Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A single-step, PCR-based method for the detection and differentiation of<i>Plasmodium vivax</i>and<i>P. falciparum</i>

1 Jan 2003

Abstract excerpt

The ability to detect and differentiate between Plasmodium falciparum and P. vivax is of great importance for the routine laboratory diagnosis of malaria, donor-blood screening and epidemiological studies. Most PCR-based methods for the discrimination of these two species require nested protocols or an additional hybridization reaction, leading to high labour costs and long turn-around times. A simple,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Malaria Research and Control
Share to Mosquito-borne diseases and control
Share to Vector-borne infectious diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12662418
DOI: 10.1179/000349803125002535

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A single-step, PCR-based method for the detection and differentiation of<i>Plasmodium vivax</i>and<i>P. falciparum</i>PMID 12662418Read ↗

Development of a Real-Time PCR Assay for Detection of <i>Plasmodium falciparum</i> , <i>Plasmodium vivax</i> , and <i>Plasmodium ovale</i> for Routine Clinical DiagnosisSemantic proximity Read ↗

Real-Time PCR for Detection and Identification of <i>Plasmodium</i> sppSemantic proximity Read ↗

Real-Time Nucleic Acid Sequence-Based Amplification Is More Convenient than Real-Time PCR for Quantification of <i>Plasmodium falciparum</i>Semantic proximity Read ↗

Detection of Four <i>Plasmodium</i> Species in Blood from Humans by 18S rRNA Gene Subunit-Based and Species-Specific Real-Time PCR AssaysSemantic proximity Read ↗

Multiplexed Real-Time PCR Assay for Discrimination of <i>Plasmodium</i> Species with Improved Sensitivity for Mixed InfectionsSemantic proximity Read ↗

Standardization of a very specific and sensitive single PCR for detection of Plasmodium vivax in low parasitized individuals and its usefulness for screening blood donorsSemantic proximity Read ↗

Detection of Four <i>Plasmodium</i> Species by Genus- and Species-Specific Loop-Mediated Isothermal Amplification for Clinical DiagnosisSemantic proximity Read ↗

An Optimized Real-Time qPCR Method for the Effective Detection of Human Malaria InfectionsSemantic proximity Read ↗

Human malaria diagnosis using a single-step direct-PCR based on the Plasmodium cytochrome oxidase III geneSemantic proximity Read ↗

Simultaneous identification of the four human Plasmodium species and quantification of Plasmodium DNA load in human blood by real-time polymerase chain reactionSemantic proximity Read ↗

Plasmodium falciparum and P. Vivax: Factors Affecting Sensitivity and Specificity of PCR-Based Diagnosis of MalariaSemantic proximity Read ↗

Real-Time PCR for Detection and Differentiation of<i>Entamoeba histolytica</i>and<i>Entamoeba dispar</i>in Fecal SamplesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.