Bioinformatics Resource for Invertebrate Vectors of Human Pathogens
All Experiments
133 items found, displaying 21 to 40.[First/Prev] 1, 2, 3, 4, 5, 6, 7 [Next/Last]
factor:
Genotype
Genotype:StrainOrLine
 
We examined patterns of gene expression in two independent colonies of both M and S molecular forms of gravid female Anopheles gambiae adults. For each colony, replicates were derived from independent RNA samples extracted from different cohorts to ensure that trends were reproducible. In addition, each replicate was derived from adults drawn from three cages to minimize the contribution of any individual cage to variation between samples. Data were obtained from a total of five biological replicates per mosquito colony. 
Using a custom microarray (Aedes detox chip), the effect on the transcription of 290 detoxification genes after exposure of Aedes aegypti larvae for 72h to sub-lethal doses of the herbicide glyphosate, the polycyclic aromatic hydrocarbon benzo[a]pyrene, and the chemical insecticides imidacloprid, permethrin and propoxur was measured in comparison to an unexposed global reference. 
Mosquitoes from a highly resistant, wild Anopheles gambiae population from Ghana were bred and selected for permethrin resistance and compared to unselected individuals using a small custom "detox chip". 
factor:
GrowthCondition
 
Microarray experiments comparing Anopheles gambiae virgins with females at 2 h, 6 h, and 24 h after mating were performed using the Affymetrix Anopheles/Plasmodium array. 
factor:
Compound:DiseaseState
 
Midguts from uninfected and Plasmodium berghei infected Anopheles gambiae mosquitoes were exposed to the anti-malarial drug chloroquine or a control. The MMC1 EST-based array was used. 
factor:
StrainOrLine:DevelopmentalStage
 
This microarray experiment aimed at comparing constitutive expression of detoxification genes between an insecticide resistant strain of Aedes aegypti (Vauclin strain) from Martinique Island (French Indies) and a susceptible strain (Bora-Bora strain). Comparison was performed at both larval stage (4th stage larvae) and adult stage (3 days-old adults, mixed sexes). Vauclin strain is highly resistant to the insecticides Permethrin and Temephos. 
Gene expression in Anopheles gambiae embryos has been profiled at many time points using the Affymetrix Anopheles/Plasmodium microarray. Time points 49h and 52h have been removed due to lack of replicates. 
factor:
OrganismPart
 
Gene expression profiles of the Anopheles gambiae embryo and serosa (shell) are compared using the Affymetrix Anopheles/Plasmodium microarray. 
The expression response of hemocytes from Aedes aegypti at three time points after infection with Escherichia coli was profiled on an array enriched with reporters for hemocyte genes. Experimental samples are compared to a uninfected control sample. Only technical replicate #1 was used in VectorBase's analysis. 
The expression response of hemocytes from Aedes aegypti at three time points after infection with Escherichia coli was profiled on an array enriched with reporters for hemocyte genes. Experimental samples are compared to a uninfected control sample. Only technical replicate #1 was used in VectorBase's analysis. 
Adult Anopheles gambiae mosquitoes were infected with Plasmodium berghei. Gene expression in midgut tissue was measured with respect to an uninfected control at 1 and 11 days post infection on a custom detoxification gene array. Expression ratios between 11 and 1 days were also determined for infected and uninfected mosquito midguts. 
Adult Anopheles gambiae mosquitoes were infected with Plasmodium berghei. Gene expression in fat body tissue was measured with respect to an uninfected control at 1 and 11 days post infection on a custom detoxification gene array. Expression ratios between 11 and 1 days were also determined for infected and uninfected mosquito fat body tissue. 
Expression profiling of three naive adult female Anopheles gambiae tissues: hemolymph (hemocytes), head and carcass (the remainder after hemolymph extraction and head removal). 
Gene expression in Plasmodium berghei infected Anopheles gambiae hemocytes was assayed with respect to infection with a midgut invasion-deficient CTRP knockout strain of the parasite. 
Expression ratios between female and male adult Aedes aegypti mosquitoes were measured using a custom EST array. This experiment has not been published, but the data and protocols have been submitted to ArrayExpress under the accession E-TABM-385
A refractory strain of Aedes aegypti, Moyo-In-Dry, was given either an infected or uninfected blood meal and gene expression was compared to a susceptible strain, DS3, under the same feeding conditions. The data and protocols have been submitted to ArrayExpress under the accession E-MTAB-64
A DNA microarray analysis of Anopheles gambiae under and constant dark (DD) conditions was undertaken to study the global regulation of genes by diel and circadian mechanisms. Adult mated, non–blood-fed female mosquitoes were collected every 4h for 48h, and RNA from heads was assayed on the Affymetrix Plasmodium/Anopheles microarray. For specialized cyclic expression analysis please see this external site
A DNA microarray analysis of Anopheles gambiae under light/dark cycle (LD) conditions was undertaken to study the global regulation of genes by diel and circadian mechanisms. Adult mated, non–blood-fed female mosquitoes were collected every 4h for 48h, and RNA from heads was assayed on the Affymetrix Plasmodium/Anopheles microarray. For specialized cyclic expression analysis please see this external site
A DNA microarray analysis of Anopheles gambiae under constant dark (DD) conditions was undertaken to study the global regulation of genes by diel and circadian mechanisms. Adult mated, non–blood-fed female mosquitoes were collected every 4h for 48h, and RNA from bodies was assayed on the Affymetrix Plasmodium/Anopheles microarray. For specialized cyclic expression analysis please see this external site
A DNA microarray analysis of Anopheles gambiae under light/dark cycle (LD) conditions was undertaken to study the global regulation of genes by diel and circadian mechanisms. Adult mated, non–blood-fed female mosquitoes were collected every 4h for 48h, and RNA from bodies was assayed on the Affymetrix Plasmodium/Anopheles microarray. For specialized cyclic expression analysis please see this external site
133 items found, displaying 21 to 40.[First/Prev] 1, 2, 3, 4, 5, 6, 7 [Next/Last]