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36 results for “Plasmodium berghei”

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zenodo40/100

Experiments for detection of Plasmodium berghei infected Anopheles stephensi mosquitoes using near-infrared spectroscopy

<p>&nbsp;</p> <p><strong>Experiments for detection of <em>Plasmodium berghei</em> infected <em>Anopheles stephensi</em> mosquitoes using near-infrared spectroscopy</strong></p> <p>This dataset contains near-infrared spectroscopy (NIRS) measurements on&nbsp;<em>Plasmodium berghei</em> infected <em>Anopheles stephensi</em> mosquitoes reared in the lab together with either oocyst counts or sporozoite counts, correponding to the two experiments undertaken:</p> <ul> <li>Experiment 1 (oocysts),&nbsp; file &quot;NIRSdata2017_Lab_AnSteph_PlasmBerg_oocysts.txt&quot;</li> <li>Experiment 2 (sporozoites), file &quot;NIRSdata2017_Lab_AnSteph_PlasmBerg_sporozoites.txt&quot;</li> </ul> <p>For further details on the experimental setup see: P.M. Esperan&ccedil;a, A.M. Blagborough, D.F. Da, F.E. Dowell, T.S. Churcher (2018) &quot;Detection of <em>Plasmodium berghei</em> infected <em>Anopheles stephensi</em> using near-infrared spectroscopy&quot;. <em>Parasites and Vector</em>, <strong>11</strong>:377. <a href="https://doi.org/10.1186/s13071-018-2960-z">https://doi.org/10.1186/s13071-018-2960-z</a>.</p> <p>The structure of the data files is as follows:</p> <ul> <li>column 1 (<strong>Scan_ID</strong>): scan identifier</li> <li>column 2 (<strong>Mosquito_ID</strong>): mosquito identifier</li> <li>column 3 (<strong>Replication</strong>): replication identifier</li> <li>column 4 (<strong>Oocysts</strong> or <strong>Sporozoites</strong>): response variable <ul> <li>for the Experiment 1, the oocyst count<em> </em>on a level-scale</li> <li>for the Experiment 2, the sporozoite count on a log-scale: 0 (no sporozoites), 1 (1&ndash;10), 2 (11&ndash;100), 3 (101&ndash;1000), 4 (&gt;1000)</li> </ul> </li> <li>columns 5 to 2155 (<strong>x350</strong> to <strong>x2500</strong>): NIRS absorbance measurements for wavelengths in the range 350 to 2500 nanometers</li> </ul> <p>&nbsp;</p>

opencc-by-sa-4.0Oct 2017View details →
zenodo40/100

A scalable CRISPR-Cas9 gene editing system facilitates CRISPR screens in the malaria parasite Plasmodium berghei - sequencing data

<p>This holds raw sequencing data, and extracted sgRNA counts&nbsp;</p>

opencc-by-4.0Oct 2024View details →
zenodo36/100

Fluorescence Microscopy Images of Hela Cell infected with Plasmodium Berghei parasite expressing mCherry in cytoplasm

<p>The purpose of our experiments was to delve into the liver stage development of the P. berghei parasite and examine the host-parasite interactions using HeLa cells. This research is primarily focused on in vitro analysis and does not extend to in vivo applications. Our study investigated the integration of fluorescent microscopy with artificial intelligence to&nbsp;<br>track and predict the developmental milestones of Plasmodium liver stage development.&nbsp;</p> <p>This is the dataset used in our study.</p>

opencc-by-4.0Apr 2024View details →
zenodo36/100

INHIBITION OF NITRIC OXIDE SYNTHESIS PROMOTES INCREASED MORTALITY DESPITE REDUCTION OF PARASITEMIA IN Plasmodium berghei-INFECTED MICE

<p><strong>Backgrounds:</strong> Nitric oxide (NO) is an important mediator molecule in inflammatory processes, but its role in the pathophysiology of malaria is still uncertain.</p> <p><strong>Methods:</strong> To investigate the NO synthesis inhibition on the oxidative changes induced by <em>Plasmodium berghei </em>infection in mice, malaria was induced in 150 animals, of which 75 animals were treated with NO inhibitor L-NAME; the remaining are sham controls. All animals underwent euthanasia after 1, 5, 10, 15 or 20 days after the infection for the collection of lungs, brain, and blood. Parasitemia was determined and the survival of the animals evaluated. Tissue samples were assayed for nitrites and nitrates (NN), thiobarbituric acid reactive substances (TBARS), and total Trolox equivalent antioxidant capacity (TEAC). A histopathological study was performed.</p> <p><strong>Results:</strong> Mortality rates in the L-NAME were always higher in relation to the controls. In brains, NN was lower in groups L-NAME. Parasitemia and its progression rate were greater in control groups. From the 5<sup>th</sup> day of infection, mice treated with L-NAME showed cerebral edema and interstitial pneumonia of greater intensity than controls.</p> <p><strong>Conclusions:</strong> Anti-inflammatory and hemodynamic effects of NO surpasses its pro-oxidant role in murine malaria.</p> <p><strong>Backgrounds:</strong> Nitric oxide (NO) is an important mediator molecule in inflammatory processes, but its role in the pathophysiology of malaria is still uncertain.</p> <p><strong>Methods:</strong> To investigate the NO synthesis inhibition on the oxidative changes induced by <em>Plasmodium berghei </em>infection in mice, malaria was induced in 150 animals, of which 75 animals were treated with NO inhibitor L-NAME; the remaining are sham controls. All animals underwent euthanasia after 1, 5, 10, 15 or 20 days after the infection for the collection of lungs, brain, and blood. Parasitemia was determined and the survival of the animals evaluated. Tissue samples were assayed for nitrites and nitrates (NN), thiobarbituric acid reactive substances (TBARS), and total Trolox equivalent antioxidant capacity (TEAC). A histopathological study was performed.</p> <p><strong>Results:</strong> Mortality rates in the L-NAME were always higher in relation to the controls. In brains, NN was lower in groups L-NAME. Parasitemia and its progression rate were greater in control groups. From the 5<sup>th</sup> day of infection, mice treated with L-NAME showed cerebral edema and interstitial pneumonia of greater intensity than controls.</p> <p><strong>Conclusions:</strong> Anti-inflammatory and hemodynamic effects of NO surpasses its pro-oxidant role in murine malaria.</p>

opencc-by-4.0Nov 2017View details →
geo24/100

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

GEO Series GSE198287. Plasmodium berghei. 4 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2022View details →
geo24/100

Whole genome RNA micro array analysis of Plasmodium berghei sporozoites infected host cells

GEO Series GSE72049. Homo sapiens. 8 samples. Type: Expression profiling by array.

openGEO-OpenSep 2016View details →
geo24/100

Transcriptome changes during inducible gametocytogenesis in Plasmodium berghei parasites

GEO Series GSE110201. Plasmodium berghei. 32 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2018View details →
geo24/100

Splenic CD4 T cells in naïve C57BL/6 mice or during Plasmodium berghei ANKA infection in C57BL/6 and B6.GzmB-/- mice.

GEO Series GSE24903. Mus musculus. 12 samples. Type: Expression profiling by array.

openGEO-OpenDec 2010View details →
geo24/100

Transcriptome of Plasmodium berghei wildtype parasites and KIN knockout parasites [RNA-seq]

GEO Series GSE69627. Plasmodium berghei. 12 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJul 2017View details →
geo24/100

The Serine/Threonine Protein Phosphatase 6 Is Required for Efficient Gametogenesis in Sexual-Stage Plasmodium berghei

GEO Series GSE271105. Plasmodium berghei ANKA. 6 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2025View details →
geo24/100

Pleiotropic Roles for the Plasmodium berghei RNA Binding Protein UIS12 in Anopheles Transmission and Sporogony

GEO Series GSE152686. Plasmodium berghei. 4 samples. Type: Expression profiling by array.

openGEO-OpenMar 2021View details →
geo24/100

A divergent cyclin/cyclin-dependent kinase complex controls progression through the atypical replicative cycles during Plasmodium berghei gametogony

GEO Series GSE144743. Plasmodium berghei. 8 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2020View details →
geo24/100

Effects of Plasmodium berghei infection on Anopheles gambiae during oocysts development

GEO Series GSE32200. Anopheles gambiae. 8 samples. Type: Expression profiling by array.

openGEO-OpenDec 2011View details →
geo24/100

Transcriptome changes during inducable gametocytogenesis in Plasmodium berghei parasites

GEO Series GSE168817. Plasmodium berghei. 28 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2021View details →
geo24/100

Differential gene expression in ap2-g and ap2-g2 mutants of Plasmodium berghei

GEO Series GSE52859. Plasmodium berghei. 8 samples. Type: Expression profiling by array.

openGEO-OpenDec 2013View details →
geo24/100

Plasmodium berghei Gametocytogenesis

GEO Series GSE53246. Plasmodium berghei. 28 samples. Type: Expression profiling by array.

openGEO-OpenDec 2013View details →
geo24/100

Global expression profiling reveals shared and distinct transcript signatures in arrested act2(-) and CDPK4(-) Plasmodium berghei gametocytes

GEO Series GSE65032. Plasmodium berghei. 4 samples. Type: Expression profiling by array.

openGEO-OpenSep 2015View details →
geo24/100

A single nucleotide polymorphism in a Plasmodium berghei ApiAP2 transcription factor alters the development of host immunity

GEO Series GSE111333. Plasmodium berghei; Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenFeb 2020View details →
geo24/100

Impact of dietary restriction (DR) on the transcriptome of the rodent malaria parasite Plasmodium berghei [microarray]

GEO Series GSE69628. Plasmodium berghei. 24 samples. Type: Expression profiling by array.

openGEO-OpenJul 2017View details →
geo24/100

Transcriptomic analysis of Plasmodium berghei apiAP2 KO mutants

GEO Series GSE80634. Plasmodium berghei. 62 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2017View details →

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