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: 14

1.

RNA Analysis for Modulation of aneuploidy in Leishmania donovani during adaptation to different in vitro and in vivo environments, and its impact on gene expression

(Submitter supplied) Purpose: Monitor modulation of aneuploidy in Leishmania donovani during adaptation to different in vitro and in vivo environments, and its impact on gene expression Importance: Aneuploidy is usually detrimental in multicellular organisms, but in several micro-organisms (fungi being the best-studied) it can be tolerated and even beneficial. Leishmania – a protozoan parasite killing more than 30,000 persons each year – is emerging as a new model for aneuploidy studies: unexpectedly high levels of aneuploidy are found in clinical isolates. more...
Organism:
Leishmania donovani
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23261
11 Samples
Download data: TXT
Series
Accession:
GSE97453
ID:
200097453
2.

Post-transcriptional regulation can harness genome instability and provide phenotypic robustness during fitness gain in the human parasite Leishmania donovani

(Submitter supplied) Genome instability has been recognized as a driver in Leishmania fitness gain in response to environmental change or chemotherapy. How genome instability generates beneficial phenotypes despite potential deleterious gene dosage effects is unknown. Here we address this important open question applying experimental evolution and integrative systems approaches on parasites adapting to in vitro culture. more...
Organism:
Leishmania donovani
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29657
15 Samples
Download data: TXT
Series
Accession:
GSE165615
ID:
200165615
3.

Comparative high-throughput gene expression analysis between cultured and sand fly vector-derived Leishmania infantum promastigotes.

(Submitter supplied) Leishmania infantum (Kinetoplastida:Trypanosomatidae) is the etiological agent of zoonotic visceral leishmaniasis in the Mediterranean basin. The motile promastigote stage infects the hematophagous sand fly vector host and amastigotes survives and multiplies within phagocytes of the mammalian host. Promastigotes are routinely cultured in liquid undefined media and are considered to mimic the environment within the sand fly gut. more...
Organism:
Leishmania infantum
Type:
Expression profiling by array
Platform:
GPL6781
1 Sample
Download data: TXT
Series
Accession:
GSE70992
ID:
200070992
4.

Transcriptional analysis of Leishmania infantum antimony resistant strains using full-genome DNA microarrays

(Submitter supplied) The aim of the experiment is to detect any gene expression modulation in an antimony resistant L.infantum Sb2000.1 strain compared to an antimony sensitive L.infantum WT strain. We want to identify the modulated genes associated with an antimony resistant phenotype. The Sb2000.1 resistant strain used is about 1000 times more resistant to SbIII than the WT sensitive strain. The full-genome DNA microarrays includes one 70-oligonucleotide probe for each gene of L. more...
Organism:
Leishmania infantum
Type:
Expression profiling by array
Platform:
GPL8804
5 Samples
Download data: GPR
Series
Accession:
GSE16965
ID:
200016965
5.

Comparative Genomic Hybridization of Leishmania major methotrexate resistant strains vs wild-type LV39

(Submitter supplied) CGH analysis of the drug resistant strain L. major MTX60.4 vs the wild-type strain LV39 The full-genome DNA microarrays includes one 70-oligonucleotides probe for each gene of L.major LV39 Keywords: drug resistance
Organism:
Leishmania major; Leishmania infantum
Type:
Genome variation profiling by array
Platform:
GPL6855
3 Samples
Download data: GPR
Series
Accession:
GSE11623
ID:
200011623
6.

Methotrexate resistant Leishmania strains

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Leishmania infantum; Leishmania major
Type:
Expression profiling by array
Platform:
GPL6855
8 Samples
Download data: GPR
Series
Accession:
GSE9949
ID:
200009949
7.

Transcriptional analysis of Leishmania major methotrexate resistant strains using full-genome DNA microarrays

(Submitter supplied) Transcriptional analysis of the drug resistant strain L. major MTX60.4 compared to the wild-type strain LV39 The full-genome DNA microarrays includes one 70-oligonucleotides probe for each gene of L.major LV39 Keywords: drug resistance
Organism:
Leishmania infantum; Leishmania major
Type:
Expression profiling by array
Platform:
GPL6855
4 Samples
Download data: GPR
Series
Accession:
GSE9948
ID:
200009948
8.

Transcriptional analysis of Leishmania infantum methotrexate resistant strains using full-genome DNA microarrays

(Submitter supplied) Transcriptional analysis of the drug resistant strain L. infantum MTX20.5 compared to the wild-type strain The full-genome DNA microarrays includes one 70-oligonucleotides probe for each gene of L. infantum Keywords: drug resistance
Organism:
Leishmania infantum; Leishmania major
Type:
Expression profiling by array
Platform:
GPL6855
4 Samples
Download data: GPR
Series
Accession:
GSE9947
ID:
200009947
9.

Whole-genome comparative RNA expression profiling of axenic and intracellular amastigote forms of Leishmania infantum

(Submitter supplied) Transcriptional analysis of L. infantum promastigote compared to L. infantum intracellular amastigote and transcriptional analysis of L. infantum promastigote compared to L. infantum axenic amastigote. The full-genome DNA microarrays includes one 70-oligonucleotides probe for each gene of L.infantum. Keywords: stage and culture condition
Organism:
Leishmania major; Leishmania infantum
Type:
Expression profiling by array
Platform:
GPL6855
10 Samples
Download data: GPR
Series
Accession:
GSE13983
ID:
200013983
10.

The expression profiles of promastigotes and axenic amastigotes in Leishmania donovani

(Submitter supplied) In this study, we examined the transcriptome of Leishmania donovani promastigotes and axenic amastigotes to identify differentially regulated mRNAs utilizing the serial analysis of gene expression Keywords: stage differentiation; axenic amastigotes
Organism:
Leishmania donovani
Type:
Expression profiling by SAGE
Platform:
GPL3252
2 Samples
Download data
Series
Accession:
GSE3835
ID:
200003835
11.

Comparative analysis of gene expression in HAT4-nulls and HAT2-heterozygous knockout cells, versus wild type Leishmania donovani cells

(Submitter supplied) Histone acetylations are known to impact gene transcription. Here, we have attempted to examine the role of Leishmania donovani histone acetyltransferases HAT4 and HAT2 in regulating global gene expression. The transcriptome of HAT4-null promastigotes (Samples 2A, 2B) and HAT2-heterozygous knockout promastigotes (Samples 3A, 3B) have been compared with the transcriptome of wild-type Leishmania promastigotes (Samples 1A, 1B) and fold change in gene expression with respect to the control wild-type has been determined.
Organism:
Leishmania donovani
Type:
Expression profiling by array
Platform:
GPL18125
6 Samples
Download data: TXT, XLS
Series
Accession:
GSE76574
ID:
200076574
12.

Simultaneous gene expression profiling in human macrophages infected with Leishmania major parasites using SAGE

(Submitter supplied) Leishmania (L) are intracellular protozoan parasites which are able to survive and replicate within the harsh and potentially hostile phago-lysosomal environment of mammalian mononuclear phagocytes. A complex interplay then takes place between the macrophage (MΦ) striving to eliminate the pathogen and the parasite struggling for its own survival. To investigate, at the transcriptional level, this host-parasite conflict in the context of monocyte-derived human MΦs (MDM) infection by L. more...
Organism:
Leishmania major; Homo sapiens
Type:
Expression profiling by SAGE
Platforms:
GPL6471 GPL4
3 Samples
Download data
Series
Accession:
GSE10442
ID:
200010442
13.

Transcriptional profiling by next generation sequencing of the spleen and splenic macrophages in the hamster model of visceral leishmaniasis

(Submitter supplied) We used next generation sequencing to examine global changes in gene expression in the spleen and splenic macrophages in a hamster model of progressive visceral leishmaniasis. We used RNA sequencing coupled with de novo transcriptome assembly, because the Syrian hamster does not have a fully sequenced and annotated reference genome. Libraries for deep sequencing were constructed from poly-A RNA isolated from the spleens or splenic macrophages of uninfected and 28-day L. more...
Organism:
Mesocricetus auratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22776
16 Samples
Download data: FA, XLSX
Series
Accession:
GSE91187
ID:
200091187
14.

Characteristics and expression of lncRNA in Drosophila aneuploidy

(Submitter supplied) Aneuploidy variation can widely affect the expression of the whole genome, which is detrimental to organisms.Long noncoding RNAs (lncRNAs) are defined as RNAs that are longer than 200 nucleotides and lack a significant open reading frame.Although only a few lncRNAs have been well described, and most of them are still functionally unknown, there is sufficient evidence that lncRNAs have important cellular functions.We provide a comprehensive description of the characteristics and expression profiles of lncRNAs in aneuploid Drosophila. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25244
15 Samples
Download data: TXT
Series
Accession:
GSE233534
ID:
200233534
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=7|blobid=MCID_66283df7f4364867151ce1cd|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