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

Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction

1 Mar 1992

Abstract excerpt

We report on the development and application of a rapid assay for detecting and typing dengue viruses. Oligonucleotide consensus primers were designed to anneal to any of the four dengue virus types and amplify a 511-bp product in a reverse transcriptase-polymerase chain reaction (PCR). First, we produced a cDNA copy of a portion of the viral genome in a reverse transcriptase reaction in the presence of primer D2...

Read the complete abstract on PubMed

Topics

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

Share to Mosquito-borne diseases and control
Share to Viral Infections and Outbreaks Research
Share to Viral Infections and Vectors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 1372617
DOI: 10.1128/jcm.30.3.545-551.1992

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

Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reactionPMID 1372617Read ↗

Rapid Diagnosis of Dengue Viremia by Reverse Transcriptase-Polymerase Chain Reaction using 3′-Noncoding Region Universal PrimersSemantic proximity Read ↗

One-step multiplex real-time RT-PCR for detection and typing of dengue virusSemantic proximity Read ↗

A new quantitative RT-PCR method for sensitive detection of dengue virus in serum samplesSemantic proximity Read ↗

Development of a fluorogenic RT-PCR system for quantitative identification of dengue virus serotypes 1–4 using conserved and serotype-specific 3′ noncoding sequencesSemantic proximity Read ↗

Development of Real-Time Reverse Transcriptase PCR Assays To Detect and Serotype Dengue VirusesSemantic proximity Read ↗

Advancing Dengue Virus Surveillance: A Rapid Multiplexed One-Step RT-PCR assay for Comprehensive Diagnosis and Serotype IdentificationSemantic proximity Read ↗

Quantitative Competitive Reverse Transcription-PCR for Quantification of Dengue Virus RNASemantic proximity Read ↗

Rapid identification of dengue virus serotypes by using polymerase chain reactionSemantic proximity Read ↗

Utility of multiplex reverse transcriptase-polymerase chain reaction for diagnosis and serotypic characterization of dengue and chikungunya viruses in clinical samplesSemantic proximity Read ↗

Development of a Singleplex Real-Time Reverse Transcriptase PCR Assay for Pan-Dengue Virus Detection and QuantificationSemantic proximity Read ↗

Early detection of dengue virus by use of reverse transcription-recombinase polymerase amplification.Semantic proximity Read ↗

Development of real time PCR for detection and quantitation of Dengue VirusesSemantic proximity Read ↗

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