Anopheles gambiae; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1321
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE18780
ID:
200018780
8.

Effect of choline kinase inhibitor hexadecyltrimethylammonium bromide on Plasmodium falciparum gene expression

(Submitter supplied) Investigations on the fundamental of malaria parasite biology, such as invasion, growth cycle, metabolism and cell signalling have uncovered a number of potential antimalarial drug targets, including choline kinase, a key enzyme involved in the synthesis of phosphatidylcholine, an important component in parasite membrane compartment. The effect on gene expression of Plasmodium falciparum K1 strain following 72 hours exposure to 2 μM (IC50 concentration) of the choline kinase inhibitor, hexadecyltrimethylammonium bromide (HDTAB) was evaluated by DNA microarray analysis. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
2 Samples
Download data: CEL
Series
Accession:
GSE54775
ID:
200054775
9.

Expression data of gene knockout Plasmodium falciparum clones

(Submitter supplied) The variant antigen, Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), expressed on the surface of P. falciparum infected Red Blood Cells (iRBCs) is a critical virulence factor for malaria. Each parasite encodes 60 antigenically distinct var genes encoding PfEMP1s, but during infection the clonal parasite population expresses only one gene at a time before switching to the expression of a new variant antigen as an immune evasion mechanism to avoid the host’s antibody responses. more...
Organism:
Anopheles gambiae; Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array
Platform:
GPL1321
13 Samples
Download data: CEL
Series
Accession:
GSE47349
ID:
200047349
10.

CpG Oligodeoxynucleotides treatment of Anopheles mosquitoes

(Submitter supplied) In the present study, we have investigated the effect of CpG Oligodeoxynucleotides (CpG-ODN) on the outcome of Plasmodium infection of the mosquito vectors Anopheles stephensi and Anopheles gambiae and on the modulation of mosquito immunity to Plasmodium. Anopheles mosquitoes inoculated with CpG-ODN showed significant reduction of Plasmodium infection rate and intensity. Microarrays were used to profile transcription of fat-body from CpG-ODN-treated mosquitoes. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
4 Samples
Download data: CEL
Series
Accession:
GSE26941
ID:
200026941
11.

Gene expression profiling of Plasmodium falciparum after co-culture with NK cells

(Submitter supplied) The aim of the study was to determine the effect of natural killer (NK) cells on the global gene expression in Plasmodium falciparum.
Organism:
Anopheles gambiae; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1321
9 Samples
Download data: CEL
Series
Accession:
GSE19010
ID:
200019010
12.

Transcript level responses of Plasmodium falciparum to antimycin A

(Submitter supplied) Abstract: The mitochondrial electron transport chain is essential to Plasmodium and is the target of the antimalarial drug atovaquone. The mitochondrial genomes of Plasmodium sp. are the most reduced known, and the majority of mitochondrial proteins are encoded in the nucleus and imported into the mitochondrion post-translationally. Many organisms have signalling pathways between the mitochondria and the nucleus to regulate the expression of nuclear-encoded mitochondrially-targeted proteins, for example in response to mitochondrial dysfunction. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
6 Samples
Download data: CEL
Series
Accession:
GSE28625
ID:
200028625
13.

Gene expression in Plasmodium falciparum NF54 and P. falciparum HOX

(Submitter supplied) P. falciparum NF54 proliferates under micro-aerophilic conditions in an environment of 3% O2, 4% CO2, 93% N2. This strain was gradually adapted to proliferate under standard tissue culture conditions of 5% CO2/95% air (~19% O2) to generate P. falciparum HOX. We compared global gene expression profiles of the two strains to identify differences, if any.
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
6 Samples
Download data: CEL
Series
Accession:
GSE33826
ID:
200033826
14.

Genome-wide Transcriptional Analysis of Genes Associated with Desiccation Stress in Anopheles gambiae

(Submitter supplied) Anopheles gambiae mosquitoes play an important role in malaria transmission. In sub-Saharan Africa, the dry season can last several months. The mechanisms for mosquito population to survive through the dry season are poorly understood. One possible mechanism is that adults increase their desiccation tolerance over the dry season. Genetic analyses have shown that inversions 2La, 2Rb, 2Rc, 2Rd and 2Ru are associated with aridity resistance, however little is known about the transcriptional response of genes in response to desiccation. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Dataset:
GDS4552
Platform:
GPL1321
19 Samples
Download data: CEL
Series
Accession:
GSE25433
ID:
200025433
15.

Transcript-level responses of Plasmodium falciparum to thiostrepton

(Submitter supplied) Abstract: The antimalarial activity of the antibiotic thiostrepton has long been attributed to inhibition of apicoplast protein synthesis through binding of apicoplast ribosomal RNA. However, the kinetics of parasite death upon thiostrepton treatment differ from those seen for other inhibitors of apicoplast housekeeping functions. We have analysed global changes in gene expression of the malaria parasite, Plasmodium falciparum, in an attempt to shed light on the responses of the parasite to this drug. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Dataset:
GDS4260
Platform:
GPL1321
6 Samples
Download data: CEL
Series
Accession:
GSE28701
ID:
200028701
16.

Genome-wide profiling of diel and circadian gene expression of the malaria vector Anopheles gambiae

(Submitter supplied) Anopheles gambiae, the primary African malarial mosquito, exhibits numerous behaviors that are under diel and circadian control, including locomotor activity, swarming, mating, host seeking, eclosion, egg laying and sugar feeding. However, little has been performed to elucidate the molecular basis for these daily rhythms. To study how gene expression is globally regulated by diel and circadian mechanisms, we have undertaken a DNA microarray analysis of A. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Dataset:
GDS4261
Platform:
GPL1321
104 Samples
Download data: CEL
Series
Accession:
GSE22585
ID:
200022585
17.

MozAtlas: A comprehensive gene expression atlas of sex- and tissue-specificity in the malaria vector, Anopheles gambiae.

(Submitter supplied) Background. The mosquito, Anopheles gambiae, is the primary vector of human malaria, a disease responsible for millions of deaths each year. To improve strategies for controlling transmission of the causative parasite, Plasmodium falciparum, we require a thorough understanding of the developmental mechanisms, physiological processes and evolutionary pressures affecting life-history traits in the mosquito. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
60 Samples
Download data: CEL
Series
Accession:
GSE21689
ID:
200021689
18.

Microarray analysis of Wolbachia infected Anopheles gambiae Sua5B cells

(Submitter supplied) Wolbachia, an endosymbiotic bacterium, is being investigated as a vector control agent in several insect species. Along with the well known classical reproductive parasitism Wolbachia employs against its host to spread within the population, it is emerging that the bacteria can protect the host against pathogens and reduced pathogen transmission. Anopheles mosquitoes, which transmit malaria, have never been found to harbour Wolbachia in nature, and despite numerous transinfection attempts, no stable line has been developed. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
9 Samples
Download data: CEL
Series
Accession:
GSE23215
ID:
200023215
19.

Gene Expression Profiling Data of African Malaria Vector Anopheles gambiae Aging

(Submitter supplied) Senescence is a biological phenomenon experienced by all living eukaryote organisms. Genome-wide gene expression associated with aging has been explored in model organisms such as Drosophila melanogaster and Caenorhabditis elegans, but this has not been well understood in African malaria vector, Anopheles gambiae. Gene expression profiling using DNA microarray allows for simultaneous study of changes in mRNA levels for thousands of genes. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array
Platform:
GPL1321
31 Samples
Download data: CEL
Series
Accession:
GSE19756
ID:
200019756
20.

Expression data from Anopheles gambiae females blood fed twice within a gonotrophic cycle

(Submitter supplied) Anopheline mosquitoes frequently take multiple blood meals in a single gonotrophic cycle. In this study we determined patterns of gene expression in Anopheles gambiae females blood fed twice within the first gonotrophic cycle.
Organism:
Anopheles gambiae; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1321
3 Samples
Download data: CEL, CHP
Series
Accession:
GSE22806
ID:
200022806
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