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Links from GEO DataSets

Items: 20

1.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [ChIP-Seq HM]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
12 Samples
Download data: BW
Series
Accession:
GSE157709
ID:
200157709
2.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [WGS-Seq]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by high throughput sequencing
Platform:
GPL26835
4 Samples
Download data: XLSX
Series
Accession:
GSE175931
ID:
200175931
3.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
117 Samples
Download data: BW
Series
Accession:
GSE149774
ID:
200149774
4.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [ChIP-Seq TF]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
18 Samples
Download data: BED, BW
Series
Accession:
GSE149773
ID:
200149773
5.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [RNA-Seq]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
83 Samples
Download data: XLSX
Series
Accession:
GSE149772
ID:
200149772
6.

PfAP2-G ChIP-seq in stage I gametocytes derived via next cycle conversion (NCC) and same cycle conversion (SCC)

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. Here we identify for the first time the direct targets of PfAP2-G and demonstrate that it dynamically binds hundreds of sites across the genome. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26920
8 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE134268
ID:
200134268
7.

Regulation of sexual differentiation is linked to invasion in malaria parasites

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21078 GPL15130
62 Samples
Download data: BED, BIGWIG, TXT
Series
Accession:
GSE125566
ID:
200125566
8.

PfAP2-G target gene promoter mutants expression timecourse

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
22 Samples
Download data: TXT
Series
Accession:
GSE121312
ID:
200121312
9.

PfAP2-G DD +Shld1 vs. -Shld1 expression timecourse

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
22 Samples
Download data: TXT
Series
Accession:
GSE120990
ID:
200120990
10.

PfAP2-G and PfAP2-I ChIP-seq in schizonts

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch that occurs from asexual multiplication to sexual differentiation is essential for transmission to mosquitos. One of the key drivers of commitment to sexual development is the transcription factor AP2-G. Although it has been hypothesised that AP2-G orchestrates this crucial cell fate decision by driving expression of gametocyte genes, the molecular mechanisms by which this occurs remain unknown. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
6 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE120488
ID:
200120488
11.

PfAP2-G ChIP-seq in committed schizonts, sexual rings, and stage I gametocytes

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
12 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE120448
ID:
200120448
12.

The PfAP2-G2 transcription factor is a critical regulator of gametocyte maturation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
44 Samples
Download data: TXT
Series
Accession:
GSE160937
ID:
200160937
13.

Plasmodium falciparum PfAP2-G2 KO gametocyte microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
28 Samples
Download data: TXT
Series
Accession:
GSE160924
ID:
200160924
14.

Plasmodium falciparum PfAP2-G2 KO asexual microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
16 Samples
Download data: TXT
Series
Accession:
GSE160923
ID:
200160923
15.

ChIP-seq on PfAP2-G2 in trophozoite and gametocyte stages of parasites.

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human host to mosquitos, where sexual fertilization occurs to complete the lifecycle. Although preventing gametocyte development would block parasite transmission, the molecular mechanisms underlying sexual commitment and gametocyte maturation are still relatively unknown. Previous studies identified an ApiAP2 protein, AP2-G2, which plays a critical role in gametocyte maturation in rodent malaria parasite Plasmodium berghei by acting as the repressor of asexual stage genes in gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21298
10 Samples
Download data: BIGWIG
Series
Accession:
GSE157753
ID:
200157753
16.

Comparison of Gametocyte producer 3D7-A subclone E5 to the gametotcyte nonprodcer strain F12 and pfap2-g deletion mutant

(Submitter supplied) Identify differentially expressed genes across the 48h intraerythrocytic development cycle of gametocyte non-producers of P. falcuparum
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL17880
32 Samples
Download data: TXT
Series
Accession:
GSE52030
ID:
200052030
17.

PFNF54-Pfs16-GFP-LUC gametocyte time course from commitment to maturity

(Submitter supplied) Plasmodium falciparum gametocytes undergo 14 days of gametocytogenesis to generate mature, transmissible gametocytes. This timecourse delineates the transcriptional profiles of gametocytes from commitment to maturity.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
16 Samples
Download data: TXT
Series
Accession:
GSE104889
ID:
200104889
18.

A G-protein-coupled receptor modulates gametogenesis via PKG-mediated signaling cascade in Plasmodium berghei

(Submitter supplied) Gametogenesis is essential for malaria parasite transmission, but the molecular mechanism of this process remains to be refined. Here, we identified a G-protein-coupled receptor 180 (GPR180) that plays a critical role in signal transduction during gametogenesis in Plasmodium. P. berghei GPR180 was predominantly expressed in gametocytes and ookinetes and associated with the plasma membrane in female gametes and ookinetes. more...
Organism:
Plasmodium berghei
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29857
4 Samples
Download data: TXT
Series
Accession:
GSE198287
ID:
200198287
19.

Transcriptional response to conditional over-expression of GDV1 in Plasmodium falciparum 3D7 wild type and F12 mutant parasites

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array
Platform:
GPL15130
28 Samples
Download data: GPR
Series
Accession:
GSE95549
ID:
200095549
20.

Transgenic Plasmodium falciparum blood stage parasites F12/GDV1-GFP-DD: control (-Shield-1;F12/GDV1-GFP-DDOFF) vs GDV1-overexpressing (+Shield-1;F12/GDV1-GFP-DDON) parasites

(Submitter supplied) Transcriptional profiling of transgenic P. falciparum blood stage parasites expressing an ectopic copy of GDV1-GFP-DD (F12/GDV1-GFP-DD). The DD (FKBP destabilisation domain) allows for the conditional expression of fusion proteins: DD fusion proteins are rapidly degraded or stably expressed in absence or presence of the stabilising ligand Shield-1, respectively (Banaszynski LA, Chen LC, Maynard-Smith LA, Ooi AG, Wandless TJ. more...
Organism:
Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array
Platform:
GPL15130
14 Samples
Download data: GPR
Series
Accession:
GSE95548
ID:
200095548
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